{"id":67,"date":"2016-12-01T23:49:34","date_gmt":"2016-12-01T22:49:34","guid":{"rendered":"http:\/\/www.biu-grimmer.de\/institute\/?page_id=67"},"modified":"2017-09-23T11:19:59","modified_gmt":"2017-09-23T10:19:59","slug":"publikationen","status":"publish","type":"page","link":"https:\/\/www.biu-grimmer.de\/institute\/?page_id=67","title":{"rendered":"Publikationen"},"content":{"rendered":"<div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2016\">2016<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2015\">2015<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2014\">2014<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2013\">2013<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2012\">2012<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2011\">2011<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2010\">2010<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2009\">2009<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2008\">2008<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2007\">2007<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2006\">2006<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2005\">2005<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2004\">2004<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2003\">2003<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2002\">2002<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2001\">2001<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#2000\">2000<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1999\">1999<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1998\">1998<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1997\">1997<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1996\">1996<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1995\">1995<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1994\">1994<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1993\">1993<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1992\">1992<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1991\">1991<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1990\">1990<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1989\">1989<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1988\">1988<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1987\">1987<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1986\">1986<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1985\">1985<\/a><\/div><div style=\"background-color: #f2f2f2;\n\t\t\tborder: 0px solid;\n\t\t\t-webkit-border-radius: 5px;\n\t\t\t-moz-border-radius: 5px;\n\t\t\tborder-radius: 5px;\n\t\t\tpadding: 5px 5px 5px 5px;\n\t\t\tmargin: 0px 10px 10px 0px;\n\t\t\tfloat: left;\n\t\t\twidth: 50px;\n\t\t\ttext-align: center;\"><a href=\"#1984\">1984<\/a><\/div>\n<h2 id=\"2016\">2016<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 257<\/span><p\/>Wohak, L.E., Krais, A.M., Kucab, J.E., Stertmann, J., Ovrebo, S., Seidel, A., Phillips, D.H. Arlt, V.M.<br\/>Carcinogenic polycyclic aromatic hydrocarbons induce CYP1A1 in human cells via a p53-dependent mechanism.<br\/>Arch. Toxicol., 90 (2016) 291-304<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 256<\/span><p\/>Sachse, B., Walter Meinl, W., Sommer, Y., Glatt, H.R., Seidel, A., Monien, B.H.<br\/>Bioactivation of suspected food carcinogens 5-hydroxymethylfurfural and furfuryl alcohol by sulfotransferases from human, mouse and rat: a comparative study.<br\/>Arch. Toxicol., 90 (2016) 137-148<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 255<\/span><p\/>Krais, A.M., Speksnijder, E.N., Melis, J.P.M., Indra, R., Moserova, M., Godschalk, R.W., van Schooten, F.-J., Seidel, A., Schmeiser, H.H., Stiborova, M., Phillips, D.H., Luijten M., and Arlt, V.M.<br\/>The impact of p53 on DNA damage and metabolic activation of the environmental carcinogen benzo[a]pyrene: effects in Trp53(+\/+), Trp53(+\/-) and Trp53(-\/-) mice.<br\/>Arch. Toxicol., 90 (2016) 839-851<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 254<\/span><p\/>V\u00f6lkel, W., Kiranoglu, M., Dettbarn, G., Jessel, S., Seidel, A., Fromme, H.<br\/>Toxicokinetic of Di-(isononyl)-cyclohexane-1,2-dicarboxylate (DINCH\u00ae) in humans following single oral administration.<br\/>Tox. Lett., 248 (2016) 16-24<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 253<\/span><p\/>Schreck, I., Grico, N., Hansjosten, I., Marquardt, C., Bormann, S., Seidel, A., Kvietkova, D. L., Pieniazek, D., Segerb\u00e4ck, D., Diabate, S., van der Horst, G. T., Oesch-Bartlomowicz, B., Oesch, F., Weiss, C.<br\/>The nucleotide excision repair protein XPC is essential for bulky DNA adducts to promote interleukin 6 expression via activation of p38-SAPK.<br\/>Oncogene, 35 (2016) 908-918<\/div>\n<h2 id=\"2015\">2015<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 252<\/span><p\/>Waizenegger, J., Lenze, D., Luckert, C., Seidel, A., Lampen, A., Hessel, S.<br\/>Dose-dependent induction of signaling pathways by the flavonoid quercetin in human primary hepatocytes: a transcriptomic study<br\/>Mol. Nutr. Food Res, 59 (2015) 1117-1129<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 251<\/span><p\/>Ehlers, A., Florian, S., Schumacher, F., Meinl, H., Lenze, D., Hummel, M., Heise, T., Seidel, A., Glatt, HR., Lampen, A.<br\/>The glucosinolate metabolite 1-methoxy-3-indolyl\u00admethyl alcohol induces a gene expression profile in mouse liver similar to the expression signature caused by known genotoxic hepatocarcinogens.<br\/>Mol. Nutr. Food Res, 59 (2015) 685-697<\/div>\n<h2 id=\"2014\">2014<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 250<\/span><p\/>Wohak, L.U.E., Krais, A.M., Kucab, J.E., Stertmann, J., \u00d8vreb\u00f8, S., Seidel, A., Phillips, D.H., and Arlt, V.M.<br\/>Carcinogenic polycyclic aromatic hydrocarbons induce CYP1A1 in human cells via a p53 dependent mechanism.<br\/>Arch. Toxicol., 90 (2014) 291-304<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 249<\/span><p\/>Kranz, J., Hessel, S., Aretz, J., Seidel, A., Petzinger, E., Geyer, J., Lampen, A.<br\/>The role of the efflux carriers Abcg2 and Abcc2 for the hepatobiliary elimination of benzo[a]pyrene and its metabolites in mice.<br\/>Chem.-Biol. Interact,  224C (2014) 36-41<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 248<\/span><p\/>Polanska, K., Dettbarn, G., Jurewicz, J., Sobala, W., Magnus, P., Seidel, A., Hanke, W.<br\/><a href=\"http:\/\/dx.doi.org\/10.1155\/2014\/408939 \" target=\"_blank\">Effect of prenatal polycyclic aromatic hydrocarbons exposure on birth outcomes: the Polish mother and child cohort study.<\/a><br\/>BioMed Research International, Article ID 408939, 10 pages, open access (2014) <\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 247<\/span><p\/>Polanska, K., Hanke, W., Dettbarn, G., Sobala, W., Gromadzinska, J., Magnus, P., Seidel, A.<br\/>Exposure of the Polish population to polycyclic aromatic hydrocarbons - a multiple urinary biomarker study among non-smoking pregnant women. <br\/>Sci. Total Environ., 487 (2014) 102-109<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 246<\/span><p\/>Westberg, E., Hedebrant, U., Haglund, J., Alsberg, T., Eriksson, J., Seidel, A., T\u00f6rnqvist, M.<br\/><a href=\"https:\/\/doi.org\/10.1007\/s00216-013-7540-7\" target=\"_blank\">Conditions for sample preparation and HPLC\/MS-MS-analysis of bulky adducts to serum albumin with diolepoxides of polycyclic aromatic hydrocarbons as models.<\/a><br\/>Anal. Bioanal. Chem., 406 (2014) 1519-1530<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 245<\/span><p\/>Schwarz, M., Behnke, A., Brandt, M., Eisentr\u00e4ger, A., Hassauer, M., Kalberlah, F., Seidel, A.<br\/><a href=\"https:\/\/doi.org\/10.1002\/ieam.1526\" target=\"_blank\">Semipolar polycyclic aromatic compounds: Identification of 15 priority substances and the need of regulatory steps under reach regulation.<\/a><br\/>Integr. Environ. Assess. Manag., 10 (2014) 415-428<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 244<\/span><p\/>Schumacher, F., Florian, S., Schnapper, A., Monien, B.\u00a0H., Mewis, I., Schreiner, M., Seidel, A., Engst, W., Glatt. H.<br\/>A secondary metabolite of Brassicales, 1-methoxy-3-indolylmethyl glucosinolate, as well as its degradation product, 1-methoxy-3-indolylmethyl alcohol, forms DNA adducts in the mouse, but in varying tissues and cells.<br\/>Arch. Toxicol., 88 (2014) 823-836<\/div>\n<h2 id=\"2013\">2013<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 243<\/span><p\/>Hessel, S., Stumkat, L., Lampen, A., and Seidel, A.<br\/>Polycyclic aromatic hydrocarbons in food - Efflux of the conjugated biomarker 1-hydroxypyrene is mediated by Breast Cancer Resistance Protein (ABCG2) in human intestinal Caco-2 cells.<br\/>Food Chem. Toxicol., 62 (2013) 797-804<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 242<\/span><p\/>Seidel, A., Steinberg, P.<br\/>Polycyclische aromatische Kohlenwasserstoffe (PAK) in Lebensmitteln \u2013 Analytische Methoden und gesetzliche H\u00f6chstmengen.<br\/>GIT Labor-Fachzeitschrift, 9 (2013) 550-555<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 241<\/span><p\/>Luckert, C., Ehlers, A., Buhrke, T., Seidel, A., Lampen, A., and Hessel, S.<br\/>Polycyclic aromatic hydrocarbons stimulate human CYP3A4 promoter activity via PXR.<br\/>Toxciol Lett., 222 (2013) 180-188<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 240<\/span><p\/>Stempin, S., Andres, S., Bumke Scheer, M., Rode, A., Nau, H., Seidel , A., and Lampen, A.<br\/>Valproic acid and its derivatives enhanced estrogenic activity but not androgenic activity in a structure dependent manner.<br\/>Reprod. Toxicol., 42C (2013) 49-57<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 239<\/span><p\/>Seidel, A., Steinberg, P., Appel, K., Lampen, A., H.M. Bolt, und Koss, G.<br\/>Kohlenwasserstoffe.<br\/>Toxikologie (Marquardt, H., Sch\u00e4fer, S., und Barth, H., Hrsg.) Wissenschaftliche Verlagsgesellschaft mbH (WVG), Stuttgart (2013) S. 593-659<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 238<\/span><p\/>Seidel, A., Steinberg, P.<br\/>Acrolein aus Lebensmitteln \u2013 Analytische Erfassung der Humanbelastung.<br\/>GIT Labor-Fachzeitschrift, 4 (2013) 231-233<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 237<\/span><p\/>Nilsson, R., Anti\u0107, R., Berni, A., Dallner, G., Dettbarn, G., Gromadzinska, J., Joksi\u0107, G., Lundin, C., Palitti, F., Prochazka, G., Rydzynski, K., Segerb\u00e4ck, D., Sou\u010dek, P., Michael Tekle, M., and Seidel, A.<br\/>Exposure to polycyclic aromatic hydrocarbons in women from Poland, Serbia, and Italy \u2013 Relation between PAH metabolite excretion, DNA damage, diet and genotype (the EU DIEPHY project). <br\/>Biomarkers, 18 (2013) 165-173<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 236<\/span><p\/>Hessel, S., John, A., Seidel, A., and Lampen, A.<br\/>Multidrug resistance-associated proteins are involved in the transport of the glutathione conjugates of the ultimate carcinogen of benzo[a]pyrene in human Caco-2 cells.<br\/>Arch. Toxicol, 87 (2013) 269-280<\/div>\n<h2 id=\"2012\">2012<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 235<\/span><p\/>Schumacher, F., Engst, W., Monien, B.H., Florian, S., Schnapper, A., Steinhauser, L., Albert, K., Frank, H., Seidel, A., and Glatt, H.<br\/>Detection of DNA adducts originating from 1-methoxy-3-indolylmethyl glucosinolate using isotope-dilution UPLC-ESI-MS\/MS.<br\/>Anal. Chem., 84 (2012) 6256-6262<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 234<\/span><p\/>Monien, B.H., Engst, W., Barknowitz, G., Seidel, A., and Glatt, H.<br\/>Mutagenicity of 5-hydroxymethylfurfural in V79 cells expressing human SULT1A1: Identification and mass spectrometric quantification of DNA adducts formed.<br\/>Chem. Res. Toxicol., 25 (2012) 1484-1492<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 233<\/span><p\/>John, A., Hessel, S., Lampen, A., and Seidel, A.<br\/>Analysis of GSH conjugates of bay- and fjord-region dihydrodiol epoxides of benzo[a]pyrene and dibenzo[a,l]pyrene and their transport in enterocyte-like Caco-2 cells.<br\/>Polycycl. Arom. Compds., 32 (2012) 221-237<\/div>\n<h2 id=\"2011\">2011<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 232<\/span><p\/>Roelofzen, J.H., van der Valk, P.G., Godschalk, R., Dettbarn, G., Seidel, A., Golsteijn, L., Anzion, R., Aben, K.K., van Schooten, F.J., Kiemeney, L.A., Scheepers, P.T.<br\/>DNA adducts in skin biopsies and 1-hydroxypyrene in urine of psoriasis patients and healthy volunteers following treatment with coal tar.<br\/>Toxicol Lett., 213 (2011) 39-44<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 231<\/span><p\/>Lagerqvist, A., Hakansson, D., Lundin, C., Prochazka, G., Dreij, K., Segerback, D., Jernstrom, B., Tornqvist, M., Frank, H., Seidel, A., Erixon, K. and Jenssen, D.<br\/>DNA repair and replication influence the number of mutations per adduct of polycyclic aromatic hydrocarbons in mammalian cells.<br\/>DNA Repair (Amst), 10 (2011) 877-886<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 230<\/span><p\/>Schubert, J., Hahn, J., Dettbarn, G., Seidel, A., Luch, A., and Schulz, T.G.<br\/>Mainstream Smoke of the Waterpipe: Does This Environmental Matrix Reveal As Significant Source of Toxic Compounds?<br\/>Toxicol. Lett., 205 (2011) 275-284<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 229<\/span><p\/>Breuer, D., Hahn, J.-U., H\u00f6ber, D., Emmel, Ch., Musanke, U., R\u00fchl, R., Spickenheuer, A., Raulf-Heimsoth, M., Bramer, R., Seidel, A., Schilling, B., Heinze, E., Kendzia, B., Marczynski, B., Welge, P., Angerer, J., Br\u00fcning, Th., and Pesch, B.<br\/>Air sampling and determination of vapours and aerosols of bitumen and polycyclic aromatic hydrocarbons in hot mastic-asphalt applications.<br\/>Arch Toxicol, 85 (Suppl 1) (2011) S11-20<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 228<\/span><p\/>Lichtenstein, N., Buchwald, K.E., Hennig, M., Bernards, M., Werner, S., Hahn, J.U., Assenmacher-Maiworm, H., Kreyenschmidt, M., Brodkorb, F., Dettbarn, G., Jacob, J., and Seidel, A.<br\/>Inhalative Exposition von Dachdeckern gegen\u00fcber 2-Naphthylamin und anderen krebserzeugenden aromatischen Aminen bei der Hei\u00dfverarbeitung von teerhaltigen Klebemassen.<br\/>Gefahrstoffe \u2013 Reinhaltung der Luft, 71 (2011) 109-207<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 227<\/span><p\/>Gminski, R., Decker, K., Heinz, C., Seidel, A., Konczol, M., Goldenberg, E., Grobety, B., Ebner, W., Giere, R. and Mersch-Sundermann, V.<br\/>Genotoxic effects of three selected black toner powders and their dimethyl sulfoxide extracts in cultured human epithelial A549 lung cells in vitro.<br\/>Environ. Mol. Mutagen., 52 (2011) 296-309<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 226<\/span><p\/>Glatt, H., Baasanjav-Gerber, C., Schumacher, F., Monien, B.H., Frank, H., Seidel, A., and Engst, W.<br\/>1-Methoxy-3-indolylmethyl glucosinolate: mechanism of bioactivation to genotoxicants for bacteria and mammalian cells.<br\/>Chem.-Biol. Interact., 192 (2011) 81-86<\/div>\n<h2 id=\"2010\">2010<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 225<\/span><p\/>Seidel, A.<br\/>Polyzyklische aromatische Kohlenwasserstoffe. In: \u201dSicherheitsrelevante Stoffe in Lebensmitteln - Toxikologie - in der praktischen Qualit\u00e4tssicherung\u201c (Steinberg, P. und Hamscher, G., Hrsg.)<br\/>Behr\u2019s Verlag (2010) p. 91-117<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 224<\/span><p\/>Lagerqvist, A., H\u00e5kansson, D., Erixon, K., Heinz Frank, Seidel, A., and Jenssen, D.<br\/>Structural requirements for mutation formation from polycyclic aromatic hydrocarbon dihydrodiol epoxides in their interaction with food chemopreventive compounds.<br\/>Food Chem. Toxicol., 49 (2010) 879-886<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 223<\/span><p\/>Singh, R., Teichert, F., Seidel, A., Roach, J., Cordell, R., Cheng, M.-K., Frank, H., Steward, W.P., Manson M.M., and Farmer, P.B.<br\/>Development of a targeted adductomic method for the determination of polycyclic aromatic hydrocarbon DNA adducts using online column-switching liquid chromatography tandem mass spectrometry.<br\/>Rapid Commun. Mass Spectrom. , 24 (2010) 2329\u20132340 <\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 222<\/span><p\/>Hessel, S., S., John, A., Seidel, A., Glatt, H., Lampen, A.<br\/>Effects of quercetin on the detoxification of the food contaminant benzo[a]pyrene in the human intestinal Caco-2 cell model, in \u201cRisk Assessment of Phytochemicals in Food: Novel Approaches\u201d<br\/>Deutsche Forschungsgemeinschaft (DFG) (G. Eisenbrand ed.), Wiley-VCH (2010) p. 404-411<\/div>\n<h2 id=\"2009\">2009<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 221<\/span><p\/>Hessel, S., John, A., Seidel, A., Lampen, A.<br\/>All-trans retinoic acid induces breast cancer resistance protein expression in Caco-2 cells and enhances the transport of benzo[a]pyrene-3-sulfate<br\/>Toxicol. Lett., 189 (Suppl.) (2009) S228, F05<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 220<\/span><p\/>Eder, C., Frankenberger, M., Stanzel, F., Seidel, A., Schramm, K.-W., Ziegler-Heitbrock, L., and Hofer Th.P.J.<br\/><a href=\"http:\/\/www.particleandfibretoxicology.com\/content\/6\/1\/27\" target=\"_blank\">Ultrafine Carbon particles down-regulate CYP1B1 expression in human monocytes.<\/a><br\/>Part Fibre Toxicol, 6 (2009) 27<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 219<\/span><p\/>Monien, B.H., M\u00fcller, C., Bakhiya, N., Donath, C., Frank, H., Seidel, A., and Glatt, H.R.<br\/>Probenecid, an inhibitor of transmembrane organic anion transporters, alters tissue distribution of DNA adducts in 1-hydroxymethylpyrene-treated rats.<br\/>Toxicology., 262 (2009) 80-85<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 218<\/span><p\/>Bakhiya, N., Monien, B., Frank, H., Seidel, A., and Glatt, H.R.<br\/>Renal organic anion transporters OAT1 and OAT3 mediate the cellular accumulation of 5-sulfooxy\u00admethylfurfural, a reactive, nephrotoxic metabolite of the Maillard product 5-hydroxy\u00admethylfurfural.<br\/>Biochem. Pharmacol., 78 (2009) 414-419<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 217<\/span><p\/>Marczynski, B., Pesch, B., Wilhelm, M., Rossbach, B., Preuss, R., Hahn, J.-U., Rabstein, S., Raulf-Heimsoth, M., Seidel, A., Rihs, H.-P., Adams, A., Scherenberg, M., Erkes, A., Engelhardt, B., Straif, K., K\u00e4fferlein, H. U., Angerer, J., and Br\u00fcning, T.<br\/>Occupational Exposure to Polycyclic Aromatic Hydrocarbons and DNA Damage by Industry \u2013 A Nationwide Study in Germany.<br\/>Arch. Tox., 83 (2009) 947-957<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 216<\/span><p\/>Monien, B.H., Frank, H., Seidel, A., and Glatt, H.<br\/>Conversion of the common food constituent, 5-hydroxymethylfurfural into a mutagenic and carcinogenic sulfuric acid ester in the mouse in vivo.<br\/>Chem Res. Toxicol., 22 (2009) 1123-1128<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 215<\/span><p\/>Kuhn, K., Nowak, B., Behnke, A., Seidel, A., and Lampen, A.<br\/>Combined chemical and effect-directed analysis of polycyclic aromatic hydrocarbons in smoked pork.<br\/>Food Addit Contam., 26 (2009) 1104-1112<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 214<\/span><p\/>Schreck, I., Chudziak, D., Schneider, S., Seidel, A., Platt, K.-L., Oesch, F., and Weiss, C. <br\/>Influence of aryl hydrocarbon- (Ah) receptor and genotoxins on DNA repair gene expression and cell survival of mouse hepatoma cells.<br\/>Toxicology, 259 (2009) 91-96<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 213<\/span><p\/>Kabler, S.L., Seidel, A., Jacob, J., Doehmer, J., Morrow, C.S., and Townsend, A.J.<br\/>Protection by human glutathione S-transferase P1 against cytotoxicity by benzo[a]pyrene or benzo[a]pyrene-7,8-dihydrodiol enantiomers in bi-transgenic cell lines that co-express rat or human cytochrome P4501A1.<br\/>Chem.-Biol. Interact., 179 (2009) 240-246<\/div>\n<h2 id=\"2008\">2008<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 212<\/span><p\/>Yagi, H., Frank, H., Seidel, A., and Jerina, D.M.<br\/>Revised assignment of absolute configuration of the cis- and trans-N6-deoxyadenosine adducts at C14 of (\u00b1)-11\u03b2,12\u03b1-dihydroxy-13\u03b1,14\u03b1-epoxy-11,12,13,14-tetrahydrodibenzo[a,l]pyrene by stereoselective synthesis.<br\/>Chem. Res. Toxicol., 21 (2008) 2379-2392<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 211<\/span><p\/>Monien, B.H., Muller, C., Engst, W., Frank, H., Seidel, A. and Glatt, H.<br\/>Time course of hepatic 1-methylpyrene DNA adducts in rats determined by isotope dilution LC-MS\/MS and 32P-postlabeling.<br\/>Chem. Res. Toxicol., 21 (2008) 2017-2025<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 210<\/span><p\/>Lagerqvist, A., H\u00e5kansson, D., Prochazka, G., Lundin, C., Dreij, K., Segerb\u00e4ck, D., Jernstr\u00f6m, B., T\u00f6rnqvist, M., Seidel, A., Erixon, K., and Jenssen, D.<br\/>Both replication bypass fidelity and repair efficiency influence the yield of mutations per target dose in intact mammalian cells induced by benzo[a]pyrene-diol-epoxide and dibenzo[a,l]pyrene-diol-epoxide.<br\/>DNA Repair., 7 (2008) 1202-1212<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 209<\/span><p\/>Glatt, H., Rost, K., Frank, H., Seidel, A., and Kollock, R.<br\/>Detoxification of promutagenic aldehydes derived from methylpyrenes by human aldehyde dehydrogenases ALDH2 and ALDH3A1.<br\/>Arch. Biochem. Biophys., 477 (2008) 196-205<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 208<\/span><p\/>Kuhn, K., Nowak, N., Klein, G., Behnke, A., Seidel, A., and Lampen, A.<br\/>Determination of polycyclic aromatic hydrocarbons in smoked pork by effect directed bioassay with confirmation by chemical analysis.<br\/>J. Food Protect., 71 (2008) 993-999<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 207<\/span><p\/>Seidel, A., Spickenheuer, A., Straif, K., Rihs, H.-P., Marczynski, B., Scherenberg, M., Dettbarn, G., Angerer, J., Wilhelm, M., Br\u00fcning, T., Jacob, J., and Pesch, B.<br\/>New biomarkers of occupational exposure to polycyclic aromatic hydrocarbons.<br\/>J. Toxicol. Environ. Health, A 71 (2008) 1\u201312<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 206<\/span><p\/>Kollock, R., Frank, H., Seidel, A., Meinl, W. and Glatt, H.<br\/>Oxidation of alcohols and reduction of aldehydes derived from methyl- and dimethylpyrenes by cDNA-expressed human alcohol dehydrogenases.<br\/>Toxicology, 245 (2008) 65-75<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 205<\/span><p\/>P\u00e4\u00e4j\u00e4rvi, G., Jernstr\u00f6m, B., Seidel, A., and Stenius U.<br\/>Anti-diol epoxide of benzo[a]pyrene induces transient Mdm2 and p53 Ser15 phosphorylation, while anti-diol epoxide of dibenzo[a,l]pyrene induces a nontransient p53 Ser15 phosphorylation.<br\/>Mol Carcinog, 47 (2008) 301-309<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 204<\/span><p\/>Mattsson, \u00c5., Malml\u00f6f, M, Seidel, A., Stenius, U., Jernstr\u00f6m, B.<br\/>H2AX, Mdm2 and p53 phosphorylations are differently affected by bay- and fjord-region diol epoxides derived from carcinogenic polycyclic aromatic hydrocarbons.<br\/>Polycyclic Aromat. Compd., 28 (2008) 392\u2013401<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 203<\/span><p\/>Kollock, R., Meinl, W., Schneider, H., Batke, M., Frank, H., Seidel, A. and Glatt, H.<br\/>Efficient oxidation of promutagenic hydroxymethylpyrenes by cDNA-expressed human alcohol dehydrogenase ADH2 and its inhibition by various agents.<br\/>Biochem. Pharmacol., 75 (2008) 527-537<\/div>\n<h2 id=\"2007\">2007<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 202<\/span><p\/>Pesch, B., Kappler, M., Straif, K., Marczynski, B., Preuss, R., Rossbach, B., Rihs, H.P., Weiss, T., Rabstein, S., Pierl, C., Scherenberg, M., Adams, A., Kafferlein, H.U., Angerer, J., Wilhelm, M., Seidel, A. and Bruning, T.<br\/>Dose-response modeling of occupational exposure to polycyclic aromatic hydrocarbons with biomarkers of exposure and effect.<br\/>Cancer Epidemiol. Biomarkers Prev., 16 (2007) 1863-1873<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 201<\/span><p\/>Bakhiya, N., Batke, M., Laake, J., Monien, B.H., Frank, H., Seidel, A., Engst, W. and Glatt, H.<br\/>Directing role of organic anion transporters in the excretion of mercapturic acids of alkylated polycyclic aromatic hydrocarbons.<br\/>Drug Metab. Dispos., 35 (2007) 1824-1831<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 200<\/span><p\/>Halter, R., Hansen, T., Seidel, A., Ziemann, C., and Borlak, J.<br\/>Importance of DNA-adduct formation and gene expression profiling of disease candidate genes in rats exposed to bitumen fumes.<br\/>J. Occup. Environ. Hyg, 4 (Suppl 1) (2007) 44-64<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 199<\/span><p\/>Yagi, H., Frank, H., Seidel, A., and Jerina, D.M.<br\/>Synthesis and absolute configuration of cis and trans opened cyclopenta[cd]pyrene 3,4-oxide N2-deoxyguanosine adducts:  conversion to phosphoramidites for oligonucleotide synthesis.<br\/>Chem. Res. Toxicol., 20 (2007) 650-661<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 198<\/span><p\/>Hansen, T., Seidel, A., and Borlak, J.<br\/>The environmental carcinogen 3-nitrobenzanthrone and its main metabolite 3-aminobenzanthrone induce production of reactive oxygen intermediates in human epithelial lung cells.<br\/>Toxicol Appl Pharmacol, 221 (2007) 222-234<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 197<\/span><p\/>Glatt, H.R., Schneider, H., Seidel, A.<br\/>Polycyclische aromatische Kohlenwasserstoffe.<br\/>Handbuch der Lebensmitteltoxikologie (H. Dunkelberg, T. Gebel, A. Hartwig, eds.), Wiley-VCH Verlag, Weinheim (2007) 1121-1155<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 196<\/span><p\/>Ebert, B., Seidel, A., and Lampen, A.<br\/>Phytochemicals induce breast cancer resistance protein in Caco-2 cells and enhance the transport of benzo[a]pyrene-3-sulfate.<br\/>Toxicol. Sci., 96 (2007) 227-236<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 195<\/span><p\/>Rihs, H.-P., John, A., Scherenberg, M., Seidel, A., and Br\u00fcning, T.<br\/>Concordance between the deduced acetylation status generated by Real-time PCR based NAT2 genotyping of seven single nucleotide polymorphisms and human NAT2 phenotypes determined with caffeine.<br\/>Clinica Chim. Acta, 376 (2007) 240-243<\/div>\n<h2 id=\"2006\">2006<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 194<\/span><p\/>Simon, R., Palme, S., Anklam E. and Collaborators: L. Delaire; V. Hanot; H. Holzer; W. Jira; C. Levasseur; F. Monteau; M.W. Obiedzinski; M. Ojala; D. Peschke; S. Ramakrishnan; C. Ranta; A. Ruthenschr\u00f6r; M. Schirmacher; A. Seidel; P. Sopelana; G. Wolz; and C. Wright<br\/>Method Validation for Determination of the 15 European-Priority Polycyclic Aromatic Hydrocarbons in Primary Smoke Condensates by Gas Chromatography\/Mass Spectrometry: Interlaboratory Study.<br\/>Journal of AOAC International, 89 (2006) 772-781<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 193<\/span><p\/>Wang, B., Sayer, J.M., Yagi, H., Frank, H., Seidel, A., and Jerina, D.M.<br\/>Facile interstrand migration of the hydrocarbon moiety of a dibenzo[a,l]pyrene 11,12-diol 13,14-epoxide adduct at N2 of deoxyguanosine in a duplex oligonucleotide.<br\/>J. Am. Chem. Soc., 128 (2006) 10079-10084<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 192<\/span><p\/>Schober, W., Luch, A., Soballa, V.J., Raab, G., Stegeman, J.J., Doehmer, J., Jacob, J. and Seidel, A.<br\/>On the species-specific biotransformation of dibenzo[a,l]pyrene.<br\/>Chem. Biol. Interact., 161 (2006) 37-48<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 191<\/span><p\/>Bakhiya, N., Stephani, M., Seidel, A., Bahn, A., Ugele, B., Burckhardt, G. and Glatt, H.R.<br\/>Uptake of chemically reactive, DNA-damaging sulfuric acid esters into renal cells by human organic anion transporters.<br\/>J. Am. Soc. Nephrol., 17 (2006) 1414-1421<\/div>\n<h2 id=\"2005\">2005<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 190<\/span><p\/>van Lipzig, M.M.H., Vermeulen, N.P.E., Gusino, R., Legler, J., Frank, H., Seidel. A. and Meerman, J.H.N.<br\/>Formation of estrogenic metabolites of benzo[a]pyrene and chrysene by cytochrome P450 activity and their combined and supra-maximal estrogenic activity. <br\/>Environ. Toxicol. Pharmacol., 19 (2005) 41-55<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 189<\/span><p\/>Musafija-Jeknic, T., Luch, A., Seidel, A., Johns, C., Pereira, C., and Baird, W.M.<br\/>Effect of nucleotide sequence on the binding of (\u2013)-anti-dibenzo[a,l]pyrene-11,12-diol 13,14-epoxide to short oligodeoxyribonucleotides.<br\/>Polycycl. Aromat. Compds., 25 (2005) 103-111<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 188<\/span><p\/>Seidel, A.<br\/>Biomonitoring of PAHs\u00a0-\u00a0Human Exposure, in \u201cThe carcinogenic effects of polycyclic aromatic hydrocarbons\u201d (Luch, A., ed.)<br\/>Imperial College Press (ICP), London (UK) (2005) p 97-136<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 187<\/span><p\/>Ebert, B., Seidel, A., and Lampen, A.<br\/>Identification of BCRP as transporter of benzo[a]-pyrene conjugates metabolically formed in Caco-2 cells and its induction by Ah-receptor agonists.<br\/>Carcinogenesis, 26 (2005) 1754-1763<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 186<\/span><p\/>Ebert, B., Jacob, J., Seidel, A., and Lampen, A.<br\/>Oltipraz, flavone and indole-3-carbinol enhance the formation and transport of sulfate conjugates of benzo[a]pyrene in human enterocytes.<br\/>Tox. Lett., 157 (2005) 140-151<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 185<\/span><p\/>Mensing, T., Marczynski, B., Engelhardt, B., Wilhelm, M., Preuss, R., Kappler, M., Angerer, J., K\u00e4fferlein, H.U., Scherenberg, M., Seidel, A., Br\u00fcning, T.<br\/>DNA adduct formation of benzo[a]pyrene in white blood cells of workers exposed to polycyclic aromatic hydrocarbons.<br\/>Int. J. Hyg. Environ. Health., 208 (2005) 173-178<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 184<\/span><p\/>Rihs, H.-P., Pesch, B., Kappler, M., Rabstein, S., Ro\u00dfbach, B., Angerer, J., Scherenberg, M., Adams, A., Wilhelm, M., Seidel, A., and Br\u00fcning, T.<br\/>Occupational exposure to polycyclic aromatic hydrocarbons in German industries: Association between ambient exposure and urinary metabolites and its modulation by enzyme polymorphisms.<br\/>Tox. Lett., 157 (2005) 241-255<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 183<\/span><p\/>Dreij, K., Seidel, A., and Jernstr\u00f6m, J.<br\/>Differential removal of DNA-adducts derived from anti-diol epoxides of dibenzo[a,l]pyrene and benzo[a]pyrene in human cells.<br\/>Chem Res. Toxicol., 18 (2005) 655-664<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 182<\/span><p\/>Marczynski, B., Preuss, R., Mensing, T., Angerer, J., Seidel, A., El Mourabit, A., Wilhelm, M., and Br\u00fcning, T.<br\/>Genotoxic risk assessment in white blood cells of occupationally exposed workers before and after alteration of the polycyclic aromatic hydrocarbon (PAH) profile in the production material: comparison with PAH air and urinary metabolite levels.<br\/>Int Arch Occup Environ Health, 78 (2005) 98-108<\/div>\n<h2 id=\"2004\">2004<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 181<\/span><p\/>Angerer, J., Ro\u00dfbach, B., und Seidel, A.<br\/>Bestandsaufnahme zur Frage des Zusammenhangs zwischen dem DNA-Adduktgehalt in wei\u00dfen Blutzellen und in humanem Lungengewebe. <br\/>Poly-cyclische aromatische Kohlenwasserstoffe \u2013 DFG Forschungsbericht (Jacob, J., und Greim, H., Hrsg.) WILEY-VCH Verlag GmbH & Co KGaA, (Weinheim) (2004) S. 77-117<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 180<\/span><p\/>Seidel, A., Angerer, J.<br\/>Nukleobasen-Addukte von PAH im Humanurin.<br\/>Poly-cyclische aromatische Kohlenwasserstoffe \u2013 DFG Forschungsbericht (Jacob, J., und Greim, H., Hrsg.) WILEY-VCH Verlag GmbH & Co KGaA, (Weinheim) (2004) S. 70-76<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 179<\/span><p\/>Jacob, J., Seidel, A.<br\/>Biomonitoring von PAH-Metaboliten im Humanurin.<br\/>Polycyclische aromatische Kohlenwasserstoffe \u2013 DFG Forschungsbericht (Jacob, J., und Greim, H., Hrsg.) WILEY-VCH Verlag GmbH & Co KGaA, (Weinheim) (2004) S. 42-69<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 178<\/span><p\/>Jacob, J., Seidel, A.<br\/>Verwendung eines auf Wirkungs\u00e4quivalenten basierenden Summenparameters f\u00fcr die Absch\u00e4tzung der PAH-Exposition und ihres Krebs erregenden Potentials.<br\/>Polycyclische aromatische Kohlenwasserstoffe \u2013 DFG Forschungsbericht (Jacob, J., und Greim, H., Hrsg.) WILEY-VCH Verlag GmbH & Co KGaA, (Weinheim) (2004) S. 8-22<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 177<\/span><p\/>Seidel, A., Frank, H., Behnke, A., Schneider, D., and Jacob, J.<br\/>Determination of dibenzo[a,l]pyrene and other fjord-region PAH isomers with mw 302 in environmental samples.<br\/>Polycycl. Aromat. Compds., 24 (2004) 759-771<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 176<\/span><p\/>Dreij, K., Bajak E., Sundberg K., Cotgreave I., Jernstr\u00f6m. B., Seidel, A. and Gusnanto A. <br\/>DNA adducts of benzo[a]pyrene- and dibenzo[a,l]pyrene-diol epoxides in human lung epithelial cells: kinetics of adduct removal, effects on cell cycle checkpoints, and gene expression.<br\/>Polycycl. Aromat. Compds., 24 (2004) 549-566<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 175<\/span><p\/>P\u00e4\u00e4rj\u00e4vi, G., Jernstr\u00f6m. B., Stenius, U., and Seidel, A.<br\/>Exposure of mammalian cells to diol epoxides from benzo[a]pyrene and dibenzo[a,l]pyrene and effects on Mdm2 and p53.<br\/>Polycycl. Aromat. Compds., 24 (2004) 537-548<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 174<\/span><p\/>Lampen, A., Ebert, B., Stumkat, L., Jacob, J., and Seidel, A.<br\/>Induction of gene expression of xenobiotic metabolism enzymes and ABC-transport proteins by PAH and a reconstituted PAH mixture in human Caco-2 cells.<br\/>Biochim. Biophys. Acta, 1681 (2004) 38-46<\/div>\n<h2 id=\"2003\">2003<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 173<\/span><p\/>Wu, J., Wu, J., Zhu, B.B., Yu, J., Zhu, H., Qiu, L., Kindy, M.S., Gu, L., Seidel, A., Li, G.M.<br\/><a href=\"http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=14602900\" target=\"_blank\">In vitro and in vivo modulations of benzo[c]phenanthrene-DNA adducts by DNA mismatch repair system.<\/a><br\/>Nucleic Acids Res., 31 (2003) 6428-6434<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 172<\/span><p\/>Arlt, V.M., Glatt, H.R., Muckel, E., Pabel, U., Sorg, B.L., Seidel, A., Frank, H., Schmeiser, H.H., and Phillips, D.H.<br\/>Activation of 3-nitrobenzanthrone and its metabolites by human acetyltransferases, sulfotransferases and cytochrome P450 expressed in Chinese hamster V79 cells.<br\/>Int. J. Cancer, 105 (2003) 583-592<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 171<\/span><p\/>Mahadevan, B., Dashwood, W.-M., Luch, A., Pecaj, A., Doehmer, J., Seidel, A., and Baird, W.M.<br\/>Mutations induced by (\u2013)-anti-11R,12S-dihydrodiol 13S,14R-epoxide of dibenzo[a,l]pyrene in the coding region of the hypoxanthine phosphoribosyltransferase (hprt) gene in Chinese hamster V79 cells.<br\/>Environ. Mol. Mutagen., 41 (2003) 131-139<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 170<\/span><p\/>Arlt V.M., Bernd L. Sorg, B.L., Osborne, M., Hewer, A., Seidel, A., Schmeiser, H.H., and Phillips, D.H.<br\/>DNA adduct formation by the ubiquitous environmental pollutant 3-nitro-benzanthrone and its metabolites in rats.<br\/>Biochem. Biophys. Res. Commun., 300 (2003) 107-114<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 169<\/span><p\/>Buesen, R., Mock, M., Nau, H., Seidel, A., Jacob, J., and Lampen, A.<br\/>Evidence for an active transport of polar [14C]-benzo[a]pyrene metabolites in human intestinal Caco-2 cells.<br\/>Chem.-biol. Interact., 142 (2003) 201-344<\/div>\n<h2 id=\"2002\">2002<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 168<\/span><p\/>Buesen, R., Mock, M., Seidel, A., Jacob, J., and Lampen, A.<br\/>Interaction between metabolism and transport of benzo[a]pyrene and its metabolites in enterocytes.<br\/>Toxicol. Appl. Pharmacol., 183 (2002) 168-178<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 167<\/span><p\/>Sundberg, K., Dreij, K., Jernstr\u00f6m, B. and Seidel, A.<br\/>Detoxification of polycyclic aromatic hydrocarbon diol epoxides by human glutathione transferases: efficiency of conjugation in intact cells relative to purified enzymes.<br\/>Polycycl. Aromat. Compds., 22 (2002) 947-953<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 166<\/span><p\/>Dreij, K., Sundberg, K., Jernstr\u00f6m, B., Johansson, A.-S., Mannervik, B., and Seidel, A.<br\/>Inactivation of carcinogenic diol epoxides of dibenzo[a,l]pyrene (dibenzo[def,p]chrysene by human alpha class glutathione transferases.<br\/>Polycycl. Aromat. Compds., 22 (2002) 823-829<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 165<\/span><p\/>Luch, A., Greim, H., Buters, J.T.M., Mahadevan, B., Baird, W.M., Doehmer, J., Seidel, A., and Glatt, H.R.<br\/>The role of cytochrome P450 1B1 in dibenzo[a,l]pyrene-induced carcinogenesis.<br\/>Polycycl. Aromat. Compds., 22 (2002) 781-789<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 164<\/span><p\/>Baird, W.M., Hooven, L.A., Mahadevan, B., Luch, A., Seidel, A., Iversen, P.L.<br\/>Responses of human cells to PAH-induced DNA damage.<br\/>Polycycl. Aromat. Compds., 22 (2002) 771-780<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 163<\/span><p\/>Jacob, J., Seidel, A.<br\/>Biomonitoring of polycyclic aromatic hydrocarbons (review) <br\/>J. Chromatogr. B, 778 (2002) 31-47<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 162<\/span><p\/>Dreij, K., Sundberg, K., Johansson, A.-S., Nordling, E., Seidel, A., Persson, E., Mannervik, B., and Jernstr\u00f6m, B.<br\/>Catalytic activities of human alpha class glutathione transferases towards carcinogenic dibenzo[a,l]pyrene diol epoxides.<br\/>Chem. Res. Toxicol., 15 (2002) 825-831<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 161<\/span><p\/>Jacob, J., Seidel, A.<br\/>Zur Problematik der Verwendung von Benzo[a]pyren als Leitkomponente f\u00fcr das PAH-bedingte karzinogene Potential in Umweltmatrices<br\/>Gefahrstoffe - Reinhaltung der Luft, 62 (2002) 239-246<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 160<\/span><p\/>Platt, K.-L., Degenhardt, C., Grupe, S., Frank, H., and Seidel, A.<br\/>Microsomal activation of anthanthrene, a hexacyclic aromatic hydrocarbon without a bay-region, to mutagenic metabolites.<br\/>Chem. Res. Toxicol., 15 (2002) 332-342<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 159<\/span><p\/>Seidel, A., Dahmann, D., Krekeler, H., and Jacob, J.<br\/>Biomonitoring of polycyclic aromatic compounds in the urine of mining workers occupationally exposed to diesel-exhaust.<br\/>Inter. J. Hyg. Environ. Health, 204 (2002) 333-338<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 158<\/span><p\/>Sundberg, K., Dreij, K., Seidel, A., and Jernstr\u00f6m, B.<br\/>Glutathione conjugation and DNA adduct formation of dibenzo[a,l]pyrene and benzo[a]pyrene diol epoxides in V79 cells stably expressing different human glutathione transferases.<br\/>Chem. Res. Toxicol., 15 (2002) 170-179<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 157<\/span><p\/>Schwerdtle, T., Seidel, A., and Hartwig, A.<br\/>Effect of soluble particulate nickel compounds on the formation and repair of stable benzo[a]pyrene DNA adducts in human lung cells. <br\/>Carcinogenesis, 23 (2002) 47-53<\/div>\n<h2 id=\"2001\">2001<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 156<\/span><p\/>Seidel, A., Grimmer, G., Dettbarn, G., and Jacob, J.<br\/>Nachweis von kanzerogenen aromatischen Aminen im Harn von Nichtrauchern.<br\/>Umweltmed. Forsch. Prax., 6 (2001) 213-220<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 155<\/span><p\/>Mahadevan, B., Luch, A., Seidel, A., Pelling, J.C., and Baird, W.M.<br\/>Effects of (\u2013)-anti-11R,12S-dihydrodiol 13S,14R-epoxide of dibenzo[a,l]pyrene on DNA adduct formation and cell cycle arrest in human diploid fibroblasts.<br\/>Carcinogenesis, 22 (2001) 161-169<\/div>\n<h2 id=\"2000\">2000<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 154<\/span><p\/>Ma, L., Landsiedel, R., Seidel, A., and Glatt, H.R.<br\/>Detection of mercapturic acids and nucleoside adducts in blood, urine and faeces of rats treated with 1-hydroxy-methylpyrene. <br\/>Polycycl. Arom. Compds., 21 (2000) 135-149<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 153<\/span><p\/>Sundberg, K., Townsend, A., Luch, A., Seidel, A., and Jernstr\u00f6m, B.<br\/>Effect of glutathione transferases on DNA-adduct formation of polycyclic aromatic hydrocarbons in mammalian cells.<br\/>Polycycl. Arom. Compds., 21 (2000) 123-133<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 152<\/span><p\/>Jacob, J., Schober, W., Raab, G., Frank, H., Luch, A., Doehmer, J., and Seidel, A.<br\/>Species dependent metabolism of benzo[c]chrysene mediated by c-DNA-expressed human, rodent and fish cytochrome P450 enzymes.<br\/>Polycycl. Arom. Compds., 21 (2000) 109-121<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 151<\/span><p\/>Luch, A., Schober, W., Greim, H., Doehmer, J., Jacob, J., Seidel, A., and Baird, W.M. <br\/>Metabolic activation of dibenzo[a,l]pyrene by cytochrome P450 enzymes to stable DNA adducts occurs exclusively through the formation of the (\u2013)-trans-(11R,12R)-dihydrodiol.<br\/>Polycycl. Arom. Compds., 21 (2000) 87-98<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 150<\/span><p\/>Borlak, J., Hansen, T., Yuan, X.Y., Sikka, H.C., Kumar, S., Schmidbauer, S., Raab, G., Frank, H., Jacob, J., and Seidel, A.<br\/>Metabolism and DNA binding of 3-nitrobenzanthrone in human fetal bronchial epithelial and alveolar typ II cells.<br\/>Polycycl. Arom. Compds., 21 (2000) 73-86<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 149<\/span><p\/>Kroth, H., Yagi, H., Seidel, A., and Jerina, D.M.<br\/>New and highly efficient synthesis of cis- and trans-opened benzo[a]pyrene 7,8-diol 9,10-epoxide adducts at the exocyclic amino group of deoxyguanosine.<br\/>J. Org. Chem., 65 (2000) 5558-5564<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 148<\/span><p\/>Doehmer, J., Krebsf\u00e4nger, N., Schober, W., Luch, A., Buters, J.T.M., Jacob, J., Seidel, A., M\u00fcrdter, T., Zanger, U.M., and Eichelbaum, M.<br\/>Building a bio-technology platform for metabolism studies in pharmacology and toxicology.<br\/>Progress in the Reduction, Refinement and Replacement of Animal Experimentation, (Balls, M., van Zeller, A.-M., and Halder, M.E., ed's), Elsevier Science B.V. (2000) pp 139-146<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 147<\/span><p\/>Buterin, T., Hess, M.T., Luneva, N., Geacintov, N.E., Amin, S., Kroth, H., Seidel, A., and Naegeli, H.<br\/>Unrepaired fjord region polycyclic aromatic hydrocarbon-DNA adducts in ras codon 61 mutational hot spots<br\/>Cancer Res., 60 (2000) 1849-1856<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 146<\/span><p\/>Li, D.N., Seidel, A., Pritchard, M.P., Wolf, C.R., and Friedberg, T.<br\/>Polymorphisms in P450 CYP1B1 affect the conversion of estradiol to the potentially carcinogenic metabolite 4-hydroxyestradiol.<br\/>Pharmacogenetics, 10 (2000) 343-353<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 145<\/span><p\/>Grimmer, G., Dettbarn, G., Seidel, A., and Jacob, J.<br\/>Detection of carcinogenic aromatic amines in the urine of non-smokers.<br\/>Sci. Total Environ., 247 (2000) 81-90<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 144<\/span><p\/>Melendez-Colon, V.J., Luch, A., Seidel, A., and Baird, W.M.<br\/>Formation of stable DNA adducts and apurinic sites upon metabolic activation of bay and fjord region polycyclic aromatic hydrocarbons in human cell cultures.<br\/>Chem. Res. Toxicol., 13 (2000) 10-17<\/div>\n<h2 id=\"1999\">1999<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 143<\/span><p\/>Sundberg, K., Seidel, A., Mannervik, B., and Jernstr\u00f6m, B.<br\/>Catalytic efficiency of glutathione transferase P1-1 variants towards bay- and fjord-region diol epoxides of polycyclic aromatic hydrocarbons.<br\/>Polycycl. Aromat. Compds., 17 (1999) 43-51<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 142<\/span><p\/>Pradhan, P., Gr\u00e4slund, A., Seidel, A., and Jernstr\u00f6m, B.<br\/>Studies on adduct formation of (+)-anti-benzo[a]pyrene 7,8-dihydrodiol 9,10-epoxide with the oligonucleotides 5'-d(CCTA TCGTTATCC) and 5'-d(CCTATCm5GTTATCC).<br\/>Polycycl. Aromat. Compds., 17 (1999) 21-32<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 141<\/span><p\/>Jacob, J., Raab, G., Soballa, V.J., Luch, A., Grimmer, G., Greim, H., Doehmer, J., Morrison, H.G., Stegeman, J.J., and Seidel, A.<br\/>Species-dependent metabolism of benzo[c]phenanthrene and dibenzo[a,l]pyrene by various CYP450 isoforms.<br\/>Polycycl. Aromat. Compds., 16 (1999) 191-203<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 140<\/span><p\/>Baird, W.M., Kaspin, L.C., Kudla, K., Seidel, A., Greim, H., and Luch, A.<br\/>Relationship of dibenzo[a,l]pyrene-DNA binding to the induction of p53, p21WAF1 and cell cycle arrest in human cells in culture.<br\/>Polycycl. Aromat. Compds., 16 (1999) 119-129<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 139<\/span><p\/>Luch, A., Coffing, S.L., Seidel, A., Greim, H., Baird, W.M., and Doehmer, J.<br\/>DNA modification induced after metabolic activation of the potent carcinogen dibenzo[a,l]pyrene in V79 Chinese hamster cells stably expressing single cytochromes P450.<br\/>Polycycl. Aromat. Compds., 16 (1999) 71-78<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 138<\/span><p\/>Pradhan, P., Gr\u00e4slund, A., Seidel, A., and Jernstr\u00f6m, B.<br\/>Implications of cytosine methylation on (+)-anti-benzo[a]pyrene 7,8-dihydrodiol 9,10-epoxide N2-dG adduct formation in 5'-d(CGT), 5'-d(CGA), and 5'-d(CGC) sequence contexts of single- and double-stranded oligonucleotides.<br\/>Chem. Res. Toxicol., 12 (1999) 816-821<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 137<\/span><p\/>Luch, A., Kishiyama, S., Seidel, A., Doehmer, J., Greim, H., and Baird, W.M.<br\/>The K-region trans-8,9-diol does not significantly contribute as an intermediate in the metabolic activation of dibenzo[a,l]pyrene to DNA-binding metabolites by human cytochrome P450 1A1 or 1B1.<br\/>Cancer Res., 59 (1999) 4603-4609<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 136<\/span><p\/>Li, K.-M., George, M., Gross, M.L., Lin, Ch.-H., Small, G.J., Jankowiak, R., Seidel, A., Kroth, H., Eleanor G. Rogan, E.L., and Cavalieri, E.L.<br\/>Structure elucidation of the adducts formed by fjord-region dibenzo[a,l]pyrene 11,12-diol 13,14-epoxides with deoxy\u00adguanosine.<br\/>Chem. Res. Toxicol., 12 (1999) 778-788<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 135<\/span><p\/>Li, K.-M., George, M., Gross, M.L., Seidel, A., Luch, A., Rogan, E.G., and Cavalieri, E.L.<br\/>Structure elucidation of the adducts formed by fjord-region dibenzo[a,l]pyrene 11,12-diol  13,14-epoxides with deoxyadenosine.<br\/>Chem. Res. Toxicol., 12 (1999) 758-767<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 134<\/span><p\/>Pal, A., Seidel, A., Xia, H., Hu, X., Oesch, F., and Singh, S.V.<br\/>Specificity of murine glutathione S-transferase isozymes in the glutathione conjugation of (-)-anti- and (+)-syn-stereoisomers of benzo[g]chrysene 11,12-dihydrodiol 13,14-epoxide.<br\/>Carcinogenesis, 20 (1999) 1997-2001<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 133<\/span><p\/>Melendez-Colon, V.J., Luch, A., Seidel, A., and Baird, W.M.<br\/>Cancer initiation by polycyclic aromatic hydrocarbons results from formation of stable DNA adducts rather than apurinic sites.<br\/>Carcinogenesis, 20 (1999) 1885-1891<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 132<\/span><p\/>Pradhan, P., Jernstr\u00f6m, B., Seidel, A., Nord\u00e9n, B., and Gr\u00e4slund, A.<br\/>Studies on the adduct heterogeneity of benzo[a]pyrene 7,8-dihydrodiol 9,10-epoxide stereo-isomers covalently bound to deoxyribooligonucleotides by induced circular dichroism and light absorption spectroscopy.<br\/>Chem. Res. Toxicol., 12 (1999) 403-411<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 131<\/span><p\/>Bluvshtein, E., Glass, G.A., Volohonsky, G., Yaakubowitz, M., Harness, E., Smorodinsky, N., Seidel, A., Frank, H., Steinberg, P., and Stark, A.A.<br\/>Inhibition of the hydrolytic and transpeptidase activities of rat kidney g-glutamyl-transpeptidase by specific monoclonal antibodies.<br\/>Eur. J. Biochem., 260 (1999) 844-854<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 130<\/span><p\/>Melendez-Colon, V.J., Luch, A., Seidel, A., and Baird, W.M.<br\/>Comparison of cytochrome P450 and peroxidase dependent metabolic activation of the potent carcinogen dibenzo[a,l]\u00adpyrene in human cell lines: formation of stable DNA adducts and absence of a detectable increase in apurinic sites.<br\/>Cancer Res., 59 (1999) 1412-1416<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 129<\/span><p\/>Luch, A., Friesel, H., Seidel, A., and Platt, K.L.<br\/>Tumor-initiating activity of the (+)-(S,S)- and (-)-(R,R)-enantiomers of trans-11,12-dihydroxy-11,12-dihydrodibenzo[a,l]pyrene in mouse skin.<br\/>Cancer Lett., 136 (1999) 119-128<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 128<\/span><p\/>Luch, A., Schober, W., Soballa, V.J., Raab, G., Greim, H., Jacob, J., Doehmer, J. and Seidel, A.<br\/>Metabolic activation of dibenzo[a,l]pyrene by human cytochrome P450 1A1 and P450 1B1 expressed in V79 Chinese hamster cells.<br\/>Chem. Res. Toxicol., 12 (1999) 353-364<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 127<\/span><p\/>Erb, C., Seidel, A., Frank, H., Platt, K.L., Oesch, F., and Klein, J.<br\/>Formation of N-methyl\u00adnicotinamide in the brain from a dihydropyridine-type pro-drug: Effect on brain choline.<br\/>Biochem. Pharmacol., 57 (1999) 681-684<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 126<\/span><p\/>Luch, A., Kudla, K., Seidel, A., Doehmer, J., Greim, H., and Baird, W.M.<br\/>The level of DNA modification by (+)-syn-(11S,12R,13S,14R)- and (-)-anti-(11R,12S,13S,14R)-dihydrodiol epoxides of dibenzo[a,l]pyrene determines the effect on the proteins p53 and p21WAF1 in the human mammary carcinoma cell line MCF-7.<br\/>Carcinogenesis, 20 (1999) 859-865<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 125<\/span><p\/>Bock, K.W., Raschko, F.T., Gschaidmeier, H., Seidel, A., Oesch, F., Grove, A.D., Ritter, J.K.<br\/>Mono- and diglucuronide formation from benzo[a]pyrene and chrysene diphenols by AHH-1 cell-expressed UDP-glucuronosyltransferase UGT1A7.<br\/>Biochem. Pharmacol., 57 (1999) 653-656<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 124<\/span><p\/>Doehmer, J., Buters, J.T.M., Luch, A., Soballa, V., Baird, W.M., Morisson, H., Stegeman, J.J., Townsend, A.J., Greenlee, W.F., Glatt, H.R., Seidel, A., Jacob, J., and Greim, H. <br\/>Molecular studies on the toxifying effects by genetically engeneered cytochromes P450. <br\/>Drug Met. Rev., 31 (1999) 423-435<\/div>\n<h2 id=\"1998\">1998<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 123<\/span><p\/>Sundberg, K., Seidel, A., Mannervik, B. and Jernstr\u00f6m, B.<br\/>Detoxification of carcinogenic fjord-region diol epoxides of polycyclic aromatic hydrocarbons by glutathione transferase P1-1 variants and glutathione.<br\/>FEBS Lett, 438 (1998) 206-210<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 122<\/span><p\/>Seidel, A., Friedberg, T., L\u00f6llmann, B., Schwierzok, A., Funk, M., Frank, H., Holler, R., Oesch, F., and Glatt, H.R.<br\/>Detoxication of optically active bay- and fjord-region polycyclic aromatic hydrocarbon dihydrodiol epoxides by human glutathione transferase P1-1 expressed in Chinese hamster V79 cells.<br\/>Carcinogenesis, 19 (1998) 1975-1981<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 121<\/span><p\/>Hu, X., Seidel, A., Frank, H., Srivastava, S.K., Xia, H., Pal, A., Zheng, S., Oesch, F., and Singh, S.V.<br\/>Differential enantioselectivity of murine glutathione S-transferase isoenzymes in the glutathione conjugation of trans-3,4-dihydroxy-1,2-oxy-1,2,3,4-tetrahydrobenzo[c]\u00adphenanthrene stereoisomers.<br\/>Ach. Biochem. Biophys., 358 (1998) 40-48<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 120<\/span><p\/>Landsiedel, R., Frank, H., Glatt, H.R., and Seidel, A.<br\/>Optical resolution of trans-dihydrodiol enantiomers of fjord-region polycyclic aromatic hydrocarbons by HPLC on a chiral cellulose-phase: relationship between elution order and absolute configuration.<br\/>J. Chromatogr. A, 822 (1998) 29-35<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 119<\/span><p\/>Khan, Q.A., Agarwal, R., Seidel, A., Frank, H., Vousden, K.H., and Dipple, A.<br\/>Effects of optical isomers of benzo[g]chrysene anti dihydrodiol epoxide on passage of MCF-7 cells through the cell cycle.<br\/>Mol. Carcinog., 23 (1998) 115-120<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 118<\/span><p\/>Luch, A., Schneider, A., Coffing, S. L., Soballa, V. J., Greim, H., Jefcoate, C.R., Greenlee, W.F., Seidel, A., Baird, W.M., and Doehmer, J.<br\/>Stable expression of human cytochrome P450 1B1 in V79 Chinese hamster cells and metabolically catalyzed DNA adduct formation of dibenzo[a,l]pyrene.<br\/>Chem. Res. Toxicol., 11 (1998) 686-695<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 117<\/span><p\/>Jankowiak, R., Ariese, F., Hewer, A., Luch, A., Zamzow, D., Hughes, N.C., Phillips, D., Seidel, A., Platt, K.L., Oesch, F., and Small, G.J.<br\/>Structure, conformations, and repair of DNA adducts from dibenzo[a,l]pyrene: 32P-Postlabeling and fluorescence studies.<br\/>Chem. Res. Toxicol., 11 (1998) 674-685<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 116<\/span><p\/>Landsiedel, R., Pabel, U., Engst, W., Ploschke, J., Seidel, A. and Glatt, H.R.<br\/>Chiral inversion of 1-hydroxymethylpyrene enantiomers mediated by enantioselective sulfotransferases.<br\/>Biochem. Biophys. Res. Commun., 247 (1998) 181-185<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 115<\/span><p\/>Seidel, A., Soballa, V.J., Raab, G., Frank, H., Grimmer, G., Greim, H., Jacob, J., and  Doehmer, J.<br\/>Regio- and stereoselectivity in the metabolism of benzo[c]phenanthrene mediated by genetically engineered V79 Chinese hamster cells expressing rat and human cytochromes P450.<br\/>Environ. Toxicol. Pharmacol., 5 (1998) 179-196<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 114<\/span><p\/>Luch, A., Platt, K.L., and Seidel, A.<br\/>Synthesis of fjord region tetraols and their use in hepatic biotransformation studies of dihydrodiols of benzo[c]chrysene, benzo[g]chrysene and dibenzo[a,l]pyrene.<br\/>Carcinogenesis, 19 (1998) 639-648<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 113<\/span><p\/>Pradhan, P., Jernstr\u00f6m, B., Seidel, A., Nord\u00e9n, B., and Gr\u00e4slund, A.<br\/>Induced circular dichroism of benzo[a]pyrene 7,8-dihydrodiol 9,10-epoxide stereoisomers covalently bound to deoxyribooligonucleotides used to probe equilibrium distribution between groove binding and intercalative adduct conformations.<br\/>Biochemistry, 37 (1998) 4664-4673<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 112<\/span><p\/>Glatt, H.R., Bartsch, I., Christoph, St., Coughtrie, M.W.H., Falany, C.N., Hagen, M., Landsiedel, R., Pabel, U., Phillips, D.H., Seidel, A., Yamazoe, Y.<br\/>Sulfotransferase-mediated activation of mutagens, studied using heterologous expression systems.<br\/>Chem.-biol. Interact., 109 (1998) 195-219<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 111<\/span><p\/>Sundberg, K., Johansson, A.S., Stenberg, G., Widersten, M., Seidel, A., Mannervik, B. and Jernstr\u00f6m, B.<br\/>Differences in the catalytic efficiencies of allelic variants of glutathione transferase P1-1 towards carcinogenic diol epoxides of polycyclic aromatic hydrocarbons.<br\/>Carcinogenesis, 19 (1998) 433-436<\/div>\n<h2 id=\"1997\">1997<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 110<\/span><p\/>Melendez-Colon, V.J., Smith, C.A., Seidel, A., Luch, A., Platt, K.L., and Baird, W.M. <br\/>Formation of stable adducts and absence of depurinating adducts upon reaction of the diol epoxides of the potent carcinogen dibenzo[a,l]pyrene with DNA in solution and in cells. <br\/>Proc. Natl. Acad. Sci. U.S.A., 94 (1997) 13542-13547<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 109<\/span><p\/>Giles, A.S., Seidel, A., and Phillips, D.H.<br\/>Covalent DNA adducts formed by benzo[c]-chrysene in mouse epidermis and by benzo[c]chrysene fjord-region diol-epoxides reacted with DNA and polynucleotides.<br\/>Chem. Res. Toxicol., 10 (1997) 1275-1284<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 108<\/span><p\/>Sundberg, K., Widersten, M., Seidel, A., Mannervik, B., and Jernstr\u00f6m, B.<br\/>Glutathione conjugation of bay- and fjord-region diol epoxides of polycyclic aromatic hydrocarbons by glutathione transferases M1b-1b and P1-1.<br\/>Chem. Res. Toxicol., 10 (1997) 1221-1227<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 107<\/span><p\/>Luch, A., Seidel, A., Glatt, H.R., and Platt, K.L.<br\/>Metabolic activation of the (+)-(S,S)- and (-)-(R,R)-enantiomers of trans-11,12-dihydroxy-11,12-dihydrodi-benzo[a,l]pyrene: stereo-selectivity, DNA adduct formation, and mutagenicity in Chinese hamster V79 cells.<br\/>Chem. Res. Toxicol., 10 (1997) 1161-1170<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 106<\/span><p\/>Funk, M., Pont\u00e9n, I., Seidel, A., and Jernstr\u00f6m, B.<br\/>Critical parameters for adduct formation of the four stereoisomeric benzo[a]pyrene 7,8-dihydrodiol 9,10-epoxides with oligo\u00adnucleotides.<br\/>Bioconjugate Chem., 8 (1997) 310-317<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 105<\/span><p\/>Steinberg, P., Heck, R., Frank, H., Odenthal, M., Dienes, H.-P., and Seidel, A.<br\/>The role of the Ha-ras gene in the malignant transformation of rat liver oval cells.<br\/>Inter. J. Cancer., 71 (1997) 680-685<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 104<\/span><p\/>Ralston, S., Coffing, S., Seidel, A., Luch, A., Platt, K.L., and Baird, W.M.<br\/>Stereoselective activation of dibenzo[a,l]pyrene and its trans-11,12-dihydrodiol to fjord region 11,12-diol 13,14-epoxides in a human mammary carcinoma MCF-7 cell-mediated V79 cell mutation assay.<br\/>Chem. Res. Toxicol., 10 (1997) 687-693<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 103<\/span><p\/>Jankowiak, R., Ariese, F., Zamzow, D., Luch, A., Kroth, H., Seidel, A., and Small, G.J. <br\/>Conformational studies of stereoisomeric tetraols derived from syn- and anti-dibenzo[a,l]pyrene diolepoxides.<br\/>Chem. Res. Toxicol., 10 (1997) 677-686<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 102<\/span><p\/>Hanelt, S., Helbig, R., Hartmann, A., Lang, M., Seidel, A., and Speit, G.<br\/>A comparative investigation of DNA adducts, DNA strand breaks and gene mutations induced by benzo[a]pyrene and (\u00b1)-benzo[a]pyrene-7,8-diol-9,10-epoxide in cultured human cells.<br\/>Mutagenesis, 390 (1997) 179-188<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 101<\/span><p\/>M\u00fcller, F., Arand, A., Frank, H., Seidel, A., Hinz, W., Winkler, L., H\u00e4nel, K., Bl\u00e9e, E., Beetham, J.K., Hammock, B.D., and Oesch, F.<br\/>Visualization of the covalent intermediate formed between microsomal epoxide hydrolase and 9,10-epoxystearic acid during enzymatic epoxide hydrolysis.<br\/>Eur. J. Biochem., 245 (1997) 490-496<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 100<\/span><p\/>Turchi, G., Glatt, H.R., Seidel, A., Puliti, A., and Sbrana, I.<br\/>Structure-activity relationship in the induction of chromosomal aberrations and spindle disturbances in Chinese hamster epithelial liver cells by regioisomeric phenanthrene quinones.<br\/>Cell Biol. Toxicol., 13 (1997) 155-165<\/div>\n<h2 id=\"1996\">1996<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 99<\/span><p\/>Kroth, H., Oesch, F., and Seidel, A.<br\/>Synthesis of stereoisomeric N6-deoxy-adenosine adducts of syn- and anti-dihydrodiol epoxides of benzo[a]pyrene and their incorporation into 18-mer DNA sequences from human Ha-ras protooncogene.<br\/>Polycycl. Arom. Compds., 11 (1996) 349-356<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 98<\/span><p\/>Landsiedel, R., Engst, W., Scholtyssek, M., Seidel, A., Glatt, H.R.<br\/>Nucleophilic displacement reactions at the benzylic position of the sulfuric acid ester 1-sulfooxymethylpyrene: Potential influence on in vivo reactivity.<br\/>Polycycl. Arom. Compds., 11 (1996) 341-348<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 97<\/span><p\/>Buchwald-Goebel, S., Oesch, F., and Seidel, A.<br\/>A tandem photochemical approach for the synthesis of biologically important metabolites of benzo[b]fluoranthene.<br\/>Polycycl. Arom. Compds., 11 (1996) 325-332<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 96<\/span><p\/>Steinberg, P., Oesch, F., and Seidel, A.<br\/>The stereoisomeric fjord-region benzo[c]-phenanthrene-3,4-dihydrodiol 1,2-oxides malignantly transform rat liver epithelial cells.<br\/>Polycycl. Arom. Compds., 10 (1996) 275-282<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 95<\/span><p\/>Baird, W.M., Ralston, S., Luch, A., Platt, K.L., and Seidel, A.<br\/>Stereoselective metabolic activation of dibenzo[a,l]pyrene in the human mammary carcinoma cell line MCF-7 results in formation of (-)-anti and (+)-syn-11,12-diol-13,14-epoxide-deoxyadenosine adducts in DNA.<br\/>Polycycl. Arom. Compds., 10 (1996) 235-242<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 94<\/span><p\/>Pfau, W., Seidel, A., Phillips, D.H., Oesch, F., and Grover, P.L.<br\/>32P-postlabelling\/ HPLC analysis of DNA adducts formed from chrysene and its metabolites.<br\/>Polycycl. Arom. Compds., 10 (1996) 219-226<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 93<\/span><p\/>Seidel, A., Sun, Z., Kroth, H., Steinbrecher, T., Oesch, F., and Friedberg, T.<br\/>DNA-polymerase action on oligonucleotide templates from human Ha-ras proto-oncogenes containing N6-deoxyadenosine adducts derived from trans addition of (+)- and (-)-anti-benzo[c]\u00adphenanthrene-3,4-dihydrodiol 1,2-oxide at Codon 61.<br\/>Polycycl. Arom. Compds., 10 (1996) 161-170<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 92<\/span><p\/>Frank, H., Luch, A., Oesch, F., and Seidel, A.<br\/>4-[4(Dimethylamino)phenylazo]-benzoate, a new red-shifted chromophore for use in the exciton chirality method: Assignment of absolute configuration to fjord-region metabolites of dibenzo[a,l]pyrene.<br\/>Polycycl. Arom. Compds., 10 (1996) 109-116<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 91<\/span><p\/>Luch, A., Seidel, A., Glatt, H.R., Oesch, F., and Platt, K.L.<br\/>Correlation of the extent of fjord-region oxidation with DNA binding and mutagenicity of the enantiomeric 11,12-dihydrodiols of dibenzo[a,l]pyrene in vitro.<br\/>Polycycl. Arom. Compds., 10 (1996) 101-108<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 90<\/span><p\/>Ponten, I., Seidel, A., Gr\u00e4slund, A., and Jernstr\u00f6m, B.<br\/>Studies on oligonucleotides modified with the enantiomers of the anti- and syn-diastereomers of benzo[a]pyrene-7,8-dihydrodiol-9,10-epoxide.<br\/>Polycycl. Arom. Compds., 10 (1996) 93-100<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 89<\/span><p\/>Degenhardt, C., Bors, W., Seidel, A., Frank, H., and Platt, K.L.<br\/>Metabolic activation of anthanthrene: Significance of stable radicals derived from its key metabolite 3-hydroxy-anthanthrene.<br\/>Polycycl. Arom. Compds., 10 (1996) 85-92<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 88<\/span><p\/>Reindl, M., Seidel, A., Frank, H. and Platt, K.L.<br\/>Detection of reactive quinones in the metabolism of polycyclic aromatic hydrocarbons by the formation of their glutathione conjugates.<br\/>Polycycl. Arom. Compds., 10 (1996) 77-84<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 87<\/span><p\/>Jernstr\u00f6m, B., Mannervik, B., Funk, M., and Seidel, A.<br\/>Glutathione conjugation of diol epoxides of polycyclic aromatic hydrocarbons catalyzed by human glutathione transferase A1-1.<br\/>Polycycl. Arom. Compds., 10 (1996) 51-57<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 86<\/span><p\/>Jacob, J., Doehmer, J., Grimmer, G., Soballa, V., Raab, G., Seidel, A., and Greim, H. <br\/>Metabolism of phenanthrene, benz[a]anthracene, benzo[a]pyrene and benzo[c]\u00adphenanthrene by eight cDNA-expressed human and rat cytochromes.<br\/>Polycycl. Arom. Compds., 10 (1996) 1-9<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 85<\/span><p\/>Speit, G., Hanelt, S., Helbig, R., Seidel, A. and Hartmann, A.<br\/>Detection of DNA effects in human cells with the comet assay and their relevance for mutagenesis.<br\/>Toxicol. Lett., 88 (1996) 91-98<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 84<\/span><p\/>Glatt, H.R., Christoph, S., Czich, A., Pauly, K., Schwierzok, A., Seidel, A., Coughtrie, M.W.H., Doehmer, J., Falany, C.N., Phillips, D.H., Yamazoe, Y., and Bartsch, I.<br\/>Rat and human sulfotransferases expressed in Ames's Salmonella typhimurium strains and Chinese hamster V79 cells for the activation of mutagens.<br\/>Control Mechanisms of Carcinogenesis (ed's J.G. Hengstler and F. Oesch), Publishing House of the Editors: J.G. Hengstler & F. Oesch (1996) p. 98-115<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 83<\/span><p\/>Jernstr\u00f6m, B., Funk, M., Frank, H., Mannervik, B., and Seidel, A. <br\/>Glutathione tranferase A1-1 catalyzed conjugation of bay- and fjord-region diol epoxides of polycyclic aromatic hydrocarbons with glutathione.<br\/>Carcinogenesis, 17 (1996) 1491-1498<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 82<\/span><p\/>Giles, A.S., Seidel, A., and Phillips, D.H.<br\/>Covalent DNA adducts formed in mouse epidermis by benzo[g]chrysene.<br\/>Carcinogenesis, 17 (1996) 1331-1336<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 81<\/span><p\/>Windsor, S.A., Tinker, M.H., Osborne, M.R. and Seidel, A.<br\/>Studies of the binding of diol-epoxide metabolites of polycyclic aromatic hydrocarbons to DNA using electro-fluorescence polarization spectroscopy.<br\/>Carcinogenesis, 17 (1996) 605-608<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 80<\/span><p\/>Jacob, J., Raab, G., Soballa, V., Holtkamp, D., Schmalix, W., Grimmer, G., Greim, H. Doehmer, J., and Seidel, A.<br\/>Cytochrome P450-mediated activation of phenanthrene in genetically engineered V79 Chinese hamster cells.<br\/>Environ. Toxicol. Pharmacol., 1 (1996) 1-11<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 79<\/span><p\/>Pont\u00e9n, I., Seidel, A., Gr\u00e4slund, A., and Jernstr\u00f6m, B.<br\/>Characterization of adducts derived from the syn-diastereomer of benzo[a]pyrene 7,8-dihydrodiol 9,10-epoxide and the oligo\u00adnucleotide 5'-d(CCTATAGATATCC).<br\/>Chem. Res. Toxicol., 9 (1996) 188-196<\/div>\n<h2 id=\"1995\">1995<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 78<\/span><p\/>Glatt, H., Bartsch I., Czich A., Seidel A. and Falany C.N.<br\/>Salmonella strains and mammalian cells genetically engineered for expression of sulfotransferases.<br\/>Toxicol. Lett., 82-3 (1995) 829-834<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 77<\/span><p\/>Ralston, S., Seidel, A., Platt, K.L., Luch, A., and Baird, W.M.<br\/>Stereochemical selectivity of activation of dibenzo[a,l]pyrene to (-)-anti- and (+)-syn-DB[a,l]P-11,12-diol-13,14-epoxide which bind extensively to deoxyadenosine residues of DNA in the human mammary carcinoma cell line MCF-7.<br\/>Carcinogenesis, 16 (1995) 2899-2907<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 76<\/span><p\/>Sbrana, I., Puliti, A., Seidel, A., Glatt, H.R., and Turchi, G.<br\/>Induction of chromosomal aberrations and spindle disturbances in Chinese hamster epithelial liver cells in culture by pyrene and benzo[a]pyrene quinones.<br\/>Mutagenesis, 10 (1995) 505-512<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 75<\/span><p\/>Du, M.Q., Seidel, A., and Phillips, D.H.<br\/>Activating mutations in human c-Ha-ras-1 protooncogene induced by the stereoisomeric fjord-region benzo[c]chrysene-9,10-diol 13,14-epoxides.<br\/>Mol. Carcinogen., 14 (1995) 160-169<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 74<\/span><p\/>Seidel, A., Oesch, F., and Steinberg, P.<br\/>Malignant transformation of the liver tumor precursor cell line OC\/CDE 22 by the four stereoisomeric fjord-region 3,4-dihydrodiol 1,2-epoxides of benzo[c]phenanthrene.<br\/>Carcinogenesis, 16 (1995) 2111-2115<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 73<\/span><p\/>Goeptar, A.R., te Koppele, J.M., Glatt, H.R., Groot, E.J., Seidel, A., Barrenscheen, M., W\u00f6lfel, C., Doehmer, J., Vermeulen, N.P.E.<br\/>The cytotoxicity of mitomycin C and adriamycin in genetically engeneered V79 cell lines and freshly isolated hepatocytes. <br\/>Chem.-Biol. Interact., 97 (1995) 149-168<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 72<\/span><p\/>Gschaidmaier, H., Seidel, A., Burchell, B. and Bock, K.W.<br\/>Formation of mono- and diglucuronides and of other glycosides of benzo[a]pyrene-3,6-quinol by V79 cell-expressed human phenol UDP-glucuronsyltransferase of the UGT1 complex (UGT1.6 and UGT1.07).<br\/>Biochem. Pharmacol., 49 (1995) 1601-1606<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 71<\/span><p\/>Funk, M., Gath, I., Seidel, A., Oesch, F., and Platt, K.L.<br\/>Conjugation of anti-dihydrodiol epoxides of benzo[a]pyrene, chrysene, benzo[c]phenanthrene and dibenz[a,h]anthracene with glutathione catalysed by cytosol and by the mu-class glutathione transferase HTP II from rat liver.<br\/>Chem. Biol. Interact., 95 (1995) 189-201<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 70<\/span><p\/>Giles, A., Seidel, A., and Phillips, D.H.<br\/>Reactivities towards DNA of the fjord-region diol-epoxides of benzo[g]chrysene and benzo[c]phenanthrene as revealed by 32P-postlabeling. <br\/>Chem. Res. Toxicol., 8 (1995) 591 - 599<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 69<\/span><p\/>Doehmer, J, Holtkamp, D, Soballa, V., Raab, G., Schmalix, W., Seidel, A., Greim, H. and Jacob, J.<br\/>Cytochrome P450 mediated reactions studied in genetically engineered V79 Chinese hamster cells.<br\/>Pharmacogenetics, 5 (1995) S91 - S96<\/div>\n<h2 id=\"1994\">1994<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 68<\/span><p\/>Glatt, H.R., Pauly, K., Frank, H., Seidel, A., Oesch, F., Harvey, R.G., and Werle-Scheider, G.<br\/>Substance-dependent sex differences in the activation of benzylic alcohols to mutagens by hepatic sulfotransferases of the rat.<br\/>Carcinogenesis, 15 (1994) 2605-2611<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 67<\/span><p\/>Luch, A., Glatt, H.R., Platt, K.L., Oesch, F., and Seidel, A.<br\/>Synthesis and mutagenicity of the diastereomeric fjord-region 11,12-dihydrodiol 13,14-epoxides of dibenzo[a,l]pyrene.<br\/>Carcinogenesis, 15 (1994) 2507-2516<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 66<\/span><p\/>Glatt, H.R., Pauly, K., Pi\u00e9e-Staffa, Seidel, A., Hornhardt, S., and Czich, A.<br\/>Activation of promutagens by endogenous and heterologous sulfotransferases expressed in continous cell cultures.<br\/>Toxicology Lett., 72 (1994) 13-21<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 65<\/span><p\/>Glatt, H.R., Werle-Schneider, G., Enders, N., Monnerjahn, S., Pudil, J., Czich, A., Seidel, A., and Schwarz, M.<br\/>1-Hydroxymethylpyrene and its sulfuric acid ester: toxicological effects in vitro and in vivo, and metabolic aspects.<br\/>Chem.-Biol. Interact., 92 (1994) 305-319<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 64<\/span><p\/>Glatt, H.R., Werle-Schneider, G., Seidel, A., and Schwarz, M.<br\/>Initiation and promotion of enzyme-altered foci in rat liver by 1-hydroxymethylpyrene.<br\/>Polycycl. Arom. Compds., 7 (1994) 153-160<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 63<\/span><p\/>Glatt, H.R., Pudil, J., Seidel, A., and Czich, A.<br\/>Stable expression of heterologous sulfo-transferase in V79 cells: activation of primary and secondary benzylic alcohols.<br\/>Polycycl. Arom. Compds., 7 (1994) 67-74<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 62<\/span><p\/>Ralston, S.L., Lau, H.H.S., Seidel, A., Luch, A., Platt, K.L., and Baird, W.M.<br\/>Identification of dibenzo[a,l]pyrene-DNA adducts formed in cells in culture and in mouse skin.<br\/>Polycycl. Arom. Compds., 6 (1994) 199-206<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 61<\/span><p\/>Seidel, A., Luch, A., Platt, K.L., Oesch, F., and Glatt, H.R.<br\/>Activated fjord-region metabolites of dibenzo[a,l]pyrene: Synthesis and mutagenic activities of the diastereomeric syn- and anti-11,12-dihydrodiol 13,14-epoxides.<br\/>Polycycl. Arom. Compds., 6 (1994) 191-198<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 60<\/span><p\/>Glatt, H.R., Seidel, A., Oesch, F., and Gumbsch, A.<br\/>Fjord-region diol-epoxides of benzo[c]chrysene are potent inducers of micronuclei in murine bone marrow.<br\/>Mutat. Res., 309 (1994) 37-43<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 59<\/span><p\/>Post, K., Seidel, A., Platt, K. L., Oesch, F., and Klein, J.<br\/>Regiospecific oxidation of dihydrodiols and reduction of quinones by rabbit liver dihydrodiol dehydrogenase.<br\/>Chem.-Biol. Interact., 90 (1994) 157-168<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 58<\/span><p\/>Funk, M., Gath, I., Seidel, A., Platt, K. L., Oesch, F. and Zeller, H.D.<br\/>Different enzyme kinetics during the glutathione conjugation of the four stereoisomeric forms of the fjord-region diolepoxide of benzo[c]phenanthrene by the acidic rat liver glutathione S-transferase HTP II.<br\/>Biochem. Pharmacol., 47 (1994) 505-514<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 57<\/span><p\/>Ralston, S.L., Lau, H.H.S., Seidel, A., Luch, A., Platt, K.L., and Baird, W.M.<br\/>The potent carcinogen dibenzo[a,l]pyrene is metabolically activated to fjord-region 11,12-diol 13,14-epoxides in human mammary carcinoma MCF-7 cell cultures.<br\/>Cancer Res., 54 (1994) 887 - 890<\/div>\n<h2 id=\"1993\">1993<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 56<\/span><p\/>Schmalix, W.A., M\u00e4ser, H., Kiefer, F., Reen, R., Wiebel, F.J., Gonzalez, F., Seidel, A., Glatt, H.R., Greim, H., and Doehmer, J.<br\/>Stable expression of human cytochrome P450 1A1 cDNA in V79 Chinese hamster cells and metabolic activation of benzo[a]pyrene.<br\/>Eur. J. Pharmacol. - Environ. Toxicol. Pharmacol. Sec., 248 (1993) 251 - 261<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 55<\/span><p\/>Glatt, H. R., Henschler, R., Frank, H., Seidel, A., Oesch, F., Yang, C. X., Abu-Shqara, E., and Harvey, R. G.<br\/>Sulfotransferase-mediated mutagenicity of 1-hydroxymethyl-pyrene and 4H-cyclopenta[def]chrysen-4-ol and its enhancement by chloride anions.<br\/>Carcinogenesis, 14 (1993) 599-602<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 54<\/span><p\/>Steinbrecher, T., Becker, A, Stezowski, J.J., Oesch, F., and Seidel, A.<br\/>Synthesis of oligo\u00addeoxynucleotides containing diastereomeric diol epoxide-N6-deoxy-adenosine adducts of polycyclic aromatic hydrocarbons.<br\/>Tetrahedron Lett., 34 (1993) 1773-1774<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 53<\/span><p\/>Jernstr\u00f6m, B., Funk, M., Steinbrecher, T., and Seidel, A.<br\/>Glutathione transferase catalyzed conjugation of diol epoxides derived from polycyclic aromatic hydrocarbons with glutathione.<br\/>Polycycl. Arom. Compds., 3 (1993) 213 - 219<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 52<\/span><p\/>Pfau, W., Lecoq, S., Hughes, N.C., Seidel, A., Platt, K.L., Grover, P.L., and Phillips, D.H. <br\/>Formation of DNA adducts by 1-hydroxy-methylpyrene in liver cells in vivo and in vitro. <br\/>Postlabelling Methods for Detection of DNA Adducts, IARC Scientific Publication No. 124, IARC, Lyon (France) (1993) pp 233 - 242<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 51<\/span><p\/>Monnerjahn, S., Seidel, A., Steinberg, P., Oesch, F., Hinz, M., Stezowski, J.J., Hewer, A., Phillips, D.H., and Glatt, H.R.<br\/>Formation of DNA adducts by 1-hydroxymethylpyrene in liver cells in vivo and in vitro.<br\/>Postlabelling Methods for Detection of DNA Adducts, IARC Scientific Publication No. 124, IARC, Lyon (France) (1993) pp 189 - 193<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 50<\/span><p\/>Glatt, H. R., Pauly, K., W\u00f6lfel, C., Dogra, S., Seidel, A., Lee, H., Harvey, R.G., Oesch, F., and Doehmer, J.<br\/>Stable expression of heterologous cytochromes P450 in V79 cells: mutagenicity studies with polycyclic aromatic hydrocarbons.<br\/>Polycyclic Aromatic Compounds: Synthesis, Properties, Analytical Measurements, Occurrence and Biological Effects (P. Garrigues and M. Lamotte, eds.) Gordon and Breach Science Publishers, Yverdon (Switzerland) (1993) pp 1167 - 1174<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 49<\/span><p\/>Lecoq, S., Platt, K.L., Seidel, A., Oesch, F., Phillips, D.H., and Grover, P.L.<br\/>Comparisons of the metabolic activation of dibenz[a,h]anthracene and picene using 32P-postlabelling.<br\/>Polycyclic Aromatic Compounds: Synthesis, Properties, Analytical Measurements, Occurrence and Biological Effects (P. Garrigues and M. Lamotte, eds.) Gordon and Breach Science Publishers, Yverdon (Switzerland) (1993) pp 921 - 928<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 48<\/span><p\/>Enders, N., Seidel, A., Monnerjahn, S. and Glatt, H.R.<br\/>Synthesis of 11 benzylic sulfate esters and their bacterial mutagenicity in dependence of the presence of chloride, bromide and acetate anions.<br\/>Polycyclic Aromatic Compounds: Synthesis, Properties, Analytical Measurements, Occurrence and Biological Effects (P. Garrigues and M. Lamotte, eds.) (Supplement to Polycyclic Aromatic Compounds, Vol. 3), Gordon and Breach Science Publishers, Yverdon (Swit (1993) pp 887 - 894<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 47<\/span><p\/>Glatt, H.R., Wameling, C., Elsberg, S., Thomas, H., Marquardt, H., Hewer, A., Phillips, D.H., Oesch, F., and Seidel, A.<br\/>\"Reverse\" diol-epoxides of chrysene: genotoxicity characteristics.<br\/>Polycyclic Aromatic Compounds: Synthesis, Properties, Analytical Measurements, Occurrence and Biological Effects (P. Garrigues and M. Lamotte, eds.) Gordon and Breach Science Publishers, Yverdon (Switzerland) (1993) pp 879 - 886<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 46<\/span><p\/>Johannes, A., Schmoldt, A., Seidel, A., and Glatt, H.R.<br\/>Sulfate conjugation of various hydroxy-PAH by rat liver sulfotransferases.<br\/>Polycyclic Aromatic Compounds: Synthesis, Properties, Analytical Measurements, Occurrence and Biological Effects (P. Garrigues and M. Lamotte, eds.) Gordon and Breach Science Publishers, Yverdon (Switzerland) (1993) pp 703 - 710<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 45<\/span><p\/>Augustin, C., Schmoldt, A., Glatt, H.R., and Seidel, A.<br\/>Various UDP-glucuronosyl-transferases involved in regiospecific conjugations of hydroxy-PAH.<br\/>Polycyclic Aromatic Compounds: Synthesis, Properties, Analytical Measurements, Occurrence and Biological Effects (P. Garrigues and M. Lamotte, eds.) Gordon and Breach Science Publishers, Yverdon (Switzerland) (1993) pp 687 - 694<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 44<\/span><p\/>Steinbrecher, T., Wameling, C., Oesch, F., and Seidel, A.<br\/>Synthesis of polycyclic aromatic hydrocarbon adducts attached to the exocyclic amino group of 2'-deoxyguanosine via nucleophilic substitution.<br\/>Polycyclic Aromatic Compounds: Synthesis, Properties, Analytical Measurements, Occurrence and Biological Effects (P. Garrigues and M. Lamotte, eds.) Gordon and Breach Science Publishers, Yverdon (Switzerland) (1993) pp 223 - 230<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 43<\/span><p\/>Funk, M., Frank, H., Platt, K. L., Oesch, F., and Seidel, A.<br\/>Synthesis and characterization of glutathione conjugates of diastereomeric bay- and fjord-region dihydrodiol epoxides.<br\/>Polycyclic Aromatic Compounds: Synthesis, Properties, Analytical Measurements, Occurrence and Biological Effects (P. Garrigues and M. Lamotte, eds.) Gordon and Breach Science Publishers, Yverdon (Switzerland) (1993) pp 207 - 214<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 42<\/span><p\/>Wameling, C., Glatt, H.R., Oesch, F., and Seidel, A.<br\/>Stereospecific synthesis of the diastereomeric \"reverse\" dihydrodiol epoxides of chrysene and picene.<br\/>Polycyclic Aromatic Compounds: Synthesis, Properties, Analytical Measurements, Occurrence and Biological Effects (P. Garrigues andM. Lamotte, eds.) Gordon and Breach Science Publishers, Yverdon (Switzerland) (1993) pp 191 - 198<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 41<\/span><p\/>Steinbrecher, T., Wameling, C., Oesch, F., and Seidel, A.<br\/>Activation of the C2 position of purine by the trifluoromethanesulfonate group: synthesis of N2-alkylated deoxyguanosines. <br\/>Angew. Chem. Int. Ed. Engl., 32 (1993) 404-406<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 40<\/span><p\/>Steinbrecher, T., Wameling, C., Oesch, F., and Seidel, A.<br\/>Die Trifluormethan- sulfonatfunktion als neue Aktivierung der C-2-Position am Purin: Synthese von N2-alkylierten Deoxyguanosinen.<br\/>Angew. Chem., 105 (1993) 408-410<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 39<\/span><p\/>Glatt, H.R., Wameling, C., Elsberg S., Thomas H., Marquardt H., Hewer A.,Phillips D.H., Oesch F., and Seidel, A.<br\/>Genotoxicity characteristics of prebay-region diol-epoxides of chrysene.<br\/>Carcinogenesis, 14 (1993) 11-19<\/div>\n<h2 id=\"1992\">1992<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 38<\/span><p\/>Bock, K.W., Gschaidmeier, H., Seidel, A., S. Baird, and Burchell, B.<br\/>Mono- and diglucuronide formation of chrysene and benzo[a]pyrene phenols by 3-methylcholanthrene-inducible phenol UDP-glucuronosyltransferase (UGT1A1).<br\/>Mol. Pharmacol., 42 (1992) 613-618<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 37<\/span><p\/>Jernstr\u00f6m, B., Seidel, A., Funk, M., Oesch, F., and Mannervik, B.<br\/>Glutathione conjugation of trans-3,4-dihydroxy 1,2-epoxy 1,2,3,4-tetrahydrobenzo[c]phenanthrene isomers by human glutathione transferases.<br\/>Carcinogenesis, 13 (1992) 1549-1555<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 36<\/span><p\/>W\u00f6lfel, C., Heinrich-Hirsch, B., Schulz-Schalge, T., Seidel, A., Frank, H., Ramp, U., W\u00e4chter, F., Wiebel, F. J., Gonzalez, F., Greim, H., and Doehmer, J.<br\/>Genetically engineered V79 chinese hamster cells for stable expression of human cytochrome P450IA2.<br\/>Eur. J. Pharmacol. - Environ. Toxicol. Pharmacol. Sec., 228 (1992) 95-102<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 35<\/span><p\/>Klein, J., Post, K., Seidel, A., Frank, H., Oesch, F., and Platt, K.L.<br\/>Quinone reduction and redox cycling catalysezed by purified rat liver dihydrodiol\/3a-hydroxysteroid dehydrogenase.<br\/>Biochem. Pharmacol., 44 (1992) 341-349<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 34<\/span><p\/>Doehmer, J., Janssens, C., Dogra, S., Doehmer, C., Seidel, A., Platt, K.-L., Oesch, F., and Glatt, H.R.<br\/>Application of stable V79 derived cell lines expressing rat cytochromes P450IAI, IA2, and IIB1.<br\/>Xenobiotica, 22 (1992) 1093-1099<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 33<\/span><p\/>Phillips, D.H., Hewer, A., Seidel, A., Steinbrecher, T., Schrode, R., Oesch, F., and Glatt, H.R.<br\/>Relationship between mutagenicity and DNA adduct formation in mammalian cells for fjord- and bay-region diol-epoxides of polycyclic aromatic hydrocarbons.<br\/>Chem.-Biol. Interactions, 80 (1992) 177-186<\/div>\n<h2 id=\"1991\">1991<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 32<\/span><p\/>Klein, J., Seidel, A., Frank, H., Oesch, F., and Platt, K.L.<br\/>Regiospecific oxidation of polycyclic aromatic dihydrodiols by rat liver dihydrodiol dehydrogenase.<br\/>Chem.-Biol. Interactions, 79 (1991) 287-303<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 31<\/span><p\/>Doehmer, J., Dogra, S., Janssens, C., Edigkaufer, M., Seidel, A., Glatt, H.R., Platt, K.-L., and Oesch, F.<br\/>Die gentechnologische Konstruktion von V79 Chinesischen Hamsterzellen zur stabilen Expression von Fremdstoff-metabolisierenden Enzymen und ihre Anwendung in Metabolismus- und Mutagenit\u00e4ts-Studien von Pharmaka und anderen Fremdstoffen. <br\/>Alternativen zu Tierexperimenten, 8 (1991) 52 - 64<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 30<\/span><p\/>Seidel, A., Bochnitschek, W., Glatt, H.R., Hodgson, R.M., Grover, P.L., and Oesch, F. <br\/>Activated Metabolites of chrysene: Synthesis of 9-Hydroxychrysene-1,2-diol and the corresponding bay-region syn- and anti-triol-epoxides.<br\/>Polynuclear Aromatic Hydrocarbons: Measurements, Means and Metabolism (ed's. M. Cooke, K. Loening and J. Meritt), Battelle Press, Columbus, OH (1991) pp 801 - 817<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 29<\/span><p\/>Ludewig, G., Dogra, S., Seidel, A., Setiabudi, F., Oesch, F., and Glatt, H.R.<br\/>Quinones derived from polycyclic aromatic hydrocarbons: Induction of diverse mutagenic and genotoxic effects in mammalian cells.<br\/>Polynuclear Aromatic Hydrocarbons: Measurements, Means and Metabolism (ed's. M. Cooke, K. Loening and J. Meritt), Battelle Press, Columbus, OH (1991) pp 545 - 556<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 28<\/span><p\/>Glatt, H. R., Seidel, A., Schrode, R., Ribeiro, O., Kirkby, C. A., Hirom, P. C., and Oesch, F.<br\/>3-Hydroxybenzo[a]pyrene-7,8-dihydrodiol compared with benzo[a]\u00adpyrene-7,8-dihydrodiol and 3-hydroxybenzo[a]pyrene with regard to muta-genicity.<br\/>Polynuclear Aromatic Hydrocarbons: Measurements, Means and Metabolism (ed's. M. Cooke, K. Loening and J. Meritt), Battelle Press, Columbus, OH (1991) pp 357 - 368<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 27<\/span><p\/>Glatt, H.R., Pi\u00e9e A., Pauly K., Steinbrecher, T., Schrode R., Oesch, F. and Seidel, A.<br\/>Fjord- and bay-region diol-epoxides investigated on stability, SOS induction in Escherichia coli, and mutagenicity in Salmonella typhimurium and mammalian cells.<br\/>Cancer Res, 51 (1991) 1659-1667<\/div>\n<h2 id=\"1990\">1990<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 26<\/span><p\/>Hradec, J., Seidel, A., Platt, K.L., Glatt, H.R., Oesch, F., and Koblyakov, V.<br\/>The Initiator tRNA acceptance assay as a short-term test for carcinogens. 6. Results with 78 polycyclic aromatic compounds.<br\/>Carcinogenesis, 11 (1990) 1921-1926<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 25<\/span><p\/>Steinberg, P., Schlemper, B., Molitor, E., Platt, K.L., Seidel, A., and Oesch, F.<br\/>Rat liver Kupffer and endothelial cell-mediated mutagenicity of polycyclic aromatic hydrocarbons and aflatoxin B1.<br\/>Environ. Health Perspect., 88 (1990) 71-76<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 24<\/span><p\/>Doehmer, J., Seidel, A., Oesch, F., and Glatt, H.R.<br\/>Genetically-engineered V79 chinese hamster cells metabolically activate the cytostatic drugs cyclophosphamide and ifosfamide.<br\/>Environ. Health Perspect., 88 (1990) 63-65<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 23<\/span><p\/>Glatt, H.R., Henschler, R., Phillips, D. H., Blake, J. W., Steinberg, P., Seidel, A., and Oesch, F.<br\/>Sulfotransferase-mediated chlorination of 1-hydroxymethylpyrene to a mutagen capable of penetrating into indicator cells.<br\/>Environ. Health Perspect., 88 (1990) 43-48<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 22<\/span><p\/>Masento, M.S., Taylor, G.W., Watson, D., Seidel, A., Bochnitschek, W., Oesch, F., and Grover, P.L.<br\/>Metabolism of 3-hydroxychrysene by rat liver microsomal preparations.<br\/>Chem.-Biol. Interactions, 74 (1990) 163-178<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 21<\/span><p\/>Dogra, S., Doehmer, J., Glatt, H.R., Siegert, P., Friedberg, T., Seidel, A., and Oesch, F.<br\/>Stable expression of rat P450IA1 cDNA in V79 Chinese hamster cells and their use in mutagenicity testing.<br\/>Mol. Pharmacol., 37 (1990) 608-613<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 20<\/span><p\/>Seidel, A., Glatt, H.R., Oesch, F., and Garrigues, P.<br\/>2,9-Dimethylpicene: Synthesis, mutagenic activity, and identification in natural samples.<br\/>Polycycl. Arom. Compds., 1 (1990) 3-14<\/div>\n<h2 id=\"1989\">1989<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 19<\/span><p\/>Knepper T., Lenhardt, S., Przybylski, M., Bosk, C., Platt, K.L., Seidel, A., and Oesch, F.<br\/>Identification and structural characterization of mono- and bis- glutathionyl conjugates from polyaromatic quinone metabolites.<br\/>Advances in Mass Spectrometry (ed. P. Longevialle), Vol. 11B (Proceedings of the 11th International Mass Spectrometry Conference held at Bordeaux 29. August - 2. September 1988), Heydon & Son, London (1989) pp 1398 - 1399<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 18<\/span><p\/>Doehmer, J., Dogra, S., Edigkaufer, M., Molitor, E., Siegert, P., Friedberg, T., Glatt, H.R., Platt, K.L., Seidel, A., Thomas, H., and Oesch, F.<br\/>Introduction of cytochrome P-450 genes into V79 Chinese hamster cells to generate new mutagenicity test systems.<br\/>Arch. Toxicol., Suppl., 13 (1989) 164 - 168<\/div>\n<h2 id=\"1987\">1988<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 17<\/span><p\/>Glatt, H.R., Hirom, P.C., Kirkby, C.A., Ribeiro, O., Seidel, A., and Oesch, F.<br\/>Complex metabolic activation pathways of polycyclic aromatic hydrocarbons: 3-Hydroxy-trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene as a proximate mutagen of 3-hydroxybenzo[a]\u00adpyrene.<br\/>Chemical Carcinogenesis (eds. F. Feo, P. Pani, A. Columbano, and R. Garcea), Plenum Publishing Corporation, New York (1988) pp 37 - 44<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 16<\/span><p\/>Platt, K.L., Petrovic, P., Seidel, A., Beermann, D., and Oesch, F.<br\/>Microsomal metabolism of picene.<br\/>Chem.-Biol. Interactions, 66 (1988) 157-175<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 15<\/span><p\/>Heidmann, M., Fonrobert, P., Przybylski, M., Platt, K.L., Seidel, A., and Oesch, F. <br\/>Conjugation reactions of polyaromatic quinones to mono- and bisglutathionyl adducts: Direct analysis by fast atom bombardment mass spectrometry.<br\/>Biomed. Environm. Mass Spectrometry, 15 (1988) 329-332<\/div>\n<h2 id=\"1986\">1987<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 14<\/span><p\/>Hodgson, R.M., Seidel, A., Bochnitschek, W., Glatt, H.R., Oesch, F., and Grover, P. L. <br\/>Formation of glutathion conjugates from chrysene diol- and triol-epoxides: Evidence for the further metabolism of the \u201cbay-region\u201d diol-epoxide of chrysene to a triol-epoxide. In: Glutathione S -Transferases and Carcinogenesis (eds. T.J. Mantle, C.B. Pickett, and J.D. Hayes)<br\/>Taylor & Francis, London (1987) pp 239 - 243<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 13<\/span><p\/>Glatt, H.R., Seidel, A., Ribeiro, O., Kirkby, C., Hirom, P., and Oesch, F.<br\/>Metabolic activation to a mutagen of 3-hydroxy-trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene, a secondary metabolite of benzo[a]pyrene.<br\/>Carcinogenesis, 8 (1987) 1621-1627<\/div>\n<h2 id=\"1985\">1986<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 12<\/span><p\/>Glatt, H.R., Henschler, R., Klein, J., Ludewig, G., Martin\u00e9, U., Pauly, K., Pi\u00e9e, A., Platt, K.L., Seidel, A., Setiabudi, S. and Utesch, D.<br\/>Multiple activation pathways of both benzene and polycyclic aromatic hydrocarbons leading to products with varying cytotoxic and genotoxic characteristics. In: Primary Changes and Control Factors in Carcinogenesis (eds. T. Friedberg, and F. Oesch)<br\/>Deutscher Fach-schriften-Verlag, Wiesbaden (Germany) (1986) pp 55 - 59<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 11<\/span><p\/>Hodgson, R. M., Weston, A., Seidel, A., Bochnitschek, W., Glatt, H. R., Oesch, F., and Grover, P. L.<br\/>Metabolism of chrysene to triols and a triol-epoxide in mouse skin and rat liver preparations.<br\/>Polynuclear Aromatic Hydrocarbons: Chemistry, Characterization and Carcinogenesis (eds. M. Cooke, and A. J. Dennis), Battelle Press, Columbus, OH (1986) pp. 387 - 399<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 10<\/span><p\/>Glatt, H. R., Seidel, A., Bochnitschek, W., Marquardt, H., Marquardt, H., Hodgson, R. M., Grover, P. L., and Oesch, F.<br\/>Mutagenicity in bacterial and mammalian cells of diol-epoxides, triol-epoxides and other metabolites of chrysene.<br\/>Polynuclear Aromatic Hydrocarbons: Chemistry, Characterization and Carcinogenesis (eds. M. Cooke , and A. J. Dennis), Battelle Press, Columbus, OH (1986) pp. 343 - 358<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 9<\/span><p\/>Hodgson, R.M., Seidel, A., Bochnitschek, W., Glatt, H.R., Oesch, F., and Grover, P.L. <br\/>Metabolism of the bay-region diol-epoxide of chrysene to a triol-epoxide and the enzyme-catalysed conjugation of these epoxides with glutathione.<br\/>Carcinogenesis, 7 (1986) 2095-2098<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 8<\/span><p\/>Phillips, D.H., Glatt, H.R., Seidel, A., Bochnitschek, W., Oesch, F., and Grover, P.L.<br\/>Mutagenic potential and DNA adducts formed by diol-epoxides, triol-epoxides and K-region epoxides of chrysene in mammalian cells.<br\/>Carcinogenesis, 7 (1986) 1739-1743<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 7<\/span><p\/>Glatt, H.R., Seidel, A., Bochnitschek, W., Marquardt, H., Marquardt, H., Hodgson, R.M., Grover, P.L., and Oesch, F.<br\/>Mutagenic and cell-transforming activities of triol-epoxides as compared to other chrysene metabolites.<br\/>Cancer Res., 46 (1986) 4556-4565<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 6<\/span><p\/>Wermuth, B., Platt, K. L., Seidel, A., and Oesch, F.<br\/>Carbonyl reductase provides the enzymatic basis of quinone detoxication in man. Biochem.<br\/>Pharmacol., 35 (1986) 1277-1282<\/div>\n<h2 id=\"1985\">1985<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 5<\/span><p\/>Hodgson, R. M., Seidel, A., Bochnitschek, W., Glatt, H.R., Oesch, F., and Grover, P.L.<br\/>The formation of 9-hydroxychrysene-1,2-diol as an intermediate in the metabolic activation of chrysene.<br\/>Carcinogenesis, 6 (1985) 135-139<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 4<\/span><p\/>Bochnitschek, W., Seidel, A., Kunz, H., and Oesch, F.<br\/><a href=\"ddd'ggg\" target=\"_blank\">Reactive metabolites of carcinogenic polycyclic hydrocarbons: Synthesis and trapping reaction of 9-hydroxybenzo[a]pyrene  4,5-oxide<\/a><br\/>Angew. Chem. Int. Ed. Engl., 24 (1985) 699-700<\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 3<\/span><p\/>Bochnitschek, W., Seidel, A., Kunz, H., and Oesch, F.<br\/>Reaktive Metabolite cancerogener polycyclischer Kohlenwasserstoffe: Synthese und Abfangreaktion von 9-Hydroxy-benzo[a]pyren-4,5-oxid<br\/>, 97 (1985) 703-704<\/div>\n<h2 id=\"1985\">1984<\/h2>\n<div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 2<\/span><p\/>Oesch, F., Glatt, H. R., Vogel, K., Seidel, A., Petrovic, P., and Platt, K. L.<br\/>Dihydrodiol dehydrogenase: A new level of control by both sequestration of proximate and inactivation of ultimate carcinogens.<br\/>Biochemical Basis of Chemical Carcinogenesis (eds. H. Greim, R. Jung, M. Kramer, H. Marquardt, and F. Oesch) Raven Press, New York, pp. 23 - 31 (1984) <\/div><div style=\"width: 90%;\n\t\t\t\t\t\t\tbackground-color: #FEFEFE;\n\t\t\t\t\t\t\t-webkit-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-moz-box-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\tbox-shadow: 0px 0px 3px 1px rgba(186,186,186,0.72);\n\t\t\t\t\t\t\t-webkit-border-radius: 2px;\n\t\t\t\t\t\t\t-moz-border-radius: 2px;\n\t\t\t\t\t\t\tborder-radius: 2px;\n\t\t\t\t\t\t\ttext-align: left;\n\t\t\t\t\t\t\tpadding: 10px 10px 10px 20px;\n\t\t\t\t\t\t\ttext-indent: -10px;\n\t\t\t\t\t\t\tmargin: 10px 10px 10px 10px;\"><span style=\"color: #C0C0C0;\">Nr. 1<\/span><p\/>Beermann, D., Petrovic, P., Seidel, A., and Oesch, F.<br\/>A facile microsynthesis of 14C-labelled picene.<br\/>J. Labelled Compds. Radiopharm., 21 (1984) 781-787<\/div>\n","protected":false},"excerpt":{"rendered":"[publication functionname='readPublicationYears']\n<h2 id=\"2016\">2016<\/h2>\n[publication functionname='readAllPublicationsYear' functionparams='2016']\n<h2 id=\"2015\">2015<\/h2>\n<p>[publication functionname=&#8217;readAllPublicationsYear&#8216; functionpar&#8230;<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-templates\/full-width.php","meta":{"footnotes":""},"class_list":["post-67","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.biu-grimmer.de\/institute\/index.php?rest_route=\/wp\/v2\/pages\/67","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.biu-grimmer.de\/institute\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.biu-grimmer.de\/institute\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.biu-grimmer.de\/institute\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.biu-grimmer.de\/institute\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=67"}],"version-history":[{"count":8,"href":"https:\/\/www.biu-grimmer.de\/institute\/index.php?rest_route=\/wp\/v2\/pages\/67\/revisions"}],"predecessor-version":[{"id":274,"href":"https:\/\/www.biu-grimmer.de\/institute\/index.php?rest_route=\/wp\/v2\/pages\/67\/revisions\/274"}],"wp:attachment":[{"href":"https:\/\/www.biu-grimmer.de\/institute\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=67"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}