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Cancer Research|May 1, 1996
Treatment of human brain tumor xenografts with O6-benzyl-2'-deoxyguanosine and BCNUS C Schold, D M Kokkinakis, J L Rudy, et al.Carcinogenesis|December 1, 1991
Comparison of the inactivation of mammalian and bacterial O6-alkylguanine-DNA alkyltransferases by O6-benzylguanine and O6-methylguanineM E Dolan, A E Pegg, L L Dumenco, et al.Biochemical Pharmacology|October 26, 1995
Human liver oxidative metabolism of O6-benzylguanineS K Roy, K R Korzekwa, F J Gonzalez, et al.Cancer Chemotherapy and Pharmacology|February 28, 2001
Inactivation of O6-alkylguanine-DNA alkyltransferase by 8-substituted O6-benzylguanine analogs in miceR B Ewesuedo, L R Wilson, H S Friedman, et al.Proceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Mouse Mos protooncogene product is present and functions during oogenesisR S Paules, R Buccione, R C Moschel, et al.Cancer Research|April 1, 1979
Comparison of metabolism-mediated binding to DNA of 7-hydroxymethyl-12-methylbenz(a)anthracene and 7, 12-dimethylbenz(a)anthraceneA Dipple, J E Tomaszewski, R C Moschel, et al.The Journal of Pharmacology and Experimental Therapeutics|February 22, 2001
Inactivation of human O(6)-alkylguanine-DNA alkyltransferase by modified oligodeoxyribonucleotides containing O(6)-benzylguanineA E Pegg, K Goodtzova, N A Loktionova, et al.Journal of Medicinal Chemistry|January 20, 1995
8-Substituted O6-benzylguanine, substituted 6(4)-(benzyloxy)pyrimidine, and related derivatives as inactivators of human O6-alkylguanine-DNA alkyltransferaseM Y Chae, K Swenn, S Kanugula, et al.Carcinogenesis|January 1, 1982
X-ray crystallographic proof of electrophilic attack at the pyrimidine/imidazole ring junction in guanosineH L Carrell, D E Zacharias, J P Glusker, et al.Journal of Medicinal Chemistry|February 4, 1994
Substituted O6-benzylguanine derivatives and their inactivation of human O6-alkylguanine-DNA alkyltransferaseM Y Chae, M G McDougall, M E Dolan, et al.Pageof 7