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Biochemical Pharmacology|December 1, 1987
Differential induction of human liver UDP-glucuronosyltransferase activities by phenobarbital-type inducersK W Bock, B S Bock-HennigArchives of Toxicology|September 1, 1982
Activating and inactivating reactions controlling 2-naphthylamine mutagenicityB S Bock-Hennig, D Ullrich, K W BockMolecular Pharmacology|April 1, 1985
Protection against toxic redox cycles between benzo(a)pyrene-3,6-quinone and its quinol by 3-methylcholanthrene-inducible formation of the quinol mono- and diglucuronideW Lilienblum, B S Bock-Hennig, K W BockXenobiotica; the Fate of Foreign Compounds in Biological Systems|November 1, 1990
Induction of drug-metabolizing enzymes by xenobioticsK W Bock, H P Lipp, B S Bock-HennigCarcinogenesis|August 1, 1994
Glucuronidation of carcinogenic arylamines and their N-hydroxy derivatives by rat and human phenol UDP-glucuronosyltransferase of the UGT1 gene complexA Orzechowski, D Schrenk, B S Bock-Hennig, et al.Chemico-Biological Interactions|August 1, 1981
Release of mutagenic metabolites of benzo[a]pyrene from the perfused rat liver after inhibition of glucuronidation and sulfation by salicylamideK W Bock, B S Bock-Hennig, W Lilienblum, et al.Toxicology|April 27, 2000
Density-dependent growth of normal and nodular hepatocytesK W Bock, H Gschaidmeier, B S Bock-Hennig, et al.Drug Metabolism Reviews|May 21, 1999
Functions and transcriptional regulation of PAH-inducible human UDP-glucuronosyltransferasesK W Bock, H Gschaidmeier, H Heel, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|April 30, 1999
Induction of human UDP glucuronosyltransferases (UGT1A6, UGT1A9, and UGT2B7) by t-butylhydroquinone and 2,3,7,8-tetrachlorodibenzo-p-dioxin in Caco-2 cellsP A Münzel, S Schmohl, H Heel, et al.Pageof 1