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Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 20, 2000
Concurrent flavin-containing monooxygenase down-regulation and cytochrome P-450 induction by dietary indoles in rat: implications for drug-drug interactionS Katchamart, D M Stresser, S S Dehal, et al.Toxicology and Applied Pharmacology|August 1, 1997
Influence of beta-naphthoflavone and methoxychlor pretreatment on the biotransformation and estrogenic activity of methoxychlor in channel catfish (Ictalurus punctatus)D Schlenk, D M Stresser, J C McCants, et al.Annals of the New York Academy of Sciences|November 18, 2000
Fluorometric high-throughput screening for inhibitors of cytochrome P450V P Miller, D M Stresser, A P Blanchard, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 1, 1994
Indole-3-carbinol induces a rat liver glutathione transferase subunit (Yc2) with high activity toward aflatoxin B1 exo-epoxide. Association with reduced levels of hepatic aflatoxin-DNA adducts in vivoD M Stresser, D E Williams, L I McLellan, et al.The Journal of Pharmacology and Experimental Therapeutics|March 1, 1995
Tissue-specific expression of flavin-containing monooxygenase (FMO) forms 1 and 2 in the rabbitS E Shehin-Johnson, D E Williams, S Larsen-Su, et al.Life Sciences|November 26, 1999
Effects of ginseng components on c-DNA-expressed cytochrome P450 enzyme catalytic activityG L Henderson, M R Harkey, M E Gershwin, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 30, 2000
Substrate-dependent modulation of CYP3A4 catalytic activity: analysis of 27 test compounds with four fluorometric substratesD M Stresser, A P Blanchard, S D Turner, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 15, 2001
The use of 3-[2-(N,N-diethyl-N-methylammonium)ethyl]-7-methoxy-4-methylcoumarin (AMMC) as a specific CYP2D6 probe in human liver microsomesN Chauret, B Dobbs, R L Lackman, et al.Xenobiotica; the Fate of Foreign Compounds in Biological Systems|March 4, 2009
Validation of cytochrome P450 time-dependent inhibition assays: a two-time point IC50 shift approach facilitates kinact assay designE S Perloff, A K Mason, S S Dehal, et al.Pageof 2