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Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 1, 1992
Purification and characterization of a cytochrome P-450 isozyme catalyzing bunitrolol 4-hydroxylation in liver microsomes of male ratsT Suzuki, S Narimatsu, S Fujita, et al.Biochemical Pharmacology|April 26, 1996
Multiple forms of human P450 expressed in Saccharomyces cerevisiae. Systematic characterization and comparison with those of the ratS Imaoka, T Yamada, T Hiroi, et al.Chemical & Pharmaceutical Bulletin|May 1, 1990
Inhibition of hepatic microsomal cytochrome P450 by cannabidiol in adult male ratsS Narimatsu, K Watanabe, T Matsunaga, et al.Toxicologic Pathology|November 7, 2001
Comparison of the levels of enzymes involved in drug metabolism between transgenic or gene-knockout and the parental miceN Ariyoshi, S Imaoka, K Nakayama, et al.Environmental Toxicology and Pharmacology|July 26, 2011
Strain differences in age-associated change in testosterone 6β-hydroxylation in Wistar and Dark Agouti ratsY Maeda, K Morita, T Tasaki, et al.FEBS Letters|July 1, 1999
Isoforms of cytochrome P450 on organic nitrate-derived nitric oxide release in human heart vesselsY Minamiyama, S Takemura, T Akiyama, et al.Journal of Hepatology|July 16, 1999
Hepatic cytochrome P450 is directly inactivated by nitric oxide, not by inflammatory cytokines, in the early phase of endotoxemiaS Takemura, Y Minamiyama, S Imaoka, et al.The Pharmacogenomics Journal|March 23, 2002
CYP2C9*3 influences the metabolism and the drug-interaction of candesartan in vitroT Hanatani, T Fukuda, M Ikeda, et al.Molecular Pharmacology|April 1, 1991
Ascorbic acid deficiency decreases specific forms of cytochrome P-450 in liver microsomes of guinea pigsY Kanazawa, M Kitada, T Mori, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 1, 1992
Cytochrome P-450 isozymes involved in the oxidative metabolism of delta 9-tetrahydrocannabinol by liver microsomes of adult female ratsS Narimatsu, K Watanabe, T Matsunaga, et al.Pageof 18