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Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 1, 1996
Participation of cytochromes P4502B and P4503A in cocaine toxicity in rat hepatocytesT S Poet, C A McQueen, J R Halpert
Biochimica Et Biophysica Acta|April 4, 1997
Functional interaction between amino-acid residues 242 and 290 in cytochromes P-450 2B1 and 2B11G R Harlow, Y A He, J R Halpert
Chemical Research in Toxicology|November 20, 2002
Substrate routes to the buried active site may vary among cytochromes P450: mutagenesis of the F-G region in P450 2B1Emily E Scott, You Qun He, James R Halpert
Biochimica Et Biophysica Acta|May 18, 1994
Epoxidation of arachidonic acid as an active-site probe of cytochrome P-450 2B isoformsR M Laethem, J R Halpert, D R Koop
Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 1, 1987
Selective inactivation by chloramphenicol of the major phenobarbital-inducible isozyme of dog liver cytochrome P-450P J Ciaccio, D B Duignan, J R Halpert
Journal of Biomolecular Structure & Dynamics|June 8, 2012
Application of 3-Dimensional Homology Modeling of Cytochrome P450 2B1 for Interpretation of Site-Directed Mutagenesis ResultsGrazyna D Szklarz, Rick L Ornstein, James R Halpert
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 1, 1995
Selectivity and kinetics of inactivation of rabbit hepatic cytochromes P450 2B4 and 2B5 by N-aralkylated derivatives of 1-aminobenzotriazoleS W Grimm, J R Bend, J R Halpert
Biochemistry|November 7, 1995
Site-directed mutagenesis as a tool for molecular modeling of cytochrome P450 2B1G D Szklarz, Y A He, J R Halpert
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