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Kenneth E Thummel

Showing results (21-30 of 159) with videos related to

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Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 21, 2004
Differences in the inhibition of cytochromes P450 3A4 and 3A5 by metabolite-inhibitor complex-forming drugsDonavon J McConn, Yvonne S Lin, Kyle Allen, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 10, 2004
Role of itraconazole metabolites in CYP3A4 inhibitionNina Isoherranen, Kent L Kunze, Kyle E Allen, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 20, 2007
Cytochrome P450 enzymes and transporters induced by anti-human immunodeficiency virus protease inhibitors in human hepatocytes: implications for predicting clinical drug interactionsVaishali Dixit, Niresh Hariparsad, Fang Li, et al.
Biochemical Pharmacology|June 14, 2006
Selective induction of intestinal CYP3A23 by 1alpha,25-dihydroxyvitamin D3 in ratsYang Xu, Kazunori Iwanaga, Changcheng Zhou, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 18, 2006
Stereochemical aspects of itraconazole metabolism in vitro and in vivoKent L Kunze, Wendel L Nelson, Evan D Kharasch, et al.
American Journal of Physiology. Renal Physiology|July 20, 2019
Renal secretion of hydrochlorothiazide involves organic anion transporter 1/3, organic cation transporter 2, and multidrug and toxin extrusion protein 2-KJia Yin, David J Wagner, Bhagwat Prasad, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 12, 2008
Intestinal human colon adenocarcinoma cell line LS180 is an excellent model to study pregnane X receptor, but not constitutive androstane receptor, mediated CYP3A4 and multidrug resistance transporter 1 induction: studies with anti-human immunodeficiency virus protease inhibitorsAnshul Gupta, Ganesh M Mugundu, Pankaj B Desai, et al.
Clinical and Translational Science|September 17, 2019
Tissue Chips in Space-Challenges and OpportunitiesCatherine K Yeung, Paul Koenig, Stefanie Countryman, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 17, 2021
Sources of Interindividual VariabilityYvonne S Lin, Kenneth E Thummel, Brice D Thompson, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 28, 2020
Modulation of Major Human Liver Microsomal Cytochromes P450 by Component Alkaloids of Goldenseal: Time-Dependent Inhibition and Allosteric EffectsMatthew G McDonald, Dan-Dan Tian, Kenneth E Thummel, et al.
Pageof 16

Showing results (21-30 of 159) with videos related to

Sort By:
Pageof 16
Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 21, 2004
Differences in the inhibition of cytochromes P450 3A4 and 3A5 by metabolite-inhibitor complex-forming drugsDonavon J McConn, Yvonne S Lin, Kyle Allen, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 10, 2004
Role of itraconazole metabolites in CYP3A4 inhibitionNina Isoherranen, Kent L Kunze, Kyle E Allen, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 20, 2007
Cytochrome P450 enzymes and transporters induced by anti-human immunodeficiency virus protease inhibitors in human hepatocytes: implications for predicting clinical drug interactionsVaishali Dixit, Niresh Hariparsad, Fang Li, et al.
Biochemical Pharmacology|June 14, 2006
Selective induction of intestinal CYP3A23 by 1alpha,25-dihydroxyvitamin D3 in ratsYang Xu, Kazunori Iwanaga, Changcheng Zhou, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 18, 2006
Stereochemical aspects of itraconazole metabolism in vitro and in vivoKent L Kunze, Wendel L Nelson, Evan D Kharasch, et al.
American Journal of Physiology. Renal Physiology|July 20, 2019
Renal secretion of hydrochlorothiazide involves organic anion transporter 1/3, organic cation transporter 2, and multidrug and toxin extrusion protein 2-KJia Yin, David J Wagner, Bhagwat Prasad, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 12, 2008
Intestinal human colon adenocarcinoma cell line LS180 is an excellent model to study pregnane X receptor, but not constitutive androstane receptor, mediated CYP3A4 and multidrug resistance transporter 1 induction: studies with anti-human immunodeficiency virus protease inhibitorsAnshul Gupta, Ganesh M Mugundu, Pankaj B Desai, et al.
Clinical and Translational Science|September 17, 2019
Tissue Chips in Space-Challenges and OpportunitiesCatherine K Yeung, Paul Koenig, Stefanie Countryman, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 17, 2021
Sources of Interindividual VariabilityYvonne S Lin, Kenneth E Thummel, Brice D Thompson, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 28, 2020
Modulation of Major Human Liver Microsomal Cytochromes P450 by Component Alkaloids of Goldenseal: Time-Dependent Inhibition and Allosteric EffectsMatthew G McDonald, Dan-Dan Tian, Kenneth E Thummel, et al.
Pageof 16