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David F V Lewis

Showing results (41-50 of 52) with videos related to

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Drug Metabolism and Drug Interactions|December 20, 2003
A molecular model of CYP2D6 constructed by homology with the CYP2C5 crystallographic template: investigation of enzyme-substrate interactionsDavid F V Lewis, Maurice Dickins, Brian G Lake, et al.
Drug Metabolism and Drug Interactions|May 20, 2003
Molecular modelling of CYP2B6 based on homology with the CYP2C5 crystal structure: analysis of enzyme-substrate interactionsDavid F V Lewis, Brian G Lake, Maurice Dickins, et al.
Drug Metabolism and Drug Interactions|February 11, 2004
Investigation of enzyme selectivity in the human CYP2C subfamily: homology modelling of CYP2C8, CYP2C9 and CYP2C19 from the CYP2C5 crystallographic templateDavid F V Lewis, Maurice Dickins, Brian G Lake, et al.
Environmental Toxicology and Chemistry|June 3, 2018
Metal toxicity in two rodent species and redox potential: Evaluation of quantitative structure-activity relationshipsDavid F V Lewis, Miloslav Dobrota, Marina G Taylor, et al.
Journal of Chemical Information and Modeling|May 24, 2011
Long-range effects of a peripheral mutation on the enzymatic activity of cytochrome P450 1A2Tao Zhang, Limin Angela Liu, David F V Lewis, et al.
Molecular Informatics|August 2, 2016
Classification Models for Predicting Cytochrome P450 Enzyme-Substrate SelectivityTao Zhang, Hao Dai, Limin Angela Liu, et al.
Chemico-Biological Interactions|May 7, 2003
Molecular modelling of human CYP1B1 substrate interactions and investigation of allelic variant effects on metabolismDavid F V Lewis, Elizabeth M J Gillam, Steven A Everett, et al.
Clinical and Experimental Pharmacology & Physiology|August 27, 2005
Inhibition of human CYP1A2 oxidation of 5,6-dimethyl-xanthenone-4-acetic acid by acridines: a molecular modelling studyJames W Paxton, Philip Kestell, Daniel Chiang, et al.
Drug Metabolism Letters|March 6, 2010
An evaluation of ondansetron binding interactions with human cytochrome P450 enzymes CYP3A4 and CYP2D6David F V Lewis, Yuko Ito, Peter J Eddershaw, et al.
Bioorganic & Medicinal Chemistry Letters|July 11, 2003
Effect of structural modification on the inhibitory selectivity of rutaecarpine derivatives on human CYP1A1, CYP1A2, and CYP1B1Ming-Jaw Don, David F V Lewis, Shu-Yun Wang, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Drug Metabolism and Drug Interactions|December 20, 2003
A molecular model of CYP2D6 constructed by homology with the CYP2C5 crystallographic template: investigation of enzyme-substrate interactionsDavid F V Lewis, Maurice Dickins, Brian G Lake, et al.
Drug Metabolism and Drug Interactions|May 20, 2003
Molecular modelling of CYP2B6 based on homology with the CYP2C5 crystal structure: analysis of enzyme-substrate interactionsDavid F V Lewis, Brian G Lake, Maurice Dickins, et al.
Drug Metabolism and Drug Interactions|February 11, 2004
Investigation of enzyme selectivity in the human CYP2C subfamily: homology modelling of CYP2C8, CYP2C9 and CYP2C19 from the CYP2C5 crystallographic templateDavid F V Lewis, Maurice Dickins, Brian G Lake, et al.
Environmental Toxicology and Chemistry|June 3, 2018
Metal toxicity in two rodent species and redox potential: Evaluation of quantitative structure-activity relationshipsDavid F V Lewis, Miloslav Dobrota, Marina G Taylor, et al.
Journal of Chemical Information and Modeling|May 24, 2011
Long-range effects of a peripheral mutation on the enzymatic activity of cytochrome P450 1A2Tao Zhang, Limin Angela Liu, David F V Lewis, et al.
Molecular Informatics|August 2, 2016
Classification Models for Predicting Cytochrome P450 Enzyme-Substrate SelectivityTao Zhang, Hao Dai, Limin Angela Liu, et al.
Chemico-Biological Interactions|May 7, 2003
Molecular modelling of human CYP1B1 substrate interactions and investigation of allelic variant effects on metabolismDavid F V Lewis, Elizabeth M J Gillam, Steven A Everett, et al.
Clinical and Experimental Pharmacology & Physiology|August 27, 2005
Inhibition of human CYP1A2 oxidation of 5,6-dimethyl-xanthenone-4-acetic acid by acridines: a molecular modelling studyJames W Paxton, Philip Kestell, Daniel Chiang, et al.
Drug Metabolism Letters|March 6, 2010
An evaluation of ondansetron binding interactions with human cytochrome P450 enzymes CYP3A4 and CYP2D6David F V Lewis, Yuko Ito, Peter J Eddershaw, et al.
Bioorganic & Medicinal Chemistry Letters|July 11, 2003
Effect of structural modification on the inhibitory selectivity of rutaecarpine derivatives on human CYP1A1, CYP1A2, and CYP1B1Ming-Jaw Don, David F V Lewis, Shu-Yun Wang, et al.
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