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D F V Lewis

Showing results (1-10 of 16) with videos related to

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Xenobiotica; the Fate of Foreign Compounds in Biological Systems|May 25, 2002
Homology modelling of human CYP2 family enzymes based on the CYP2C5 crystal structureD F V Lewis
Ernst Schering Research Foundation Workshop|April 27, 2002
Modelling human cytochrome P450-substrate interactionsD F V Lewis
Toxicology|December 26, 2001
Factors influencing rates and clearance in P450-mediated reactions: QSARs for substrates of the xenobiotic-metabolizing hepatic microsomal P450sD F V Lewis, M Dickins
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|June 12, 2009
Human P450s involved in drug metabolism and the use of structural modelling for understanding substrate selectivity and binding affinityD F V Lewis, Y Ito
Drug Metabolism and Drug Interactions|September 12, 2002
Molecular orbital calculations and nicotine metabolism: a rationale for experimentally observed metabolite ratiosD F V Lewis, J W Gorrod
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|August 7, 2002
Species differences in coumarin metabolism: a molecular modelling evaluation of CYP2A interactionsD F V Lewis, B G Lake
Journal of Inorganic Biochemistry|July 31, 2003
Functional interaction of cytochrome P450 with its redox partners: a critical assessment and update of the topology of predicted contact regionsP Hlavica, J Schulze, D F V Lewis
The Journal of Steroid Biochemistry and Molecular Biology|April 25, 2003
Homology modelling of the nuclear receptors: human oestrogen receptorbeta (hERbeta), the human pregnane-X-receptor (PXR), the Ah receptor (AhR) and the constitutive androstane receptor (CAR) ligand binding domains from the human oestrogen receptor alpha (hERalpha) crystal structure, and the human peroxisome proliferator activated receptor alpha (PPARalpha) ligand binding domain from the human PPARgamma crystal structureM N Jacobs, M Dickins, D F V Lewis
Toxicology in Vitro : an International Journal Published in Association with BIBRA|May 22, 2002
Molecular modelling of the peroxisome proliferator-activated receptor alpha (PPAR alpha) from human, rat and mouse, based on homology with the human PPAR gamma crystal structureD F V Lewis, M N Jacobs, M Dickins, et al.
Toxicology|June 14, 2002
Quantitative structure--activity relationships for inducers of cytochromes P450 and nuclear receptor ligands involved in P450 regulation within the CYP1, CYP2, CYP3 and CYP4 familiesD F V Lewis, M N Jacobs, M Dickins, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|May 25, 2002
Homology modelling of human CYP2 family enzymes based on the CYP2C5 crystal structureD F V Lewis
Ernst Schering Research Foundation Workshop|April 27, 2002
Modelling human cytochrome P450-substrate interactionsD F V Lewis
Toxicology|December 26, 2001
Factors influencing rates and clearance in P450-mediated reactions: QSARs for substrates of the xenobiotic-metabolizing hepatic microsomal P450sD F V Lewis, M Dickins
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|June 12, 2009
Human P450s involved in drug metabolism and the use of structural modelling for understanding substrate selectivity and binding affinityD F V Lewis, Y Ito
Drug Metabolism and Drug Interactions|September 12, 2002
Molecular orbital calculations and nicotine metabolism: a rationale for experimentally observed metabolite ratiosD F V Lewis, J W Gorrod
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|August 7, 2002
Species differences in coumarin metabolism: a molecular modelling evaluation of CYP2A interactionsD F V Lewis, B G Lake
Journal of Inorganic Biochemistry|July 31, 2003
Functional interaction of cytochrome P450 with its redox partners: a critical assessment and update of the topology of predicted contact regionsP Hlavica, J Schulze, D F V Lewis
The Journal of Steroid Biochemistry and Molecular Biology|April 25, 2003
Homology modelling of the nuclear receptors: human oestrogen receptorbeta (hERbeta), the human pregnane-X-receptor (PXR), the Ah receptor (AhR) and the constitutive androstane receptor (CAR) ligand binding domains from the human oestrogen receptor alpha (hERalpha) crystal structure, and the human peroxisome proliferator activated receptor alpha (PPARalpha) ligand binding domain from the human PPARgamma crystal structureM N Jacobs, M Dickins, D F V Lewis
Toxicology in Vitro : an International Journal Published in Association with BIBRA|May 22, 2002
Molecular modelling of the peroxisome proliferator-activated receptor alpha (PPAR alpha) from human, rat and mouse, based on homology with the human PPAR gamma crystal structureD F V Lewis, M N Jacobs, M Dickins, et al.
Toxicology|June 14, 2002
Quantitative structure--activity relationships for inducers of cytochromes P450 and nuclear receptor ligands involved in P450 regulation within the CYP1, CYP2, CYP3 and CYP4 familiesD F V Lewis, M N Jacobs, M Dickins, et al.
Pageof 2