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Journal of Enzyme Inhibition and Medicinal Chemistry
|
March 22, 2007
Quantitative structure-activity relationships (QSARs) in inhibitors of various cytochromes P450: the importance of compound lipophilicity
David F V Lewis, Brian G Lake, Maurice Dickins
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
April 14, 2005
Molecular modelling of human microsomal epoxide hydrolase (EH) by homology with a fungal (Aspergillus niger) EH crystal structure of 1.8 A resolution: structure-activity relationships in epoxides inhibiting EH activity
David F V Lewis, Brian G Lake, Michael G Bird
Drug Metabolism and Drug Interactions
|
July 18, 2006
Quantitative structure-activity relationships (QSARs) within cytochromes P450 2B (CYP2B) subfamily enzymes: the importance of lipophilicity for binding and metabolism
David F V Lewis, Brian G Lake, Yuko Ito, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
October 25, 2006
Lipophilicity relationships in inhibitors of CYP2C9 and CYP2C19 enzymes
David F V Lewis, Brian G Lake, Yuko Ito, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
August 20, 2013
Evaluation of the utility of the lifetime mouse bioassay in the identification of cancer hazards for humans
Thomas G Osimitz, Wiebke Droege, Alan R Boobis, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
December 20, 2008
In vitro assays for induction of drug metabolism
Brian G Lake, Roger J Price, Amanda M Giddings, et al.
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 interactions
David F V Lewis, Maurice Dickins, Brian G Lake, et al.
Environmental Toxicology and Pharmacology
|
July 26, 2011
Dose-related effects of the peroxisome proliferator methylclofenapate in rat liver
Brian G Lake, Paul C Rumsby, Morag E Cunninghame, 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 interactions
David 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 template
David F V Lewis, Maurice Dickins, Brian G Lake, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 78) with videos related to
Sort By:
Page
of 8
Journal of Enzyme Inhibition and Medicinal Chemistry
|
March 22, 2007
Quantitative structure-activity relationships (QSARs) in inhibitors of various cytochromes P450: the importance of compound lipophilicity
David F V Lewis, Brian G Lake, Maurice Dickins
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
April 14, 2005
Molecular modelling of human microsomal epoxide hydrolase (EH) by homology with a fungal (Aspergillus niger) EH crystal structure of 1.8 A resolution: structure-activity relationships in epoxides inhibiting EH activity
David F V Lewis, Brian G Lake, Michael G Bird
Drug Metabolism and Drug Interactions
|
July 18, 2006
Quantitative structure-activity relationships (QSARs) within cytochromes P450 2B (CYP2B) subfamily enzymes: the importance of lipophilicity for binding and metabolism
David F V Lewis, Brian G Lake, Yuko Ito, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
October 25, 2006
Lipophilicity relationships in inhibitors of CYP2C9 and CYP2C19 enzymes
David F V Lewis, Brian G Lake, Yuko Ito, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
August 20, 2013
Evaluation of the utility of the lifetime mouse bioassay in the identification of cancer hazards for humans
Thomas G Osimitz, Wiebke Droege, Alan R Boobis, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
December 20, 2008
In vitro assays for induction of drug metabolism
Brian G Lake, Roger J Price, Amanda M Giddings, et al.
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 interactions
David F V Lewis, Maurice Dickins, Brian G Lake, et al.
Environmental Toxicology and Pharmacology
|
July 26, 2011
Dose-related effects of the peroxisome proliferator methylclofenapate in rat liver
Brian G Lake, Paul C Rumsby, Morag E Cunninghame, 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 interactions
David 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 template
David F V Lewis, Maurice Dickins, Brian G Lake, et al.
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of 8