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Journal of Enzyme Inhibition
|
March 28, 2002
Quantitative structure-activity relationships (QSARs) within series of inhibitors for mammalian cytochromes P450 (CYPs)
D F Lewis, M Dickins
Journal of Computer-Aided Molecular Design
|
June 1, 1992
The sequence homologies of cytochromes P-450 and active-site geometries
D F Lewis, H Moereels
European Journal of Biochemistry
|
September 18, 2001
Allosteric phenomena in cytochrome P450-catalyzed monooxygenations
P Hlavica, D F Lewis
Clinics in Perinatology
|
January 31, 2002
Tocolytic therapy with preterm premature rupture of membranes
T Fontenot, D F Lewis
Applied and Environmental Microbiology
|
June 1, 1984
Caffeine inhibition of aflatoxin synthesis: probable site of action
R L Buchanan, D F Lewis
Prostaglandins, Leukotrienes, and Essential Fatty Acids
|
January 1, 1992
Activation of 15-lipoxygenase by low density lipoprotein in vascular endothelial cells. Relationship to the oxidative modification of low density lipoprotein
C K Derian, D F Lewis
Toxicology
|
May 19, 1998
Molecular modelling and quantitative structure-activity relationship studies on the interaction of omeprazole with cytochrome P450 isozymes
D F Lewis, B G Lake
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
June 1, 1987
Molecular electrostatic potential energies and methylation of DNA bases: a molecular orbital-generated quantitative structure-activity relationship
D F Lewis, V S Griffiths
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
July 27, 2010
Molecular modelling of the rat peroxisome proliferator-activated receptor -alpha (rPPARalpha) by homology with the human retinoic acid X receptor alpha (hRXRalpha) and investigation of ligand binding interactions I: QSARs
D F Lewis, B G Lake
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
December 20, 1999
Molecular modelling of CYP4A subfamily members based on sequence homology with CYP102
D F Lewis, B G Lake
Page
of 18
Search research articles
Search
Showing results (21-30 of 180) with videos related to
Sort By:
Page
of 18
Journal of Enzyme Inhibition
|
March 28, 2002
Quantitative structure-activity relationships (QSARs) within series of inhibitors for mammalian cytochromes P450 (CYPs)
D F Lewis, M Dickins
Journal of Computer-Aided Molecular Design
|
June 1, 1992
The sequence homologies of cytochromes P-450 and active-site geometries
D F Lewis, H Moereels
European Journal of Biochemistry
|
September 18, 2001
Allosteric phenomena in cytochrome P450-catalyzed monooxygenations
P Hlavica, D F Lewis
Clinics in Perinatology
|
January 31, 2002
Tocolytic therapy with preterm premature rupture of membranes
T Fontenot, D F Lewis
Applied and Environmental Microbiology
|
June 1, 1984
Caffeine inhibition of aflatoxin synthesis: probable site of action
R L Buchanan, D F Lewis
Prostaglandins, Leukotrienes, and Essential Fatty Acids
|
January 1, 1992
Activation of 15-lipoxygenase by low density lipoprotein in vascular endothelial cells. Relationship to the oxidative modification of low density lipoprotein
C K Derian, D F Lewis
Toxicology
|
May 19, 1998
Molecular modelling and quantitative structure-activity relationship studies on the interaction of omeprazole with cytochrome P450 isozymes
D F Lewis, B G Lake
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
June 1, 1987
Molecular electrostatic potential energies and methylation of DNA bases: a molecular orbital-generated quantitative structure-activity relationship
D F Lewis, V S Griffiths
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
July 27, 2010
Molecular modelling of the rat peroxisome proliferator-activated receptor -alpha (rPPARalpha) by homology with the human retinoic acid X receptor alpha (hRXRalpha) and investigation of ligand binding interactions I: QSARs
D F Lewis, B G Lake
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
December 20, 1999
Molecular modelling of CYP4A subfamily members based on sequence homology with CYP102
D F Lewis, B G Lake
Page
of 18