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Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
June 22, 1999
Molecular modelling of CYP2B6, the human CYP2B isoform, by homology with the substrate-bound CYP102 crystal structure: evaluation of CYP2B6 substrate characteristics, the cytochrome b5 binding site and comparisons with CYP2B1 and CYP2B4
D F Lewis, B G Lake, M Dickins, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
April 29, 1999
A reporter gene assay to assess the molecular mechanisms of xenobiotic-dependent induction of the human CYP3A4 gene in vitro
M S Ogg, J M Williams, M Tarbit, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
May 9, 1998
Molecular modelling of human CYP2C subfamily enzymes CYP2C9 and CYP2C19: rationalization of substrate specificity and site-directed mutagenesis experiments in the CYP2C subfamily
D F Lewis, M Dickins, R J Weaver, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
January 23, 2003
Homology modelling of human CYP2E1 based on the CYP2C5 crystal structure: investigation of enzyme-substrate and enzyme-inhibitor interactions
D F V Lewis, B G Lake, M G Bird, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
February 5, 2000
Molecular modelling of human CYP2E1 by homology with the CYP102 haemoprotein domain: investigation of the interactions of substrates and inhibitors within the putative active site of the human CYP2E1 isoform
D F Lewis, M G Bird, M Dickins, et al.
Molecular Pharmacology
|
May 1, 1993
Isolation and expression of a cDNA coding for rat kidney cytosolic cysteine conjugate beta-lyase
S J Perry, M A Schofield, M MacFarlane, et al.
Toxicology
|
January 29, 1993
Dose-dependent induction or depression of cysteine conjugate beta-lyase in rat kidney by N-acetyl-S-(1,2,3,4,4-pentachloro-1,3-butadienyl)-L-cysteine
M MacFarlane, M Schofield, N Parker, et al.
Toxicology
|
December 30, 1999
Molecular modelling of CYP1 family enzymes CYP1A1, CYP1A2, CYP1A6 and CYP1B1 based on sequence homology with CYP102
D F Lewis, B G Lake, S G George, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
August 22, 2001
Carbamazepine: a 'blind' assessment of CVP-associated metabolism and interactions in human liver-derived in vitro systems
O Pelkonen, P Myllynen, P Taavitsainen, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
April 17, 2001
An assessment of human liver-derived in vitro systems to predict the in vivo metabolism and clearance of almokalant
T B Andersson, H Sjöberg, K J Hoffmann, et al.
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of 3
Search research articles
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Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
June 22, 1999
Molecular modelling of CYP2B6, the human CYP2B isoform, by homology with the substrate-bound CYP102 crystal structure: evaluation of CYP2B6 substrate characteristics, the cytochrome b5 binding site and comparisons with CYP2B1 and CYP2B4
D F Lewis, B G Lake, M Dickins, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
April 29, 1999
A reporter gene assay to assess the molecular mechanisms of xenobiotic-dependent induction of the human CYP3A4 gene in vitro
M S Ogg, J M Williams, M Tarbit, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
May 9, 1998
Molecular modelling of human CYP2C subfamily enzymes CYP2C9 and CYP2C19: rationalization of substrate specificity and site-directed mutagenesis experiments in the CYP2C subfamily
D F Lewis, M Dickins, R J Weaver, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
January 23, 2003
Homology modelling of human CYP2E1 based on the CYP2C5 crystal structure: investigation of enzyme-substrate and enzyme-inhibitor interactions
D F V Lewis, B G Lake, M G Bird, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
February 5, 2000
Molecular modelling of human CYP2E1 by homology with the CYP102 haemoprotein domain: investigation of the interactions of substrates and inhibitors within the putative active site of the human CYP2E1 isoform
D F Lewis, M G Bird, M Dickins, et al.
Molecular Pharmacology
|
May 1, 1993
Isolation and expression of a cDNA coding for rat kidney cytosolic cysteine conjugate beta-lyase
S J Perry, M A Schofield, M MacFarlane, et al.
Toxicology
|
January 29, 1993
Dose-dependent induction or depression of cysteine conjugate beta-lyase in rat kidney by N-acetyl-S-(1,2,3,4,4-pentachloro-1,3-butadienyl)-L-cysteine
M MacFarlane, M Schofield, N Parker, et al.
Toxicology
|
December 30, 1999
Molecular modelling of CYP1 family enzymes CYP1A1, CYP1A2, CYP1A6 and CYP1B1 based on sequence homology with CYP102
D F Lewis, B G Lake, S G George, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
August 22, 2001
Carbamazepine: a 'blind' assessment of CVP-associated metabolism and interactions in human liver-derived in vitro systems
O Pelkonen, P Myllynen, P Taavitsainen, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
April 17, 2001
An assessment of human liver-derived in vitro systems to predict the in vivo metabolism and clearance of almokalant
T B Andersson, H Sjöberg, K J Hoffmann, et al.
Page
of 3