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British Journal of Clinical Pharmacology
|
March 18, 2004
Database analyses for the prediction of in vivo drug-drug interactions from in vitro data
Kiyomi Ito, Hayley S Brown, J Brian Houston
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
November 16, 2002
Quinidine and haloperidol as modifiers of CYP3A4 activity: multisite kinetic model approach
Aleksandra Galetin, Stephen E Clarke, J Brian Houston
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
August 16, 2003
Multisite kinetic analysis of interactions between prototypical CYP3A4 subgroup substrates: midazolam, testosterone, and nifedipine
Aleksandra Galetin, Stephen E Clarke, J Brian Houston
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
November 30, 2006
Evaluation of cryopreserved human hepatocytes as an alternative in vitro system to microsomes for the prediction of metabolic clearance
Hayley S Brown, Michael Griffin, J Brian Houston
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
January 17, 2012
Evaluation of the novel in vitro systems for hepatic drug clearance and assessment of their predictive utility
J Brian Houston, Karen Rowland-Yeo, Ugo Zanelli
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
July 21, 2011
Predictive utility of in vitro rifampin induction data generated in fresh and cryopreserved human hepatocytes, Fa2N-4, and HepaRG cells
Ian E Templeton, J Brian Houston, Aleksandra Galetin
The Journal of Pharmacology and Experimental Therapeutics
|
December 2, 2004
Predictive models of CYP3A4 Heteroactivation: in vitro-in vivo scaling and pharmacophore modeling
Ann-Charlotte Egnell, J Brian Houston, C Scott Boyer
The Journal of Pharmacology and Experimental Therapeutics
|
March 24, 2005
CYP3A4 substrate selection and substitution in the prediction of potential drug-drug interactions
Aleksandra Galetin, Kiyomi Ito, David Hallifax, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
October 14, 2005
Prediction of time-dependent CYP3A4 drug-drug interactions: impact of enzyme degradation, parallel elimination pathways, and intestinal inhibition
Aleksandra Galetin, Howard Burt, Laura Gibbons, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
April 7, 2010
Prediction of human intestinal first-pass metabolism of 25 CYP3A substrates from in vitro clearance and permeability data
Michael Gertz, Anthony Harrison, J Brian Houston, et al.
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Search research articles
Search
Showing results (41-50 of 125) with videos related to
Sort By:
Page
of 13
British Journal of Clinical Pharmacology
|
March 18, 2004
Database analyses for the prediction of in vivo drug-drug interactions from in vitro data
Kiyomi Ito, Hayley S Brown, J Brian Houston
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
November 16, 2002
Quinidine and haloperidol as modifiers of CYP3A4 activity: multisite kinetic model approach
Aleksandra Galetin, Stephen E Clarke, J Brian Houston
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
August 16, 2003
Multisite kinetic analysis of interactions between prototypical CYP3A4 subgroup substrates: midazolam, testosterone, and nifedipine
Aleksandra Galetin, Stephen E Clarke, J Brian Houston
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
November 30, 2006
Evaluation of cryopreserved human hepatocytes as an alternative in vitro system to microsomes for the prediction of metabolic clearance
Hayley S Brown, Michael Griffin, J Brian Houston
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
January 17, 2012
Evaluation of the novel in vitro systems for hepatic drug clearance and assessment of their predictive utility
J Brian Houston, Karen Rowland-Yeo, Ugo Zanelli
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
July 21, 2011
Predictive utility of in vitro rifampin induction data generated in fresh and cryopreserved human hepatocytes, Fa2N-4, and HepaRG cells
Ian E Templeton, J Brian Houston, Aleksandra Galetin
The Journal of Pharmacology and Experimental Therapeutics
|
December 2, 2004
Predictive models of CYP3A4 Heteroactivation: in vitro-in vivo scaling and pharmacophore modeling
Ann-Charlotte Egnell, J Brian Houston, C Scott Boyer
The Journal of Pharmacology and Experimental Therapeutics
|
March 24, 2005
CYP3A4 substrate selection and substitution in the prediction of potential drug-drug interactions
Aleksandra Galetin, Kiyomi Ito, David Hallifax, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
October 14, 2005
Prediction of time-dependent CYP3A4 drug-drug interactions: impact of enzyme degradation, parallel elimination pathways, and intestinal inhibition
Aleksandra Galetin, Howard Burt, Laura Gibbons, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
April 7, 2010
Prediction of human intestinal first-pass metabolism of 25 CYP3A substrates from in vitro clearance and permeability data
Michael Gertz, Anthony Harrison, J Brian Houston, et al.
Page
of 13