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Clinical and Experimental Pharmacology & Physiology
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October 9, 2002
Evolution of drug metabolism: hitchhiking the technology bandwagon
John O Miners
British Journal of Clinical Pharmacology
|
November 26, 2002
In vitro-in vivo correlations for drugs eliminated by glucuronidation: investigations with the model substrate zidovudine
Sam Boase, John O Miners
Methods in Molecular Biology (Clifton, N.J.)
|
February 14, 2014
Enzyme kinetics of uridine diphosphate glucuronosyltransferases (UGTs)
Jin Zhou, John O Miners
British Journal of Clinical Pharmacology
|
August 8, 2006
Relationships between the adverse effects of drugs and genetic polymorphism in genes encoding drug metabolizing enzymes
John O Miners, Richard O Day
Current Topics in Medicinal Chemistry
|
September 20, 2013
Generation, validation, and application of a P450 homology model
Benjamin C Lewis, John O Miners
In Silico Pharmacology
|
December 18, 2014
Molecular dynamics simulations: from structure function relationships to drug discovery
Pramod C Nair, John O Miners
Clinical Pharmacology and Therapeutics
|
December 22, 2025
Reply to "Minor Contribution of UGT1A1 Inhibition to Atazanavir-Related Bilirubin Elevation Supported by Conservative PBPK Modeling and Clinical Data"
John O Miners, Thomas M Polasek
Expert Opinion on Drug Metabolism & Toxicology
|
June 2, 2007
In vitro approaches to investigate mechanism-based inactivation of CYP enzymes
Thomas M Polasek, John O Miners
Drug Metabolism Reviews
|
September 29, 2009
Renal UDP-glucuronosyltransferases and the glucuronidation of xenobiotics and endogenous mediators
Kathleen M Knights, John O Miners
Clinical Pharmacology and Therapeutics
|
May 26, 2025
Caution with PBPK Modeling Based on the In Vitro Kinetics for Bilirubin Hepatic Uptake and Glucuronidation: Commentary on Dong et al
John O Miners, Thomas M Polasek
Page
of 14
Search research articles
Search
Showing results (1-10 of 136) with videos related to
Sort By:
Page
of 14
Clinical and Experimental Pharmacology & Physiology
|
October 9, 2002
Evolution of drug metabolism: hitchhiking the technology bandwagon
John O Miners
British Journal of Clinical Pharmacology
|
November 26, 2002
In vitro-in vivo correlations for drugs eliminated by glucuronidation: investigations with the model substrate zidovudine
Sam Boase, John O Miners
Methods in Molecular Biology (Clifton, N.J.)
|
February 14, 2014
Enzyme kinetics of uridine diphosphate glucuronosyltransferases (UGTs)
Jin Zhou, John O Miners
British Journal of Clinical Pharmacology
|
August 8, 2006
Relationships between the adverse effects of drugs and genetic polymorphism in genes encoding drug metabolizing enzymes
John O Miners, Richard O Day
Current Topics in Medicinal Chemistry
|
September 20, 2013
Generation, validation, and application of a P450 homology model
Benjamin C Lewis, John O Miners
In Silico Pharmacology
|
December 18, 2014
Molecular dynamics simulations: from structure function relationships to drug discovery
Pramod C Nair, John O Miners
Clinical Pharmacology and Therapeutics
|
December 22, 2025
Reply to "Minor Contribution of UGT1A1 Inhibition to Atazanavir-Related Bilirubin Elevation Supported by Conservative PBPK Modeling and Clinical Data"
John O Miners, Thomas M Polasek
Expert Opinion on Drug Metabolism & Toxicology
|
June 2, 2007
In vitro approaches to investigate mechanism-based inactivation of CYP enzymes
Thomas M Polasek, John O Miners
Drug Metabolism Reviews
|
September 29, 2009
Renal UDP-glucuronosyltransferases and the glucuronidation of xenobiotics and endogenous mediators
Kathleen M Knights, John O Miners
Clinical Pharmacology and Therapeutics
|
May 26, 2025
Caution with PBPK Modeling Based on the In Vitro Kinetics for Bilirubin Hepatic Uptake and Glucuronidation: Commentary on Dong et al
John O Miners, Thomas M Polasek
Page
of 14