Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Maurel

Showing results (91-100 of 142) with videos related to

Pageof 15
Sort By:
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 1, 1989
Metabolism of cyclosporin A. IV. Purification and identification of the rifampicin-inducible human liver cytochrome P-450 (cyclosporin A oxidase) as a product of P450IIIA gene subfamilyJ Combalbert, I Fabre, G Fabre, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 1, 1990
Cyclosporin A drug interactions. Screening for inducers and inhibitors of cytochrome P-450 (cyclosporin A oxidase) in primary cultures of human hepatocytes and in liver microsomesL Pichard, I Fabre, G Fabre, et al.
Gastroenterology|September 1, 1990
Omeprazole is an aryl hydrocarbon-like inducer of human hepatic cytochrome P450D Diaz, I Fabre, M Daujat, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 19, 2001
Calcium channel modulators of the dihydropyridine family are human pregnane X receptor activators and inducers of CYP3A, CYP2B, and CYP2C in human hepatocytesL Drocourt, J M Pascussi, E Assenat, et al.
Chemico-Biological Interactions|December 24, 1997
Preclinical evaluation of drug-drug interaction potential: present status of the application of primary human hepatocytes in the evaluation of cytochrome P450 inductionA P Li, P Maurel, M J Gomez-Lechon, et al.
Biochemical Pharmacology|February 24, 1993
Human liver microsomal cytochrome P450 3A isozymes mediated vindesine biotransformation. Metabolic drug interactionsX J Zhou, X R Zhou-Pan, T Gauthier, et al.
Biochemical and Biophysical Research Communications|July 15, 1999
Evidence for the presence of a functional pregnane X receptor response element in the CYP3A7 promoter geneJ M Pascussi, Y Jounaidi, L Drocourt, et al.
Biochemical and Biophysical Research Communications|April 17, 1995
Evidence for the ligand-independent activation of the AH receptorP Lesca, B Peryt, G Larrieu, et al.
Transplantation Proceedings|February 1, 1991
Molecular mechanism of cyclosporine A drug interactions: inducers and inhibitors of cytochrome P450 screening in primary cultures of human hepatocytesL Pichard, J M Fabre, J Domergue, et al.
The Journal of General Virology|October 21, 1998
In vitro infection of adult normal human hepatocytes in primary culture by hepatitis C virusC Fournier, C Sureau, J Coste, et al.
Pageof 15

Showing results (91-100 of 142) with videos related to

Sort By:
Pageof 15
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 1, 1989
Metabolism of cyclosporin A. IV. Purification and identification of the rifampicin-inducible human liver cytochrome P-450 (cyclosporin A oxidase) as a product of P450IIIA gene subfamilyJ Combalbert, I Fabre, G Fabre, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 1, 1990
Cyclosporin A drug interactions. Screening for inducers and inhibitors of cytochrome P-450 (cyclosporin A oxidase) in primary cultures of human hepatocytes and in liver microsomesL Pichard, I Fabre, G Fabre, et al.
Gastroenterology|September 1, 1990
Omeprazole is an aryl hydrocarbon-like inducer of human hepatic cytochrome P450D Diaz, I Fabre, M Daujat, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 19, 2001
Calcium channel modulators of the dihydropyridine family are human pregnane X receptor activators and inducers of CYP3A, CYP2B, and CYP2C in human hepatocytesL Drocourt, J M Pascussi, E Assenat, et al.
Chemico-Biological Interactions|December 24, 1997
Preclinical evaluation of drug-drug interaction potential: present status of the application of primary human hepatocytes in the evaluation of cytochrome P450 inductionA P Li, P Maurel, M J Gomez-Lechon, et al.
Biochemical Pharmacology|February 24, 1993
Human liver microsomal cytochrome P450 3A isozymes mediated vindesine biotransformation. Metabolic drug interactionsX J Zhou, X R Zhou-Pan, T Gauthier, et al.
Biochemical and Biophysical Research Communications|July 15, 1999
Evidence for the presence of a functional pregnane X receptor response element in the CYP3A7 promoter geneJ M Pascussi, Y Jounaidi, L Drocourt, et al.
Biochemical and Biophysical Research Communications|April 17, 1995
Evidence for the ligand-independent activation of the AH receptorP Lesca, B Peryt, G Larrieu, et al.
Transplantation Proceedings|February 1, 1991
Molecular mechanism of cyclosporine A drug interactions: inducers and inhibitors of cytochrome P450 screening in primary cultures of human hepatocytesL Pichard, J M Fabre, J Domergue, et al.
The Journal of General Virology|October 21, 1998
In vitro infection of adult normal human hepatocytes in primary culture by hepatitis C virusC Fournier, C Sureau, J Coste, et al.
Pageof 15