Search research articles
Contact Us
Filters
Showing results (131-140 of 171) with videos related to
Page
of 18
Sort By:
Biochimie
|
January 1, 1994
The human testis determining factor SRY: a new member of the HMG box protein family
S Soullier, F Poulat, B Boizet-Bonhoure, et al.
The Journal of Membrane Biology
|
May 16, 1998
Interactions of primary amphipathic vector peptides with membranes. Conformational consequences and influence on cellular localization
P Vidal, L Chaloin, A Heitz, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society
|
June 10, 1998
Capping and dynamic relation between domains 1 and 2 of gelsolin
J Feinberg, O Kwiatek, C Astier, et al.
Biophysical Journal
|
May 12, 2009
Structural information from functional measurements: single-channel studies on gramicidin analogues
J T Durkin, O S Andersen, E R Blout, et al.
Peptide Research
|
March 1, 1992
Endothelin 1: conformation and aggregation
B Calas, M C Harricane, L Guimard, et al.
Biochemistry
|
June 16, 1992
Gramicidin channels that have no tryptophan residues
V Fonseca, P Daumas, L Ranjalahy-Rasoloarijao, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
August 11, 1998
The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A. Implications for drug-drug interactions and pharmacological activity of the main metabolite
V Fischer, A Rodríguez-Gascón, F Heitz, et al.
Biology of the Neonate
|
January 1, 1988
Left ventricular diastolic function during the first month of life
J C Fouron, F Heitz, A M Carceller, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 4, 1999
The 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor fluvastatin: effect on human cytochrome P-450 and implications for metabolic drug interactions
V Fischer, L Johanson, F Heitz, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 1, 1994
The polymorphic cytochrome P-4502D6 is involved in the metabolism of both 5-hydroxytryptamine antagonists, tropisetron and ondansetron
V Fischer, A E Vickers, F Heitz, et al.
Page
of 18
Search research articles
Search
Showing results (131-140 of 171) with videos related to
Sort By:
Page
of 18
Biochimie
|
January 1, 1994
The human testis determining factor SRY: a new member of the HMG box protein family
S Soullier, F Poulat, B Boizet-Bonhoure, et al.
The Journal of Membrane Biology
|
May 16, 1998
Interactions of primary amphipathic vector peptides with membranes. Conformational consequences and influence on cellular localization
P Vidal, L Chaloin, A Heitz, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society
|
June 10, 1998
Capping and dynamic relation between domains 1 and 2 of gelsolin
J Feinberg, O Kwiatek, C Astier, et al.
Biophysical Journal
|
May 12, 2009
Structural information from functional measurements: single-channel studies on gramicidin analogues
J T Durkin, O S Andersen, E R Blout, et al.
Peptide Research
|
March 1, 1992
Endothelin 1: conformation and aggregation
B Calas, M C Harricane, L Guimard, et al.
Biochemistry
|
June 16, 1992
Gramicidin channels that have no tryptophan residues
V Fonseca, P Daumas, L Ranjalahy-Rasoloarijao, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
August 11, 1998
The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A. Implications for drug-drug interactions and pharmacological activity of the main metabolite
V Fischer, A Rodríguez-Gascón, F Heitz, et al.
Biology of the Neonate
|
January 1, 1988
Left ventricular diastolic function during the first month of life
J C Fouron, F Heitz, A M Carceller, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 4, 1999
The 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor fluvastatin: effect on human cytochrome P-450 and implications for metabolic drug interactions
V Fischer, L Johanson, F Heitz, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 1, 1994
The polymorphic cytochrome P-4502D6 is involved in the metabolism of both 5-hydroxytryptamine antagonists, tropisetron and ondansetron
V Fischer, A E Vickers, F Heitz, et al.
Page
of 18