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B Testa

Showing results (201-210 of 212) with videos related to

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Journal of Medicinal Chemistry|April 4, 1998
Molecular properties and pharmacokinetic behavior of cetirizine, a zwitterionic H1-receptor antagonistA Pagliara, B Testa, P A Carrupt, et al.
Biochemical Pharmacology|July 12, 1996
Inhibition of [3H]dopamine uptake into striatal synaptosomes by isoquinoline derivatives structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridineK S McNaught, U Thull, P A Carrupt, et al.
Biochemical Pharmacology|November 27, 1995
Inhibition of complex I by isoquinoline derivatives structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)K S McNaught, U Thull, P A Carrupt, et al.
Neuroscience Letters|March 8, 1996
Toxicity to PC12 cells of isoquinoline derivatives structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridineK S McNaught, U Thull, P A Carrupt, et al.
Biochemical Pharmacology|June 14, 1996
Effects of isoquinoline derivatives structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) on mitochondrial respirationK S McNaught, U Thull, P A Carrupt, et al.
International Immunology|January 14, 1999
Molecular modeling of hen egg lysozyme HEL[52-61] peptide binding to I-Ak MHC class II moleculeP Weber, I Raynaud, L Ettouati, et al.
Journal of Biological Regulators and Homeostatic Agents|January 6, 2012
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutismD Minella, F Wannenes, M Biancolella, et al.
International Journal of Tissue Reactions|January 1, 1993
Clinical pharmacology of oxicams: new insights into the mechanisms of their dose-dependent toxicityE Albengres, S Urien, J Barre, et al.
Molecular Pharmacology|July 11, 1998
Ligand specificity of the genetic variants of human alpha1-acid glycoprotein: generation of a three-dimensional quantitative structure-activity relationship model for drug binding to the A variantF Hervé, G Caron, J C Duché, et al.
Journal of Medicinal Chemistry|August 1, 1997
H3-receptor antagonists: synthesis and structure-activity relationships of para- and meta-substituted 4(5)-phenyl-2-[[2-[4(5)-imidazolyl]ethyl]thio]imidazolesM Mor, F Bordi, C Silva, et al.
Pageof 22

Showing results (201-210 of 212) with videos related to

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Pageof 22
Journal of Medicinal Chemistry|April 4, 1998
Molecular properties and pharmacokinetic behavior of cetirizine, a zwitterionic H1-receptor antagonistA Pagliara, B Testa, P A Carrupt, et al.
Biochemical Pharmacology|July 12, 1996
Inhibition of [3H]dopamine uptake into striatal synaptosomes by isoquinoline derivatives structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridineK S McNaught, U Thull, P A Carrupt, et al.
Biochemical Pharmacology|November 27, 1995
Inhibition of complex I by isoquinoline derivatives structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)K S McNaught, U Thull, P A Carrupt, et al.
Neuroscience Letters|March 8, 1996
Toxicity to PC12 cells of isoquinoline derivatives structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridineK S McNaught, U Thull, P A Carrupt, et al.
Biochemical Pharmacology|June 14, 1996
Effects of isoquinoline derivatives structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) on mitochondrial respirationK S McNaught, U Thull, P A Carrupt, et al.
International Immunology|January 14, 1999
Molecular modeling of hen egg lysozyme HEL[52-61] peptide binding to I-Ak MHC class II moleculeP Weber, I Raynaud, L Ettouati, et al.
Journal of Biological Regulators and Homeostatic Agents|January 6, 2012
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutismD Minella, F Wannenes, M Biancolella, et al.
International Journal of Tissue Reactions|January 1, 1993
Clinical pharmacology of oxicams: new insights into the mechanisms of their dose-dependent toxicityE Albengres, S Urien, J Barre, et al.
Molecular Pharmacology|July 11, 1998
Ligand specificity of the genetic variants of human alpha1-acid glycoprotein: generation of a three-dimensional quantitative structure-activity relationship model for drug binding to the A variantF Hervé, G Caron, J C Duché, et al.
Journal of Medicinal Chemistry|August 1, 1997
H3-receptor antagonists: synthesis and structure-activity relationships of para- and meta-substituted 4(5)-phenyl-2-[[2-[4(5)-imidazolyl]ethyl]thio]imidazolesM Mor, F Bordi, C Silva, et al.
Pageof 22