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F Broly

Showing results (31-40 of 68) with videos related to

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Leukemia|February 13, 2004
A case of refractory anemia with 17p- syndrome following azathioprine treatment for heart transplantationS Depil, P Lepelley, V Soenen, et al.
Skin Pharmacology and Applied Skin Physiology|October 7, 2003
N-acetyltransferase 2 acetylation polymorphism: prevalence of slow acetylators does not differ between atopic dermatitis patients and healthy subjectsH Brocvielle, P Muret, A-C Goydadin, et al.
Molecular Biology Reports|October 12, 2012
Study of NAT2 genetic polymorphism in West African subjects: example of an healthy non-smoker Senegalese populationA Touré, C Diop, M Cabral, et al.
Pharmacogenetics|June 22, 2000
Molecular analysis of the N-acetyltransferase 1 gene (NAT1*) using polymerase chain reaction-restriction fragment-single strand conformation polymorphism assayJ M Lo-Guidice, D Allorge, D Chevalier, et al.
Human Mutation|April 11, 2001
Detection of known and two novel (M331I and R464S) missense mutations in the human CYP1A1 gene in a French Caucasian populationD Chevalier, D Allorge, J M Lo-Guidice, et al.
British Journal of Clinical Pharmacology|December 14, 1999
Thiopurine methyltransferase activity and its relationship to the occurrence of rejection episodes in paediatric renal transplant recipients treated with azathioprineT Dervieux, Y Médard, V Baudouin, et al.
Human Genetics|November 1, 1995
A nonsense mutation in the cytochrome P450 CYP2D6 gene identified in a Caucasian with an enzyme deficiencyF Broly, D Marez, J M Lo Guidice, et al.
Human Mutation|November 3, 2000
Identification of 6 new polymorphisms, g.11177G>A, g.14622C>T (R49C), g.17540T>C, g.17639T>C, g.30929T>C, g.31074G>A (R454Q), in the human microsomal epoxide hydrolase gene (EPHX1) in a French populationF Belmahdi, D Chevalier, J M Lo-Guidice, et al.
Human Mutation|April 11, 2001
Five novel natural allelic variants-951A>C, 1042G>A (D348N), 1156A>T (I386F), 1217G>A (C406Y) and 1291C>T (C431Y)-of the human CYP1A2 gene in a French Caucasian populationD Chevalier, C Cauffiez, D Allorge, et al.
European Journal of Clinical Pharmacology|January 19, 2000
Drug extrapyramidal side effects. CYP2D6 genotypes and phenotypesP Vandel, E Haffen, S Vandel, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
Leukemia|February 13, 2004
A case of refractory anemia with 17p- syndrome following azathioprine treatment for heart transplantationS Depil, P Lepelley, V Soenen, et al.
Skin Pharmacology and Applied Skin Physiology|October 7, 2003
N-acetyltransferase 2 acetylation polymorphism: prevalence of slow acetylators does not differ between atopic dermatitis patients and healthy subjectsH Brocvielle, P Muret, A-C Goydadin, et al.
Molecular Biology Reports|October 12, 2012
Study of NAT2 genetic polymorphism in West African subjects: example of an healthy non-smoker Senegalese populationA Touré, C Diop, M Cabral, et al.
Pharmacogenetics|June 22, 2000
Molecular analysis of the N-acetyltransferase 1 gene (NAT1*) using polymerase chain reaction-restriction fragment-single strand conformation polymorphism assayJ M Lo-Guidice, D Allorge, D Chevalier, et al.
Human Mutation|April 11, 2001
Detection of known and two novel (M331I and R464S) missense mutations in the human CYP1A1 gene in a French Caucasian populationD Chevalier, D Allorge, J M Lo-Guidice, et al.
British Journal of Clinical Pharmacology|December 14, 1999
Thiopurine methyltransferase activity and its relationship to the occurrence of rejection episodes in paediatric renal transplant recipients treated with azathioprineT Dervieux, Y Médard, V Baudouin, et al.
Human Genetics|November 1, 1995
A nonsense mutation in the cytochrome P450 CYP2D6 gene identified in a Caucasian with an enzyme deficiencyF Broly, D Marez, J M Lo Guidice, et al.
Human Mutation|November 3, 2000
Identification of 6 new polymorphisms, g.11177G>A, g.14622C>T (R49C), g.17540T>C, g.17639T>C, g.30929T>C, g.31074G>A (R454Q), in the human microsomal epoxide hydrolase gene (EPHX1) in a French populationF Belmahdi, D Chevalier, J M Lo-Guidice, et al.
Human Mutation|April 11, 2001
Five novel natural allelic variants-951A>C, 1042G>A (D348N), 1156A>T (I386F), 1217G>A (C406Y) and 1291C>T (C431Y)-of the human CYP1A2 gene in a French Caucasian populationD Chevalier, C Cauffiez, D Allorge, et al.
European Journal of Clinical Pharmacology|January 19, 2000
Drug extrapyramidal side effects. CYP2D6 genotypes and phenotypesP Vandel, E Haffen, S Vandel, et al.
Pageof 7