Chevalier D - Search Results

1

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 population.

Chevalier D, Cauffiez C, Allorge D, Lo-Guidice JM, Lhermitte M, Lafitte JJ, Broly F. Chevalier D, et al. Hum Mutat. 2001 Apr;17(4):355-6. Hum Mutat. 2001. PMID: 11295848 No abstract available.

2

Identification of a novel splice-site mutation in the CYP1A2 gene.

Allorge D, Chevalier D, Lo-Guidice JM, Cauffiez C, Suard F, Baumann P, Eap CB, Broly F. Allorge D, et al. Among authors: chevalier d. Br J Clin Pharmacol. 2003 Sep;56(3):341-4. doi: 10.1046/j.1365-2125.2003.01858.x. Br J Clin Pharmacol. 2003. PMID: 12919186 Free PMC article.

3

First report of a genetic polymorphism of the cytochrome P450 3A43 (CYP3A43) gene: identification of a loss-of-function variant.

Cauffiez C, Lo-Guidice JM, Chevalier D, Allorge D, Hamdan R, Lhermitte M, Lafitte JJ, Colombel JF, Libersa C, Broly F. Cauffiez C, et al. Among authors: chevalier d. Hum Mutat. 2004 Jan;23(1):101. doi: 10.1002/humu.9211. Hum Mutat. 2004. PMID: 14695544

4

Molecular analysis of the CYP2F1 gene: identification of a frequent non-functional allelic variant.

Tournel G, Cauffiez C, Billaut-Laden I, Allorge D, Chevalier D, Bonnifet F, Mensier E, Lafitte JJ, Lhermitte M, Broly F, Lo-Guidice JM. Tournel G, et al. Among authors: chevalier d. Mutat Res. 2007 Apr 1;617(1-2):79-89. doi: 10.1016/j.mrfmmm.2007.01.007. Epub 2007 Jan 25. Mutat Res. 2007. PMID: 17327131

5

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 population.

Belmahdi F, Chevalier D, Lo-Guidice JM, Allorge D, Cauffiez C, Lafitte JJ, Broly F. Belmahdi F, et al. Among authors: chevalier d. Hum Mutat. 2000 Nov;16(5):450. doi: 10.1002/1098-1004(200011)16:5<450::AID-HUMU28>3.0.CO;2-1. Hum Mutat. 2000. PMID: 11058921 No abstract available.

6

Characterization of new mutations in the coding sequence and 5'-untranslated region of the human prostacylcin synthase gene (CYP8A1).

Chevalier D, Cauffiez C, Bernard C, Lo-Guidice JM, Allorge D, Fazio F, Ferrari N, Libersa C, Lhermitte M, D'Halluin JC, Broly F. Chevalier D, et al. Among authors: d halluin jc. Hum Genet. 2001 Feb;108(2):148-55. doi: 10.1007/s004390000444. Hum Genet. 2001. PMID: 11281454

7

Detection of known and two novel (M331I and R464S) missense mutations in the human CYP1A1 gene in a French Caucasian population.

Chevalier D, Allorge D, Lo-Guidice JM, Cauffiez C, Lhermitte M, Lafitte JJ, Broly F. Chevalier D, et al. Hum Mutat. 2001 Apr;17(4):355. Hum Mutat. 2001. PMID: 11295847 No abstract available.

8

Identification of genetic variants in the human thromboxane synthase gene (CYP5A1).

Chevalier D, Lo-Guidice JM, Sergent E, Allorge D, Debuysère H, Ferrari N, Libersa C, Lhermitte M, Broly F. Chevalier D, et al. Mutat Res. 2001 Jan;432(3-4):61-7. doi: 10.1016/s1383-5726(00)00004-2. Mutat Res. 2001. PMID: 11465543

9

Characterisation of novel defective thiopurine S-methyltransferase allelic variants.

Garat A, Cauffiez C, Renault N, Lo-Guidice JM, Allorge D, Chevalier D, Houdret N, Chavatte P, Loriot MA, Gala JL, Broly F. Garat A, et al. Among authors: chevalier d. Biochem Pharmacol. 2008 Aug 1;76(3):404-15. doi: 10.1016/j.bcp.2008.05.009. Epub 2008 May 18. Biochem Pharmacol. 2008. PMID: 18602085

10

Genetic polymorphism of the human cytochrome P450 CYP4B1: evidence for a non-functional allelic variant.

Lo-Guidice JM, Allorge D, Cauffiez C, Chevalier D, Lafitte JJ, Lhermitte M, Broly F. Lo-Guidice JM, et al. Among authors: chevalier d. Pharmacogenetics. 2002 Jul;12(5):367-74. doi: 10.1097/00008571-200207000-00004. Pharmacogenetics. 2002. PMID: 12142726

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