Allorge D - Search Results

1

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: allorge 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

2

The potential of keratinized matrices for the retrospective exploration of repeated ayahuasca use by patients.

Gish A, Hakim F, Richeval C, Lecot J, Bruneau C, Allorge D, Gaulier JM, Le Roux G. Gish A, et al. Among authors: allorge d. Clin Toxicol (Phila). 2023 Nov;61(11):1010-1011. doi: 10.1080/15563650.2023.2282943. Epub 2023 Dec 19. Clin Toxicol (Phila). 2023. PMID: 38038972 No abstract available.

3

Molecular analysis of the N-acetyltransferase 1 gene (NAT1*) using polymerase chain reaction-restriction fragment-single strand conformation polymorphism assay.

Lo-Guidice JM, Allorge D, Chevalier D, Debuysère H, Fazio F, Lafitte LJ, Broly F. Lo-Guidice JM, et al. Among authors: allorge d. Pharmacogenetics. 2000 Jun;10(4):293-300. doi: 10.1097/00008571-200006000-00003. Pharmacogenetics. 2000. PMID: 10862520

4

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: allorge 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.

5

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, allorge d. Hum Genet. 2001 Feb;108(2):148-55. doi: 10.1007/s004390000444. Hum Genet. 2001. PMID: 11281454

6

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. Among authors: allorge d. Hum Mutat. 2001 Apr;17(4):355. Hum Mutat. 2001. PMID: 11295847 No abstract available.

7

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. Among authors: allorge d. Hum Mutat. 2001 Apr;17(4):355-6. Hum Mutat. 2001. PMID: 11295848 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. Among authors: allorge d. Mutat Res. 2001 Jan;432(3-4):61-7. doi: 10.1016/s1383-5726(00)00004-2. Mutat Res. 2001. PMID: 11465543

9

In-vitro analysis of the contribution of CYP2D6.35 to ultra-rapid metabolism.

Allorge D, Harlow J, Boulet O, Hayhurst GP, Chowdry J, Roth E, Crewe K, Lo-Guidice JM, Lhermitte M, Broly F, Tucker GT, Ellis SW. Allorge D, et al. Pharmacogenetics. 2001 Nov;11(8):739-41. doi: 10.1097/00008571-200111000-00014. Pharmacogenetics. 2001. PMID: 11692084 Review.

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: allorge d. Pharmacogenetics. 2002 Jul;12(5):367-74. doi: 10.1097/00008571-200207000-00004. Pharmacogenetics. 2002. PMID: 12142726

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