Lhermitte M - Search Results

1

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. Among authors: lhermitte m. Pharmacogenetics. 2001 Nov;11(8):739-41. doi: 10.1097/00008571-200111000-00014. Pharmacogenetics. 2001. PMID: 11692084 Review.

2

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

3

Functional analysis of CYP2D6.31 variant: homology modeling suggests possible disruption of redox partner interaction by Arg440His substitution.

Allorge D, Bréant D, Harlow J, Chowdry J, Lo-Guidice JM, Chevalier D, Cauffiez C, Lhermitte M, Blaney FE, Tucker GT, Broly F, Ellis SW. Allorge D, et al. Among authors: lhermitte m. Proteins. 2005 May 1;59(2):339-46. doi: 10.1002/prot.20399. Proteins. 2005. PMID: 15726636

4

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: lhermitte m. Hum Mutat. 2001 Apr;17(4):355. Hum Mutat. 2001. PMID: 11295847 No abstract available.

5

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: lhermitte m. Hum Mutat. 2001 Apr;17(4):355-6. Hum Mutat. 2001. PMID: 11295848 No abstract available.

6

Ethnic differences in the distribution of CYP3A5 gene polymorphisms.

Quaranta S, Chevalier D, Allorge D, Lo-Guidice JM, Migot-Nabias F, Kenani A, Imbenotte M, Broly F, Lacarelle B, Lhermitte M. Quaranta S, et al. Among authors: lhermitte m. Xenobiotica. 2006 Dec;36(12):1191-200. doi: 10.1080/00498250600944300. Xenobiotica. 2006. PMID: 17162466

7

In vitro characterization of four novel non-functional variants of the thiopurine S-methyltransferase.

Hamdan-Khalil R, Allorge D, Lo-Guidice JM, Cauffiez C, Chevalier D, Spire C, Houdret N, Libersa C, Lhermitte M, Colombel JF, Gala JL, Broly F. Hamdan-Khalil R, et al. Among authors: lhermitte m. Biochem Biophys Res Commun. 2003 Oct 3;309(4):1005-10. doi: 10.1016/j.bbrc.2003.08.103. Biochem Biophys Res Commun. 2003. PMID: 13679074

8

Genetic polymorphism of the human cytochrome CYP2A13 in a French population: implication in lung cancer susceptibility.

Cauffiez C, Lo-Guidice JM, Quaranta S, Allorge D, Chevalier D, Cenée S, Hamdan R, Lhermitte M, Lafitte JJ, Libersa C, Colombel JF, Stücker I, Broly F. Cauffiez C, et al. Among authors: lhermitte m. Biochem Biophys Res Commun. 2004 Apr 30;317(2):662-9. doi: 10.1016/j.bbrc.2004.03.092. Biochem Biophys Res Commun. 2004. PMID: 15063809

9

Functional characterization of genetic polymorphisms identified in the human cytochrome P450 4F12 (CYP4F12) promoter region.

Cauffiez C, Klinzig F, Rat E, Tournel G, Allorge D, Chevalier D, Lovecchio T, Pottier N, Colombel JF, Lhermitte M, D'Halluin JC, Broly F, Lo-Guidice JM. Cauffiez C, et al. Among authors: lhermitte m. Biochem Pharmacol. 2004 Jun 15;67(12):2231-8. doi: 10.1016/j.bcp.2004.02.033. Biochem Pharmacol. 2004. PMID: 15163554

10

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: lhermitte m. 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

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