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Identification by single-strand conformational polymorphism analysis of known and new mutations of the CYP3A5 gene in a French population.
Quaranta S, Chevalier D, Bourgarel-Rey V, Allorge D, Solas C, Lo-Guidice JM, Sampol-Manos E, Vacher-Coponat H, Moal V, Broly F, Lhermitte M, Lacarelle B. Quaranta S, et al. Among authors: lhermitte m. Toxicol Lett. 2006 Jul 1;164(2):177-84. doi: 10.1016/j.toxlet.2005.12.007. Epub 2006 Jan 25. Toxicol Lett. 2006. PMID: 16442753
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
Sequence analysis, frequency and ethnic distribution of VNTR polymorphism in the 5'-untranslated region of the human prostacyclin synthase gene (CYP8A1).
Chevalier D, Allorge D, Lo-Guidice JM, Cauffiez C, Lepetit C, Migot-Nabias F, Kenani A, Lhermitte M, Broly F. Chevalier D, et al. Among authors: lhermitte m. Prostaglandins Other Lipid Mediat. 2002 Sep;70(1-2):31-7. doi: 10.1016/s0090-6980(02)00016-3. Prostaglandins Other Lipid Mediat. 2002. PMID: 12428676
Evidence for a functional genetic polymorphism of the human retinoic acid-metabolizing enzyme CYP26A1, an enzyme that may be involved in spina bifida.
Rat E, Billaut-Laden I, Allorge D, Lo-Guidice JM, Tellier M, Cauffiez C, Jonckheere N, van Seuningen I, Lhermitte M, Romano A, Guéant JL, Broly F. Rat E, et al. Among authors: lhermitte m. Birth Defects Res A Clin Mol Teratol. 2006 Jun;76(6):491-8. doi: 10.1002/bdra.20275. Birth Defects Res A Clin Mol Teratol. 2006. PMID: 16933217
173 results