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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: broly f. 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
Genetic polymorphism of CYP2U1, a cytochrome P450 involved in fatty acids hydroxylation.
Devos A, Lino Cardenas CL, Glowacki F, Engels A, Lo-Guidice JM, Chevalier D, Allorge D, Broly F, Cauffiez C. Devos A, et al. Among authors: broly f. Prostaglandins Leukot Essent Fatty Acids. 2010 Aug;83(2):105-10. doi: 10.1016/j.plefa.2010.06.005. Epub 2010 Jul 13. Prostaglandins Leukot Essent Fatty Acids. 2010. PMID: 20630735
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: broly f. 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
132 results