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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: cauffiez c. 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.
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: cauffiez c. 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
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: cauffiez c. 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.
64 results