Vaxillaire M - Search Results

1

Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes.

Bonnefond A, Clément N, Fawcett K, Yengo L, Vaillant E, Guillaume JL, Dechaume A, Payne F, Roussel R, Czernichow S, Hercberg S, Hadjadj S, Balkau B, Marre M, Lantieri O, Langenberg C, Bouatia-Naji N; Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC); Charpentier G, Vaxillaire M, Rocheleau G, Wareham NJ, Sladek R, McCarthy MI, Dina C, Barroso I, Jockers R, Froguel P. Bonnefond A, et al. Among authors: vaxillaire m. Nat Genet. 2012 Jan 29;44(3):297-301. doi: 10.1038/ng.1053. Nat Genet. 2012. PMID: 22286214 Free PMC article.

2

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus.

Froguel P, Vaxillaire M, Sun F, Velho G, Zouali H, Butel MO, Lesage S, Vionnet N, Clément K, Fougerousse F, et al. Froguel P, et al. Among authors: vaxillaire m. Nature. 1992 Mar 12;356(6365):162-4. doi: 10.1038/356162a0. Nature. 1992. PMID: 1545870

3

Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM.

Lesage S, Hani EH, Philippi A, Vaxillaire M, Hager J, Passa P, Demenais F, Froguel P, Vionnet N. Lesage S, et al. Among authors: vaxillaire m. Diabetes. 1995 Oct;44(10):1243-7. doi: 10.2337/diab.44.10.1243. Diabetes. 1995. PMID: 7556965

4

A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q.

Vaxillaire M, Boccio V, Philippi A, Vigouroux C, Terwilliger J, Passa P, Beckmann JS, Velho G, Lathrop GM, Froguel P. Vaxillaire M, et al. Nat Genet. 1995 Apr;9(4):418-23. doi: 10.1038/ng0495-418. Nat Genet. 1995. PMID: 7795649

5

Diabetes complications in NIDDM kindreds linked to the MODY3 locus on chromosome 12q.

Velho G, Vaxillaire M, Boccio V, Charpentier G, Froguel P. Velho G, et al. Among authors: vaxillaire m. Diabetes Care. 1996 Sep;19(9):915-9. doi: 10.2337/diacare.19.9.915. Diabetes Care. 1996. PMID: 8875082

6

Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3).

Vaxillaire M, Rouard M, Yamagata K, Oda N, Kaisaki PJ, Boriraj VV, Chevre JC, Boccio V, Cox RD, Lathrop GM, Dussoix P, Philippe J, Timsit J, Charpentier G, Velho G, Bell GI, Froguel P. Vaxillaire M, et al. Hum Mol Genet. 1997 Apr;6(4):583-6. doi: 10.1093/hmg/6.4.583. Hum Mol Genet. 1997. PMID: 9097962

7

An automated fluorescent single-strand conformation polymorphism technique for screening mutations in the hepatocyte nuclear factor-1alpha gene (maturity-onset diabetes of the young).

Boutin P, Chèvre JC, Hani EH, Gomis R, Pardini VC, Guillausseau PJ, Vaxillaire M, Velho G, Froguel P. Boutin P, et al. Among authors: vaxillaire m. Diabetes. 1997 Dec;46(12):2108-9. doi: 10.2337/diab.46.12.2108. Diabetes. 1997. PMID: 9392505 No abstract available.

8

Mutation screening in 18 Caucasian families suggest the existence of other MODY genes.

Chèvre JC, Hani EH, Boutin P, Vaxillaire M, Blanché H, Vionnet N, Pardini VC, Timsit J, Larger E, Charpentier G, Beckers D, Maes M, Bellanné-Chantelot C, Velho G, Froguel P. Chèvre JC, et al. Among authors: vaxillaire m. Diabetologia. 1998 Sep;41(9):1017-23. doi: 10.1007/s001250051025. Diabetologia. 1998. PMID: 9754819

9

Anatomy of a homeoprotein revealed by the analysis of human MODY3 mutations.

Vaxillaire M, Abderrahmani A, Boutin P, Bailleul B, Froguel P, Yaniv M, Pontoglio M. Vaxillaire M, et al. J Biol Chem. 1999 Dec 10;274(50):35639-46. doi: 10.1074/jbc.274.50.35639. J Biol Chem. 1999. PMID: 10585442 Free article.

10

Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians.

Abderrahmani A, Chèvre JC, Otabe S, Chikri M, Hani EH, Vaxillaire M, Hinokio Y, Horikawa Y, Bell GI, Froguel P. Abderrahmani A, et al. Among authors: vaxillaire m. Diabetes. 2000 Feb;49(2):306-8. doi: 10.2337/diabetes.49.2.306. Diabetes. 2000. PMID: 10868949

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