Vaxillaire M - Search Results

1

A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels.

Bouatia-Naji N, Rocheleau G, Van Lommel L, Lemaire K, Schuit F, Cavalcanti-Proença C, Marchand M, Hartikainen AL, Sovio U, De Graeve F, Rung J, Vaxillaire M, Tichet J, Marre M, Balkau B, Weill J, Elliott P, Jarvelin MR, Meyre D, Polychronakos C, Dina C, Sladek R, Froguel P. Bouatia-Naji N, et al. Among authors: vaxillaire m. Science. 2008 May 23;320(5879):1085-8. doi: 10.1126/science.1156849. Epub 2008 May 1. Science. 2008. PMID: 18451265 Free article.

2

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

3

Arginine-induced insulin release in glucokinase-deficient subjects.

Pueyo ME, Clement K, Vaxillaire M, Passa P, Froguel P, Robert JJ, Velho G. Pueyo ME, et al. Among authors: vaxillaire m. Diabetes Care. 1994 Sep;17(9):1015-21. doi: 10.2337/diacare.17.9.1015. Diabetes Care. 1994. PMID: 7988299

4

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus.

Froguel P, Zouali H, Vionnet N, Velho G, Vaxillaire M, Sun F, Lesage S, Stoffel M, Takeda J, Passa P, et al. Froguel P, et al. Among authors: vaxillaire m. N Engl J Med. 1993 Mar 11;328(10):697-702. doi: 10.1056/NEJM199303113281005. N Engl J Med. 1993. PMID: 8433729 Free article.

5

Assessment of insulin sensitivity in glucokinase-deficient subjects.

Clément K, Pueyo ME, Vaxillaire M, Rakotoambinina B, Thuillier F, Passa P, Froguel P, Robert JJ, Velho G. Clément K, et al. Among authors: vaxillaire m. Diabetologia. 1996 Jan;39(1):82-90. doi: 10.1007/BF00400417. Diabetologia. 1996. PMID: 8720607

6

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

7

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

8

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.

9

Insulin secretion and insulin sensitivity in diabetic and non-diabetic subjects with hepatic nuclear factor-1alpha (maturity-onset diabetes of the young-3) mutations.

Vaxillaire M, Pueyo ME, Clément K, Fiet J, Timsit J, Philippe J, Robert JJ, Tappy L, Froguel P, Velho G. Vaxillaire M, et al. Eur J Endocrinol. 1999 Dec;141(6):609-18. doi: 10.1530/eje.0.1410609. Eur J Endocrinol. 1999. PMID: 10601964

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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