Vaxillaire M - Search Results

1

Type 2 diabetes-related genetic risk scores associated with variations in fasting plasma glucose and development of impaired glucose homeostasis in the prospective DESIR study.

Vaxillaire M, Yengo L, Lobbens S, Rocheleau G, Eury E, Lantieri O, Marre M, Balkau B, Bonnefond A, Froguel P. Vaxillaire M, et al. Diabetologia. 2014 Aug;57(8):1601-10. doi: 10.1007/s00125-014-3277-x. Epub 2014 Jun 4. Diabetologia. 2014. PMID: 24893864

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

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.

4

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

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 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families.

Velho G, Blanché H, Vaxillaire M, Bellanné-Chantelot C, Pardini VC, Timsit J, Passa P, Deschamps I, Robert JJ, Weber IT, Marotta D, Pilkis SJ, Lipkind GM, Bell GI, Froguel P. Velho G, et al. Among authors: vaxillaire m. Diabetologia. 1997 Feb;40(2):217-24. doi: 10.1007/s001250050666. Diabetologia. 1997. PMID: 9049484

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

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

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

No evidence for linkage or for diabetes-associated mutations in the activin type 2B receptor gene (ACVR2B) in French patients with mature-onset diabetes of the young or type 2 diabetes.

Dupont S, Hani EH, Cras-Méneur C, De Matos F, Lobbens S, Lecoeur C, Vaxillaire M, Scharfmann R, Froguel P. Dupont S, et al. Among authors: vaxillaire m. Diabetes. 2001 May;50(5):1219-21. doi: 10.2337/diabetes.50.5.1219. Diabetes. 2001. PMID: 11334431

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