Vaxillaire M - Search Results

1

Pathogenic variants in actionable MODY genes are associated with type 2 diabetes.

Bonnefond A, Boissel M, Bolze A, Durand E, Toussaint B, Vaillant E, Gaget S, Graeve F, Dechaume A, Allegaert F, Guilcher DL, Yengo L, Dhennin V, Borys JM, Lu JT, Cirulli ET, Elhanan G, Roussel R, Balkau B, Marre M, Franc S, Charpentier G, Vaxillaire M, Canouil M, Washington NL, Grzymski JJ, Froguel P. Bonnefond A, et al. Among authors: vaxillaire m. Nat Metab. 2020 Oct;2(10):1126-1134. doi: 10.1038/s42255-020-00294-3. Epub 2020 Oct 12. Nat Metab. 2020. PMID: 33046911 Free 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

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

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

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

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

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

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