Vaxillaire M - Search Results

1

Human mutation within Per-Arnt-Sim (PAS) domain-containing protein kinase (PASK) causes basal insulin hypersecretion.

Semplici F, Vaxillaire M, Fogarty S, Semache M, Bonnefond A, Fontés G, Philippe J, Meur G, Diraison F, Sessions RB, Rutter J, Poitout V, Froguel P, Rutter GA. Semplici F, et al. Among authors: vaxillaire m. J Biol Chem. 2011 Dec 23;286(51):44005-44014. doi: 10.1074/jbc.M111.254995. Epub 2011 Nov 7. J Biol Chem. 2011. PMID: 22065581 Free PMC 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

Structure/function studies of human beta-cell glucokinase. Enzymatic properties of a sequence polymorphism, mutations associated with diabetes, and other site-directed mutants.

Takeda J, Gidh-Jain M, Xu LZ, Froguel P, Velho G, Vaxillaire M, Cohen D, Shimada F, Makino H, Nishi S, et al. Takeda J, et al. Among authors: vaxillaire m. J Biol Chem. 1993 Jul 15;268(20):15200-4. J Biol Chem. 1993. PMID: 8325892 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

Diagnostic heterogeneity of diabetes in lean young adults: classification based on immunological and genetic parameters.

Dussoix P, Vaxillaire M, Iynedjian PB, Tiercy JM, Ruiz J, Spinas GA, Berger W, Zahnd G, Froguel P, Philippe J. Dussoix P, et al. Among authors: vaxillaire m. Diabetes. 1997 Apr;46(4):622-31. doi: 10.2337/diab.46.4.622. Diabetes. 1997. PMID: 9075802

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

Glucose utilization and production in patients with maturity-onset diabetes of the young caused by a mutation of the hepatocyte nuclear factor-1alpha gene.

Surmely JF, Guenat E, Philippe J, Dussoix P, Schneiter P, Temler E, Vaxillaire M, Froguel P, Jéquier E, Tappy L. Surmely JF, et al. Among authors: vaxillaire m. Diabetes. 1998 Sep;47(9):1459-63. doi: 10.2337/diabetes.47.9.1459. Diabetes. 1998. PMID: 9726235

8

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.

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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