Vionnet N - Search Results

1

A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus.

Hani EH, Suaud L, Boutin P, Chèvre JC, Durand E, Philippi A, Demenais F, Vionnet N, Furuta H, Velho G, Bell GI, Laine B, Froguel P. Hani EH, et al. Among authors: vionnet n. J Clin Invest. 1998 Feb 1;101(3):521-6. doi: 10.1172/JCI1403. J Clin Invest. 1998. PMID: 9449683 Free PMC article.

2

Indication for genetic linkage of the phosphoenolpyruvate carboxykinase (PCK1) gene region on chromosome 20q to non-insulin-dependent diabetes mellitus.

Hani EH, Zouali H, Philippi A, Beaudoin JC, Vionnet N, Passa P, Demenais F, Froguel P. Hani EH, et al. Among authors: vionnet n. Diabetes Metab. 1996 Dec;22(6):451-4. Diabetes Metab. 1996. PMID: 8985654

3

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: vionnet n. Diabetologia. 1998 Sep;41(9):1017-23. doi: 10.1007/s001250051025. Diabetologia. 1998. PMID: 9754819

4

[Genetic risk of non-insulin-dependent diabetes].

Vionnet N, Froguel P. Vionnet N, et al. Journ Annu Diabetol Hotel Dieu. 1998:223-40. Journ Annu Diabetol Hotel Dieu. 1998. PMID: 9773623 Review. French. No abstract available.

5

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: vionnet n. Diabetes. 1995 Oct;44(10):1243-7. doi: 10.2337/diab.44.10.1243. Diabetes. 1995. PMID: 7556965

6

Genetics of non-insulin-dependent diabetes mellitus: from genes to the disease.

Froguel P, Vionnet N. Froguel P, et al. Among authors: vionnet n. Adv Nephrol Necker Hosp. 1995;24:157-63. Adv Nephrol Necker Hosp. 1995. PMID: 7572407 Review. No abstract available.

7

A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus.

Hager J, Hansen L, Vaisse C, Vionnet N, Philippi A, Poller W, Velho G, Carcassi C, Contu L, Julier C, et al. Hager J, et al. Among authors: vionnet n. Nat Genet. 1995 Mar;9(3):299-304. doi: 10.1038/ng0395-299. Nat Genet. 1995. PMID: 7773293

8

Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.

Velho G, Byrne MM, Clément K, Sturis J, Pueyo ME, Blanché H, Vionnet N, Fiet J, Passa P, Robert JJ, Polonsky KS, Froguel P. Velho G, et al. Among authors: vionnet n. Diabetes. 1996 Apr;45(4):478-87. doi: 10.2337/diab.45.4.478. Diabetes. 1996. PMID: 8603770

9

Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians.

Hani EH, Clément K, Velho G, Vionnet N, Hager J, Philippi A, Dina C, Inoue H, Permutt MA, Basdevant A, North M, Demenais F, Guy-Grand B, Froguel P. Hani EH, et al. Among authors: vionnet n. Diabetes. 1997 Apr;46(4):688-94. doi: 10.2337/diab.46.4.688. Diabetes. 1997. PMID: 9075812

10

Genetic analyses of glucose transporter genes in French non-insulin-dependent diabetic families.

Lesage S, Zouali H, Vionnet N, Philippi A, Velho G, Serradas P, Passa P, Demenais F, Froguel P. Lesage S, et al. Among authors: vionnet n. Diabetes Metab. 1997 Apr;23(2):137-42. Diabetes Metab. 1997. PMID: 9137902

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