Velho G - Search Results

1

The common -866G>A variant in the promoter of UCP2 is associated with decreased risk of coronary artery disease in type 2 diabetic men.

Cheurfa N, Dubois-Laforgue D, Ferrarezi DA, Reis AF, Brenner GM, Bouché C, Le Feuvre C, Fumeron F, Timsit J, Marre M, Velho G. Cheurfa N, et al. Among authors: velho g. Diabetes. 2008 Apr;57(4):1063-8. doi: 10.2337/db07-1292. Epub 2008 Jan 11. Diabetes. 2008. PMID: 18192542 Free article.

2

Linkage analysis and molecular scanning of glucokinase gene in NIDDM families.

Zouali H, Vaxillaire M, Lesage S, Sun F, Velho G, Vionnet N, Chiu K, Passa P, Permutt A, Demenais F, et al. Zouali H, et al. Among authors: velho g. Diabetes. 1993 Sep;42(9):1238-45. doi: 10.2337/diab.42.9.1238. Diabetes. 1993. PMID: 8349034

3

Lipoprotein(a) in diabetic patients and normoglycemic relatives in familial NIDDM.

Velho G, Erlich D, Turpin E, Néel D, Cohen D, Froguel P, Passa P. Velho G, et al. Diabetes Care. 1993 May;16(5):742-7. doi: 10.2337/diacare.16.5.742. Diabetes Care. 1993. PMID: 8495614

4

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. Diabetes Care. 1996 Sep;19(9):915-9. doi: 10.2337/diacare.19.9.915. Diabetes Care. 1996. PMID: 8875082

5

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: velho g. Diabetes. 1997 Apr;46(4):688-94. doi: 10.2337/diab.46.4.688. Diabetes. 1997. PMID: 9075812

6

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. Among authors: velho g. Eur J Endocrinol. 1999 Dec;141(6):609-18. doi: 10.1530/eje.0.1410609. Eur J Endocrinol. 1999. PMID: 10601964

7

Identification of a novel Tru9 I polymorphism in the human vitamin D receptor gene.

Ye WZ, Reis AF, Velho G. Ye WZ, et al. Among authors: velho g. J Hum Genet. 2000;45(1):56-7. doi: 10.1007/s100380050011. J Hum Genet. 2000. PMID: 10697965

8

Mutations in the insulin promoter factor-1 gene in late-onset type 2 diabetes mellitus.

Reis AF, Ye WZ, Dubois-Laforgue D, Bellanné-Chantelot C, Timsit J, Velho G. Reis AF, et al. Among authors: velho g. Eur J Endocrinol. 2000 Oct;143(4):511-3. doi: 10.1530/eje.0.1430511. Eur J Endocrinol. 2000. PMID: 11022198 Clinical Trial.

9

Association of a variant in exon 31 of the sulfonylurea receptor 1 (SUR1) gene with type 2 diabetes mellitus in French Caucasians.

Reis AF, Ye WZ, Dubois-Laforgue D, Bellanné-Chantelot C, Timsit J, Velho G. Reis AF, et al. Among authors: velho g. Hum Genet. 2000 Aug;107(2):138-44. doi: 10.1007/s004390000345. Hum Genet. 2000. PMID: 11030411

10

Variations in the vitamin D-binding protein (Gc locus) and risk of type 2 diabetes mellitus in French Caucasians.

Ye WZ, Dubois-Laforgue D, Bellanné-Chantelot C, Timsit J, Velho G. Ye WZ, et al. Among authors: velho g. Metabolism. 2001 Mar;50(3):366-9. doi: 10.1053/meta.2001.20172. Metabolism. 2001. PMID: 11230793

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