Vigouroux C - Search Results

1

Search for a third susceptibility gene for maturity-onset diabetes of the young. Studies with eleven candidate genes.

Vaxillaire M, Vionnet N, Vigouroux C, Sun F, Espinosa R 3rd, Lebeau MM, Stoffel M, Lehto M, Beckmann JS, Detheux M, et al. Vaxillaire M, et al. Among authors: vigouroux c. Diabetes. 1994 Mar;43(3):389-95. doi: 10.2337/diab.43.3.389. Diabetes. 1994. PMID: 7508874

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. Among authors: vigouroux c. Nat Genet. 1995 Apr;9(4):418-23. doi: 10.1038/ng0495-418. Nat Genet. 1995. PMID: 7795649

3

Genetic exclusion of 14 candidate genes in lipoatropic diabetes using linkage analysis in 10 consanguineous families.

Vigouroux C, Khallouf E, Bourut C, Robert JJ, de Kerdanet M, Tubiana-Rufi N, Fauré S, Weissenbach J, Capeau J, Magré J. Vigouroux C, et al. J Clin Endocrinol Metab. 1997 Oct;82(10):3438-44. doi: 10.1210/jcem.82.10.4292. J Clin Endocrinol Metab. 1997. PMID: 9329383

4

Dominant transmission of insulin resistance in a type A family resulting from a heterozygous nonsense mutation in the insulin receptor gene and associated with decreased mRNA level and insulin binding sites.

Magré J, Karayanni C, Hadjiathanasiou CG, Desbois-Mouthon C, Meier M, Vigouroux C, Stavrinadis C, Sinaniotis C, Caron M, Capeau J. Magré J, et al. Among authors: vigouroux c. Diabetes. 1997 Nov;46(11):1901-3. doi: 10.2337/diab.46.11.1901. Diabetes. 1997. PMID: 9356044 No abstract available.

5

Human hormone-sensitive lipase: genetic mapping, identification of a new dinucleotide repeat, and association with obesity and NIDDM.

Magré J, Laurell H, Fizames C, Antoine PJ, Dib C, Vigouroux C, Bourut C, Capeau J, Weissenbach J, Langin D. Magré J, et al. Among authors: vigouroux c. Diabetes. 1998 Feb;47(2):284-6. doi: 10.2337/diab.47.2.284. Diabetes. 1998. PMID: 9519728 No abstract available.

6

Human peroxisome proliferator-activated receptor-gamma2: genetic mapping, identification of a variant in the coding sequence, and exclusion as the gene responsible for lipoatrophic diabetes.

Vigouroux C, Fajas L, Khallouf E, Meier M, Gyapay G, Lascols O, Auwerx J, Weissenbach J, Capeau J, Magré J. Vigouroux C, et al. Diabetes. 1998 Mar;47(3):490-2. doi: 10.2337/diabetes.47.3.490. Diabetes. 1998. PMID: 9519760 No abstract available.

7

Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophy.

Vigouroux C, Magré J, Vantyghem MC, Bourut C, Lascols O, Shackleton S, Lloyd DJ, Guerci B, Padova G, Valensi P, Grimaldi A, Piquemal R, Touraine P, Trembath RC, Capeau J. Vigouroux C, et al. Diabetes. 2000 Nov;49(11):1958-62. doi: 10.2337/diabetes.49.11.1958. Diabetes. 2000. PMID: 11078466

8

Prevalence of mutations in AGPAT2 among human lipodystrophies.

Magré J, Delépine M, Van Maldergem L, Robert JJ, Maassen JA, Meier M, Panz VR, Kim CA, Tubiana-Rufi N, Czernichow P, Seemanova E, Buchanan CR, Lacombe D, Vigouroux C, Lascols O, Kahn CR, Capeau J, Lathrop M. Magré J, et al. Among authors: vigouroux c. Diabetes. 2003 Jun;52(6):1573-8. doi: 10.2337/diabetes.52.6.1573. Diabetes. 2003. PMID: 12765973

9

Etiological investigations in apparent type 2 diabetes: when to search for lamin A/C mutations?

Donadille B, Lascols O, Capeau J, Vigouroux C. Donadille B, et al. Among authors: vigouroux c. Diabetes Metab. 2005 Dec;31(6):527-32. doi: 10.1016/s1262-3636(07)70227-6. Diabetes Metab. 2005. PMID: 16357800 Review.

10

Diabetes, insulin resistance and dyslipidaemia in lipodystrophic HIV-infected patients on highly active antiretroviral therapy (HAART).

Vigouroux C, Gharakhanian S, Salhi Y, Nguyen TH, Chevenne D, Capeau J, Rozenbaum W. Vigouroux C, et al. Diabetes Metab. 1999 Sep;25(3):225-32. Diabetes Metab. 1999. PMID: 10499191

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