1 - 25 of 61 results for author:"Vaxillaire M." in Literature citations
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| Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene. Bonnefond A., Philippe J., Durand E., Dechaume A., Huyvaert M., Montagne L., Marre M., Balkau B., Fajardy I., Vambergue A. et al. PLoS ONE 7:e37423-e37423(2012) · Mapped (3) |
| Glucose-dependent regulation of NR2F2 promoter and influence of SNP-rs3743462 on whole body insulin sensitivity. Boutant M., Ramos O.H., Lecoeur C., Vaillant E., Philippe J., Zhang P., Perilhou A., Valcarcel B., Sebert S., Jarvelin M.R. et al. PLoS ONE 7:e35810-e35810(2012) · Mapped (3) |
| Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes. Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC) Nat. Genet. 44:297-301(2012) · Mapped (2) |
| 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., Fontes G., Philippe J., Meur G., Diraison F., Sessions R.B. et al. J. Biol. Chem. 286:44005-44014(2011) · Mapped (9) |
| Mechanism of KATP hyperactivity and sulfonylurea tolerance due to a diabetogenic mutation in L0 helix of sulfonylurea receptor 1 (ABCC8). Babenko A.P., Vaxillaire M. FEBS Lett. 585:3555-3559(2011) · Mapped (3) |
| A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes. Thanabalasingham G., Shah N., Vaxillaire M., Hansen T., Tuomi T., Gasperikova D., Szopa M., Tjora E., James T.J., Kokko P. et al. Diabetologia 54:2801-2810(2011) · Mapped (20) |
| Disruption of a novel Kruppel-like transcription factor p300-regulated pathway for insulin biosynthesis revealed by studies of the c.-331 INS mutation found in neonatal diabetes mellitus. Bonnefond A., Lomberk G., Buttar N., Busiah K., Vaillant E., Lobbens S., Yengo L., Dechaume A., Mignot B., Simon A. et al. J. Biol. Chem. 286:28414-28424(2011) · Mapped (8) |
| Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations. Gonsorcikova L., Vaxillaire M., Pruhova S., Dechaume A., Dusatkova P., Cinek O., Pedersen O., Froguel P., Hansen T., Lebl J. Pediatr Diabetes 12:266-269(2011) · Mapped (3) |
| Conserved intramolecular disulfide bond is critical to trafficking and fate of ATP-binding cassette (ABC) transporters ABCB6 and sulfonylurea receptor 1 (SUR1)/ABCC8. Fukuda Y., Aguilar-Bryan L., Vaxillaire M., Dechaume A., Wang Y., Dean M., Moitra K., Bryan J., Schuetz J.D. J. Biol. Chem. 286:8481-8492(2011) · Mapped (11) |
| Genetic and functional assessment of the role of the rs13431652-A and rs573225-A alleles in the G6PC2 promoter that are strongly associated with elevated fasting glucose levels. Bouatia-Naji N., Bonnefond A., Baerenwald D.A., Marchand M., Bugliani M., Marchetti P., Pattou F., Printz R.L., Flemming B.P., Umunakwe O.C. et al. Diabetes 59:2662-2671(2010) · Mapped (2) |
| Study of TNFalpha -308G/A and IL6 -174G/C polymorphisms in type 2 diabetes and obesity risk in the Tunisian population. Bouhaha R., Baroudi T., Ennafaa H., Vaillant E., Abid H., Sassi R., Vatin V., Froguel P., Gaaied A.B., Meyre D. et al. Clin. Biochem. 43:549-552(2010) · Mapped (5) |
| Insulin gene mutations resulting in early-onset diabetes: marked differences in clinical presentation, metabolic status, and pathogenic effect through endoplasmic reticulum retention. Meur G., Simon A., Harun N., Virally M., Dechaume A., Bonnefond A., Fetita S., Tarasov A.I., Guillausseau P.J., Boesgaard T.W. et al. Diabetes 59:653-661(2010) · Mapped (3) |
| Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia. Rung J., Cauchi S., Albrechtsen A., Shen L., Rocheleau G., Cavalcanti-Proenca C., Bacot F., Balkau B., Belisle A., Borch-Johnsen K. et al. Nat. Genet. 41:1110-1115(2009) · Mapped (40) |
| Genetic variant in HK1 is associated with a proanemic state and A1C but not other glycemic control-related traits. Bonnefond A., Vaxillaire M., Labrune Y., Lecoeur C., Chevre J.C., Bouatia-Naji N., Cauchi S., Balkau B., Marre M., Tichet J. et al. Diabetes 58:2687-2697(2009) · Mapped (24) |
| The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects. Choquet H., Cavalcanti-Proenca C., Lecoeur C., Dina C., Cauchi S., Vaxillaire M., Hadjadj S., Horber F., Potoczna N., Charpentier G. et al. Hum. Mol. Genet. 18:2495-2501(2009) · Mapped (1) |
| Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: a case-control study. Ezzidi I., Mtiraoui N., Cauchi S., Vaillant E., Dechaume A., Chaieb M., Kacem M., Almawi W.Y., Froguel P., Mahjoub T. et al. BMC Med. Genet. 10:33-33(2009) · Mapped (43) |
| Mutations in the ABCC8 gene can cause autoantibody-negative insulin-dependent diabetes. Hartemann-Heurtier A., Simon A., Bellanne-Chantelot C., Reynaud R., Cave H., Polak M., Vaxillaire M., Grimaldi A. Diabetes Metab. 35:233-235(2009) · Mapped (3) |
| G-allele of intronic rs10830963 in MTNR1B confers increased risk of impaired fasting glycemia and type 2 diabetes through an impaired glucose-stimulated insulin release: studies involving 19,605 Europeans. Sparso T., Bonnefond A., Andersson E., Bouatia-Naji N., Holmkvist J., Wegner L., Grarup N., Gjesing A.P., Banasik K., Cavalcanti-Proenca C. et al. Diabetes 58:1450-1456(2009) · Mapped (2) |
| Functional and genetic analysis in type 2 diabetes of liver X receptor alleles--a cohort study. Dahlman I., Nilsson M., Gu H.F., Lecoeur C., Efendic S., Ostenson C.G., Brismar K., Gustafsson J.A., Froguel P., Vaxillaire M. et al. BMC Med. Genet. 10:27-27(2009) · Mapped (14) |
| TCF7L2 is associated with type 2 diabetes in nonobese individuals from Tunisia. Bouhaha R., Choquet H., Meyre D., Abid Kamoun H., Ennafaa H., Baroudi T., Sassi R., Vaxillaire M., Elgaaied A., Froguel P. et al. Pathol. Biol. 58:426-429(2010) · Mapped (31) |
| Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction. Bonnefond A., Bouatia-Naji N., Simon A., Saint-Martin C., Dechaume A., de Lonlay P., Polak M., Bellanne-Chantelot C., Froguel P., Vaxillaire M. Diabetologia 52:982-985(2009) · Mapped (2) |
| A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk. Bouatia-Naji N., Bonnefond A., Cavalcanti-Proenca C., Sparso T., Holmkvist J., Marchand M., Delplanque J., Lobbens S., Rocheleau G., Durand E. et al. Nat. Genet. 41:89-94(2009) · Mapped (2) |
| Estrogen receptor alpha gene variants associate with type 2 diabetes and fasting plasma glucose. Dahlman I., Vaxillaire M., Nilsson M., Lecoeur C., Gu H.F., Cavalcanti-Proenca C., Efendic S., Ostenson C.G., Brismar K., Charpentier G. et al. Pharmacogenet. Genomics 18:967-975(2008) · Mapped (61) |
| Predicting diabetes: clinical, biological, and genetic approaches: data from the Epidemiological Study on the Insulin Resistance Syndrome (DESIR). Balkau B., Lange C., Fezeu L., Tichet J., de Lauzon-Guillain B., Czernichow S., Fumeron F., Froguel P., Vaxillaire M., Cauchi S. et al. Diabetes Care 31:2056-2061(2008) · Mapped (38) |
| Effect of ENPP1/PC-1-K121Q and PPARgamma-Pro12Ala polymorphisms on the genetic susceptibility to T2D in the Tunisian population. Bouhaha R., Meyre D., Kamoun H.A., Ennafaa H., Vaillant E., Sassi R., Baroudi T., Vatin V., Froguel P., Elgaaied A. et al. Diabetes Res. Clin. Pract. 81:278-283(2008) · Mapped (13) |