1 - 25 of 39 results for author:"Velho G." in Literature citations
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| Allelic variations in superoxide dismutase-1 (SOD1) gene and renal and cardiovascular morbidity and mortality in type 2 diabetic subjects. Neves A.L., Mohammedi K., Emery N., Roussel R., Fumeron F., Marre M., Velho G. Mol. Genet. Metab. 106:359-365(2012) · Mapped (2) |
| Allelic variations in the vitamin D receptor gene, insulin secretion and parents' heights are independently associated with height in obese children and adolescents. Ferrarezi D.A., Bellili-Munoz N., Nicolau C., Cheurfa N., Guazzelli I.C., Frazzatto E., Velho G., Villares S.M. Metab. Clin. Exp. 61:1413-1421(2012) · Mapped (6) |
| Association of ADIPOQ variants, total and high molecular weight adiponectin levels with coronary artery disease in diabetic and non-diabetic Brazilian subjects. Oliveira C.S., Saddi-Rosa P., Crispim F., Canani L.H., Gerchman F., Giuffrida F.M., Vieira J.G., Velho G., Reis A.F. J. Diabetes Complicat. 26:94-98(2012) · Mapped (3) |
| Dietary fat intake and polymorphisms at the PPARG locus modulate BMI and type 2 diabetes risk in the D.E.S.I.R. prospective study. Lamri A., Abi Khalil C., Jaziri R., Velho G., Lantieri O., Vol S., Froguel P., Balkau B., Marre M., Fumeron F. Int J Obes (Lond) 36:218-224(2012) · Mapped (9) |
| Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome. Reis A.F., Kannengiesser C., Jennane F., Manna T.D., Cheurfa N., Oudin C., Savoldelli R.D., Oliveira C., Grandchamp B., Kok F. et al. Pediatr Diabetes 12:187-191(2011) · Mapped (3) |
| Decreased insulin secretion and increased risk of type 2 diabetes associated with allelic variations of the WFS1 gene: the Data from Epidemiological Study on the Insulin Resistance Syndrome (DESIR) prospective study. Cheurfa N., Brenner G.M., Reis A.F., Dubois-Laforgue D., Roussel R., Tichet J., Lantieri O., Balkau B., Fumeron F., Timsit J. et al. Diabetologia 54:554-562(2011) · Mapped (2) |
| Association of common variants in NPPA and NPPB with blood pressure does not translate into kidney damage in a general population study. Maimaitiming S., Roussel R., Hadjadj S., Fumeron F., Aubert R., Emery N., Velho G., Mohammedi K., Travert F., Tichet J. et al. J. Hypertens. 28:1230-1233(2010) · Mapped (2) |
| Genetic variability at the six transmembrane protein of prostate 2 locus and the metabolic syndrome: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study. Miot A., Maimaitiming S., Emery N., Bellili N., Roussel R., Tichet J., Velho G., Balkau B., Marre M., Fumeron F. J. Clin. Endocrinol. Metab. 95:2942-2947(2010) · Mapped (1) |
| HNF1alpha mutations are present in half of clinically defined MODY patients in South-Brazilian individuals. Maraschin J.d.e. F., Kannengiesser C., Murussi N., Campagnolo N., Canani L.H., Gross J.L., Velho G., Grandchamp B., Silveiro S.P. Arq Bras Endocrinol Metabol 52:1326-1331(2008) · Mapped (20) |
| Long-term follow-up of oral glucose tolerance test-derived glucose tolerance and insulin secretion and insulin sensitivity indexes in subjects with glucokinase mutations (MODY2). Martin D., Bellanne-Chantelot C., Deschamps I., Froguel P., Robert J.J., Velho G. Diabetes Care 31:1321-1323(2008) · Mapped (3) |
| 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 D.A., Reis A.F., Brenner G.M., Bouche C., Le Feuvre C., Fumeron F., Timsit J., Marre M. et al. Diabetes 57:1063-1068(2008) · Mapped (1) |
| The type and the position of HNF1A mutation modulate age at diagnosis of diabetes in patients with maturity-onset diabetes of the young (MODY)-3. Bellanne-Chantelot C., Carette C., Riveline J.P., Valero R., Gautier J.F., Larger E., Reznik Y., Ducluzeau P.H., Sola A., Hartemann-Heurtier A. et al. Diabetes 57:503-508(2008) · Mapped (18) |
| The Ala45Thr polymorphism of NEUROD1 is associated with type 1 diabetes in Brazilian women. Oliveira C.S., Hauache O.M., Vieira J.G., Maciel R.M., Sjoroos M., Canani L.H., Velho G., Gross J.L., Reis A.F. Diabetes Metab. 31:599-602(2005) · Mapped (3) |
| Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5. Bellanne-Chantelot C., Clauin S., Chauveau D., Collin P., Daumont M., Douillard C., Dubois-Laforgue D., Dusselier L., Gautier J.-F., Jadoul M. et al. Diabetes 54:3126-3132(2005) · UniProtKB (1) |
| The Gly482Ser polymorphism in the peroxisome proliferator-activated receptor-gamma coactivator-1 gene is associated with hypertension in type 2 diabetic men. Cheurfa N., Reis A.F., Dubois-Laforgue D., Bellanne-Chantelot C., Timsit J., Velho G. Diabetologia 47:1980-1983(2004) · Mapped (10) |
| A polymorphism in the promoter of UCP2 gene modulates lipid levels in patients with type 2 diabetes. Reis A.F., Dubois-Laforgue D., Bellanne-Chantelot C., Timsit J., Velho G. Mol. Genet. Metab. 82:339-344(2004) · Mapped (1) |
| Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations. Bellanne-Chantelot C., Chauveau D., Gautier J.-F., Dubois-Laforgue D., Clauin S., Beaufils S., Wilhelm J.-M., Boitard C., Noeel L.-H., Velho G. et al. Ann. Intern. Med. 140:510-517(2004) · UniProtKB (1) · Mapped (2) |
| The N363S polymorphism in the glucocorticoid receptor gene is associated with overweight in subjects with type 2 diabetes mellitus. Roussel R., Reis A.F., Dubois-Laforgue D., Bellanne-Chantelot C., Timsit J., Velho G. Clin. Endocrinol. (Oxf) 59:237-241(2003) · Mapped (12) |
| Allelic variation in exon 18 of the sulfonylurea receptor 1 (SUR1) gene, insulin secretion and insulin sensitivity in nondiabetic relatives of type 2 diabetic subjects. Reis A.F., Hani E.H., Beressi N., Robert J.J., Bresson J.L., Froguel P., Velho G. Diabetes Metab. 28:209-215(2002) · Mapped (3) |
| Sulfonylurea receptor -1 (SUR1): genetic and metabolic evidences for a role in the susceptibility to type 2 diabetes mellitus. Reis A.F., Velho G. Diabetes Metab. 28:14-19(2002) · Mapped (3) |
| Vitamin D receptor gene polymorphisms are associated with obesity in type 2 diabetic subjects with early age of onset. Ye W.Z., Reis A.F., Dubois-Laforgue D., Bellanne-Chantelot C., Timsit J., Velho G. Eur. J. Endocrinol. 145:181-186(2001) · Mapped (6) |
| HNF1alpha controls renal glucose reabsorption in mouse and man. Pontoglio M., Prie D., Cheret C., Doyen A., Leroy C., Froguel P., Velho G., Yaniv M., Friedlander G. |
| Variations in the vitamin D-binding protein (Gc locus) and risk of type 2 diabetes mellitus in French Caucasians. Ye W.Z., Dubois-Laforgue D., Bellanne-Chantelot C., Timsit J., Velho G. Metab. Clin. Exp. 50:366-369(2001) · Mapped (2) |
| Association of a variant in exon 31 of the sulfonylurea receptor 1 (SUR1) gene with type 2 diabetes mellitus in French Caucasians. Reis A.F., Ye W.Z., Dubois-Laforgue D., Bellanne-Chantelot C., Timsit J., Velho G. Hum. Genet. 107:138-144(2000) · Mapped (5) |
| Mutations in the insulin promoter factor-1 gene in late-onset type 2 diabetes mellitus. Reis A.F., Ye W.Z., Dubois-Laforgue D., Bellanne-Chantelot C., Timsit J., Velho G. Eur. J. Endocrinol. 143:511-513(2000) · Mapped (1) |