1 - 25 of 179 results for author:"Bell G.I." in Literature citations
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| Association of the KCNJ11 variant E23K with type 2 diabetes in Indo-Trinidadians. Boodram L.G., Miyake K., Hayes M.G., Bell G.I., Cockburn B.N. West Indian Med J 60:604-607(2011) · Mapped (3) |
| Alterations in TCF7L2 expression define its role as a key regulator of glucose metabolism. Savic D., Ye H., Aneas I., Park S.Y., Bell G.I., Nobrega M.A. Genome Res. 21:1417-1425(2011) · Mapped (47) |
| HLA-DQ haplotypes differ by ethnicity in patients with childhood-onset diabetes. Lipton R.B., Drum M., Greeley S.A., Danielson K.K., Bell G.I., Hagopian W.A. Pediatr Diabetes 12:388-395(2011) · Mapped (330) |
| Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene. Stoy J., Steiner D.F., Park S.Y., Ye H., Philipson L.H., Bell G.I. Rev Endocr Metab Disord 11:205-215(2010) · Mapped (3) |
| Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60. Fajans S.S., Bell G.I., Paz V.P., Below J.E., Cox N.J., Martin C., Thomas I.H., Chen M. Transl Res 156:7-14(2010) · Mapped (1) |
| Calpain-10 is a component of the obesity-related quantitative trait locus Adip1. Cheverud J.M., Fawcett G.L., Jarvis J.P., Norgard E.A., Pavlicev M., Pletscher L.S., Polonsky K.S., Ye H., Bell G.I., Semenkovich C.F. J. Lipid Res. 51:907-913(2010) · Mapped (3) |
| Mutant proinsulin proteins associated with neonatal diabetes are retained in the endoplasmic reticulum and not efficiently secreted. Park S.Y., Ye H., Steiner D.F., Bell G.I. Biochem. Biophys. Res. Commun. 391:1449-1454(2010) · Mapped (4) |
| TCF7L2 variant rs7903146 affects the risk of type 2 diabetes by modulating incretin action. Villareal D.T., Robertson H., Bell G.I., Patterson B.W., Tran H., Wice B., Polonsky K.S. Diabetes 59:479-485(2010) · Mapped (31) |
| Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome. Kawai T., Ng M.C., Hayes M.G., Yoshiuchi I., Tsuchiya T., Robertson H., Cox N.J., Polonsky K.S., Bell G.I., Ehrmann D.A. Diabetes Res. Clin. Pract. 86:186-192(2009) · Mapped (1) |
| Kir6.2 variant E23K increases ATP-sensitive K+ channel activity and is associated with impaired insulin release and enhanced insulin sensitivity in adults with normal glucose tolerance. Villareal D.T., Koster J.C., Robertson H., Akrouh A., Miyake K., Bell G.I., Patterson B.W., Nichols C.G., Polonsky K.S. Diabetes 58:1869-1878(2009) · Mapped (3) |
| Diagnosis and treatment of neonatal diabetes: a United States experience. Stoy J., Greeley S.A., Paz V.P., Ye H., Pastore A.N., Skowron K.B., Lipton R.B., Cogen F.R., Bell G.I., Philipson L.H. Pediatr Diabetes 9:450-459(2008) · Mapped (6) |
| Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. Molven A., Ringdal M., Nordbo A.M., Raeder H., Stoy J., Lipkind G.M., Steiner D.F., Philipson L.H., Bergmann I., Aarskog D. et al. |
| Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood. Edghill E.L., Flanagan S.E., Patch A.M., Boustred C., Parrish A., Shields B., Shepherd M.H., Hussain K., Kapoor R.R., Malecki M. et al. |
| Macrosomia and neonatal hypoglycaemia in RW pedigree subjects with a mutation (Q268X) in the gene encoding hepatocyte nuclear factor 4alpha (HNF4A). Fajans S.S., Bell G.I. Diabetologia 50:2600-2601(2007) · Mapped (9) |
| Insulin gene mutations as a cause of permanent neonatal diabetes. Stoy J., Edghill E.L., Flanagan S.E., Ye H., Paz V.P., Pluzhnikov A., Below J.E., Hayes M.G., Cox N.J., Lipkind G.M. et al. Proc. Natl. Acad. Sci. U.S.A. 104:15040-15044(2007) · UniProtKB (1) · Mapped (10) |
| Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses. Tsuchiya T., Schwarz P.E., Bosque-Plata L.D., Geoffrey Hayes M., Dina C., Froguel P., Wayne Towers G., Fischer S., Temelkova-Kurktschiev T., Rietzsch H. et al. Mol. Genet. Metab. 89:174-184(2006) · Mapped (2) |
| Common polymorphisms of calpain-10 are associated with abdominal obesity in subjects at high risk of type 2 diabetes. Pihlajamaki J., Salmenniemi U., Vanttinen M., Ruotsalainen E., Kuusisto J., Vauhkonen I., Kainulainen S., Ng M.C., Cox N.J., Bell G.I. et al. Diabetologia 49:1560-1566(2006) · Mapped (2) |
| Treatment of hyperglycemia in a 7-year-old child diagnosed with neonatal diabetes. Hathout E., Mace J., Bell G.I., Njolstad P.R. Diabetes Care 29:1458-1458(2006) · Mapped (3) |
| Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees. Fajans S.S., Bell G.I. Diabetologia 49:1106-1108(2006) · Mapped (9) |
| The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population. Ng M.C., Miyake K., So W.Y., Poon E.W., Lam V.K., Li J.K., Cox N.J., Bell G.I., Chan J.C. Diabetologia 48:2018-2024(2005) · Mapped (3) |
| Subcellular recruitment by TSG118 and TSPYL implicates a role for zinc finger protein 106 in a novel developmental pathway. Grasberger H., Bell G.I. Int. J. Biochem. Cell Biol. 37:1421-1437(2005) · UniProtKB (2) · Mapped (2) |
| Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population. Iwasaki N., Horikawa Y., Tsuchiya T., Kitamura Y., Nakamura T., Tanizawa Y., Oka Y., Hara K., Kadowaki T., Awata T. et al. J. Hum. Genet. 50:92-98(2005) · Mapped (2) |
| Dual promoter structure of ZFP106: regulation by myogenin and nuclear respiratory factor-1. Grasberger H., Ye H., Mashima H., Bell G.I. Gene 344:143-159(2005) · Mapped (8) |
| Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy. Sagen J.V., Raeder H., Hathout E., Shehadeh N., Gudmundsson K., Baevre H., Abuelo D., Phornphutkul C., Molnes J., Bell G.I. et al. |
| Association of the (AU)AT-rich element polymorphism in PPP1R3 with hormonal and metabolic features of polycystic ovary syndrome. Alcoser S.Y., Hara M., Bell G.I., Ehrmann D.A. J. Clin. Endocrinol. Metab. 89:2973-2976(2004) · Mapped (1) |