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Journal Abstract Search

148 related items for PubMed ID: 15579791

  • 1. Polymorphisms of the SUR1 (ABCC8) and Kir6.2 (KCNJ11) genes predict the conversion from impaired glucose tolerance to type 2 diabetes. The Finnish Diabetes Prevention Study.
    Laukkanen O, Pihlajamäki J, Lindström J, Eriksson J, Valle TT, Hämäläinen H, Ilanne-Parikka P, Keinänen-Kiukaanniemi S, Tuomilehto J, Uusitupa M, Laakso M, Finnish Diabetes Prevention Study Group.
    J Clin Endocrinol Metab; 2004 Dec; 89(12):6286-90. PubMed ID: 15579791
    [Abstract] [Full Text] [Related]

  • 2. Type 2 diabetes-associated missense polymorphisms KCNJ11 E23K and ABCC8 A1369S influence progression to diabetes and response to interventions in the Diabetes Prevention Program.
    Florez JC, Jablonski KA, Kahn SE, Franks PW, Dabelea D, Hamman RF, Knowler WC, Nathan DM, Altshuler D.
    Diabetes; 2007 Feb; 56(2):531-6. PubMed ID: 17259403
    [Abstract] [Full Text] [Related]

  • 3. Physical activity modifies the effect of SNPs in the SLC2A2 (GLUT2) and ABCC8 (SUR1) genes on the risk of developing type 2 diabetes.
    Kilpeläinen TO, Lakka TA, Laaksonen DE, Laukkanen O, Lindström J, Eriksson JG, Valle TT, Hämäläinen H, Aunola S, Ilanne-Parikka P, Keinänen-Kiukaanniemi S, Tuomilehto J, Uusitupa M, Laakso M, Finnish Diabetes Prevention Study Group.
    Physiol Genomics; 2007 Oct 22; 31(2):264-72. PubMed ID: 17636114
    [Abstract] [Full Text] [Related]

  • 4. Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region.
    Florez JC, Burtt N, de Bakker PI, Almgren P, Tuomi T, Holmkvist J, Gaudet D, Hudson TJ, Schaffner SF, Daly MJ, Hirschhorn JN, Groop L, Altshuler D.
    Diabetes; 2004 May 22; 53(5):1360-8. PubMed ID: 15111507
    [Abstract] [Full Text] [Related]

  • 5. Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes.
    Gloyn AL, Weedon MN, Owen KR, Turner MJ, Knight BA, Hitman G, Walker M, Levy JC, Sampson M, Halford S, McCarthy MI, Hattersley AT, Frayling TM.
    Diabetes; 2003 Feb 22; 52(2):568-72. PubMed ID: 12540637
    [Abstract] [Full Text] [Related]

  • 6. Association studies of variants in promoter and coding regions of beta-cell ATP-sensitive K-channel genes SUR1 and Kir6.2 with Type 2 diabetes mellitus (UKPDS 53).
    Gloyn AL, Hashim Y, Ashcroft SJ, Ashfield R, Wiltshire S, Turner RC, UK Prospective Diabetes Study (UKPDS 53).
    Diabet Med; 2001 Mar 22; 18(3):206-12. PubMed ID: 11318841
    [Abstract] [Full Text] [Related]

  • 7. Effects of single nucleotide polymorphisms in K(ATP) channel genes on type 2 diabetes in a Turkish population.
    Gonen MS, Arikoglu H, Erkoc Kaya D, Ozdemir H, Ipekci SH, Arslan A, Kayis SA, Gogebakan B.
    Arch Med Res; 2012 May 22; 43(4):317-23. PubMed ID: 22704848
    [Abstract] [Full Text] [Related]

  • 8. Common variants in the ATP-sensitive K+ channel genes KCNJ11 (Kir6.2) and ABCC8 (SUR1) in relation to glucose intolerance: population-based studies and meta-analyses.
    van Dam RM, Hoebee B, Seidell JC, Schaap MM, de Bruin TW, Feskens EJ.
    Diabet Med; 2005 May 22; 22(5):590-8. PubMed ID: 15842514
    [Abstract] [Full Text] [Related]

  • 9. Association of adiponectin (AdipoQ) and sulphonylurea receptor (ABCC8) gene polymorphisms with Type 2 Diabetes in North Indian population of Punjab.
    Matharoo K, Arora P, Bhanwer AJ.
    Gene; 2013 Sep 15; 527(1):228-34. PubMed ID: 23764562
    [Abstract] [Full Text] [Related]

  • 10. Sulfonylurea receptor 1 gene variants are associated with gestational diabetes and type 2 diabetes but not with altered secretion of insulin.
    Rissanen J, Markkanen A, Kärkkäinen P, Pihlajamäki J, Kekäläinen P, Mykkänen L, Kuusisto J, Karhapää P, Niskanen L, Laakso M.
    Diabetes Care; 2000 Jan 15; 23(1):70-3. PubMed ID: 10857971
    [Abstract] [Full Text] [Related]

  • 11. A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes.
    Proks P, Arnold AL, Bruining J, Girard C, Flanagan SE, Larkin B, Colclough K, Hattersley AT, Ashcroft FM, Ellard S.
    Hum Mol Genet; 2006 Jun 01; 15(11):1793-800. PubMed ID: 16613899
    [Abstract] [Full Text] [Related]

  • 12. Coexpression of the type 2 diabetes susceptibility gene variants KCNJ11 E23K and ABCC8 S1369A alter the ATP and sulfonylurea sensitivities of the ATP-sensitive K(+) channel.
    Hamming KS, Soliman D, Matemisz LC, Niazi O, Lang Y, Gloyn AL, Light PE.
    Diabetes; 2009 Oct 01; 58(10):2419-24. PubMed ID: 19587354
    [Abstract] [Full Text] [Related]

  • 13. Mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes mellitus and hyperinsulinism.
    Gloyn AL, Siddiqui J, Ellard S.
    Hum Mutat; 2006 Mar 01; 27(3):220-31. PubMed ID: 16416420
    [Abstract] [Full Text] [Related]

  • 14. Sulfonylurea receptor -1 (SUR1): genetic and metabolic evidences for a role in the susceptibility to type 2 diabetes mellitus.
    Reis AF, Velho G.
    Diabetes Metab; 2002 Feb 01; 28(1):14-9. PubMed ID: 11938023
    [Abstract] [Full Text] [Related]

  • 15. Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.
    Yokoi N, Kanamori M, Horikawa Y, Takeda J, Sanke T, Furuta H, Nanjo K, Mori H, Kasuga M, Hara K, Kadowaki T, Tanizawa Y, Oka Y, Iwami Y, Ohgawara H, Yamada Y, Seino Y, Yano H, Cox NJ, Seino S.
    Diabetes; 2006 Aug 01; 55(8):2379-86. PubMed ID: 16873704
    [Abstract] [Full Text] [Related]

  • 16. Genetic variations in the pancreatic ATP-sensitive potassium channel, beta-cell dysfunction, and susceptibility to type 2 diabetes.
    Chistiakov DA, Potapov VA, Khodirev DC, Shamkhalova MS, Shestakova MV, Nosikov VV.
    Acta Diabetol; 2009 Mar 01; 46(1):43-9. PubMed ID: 18758683
    [Abstract] [Full Text] [Related]

  • 17. [Polymorphism of the sulfonylurea receptor gene in type 2 diabetes mellitus].
    Owecki M, Horst-Sikorska W, Kaczmarek M, Słomski R, Sowiński J.
    Pol Arch Med Wewn; 2003 Feb 01; 109(2):143-8. PubMed ID: 12879777
    [Abstract] [Full Text] [Related]

  • 18. New ABCC8 mutations in relapsing neonatal diabetes and clinical features.
    Vaxillaire M, Dechaume A, Busiah K, Cavé H, Pereira S, Scharfmann R, de Nanclares GP, Castano L, Froguel P, Polak M, SUR1-Neonatal Diabetes Study Group.
    Diabetes; 2007 Jun 01; 56(6):1737-41. PubMed ID: 17389331
    [Abstract] [Full Text] [Related]

  • 19. Effect of genetic variants in KCNJ11, ABCC8, PPARG and HNF4A loci on the susceptibility of type 2 diabetes in Chinese Han population.
    Wang F, Han XY, Ren Q, Zhang XY, Han LC, Luo YY, Zhou XH, Ji LN.
    Chin Med J (Engl); 2009 Oct 20; 122(20):2477-82. PubMed ID: 20079163
    [Abstract] [Full Text] [Related]

  • 20. [Study on the relationship between sulfonylurea receptor 1 gene polymorphism and type 2 diabetes mellitus].
    Wang JS, Zhou L, Cheng JL, Shen MY.
    Yi Chuan; 2004 Jan 20; 26(1):8-12. PubMed ID: 15626659
    [Abstract] [Full Text] [Related]

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