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293 related items for PubMed ID: 28587604

  • 1. KCNJ11, ABCC8 and TCF7L2 polymorphisms and the response to sulfonylurea treatment in patients with type 2 diabetes: a bioinformatics assessment.
    Song J, Yang Y, Mauvais-Jarvis F, Wang YP, Niu T.
    BMC Med Genet; 2017 Jun 06; 18(1):64. PubMed ID: 28587604
    [Abstract] [Full Text] [Related]

  • 2. 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 06; 43(4):317-23. PubMed ID: 22704848
    [Abstract] [Full Text] [Related]

  • 3. An analysis of the relationship between ABCC8 and KCNJ11 gene polymorphisms and diabetic retinopathy in Turkish population.
    Alp E, Doguizi S, Mutlu Icduygu F, Akgun E, Sekeroglu MA, Ozer MA.
    Ophthalmic Genet; 2024 Apr 06; 45(2):126-132. PubMed ID: 38411150
    [Abstract] [Full Text] [Related]

  • 4. 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 06; 52(2):568-72. PubMed ID: 12540637
    [Abstract] [Full Text] [Related]

  • 5. 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 06; 56(2):531-6. PubMed ID: 17259403
    [Abstract] [Full Text] [Related]

  • 6. Search for Pharmacoepigenetic Correlations in Type 2 Diabetes Under Sulfonylurea Treatment.
    Karaglani M, Ragia G, Panagopoulou M, Balgkouranidou I, Nena E, Kolios G, Papanas N, Manolopoulos VG, Chatzaki E.
    Exp Clin Endocrinol Diabetes; 2019 Apr 06; 127(4):226-233. PubMed ID: 29396966
    [Abstract] [Full Text] [Related]

  • 7. 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 06; 46(1):43-9. PubMed ID: 18758683
    [Abstract] [Full Text] [Related]

  • 8. Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of KATP-Channel Neonatal Diabetes Mellitus in Vietnam National Children's Hospital.
    Ngoc CTB, Dien TM, De Franco E, Ellard S, Houghton JAL, Lan NN, Thao BP, Khanh NN, Flanagan SE, Craig ME, Dung VC.
    Front Endocrinol (Lausanne); 2021 Mar 06; 12():727083. PubMed ID: 34566892
    [Abstract] [Full Text] [Related]

  • 9. Meta-analysis of association of common variants in the KCNJ11-ABCC8 region with type 2 diabetes.
    Qin LJ, Lv Y, Huang QY.
    Genet Mol Res; 2013 Aug 20; 12(3):2990-3002. PubMed ID: 24065655
    [Abstract] [Full Text] [Related]

  • 10. Functional characterization of activating mutations in the sulfonylurea receptor 1 (ABCC8) causing neonatal diabetes mellitus in Asian Indian children.
    Balamurugan K, Kavitha B, Yang Z, Mohan V, Radha V, Shyng SL.
    Pediatr Diabetes; 2019 Jun 20; 20(4):397-407. PubMed ID: 30861254
    [Abstract] [Full Text] [Related]

  • 11. 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 20; 58(10):2419-24. PubMed ID: 19587354
    [Abstract] [Full Text] [Related]

  • 12. 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 20; 22(5):590-8. PubMed ID: 15842514
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Identification of ABCC8 as a contributory gene to impaired early-phase insulin secretion in NZO mice.
    Andrikopoulos S, Fam BC, Holdsworth A, Visinoni S, Ruan Z, Stathopoulos M, Thorburn AW, Joannides CN, Cancilla M, Balmer L, Proietto J, Morahan G.
    J Endocrinol; 2016 Jan 20; 228(1):61-73. PubMed ID: 26493453
    [Abstract] [Full Text] [Related]

  • 15. CYP2C9, KCNJ11 and ABCC8 polymorphisms and the response to sulphonylurea treatment in type 2 diabetes patients.
    Klen J, Dolžan V, Janež A.
    Eur J Clin Pharmacol; 2014 Apr 20; 70(4):421-8. PubMed ID: 24442125
    [Abstract] [Full Text] [Related]

  • 16. Genetics of type 2 diabetes mellitus and other specific types of diabetes; its role in treatment modalities.
    Kota SK, Meher LK, Jammula S, Kota SK, Modi KD.
    Diabetes Metab Syndr; 2012 Apr 20; 6(1):54-8. PubMed ID: 23014256
    [Abstract] [Full Text] [Related]

  • 17. Association of KCNJ11 and ABCC8 single-nucleotide polymorphisms with type 2 diabetes mellitus in a Kinh Vietnamese population.
    Tran NQ, Truong SD, Ma PT, Hoang CK, Le BH, Dinh TTN, Van Tran L, Tran TV, Le LHG, Le KT, Nguyen HT, Vu HA, Mai TP, Do MD.
    Medicine (Baltimore); 2022 Nov 18; 101(46):e31653. PubMed ID: 36401380
    [Abstract] [Full Text] [Related]

  • 18. Activating mutations in the ABCC8 gene in neonatal diabetes mellitus.
    Babenko AP, Polak M, Cavé H, Busiah K, Czernichow P, Scharfmann R, Bryan J, Aguilar-Bryan L, Vaxillaire M, Froguel P.
    N Engl J Med; 2006 Aug 03; 355(5):456-66. PubMed ID: 16885549
    [Abstract] [Full Text] [Related]

  • 19. Replication of KCNJ11 (p.E23K) and ABCC8 (p.S1369A) Association in Russian Diabetes Mellitus 2 Type Cohort and Meta-Analysis.
    Sokolova EA, Bondar IA, Shabelnikova OY, Pyankova OV, Filipenko ML.
    PLoS One; 2015 Aug 03; 10(5):e0124662. PubMed ID: 25955821
    [Abstract] [Full Text] [Related]

  • 20. ABCC8 polymorphisms are associated with triglyceride concentration in type 2 diabetics on sulfonylurea therapy.
    Nikolac N, Simundic AM, Saracevic A, Katalinic D.
    Genet Test Mol Biomarkers; 2012 Aug 03; 16(8):924-30. PubMed ID: 22533711
    [Abstract] [Full Text] [Related]

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