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303 related items for PubMed ID: 16595597
21. Gene-gene interactions between HNF4A and KCNJ11 in predicting Type 2 diabetes in women. Qi L, van Dam RM, Asselbergs FW, Hu FB. Diabet Med; 2007 Nov; 24(11):1187-91. PubMed ID: 17894829 [Abstract] [Full Text] [Related]
22. 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; 53(5):1360-8. PubMed ID: 15111507 [Abstract] [Full Text] [Related]
23. Successful sulfonylurea treatment of a neonate with neonatal diabetes mellitus due to a new KCNJ11 mutation. Ješić MM, Ješić MD, Maglajlić S, Sajić S, Necić S. Diabetes Res Clin Pract; 2011 Jan; 91(1):e1-3. PubMed ID: 21056492 [Abstract] [Full Text] [Related]
24. 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 DT, Koster JC, Robertson H, Akrouh A, Miyake K, Bell GI, Patterson BW, Nichols CG, Polonsky KS. Diabetes; 2009 Aug; 58(8):1869-78. PubMed ID: 19491206 [Abstract] [Full Text] [Related]
25. 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; 18(3):206-12. PubMed ID: 11318841 [Abstract] [Full Text] [Related]
26. 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; 46(1):43-9. PubMed ID: 18758683 [Abstract] [Full Text] [Related]
28. Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polygenic basis of Type II diabetes mellitus in Caucasians. Hani EH, Boutin P, Durand E, Inoue H, Permutt MA, Velho G, Froguel P. Diabetologia; 1998 Dec; 41(12):1511-5. PubMed ID: 9867219 [Abstract] [Full Text] [Related]
29. Chronic antidiabetic sulfonylureas in vivo: reversible effects on mouse pancreatic beta-cells. Remedi MS, Nichols CG. PLoS Med; 2008 Oct 28; 5(10):e206. PubMed ID: 18959471 [Abstract] [Full Text] [Related]
30. Variations in insulin secretion in carriers of the E23K variant in the KIR6.2 subunit of the ATP-sensitive K(+) channel in the beta-cell. 't Hart LM, van Haeften TW, Dekker JM, Bot M, Heine RJ, Maassen JA. Diabetes; 2002 Oct 28; 51(10):3135-8. PubMed ID: 12351459 [Abstract] [Full Text] [Related]
31. 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 28; 22(5):590-8. PubMed ID: 15842514 [Abstract] [Full Text] [Related]
32. Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels. Barber TM, Bennett AJ, Gloyn AL, Groves CJ, Sovio U, Ruokonen A, Martikainen H, Pouta A, Taponen S, Weedon MN, Hartikainen AL, Wass JA, Järvelin MR, Zeggini E, Franks S, McCarthy MI. Eur J Hum Genet; 2007 Jun 28; 15(6):679-84. PubMed ID: 17342155 [Abstract] [Full Text] [Related]
33. ABCC8 polymorphism (Ser1369Ala): influence on severe hypoglycemia due to sulfonylureas. Sato R, Watanabe H, Genma R, Takeuchi M, Maekawa M, Nakamura H. Pharmacogenomics; 2010 Dec 28; 11(12):1743-50. PubMed ID: 21142918 [Abstract] [Full Text] [Related]
34. Impact of Kir6.2 E23K polymorphism on the development of type 2 diabetes in a general Japanese population: The Hisayama Study. Doi Y, Kubo M, Ninomiya T, Yonemoto K, Iwase M, Arima H, Hata J, Tanizaki Y, Iida M, Kiyohara Y. Diabetes; 2007 Nov 28; 56(11):2829-33. PubMed ID: 17965318 [Abstract] [Full Text] [Related]
35. Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes. Babiker T, Vedovato N, Patel K, Thomas N, Finn R, Männikkö R, Chakera AJ, Flanagan SE, Shepherd MH, Ellard S, Ashcroft FM, Hattersley AT. Diabetologia; 2016 Jun 28; 59(6):1162-6. PubMed ID: 27033559 [Abstract] [Full Text] [Related]
36. Sulfonylurea receptor gene 16-3 polymorphism - association with sulfonylurea or insulin treatment in type 2 diabetic subjects. Zychma MJ, Gumprecht J, Strojek K, Grzeszczak W, Moczulski D, Trautsolt W, Karasek D. Med Sci Monit; 2002 Jul 28; 8(7):CR512-5. PubMed ID: 12118200 [Abstract] [Full Text] [Related]
37. Association of KCNJ11 and ABCC8 genetic polymorphisms with response to repaglinide in Chinese diabetic patients. He YY, Zhang R, Shao XY, Hu C, Wang CR, Lu JX, Bao YQ, Jia WP, Xiang KS. Acta Pharmacol Sin; 2008 Aug 28; 29(8):983-9. PubMed ID: 18664331 [Abstract] [Full Text] [Related]
38. Type II diabetic subjects with secondary failure: treatment with prebreakfast mixed ultralente and regular insulin with a sulfonylurea. Kabadi UM, Kabadi MU. J Fam Pract; 1991 Oct 28; 33(4):349-53. PubMed ID: 1919450 [Abstract] [Full Text] [Related]
39. 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 Oct 28; 6(1):54-8. PubMed ID: 23014256 [Abstract] [Full Text] [Related]
40. Genetic study of Saudi diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes. Alsmadi O, Al-Rubeaan K, Wakil SM, Imtiaz F, Mohamed G, Al-Saud H, Al-Saud NA, Aldaghri N, Mohammad S, Meyer BF. Diabetes Metab Res Rev; 2008 Feb 28; 24(2):137-40. PubMed ID: 17922473 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]