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138 related items for PubMed ID: 17922473
21. Association of TCF7L2 polymorphism with diabetes mellitus, metabolic syndrome, and markers of beta cell function and insulin resistance in a population-based sample of Emirati subjects. Saadi H, Nagelkerke N, Carruthers SG, Benedict S, Abdulkhalek S, Reed R, Lukic M, Nicholls MG. Diabetes Res Clin Pract; 2008 Jun; 80(3):392-8. PubMed ID: 18282631 [Abstract] [Full Text] [Related]
22. Lack of genetic susceptibility of KCNJ11 E23K polymorphism with risk of type 2 diabetes in an Iranian population. Keshavarz P, Habibipour R, Ghasemi M, Kazemnezhad E, Alizadeh M, Omami MH. Endocr Res; 2014 Jun; 39(3):120-5. PubMed ID: 24460047 [Abstract] [Full Text] [Related]
23. Association of Gly972Arg polymorphism of IRS1 gene with type 2 diabetes mellitus in lean participants of a national health survey in Mexico: a candidate gene study. Burguete-Garcia AI, Cruz-Lopez M, Madrid-Marina V, Lopez-Ridaura R, Hernández-Avila M, Cortina B, Gómez RE, Velasco-Mondragón E. Metabolism; 2010 Jan; 59(1):38-45. PubMed ID: 19716569 [Abstract] [Full Text] [Related]
24. Loci of TCF7L2, HHEX and IDE on chromosome 10q and the susceptibility of their genetic polymorphisms to type 2 diabetes. Nordman S, Ostenson CG, Efendic S, Gu HF. Exp Clin Endocrinol Diabetes; 2009 Apr; 117(4):186-90. PubMed ID: 19053027 [Abstract] [Full Text] [Related]
25. HHEX gene polymorphisms are associated with type 2 diabetes in the Dutch Breda cohort. van Vliet-Ostaptchouk JV, Onland-Moret NC, van Haeften TW, Franke L, Elbers CC, Shiri-Sverdlov R, van der Schouw YT, Hofker MH, Wijmenga C. Eur J Hum Genet; 2008 May; 16(5):652-6. PubMed ID: 18231124 [Abstract] [Full Text] [Related]
26. The E23K and A190A variations of the KCNJ11 gene are associated with early-onset type 2 diabetes and blood pressure in the Chinese population. Zhuang L, Zhao Y, Zhao W, Li M, Yu M, Lu M, Zhang R, Ge X, Zheng T, Li C, Yin J, Yin J, Bao Y, Liu L, Jia W, Liu Y. Mol Cell Biochem; 2015 Jun; 404(1-2):133-41. PubMed ID: 25725792 [Abstract] [Full Text] [Related]
27. The KCNJ11 E23K polymorphism and progression of glycaemia in Southern Chinese: a long-term prospective study. Cheung CY, Tso AW, Cheung BM, Xu A, Fong CH, Ong KL, Law LS, Wat NM, Janus ED, Sham PC, Lam KS. PLoS One; 2011 Jun; 6(12):e28598. PubMed ID: 22163043 [Abstract] [Full Text] [Related]
28. EDN1 Lys198Asn is associated with diabetic retinopathy in type 2 diabetes. Li H, Louey JW, Choy KW, Liu DT, Chan WM, Chan YM, Fung NS, Fan BJ, Baum L, Chan JC, Lam DS, Pang CP. Mol Vis; 2008 Sep 15; 14():1698-704. PubMed ID: 18806884 [Abstract] [Full Text] [Related]
29. SNPs in PPARG associate with type 2 diabetes and interact with physical activity. Kilpeläinen TO, Lakka TA, Laaksonen DE, Lindström J, Eriksson JG, Valle TT, Hämäläinen H, Ilanne-Parikka P, Keinänen-Kiukaanniemi S, Lindi V, Tuomilehto J, Uusitupa M, Laakso M. Med Sci Sports Exerc; 2008 Jan 15; 40(1):25-33. PubMed ID: 18091023 [Abstract] [Full Text] [Related]
30. Association of KCNJ11 with impaired glucose regulation in essential hypertension. Wang Y, Zhou XO, Zhang Y, Gao PJ, Zhu DL. Genet Mol Res; 2011 Jun 14; 10(2):1111-9. PubMed ID: 21710463 [Abstract] [Full Text] [Related]
31. ACE I/D and MTHFR C677T polymorphisms are significantly associated with type 2 diabetes in Arab ethnicity: a meta-analysis. Al-Rubeaan K, Siddiqui K, Saeb AT, Nazir N, Al-Naqeb D, Al-Qasim S. Gene; 2013 May 15; 520(2):166-77. PubMed ID: 23458876 [Abstract] [Full Text] [Related]
32. 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 May 15; 10(5):e0124662. PubMed ID: 25955821 [Abstract] [Full Text] [Related]
33. Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population. Alsmadi O, Al-Rubeaan K, Mohamed G, Alkayal F, Al-Saud H, Al-Saud NA, Al-Daghri N, Mohammad S, Meyer BF. BMC Med Genet; 2008 Jul 26; 9():72. PubMed ID: 18655717 [Abstract] [Full Text] [Related]
34. Association of the KCNJ11 variant E23K with type 2 diabetes in Indo-Trinidadians. Boodram LG, Miyake K, Hayes MG, Bell GI, Cockburn BN. West Indian Med J; 2011 Dec 26; 60(6):604-7. PubMed ID: 22512215 [Abstract] [Full Text] [Related]
35. Prediabetes is associated with genetic variations in the gene encoding the Kir6.2 subunit of the pancreatic ATP-sensitive potassium channel (KCNJ11): A case-control study in a Han Chinese youth population. Xu M, Hu H, Deng D, Chen M, Xu Z, Wang Y. J Diabetes; 2018 Feb 26; 10(2):121-129. PubMed ID: 28449408 [Abstract] [Full Text] [Related]
36. An insertion/deletion polymorphism in the alpha2B adrenoceptor gene is associated with age at onset of type 2 diabetes mellitus. Papazoglou D, Papanas N, Papatheodorou K, Kotsiou S, Christakidis D, Maltezos E. Exp Clin Endocrinol Diabetes; 2006 Sep 26; 114(8):424-7. PubMed ID: 17039423 [Abstract] [Full Text] [Related]
37. Family history of type 2 diabetes is increased in patients with type 1 diabetes. Barone B, Rodacki M, Zajdenverg L, Almeida MH, Cabizuca CA, Barreto D, de Araújo LF, Kupfer R, Milech A, Oliveira JE. Diabetes Res Clin Pract; 2008 Oct 26; 82(1):e1-4. PubMed ID: 18835018 [Abstract] [Full Text] [Related]
38. The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetes. Nielsen EM, Hansen L, Carstensen B, Echwald SM, Drivsholm T, Glümer C, Thorsteinsson B, Borch-Johnsen K, Hansen T, Pedersen O. Diabetes; 2003 Feb 26; 52(2):573-7. PubMed ID: 12540638 [Abstract] [Full Text] [Related]
39. Association between KCNJ11 E23K polymorphism and the risk of type 2 diabetes mellitus: A global meta-analysis. Ren Y, Zhu W, Shi J, Shao A, Cheng Y, Liu Y. J Diabetes Complications; 2022 May 26; 36(5):108170. PubMed ID: 35305868 [Abstract] [Full Text] [Related]
40. CHOP T/C and C/T haplotypes contribute to early-onset type 2 diabetes in Italians. Gragnoli C. J Cell Physiol; 2008 Nov 26; 217(2):291-5. PubMed ID: 18680108 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]