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221 related items for PubMed ID: 21641671
21. [Insulin receptor substrate-1 and glucose transporter gene polymorphisms in noninsulin-dependent diabetes mellitus]. Liu Z, Guan T, Chen Z. Zhonghua Yi Xue Za Zhi; 1998 Sep; 78(9):662-5. PubMed ID: 11038788 [Abstract] [Full Text] [Related]
22. Correlation of the TCF7L2 (rs7903146) polymorphism with an enhanced risk of type 2 diabetes mellitus: a meta-analysis. Guan Y, Yan LH, Liu XY, Zhu XY, Wang SZ, Chen LM. Genet Mol Res; 2016 Aug 26; 15(3):. PubMed ID: 27706609 [Abstract] [Full Text] [Related]
25. [Association of polymorphism in neurogenic differentiation factor 1 gene with type 2 diabetes]. Ye L, Xu Y, Zhu Y, Fan Y, Deng H, Zhang J. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Dec 26; 19(6):484-7. PubMed ID: 12476420 [Abstract] [Full Text] [Related]
27. Lack of association between the CC genotype of the rs7903146 polymorphism in the TCF7L2 gene and rheumatoid arthritis. Mota LM, Rabelo Fde S, Lima FA, Lima RA, Carvalho JF, Barra GB, Amato AA. Rev Bras Reumatol; 2012 Aug 26; 52(4):523-8. PubMed ID: 22885420 [Abstract] [Full Text] [Related]
28. [The relationship of methylenetetrahydrofolate reductase gene polymorphism and plasma homocysteine levels in type 2 diabetes mellitus patients with diabetic retinopathy]. Sun J, Xu Y, Zhu Y, Lu H, Deng H, Fan Y, Sun S, Zhang Y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr 26; 20(2):131-4. PubMed ID: 12673582 [Abstract] [Full Text] [Related]
29. [Relationships of angiotensinogen gene M235T variant with diabetic nephropathy in Chinese type 2 diabetes mellitus]. Wang J, Zhu X, Yang L, Zhou W, Li H, Fu H, Zhu L, Yuan S. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct 26; 16(5):299-302. PubMed ID: 10514536 [Abstract] [Full Text] [Related]
30. The TCF7L2 rs7903146 (C/T) polymorphism is associated with risk to type 2 diabetes mellitus in Southern-Brazil. Assmann TS, Duarte GC, Rheinheimer J, Cruz LA, Canani LH, Crispim D. Arq Bras Endocrinol Metabol; 2014 Dec 26; 58(9):918-25. PubMed ID: 25627047 [Abstract] [Full Text] [Related]
31. Transcription factor 7-like 2 (TCF7L2) gene polymorphism and clinical phenotype in end-stage renal disease patients. Buraczynska M, Zukowski P, Ksiazek P, Kuczmaszewska A, Janicka J, Zaluska W. Mol Biol Rep; 2014 Jun 26; 41(6):4063-8. PubMed ID: 24574000 [Abstract] [Full Text] [Related]
33. 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 26; 117(4):186-90. PubMed ID: 19053027 [Abstract] [Full Text] [Related]
34. Meta-analysis of the association between the rs7903146 polymorphism at the TCF7L2 locus and type 2 diabetes mellitus susceptibility. Liu XH, Xie CG, An Y, Zhang XX, Wu WB. Genet Mol Res; 2015 Dec 14; 14(4):16856-62. PubMed ID: 26681031 [Abstract] [Full Text] [Related]
37. The C677T methylenetetrahydrofolate reductase gene mutation and nephropathy in type 2 diabetes mellitus. Ksiazek P, Bednarek-Skublewska A, Buraczyńska M. Med Sci Monit; 2004 Feb 14; 10(2):BR47-51. PubMed ID: 14737040 [Abstract] [Full Text] [Related]
38. [Polymorphism of aldose reductase gene and susceptibility to retinopathy and nephropathy in Caucasians with type 1 diabetes]. Fanelli A, Hadjadj S, Gallois Y, Fumeron F, Betoule D, Grandchamp B, Marre M. Arch Mal Coeur Vaiss; 2002 Feb 14; 95(7-8):701-8. PubMed ID: 12365083 [Abstract] [Full Text] [Related]
39. Genetic association of interleukin-1beta (-511C/T) and interleukin-1 receptor antagonist (86 bp repeat) polymorphisms with Type 2 diabetes mellitus in North Indians. Achyut BR, Srivastava A, Bhattacharya S, Mittal B. Clin Chim Acta; 2007 Feb 14; 377(1-2):163-9. PubMed ID: 17069782 [Abstract] [Full Text] [Related]
40. Using gene-network landscape to dissect genotype effects of TCF7L2 genetic variant on diabetes and cardiovascular risk. Vaquero AR, Ferreira NE, Omae SV, Rodrigues MV, Teixeira SK, Krieger JE, Pereira AC. Physiol Genomics; 2012 Oct 02; 44(19):903-14. PubMed ID: 22872755 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]