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411 related items for PubMed ID: 18401556
1. Endothelial nitric oxide synthase gene haplotypes and diabetic nephropathy among Asian Indians. Ahluwalia TS, Ahuja M, Rai TS, Kohli HS, Sud K, Bhansali A, Khullar M. Mol Cell Biochem; 2008 Jul; 314(1-2):9-17. PubMed ID: 18401556 [Abstract] [Full Text] [Related]
2. Endothelial nitric oxide synthase gene polymorphism and type 2 diabetic retinopathy among Asian Indians. Cheema BS, kohli HS, Sharma R, Bhansali A, Khullar M. Acta Diabetol; 2012 Dec; 49(6):481-8. PubMed ID: 23085930 [Abstract] [Full Text] [Related]
8. Endothelial nitric oxide synthase gene polymorphisms and renal responsiveness to RAS inhibition therapy in type 2 diabetic Asian Indians. Cheema BS, Kohli HS, Sharma R, Bhansali A, Khullar M. Diabetes Res Clin Pract; 2013 Mar 30; 99(3):335-42. PubMed ID: 23260854 [Abstract] [Full Text] [Related]
9. Association of (-)786T-C mutation of endothelial nitric oxide synthase gene with insulin resistance. Ohtoshi K, Yamasaki Y, Gorogawa S, Hayaishi-Okano R, Node K, Matsuhisa M, Kajimoto Y, Hori M. Diabetologia; 2002 Nov 30; 45(11):1594-601. PubMed ID: 12436344 [Abstract] [Full Text] [Related]
11. Risk of advanced diabetic nephropathy in type 1 diabetes is associated with endothelial nitric oxide synthase gene polymorphism. Zanchi A, Moczulski DK, Hanna LS, Wantman M, Warram JH, Krolewski AS. Kidney Int; 2000 Feb 30; 57(2):405-13. PubMed ID: 10652017 [Abstract] [Full Text] [Related]
12. Influence of endothelial nitric oxide synthase gene polymorphisms (-786T>C, 4a4b, 894G>T) in Korean patients with coronary artery disease. Kim IJ, Bae J, Lim SW, Cha DH, Cho HJ, Kim S, Yang DH, Hwang SG, Oh D, Kim NK. Thromb Res; 2007 Feb 30; 119(5):579-85. PubMed ID: 16842840 [Abstract] [Full Text] [Related]
13. Relationship of endothelial nitric oxide synthase (eNOS) gene polymorphisms with diabetic retinopathy in Caucasians with type 2 diabetes. Santos KG, Crispim D, Canani LH, Ferrugem PT, Gross JL, Roisenberg I. Ophthalmic Genet; 2012 Mar 30; 33(1):23-7. PubMed ID: 22017289 [Abstract] [Full Text] [Related]
14. Association of endothelial nitric oxide synthase gene variants (-786 T>C, intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A case-control study with haplotype and in silico analysis. Azani A, Hosseinzadeh A, Azadkhah R, Zonouzi AAP, Zonouzi AP, Aftabi Y, Khani H, Heidary L, Danaii S, Bargahi N, Pouladi N, Hosseini SM. Eur J Obstet Gynecol Reprod Biol; 2017 Aug 30; 215():93-100. PubMed ID: 28605668 [Abstract] [Full Text] [Related]
15. Association of BglII Polymorphism in ITGA2 and (894G/T and -786T/C) Polymorphisms in eNOS Gene With Stroke Susceptibility in Tunisian Patients α2 Gene Polymorphism in α2β1 Integrin and eNOS Gene Variants and Stroke. Jalel A, Midani F, Fredj SH, Messaoud T, Hentati F, Soualmia H. Biol Res Nurs; 2021 Jul 30; 23(3):408-417. PubMed ID: 33297767 [Abstract] [Full Text] [Related]
16. Association of endothelial nitric oxide synthase polymorphisms with coronary artery disease in Korean individuals with or without diabetes mellitus. Bae J, Kim IJ, Hong SH, Sung JH, Lim SW, Cha DH, Cho YW, Oh D, Kim NK. Exp Ther Med; 2010 Jul 30; 1(4):719-724. PubMed ID: 22993595 [Abstract] [Full Text] [Related]
18. Comprehensive insight into functional interaction between GNB3 C825T and eNOS T-786C, G894T gene polymorphisms and association with susceptibility to diabetic erectile dysfunction. Ben Khedher MR, Abid M, Jamoussi K, Hammami M. Andrology; 2018 Nov 30; 6(6):865-873. PubMed ID: 30101547 [Abstract] [Full Text] [Related]
19. Effects of the T-786C, G894T, and Intron 4 VNTR (4a/b) polymorphisms of the endothelial nitric oxide synthase gene on the risk of prostate cancer. Safarinejad MR, Safarinejad S, Shafiei N, Safarinejad S. Urol Oncol; 2013 Oct 30; 31(7):1132-40. PubMed ID: 22317880 [Abstract] [Full Text] [Related]
20. Association of eNOS polymorphisms (-786T>C, 4a4b, 894G>T) with colorectal cancer susceptibility in the Korean population. Jang MJ, Jeon YJ, Kim JW, Chong SY, Hong SP, Oh D, Cho YK, Chung KW, Kim NK. Gene; 2013 Jan 10; 512(2):275-81. PubMed ID: 23137631 [Abstract] [Full Text] [Related] Page: [Next] [New Search]