These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
188 related articles for article (PubMed ID: 34662360)
1. Association between nitric oxide synthase T-786C genetic polymorphism and chronic kidney disease: Meta-analysis incorporating trial sequential analysis. Hsiao PJ; Chiu CC; Tsai DJ; Ko PS; Chen YK; Cheng H; Su W; Lu KC; Su SL PLoS One; 2021; 16(10):e0258789. PubMed ID: 34662360 [TBL] [Abstract][Full Text] [Related]
2. Endothelial nitric oxide synthase gene single nucleotide polymorphisms and the risk of hypertension: A meta-analysis involving 63,258 subjects. Xie X; Shi X; Xun X; Rao L Clin Exp Hypertens; 2017; 39(2):175-182. PubMed ID: 28287883 [TBL] [Abstract][Full Text] [Related]
3. An updated meta-analysis of endothelial nitric oxide synthase gene: three well-characterized polymorphisms with ischemic stroke. Yao YS; Chang WW; Jin YL; He LP Gene; 2013 Oct; 528(2):84-92. PubMed ID: 23845784 [TBL] [Abstract][Full Text] [Related]
4. The Endothelial Nitric Oxide Synthase Gene T-786C Polymorphism Increases Myocardial Infarction Risk: A Meta-Analysis. Kong XZ; Zhang ZY; Wei LH; Li R; Yu J Med Sci Monit; 2017 Feb; 23():759-766. PubMed ID: 28188309 [TBL] [Abstract][Full Text] [Related]
5. Association between endothelial nitric oxide synthase gene polymorphism (T-786C) and ischemic stroke susceptibility: a meta-analysis. Liu R; Geng P; Ma M; Yu S; Wang X; Zhang W; Di H Int J Neurosci; 2014 Sep; 124(9):642-51. PubMed ID: 24325389 [TBL] [Abstract][Full Text] [Related]
6. T-786C polymorphism in the endothelial nitric oxide synthase gene is associated with increased risk of coronary artery disease in a Chinese population. Han Y; Xu W; Zhang W; Liu N; Ji Y Pharmacology; 2010; 85(4):211-6. PubMed ID: 20215811 [TBL] [Abstract][Full Text] [Related]
7. PPARG Pro12Ala Polymorphism with CKD in Asians: A Meta-Analysis Combined with a Case-Control Study-A Key for Reaching Null Association. Chen HC; Chen WT; Sung TL; Tsai DJ; Lin C; Su H; Lin YF; Chiu HY; Su SL Genes (Basel); 2020 Jun; 11(6):. PubMed ID: 32604723 [TBL] [Abstract][Full Text] [Related]
8. Association between the - 786T>C 1polymorphism in the promoter region of endothelial nitric oxide synthase (eNOS) and risk of coronary artery disease: a systematic review and meta-analysis. Liu D; Jiang Z; Dai L; Zhang X; Yan C; Han Y Gene; 2014 Jul; 545(1):175-83. PubMed ID: 24135644 [TBL] [Abstract][Full Text] [Related]
9. The T -786C, G894T, and Intron 4 VNTR (4a/b) Polymorphisms of the Endothelial Nitric Oxide Synthase Gene in Prostate Cancer Cases. Diler SB; Öden A Genetika; 2016 Feb; 52(2):249-54. PubMed ID: 27215040 [TBL] [Abstract][Full Text] [Related]
10. The G894t, T-786c and 4b/a polymorphisms in Enos gene and cancer risk: a meta-analysis. Zhang L; Chen LM; Wang MN; Chen XJ; Li N; Huang YD; Chen M J Evid Based Med; 2014 Dec; 7(4):263-9. PubMed ID: 25586457 [TBL] [Abstract][Full Text] [Related]
11. Decisive evidence corroborates a null relationship between MTHFR C677T and chronic kidney disease: A case-control study and a meta-analysis. Chang HL; Chen GR; Hsiao PJ; Chiu CC; Tai MC; Kao CC; Tsai DJ; Su H; Chen YH; Chen WT; Su SL Medicine (Baltimore); 2020 Jul; 99(29):e21045. PubMed ID: 32702845 [TBL] [Abstract][Full Text] [Related]
12. Promoter polymorphism T-786C, 894G→T at exon 7 of endothelial nitric oxide synthase gene are associated with risk of osteoporosis in Sichuan region male residents. Gu Z; Zhang Y; Qiu G Int J Clin Exp Pathol; 2015; 8(11):15270-4. PubMed ID: 26823879 [TBL] [Abstract][Full Text] [Related]
13. Endothelial nitric oxide synthase (eNOS) T-786C, 4a4b, and G894T polymorphisms and male infertility: study for idiopathic asthenozoospermia and meta-analysis. Song P; Zou S; Chen T; Chen J; Wang Y; Yang J; Song Z; Jiang H; Shi H; Huang Y; Li Z; Shi Y; Hu H Biol Reprod; 2015 Feb; 92(2):38. PubMed ID: 25505202 [TBL] [Abstract][Full Text] [Related]
14. Endothelial Nitric Oxide Synthase T-786C and G-894T Gene Polymorphisms: A Risk Assessment of Coronary Heart Disease. Jaishankar T; Shivasekar M; Vinodhini VM J Assoc Physicians India; 2023 Sep; 71(9):45-50. PubMed ID: 38700301 [TBL] [Abstract][Full Text] [Related]
15. Endothelial nitric oxide synthase gene polymorphisms and risk of diabetic nephropathy: a systematic review and meta-analysis. Dellamea BS; Pinto LC; Leitão CB; Santos KG; Canani LH BMC Med Genet; 2014 Jan; 15():9. PubMed ID: 24433471 [TBL] [Abstract][Full Text] [Related]
16. 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; 6(6):865-873. PubMed ID: 30101547 [TBL] [Abstract][Full Text] [Related]
17. 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; 215():93-100. PubMed ID: 28605668 [TBL] [Abstract][Full Text] [Related]
18. Endothelial nitric oxide synthase gene polymorphisms (G894T, 4b/a and T-786C) and preeclampsia: meta-analysis of 18 case-control studies. Chen H; Zhao G; Sun M; Wang H; Liu J; Gao W; Meng T DNA Cell Biol; 2012 Jun; 31(6):1136-45. PubMed ID: 22054068 [TBL] [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; 31(7):1132-40. PubMed ID: 22317880 [TBL] [Abstract][Full Text] [Related]
20. Endothelial nitric oxide gene T-786C polymorphism and subarachnoid hemorrhage in Korean population. Song MK; Kim MK; Kim TS; Joo SP; Park MS; Kim BC; Cho KH J Korean Med Sci; 2006 Oct; 21(5):922-6. PubMed ID: 17043430 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]