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421 related items for PubMed ID: 19730129

  • 1. Distribution of endothelial nitric oxide synthase gene polymorphisms in Turkish population.
    Sinici I, Karahan S, Atalar E.
    J Investig Med; 2009 Oct; 57(7):769-76. PubMed ID: 19730129
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. eNOS gene intron 4 VNTR and exon 7-G894T polymorphisms in Turkish men with erectile dysfunction: a case control study.
    Erol B, Bozdogan G, Akduman B, Dursun A, Bozdogan S, Onem K, Mungan A.
    J Sex Med; 2009 May; 6(5):1423-9. PubMed ID: 19473288
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Association of the genetic variants of endothelial nitric oxide synthase gene with angiographically defined coronary artery disease and myocardial infarction in South Indian patients with type 2 diabetes mellitus.
    Narne P, Ponnaluri KC, Singh S, Siraj M, Ishaq M.
    J Diabetes Complications; 2013 Feb; 27(3):255-61. PubMed ID: 23182401
    [Abstract] [Full Text] [Related]

  • 6. Endothelial nitric oxide gene polymorphism and risk of systemic sclerosis: predisposition effect of T-786C promoter and protective effect of 27 bp repeats in Intron 4.
    Sinici I, Kalyoncu U, Karahan S, Kiraz S, Atalar E.
    Clin Exp Rheumatol; 2010 Feb; 28(2):169-75. PubMed ID: 20406610
    [Abstract] [Full Text] [Related]

  • 7. Endothelial nitric oxide synthase gene haplotype association with systemic lupus erythematosus.
    Alfadhli S, AlTamimy B, AlSaeid K, Haider M.
    Lupus; 2011 Jun; 20(7):700-8. PubMed ID: 21478289
    [Abstract] [Full Text] [Related]

  • 8. Association of the G894T polymorphism of the endothelial nitric oxide synthase gene with diabetic foot syndrome foot ulcer, diabetic complications, and comorbid vascular diseases: a Turkish case-control study.
    Corapcioglu D, Sahin M, Emral R, Celebi ZK, Sener O, Gedik VT.
    Genet Test Mol Biomarkers; 2010 Aug; 14(4):483-8. PubMed ID: 20642368
    [Abstract] [Full Text] [Related]

  • 9. The role of endothelial nitric oxide synthase (eNOS) T-786C, G894T, and 4a/b gene polymorphisms in the risk of idiopathic male infertility.
    Safarinejad MR, Shafiei N, Safarinejad S.
    Mol Reprod Dev; 2010 Aug; 77(8):720-7. PubMed ID: 20586099
    [Abstract] [Full Text] [Related]

  • 10. T-786C polymorphism in promoter of eNOS gene as genetic risk factor in patients with erectile dysfunction in Turkish population.
    Sinici I, Güven EO, Serefoğlu E, Hayran M.
    Urology; 2010 Apr; 75(4):955-60. PubMed ID: 19800665
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Endothelial nitric oxide synthase haplotypes associated with aura in patients with migraine.
    Gonçalves FM, Martins-Oliveira A, Speciali JG, Luizon MR, Izidoro-Toledo TC, Silva PS, Dach F, Tanus-Santos JE.
    DNA Cell Biol; 2011 Jun; 30(6):363-9. PubMed ID: 21332392
    [Abstract] [Full Text] [Related]

  • 13. Association study of the endothelial nitric oxide synthase gene polymorphisms with essential hypertension in northern Han Chinese.
    Zhao Q, Su SY, Chen SF, Li B, Gu DF.
    Chin Med J (Engl); 2006 Jul 05; 119(13):1065-71. PubMed ID: 16834924
    [Abstract] [Full Text] [Related]

  • 14. Protective role of 27bp repeat polymorphism in intron 4 of eNOS gene in lacunar infarction.
    Yemişçi M, Sinici I, Ozkara HA, Hayran M, Ay H, Celtikçi B, Onder E, Büyükşerbetci G, Kaya EB, Tokgözoglu L, Dalkara T.
    Free Radic Res; 2009 Mar 05; 43(3):272-9. PubMed ID: 19184759
    [Abstract] [Full Text] [Related]

  • 15. Association between achalasia and nitric oxide synthase gene polymorphisms.
    Mearin F, García-González MA, Strunk M, Zárate N, Malagelada JR, Lanas A.
    Am J Gastroenterol; 2006 Sep 05; 101(9):1979-84. PubMed ID: 16848803
    [Abstract] [Full Text] [Related]

  • 16. Endothelial nitric oxide synthase genotype and haplotype are not associated with diabetic retinopathy in diabetes type 2 patients.
    de Syllos RW, Sandrim VC, Lisboa HR, Tres GS, Tanus-Santos JE.
    Nitric Oxide; 2006 Dec 05; 15(4):417-22. PubMed ID: 16581274
    [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 05; 215():93-100. PubMed ID: 28605668
    [Abstract] [Full Text] [Related]

  • 18. Endothelial nitric oxide synthase haplotypes associated with hypertension do not predispose to cardiac hypertrophy.
    Vasconcellos V, Lacchini R, Jacob-Ferreira AL, Sales ML, Ferreira-Sae MC, Schreiber R, Nadruz W, Tanus-Santos JE.
    DNA Cell Biol; 2010 Apr 05; 29(4):171-6. PubMed ID: 20070154
    [Abstract] [Full Text] [Related]

  • 19. Endothelial nitric oxide synthase Glu298Asp, 4b/a, and -786T>C gene polymorphisms and the risk of ischemic stroke.
    Saidi S, Mallat SG, Almawi WY, Mahjoub T.
    Acta Neurol Scand; 2010 Feb 05; 121(2):114-9. PubMed ID: 19804474
    [Abstract] [Full Text] [Related]

  • 20. Polymorphisms in the endothelial nitric oxide synthase gene are associated with Behçet's disease.
    Karasneh JA, Hajeer AH, Silman A, Worthington J, Ollier WE, Gul A.
    Rheumatology (Oxford); 2005 May 05; 44(5):614-7. PubMed ID: 15705632
    [Abstract] [Full Text] [Related]

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