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271 related items for PubMed ID: 29359785

  • 1. The association between an endothelial nitric oxide synthase gene polymorphism and coronary heart disease in young people and the underlying mechanism.
    Chen XJ, Qiu CG, Kong XD, Ren SM, Dong JZ, Gu HP, Chen YW, Tao HL, Sarbesh J.
    Mol Med Rep; 2018 Mar; 17(3):3928-3934. PubMed ID: 29359785
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  • 2. Association of endothelial nitric oxide synthase gene G894T polymorphism and serum nitric oxide levels in patients with preeclampsia and gestational hypertension.
    Sakar MN, Atay AE, Demir S, Bakir VL, Demir B, Balsak D, Akay E, Ulusoy AI, Verit FF.
    J Matern Fetal Neonatal Med; 2015 Nov; 28(16):1907-11. PubMed ID: 25275587
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  • 3. The association of endothelial nitric oxide synthase gene G894T polymorphism and serum nitric oxide concentration with microalbuminuria in patients with gestational diabetes.
    Atay AE, Akbas H, Tumer C, Sakar MN, Esen B, Incebiyik A, Simsek S, Sit D.
    Clin Nephrol; 2014 Feb; 81(2):105-11. PubMed ID: 24403014
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  • 4. [Association between G894T mutation in endothelial nitric oxide synthase gene and premature coronary heart disease].
    Jia CQ, Ning Y, Liu TT, Liu ZL.
    Zhonghua Liu Xing Bing Xue Za Zhi; 2005 Jan; 26(1):51-3. PubMed ID: 15921596
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  • 5. Investigation of the relationships between eNOS T786C, G894T, intron 4 VNTR (4a/b) gene variations and prostate cancer development and progression.
    Alkanli N, Ay A, Cevik G.
    Nitric Oxide; 2024 Nov 01; 152():69-77. PubMed ID: 39322022
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  • 6. 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 01; 31(7):1132-40. PubMed ID: 22317880
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  • 7. Endothelial nitric oxide synthase (eNOS) Glu298-->Asp polymorphism (G894T) among south Indians.
    Nishevitha NS, Angeline T, Jeyaraj N.
    Indian J Med Res; 2009 Jan 01; 129(1):68-71. PubMed ID: 19287060
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  • 9. [The G894T mutation of the endothelial nitric oxide synthase gene is associated with coronary atherosclerotic heart disease in Chinese].
    Wei D, Shan J, Chen Z, Shi Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Dec 01; 19(6):471-4. PubMed ID: 12476417
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  • 13. Association of endothelial nitric oxide synthase gene G894T polymorphism with blood oxygen transport.
    Zinchuk V, Zhadko D.
    Nitric Oxide; 2019 Mar 01; 84():45-49. PubMed ID: 30641122
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  • 14. The correlation between gene polymorphisms of endothelial nitric oxide synthase and aneurismal subarachnoid hemorrhage.
    Zhe Z, Bo Y.
    Neurosurg Rev; 2019 Jun 01; 42(2):493-498. PubMed ID: 29948497
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  • 15. Autopsy and postmortem examination case study on genetic risk factors for cardiac death: polymorphisms of endothelial nitric oxide synthase gene Glu298Asp variant and T-786C mutation, human paraoxonase 1 (PON1) gene and alpha2beta-adrenergic receptor gene.
    Ameno K, Ameno S, Kinoshita H, Jamal M, Wang W, Kumihashi M, Uekita I, Ijiri I.
    Vojnosanit Pregl; 2006 Apr 01; 63(4):357-61; discussion 362-3. PubMed ID: 16683402
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  • 16. 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 01; 71(9):45-50. PubMed ID: 38700301
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  • 18. Hyperhomocysteinemia, endothelial nitric oxide synthase polymorphism, and risk of coronary artery disease.
    Kerkeni M, Addad F, Chauffert M, Myara A, Ben Farhat M, Miled A, Maaroufi K, Trivin F.
    Clin Chem; 2006 Jan 01; 52(1):53-8. PubMed ID: 16284093
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  • 19. Endothelial Nitric Oxide Synthase G894T Polymorphism Associates with Disease Severity in Puumala Hantavirus Infection.
    Koskela S, Laine O, Mäkelä S, Pessi T, Tuomisto S, Huhtala H, Karhunen PJ, Pörsti I, Mustonen J.
    PLoS One; 2015 Jan 01; 10(11):e0142872. PubMed ID: 26561052
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  • 20. 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 01; 52(2):249-54. PubMed ID: 27215040
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