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Journal Abstract Search

225 related items for PubMed ID: 15918973

  • 1. [A study of the association of iNOS and eNOS gene polymorphism with portal hypertension in liver cirrhosis].
    Cheng YQ, Lin JS, Wang WQ, Xiong P, Jiang XD.
    Zhonghua Gan Zang Bing Za Zhi; 2005 May; 13(5):366-9. PubMed ID: 15918973
    [Abstract] [Full Text] [Related]

  • 2. [Polymorphism of NOS2A promoter -969(G>C) is associated with portal hypertension of liver cirrhosis].
    Cheng YQ, Wang WQ, Lin JS, Xiong P, Jiang XD.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):591-5. PubMed ID: 15583989
    [Abstract] [Full Text] [Related]

  • 3. [The association between polymorphism of endothelial nitric oxide synthase gene and cirrhotic portal hypertension].
    Cheng YQ, Lin JS, Liao JZ, Liang KH, Xiong P.
    Zhonghua Yi Xue Za Zhi; 2003 Jul 10; 83(13):1116-21. PubMed ID: 12921626
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  • 6. 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 10; 101(9):1979-84. PubMed ID: 16848803
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  • 7. 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 Sep 10; 119(5):579-85. PubMed ID: 16842840
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  • 10. Allelic polymorphism of endothelial NO-synthase gene and its functional manifestations.
    Dosenko VE, Zagoriy VY, Haytovich NV, Gordok OA, Moibenko AA.
    Acta Biochim Pol; 2006 Sep 10; 53(2):299-302. PubMed ID: 16733564
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  • 11. [Effect of polymorphism of transforming growth factor beta1 gene on HBV-induced liver cirrhosis].
    Yang ZX, Wang H, Gao CF, Xu LL, Zhao WJ.
    Zhonghua Yi Xue Za Zhi; 2005 Apr 20; 85(15):1021-6. PubMed ID: 16029542
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  • 12. [Estrogen receptor gene polymorphisms and HBV-induced liver cirrhosis].
    Xie JP, Gong XQ, Tan DM, Liu F, Zhou JL.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Jun 20; 31(3):379-82. PubMed ID: 16859128
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  • 13. Association analysis of endothelial nitric oxide synthase gene polymorphism with primary hypertension in a Singapore population.
    Moe KT, Lim ST, Wong P, Chua T, DeSilva DA, Koh TH, Wong MC, Chin-Dusting J.
    J Hum Hypertens; 2006 Dec 20; 20(12):956-63. PubMed ID: 17024134
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  • 14. eNOS G894T polymorphism and abdominal aortic aneurysms.
    Atli FH, Manduz S, Katrancioglu N, Ozum U, Disli OM, Atahan E, Ozdemir O, Dogan K, Berkan O.
    Angiology; 2010 Feb 20; 61(2):125-30. PubMed ID: 19638352
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  • 15. Influence of eNOS gene polymorphisms (894G/T; - 786C/T) on postoperative hemodynamics after cardiac surgery.
    Liakopoulos OJ, Dörge H, Popov AF, Schmitto JD, Cattaruzza M, Schoendube FA.
    Thorac Cardiovasc Surg; 2006 Jun 20; 54(4):233-8. PubMed ID: 16755443
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  • 16. Relations between eNOS Glu298Asp polymorphism and progression of diabetic nephropathy.
    Shin Shin Y, Baek SH, Chang KY, Park CW, Yang CW, Jin DC, Kim YS, Chang YS, Bang BK.
    Diabetes Res Clin Pract; 2004 Sep 20; 65(3):257-65. PubMed ID: 15331206
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  • 17. 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 20; 75(4):955-60. PubMed ID: 19800665
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  • 18. Endothelial nitric oxide synthase 894G→T but not -786T→C gene polymorphism is associated with organ dysfunction and increased mortality in patients with severe sepsis.
    Ma P, Zhu Y, Qiu H, Liu J, Wang Y, Zeng L.
    J Trauma; 2011 Oct 20; 71(4):872-7. PubMed ID: 21336191
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  • 19. [Association between endothelial nitric oxide synthase gene (G894T) polymorphism and essential hypertension in Uygur populations].
    Zhang LP, Wang SZ, Zhao XX, Lian B, Wang XF, Lin RY, Lu DR, Jin L.
    Zhonghua Xin Xue Guan Bing Za Zhi; 2006 May 20; 34(5):403-6. PubMed ID: 16776950
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  • 20. Role of nitric oxide synthase genes in hepatitis E virus infection.
    Hazam RK, Deka M, Kar P.
    J Viral Hepat; 2014 May 20; 21(9):671-9. PubMed ID: 24215170
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