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Journal Abstract Search

109 related items for PubMed ID: 21382364

  • 21.
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  • 22. Adiponectin and resistin gene polymorphisms in association with their respective adipokine levels.
    Lau CH, Muniandy S.
    Ann Hum Genet; 2011 May; 75(3):370-82. PubMed ID: 21323646
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  • 23.
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  • 24. Polymorphisms of cytochrome P450 1A1, cigarette smoking and risk of coronary artery disease.
    Yeh CC, Sung FC, Kuo LT, Hsu WP, Chu HY.
    Mutat Res; 2009 Jul 10; 667(1-2):77-81. PubMed ID: 19563927
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  • 28. Arginase-1 Variants and the Risk of Familial Coronary Artery Disease in Subjects Originating from Pakistan.
    Shah SFA, Khan MJ, Iqbal T, Akram S, Waheed F, Satti HS, Rafiq MA, Hussain S.
    Genet Test Mol Biomarkers; 2019 Jan 10; 23(1):32-38. PubMed ID: 30526064
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  • 31. Association between apolipoprotein E polymorphism and coronary artery disease in the Kermanshah population in Iran.
    Kharrazi H, Vaisi Raygani A, Sabokroh AR, Pourmotabbed T.
    Clin Biochem; 2006 Jun 10; 39(6):613-6. PubMed ID: 16545358
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  • 32. The G894T polymorphism on endothelial nitric oxide synthase gene is associated with premature coronary artery disease in a Turkish population.
    Cam SF, Sekuri C, Tengiz I, Ercan E, Sagcan A, Akin M, Berdeli A.
    Thromb Res; 2005 Jun 10; 116(4):287-92. PubMed ID: 16038712
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  • 33. [Association of PAI-1 gene polymorphism with prognosis of coronary artery disease].
    Zhang AY, Ji XW, Guan LX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr 10; 25(2):233-5. PubMed ID: 18393255
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  • 34. Synergistic Effects of Weighted Genetic Risk Scores and Resistin and sST2 Levels on the Prognostication of Long-Term Outcomes in Patients with Coronary Artery Disease.
    Chou HH, Hsu LA, Juang JJ, Chiang FT, Teng MS, Wu S, Ko YL.
    Int J Mol Sci; 2022 Apr 13; 23(8):. PubMed ID: 35457109
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  • 35. The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease.
    Kadziela J, Janas J, Dzielińska Z, Szperl M, Gaździk D, Chotkowska E, Piotrowski W, Ruzyłło W.
    Kardiol Pol; 2003 Jul 13; 59(7):17-26; discussion 26. PubMed ID: 14560345
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  • 36. Multiple less common genetic variants explain the association of the cholesteryl ester transfer protein gene with coronary artery disease.
    Horne BD, Camp NJ, Anderson JL, Mower CP, Clarke JL, Kolek MJ, Carlquist JF, Intermountain Heart Collaborative Study Group.
    J Am Coll Cardiol; 2007 May 22; 49(20):2053-60. PubMed ID: 17512363
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  • 37. Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.
    Rahimi Z, Nomani H, Mozafari H, Vaisi-Raygani A, Madani H, Malek-Khosravi S, Parsian A.
    Blood Coagul Fibrinolysis; 2009 Jun 22; 20(4):252-6. PubMed ID: 19349859
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  • 38. Gene--nutrition interactions in coronary artery disease: correlation between the MTHFR C677T polymorphism and folate and homocysteine status in a Korean population.
    Huh HJ, Chi HS, Shim EH, Jang S, Park CJ.
    Thromb Res; 2006 Jun 22; 117(5):501-6. PubMed ID: 15935452
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  • 39. Association of RETN C-420G single nucleotide polymorphism with type 2 diabetes mellitus in Pakistani Punjabi Rajput population.
    Nadeem A, Mumtaz S, Saif MW, Naveed AK, Aslam M, Mansoor Q, Siddiqui A, Ismail M.
    J Pak Med Assoc; 2018 Nov 22; 68(11):1584-1589. PubMed ID: 30410133
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  • 40. Variants of resistin gene and the risk of idiopathic dilated cardiomyopathy in Pakistan.
    Hussain S, Haroon J, Ejaz S, Javed Q.
    Meta Gene; 2016 Sep 22; 9():37-41. PubMed ID: 27114921
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