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Journal Abstract Search

228 related items for PubMed ID: 23357300

  • 1. Role of inflammatory gene polymorphisms in left ventricular dysfunction (LVD) susceptibility in coronary artery disease (CAD) patients.
    Mishra A, Srivastava A, Mittal T, Garg N, Mittal B.
    Cytokine; 2013 Mar; 61(3):856-61. PubMed ID: 23357300
    [Abstract] [Full Text] [Related]

  • 2. Genetic predisposition to left ventricular dysfunction: a multigenic and multi-analytical approach.
    Mishra A, Srivastava A, Mittal T, Garg N, Mittal B.
    Gene; 2014 Aug 10; 546(2):309-17. PubMed ID: 24875414
    [Abstract] [Full Text] [Related]

  • 3. Association of matrix metalloproteinases (MMP2, MMP7 and MMP9) genetic variants with left ventricular dysfunction in coronary artery disease patients.
    Mishra A, Srivastava A, Mittal T, Garg N, Mittal B.
    Clin Chim Acta; 2012 Oct 09; 413(19-20):1668-74. PubMed ID: 22664146
    [Abstract] [Full Text] [Related]

  • 4. The functional -94 insertion/deletion ATTG polymorphism in the promoter region of NFKB1 gene increases the risk of sporadic colorectal cancer.
    Mohd Suzairi MS, Tan SC, Ahmad Aizat AA, Mohd Aminudin M, Siti Nurfatimah MS, Andee ZD, Ankathil R.
    Cancer Epidemiol; 2013 Oct 09; 37(5):634-8. PubMed ID: 23806437
    [Abstract] [Full Text] [Related]

  • 5. Genetic Variation in NFKB1 and NFKBIA and Susceptibility to Coronary Artery Disease in a Chinese Uygur Population.
    Lai HM, Li XM, Yang YN, Ma YT, Xu R, Pan S, Zhai H, Liu F, Chen BD, Zhao Q.
    PLoS One; 2015 Oct 09; 10(6):e0129144. PubMed ID: 26075620
    [Abstract] [Full Text] [Related]

  • 6. -94 ATTG insertion/deletion polymorphism of the NFKB1 gene is associated with coronary artery disease in Han and Uygur women in China.
    Yang YN, Zhang JY, Ma YT, Xie X, Li XM, Liu F, Chen BD, Dong XH, Zheng YY, Pan S, Zhai H, Li DZ, Chen QJ.
    Genet Test Mol Biomarkers; 2014 Jun 09; 18(6):430-8. PubMed ID: 24818816
    [Abstract] [Full Text] [Related]

  • 7. Role of common sarcomeric gene polymorphisms in genetic susceptibility to left ventricular dysfunction.
    Kumar S, Mishra A, Srivastava A, Bhatt M, Garg N, Agarwal SK, Pande S, Mittal B.
    J Genet; 2016 Jun 09; 95(2):263-72. PubMed ID: 27350668
    [Abstract] [Full Text] [Related]

  • 8. Role of angiotensin II type I (AT1 A1166C) receptor polymorphism in susceptibility of left ventricular dysfunction.
    Mishra A, Srivastava A, Kumar S, Mittal T, Garg N, Agarwal SK, Pande S, Mittal B.
    Indian Heart J; 2015 Jun 09; 67(3):214-21. PubMed ID: 26138177
    [Abstract] [Full Text] [Related]

  • 9. Mutant DD genotype of NFKB1 gene is associated with the susceptibility and severity of coronary artery disease.
    Luo JY, Li XM, Zhou Y, Zhao Q, Chen BD, Liu F, Chen XC, Zheng H, Ma YT, Gao XM, Yang YN.
    J Mol Cell Cardiol; 2017 Feb 09; 103():56-64. PubMed ID: 28088561
    [Abstract] [Full Text] [Related]

  • 10. The functional 4-bp insertion/deletion ATTG polymorphism in the promoter region of NF-KB1 reduces the risk of BC.
    Eskandari-Nasab E, Hashemi M, Ebrahimi M, Amininia S.
    Cancer Biomark; 2016 Feb 09; 16(1):109-15. PubMed ID: 26835711
    [Abstract] [Full Text] [Related]

  • 11. Association Between the NFKB1-94ins/del ATTG Polymorphism (rs28362491) and Coronary Artery Disease: A Systematic Review and Meta-Analysis.
    Chen QJ, Lai HM, Zhao L, Ma YT, Li XM, Zhai H, Zhou Y, He CH, Chen BD, Liu F, Yang YN.
    Genet Test Mol Biomarkers; 2016 Mar 09; 20(3):105-11. PubMed ID: 26799199
    [Abstract] [Full Text] [Related]

  • 12. Association of NFKB1 -94ins/del ATTG promoter polymorphism with susceptibility to and phenotype of Graves' disease.
    Kurylowicz A, Hiromatsu Y, Jurecka-Lubieniecka B, Kula D, Kowalska M, Ichimura M, Koga H, Kaku H, Bar-Andziak E, Nauman J, Jarzab B, Ploski R, Bednarczuk T.
    Genes Immun; 2007 Oct 09; 8(7):532-8. PubMed ID: 17690684
    [Abstract] [Full Text] [Related]

  • 13. A functional insertion/deletion polymorphism (-94 ins/del ATTG) in the promoter region of the NFKB1 gene is related to the risk of renal cell carcinoma.
    Cai H, Sun L, Cui L, Cao Q, Qin C, Zhang G, Mao X, Wang M, Zhang Z, Shao P, Yin C.
    Urol Int; 2013 Oct 09; 91(2):206-12. PubMed ID: 23295440
    [Abstract] [Full Text] [Related]

  • 14. -94 ins/del ATTG NFKB1 gene variant is associated with lower susceptibility to myocardial infarction.
    Boccardi V, Rizzo MR, Marfella R, Papa M, Esposito A, Portoghese M, Paolisso G, Barbieri M.
    Nutr Metab Cardiovasc Dis; 2011 Sep 09; 21(9):679-84. PubMed ID: 20304615
    [Abstract] [Full Text] [Related]

  • 15. Involvement of -308 TNF-alpha and 1267 Hsp70-2 polymorphisms and zinc status in the susceptibility of coronary artery disease (CAD) in old patients.
    Giacconi R, Cipriano C, Muti E, Costarelli L, Malavolta M, Caruso C, Lio D, Mocchegiani E.
    Biogerontology; 2006 Sep 09; 7(5-6):347-56. PubMed ID: 16953332
    [Abstract] [Full Text] [Related]

  • 16. Polymorphism of the NFKB1 affects the serum inflammatory levels of IL-6 in Hashimoto thyroiditis in a Turkish population.
    Koc A, Batar B, Celik O, Onaran I, Tasan E, Sultuybek GK.
    Immunobiology; 2014 Jul 09; 219(7):531-6. PubMed ID: 24703107
    [Abstract] [Full Text] [Related]

  • 17. Association of natriuretic peptide polymorphisms with left ventricular dysfunction in southern Han Chinese coronary artery disease patients.
    Wu Z, Xu M, Sheng H, Lou Y, Su X, Chen Y, Lu L, Liu Y, Jin W.
    Int J Clin Exp Pathol; 2014 Jul 09; 7(10):7148-57. PubMed ID: 25400811
    [Abstract] [Full Text] [Related]

  • 18. A functional promoter polymorphism in NFKB1 increases susceptibility to endometriosis.
    Zhou B, Rao L, Peng Y, Wang Y, Qie M, Zhang Z, Song Y, Zhang L.
    DNA Cell Biol; 2010 May 09; 29(5):235-9. PubMed ID: 20218898
    [Abstract] [Full Text] [Related]

  • 19. NFKB1 polymorphism is associated with age-related gene methylation in Helicobacter pylori-infected subjects.
    Arisawa T, Tahara T, Shiroeda H, Yamada H, Nomura T, Hayashi R, Saito T, Fukuyama T, Otsuka T, Nakamura M, Toshikuni N, Tsuchishima M, Shibata T.
    Int J Mol Med; 2012 Aug 09; 30(2):255-62. PubMed ID: 22614238
    [Abstract] [Full Text] [Related]

  • 20. Polymorphisms in inflammation-related genes and the risk of primary varicose veins in ethnic Russians.
    Shadrina A, Voronina E, Smetanina M, Tsepilov Y, Sevost'ianova K, Shevela A, Seliverstov E, Zakharova E, Ilyukhin E, Kirienko A, Zolotukhin I, Filipenko M.
    Immunol Res; 2018 Feb 09; 66(1):141-150. PubMed ID: 29247331
    [Abstract] [Full Text] [Related]

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