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231 related items for PubMed ID: 24818816

  • 1. -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; 18(6):430-8. PubMed ID: 24818816
    [Abstract] [Full Text] [Related]

  • 2. 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 Jun; 10(6):e0129144. PubMed ID: 26075620
    [Abstract] [Full Text] [Related]

  • 3. 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; 20(3):105-11. PubMed ID: 26799199
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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 Mar; 16(1):109-15. PubMed ID: 26835711
    [Abstract] [Full Text] [Related]

  • 6. 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; 103():56-64. PubMed ID: 28088561
    [Abstract] [Full Text] [Related]

  • 7. NFKB1 gene rs28362491 ins/del variation is associated with higher susceptibility to myocardial infarction in a Chinese Han population.
    Luo JY, Li YH, Fang BB, Tian T, Liu F, Li XM, Gao XM, Yang YN.
    Sci Rep; 2020 Nov 11; 10(1):19518. PubMed ID: 33177541
    [Abstract] [Full Text] [Related]

  • 8. 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 11; 37(5):634-8. PubMed ID: 23806437
    [Abstract] [Full Text] [Related]

  • 9. Association between genetic polymorphism in NFKB1 and NFKBIA and coronary artery disease in a Chinese Han population.
    Lai H, Chen Q, Li X, Ma Y, Xu R, Zhai H, Liu F, Chen B, Yang Y.
    Int J Clin Exp Med; 2015 Oct 11; 8(11):21487-96. PubMed ID: 26885097
    [Abstract] [Full Text] [Related]

  • 10. 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 11; 29(5):235-9. PubMed ID: 20218898
    [Abstract] [Full Text] [Related]

  • 11. Association and interaction of NFKB1 rs28362491 insertion/deletion ATTG polymorphism and PPP1R13L and CD3EAP related to lung cancer risk in a Chinese population.
    Yin J, Wang H, Vogel U, Wang C, Hou W, Ma Y.
    Tumour Biol; 2016 Apr 11; 37(4):5467-73. PubMed ID: 26563375
    [Abstract] [Full Text] [Related]

  • 12. A novel polymorphism of the CYP2J2 gene is associated with coronary artery disease in Uygur population in China.
    Zhu Q, Fu Z, Ma Y, Yang H, Huang D, Xie X, Liu F, Zheng Y, Cha E.
    Clin Biochem; 2013 Aug 11; 46(12):1047-1054. PubMed ID: 23684773
    [Abstract] [Full Text] [Related]

  • 13. NFKB1 -94 insertion/deletion ATTG polymorphism contributes to risk of systemic lupus erythematosus.
    Gao M, Wang CH, Sima X, Han XM.
    DNA Cell Biol; 2012 Apr 11; 31(4):611-5. PubMed ID: 22013908
    [Abstract] [Full Text] [Related]

  • 14. The NFKB1 ATTG ins/del polymorphism and risk of coronary heart disease in three independent populations.
    Vogel U, Jensen MK, Due KM, Rimm EB, Wallin H, Nielsen MR, Pedersen AP, Tjønneland A, Overvad K.
    Atherosclerosis; 2011 Nov 11; 219(1):200-4. PubMed ID: 21726863
    [Abstract] [Full Text] [Related]

  • 15. Functional promoter -94 ins/del ATTG polymorphism in NFKB1 gene is associated with bladder cancer risk in a Chinese population.
    Li P, Gu J, Yang X, Cai H, Tao J, Yang X, Lu Q, Wang Z, Yin C, Gu M.
    PLoS One; 2013 Nov 11; 8(8):e71604. PubMed ID: 23977085
    [Abstract] [Full Text] [Related]

  • 16. NFKB1 Gene Mutant Was Associated with Prognosis of Coronary Artery Disease and Exacerbated Endothelial Mitochondrial Fission and Dysfunction.
    Luo JY, Liu F, Fang BB, Tian T, Li YH, Zhang T, Li XM, Yang YN.
    Oxid Med Cell Longev; 2022 Nov 11; 2022():9494926. PubMed ID: 36317060
    [Abstract] [Full Text] [Related]

  • 17. NFKB1 promoter -94 insertion/deletion ATTG polymorphism (rs28362491) is associated with severity and disease progression of rheumatoid arthritis through interleukin-6 levels modulation in Egyptian patients.
    Elkhawaga SY, Gomaa MH, Elsayed MM, Ebeed AA.
    Clin Rheumatol; 2021 Jul 11; 40(7):2927-2937. PubMed ID: 33459954
    [Abstract] [Full Text] [Related]

  • 18. NFKB1 gene rs28362491 polymorphism is associated with the susceptibility of acute coronary syndrome.
    Jin SY, Luo JY, Li XM, Liu F, Ma YT, Gao XM, Yang YN.
    Biosci Rep; 2019 Apr 30; 39(4):. PubMed ID: 30910844
    [Abstract] [Full Text] [Related]

  • 19. The association between CYP1A1 genetic polymorphisms and coronary artery disease in the Uygur and Han of China.
    Zou JG, Ma YT, Xie X, Yang YN, Pan S, Adi D, Liu F, Chen BD.
    Lipids Health Dis; 2014 Sep 05; 13():145. PubMed ID: 25189712
    [Abstract] [Full Text] [Related]

  • 20. Functional polymorphism of the NFKB1 gene promoter is related to the risk of dilated cardiomyopathy.
    Zhou B, Rao L, Peng Y, Wang Y, Li Y, Gao L, Chen Y, Xue H, Song Y, Liao M, Zhang L.
    BMC Med Genet; 2009 May 31; 10():47. PubMed ID: 19480714
    [Abstract] [Full Text] [Related]

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