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Journal Abstract Search

204 related items for PubMed ID: 27507606

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  • 6. Variations in Toll-like receptor and nuclear factor-kappa B genes and the risk of glioma.
    Kına I, Sultuybek GK, Soydas T, Yenmis G, Biceroglu H, Dirican A, Uzan M, Ulutin T.
    Br J Neurosurg; 2019 Apr; 33(2):165-170. PubMed ID: 30450997
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  • 9. 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; 30(2):255-62. PubMed ID: 22614238
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  • 12. 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; 40(7):2927-2937. PubMed ID: 33459954
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  • 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 Jul; 91(2):206-12. PubMed ID: 23295440
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  • 14. 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
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  • 15. 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 Mar; 10(6):e0129144. PubMed ID: 26075620
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  • 17. Genetic polymorphisms in inflammatory response genes and their associations with breast cancer risk.
    Wang Z, Liu QL, Sun W, Yang CJ, Tang L, Zhang X, Zhong XM.
    Croat Med J; 2014 Dec; 55(6):638-46. PubMed ID: 25559835
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  • 19. Association between TLR2 polymorphisms (- 196-174 Ins/Del, R677W, R753Q, and P631H) and schizophrenia in a Tunisian population.
    Aflouk Y, Inoubli O, Saoud H, Zaafrane F, Gaha L, Bel Hadj Jrad B.
    Immunol Res; 2021 Dec; 69(6):541-552. PubMed ID: 34546527
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  • 20. Co-stimulatory CD28 and transcription factor NFKB1 gene variants affect idiopathic recurrent miscarriages.
    Misra MK, Singh B, Mishra A, Agrawal S.
    J Hum Genet; 2016 Dec; 61(12):1035-1041. PubMed ID: 27488439
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