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Journal Abstract Search

158 related items for PubMed ID: 25806576

  • 1. The polymorphisms of tumor necrosis factor-induced protein 3 gene may contribute to the susceptibility of chronic primary immune thrombocytopenia in Chinese population.
    Zhou H, Yang J, Liu L, Zhang D, Zhou K, Li H, Zhao H, Han L, Zhou J, Liu X, Song Y, Yang R.
    Platelets; 2016; 27(1):26-31. PubMed ID: 25806576
    [Abstract] [Full Text] [Related]

  • 2. Association between TNFAIP3 nonsynonymous single-nucleotide polymorphism rs2230926 and chronic hepatitis B virus infection in a Chinese Han population.
    Zhang P, Li N, Zhu Q, Li F, Yang C, Zeng X, Lv Y, Zhou Z, Han Q, Liu Z.
    Virol J; 2015 Feb 28; 12():33. PubMed ID: 25890346
    [Abstract] [Full Text] [Related]

  • 3. Genetic association study of TNFAIP3, IFIH1, IRF5 polymorphisms with polymyositis/dermatomyositis in Chinese Han population.
    Chen S, Wang Q, Wu Z, Li Y, Li P, Sun F, Zheng W, Wu Q, Wu C, Deng C, Zhang F, Li Y.
    PLoS One; 2014 Feb 28; 9(10):e110044. PubMed ID: 25337792
    [Abstract] [Full Text] [Related]

  • 4. PTPN22 -1123G > C polymorphism is associated with susceptibility to primary immune thrombocytopenia in Chinese population.
    Ge J, Li H, Gu D, Du W, Xue F, Sui T, Xu J, Yang R.
    Platelets; 2013 Feb 28; 24(6):448-53. PubMed ID: 23098231
    [Abstract] [Full Text] [Related]

  • 5. Single nucleotide polymorphisms in TNFAIP3 were associated with the risks of rheumatoid arthritis in northern Chinese Han population.
    Zhang X, Li W, Zhang X, Zhao L, Zhang X, Jiang L, Guo Y, Zhang J, Liang Z, Wang X.
    BMC Med Genet; 2014 May 15; 15():56. PubMed ID: 24884566
    [Abstract] [Full Text] [Related]

  • 6. TNFAIP3 rs2230926 polymorphisms in rheumatoid arthritis of southern Chinese Han population: a case-control study.
    Hao G, Li Y, Liu J, Wo M.
    Int J Clin Exp Pathol; 2014 May 15; 7(12):8958-61. PubMed ID: 25674272
    [Abstract] [Full Text] [Related]

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  • 8. Decreased Frequency of IL-17F rs763780 Site Allele G is Associated With Genetic Susceptibility to Immune Thrombocytopenia in a Chinese Population.
    Li H, Zhou Z, Tai W, Feng W, Zhang D, Gu X, Yang R.
    Clin Appl Thromb Hemost; 2017 Jul 15; 23(5):466-471. PubMed ID: 26620416
    [Abstract] [Full Text] [Related]

  • 9. TNFAIP3 gene polymorphisms associated with differential susceptibility to rheumatoid arthritis and systemic lupus erythematosus in the Korean population.
    Kim SK, Choe JY, Bae J, Chae SC, Park DJ, Kwak SG, Lee SS.
    Rheumatology (Oxford); 2014 Jun 15; 53(6):1009-13. PubMed ID: 24489017
    [Abstract] [Full Text] [Related]

  • 10. TNF-α promoter single nucleotide polymorphisms and haplotypes associate with susceptibility of immune thrombocytopenia in Chinese adults.
    Wang N, Li GN, Wang XB, Liang T, Hu L.
    Hum Immunol; 2014 Sep 15; 75(9):980-5. PubMed ID: 25158149
    [Abstract] [Full Text] [Related]

  • 11. Mesenchymal stem cell deficiency influences megakaryocytopoiesis through the TNFAIP3/NF-κB/SMAD pathway in patients with immune thrombocytopenia.
    He Y, Xu LL, Feng FE, Wang QM, Zhu XL, Wang CC, Zhang JM, Fu HX, Xu LP, Liu KY, Huang XJ, Zhang XH.
    Br J Haematol; 2018 Feb 15; 180(3):395-411. PubMed ID: 29327472
    [Abstract] [Full Text] [Related]

  • 12. Polymorphisms of TNFAIP3 gene in a Chinese Han population with fuchs heterochromic iridocyclitis.
    Li H, Hou S, Du L, Zhou Q, Kijlstra A, Liu Q.
    Ophthalmic Genet; 2014 Jun 15; 35(2):63-7. PubMed ID: 23463983
    [Abstract] [Full Text] [Related]

  • 13. Analysis of gender differences in genetic risk: association of TNFAIP3 polymorphism with male childhood-onset systemic lupus erythematosus in the Japanese population.
    Kadota K, Mori M, Yanagimachi M, Miyamae T, Hara T, Kanetaka T, Nozawa T, Kikuchi M, Hara R, Imagawa T, Kaneko T, Yokota S.
    PLoS One; 2013 Jun 15; 8(8):e72551. PubMed ID: 24023622
    [Abstract] [Full Text] [Related]

  • 14. Association of the TNFAIP3 rs5029939 variant with systemic sclerosis in the European Caucasian population.
    Dieudé P, Guedj M, Wipff J, Ruiz B, Riemekasten G, Matucci-Cerinic M, Melchers I, Hachulla E, Airo P, Diot E, Hunzelmann N, Cabane J, Mouthon L, Cracowski JL, Riccieri V, Distler J, Meyer O, Kahan A, Boileau C, Allanore Y.
    Ann Rheum Dis; 2010 Nov 15; 69(11):1958-64. PubMed ID: 20511617
    [Abstract] [Full Text] [Related]

  • 15. Brief report: candidate gene study in systemic sclerosis identifies a rare and functional variant of the TNFAIP3 locus as a risk factor for polyautoimmunity.
    Koumakis E, Giraud M, Dieudé P, Cohignac V, Cuomo G, Airò P, Hachulla E, Matucci-Cerinic M, Diot E, Caramaschi P, Mouthon L, Riccieri V, Cracowski JL, Tiev KP, Francès C, Amoura Z, Sibilia J, Cosnes A, Carpentier P, Valentini G, Manetti M, Guiducci S, Meyer O, Kahan A, Boileau C, Chiocchia G, Allanore Y.
    Arthritis Rheum; 2012 Aug 15; 64(8):2746-52. PubMed ID: 22488580
    [Abstract] [Full Text] [Related]

  • 16. Polymorphisms of the TNFAIP3 region and Graves' disease.
    Song RH, Yu ZY, Wang Q, Muhali FS, Jiang WJ, Xiao L, Shi XH, He ST, Xu J, Zhang JA.
    Autoimmunity; 2014 Nov 15; 47(7):459-65. PubMed ID: 24798189
    [Abstract] [Full Text] [Related]

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  • 18. Single nucleotide polymorphisms at the TNFAIP3/A20 locus and susceptibility/resistance to inflammatory and autoimmune diseases.
    Mele A, Cervantes JR, Chien V, Friedman D, Ferran C.
    Adv Exp Med Biol; 2014 Nov 15; 809():163-83. PubMed ID: 25302371
    [Abstract] [Full Text] [Related]

  • 19. TNFAIP3 gene polymorphisms confer risk for Behcet's disease in a Chinese Han population.
    Li H, Liu Q, Hou S, Du L, Zhou Q, Zhou Y, Kijlstra A, Li Z, Yang P.
    Hum Genet; 2013 Mar 15; 132(3):293-300. PubMed ID: 23161053
    [Abstract] [Full Text] [Related]

  • 20. Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus.
    Musone SL, Taylor KE, Lu TT, Nititham J, Ferreira RC, Ortmann W, Shifrin N, Petri MA, Kamboh MI, Manzi S, Seldin MF, Gregersen PK, Behrens TW, Ma A, Kwok PY, Criswell LA.
    Nat Genet; 2008 Sep 15; 40(9):1062-4. PubMed ID: 19165919
    [Abstract] [Full Text] [Related]

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