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Journal Abstract Search


198 related items for PubMed ID: 20438790

  • 21. FGFR1OP tagSNP but not CCR6 polymorphisms are associated with Vogt-Koyanagi-Harada syndrome in Chinese Han.
    Yi X, Du L, Hou S, Li F, Chen Y, Kijlstra A, Yang P.
    PLoS One; 2013; 8(7):e69358. PubMed ID: 23935994
    [Abstract] [Full Text] [Related]

  • 22. TRAF5 and TRAF3IP2 gene polymorphisms are associated with Behçet's disease and Vogt-Koyanagi-Harada syndrome: a case-control study.
    Xiang Q, Chen L, Hou S, Fang J, Zhou Y, Bai L, Liu Y, Kijlstra A, Yang P.
    PLoS One; 2014; 9(1):e84214. PubMed ID: 24416204
    [Abstract] [Full Text] [Related]

  • 23. Monocyte chemoattractant protein (MCP)-1 -2518 A/G SNP in Chinese Han patients with VKH syndrome.
    Hou S, Yang P, Xie L, Du L, Zhou H, Jiang Z.
    Mol Vis; 2009 Aug 08; 15():1537-41. PubMed ID: 19668598
    [Abstract] [Full Text] [Related]

  • 24. A functional variant of pre-miRNA-196a2 confers risk for Behcet's disease but not for Vogt-Koyanagi-Harada syndrome or AAU in ankylosing spondylitis.
    Qi J, Hou S, Zhang Q, Liao D, Wei L, Fang J, Zhou Y, Kijlstra A, Yang P.
    Hum Genet; 2013 Dec 08; 132(12):1395-404. PubMed ID: 23928854
    [Abstract] [Full Text] [Related]

  • 25. Small ubiquitin-like modifier 4 (SUMO4) polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome in the Chinese Han population.
    Hou S, Yang P, Du L, Zhou H, Lin X, Liu X, Kijlstra A.
    Mol Vis; 2008 Dec 08; 14():2597-603. PubMed ID: 19122825
    [Abstract] [Full Text] [Related]

  • 26. Association of macrophage migration inhibitory factor gene polymorphisms with Behçet's disease in a Han Chinese population.
    Zheng X, Wang D, Hou S, Zhang C, Lei B, Xiao X, Kijlstra A, Yang P.
    Ophthalmology; 2012 Dec 08; 119(12):2514-8. PubMed ID: 22939113
    [Abstract] [Full Text] [Related]

  • 27. Interactions between IL17A, IL23R, and STAT4 polymorphisms confer susceptibility to intestinal Behcet's disease in Korean population.
    Kim ES, Kim SW, Moon CM, Park JJ, Kim TI, Kim WH, Cheon JH.
    Life Sci; 2012 May 22; 90(19-20):740-6. PubMed ID: 22483685
    [Abstract] [Full Text] [Related]

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  • 30. TNFAIP3 gene polymorphisms in a Chinese Han population with Vogt-Koyanagi-Harada syndrome.
    Li H, Liu Q, Hou S, Du L, Zhou Q, Zhou Y, Kijlstra A, Yang P.
    PLoS One; 2013 May 22; 8(3):e59515. PubMed ID: 23555688
    [Abstract] [Full Text] [Related]

  • 31. Polymorphisms in genetics of vitamin D metabolism confer susceptibility to ocular Behçet disease in a Chinese Han population.
    Fang J, Hou S, Xiang Q, Qi J, Yu H, Shi Y, Zhou Y, Kijlstra A, Yang P.
    Am J Ophthalmol; 2014 Feb 22; 157(2):488-494.e6. PubMed ID: 24184224
    [Abstract] [Full Text] [Related]

  • 32. FAS Gene Copy Numbers are Associated with Susceptibility to Behçet Disease and VKH Syndrome in Han Chinese.
    Yu H, Luo L, Wu L, Zheng M, Zhang L, Liu Y, Li H, Cao Q, Kijlstra A, Yang P.
    Hum Mutat; 2015 Nov 22; 36(11):1064-9. PubMed ID: 26136352
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  • 34. Association of STAT4 gene polymorphism with increased susceptibility of rheumatoid arthritis in a northern Chinese Han subpopulation.
    Zhao Y, Liu X, Liu X, Su Y, Li Y, Zhang X, Zhu L, Wang S, Wang T, Jiang Q, Liu X, Li X, Huang C, Jia R, Lu X, Guo J, Li Z.
    Int J Rheum Dis; 2013 Apr 22; 16(2):178-84. PubMed ID: 23773642
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  • 36. Genetic variations of IL17F and IL23A show associations with Behçet's disease and Vogt-Koyanagi-Harada syndrome.
    Hou S, Liao D, Zhang J, Fang J, Chen L, Qi J, Zhang Q, Liu Y, Bai L, Zhou Y, Kijlstra A, Yang P.
    Ophthalmology; 2015 Mar 22; 122(3):518-23. PubMed ID: 25439430
    [Abstract] [Full Text] [Related]

  • 37. Association Between Interleukin 35 Gene Single Nucleotide Polymorphisms and the Uveitis Immune Status in a Chinese Han Population.
    Feng M, Zhou S, Liu T, Yu Y, Su Q, Li X, Zhang M, Xie X, Liu T, Lin W.
    Front Immunol; 2021 Mar 22; 12():758554. PubMed ID: 34950136
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  • 39. Genetic analysis of innate immunity in Behcet's disease identifies an association with IL-37 and IL-18RAP.
    Tan H, Deng B, Yu H, Yang Y, Ding L, Zhang Q, Qin J, Kijlstra A, Chen R, Yang P.
    Sci Rep; 2016 Oct 24; 6():35802. PubMed ID: 27775096
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  • 40. Association of the C2-CFB locus with non-infectious uveitis, specifically predisposed to Vogt-Koyanagi-Harada disease.
    Yang M, Fan JJ, Wang J, Zhao Y, Teng Y, Liu P.
    Immunol Res; 2016 Apr 24; 64(2):610-8. PubMed ID: 26671509
    [Abstract] [Full Text] [Related]


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