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Journal Abstract Search

190 related items for PubMed ID: 19122825

  • 1. 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; 14():2597-603. PubMed ID: 19122825
    [Abstract] [Full Text] [Related]

  • 2. Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome.
    Li K, Yang P, Zhao M, Hou S, Du L, Zhou H, Kijlstra A.
    Mol Vis; 2009 May 11; 15():955-61. PubMed ID: 19452015
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  • 3. PDCD1 genes may protect against extraocular manifestations in Chinese Han patients with Vogt-Koyanagi-Harada syndrome.
    Meng Q, Liu X, Yang P, Hou S, Du L, Zhou H, Kijlstra A.
    Mol Vis; 2009 May 11; 15():386-92. PubMed ID: 19234630
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  • 4. JAK1, but not JAK2 and STAT3, confers susceptibility to Vogt-Koyanagi-Harada (VKH) syndrome in a Han Chinese population.
    Hu K, Hou S, Li F, Xiang Q, Kijlstra A, Yang P.
    Invest Ophthalmol Vis Sci; 2013 May 09; 54(5):3360-5. PubMed ID: 23611997
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  • 5. A variant of CLEC16A gene confers protection for Vogt-Koyanagi-Harada syndrome but not for Behcet's disease in a Chinese Han population.
    Li K, Hou S, Qi J, Kijlstra A, Yang P.
    Exp Eye Res; 2015 Mar 09; 132():225-30. PubMed ID: 25576669
    [Abstract] [Full Text] [Related]

  • 6. MIF gene polymorphisms confer susceptibility to Vogt-Koyanagi-Harada syndrome in a Han Chinese population.
    Zhang C, Liu S, Hou S, Lei B, Zheng X, Xiao X, Kijlstra A, Yang P.
    Invest Ophthalmol Vis Sci; 2013 Nov 21; 54(12):7734-8. PubMed ID: 24194192
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  • 15. No association between Bach2 gene polymorphisms with Vogt-Koyanagi-Harada syndrome (VKH) and Behcet's disease (BD) in a Chinese Han population.
    Gao X, Tan X, Qin J, Lv S, Hou S, Kijlstra A, Yang P.
    Br J Ophthalmol; 2015 Aug 21; 99(8):1150-4. PubMed ID: 25873652
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  • 16. A shared HLA-DRB1 epitope in the DR beta first domain is associated with Vogt-Koyanagi-Harada syndrome in Indian patients.
    Tiercy JM, Rathinam SR, Gex-Fabry M, Baglivo E.
    Mol Vis; 2010 Mar 05; 16():353-8. PubMed ID: 20216938
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  • 19. Association of a TNIP1 polymorphism with Vogt-Koyanagi-Harada syndrome but not with ocular Behcet's disease in Han Chinese.
    Shi Y, Jia Y, Hou S, Fang J, Zhou Y, Kijlstra A, Yang P.
    PLoS One; 2014 Mar 05; 9(5):e95573. PubMed ID: 24788730
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