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Journal Abstract Search

201 related items for PubMed ID: 31669406

  • 1. Uveitis genetics.
    Hou S, Li N, Liao X, Kijlstra A, Yang P.
    Exp Eye Res; 2020 Jan; 190():107853. PubMed ID: 31669406
    [Abstract] [Full Text] [Related]

  • 2. Molecular Genetic Advances in Uveitis.
    Hou S, Kijlstra A, Yang P.
    Prog Mol Biol Transl Sci; 2015 Jan; 134():283-98. PubMed ID: 26310161
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  • 4. 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; 122(3):518-23. PubMed ID: 25439430
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  • 8. Decreased microRNA-155 expression in ocular Behcet's disease but not in Vogt Koyanagi Harada syndrome.
    Zhou Q, Xiao X, Wang C, Zhang X, Li F, Zhou Y, Kijlstra A, Yang P.
    Invest Ophthalmol Vis Sci; 2012 Aug 17; 53(9):5665-74. PubMed ID: 22815348
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  • 9. miR-23a, miR-146a and miR-301a confer predisposition to Vogt-Koyanagi-Harada syndrome but not to Behcet's disease.
    Hou S, Ye Z, Liao D, Bai L, Liu Y, Zhang J, Kijlstra A, Yang P.
    Sci Rep; 2016 Jan 28; 6():20057. PubMed ID: 26818976
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  • 12. Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population.
    Chen Y, Yang P, Li F, Hou S, Jiang Z, Shu Q, Kijlstra A.
    Curr Eye Res; 2012 Apr 28; 37(4):312-7. PubMed ID: 22440163
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  • 13. UVEOGENE: An SNP database for investigations on genetic factors associated with uveitis and their relationship with other systemic autoimmune diseases.
    Wang Q, Su G, Tan X, Deng J, Du L, Huang X, Lv M, Yi S, Hou S, Kijlstra A, Yang P.
    Hum Mutat; 2019 Mar 28; 40(3):258-266. PubMed ID: 30614601
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  • 14. Decreased expression of A20 is associated with ocular Behcet's disease (BD) but not with Vogt-Koyanagi-Harada (VKH) disease.
    He Y, Wang C, Su G, Deng B, Ye Z, Huang Y, Yuan G, Aize K, Li H, Yang P.
    Br J Ophthalmol; 2018 Aug 28; 102(8):1167-1172. PubMed ID: 29699987
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  • 15. 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 28; 132(12):1395-404. PubMed ID: 23928854
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  • 17. Epigenetic Modifications and Therapy in Uveitis.
    Zou Y, Li JJ, Xue W, Kong X, Duan H, Li Y, Wei L.
    Front Cell Dev Biol; 2021 Dec 28; 9():758240. PubMed ID: 34869347
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  • 18. 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 Dec 28; 9(1):e84214. PubMed ID: 24416204
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  • 19. Gut microbial signatures and their functions in Behcet's uveitis and Vogt-Koyanagi-Harada disease.
    Wang Q, Wu S, Ye X, Tan S, Huang F, Su G, Kijlstra A, Yang P.
    J Autoimmun; 2023 May 28; 137():103055. PubMed ID: 37208257
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  • 20. Genetics in Behcet's Disease: An Update Review.
    Gao Y, Zhong Z, Yang P.
    Front Ophthalmol (Lausanne); 2022 May 28; 2():916887. PubMed ID: 38983559
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