[1] |
Yang P, Zhang Z, Zhou H, et al. Clinical patterns and characteristics of uveitis in a tertiary center for uveitis in China[J]. Curr Eye Res,2005,30(11):943-948.
|
[2] |
杨培增,张震,王红,等. 葡萄膜炎的临床类型及病因探讨[J]. 中华眼底病杂志,2002,18(4):253-255.
|
[3] |
de Menthon M, Lavalley MP, Maldini C, et al. HLA-B51/B5 and the risk of Behcet′s disease: a systematic review and meta-analysis of case-control genetic association studies[J]. Arthritis Rheum,2009,61(10):1287-1296.
|
[4] |
Hou S, Yang P, Du L, et al. SUMO4 gene polymorphisms in Chinese Han patients with Behcet′s disease[J]. Clin Immunol, 2008,129(1):170-175.
|
[5] |
Yang P, Ren Y, Li B, et al. Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients[J]. Ophthalmology, 2007,114(3):606-614.
|
[6] |
Shi T, Lv W, Zhang L, et al. Association of HLA-DR4/HLA-DRB1*04 with Vogt-Koyanagi-Harada disease: a systematic review and meta-analysis[J]. Sci Rep,2014,4:6887.
|
[7] |
闵寒毅,刘英,牛妮芳,等. 我国汉族Vogt-Koyanagi-Harada综合征患者人类白细胞抗原DQB1等位基因多态性研究[J]. 中华眼科杂志,2007,43(4):355-360.
|
[8] |
闵寒毅,刘英,牛妮芳,等. 我国汉族Vogt-小柳原田综合征患者人类白细胞抗原-DQB1基因启动子区单核苷酸多态性的研究[J]. 中华眼科杂志,2008,44(10):870-875.
|
[9] |
Hu K, Yang P, Jiang Z, et al. STAT4 polymorphism in a Chinese Han population with Vogt-Koyanagi-Harada syndrome and Behcet′s disease[J]. Hum Immunol,2010,71(7):723-726.
|
[10] |
Hou S, Yang Z, Du L, et al. Identification of a susceptibility locus in STAT4 for Behcet′s disease in Han Chinese in a genome-wide association study[J]. Arthritis Rheum,2012,64(12):4104-4113.
|
[11] |
Hou S, Shu Q, Jiang Z, et al. Replication study confirms the association between UBAC2 and Behcet′s disease in two independent Chinese sets of patients and controls[J]. Arthritis Res Ther,2012,14(2):R70.
|
[12] |
Fei Y, Webb R, Cobb BL, et al. Identification of novel genetic susceptibility loci for Behcet′s disease using a genome-wide association study[J]. Arthritis Res Ther,2009,11(3):R66.
|
[13] |
Hou S, Xiao X, Li F, et al. Two-stage association study identifies three associated variants in CCR1 gene for Behcet′s disease in Chinese Han[J]. Hum Genet,2012,131(12):1841-1850.
|
[14] |
Du L, Yang P, Hou S, et al. Association of the CTLA-4 gene and Vogt-Koyanagi-Harada syndrome[J]. Clin Immunol,2008, 127(1):43-48.
|
[15] |
Wu Z, Chen H, Sun F, et al. PTPN2 rs1893217 single-nucleotide polymorphism is associated with risk of Behcet′s disease in a Chinese Han population[J]. Clin Exp Rheumatol,2014,32(4 Suppl 84):S20-26.
|
[16] |
Zhang Q, Qi J, Hou S, et al. A functional variant of PTPN22 confers risk for Vogt-Koyanagi-Harada syndrome but not for ankylosing spondylitis[J]. PLoS One,2014,9(5):e96943.
|
[17] |
Li X, Bai L, Fang J, et al. Genetic variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet′s disease and VKH syndrome[J]. PLoS One,2014,9(5):e98373.
|
[18] |
Chi W, Yang P, Li B, et al. IL-23 promotes CD4+T cells to produce IL-17 in Vogt-Koyanagi-Harada disease[J]. J Allergy Clin Immunol,2007,119(5):1218-1224.
|
[19] |
Chi W, Zhu X, Yang P, et al. Upregulated IL-23 and IL-17 in Behcet patients with active uveitis[J]. Invest Ophthalmol Vis Sci,2008,49(7):3058-3064.
|
[20] |
Jiang Z, Yang P, Hou S, et al. IL23R gene confers susceptibility to Behcet′s disease in a Chinese Han population[J]. Ann Rheum Dis,2010,69(7):1325-1328.
|
[21] |
Shu Q, Yang P, Hou S, et al. IL-17 gene polymorphism is associated with Vogt-Koyanagi-Harada disease but not with Behcet′s disease in a Chinese Han population[J]. Hum Immunol, 2010,71(10):988-991.
|
[22] |
Cho ML, Kang JW, Moon YM, et al. STAT3 and NF-kappaB signal pathway is required for IL-23-mediated IL-17 production in spontaneous arthritis animal model IL-1 receptor antagonist-deficient mice[J]. J Immunol,2006,176(9):5652-5661.
|
[23] |
Hu K, Hou S, Li F, et al. JAK1, but not JAK2 and STAT3, confers susceptibility to Vogt-Koyanagi-Harada (VKH) syndrome in a Han Chinese population[J]. Invest Ophthalmol Vis Sci,2013,54(5):3360-3365.
|
[24] |
Hou S, Qi J, Zhang Q, et al. Genetic variants in the JAK1 gene confer higher risk of Behcet′s disease with ocular involvement in Han Chinese[J]. Hum Genet,2013,132(9):1049-1058.
|
[25] |
Hu K, Hou S, Jiang Z, et al. JAK2 and STAT3 polymorphisms in a Han Chinese population with Behcet′s disease[J]. Invest Ophthalmol Vis Sci,2012,53(1):538-541.
|
[26] |
Hou S, Du L, Lei B, et al. Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3[J]. Nat Genet,2014,46(9):1007-1011.
|
[27] |
Chen F, Hou S, Jiang Z, et al. CD40 gene polymorphisms confer risk to Behcet′s disease but not to Vogt-Koyanagi-Harada syndrome in a Han Chinese population[J]. Rheumatology (Oxford), 2012,51(1):47-51.
|
[28] |
Xiang Q, Chen L, Hou S, et al. TRAF5 and TRAF3IP2 gene polymorphisms are associated with Behcet′s disease and Vogt-Koyanagi-Harada syndrome: a case-control study[J]. PLoS One 2014,9(1):e84214.
|
[29] |
Chu M, Yang P, Hu R, et al. Elevated serum osteopontin levels and genetic polymorphisms of osteopontin are associated with Vogt-Koyanagi-Harada disease[J]. Invest Ophthalmol Vis Sci,2011,52(10):7084-7089.
|
[30] |
Tian Y, Wang C, Ye Z, et al. Effect of 1,25-Dihydroxyvitamin D3 on Th17 and Th1 Response in Patients with Behcet′s Disease[J]. Invest Ophthalmol Vis Sci,2012,53(10):6434-6441.
|
[31] |
Fang J, Hou S, Xiang Q, et al. Polymorphisms in genetics of Vitamin D metabolism confer susceptibility to ocular Behcet′s disease in a Chinese Han population[J]. Am J Ophthalmol,2014,157(2):488-494.
|
[32] |
Fang J, Hu R, Hou S, et al. Association of TLR2 gene polymorphisms with ocular Behcet′s disease in a Chinese Han population[J]. Invest Ophthalmol Vis Sci,2013,54(13):8384-8392.
|
[33] |
Li H, Liu Q, Hou S, et al. TNFAIP3 gene polymorphisms confer risk for Behcet′s disease in a Chinese Han population[J]. Hum Genet,2013,132(3):293-300.
|
[34] |
Li H, Liu Q, Hou S, et al. TNFAIP3 gene polymorphisms in a Chinese Han population with Vogt-Koyanagi-Harada syndrome[J]. PLoS One,2013,8(3):e59515.
|
[35] |
Shi Y, Jia Y, Hou S, et al. Association of a TNIP1 polymorphism with Vogt-Koyanagi-Harada syndrome but not with ocular Behcet′s disease in Han Chinese[J]. PLoS One,2014,9(5):e95573.
|
[36] |
Wu Z, Zheng W, Xu J, et al. IL10 polymorphisms associated with Behcet′s disease in Chinese Han[J]. Hum Immunol,2014, 75(3):271-276.
|
[37] |
Li W, Saraiya AA, Wang CC. Gene regulation in Giardia lambia involves a putative microRNA derived from a small nucleolar RNA[J]. PLoS Negl Trop Dis,2011,5(10):e1338.
|
[38] |
Kawahara H, Imai T, Okano H. MicroRNAs in Neural Stem Cells and Neurogenesis[J]. Front Neurosci,2012,6:30.
|
[39] |
Fulci V, Scappucci G, Sebastiani G, et al. miR-223 is overexpressed in T-lymphocytes of patients affected by rheumatoid arthritis[J]. Hum Immunol,2010,71(2):206-211.
|
[40] |
Paraboschi EM, Solda G, Gemmati D, et al. Genetic association and altered gene expression of mir-155 in multiple sclerosis patients[J]. Int J Mol Sci,2011,12(12):8695-8712.
|
[41] |
Zhou Q, Xiao X, Wang C, et al. Decreased microRNA-155 expression in ocular Behcet′s disease but not in Vogt Koyanagi Harada syndrome[J]. Invest Ophthalmol Vis Sci,2012,53(9):5665-5674.
|
[42] |
Zhou Q, Hou S, Liang L, et al. MicroRNA-146a and Ets-1 gene polymorphisms in ocular Behcet′s disease and Vogt-Koyanagi-Harada syndrome[J]. Ann Rheum Dis,2014,73(1):170-176.
|
[43] |
Qi J, Hou S, Zhang Q, et al. 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[J]. Hum Genet,2013,132(12):1395-1404.
|
[44] |
Yu H, Liu Y, Bai L, et al. Predisposition to Behcet′s disease and VKH syndrome by genetic variants of miR-182[J]. J Mol Med (Berl),2014,92(9):961-967.
|
[45] |
Hou S, Qi J, Liao D, et al. Copy number variations of C4 are associated with Behcet′s disease but not with ankylosing spondylitis associated with acute anterior uveitis[J]. Arthritis Rheum,2013,65(11):2963-2970.
|
[46] |
Hou S, Qi J, Liao D, et al. High C4 gene copy numbers protects against Vogt-Koyanagi-Harada syndrome in Chinese Han[J]. Br J Ophthalmol,2014,98(12):1733-1737.
|