212 related articles for article (PubMed ID: 19234630)
1. 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; 15():386-92. PubMed ID: 19234630
[TBL] [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; 15():955-61. PubMed ID: 19452015
[TBL] [Abstract][Full Text] [Related]
3. 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
[TBL] [Abstract][Full Text] [Related]
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; 54(5):3360-5. PubMed ID: 23611997
[TBL] [Abstract][Full Text] [Related]
5. 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; 54(12):7734-8. PubMed ID: 24194192
[TBL] [Abstract][Full Text] [Related]
6. [Association of HLA-DRB genes with Vogt-Koyanagi-Harada syndrome in a Chinese Han population].
Zhang M; Qiu C; Hu T
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2000 Feb; 22(1):36-40. PubMed ID: 12903490
[TBL] [Abstract][Full Text] [Related]
7. 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; 132():225-30. PubMed ID: 25576669
[TBL] [Abstract][Full Text] [Related]
8. Polymorphisms of IL23R and Vogt-Koyanagi-Harada syndrome in a Chinese Han population.
Jiang Z; Yang P; Hou S; Li F; Zhou H
Hum Immunol; 2010 Apr; 71(4):414-7. PubMed ID: 20116410
[TBL] [Abstract][Full Text] [Related]
9. 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; 16():353-8. PubMed ID: 20216938
[TBL] [Abstract][Full Text] [Related]
10. [The association of HLA-DR4 gene subtypes with Vogt-Koyanagi-Harada syndrome].
Xiao T; Jiang Y; You X
Zhonghua Yan Ke Za Zhi; 1997 Jul; 33(4):268-71. PubMed ID: 10451958
[TBL] [Abstract][Full Text] [Related]
11. HLA-DRB1 typing of Vogt-Koyanagi-Harada's disease by PCR-RFLP and the strong association with DRB1*0405 and DRB1*0410.
Shindo Y; Inoko H; Yamamoto T; Ohno S
Br J Ophthalmol; 1994 Mar; 78(3):223-6. PubMed ID: 7908535
[TBL] [Abstract][Full Text] [Related]
12.
Xu L; Zhao T; Yuan G; Hou S; Zeng W; Chen F
Mol Vis; 2019; 25():834-842. PubMed ID: 31908401
[TBL] [Abstract][Full Text] [Related]
13. 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
[TBL] [Abstract][Full Text] [Related]
14. HLA class II genes in Vogt-Koyanagi-Harada disease.
Islam SM; Numaga J; Fujino Y; Hirata R; Matsuki K; Maeda H; Masuda K
Invest Ophthalmol Vis Sci; 1994 Oct; 35(11):3890-6. PubMed ID: 7928186
[TBL] [Abstract][Full Text] [Related]
15. 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; 9(5):e95573. PubMed ID: 24788730
[TBL] [Abstract][Full Text] [Related]
16. [Single nucleotide polymorphisms of promoter of human leukocyte antigen-DQB1 alleles in Chinese Han patients with Vogt-Koyanagi-Harada syndrome].
Min HY; Niu NF; Liu Y; Zhang MF; Zhu XL; Zhao JL
Zhonghua Yan Ke Za Zhi; 2008 Oct; 44(10):870-5. PubMed ID: 19176112
[TBL] [Abstract][Full Text] [Related]
17. 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; 15():1537-41. PubMed ID: 19668598
[TBL] [Abstract][Full Text] [Related]
18. 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; 99(8):1150-4. PubMed ID: 25873652
[TBL] [Abstract][Full Text] [Related]
19. CD40 gene polymorphisms confer risk of Behcet's disease but not of Vogt-Koyanagi-Harada syndrome in a Han Chinese population.
Chen F; Hou S; Jiang Z; Chen Y; Kijlstra A; Rosenbaum JT; Yang P
Rheumatology (Oxford); 2012 Jan; 51(1):47-51. PubMed ID: 22087016
[TBL] [Abstract][Full Text] [Related]
20. Association of the CTLA-4 gene with Vogt-Koyanagi-Harada syndrome.
Du L; Yang P; Hou S; Lin X; Zhou H; Huang X; Wang L; Kijlstra A
Clin Immunol; 2008 Apr; 127(1):43-8. PubMed ID: 18282809
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]