186 related articles for article (PubMed ID: 37221558)
1. Association of ZC3HAV1 single nucleotide polymorphisms with the susceptibility of Vogt-Koyanagi-Harada Disease.
Wu Q; Zhong Z; Zhou C; Cao Q; Su G; Yang P
BMC Med Genomics; 2023 May; 16(1):113. PubMed ID: 37221558
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
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. Genetic association of PRKCD and CARD9 polymorphisms with Vogt-Koyanagi-Harada disease in the Chinese Han population.
Zhou C; Cai S; Xie Y; Zeng Z; Zhang J; Su G; Wu Q; Ye X; Cao Q; Yang P; Hu J
Hum Genomics; 2023 Feb; 17(1):9. PubMed ID: 36782298
[TBL] [Abstract][Full Text] [Related]
6. Association of TNFSF4 Polymorphisms with Vogt-Koyanagi-Harada and Behcet's Disease in Han Chinese.
Lu S; Song S; Hou S; Li H; Yang P
Sci Rep; 2016 Nov; 6():37257. PubMed ID: 27872495
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9.
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]
10. CFI-rs7356506 polymorphisms associated with Vogt-Koyanagi-Harada syndrome.
Dai ML; Huang XF; Wang QF; Cai WJ; Jin ZB; Wang Y
Mol Vis; 2016; 22():9-17. PubMed ID: 26900322
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The Association of Chemokine Gene Polymorphisms with VKH and Behcet's Disease in a Chinese Han Population.
Huang Y; Yu H; Cao Q; Deng J; Huang X; Kijlstra A; Yang P
Biomed Res Int; 2017; 2017():1274960. PubMed ID: 28589131
[TBL] [Abstract][Full Text] [Related]
13. Variants in IL23R-C1orf141 and ADO-ZNF365-EGR2 are associated with susceptibility to Vogt-Koyanagi-Harada disease in Japanese population.
Sakono T; Meguro A; Takeuchi M; Yamane T; Teshigawara T; Kitaichi N; Horie Y; Namba K; Ohno S; Nakao K; Sakamoto T; Sakai T; Nakano T; Keino H; Okada AA; Takeda A; Ito T; Mashimo H; Ohguro N; Oono S; Enaida H; Okinami S; Horita N; Ota M; Mizuki N
PLoS One; 2020; 15(5):e0233464. PubMed ID: 32437414
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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; 8(3):e59515. PubMed ID: 23555688
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. 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]
20. 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; 37(4):312-7. PubMed ID: 22440163
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
