181 related articles for article (PubMed ID: 22876110)
1. Complement factor H and interleukin gene polymorphisms in patients with non-infectious intermediate and posterior uveitis.
Yang MM; Lai TY; Tam PO; Chiang SW; Chan CK; Luk FO; Ng TK; Pang CP
Mol Vis; 2012; 18():1865-72. PubMed ID: 22876110
[TBL] [Abstract][Full Text] [Related]
2. CFH 184G as a genetic risk marker for anterior uveitis in Chinese females.
Yang MM; Lai TY; Tam PO; Chiang SW; Chan CK; Luk FO; Ng TK; Pang CP
Mol Vis; 2011; 17():2655-64. PubMed ID: 22065918
[TBL] [Abstract][Full Text] [Related]
3. Association of the C2-CFB locus with non-infectious uveitis, specifically predisposed to Vogt-Koyanagi-Harada disease.
Yang M; Fan JJ; Wang J; Zhao Y; Teng Y; Liu P
Immunol Res; 2016 Apr; 64(2):610-8. PubMed ID: 26671509
[TBL] [Abstract][Full Text] [Related]
4. Association of CD59 and CFH polymorphisms with acute anterior uveitis in Chinese population.
Wang QF; Huang XF; Zheng ZL; Dai ML; Cai WJ; Yang MM; Jin ZB; Wang YQ
Eye (Lond); 2016 Nov; 30(11):1452-1457. PubMed ID: 27419833
[TBL] [Abstract][Full Text] [Related]
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; 132():225-30. PubMed ID: 25576669
[TBL] [Abstract][Full Text] [Related]
6. Association of CFH and SERPING1 polymorphisms with anterior uveitis.
Yang MM; Lai TY; Tam PO; Chiang SW; Ng TK; Rong SS; Pang CP
Br J Ophthalmol; 2013 Nov; 97(11):1475-80. PubMed ID: 23966370
[TBL] [Abstract][Full Text] [Related]
7. Association of TLR2 gene polymorphisms with ocular Behcet's disease in a Chinese Han population.
Fang J; Hu R; Hou S; Ye Z; Xiang Q; Qi J; Zhou Y; Kijlstra A; Yang P
Invest Ophthalmol Vis Sci; 2013 Dec; 54(13):8384-92. PubMed ID: 24255044
[TBL] [Abstract][Full Text] [Related]
8. Interleukin-10 gene polymorphisms are associated with Behcet's disease but not with Vogt-Koyanagi-Harada syndrome in the Chinese Han population.
Hu J; Hou S; Zhu X; Fang J; Zhou Y; Liu Y; Bai L; Kijlstra A; Yang P
Mol Vis; 2015; 21():589-603. PubMed ID: 26015771
[TBL] [Abstract][Full Text] [Related]
9. Polymorphisms in genetics of vitamin D metabolism confer susceptibility to ocular Behçet disease in a Chinese Han population.
Fang J; Hou S; Xiang Q; Qi J; Yu H; Shi Y; Zhou Y; Kijlstra A; Yang P
Am J Ophthalmol; 2014 Feb; 157(2):488-494.e6. PubMed ID: 24184224
[TBL] [Abstract][Full Text] [Related]
10. Ubiquitin Associated and SH3 Domain Containing B (UBASH3B) Gene Association with Behcet's Disease in Iranian Population.
Shahriyari E; Bonyadi M; Jabbarpoor Bonyadi MH; Soheilian M; Yaseri M; Ebrahimiadib N
Curr Eye Res; 2019 Feb; 44(2):200-205. PubMed ID: 30289285
[TBL] [Abstract][Full Text] [Related]
11. Genetic analysis of innate immunity in Behcet's disease identifies an association with IL-37 and IL-18RAP.
Tan H; Deng B; Yu H; Yang Y; Ding L; Zhang Q; Qin J; Kijlstra A; Chen R; Yang P
Sci Rep; 2016 Oct; 6():35802. PubMed ID: 27775096
[TBL] [Abstract][Full Text] [Related]
12.
Yang MM; Sun HY; Meng T; Qiu SH; Zeng QQ; Ng TK; Jiang L; Deng TM; Zeng AN; Wang J; Luo XL
Front Immunol; 2021; 12():608723. PubMed ID: 33643312
[No Abstract] [Full Text] [Related]
13. 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]
14. 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; 132(12):1395-404. PubMed ID: 23928854
[TBL] [Abstract][Full Text] [Related]
15. STAT4 polymorphism in a Chinese Han population with Vogt-Koyanagi-Harada syndrome and Behçet's disease.
Hu K; Yang P; Jiang Z; Hou S; Du L; Li F
Hum Immunol; 2010 Jul; 71(7):723-6. PubMed ID: 20438790
[TBL] [Abstract][Full Text] [Related]
16. Copy number variations and gene polymorphisms of complement components in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome.
Xu D; Hou S; Zhang J; Jiang Y; Kijlstra A; Yang P
Sci Rep; 2015 Aug; 5():12989. PubMed ID: 26269006
[TBL] [Abstract][Full Text] [Related]
17. Association of complement factor H tyrosine 402 histidine genotype with posterior involvement in sarcoid-related uveitis.
Thompson IA; Liu B; Sen HN; Jiao X; Katamay R; Li Z; Hu M; Hejtmancik F; Nussenblatt RB
Am J Ophthalmol; 2013 Jun; 155(6):1068-1074.e1. PubMed ID: 23497844
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Genetic variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's disease and VKH syndrome.
Li X; Bai L; Fang J; Hou S; Zhou Q; Yu H; Kijlstra A; Yang P
PLoS One; 2014; 9(5):e98373. PubMed ID: 24859272
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
