160 related articles for article (PubMed ID: 21331694)
1. Evaluation of NLRP1 gene polymorphisms in Vogt-Koyanagi-Harada disease.
Horie Y; Saito W; Kitaichi N; Miura T; Ishida S; Ohno S
Jpn J Ophthalmol; 2011 Jan; 55(1):57-61. PubMed ID: 21331694
[TBL] [Abstract][Full Text] [Related]
2. Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.
Horie Y; Kitaichi N; Katsuyama Y; Yoshida K; Miura T; Ota M; Asukata Y; Inoko H; Mizuki N; Ishida S; Ohno S
Mol Vis; 2009 Jun; 15():1115-9. PubMed ID: 19503742
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Association of NLRP1 genetic variants and mRNA overexpression with generalized vitiligo and disease activity in a Gujarat population.
Dwivedi M; Laddha NC; Mansuri MS; Marfatia YS; Begum R
Br J Dermatol; 2013 Nov; 169(5):1114-25. PubMed ID: 23773036
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. 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; 9(1):e84214. PubMed ID: 24416204
[TBL] [Abstract][Full Text] [Related]
10. NLRP1 gene polymorphism influences gene transcription and is a risk factor for rheumatoid arthritis in han chinese.
Sui J; Li H; Fang Y; Liu Y; Li M; Zhong B; Yang F; Zou Q; Wu Y
Arthritis Rheum; 2012 Mar; 64(3):647-54. PubMed ID: 21976003
[TBL] [Abstract][Full Text] [Related]
11. Association Study of
Ohno 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; Fukuhara T; Mashimo H; Ohguro N; Oono S; Enaida H; Okinami S; Mizuki N
Ocul Immunol Inflamm; 2019; 27(5):699-705. PubMed ID: 30395750
[No Abstract] [Full Text] [Related]
12. 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]
13. 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]
14. Polymorphism of IFN-gamma gene and Vogt-Koyanagi-Harada disease.
Horie Y; Kitaichi N; Takemoto Y; Namba K; Yoshida K; Hirose S; Hasumi Y; Ota M; Inoko H; Mizuki N; Ohno S
Mol Vis; 2007 Dec; 13():2334-8. PubMed ID: 18199975
[TBL] [Abstract][Full Text] [Related]
15. Investigation of association between TLR9 gene polymorphisms and VKH in Japanese patients.
Ito R; Ota M; Meguro A; Katsuyama Y; Uemoto R; Nomura E; Nishide T; Kitaichi N; Horie Y; Namba K; Ohno S; Inoko H; Mizuki N
Ocul Immunol Inflamm; 2011 Jun; 19(3):202-5. PubMed ID: 21595536
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Case Series: Gene Expression Analysis in Canine Vogt-Koyanagi-Harada/Uveodermatologic Syndrome and Vitiligo Reveals Conserved Immunopathogenesis Pathways Between Dog and Human Autoimmune Pigmentary Disorders.
Egbeto IA; Garelli CJ; Piedra-Mora C; Wong NB; David CN; Robinson NA; Richmond JM
Front Immunol; 2020; 11():590558. PubMed ID: 33384688
[TBL] [Abstract][Full Text] [Related]
19. Elevated serum osteopontin levels and genetic polymorphisms of osteopontin are associated with Vogt-Koyanagi-Harada disease.
Chu M; Yang P; Hu R; Hou S; Li F; Chen Y; Kijlstra A
Invest Ophthalmol Vis Sci; 2011 Sep; 52(10):7084-9. PubMed ID: 21810982
[TBL] [Abstract][Full Text] [Related]
20. NLRP1, PTPN22 and PADI4 gene polymorphisms and rheumatoid arthritis in ACPA-positive Singaporean Chinese.
Goh LL; Yong MY; See WQ; Chee EYW; Lim PQ; Koh ET; Leong KP;
Rheumatol Int; 2017 Aug; 37(8):1295-1302. PubMed ID: 28653215
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]