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Items: 1 to 20 of 128

1.

Two Genetic Variations in the IRF8 region are associated with Behçet's disease in Han Chinese.

Jiang Y, Wang H, Yu H, Li L, Xu D, Hou S, Kijlstra A, Yang P.

Sci Rep. 2016 Jan 22;6:19651. doi: 10.1038/srep19651.

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. doi: 10.1016/j.exer.2015.01.004. Epub 2015 Jan 7.

PMID:
25576669
3.

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 May 2;9(5):e95573. doi: 10.1371/journal.pone.0095573. eCollection 2014.

4.

Copy number variants and genetic polymorphisms in TBX21, GATA3, Rorc, Foxp3 and susceptibility to Behcet's disease and Vogt-Koyanagi-Harada syndrome.

Liao D, Hou S, Zhang J, Fang J, Liu Y, Bai L, Cao Q, Kijlstra A, Yang P.

Sci Rep. 2015 Apr 15;5:9511. doi: 10.1038/srep09511.

5.

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 Jan 8;9(1):e84214. doi: 10.1371/journal.pone.0084214. eCollection 2014.

6.

MicroRNA-146a and Ets-1 gene polymorphisms in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome.

Zhou Q, Hou S, Liang L, Li X, Tan X, Wei L, Lei B, Kijlstra A, Yang P.

Ann Rheum Dis. 2014 Jan;73(1):170-6. doi: 10.1136/annrheumdis-2012-201627. Epub 2012 Dec 25.

PMID:
23268366
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 30;54(13):8384-92. doi: 10.1167/iovs.13-12878.

PMID:
24255044
8.

Association of ATG5 Gene Polymorphisms With Behçet's Disease and ATG10 Gene Polymorphisms With VKH Syndrome in a Chinese Han Population.

Zheng M, Yu H, Zhang L, Li H, Liu Y, Kijlstra A, Yang P.

Invest Ophthalmol Vis Sci. 2015 Dec;56(13):8280-7. doi: 10.1167/iovs.15-18035.

PMID:
26747760
9.

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. doi: 10.1016/j.humimm.2010.04.007. Epub 2010 May 14.

PMID:
20438790
10.

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 May 22;21:589-603. eCollection 2015.

11.

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. doi: 10.1093/rheumatology/ker345. Epub 2011 Nov 15.

PMID:
22087016
12.

Association of a NOS3 gene polymorphism with Behçet's disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese.

Zhou Y, Yu H, Hou S, Fang J, Qin J, Yuan G, Kijlstra A, Yang P.

Mol Vis. 2016 Apr 3;22:311-8. eCollection 2016.

13.

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 May 23;9(5):e98373. doi: 10.1371/journal.pone.0098373. eCollection 2014.

14.

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. doi: 10.1136/bjophthalmol-2014-306163. Epub 2015 Apr 14.

PMID:
25873652
15.

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 24;6:35802. doi: 10.1038/srep35802.

16.

Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182.

Yu H, Liu Y, Bai L, Kijlstra A, Yang P.

J Mol Med (Berl). 2014 Sep;92(9):961-7. doi: 10.1007/s00109-014-1159-9. Epub 2014 May 8.

PMID:
24801147
17.

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. doi: 10.3109/02713683.2011.635398.

PMID:
22440163
18.

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. doi: 10.1007/s00439-013-1346-8. Epub 2013 Aug 9.

PMID:
23928854
19.

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 13;5:12989. doi: 10.1038/srep12989.

20.

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 22;6:37257. doi: 10.1038/srep37257.

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