Bai L - Search Results

1

TNF receptor-associated factor 5 gene confers genetic predisposition to acute anterior uveitis and pediatric uveitis.

Xiang Q, Chen L, Fang J, Hou S, Wei L, Bai L, Liu Y, Zhou Y, Kijlstra A, Yang P. Xiang Q, et al. Among authors: bai l. Arthritis Res Ther. 2013;15(5):R113. doi: 10.1186/ar4293. Arthritis Res Ther. 2013. PMID: 24020968 Free PMC article.

2

Copy number variations of complement component C4 are associated with Behçet's disease but not with ankylosing spondylitis associated with acute anterior uveitis.

Hou S, Qi J, Liao D, Zhang Q, Fang J, Zhou Y, Liu Y, Bai L, Zhang M, Kijlstra A, Yang P. Hou S, et al. Among authors: bai l. Arthritis Rheum. 2013 Nov;65(11):2963-70. doi: 10.1002/art.38116. Arthritis Rheum. 2013. PMID: 23918728 Free article.

3

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. Xiang Q, et al. Among authors: bai l. PLoS One. 2014 Jan 8;9(1):e84214. doi: 10.1371/journal.pone.0084214. eCollection 2014. PLoS One. 2014. PMID: 24416204 Free PMC article.

4

MicroRNA-146a and Ets-1 gene polymorphisms are associated with pediatric uveitis.

Wei L, Zhou Q, Hou S, Bai L, Liu Y, Qi J, Xiang Q, Zhou Y, Kijlstra A, Yang P. Wei L, et al. Among authors: bai l. PLoS One. 2014 Mar 21;9(3):e91199. doi: 10.1371/journal.pone.0091199. eCollection 2014. PLoS One. 2014. PMID: 24658012 Free PMC article.

5

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

Yu H, Liu Y, Bai L, Kijlstra A, Yang P. Yu H, et al. Among authors: bai l. J Mol Med (Berl). 2014 Sep;92(9):961-7. doi: 10.1007/s00109-014-1159-9. Epub 2014 May 8. J Mol Med (Berl). 2014. PMID: 24801147

6

Association of T-Bet, GATA-3, RORC, and FOXP3 Copy Number Variations With Acute Anterior Uveitis With or Without Ankylosing Spondylitis in Chinese Han.

Bai L, Liu Y, Hou S, Liao D, Kijlstra A, Yang P. Bai L, et al. Invest Ophthalmol Vis Sci. 2016 Apr;57(4):1847-52. doi: 10.1167/iovs.15-17960. Invest Ophthalmol Vis Sci. 2016. PMID: 27082299

7

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. Li X, et al. Among authors: bai l. PLoS One. 2014 May 23;9(5):e98373. doi: 10.1371/journal.pone.0098373. eCollection 2014. PLoS One. 2014. PMID: 24859272 Free PMC article. Clinical Trial.

8

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. Liao D, et al. Among authors: bai l. Sci Rep. 2015 Apr 15;5:9511. doi: 10.1038/srep09511. Sci Rep. 2015. PMID: 25873156 Free PMC article.

9

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. Hu J, et al. Among authors: bai l. Mol Vis. 2015 May 22;21:589-603. eCollection 2015. Mol Vis. 2015. PMID: 26015771 Free PMC article.

10

Genetic variations of IL17F and IL23A show associations with Behçet's disease and Vogt-Koyanagi-Harada syndrome.

Hou S, Liao D, Zhang J, Fang J, Chen L, Qi J, Zhang Q, Liu Y, Bai L, Zhou Y, Kijlstra A, Yang P. Hou S, et al. Among authors: bai l. Ophthalmology. 2015 Mar;122(3):518-23. doi: 10.1016/j.ophtha.2014.09.025. Epub 2014 Nov 15. Ophthalmology. 2015. PMID: 25439430

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