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Page 1
Did you mean wenjuan zhang (789 results)?
Scleral HIF-1α is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis.
Zhao F, Zhang D, Zhou Q, Zhao F, He M, Yang Z, Su Y, Zhai Y, Yan J, Zhang G, Xue A, Tang J, Han X, Shi Y, Zhu Y, Liu T, Zhuang W, Huang L, Hong Y, Wu D, Li Y, Lu Q, Chen W, Jiao S, Wang Q, Srinivasalu N, Wen Y, Zeng C, Qu J, Zhou X. Zhao F, et al. Among authors: zhuang w. EBioMedicine. 2020 Jul;57:102878. doi: 10.1016/j.ebiom.2020.102878. Epub 2020 Jul 8. EBioMedicine. 2020. PMID: 32652319 Free PMC article.
Identification of Novel Risk Loci for Behçet's Disease-Related Uveitis in a Chinese Population in a Genome-Wide Association Study.
Su G, Zhong Z, Zhou Q, Du L, Ye Z, Li F, Zhuang W, Wang C, Liang L, Ji Y, Cao Q, Wang Q, Chang R, Tan H, Yi S, Li Y, Feng X, Liao W, Zhang W, Shu J, Tan S, Xu J, Pan S, Li H, Shi J, Chen Z, Zhu Y, Ye X, Tan X, Zhang J, Liu Z, Huang F, Yuan G, Pang T, Liu Y, Ding J, Gao Y, Zhang M, Chi W, Liu X, Wang Y, Chen L, Meguro A, Takeuchi M, Mizuki N, Ohno S, Zuo X, Kijlstra A, Yang P. Su G, et al. Among authors: zhuang w. Arthritis Rheumatol. 2022 Apr;74(4):671-681. doi: 10.1002/art.41998. Epub 2022 Feb 14. Arthritis Rheumatol. 2022. PMID: 34652073
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.
Hou S, Du L, Lei B, Pang CP, Zhang M, Zhuang W, Zhang M, Huang L, Gong B, Wang M, Zhang Q, Hu K, Zhou Q, Qi J, Wang C, Tian Y, Ye Z, Liang L, Yu H, Li H, Zhou Y, Cao Q, Liu Y, Bai L, Liao D, Kijlstra A, Xu J, Yang Z, Yang P. Hou S, et al. Among authors: zhuang w. Nat Genet. 2014 Sep;46(9):1007-11. doi: 10.1038/ng.3061. Epub 2014 Aug 10. Nat Genet. 2014. PMID: 25108386
Development and Evaluation of Diagnostic Criteria for Vogt-Koyanagi-Harada Disease.
Yang P, Zhong Y, Du L, Chi W, Chen L, Zhang R, Zhang M, Wang H, Lu H, Yang L, Zhuang W, Yang Y, Xing L, Feng L, Jiang Z, Zhang X, Wang Y, Zhong H, Jiang L, Zhao C, Li F, Cao S, Liu X, Chen X, Shi Y, Zhao W, Kijlstra A. Yang P, et al. Among authors: zhuang w. JAMA Ophthalmol. 2018 Sep 1;136(9):1025-1031. doi: 10.1001/jamaophthalmol.2018.2664. JAMA Ophthalmol. 2018. PMID: 29978190 Free PMC article.
FGFR2 mutation in a Chinese family with unusual Crouzon syndrome.
Li ZL, Chen X, Zhuang WJ, Zhao W, Liu YN, Zhang FX, Ha RS, Wu JH, Zhao C, Sheng XL. Li ZL, et al. Int J Ophthalmol. 2016 Oct 18;9(10):1403-1408. doi: 10.18240/ijo.2016.10.06. eCollection 2016. Int J Ophthalmol. 2016. PMID: 27803855 Free PMC article.
40 results