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Clinical Genetics|April 5, 2019
Whole-exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndromeXue-Bi Cai, Kun-Chao Wu, Xiao Zhang, et al.
Investigative Ophthalmology & Visual Science|March 30, 2019
Deletion of miR-182 Leads to Retinal Dysfunction in MiceKun-Chao Wu, Xue-Jiao Chen, Guang-Hui Jin, et al.
Heliyon|December 25, 2023
Identification of a novel ferroptosis-related gene signature associated with retinal degeneration induced by light damage in miceXin-Lan Lei, Qiao-Li Yang, Yong-Zhao Wei, et al.
Investigative Ophthalmology & Visual Science|February 3, 2017
Toll-Like Receptor 3 Activation Initiates Photoreceptor Cell Death In Vivo and In VitroMei-Ling Gao, Kun-Chao Wu, Wen-Li Deng, et al.
Molecular Therapy. Nucleic Acids|December 27, 2019
The Circular RNome of Developmental Retina in MiceXue-Jiao Chen, Zi-Cheng Zhang, Xiao-Yun Wang, et al.
Human Mutation|April 19, 2019
Functional characterization of CEP250 variant identified in nonsyndromic retinitis pigmentosaXiu-Feng Huang, Lue Xiang, Xiao-Long Fang, et al.
Investigative Ophthalmology & Visual Science|April 28, 2022
Depletion of miR-96 Delays, But Does Not Arrest, Photoreceptor Development in MiceLue Xiang, Juan Zhang, Feng-Qin Rao, et al.
Experimental & Molecular Medicine|April 28, 2018
Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataractXiu-Feng Huang, Lue Xiang, Wan Cheng, et al.
Investigative Ophthalmology & Visual Science|March 17, 2020
Ablation of Mature miR-183 Leads to Retinal Dysfunction in MiceChang-Jun Zhang, Lue Xiang, Xue-Jiao Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 5, 2017
Trio-based exome sequencing arrests de novo mutations in early-onset high myopiaZi-Bing Jin, Jinyu Wu, Xiu-Feng Huang, et al.
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