Cell Development Deficiency and Gene Expression Dysregulation of Trisomy 21 Retina Revealed by Single-Nucleus RNA Sequencing by Fang-Yuan Hu, Fang-Yuan Hu, Fang-Yuan Hu, Feng-Juan Gao, Feng-Juan Gao, Feng-Juan Gao, Ping Xu, Ping Xu, Ping Xu, Sheng-Hai Zhang, Sheng-Hai Zhang, Sheng-Hai Zhang, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu

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Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family by Yu-He Qi, Feng-Juan Gao, Fang-Yuan Hu, Sheng-Hai Zhang, Sheng-Hai Zhang, Sheng-Hai Zhang, Jun-Yi Chen, Wan-Jing Huang, Guo-Hong Tian, Min Wang, De-Kang Gan, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu, Ge-Zhi Xu, Ge-Zhi Xu, Ge-Zhi Xu

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High pressure-induced mtDNA alterations in retinal ganglion cells and subsequent apoptosis by Sheng-Hai Zhang, Sheng-Hai Zhang, Feng-Juan Gao, Zhong-Mou Sun, Ping Xu, Jun-Yi Chen, Xing-Huai Sun, Xing-Huai Sun, Xing-Huai Sun, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu

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Mutational spectrum in a Chinese cohort with congenital cataracts by Hong‐Li Liu, Dao‐Wei Zhang, Fang‐Yuan Hu, Ping Xu, Sheng‐Hai Zhang, Ji‐Hong Wu

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Mutation Spectrum of Stickler Syndrome Type I and Genotype-phenotype Analysis in East Asian Population: a systematic review by Dan-Dan Wang, Feng-Juan Gao, Fang-Yuan Hu, Sheng-Hai Zhang, Ping Xu, Ji-Hong Wu

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The Precise Diagnosis of Wolfram Syndrome Type 1 Based on Next-Generation Sequencing by Dan-Dan Wang, Dan-Dan Wang, Dan-Dan Wang, Fang-Yuan Hu, Fang-Yuan Hu, Fang-Yuan Hu, Feng-Juan Gao, Feng-Juan Gao, Feng-Juan Gao, Sheng-Hai Zhang, Sheng-Hai Zhang, Sheng-Hai Zhang, Ping Xu, Ping Xu, Ping Xu, Guo-Hong Tian, Guo-Hong Tian, Guo-Hong Tian, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu

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Quercetin Declines Apoptosis, Ameliorates Mitochondrial Function and Improves Retinal Ganglion Cell Survival and Function in In Vivo Model of Glaucoma in Rat and Retinal Ganglion C... by Feng-Juan Gao, Sheng-Hai Zhang, Sheng-Hai Zhang, Sheng-Hai Zhang, Sheng-Hai Zhang, Ping Xu, Ping Xu, Ping Xu, Ping Xu, Bo-Qi Yang, Bo-Qi Yang, Bo-Qi Yang, Bo-Qi Yang, Rong Zhang, Rong Zhang, Rong Zhang, Rong Zhang, Yun Cheng, Yun Cheng, Yun Cheng, Yun Cheng, Xu-Jiao Zhou, Xu-Jiao Zhou, Xu-Jiao Zhou, Xu-Jiao Zhou, Wan-Jing Huang, Min Wang, Jun-Yi Chen, Xing-Huai Sun, Xing-Huai Sun, Xing-Huai Sun, Xing-Huai Sun, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu

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Involvement of the MEK-ERK/p38-CREB/c-fos signaling pathway in Kir channel inhibition-induced rat retinal Müller cell gliosis by Feng Gao, Fang Li, Yanying Miao, Lin-Jie Xu, Yuan Zhao, Qian Li, Sheng-Hai Zhang, Jihong Wu, Xing-Huai Sun, Zhongfeng Wang

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Genetic Characteristics and Variation Spectrum of USH2A-Related Retinitis Pigmentosa and Usher Syndrome by Wei Li, Wei Li, Xiao-Sen Jiang, Xiao-Sen Jiang, Dong-Ming Han, Dong-Ming Han, Jia-Yu Gao, Jia-Yu Gao, Zheng-Tao Yang, Zheng-Tao Yang, Li Jiang, Qian Zhang, Qian Zhang, Sheng-Hai Zhang, Sheng-Hai Zhang, Ya Gao, Ji-Hong Wu, Ji-Hong Wu, Jian-Kang Li

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ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants by Fang-Yuan Hu, Fang-Yuan Hu, Fang-Yuan Hu, Fang-Yuan Hu, Jian-kang Li, Jian-kang Li, Feng-Juan Gao, Feng-Juan Gao, Feng-Juan Gao, Feng-Juan Gao, Yu-He Qi, Yu-He Qi, Yu-He Qi, Yu-He Qi, Ping Xu, Ping Xu, Ping Xu, Ping Xu, Yong-Jin Zhang, Yong-Jin Zhang, Yong-Jin Zhang, Yong-Jin Zhang, Dan-Dan Wang, Dan-Dan Wang, Dan-Dan Wang, Dan-Dan Wang, Lu-Sheng Wang, Wei Li, Wei Li, Min Wang, Min Wang, Min Wang, Min Wang, Fang Chen, Fang Chen, Fang Chen, Si-Mai Shen, Ge-Zhi Xu, Ge-Zhi Xu, Ge-Zhi Xu, Ge-Zhi Xu, Sheng-Hai Zhang, Sheng-Hai Zhang, Sheng-Hai Zhang, Sheng-Hai Zhang, Qing Chang, Qing Chang, Qing Chang, Qing Chang, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu, Ji-Hong Wu

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Cumulative mtDNA damage and mutations contribute to the progressive loss of RGCs in a rat model of glaucoma by Ji-hong Wu, Sheng-hai Zhang, John M. Nickerson, Feng-juan Gao, Zhongmou Sun, Xin-ya Chen, Shu-jie Zhang, Rong Zhang, Feng Gao, Jun-yi Chen, Yi Luo, Yan Wang, Xing-huai Sun

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