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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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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Screw-Dislocation-Driven Hierarchical Superstructures of Ag-Ag₂O-AgO Nanoparticles by Hua Yang, Jing Ru Zhang, Wentao Cao, Jin Zhen, 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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Calpastatin participates in the regulation of cell migration in BAP1-deficient uveal melanoma cells by Han Yue, Feng-Xi Meng, Jiang Qian, Bin-Bin Xu, Gang Li, 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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Mutation Analysis of the RPGR Gene in a Chinese Cohort by Hong-Li Liu, Hong-Li Liu, Hong-Li Liu, Hong-Li Liu, Feng-Guan Gao, Feng-Guan Gao, Feng-Guan Gao, Feng-Guan Gao, Dan-Dan Wang, Dan-Dan Wang, Dan-Dan Wang, Dan-Dan Wang, Fang-Yuan Hu, Fang-Yuan Hu, Fang-Yuan Hu, Fang-Yuan Hu, Ping Xu, Ping Xu, Ping Xu, Ping Xu, Qing Chang, Qing Chang, Qing Chang, Qing Chang, Ge-Zhi Xu, Ge-Zhi Xu, Ge-Zhi Xu, Ge-Zhi Xu, Ji-Hong Wu, 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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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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Out-of-Substrate Ag–Ag2O Nanoplates: Surfactantless Photochemical Synthesis, Structural Evolution, and Mechanistic Study by Meng Yin Li, Yao Quan Mao, Su Ke Yang, Ting Ting Dai, Hua Yang, Feng Feng, Tao Wu, Muzi Chen, Guo Qin Xu, Ji Hong Wu

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Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses by Feng-Juan Gao, Guo-Hong Tian, Fang-Yuan Hu, Dan-Dan Wang, Jian-Kang Li, Qing Chang, Fang Chen, Ge-Zhi Xu, Wei Liu, Ji-Hong Wu

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Mutation spectrum in a cohort with familial exudative vitreoretinopathy by Ning Qu, Wei Li, Dong‐Ming Han, Jia‐Yu Gao, Zheng‐Tao Yang, Li Jiang, Tian‐Bin Liu, Yan‐Xian Chen, Xiao‐Sen Jiang, Liang Zhou, Ji‐Hong Wu, Xin Huang

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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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Expanding the clinical and genetic spectrum of Heimler syndrome by Feng-Juan Gao, Fang-Yuan Hu, Ping Xu, Yu-He Qi, Jian-Kang Li, Yong-Jin Zhang, Fang Chen, Qing Chang, Fang Song, Si-Mai Shen, Ge-Zhi Xu, 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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