Expression and Distribution of Mesencephalic Astrocyte-Derived Neurotrophic Factor in the Retina and Optic Nerve

por Gao, Feng-Juan, Zhang, Sheng-Hai, Li, Ting-Ting, Wu, Ji-Hong, Wu, Qiang
Publicado 2017

Cell Development Deficiency and Gene Expression Dysregulation of Trisomy 21 Retina Revealed by Single-Nucleus RNA Sequencing

por Hu, Fang-Yuan, Gao, Feng-Juan, Xu, Ping, Zhang, Sheng-Hai, Wu, Ji-Hong
Publicado 2020

Mutational spectrum in a Chinese cohort with congenital cataracts

por Liu, Hong‐Li, Zhang, Dao‐Wei, Hu, Fang‐Yuan, Xu, Ping, Zhang, Sheng‐Hai, Wu, Ji‐Hong
Publicado 2023

Mutation Spectrum of Stickler Syndrome Type I and Genotype-phenotype Analysis in East Asian Population: a systematic review

por Wang, Dan-Dan, Gao, Feng-Juan, Hu, Fang-Yuan, Zhang, Sheng-Hai, Xu, Ping, Wu, Ji-Hong
Publicado 2020

High Pressure-Induced mtDNA Alterations in Retinal Ganglion Cells and Subsequent Apoptosis

por Zhang, Sheng-Hai, Gao, Feng-Juan, Sun, Zhong-Mou, Xu, Ping, Chen, Jun-Yi, Sun, Xing-Huai, Wu, Ji-Hong
Publicado 2016

The Precise Diagnosis of Wolfram Syndrome Type 1 Based on Next-Generation Sequencing

por Wang, Dan-Dan, Hu, Fang-Yuan, Gao, Feng-Juan, Zhang, Sheng-Hai, Xu, Ping, Tian, Guo-Hong, Wu, Ji-Hong
Publicado 2019

Novel variants of ABCA4 in Han Chinese families with Stargardt disease

por Hu, Fang-Yuan, Gao, Feng-Juan, Li, Jian-kang, Xu, Ping, Wang, Dan-Dan, Zhang, Sheng-Hai, Wu, Ji-Hong
Publicado 2020

Involvement of the MEK-ERK/p38-CREB/c-fos signaling pathway in Kir channel inhibition-induced rat retinal Müller cell gliosis

por Gao, Feng, Li, Fang, Miao, Yanying, Xu, Lin-Jie, Zhao, Yuan, Li, Qian, Zhang, Sheng-Hai, Wu, Jihong, Sun, Xing-Huai, Wang, Zhongfeng
Publicado 2017

Genotypic spectrum and phenotype correlations of EYS-associated disease in a Chinese cohort

por Gao, Feng-Juan, Wang, Dan-Dan, Hu, Fang-Yuan, Xu, Ping, Chang, Qing, Li, Jian-Kang, Liu, Wei, Zhang, Sheng-Hai, Xu, Ge-Zhi, Wu, Ji-Hong
Publicado 2021

Targeting circular RNA-ZRANB1 for therapeutic intervention in retinal neurodegeneration

por Wang, Jia-Jian, Shan, Kun, Liu, Bai-Hui, Liu, Chang, Zhou, Rong-Mei, Li, Xiu-Miao, Dong, Rui, Zhang, Shu-Jie, Zhang, Sheng-Hai, Wu, Ji-Hong, Yan, Biao
Publicado 2018

Genetic Characteristics and Variation Spectrum of USH2A-Related Retinitis Pigmentosa and Usher Syndrome

por Li, Wei, Jiang, Xiao-Sen, Han, Dong-Ming, Gao, Jia-Yu, Yang, Zheng-Tao, Jiang, Li, Zhang, Qian, Zhang, Sheng-Hai, Gao, Ya, Wu, Ji-Hong, Li, Jian-Kang
Publicado 2022

Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family

por Qi, Yu-He, Gao, Feng-Juan, Hu, Fang-Yuan, Zhang, Sheng-Hai, Chen, Jun-Yi, Huang, Wan-Jing, Tian, Guo-Hong, Wang, Min, Gan, De-Kang, Wu, Ji-Hong, Xu, Ge-Zhi
Publicado 2017

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...

por Gao, Feng-Juan, Zhang, Sheng-Hai, Xu, Ping, Yang, Bo-Qi, Zhang, Rong, Cheng, Yun, Zhou, Xu-Jiao, Huang, Wan-Jing, Wang, Min, Chen, Jun-Yi, Sun, Xing-Huai, Wu, Ji-Hong
Publicado 2017

Targeted next-generation sequencing analysis identifies novel mutations in families with severe familial exudative vitreoretinopathy

por Huang, Xiao-Yan, Zhuang, Hong, Wu, Ji-Hong, Li, Jian-Kang, Hu, Fang-Yuan, Zheng, Yu, Tellier, Laurent Christian Asker M., Zhang, Sheng-Hai, Gao, Feng-Juan, Zhang, Jian-Guo, Xu, Ge-Zhi
Publicado 2017

Panel‐based targeted exome sequencing reveals novel candidate susceptibility loci for age‐related cataracts in Chinese Cohort

por Li, Jian-Kang, Li, Li‐Li, Li, Wei, Wang, Zi‐Wei, Gao, Feng‐Juan, Hu, Fang-Yuan, Zhang, Sheng‐Hai, Qu, Shou-Fang, Huang, Jie, Wang, Lu-Sheng, Wu, Ji-Hong, Chen, Fang
Publicado 2020

Clinical and Genetic Characteristics of Chinese Patients with Occult Macular Dystrophy

por Wang, Dan-Dan, Gao, Feng-Juan, Li, Jian-Kang, Chen, Fang, Hu, Fang-Yuan, Xu, Ge-Zhi, Zhang, Jian-Guo, Sun, Hao-Xiang, Zhang, Sheng-Hai, Xu, Ping, Tian, Guo-Hong, Wu, Ji-Hong
Publicado 2020

Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population

por Gao, Feng-Juan, Wang, Dan-Dan, Li, Jian-Kang, Hu, Fang-Yuan, Xu, Ping, Chen, Fang, Qi, Yu-He, Liu, Wei, Li, Wei, Zhang, Sheng-Hai, Chang, Qing, Xu, Ge-Zhi, Wu, Ji-Hong
Publicado 2021

Mutation Screening of mtDNA Combined Targeted Exon Sequencing in a Cohort With Suspected Hereditary Optic Neuropathy

por Li, Jian-Kang, Li, Wei, Gao, Feng-Juan, Qu, Shou-Fang, Hu, Fang-Yuan, Zhang, Sheng-Hai, Li, Li-Li, Wang, Zi-Wei, Qiu, Yong, Wang, Lu-Sheng, Huang, Jie, Wu, Ji-Hong, Chen, Fang
Publicado 2020

ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants

por Hu, Fang-Yuan, Li, Jian-kang, Gao, Feng-Juan, Qi, Yu-He, Xu, Ping, Zhang, Yong-Jin, Wang, Dan-Dan, Wang, Lu-Sheng, Li, Wei, Wang, Min, Chen, Fang, Shen, Si-Mai, Xu, Ge-Zhi, Zhang, Sheng-Hai, Chang, Qing, Wu, Ji-Hong
Publicado 2019