P. Xu

发表

Asiatic Acid Prevents Retinal Ganglion Cell Apoptosis in a Rat Model of Glaucoma

Xinghuai Sun, Feng-Juan Gao, Jihong Wu, 2018, Front. Neurosci..

Patient-derived three-dimensional cortical neurospheres to model Parkinson’s disease

K. Rhodes, V. Khurana, W. Raja, 2021, bioRxiv.

Comprehensive analysis of genetic and clinical characteristics of 30 patients with X‐linked juvenile retinoschisis in China

Jian-kang Li, Feng-Juan Gao, Jihong Wu, 2020, Acta ophthalmologica.

Novel variants associated with Stargardt disease in Chinese patients.

Jian-kang Li, Feng-Juan Gao, Fangyuan Hu, 2020, Gene.

Genetic and Clinical Findings in a Large Cohort of Chinese Patients with Suspected Retinitis Pigmentosa.

W. Liu, Jian-kang Li, Wei Li, 2019, Ophthalmology.

Amniotic Membrane Enhances the Characteristics and Function of Stem Cell-Derived Retinal Pigment Epithelium Sheets by Inhibiting the Epithelial-Mesenchymal Transition.

X. Zhong, Dandan Zheng, Bingbing Xie, 2022, Acta biomaterialia.

Mutation spectrum of the bestrophin-1 gene in a large Chinese cohort with bestrophinopathy

Jian-kang Li, Wei Li, Feng-Juan Gao, 2019, British Journal of Ophthalmology.

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

Fang Chen, Jian-kang Li, Wei Li, 2019, Front. Genet..

Novel variants of ABCA4 in Han Chinese families with Stargardt disease

Jian-kang Li, Feng-Juan Gao, Shenghai Zhang, 2020, BMC medical genetics.

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

Feng-Juan Gao, Shenghai Zhang, Jihong Wu, 2016, Front. Cell. Neurosci..

Clinical and Genetic Characteristics of Chinese Patients with Occult Macular Dystrophy

Jian-kang Li, Feng-Juan Gao, Shenghai Zhang, 2020, Investigative ophthalmology & visual science.

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

Jian-kang Li, Feng-Juan Gao, Fangyuan Hu, 2021, Eye.

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 Cell Culture In Vitro

Feng-Juan Gao, Shenghai Zhang, Jihong Wu, 2017, Front. Mol. Neurosci..

Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population

Jian-kang Li, Wei Li, Feng-Juan Gao, 2021, Orphanet Journal of Rare Diseases.

Regulation of mitophagy by metformin improves the structure and function of retinal ganglion cells following excitotoxicity-induced retinal injury.

Jihong Wu, Ping Xu, Fang-Yuan Hu, 2022, Experimental eye research.

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

Feng-Juan Gao, Shenghai Zhang, Jihong Wu, 2019, Front. Genet..

Nobiletin protects retinal ganglion cells in models of ocular hypertension in vivo and hypoxia in vitro

Feng-Juan Gao, Jihong Wu, Ping Xu, 2022, Laboratory Investigation.

Prevalence and genetic–phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease

Jian-kang Li, Wei Li, Feng-Juan Gao, 2020, British Journal of Ophthalmology.

Next‐generation sequencing‐aided precise diagnosis of Stickler syndrome type I

Jian-kang Li, Feng-Juan Gao, Shenghai Zhang, 2019, Acta ophthalmologica.

Clinical and Genetic Analysis of Retinitis Pigmentosa with Primary Angle Closure Glaucoma in the Chinese Population

Feng-Juan Gao, Jihong Wu, Ping Xu, 2022, Current eye research.

Mutation Analysis of the RPGR Gene in a Chinese Cohort

Jihong Wu, F. Gao, Dan-Dan Wang, 2022, Frontiers in Genetics.

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

Jihong Wu, Feng-Juan Gao, Shenghai Zhang, 2020, Frontiers in Bioengineering and Biotechnology.

Single cell RNA sequencing reveals cellular diversity of trisomy 21 retina

Fang Chen, Xinghuai Sun, Jixing Zhong, 2019, bioRxiv.

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

Jian-kang Li, Feng-Juan Gao, Shenghai Zhang, 2021, Eye.

Comparative analysis of retinal ganglion cell damage in three glaucomatous rat models

Xinghuai Sun, Feng-Juan Gao, Jihong Wu, 2018, Experimental eye research.

Expanding the clinical and genetic spectrum of Heimler syndrome

F. Song, Jian-kang Li, Feng-Juan Gao, 2019, Orphanet Journal of Rare Diseases.

Single cell RNA-seq reveals cellular diversity and developmental characteristics of human infant retina

Fang Chen, Xinghuai Sun, Jixing Zhong, 2019, bioRxiv.

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

Jihong Wu, Feng-Juan Gao, Shenghai Zhang, 2020, BMC Medical Genetics.

Mutational spectrum in a Chinese cohort with congenital cataracts

Shenmin Zhang, Jihong Wu, Honglong Liu, 2023, Molecular genetics & genomic medicine.