Yihua Zhu

发表

Identification of miRNAs associated with tumorigenesis of retinoblastoma by miRNA microarray analysis

J. Cheng, Juhua Yang, Jianhua Xu, 2008, Child's Nervous System.

Analysis of TGFBI gene mutations in Chinese patients with corneal dystrophies and review of the literature

Juhua Yang, Xu Ma, Yihua Zhu, 2010, Molecular vision.

Antiproliferative and Apoptotic Effects of Indomethacin on Human Retinoblastoma Cell Line Y79 and the Involvement of ß-Catenin, Nuclear Factor-κB and Akt Signaling Pathways

Hao Chen, Yihua Zhu, Yijun Wu, 2013, Ophthalmic Research.

Fenofibrate Ameliorated Systemic and Retinal Inflammation and Modulated Gut Microbiota in High-Fat Diet-Induced Mice

Yajun Wu, Yihua Zhu, Xiaomei Liu, 2022, Frontiers in Cellular and Infection Microbiology.

Protective Effects of Trimetazidine in Retarding Selenite-Induced Lens Opacification

Feng Gu, Yihua Zhu, Yanghui Xiu, 2019, Current eye research.

Identification of a novel GJA3 mutation in a large Chinese family with congenital cataract using targeted exome sequencing

Feng Gu, Yihua Zhu, Junzhao Zhao, 2017, PloS one.

Mutation screening of crystallin genes in Chinese families with congenital cataracts

Zongfu Cao, Juhua Yang, Lijuan Liu, 2019, Molecular vision.

A novel de novo duplication mutation of PAX6 in a Chinese family with aniridia and other ocular abnormalities

Juhua Yang, Kanxing Zhao, Yihua Zhu, 2014, Scientific Reports.

Forkhead Domain Inhibitor-6 Suppresses Corneal Neovascularization and Subsequent Fibrosis After Alkali Burn in Rats

N. Fan, Man Yu, Yihua Zhu, 2022, Investigative ophthalmology & visual science.

Identification of a novel idiopathic congenital nystagmus-causing missense mutation, p.G296C, in the FRMD7 gene

Feng Gu, Yihua Zhu, Junzhao Zhao, 2018, Molecular medicine reports.

Optical Coherence Tomography Angiography in Posner-Schlossman Syndrome – A Preliminary Study

Xiaoyong Chen, Yihua Zhu, Jinyuan Chen, 2022, Ocular immunology and inflammation.

Investigation of Accuracy and Influence Factors of Predicting Lenticule Thickness in Small Incision Lenticule Extraction by Machine Learning Models

Ying Chen, Yihua Zhu, Huihang Wang, 2023, Journal of personalized medicine.

Identification of candidate cancer genes involved in human retinoblastoma by data mining

Wei Xiong, W. Xiong, Juhua Yang, 2008, Child's Nervous System.

Novel mutations in HSF4 cause congenital cataracts in Chinese families

Zongfu Cao, Juhua Yang, Lijuan Liu, 2018, BMC Medical Genetics.

Mitochondrial quality control protects photoreceptors against oxidative stress in the H2O2-induced models of retinal degeneration diseases

Juhua Yang, Yihua Zhu, Xiaole Chen, 2021, Cell Death & Disease.

Identifcation of a Novel Mutation p.I240T in the FRMD7 gene in a Family with Congenital Nystagmus

Feng Gu, Z. Wang, Juhua Yang, 2013, Scientific Reports.

The effect of human gene therapy for RPE65-associated Leber’s congenital amaurosis on visual function: a systematic review and meta-analysis

Yihua Zhu, Radouil Tzekov, Wensheng Li, 2020, Orphanet Journal of Rare Diseases.

Clinical characteristics, rates of blindness, and geographic features of primary angle-closure disease in hospitals of the Chinese Glaucoma Study Consortium.

Ningli Wang, Kaijun Li, Li Tang, 2021, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

Analysis of ocular biometric parameters in patients with primary angle closure diseases at different refractive status

N. Fan, Yihua Zhu, Lijun Zhao, 2023, Journal of evidence-based medicine.

Novel A14841G mutation is associated with high penetrance of LHON/C4171A family.

Juhua Yang, Xu Ma, Yihua Zhu, 2009, Biochemical and biophysical research communications.

Confirmation of the mitochondrial ND1 gene mutation G3635A as a primary LHON mutation.

Juhua Yang, Lijuan Liu, Xu Ma, 2009, Biochemical and biophysical research communications.

Clinical characteristics, rates of blindness, and geographic features of primary angle-closure disease in hospitals of the Chinese Glaucoma Study Consortium.

Ningli Wang, Yinong Zhang, Kaijun Li, 2021, Canadian Journal of Ophthalmology-journal Canadien D Ophtalmologie.

AZD6738 Inhibits fibrotic response of conjunctival fibroblasts by regulating checkpoint kinase 1/P53 and PI3K/AKT pathways

Yihua Zhu, Longxiang Huang, Chunlin Lan, 2022, Frontiers in Pharmacology.

Protective Effects of Nicotinamide Riboside on H2O2-induced Oxidative Damage in Lens Epithelial Cells

Juhua Yang, Yihua Zhu, Xiaole Chen, 2020, Current eye research.

A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract

Zongfu Cao, Feng Gu, Juhua Yang, 2008, Molecular vision.

Structure‒function‒pathogenicity analysis of C-terminal myocilin missense variants based on experiments and 3D models

Juhua Yang, Yihua Zhu, Xiaojiang Lin, 2022, Frontiers in Genetics.

The novel G10680A mutation is associated with complete penetrance of the LHON/T14484C family.

Zongfu Cao, Juhua Yang, Xu Ma, 2009, Mitochondrion.

China Glaucoma Treatment Pattern Study I–Primary Angle-Closure Glaucoma: protocol for a multicentre, retrospective, observational study

M. He, Yihua Zhu, Jinyuan Chen, 2023, BMJ Open.

Identification of a novel GJA3 mutation in a large Chinese family with congenital cataract using targeted exome sequencing

Feng Gu, Yihua Zhu, Junzhao Zhao, 2017, PloS one.

Zonule-Associated Gene Variants in Isolated Ectopia Lentis and Glaucoma

X. Jiao, J. Hejtmancik, Yihua Zhu, 2023, Journal of glaucoma.

A novel causative mutation for congenital cataract and its underlying pathogenesis

Xun Xu, Yihua Zhu, Kangni Wu, 2019, Ophthalmic genetics.

Clinical observation of phacoemulsification under the low perfusion pattern and low negative pressure in patients with low corneal endothelial cell density

Yihua Zhu, Q. Ye, Yi-hua Yao, 2023, BMC Ophthalmology.