Lue Xiang

State Key Laboratory of Ophthalmology, Wenzhou Medical University

Affiliated withWenzhou Medical University

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 1	2023

Other Publications

Article	Year
AAV-mediated lysophosphatidylcholine acyltransferase 1 (Lpcat1) gene replacement therapy rescues retinal degeneration in rd11 mice. Investigative ophthalmology & visual science\| PubMed ID: 24557352	2014
SLC7A14 linked to autosomal recessive retinitis pigmentosa. Nature communications\| PubMed ID: 24670872	2014
A novel Bruch's membrane-mimetic electrospun substrate scaffold for human retinal pigment epithelium cells. Biomaterials\| PubMed ID: 25220295	2014
A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal Degeneration. PloS one\| PubMed ID: 26930483	2016
Toll-Like Receptor 3 Activation Initiates Photoreceptor Cell Death In Vivo and In Vitro. Investigative ophthalmology & visual science\| PubMed ID: 28152141	2017
Targeted RP9 ablation and mutagenesis in mouse photoreceptor cells by CRISPR-Cas9. Scientific reports\| PubMed ID: 28216641	2017
Trio-based exome sequencing arrests de novo mutations in early-onset high myopia. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 28373534	2017
miR-183/96 plays a pivotal regulatory role in mouse photoreceptor maturation and maintenance. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 28559309	2017
Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract. Experimental & molecular medicine\| PubMed ID: 29700284	2018
Versatile Genome Engineering Techniques Advance Human Ocular Disease Researches in Zebrafish. Frontiers in cell and developmental biology\| PubMed ID: 30050903	2018
Deletion of miR-182 Leads to Retinal Dysfunction in Mice. Investigative ophthalmology & visual science\| PubMed ID: 30924851	2019
Whole-exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndrome. Clinical genetics\| PubMed ID: 30945270	2019
Functional characterization of CEP250 variant identified in nonsyndromic retinitis pigmentosa. Human mutation\| PubMed ID: 30998843	2019
Targeting neuronal and glial cell types with synthetic promoter AAVs in mice, non-human primates and humans. Nature neuroscience\| PubMed ID: 31285614	2019
The Circular RNome of Developmental Retina in Mice. Molecular therapy. Nucleic acids\| PubMed ID: 31877410	2020
Is Indispensable in Zebrafish Retinas. Frontiers in cell and developmental biology\| PubMed ID: 31921845	2019
Ablation of Mature miR-183 Leads to Retinal Dysfunction in Mice. Investigative ophthalmology & visual science\| PubMed ID: 32176259	2020
MLL5 is involved in retinal photoreceptor maturation through facilitating CRX-mediated photoreceptor gene transactivation. iScience\| PubMed ID: 35359806	2022
Depletion of miR-96 Delays, But Does Not Arrest, Photoreceptor Development in Mice. Investigative ophthalmology & visual science\| PubMed ID: 35481839	2022