Jineng Lv

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
Identification of a novel GJA8 (Cx50) point mutation causes human dominant congenital cataracts. Scientific reports\| PubMed ID: 24535056	2014
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
Identification of false-negative mutations missed by next-generation sequencing in retinitis pigmentosa patients: a complementary approach to clinical genetic diagnostic testing. Genetics in medicine : official journal of the American College of Medical Genetics\| PubMed ID: 25569437	2015
Targeted RP9 ablation and mutagenesis in mouse photoreceptor cells by CRISPR-Cas9. Scientific reports\| PubMed ID: 28216641	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
Gene Correction Reverses Ciliopathy and Photoreceptor Loss in iPSC-Derived Retinal Organoids from Retinitis Pigmentosa Patients. Stem cell reports\| PubMed ID: 29526738	2018
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
Nonhuman Primate Model of Oculocutaneous Albinism with and Mutations. Research (Washington, D.C.)\| PubMed ID: 32259106	2020
Generation of Nonhuman Primate Model of Cone Dysfunction through AAV-Mediated Ablation. Molecular therapy. Methods & clinical development\| PubMed ID: 32953936	2020
Engineered FnCas12a with enhanced activity through directional evolution in human cells. The Journal of biological chemistry\| PubMed ID: 33567342	2021
Human cell based directed evolution of adenine base editors with improved efficiency. Nature communications\| PubMed ID: 34625552	2021
Two high-fidelity variants: efSaCas9 and SaCas9-HF, which one is better? Gene therapy\| PubMed ID: 35095097	2022
Depletion of miR-96 Delays, But Does Not Arrest, Photoreceptor Development in Mice. Investigative ophthalmology & visual science\| PubMed ID: 35481839	2022
Can SpRY recognize any PAM in human cells? Journal of Zhejiang University. Science. B\| PubMed ID: 35557039	2022
Identification of RPGR ORF15 mutation for X-linked retinitis pigmentosa in a large Chinese family and in vitro correction with prime editor. Gene therapy\| PubMed ID: 35794468	2022
A precise and efficient adenine base editor. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 35821638	2022