Kun-chao Wu
China
Last Updated: 09/26/2026
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Found 21 publications
Identification and validation of a novel ferroptosis-related gene signature associated with inherited retinal degeneration in Rd10 mice.
Journal: Scientific reports
Published: October 14, 2025
Recurrence of macular edema in patients with branch retinal vein occlusion: a proteomic study.
Journal: BMC ophthalmology
Published: December 28, 2023
Identification of a novel ferroptosis-related gene signature associated with retinal degeneration induced by light damage in mice.
Journal: Heliyon
Published: February 22, 2023
Depletion of miR-96 Delays, But Does Not Arrest, Photoreceptor Development in Mice.
Journal: Investigative ophthalmology & visual science
Published: April 28, 2022
Human embryonic stem cell-derived organoid retinoblastoma reveals a cancerous origin.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: December 15, 2020
Generation of Nonhuman Primate Model of Cone Dysfunction through In Situ AAV-Mediated CNGB3 Ablation.
Journal: Molecular therapy. Methods & clinical development
Published: June 15, 2020
Ablation of Mature miR-183 Leads to Retinal Dysfunction in Mice.
Journal: Investigative ophthalmology & visual science
Published: March 17, 2020
Nonhuman Primate Model of Oculocutaneous Albinism with TYR and OCA2 Mutations.
Journal: Research (Washington, D.C.)
Published: October 31, 2019
The Circular RNome of Developmental Retina in Mice.
Journal: Molecular therapy. Nucleic acids
Published: May 09, 2019
Deletion of miR-182 Leads to Retinal Dysfunction in Mice.
Journal: Investigative ophthalmology & visual science
Published: March 30, 2019
Whole-exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndrome.
Journal: Clinical genetics
Published: November 19, 2018
Last Updated: 09/26/2026