Guanjie Gao

State Key Laboratory Of Ophthalmology, Guangdong Provincial Key Laboratory Of Ophthalmology And Visual Science
Guangzhou, 510060, China

Last Updated: 09/26/2026

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Found 14 publications

Exogenous photoreceptor-specific N-glycosylated PROM1 rescues retinal degeneration in patient and mouse models.

Exogenous photoreceptor-specific N-glycosylated PROM1 rescues retinal degeneration in patient and mouse models.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: August 05, 2025

Subretinal suspensions of hiPSC-derived retinal pigment epithelium cells form functional monolayers in NOD-SCID mice facilitating treatment of advanced retinal diseases.

Subretinal suspensions of hiPSC-derived retinal pigment epithelium cells form functional monolayers in NOD-SCID mice facilitating treatment of advanced retinal diseases.

Journal: Regenerative therapy

Published: April 11, 2025

Human CRX regulates photoreceptor cells development via bidirectional transcriptional control in retinal organoids.

Human CRX regulates photoreceptor cells development via bidirectional transcriptional control in retinal organoids.

Journal: Stem cell reports

Published: March 27, 2025

Longitudinal analysis of retinal cell state transitions in RB1-deficient retinal organoids reveals the nascent cone precursors are the earliest cell-origin of human retinoblastoma.

Longitudinal analysis of retinal cell state transitions in RB1-deficient retinal organoids reveals the nascent cone precursors are the earliest cell-origin of human retinoblastoma.

Journal: Cell death & disease

Published: March 10, 2025

Dynamic molecular and cellular characteristics of VSX2-positive retinal progenitor cells in human retinal organoids.

Dynamic molecular and cellular characteristics of VSX2-positive retinal progenitor cells in human retinal organoids.

Journal: Stem cell research & therapy

Published: December 13, 2024

Ion channels research in hPSC-RPE cells: bridging benchwork to clinical applications.

Ion channels research in hPSC-RPE cells: bridging benchwork to clinical applications.

Journal: Journal of translational medicine

Published: August 17, 2024

Biallelic CLCN2 mutations cause retinal degeneration by impairing retinal pigment epithelium phagocytosis and chloride channel function.

Biallelic CLCN2 mutations cause retinal degeneration by impairing retinal pigment epithelium phagocytosis and chloride channel function.

Journal: Human genetics

Published: November 07, 2022

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

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

Journal: Acta biomaterialia

Published: March 07, 2022

Generation of an RCVRN-eGFP Reporter hiPSC Line by CRISPR/Cas9 to Monitor Photoreceptor Cell Development and Facilitate the Cell Enrichment for Transplantation.

Generation of an RCVRN-eGFP Reporter hiPSC Line by CRISPR/Cas9 to Monitor Photoreceptor Cell Development and Facilitate the Cell Enrichment for Transplantation.

Journal: Frontiers in cell and developmental biology

Published: February 06, 2022

Spatial and Temporal Development of Müller Glial Cells in hiPSC-Derived Retinal Organoids Facilitates the Cell Enrichment and Transcriptome Analysis.

Spatial and Temporal Development of Müller Glial Cells in hiPSC-Derived Retinal Organoids Facilitates the Cell Enrichment and Transcriptome Analysis.

Journal: Frontiers in cellular neuroscience

Published: November 23, 2021

Establishment of a Rapid Lesion-Controllable Retinal Degeneration Monkey Model for Preclinical Stem Cell Therapy.

Establishment of a Rapid Lesion-Controllable Retinal Degeneration Monkey Model for Preclinical Stem Cell Therapy.

Journal: Cells

Published: August 19, 2020

Generation and Characterization of Induced Pluripotent Stem Cells and Retinal Organoids From a Leber's Congenital Amaurosis Patient With Novel RPE65 Mutations.

Generation and Characterization of Induced Pluripotent Stem Cells and Retinal Organoids From a Leber's Congenital Amaurosis Patient With Novel RPE65 Mutations.

Journal: Frontiers in molecular neuroscience

Published: March 21, 2019

Showing 1-12 of 14

Last Updated: 09/26/2026