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Scientific Reports|June 10, 2022
AAV2-mediated gene therapy for Bietti crystalline dystrophy provides functional CYP4V2 in multiple relevant cell modelsJiang-Hui Wang, Grace E Lidgerwood, Maciej Daniszewski, et al.
Scientific Reports|August 11, 2016
Enriched retinal ganglion cells derived from human embryonic stem cellsKatherine P Gill, Sandy S C Hung, Alexei Sharov, et al.
NAR Genomics and Bioinformatics|February 12, 2021
Comparative performance of the BGI and Illumina sequencing technology for single-cell RNA-sequencingAnne Senabouth, Stacey Andersen, Qianyu Shi, et al.
Aging|April 30, 2017
Mitochondrial replacement in an iPSC model of Leber's hereditary optic neuropathyRaymond C B Wong, Shiang Y Lim, Sandy S C Hung, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 8, 2017
Drusen in patient-derived hiPSC-RPE models of macular dystrophiesChad A Galloway, Sonal Dalvi, Sandy S C Hung, et al.
Aging|February 16, 2023
Knockout of AMD-associated gene <i>POLDIP2</i> reduces mitochondrial superoxide in human retinal pigment epithelial cellsTu Nguyen, Daniel Urrutia-Cabrera, Luozixian Wang, et al.
Investigative Ophthalmology & Visual Science|July 2, 2016
AAV-Mediated CRISPR/Cas Gene Editing of Retinal Cells In VivoSandy S C Hung, Vicki Chrysostomou, Fan Li, et al.
Frontiers in Cellular Neuroscience|November 2, 2020
Comparison of CRISPR/Cas Endonucleases for <i>in vivo</i> Retinal Gene EditingFan Li, Kristof Wing, Jiang-Hui Wang, et al.
Human Gene Therapy|August 3, 2019
Utility of Self-Destructing CRISPR/Cas Constructs for Targeted Gene Editing in the RetinaFan Li, Sandy S C Hung, Mohd Khairul Nizam Mohd Khalid, et al.
BMC Medical Genomics|July 25, 2018
Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritisElisabeth De Smit, Samuel W Lukowski, Lisa Anderson, et al.
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