Xiufeng Zhong

This study demonstrates that gene therapy using AAV vectors can rescue retinal degeneration in PROM1-IRD patient and mouse models by restoring PROM1 expression and photoreceptor structure.

This study identifies ATOH7+ nascent cone precursors as the earliest cell-of-origin for human retinoblastoma using RB1-deficient retinal organoids and scRNA-seq.

This study identifies EVs from human retinal organoids and shows they regulate gene expression in retinal progenitors through miRNA cargo.