Lue Xiang

AAV-mediated lysophosphatidylcholine acyltransferase 1 (Lpcat1) gene replacement therapy rescues retinal degeneration in rd11 mice.

SLC7A14 linked to autosomal recessive retinitis pigmentosa.

A novel Bruch's membrane-mimetic electrospun substrate scaffold for human retinal pigment epithelium cells.

A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal Degeneration.

Toll-Like Receptor 3 Activation Initiates Photoreceptor Cell Death In Vivo and In Vitro.

Targeted RP9 ablation and mutagenesis in mouse photoreceptor cells by CRISPR-Cas9.

Trio-based exome sequencing arrests de novo mutations in early-onset high myopia.

miR-183/96 plays a pivotal regulatory role in mouse photoreceptor maturation and maintenance.

Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.

Versatile Genome Engineering Techniques Advance Human Ocular Disease Researches in Zebrafish.

Deletion of miR-182 Leads to Retinal Dysfunction in Mice.

Whole-exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndrome.

Functional characterization of CEP250 variant identified in nonsyndromic retinitis pigmentosa.

Targeting neuronal and glial cell types with synthetic promoter AAVs in mice, non-human primates and humans.

The Circular RNome of Developmental Retina in Mice.

Is Indispensable in Zebrafish Retinas.

Ablation of Mature miR-183 Leads to Retinal Dysfunction in Mice.

MLL5 is involved in retinal photoreceptor maturation through facilitating CRX-mediated photoreceptor gene transactivation.

Depletion of miR-96 Delays, But Does Not Arrest, Photoreceptor Development in Mice.