Houbin Zhang

Mistrafficking of prenylated proteins causes retinitis pigmentosa 2.

Retinitis Pigmentosa: Disease Mechanisms, Diagnosis, and Therapies.

Whole-exome Sequencing Analysis Identifies Mutations in the EYS Gene in Retinitis Pigmentosa in the Indian Population.

Arf-like Protein 3 (ARL3) Regulates Protein Trafficking and Ciliogenesis in Mouse Photoreceptors.

Associations of 6p21.3 Region with Age-related Macular Degeneration and Polypoidal Choroidal Vasculopathy.

A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy.

A novel deletion downstream of the PAX6 gene identified in a Chinese family with congenital aniridia.

Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis.

Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa.

Identification of a novel homozygous variant in the CNGA1 gene in a Chinese family with autosomal recessive retinitis pigmentosa.

An improved method for preparation of mouse retinal cryosections.

A novel missense variant in cathepsin C gene leads to PLS in a Chinese patient: A case report and literature review.

Inhibition of mTOR signaling by rapamycin protects photoreceptors from degeneration in mice.

A quick protocol for the preparation of mouse retinal cryosections for immunohistochemistry.

Exogenous PDE5 Expression Rescues Photoreceptors in Mice.

Identification of a novel compound heterozygous variant in a patient with autosomal recessive retinitis pigmentosa.

Characterization of two novel knock-in mouse models of syndromic retinal ciliopathy carrying hypomorphic mutations.

Cholesterol homeostasis regulated by ABCA1 is critical for retinal ganglion cell survival.

Automatic counting of retinal ganglion cells in the entire mouse retina based on improved YOLOv5.

Improved methods for isolating the mouse retinal vasculature.

Deep Sc-RNA sequencing decoding the molecular dynamic architecture of the human retina.

Rhodopsin-associated retinal dystrophy: Disease mechanisms and therapeutic strategies.

Leukemia Inhibitory Factor Protects against Degeneration of Cone Photoreceptors Caused by RPE65 Deficiency.

Association of variants in GJA8 with familial acorea-microphthalmia-cataract syndrome.

A new mouse-fixation device for IOP measurement in awake mice.

Erratum to: Cholesterol homeostasis regulated by ABCA1 is critical for retinal ganglion cell survival.

Exome Sequencing Identified a Recessive RDH12 Mutation in a Family with Severe Early-Onset Retinitis Pigmentosa.

Binary Function of ARL3-GTP Revealed by Gene Knockouts.