Chunqiao Liu

A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma.

A Spatiotemporal Requirement for Prickle 1-Mediated PCP Signaling in Eyelid Morphogenesis and Homeostasis.

Ocular surface pathogenesis associated with precocious eyelid opening and necrotic autologous tissue in mouse with disruption of Prickle 1 gene.

D609 protects retinal pigmented epithelium as a potential therapy for age-related macular degeneration.

Malformation of Tear Ducts Underlies the Epiphora and Precocious Eyelid Opening in Prickle 1 Mutant Mice: Genetic Implications for Tear Duct Genesis.

Ontogenesis of the tear drainage system requires Prickle1-driven polarized basement membrane deposition.

Loss of FOXC1 contributes to the corneal epithelial fate switch and pathogenesis.

Low-dose PCB126 exposure disrupts cardiac metabolism and causes hypertrophy and fibrosis in mice.

dsRNA Induced IFNβ-MMP13 Axis Drives Corneal Wound Healing.

The mA reader YTHDF2 is a negative regulator for dendrite development and maintenance of retinal ganglion cells.

Comprehensive 3D epigenomic maps define limbal stem/progenitor cell function and identity.

Tmem138 is localized to the connecting cilium essential for rhodopsin localization and outer segment biogenesis.

Single-cell characterization of malignant phenotypes and microenvironment alteration in retinoblastoma.

IL-4 induces reparative phenotype of RPE cells and protects against retinal neurodegeneration via Nrf2 activation.

Single-Cell Characterization of the Frizzled 5 (Fz5) Mutant Mouse and Human Persistent Fetal Vasculature (PFV).