L. Xie

Clinical and genetic features of a dominantly-inherited microphthalmia pedigree from China

K. Xia, Zhengmao Hu, Changhong Yu, 2009, Molecular vision.

An R124C mutation in TGFBI caused lattice corneal dystrophy type I with a variable phenotype in three Chinese families

Lixin Xie, Zhe Liu, Yi-qiang Wang, 2008, Molecular vision.

MicroRNA-30a Regulation of Epithelial-Mesenchymal Transition in Diabetic Cataracts Through Targeting SNAI1

P. Tsonis, Ye Wang, Yusen Huang, 2017, Scientific Reports.

Hyperglycemia induces tear reduction and dry eye in diabetic mice through the norepinephrine-α1AR -mitochondrial impairment axis of lacrimal gland.

Qingjun Zhou, Xiaofei Bai, Mingli Qu, 2023, The American journal of pathology.

A novel locus for congenital simple microphthalmia family mapping to 17p12-q12.

K. Xia, Q. Pan, W. Su, 2011, Investigative ophthalmology & visual science.

Effect of TRPM8 Functional Loss on Corneal Epithelial Wound Healing in Mice

Qingjun Zhou, Ting Liu, X. Qi, 2023, Investigative ophthalmology & visual science.

A Novel CRYGD Mutation (p.Trp43Arg) Causing Autosomal Dominant Congenital Cataract in a Chinese Family

Binbin Wang, Jing Wang, Sirui Zhou, 2011, Human mutation.

ECM‐Like Adhesive Hydrogel for the Regeneration of Large Corneal Stromal Defects

Wei Zhang, Lizhi Hu, W. Shi, 2023, Advanced healthcare materials.