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Journal of Neurochemistry|December 15, 2018
Tmem30a deficiency leads to retinal rod bipolar cell degenerationYeming Yang, Wenjing Liu, Kuanxiang Sun, et al.Genetic Testing and Molecular Biomarkers|April 7, 2017
Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital GlaucomaYeming Yang, Lin Zhang, Shujin Li, et al.Journal of Cellular Physiology|May 9, 2022
Specific ablation of Hippo signalling component Yap1 in retinal progenitors and Müller cells results in late onset retinal degenerationYeming Yang, Xiaoyan Jiang, Xiao Li, et al.Biomed Research International|June 30, 2020
Disease Mutation Study Identifies Critical Residues for Phosphatidylserine Flippase ATP11AKuanxiang Sun, Wanli Tian, Xiao Li, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|April 25, 2021
The phosphatidylserine flippase β-subunit Tmem30a is essential for normal insulin maturation and secretionYeming Yang, Kuanxiang Sun, Wenjing Liu, et al.Molecular Medicine Reports|April 23, 2020
Identification of novel USH2A mutations in patients with autosomal recessive retinitis pigmentosa via targeted next‑generation sequencingXiong Zhu, Xiao Li, Wanli Tian, et al.Genetic Testing and Molecular Biomarkers|June 30, 2018
Targeted Next Generation Sequencing Revealed Novel PRPF31 Mutations in Autosomal Dominant Retinitis PigmentosaDan Xie, Kun Peng, Qian Yi, et al.Investigative Ophthalmology & Visual Science|December 27, 2024
Mettl3-Mediated m6A Modification is Essential for Visual Function and Retinal Photoreceptor SurvivalXiaoyan Jiang, Kuanxiang Sun, Yudi Fan, et al.Journal of Genetics and Genomics = Yi Chuan Xue Bao|March 19, 2022
Loss of Wtap results in cerebellar ataxia and degeneration of Purkinje cellsYeming Yang, Guo Huang, Xiaoyan Jiang, et al.Journal of Cell Science|February 11, 2022
LMBR1L regulates the proliferation and migration of endothelial cells through Norrin/β-catenin signalingWenjing Liu, Xiaoyan Jiang, Xiao Li, et al.Pageof 5