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Science Advances|January 22, 2025
WWC proteins-mediated compensatory mechanism restricts schwannomatosis driven by <i>NF2</i> loss of functionXueying Wang, Rui Zhu, Pengcheng Yu, et al.Molecular Therapy. Nucleic Acids|August 29, 2022
Precise detection of CRISPR-Cas9 editing in hair cells in the treatment of autosomal dominant hearing lossChong Cui, Daqi Wang, Bowei Huang, et al.Journal of Genetics and Genomics = Yi Chuan Xue Bao|February 14, 2026
Natural history and phenotype-genotype correlations in GJB2-related hearing loss: a systematic and comprehensive reviewLiheng Chen, Cheng Wen, Weitao Li, et al.Molecular Genetics and Genomics : MGG|August 31, 2025
Prevalence and spectrum of STRC variants in 1015 sensorineural hearing loss patients: insights from the Chinese populationLuo Guo, Sha Yu, Wenrui Zhao, et al.Biorxiv : the Preprint Server for Biology|November 14, 2023
Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutationWenliang Zhu, Wan Du, Arun Prabhu Rameshbabu, et al.Science Translational Medicine|July 10, 2024
Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutationWenliang Zhu, Wan Du, Arun Prabhu Rameshbabu, et al.Nature Communications|December 5, 2019
Renewed proliferation in adult mouse cochlea and regeneration of hair cellsYilai Shu, Wenyan Li, Mingqian Huang, et al.Molecular Therapy. Nucleic Acids|February 26, 2024
Hair cell-specific Myo15 promoter-mediated gene therapy rescues hearing in DFNB9 mouse modelHui Wang, MengZhao Xun, Honghai Tang, et al.Nature Biotechnology|October 31, 2014
Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing in vitro and in vivoJohn A Zuris, David B Thompson, Yilai Shu, et al.Science Translational Medicine|July 20, 2022
Rescue of autosomal dominant hearing loss by in vivo delivery of mini dCas13X-derived RNA base editorQingquan Xiao, Zhijiao Xu, Yuanyuan Xue, et al.Pageof 13