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Molecular Therapy. Methods & Clinical Development|September 2, 2025
Erratum: Preclinical evaluation of the efficacy and safety of AAV1-hOTOF in mice and nonhuman primatesLonglong Zhang, Hui Wang, Mengzhao Xun, et al.Cellular and Molecular Life Sciences : CMLS|May 13, 2023
The pathogenesis of common Gjb2 mutations associated with human hereditary deafness in miceQing Li, Chong Cui, Rongyu Liao, et al.Research (Washington, D.C.)|April 26, 2024
Engineering of the AAV-Compatible Hair Cell-Specific Small-Size Myo15 Promoter for Gene Therapy in the Inner EarShao Wei Hu, Jun Lv, Zijing Wang, et al.Signal Transduction and Targeted Therapy|March 14, 2022
Preventing autosomal-dominant hearing loss in Bth mice with CRISPR/CasRx-based RNA editingZiwen Zheng, Guo Li, Chong Cui, et al.Nature Biomedical Engineering|August 12, 2024
A base editor for the long-term restoration of auditory function in mice with recessive profound deafnessChong Cui, Shengyi Wang, Daqi Wang, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|June 26, 2021
Gene editing in a Myo6 semi-dominant mouse model rescues auditory functionYuanyuan Xue, Xinde Hu, Daqi Wang, et al.Trends in Molecular Medicine|September 4, 2025
Clinical gene therapy restores hearing: a paradigm shiftShuang Han, Ziting Chen, Daqi Wang, et al.Lancet (London, England)|January 27, 2024
AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trialJun Lv, Hui Wang, Xiaoting Cheng, et al.Nature Medicine|June 26, 2026
Re-administration of AAV-mediated gene therapy for OTOF-related deafness: a single-arm trialXintai Fan, Longlong Zhang, Ziwen Gao, et al.Nature Medicine|June 5, 2024
Bilateral gene therapy in children with autosomal recessive deafness 9: single-arm trial resultsHui Wang, Yuxin Chen, Jun Lv, et al.Pageof 13