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BMC Medical Genomics|October 18, 2024
Identification of a novel FGF3 variant and a new phenotype in three LAMM syndrome familiesQiang Du, Yike Zhang, Rujian Hong, 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 5, 2024
Bilateral gene therapy in children with autosomal recessive deafness 9: single-arm trial resultsHui Wang, Yuxin Chen, Jun Lv, et al.Nature Human Behaviour|May 2, 2025
Preliminary evidence for enhanced auditory cortex activation and mental development after gene therapy in children with autosomal recessive deafness 9Jiajia Zhang, Zengzhi Guo, Changjie Pan, et al.Nature Communications|August 5, 2025
PAM-flexible adenine base editing rescues hearing loss in a humanized MPZL2 mouse model harboring an East Asian founder mutationShao Wei Hu, Sohyang Jeong, Luoying Jiang, et al.The New England Journal of Medicine|January 21, 2016
Mutations in TUBB8 and Human Oocyte Meiotic ArrestRuizhi Feng, Qing Sang, Yanping Kuang, et al.JAMA Neurology|July 21, 2025
Gene Therapy vs Cochlear Implantation in Restoring Hearing Function and Speech Perception for Individuals With Congenital DeafnessXiaoting Cheng, Jiake Zhong, Jiajia Zhang, et al.Nature Cancer|November 14, 2024
Single-cell transcriptomic landscape deciphers olfactory neuroblastoma subtypes and intra-tumoral heterogeneityJingyi Yang, Xiaole Song, Huankang Zhang, et al.Nature|April 22, 2026
Multicentre gene therapy for OTOF-related deafness followed up to 2.5 yearsLuoying Jiang, Xiaoting Cheng, Jun Lv, et al.Med (New York, N.Y.)|October 24, 2025
International expert consensus on gene therapy for hereditary hearing loss: Based on clinical trialsXintai Fan, Ziwen Gao, Jiake Zhong, et al.Pageof 8