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Proceedings of the National Academy of Sciences of the United States of America|January 25, 2013
Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noiseDenise Yan, Yan Zhu, Tom Walsh, 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.American Journal of Human Genetics|May 11, 2010
A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing lossAsli Sirmaci, Seyra Erbek, Justin Price, et al.Human Genetics|November 3, 2017
Creation of miniature pig model of human Waardenburg syndrome type 2A by ENU mutagenesisTang Hai, Weiwei Guo, Jing Yao, 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.American Journal of Human Genetics|November 6, 2012
Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing lossKemal O Yariz, Duygu Duman, Celia Zazo Seco, 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|April 22, 2026
Multicentre gene therapy for OTOF-related deafness followed up to 2.5 yearsLuoying Jiang, Xiaoting Cheng, Jun Lv, et al.The New England Journal of Medicine|February 29, 2020
Clinical Characteristics of Coronavirus Disease 2019 in ChinaWei-Jie Guan, Zheng-Yi Ni, Yu Hu, et al.Pageof 52