Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c
出版年份 2017 全文链接
标题
Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c
作者
关键词
-
出版物
NATURE BIOTECHNOLOGY
Volume 35, Issue 3, Pages 264-272
出版商
Springer Nature
发表日期
2017-02-07
DOI
10.1038/nbt.3801
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Gene Therapy Restores Hair Cell Stereocilia Morphology in Inner Ears of Deaf Whirler Mice
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- Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness
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- Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48
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- Targeting of the Hair Cell Proteins Cadherin 23, Harmonin, Myosin XVa, Espin, and Prestin in an Epithelial Cell Model
- (2010) L. Zheng et al. JOURNAL OF NEUROSCIENCE
- Tonotopic Gradient in the Developmental Acquisition of Sensory Transduction in Outer Hair Cells of the Mouse Cochlea
- (2009) Andrea Lelli et al. JOURNAL OF NEUROPHYSIOLOGY
- Harmonin Mutations Cause Mechanotransduction Defects in Cochlear Hair Cells
- (2009) Nicolas Grillet et al. NEURON
- Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells
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- A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth
- (2008) G. Lefevre et al. DEVELOPMENT
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