Template-independent genome editing in the Pcdh15 mouse, a model of human DFNB23 nonsyndromic deafness-Reference-Cited by-同舟云学术

Template-independent genome editing in the Pcdh15 mouse, a model of human DFNB23 nonsyndromic deafness

Published:2022-07 Issue:2 Volume:40 Page:111061
ISSN:2211-1247
Container-title:Cell Reports
language:en
Short-container-title:Cell Reports

Author:

Liu Lian,Zou Linzhi,Li Kuan,Hou Hanqing,Hu Qun,Liu Shuang,Li Jie,Song Chenmeng,Chen Jiaofeng,Wang Shufeng,Wang Yangzhen,Li Changri,Du Haibo,Li Jun-Liszt^ORCID,Chen Fangyi,Xu Zhigang,Sun Wenzhi,Sun Qianwen,Xiong Wei^ORCID

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference52 articles.

1. The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15;Ahmed;J. Neurosci.,2006

2. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23;Ahmed;Hum. Mol. Genet.,2003

3. Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model;Akil;Proc. Natl. Acad. Sci. USA,2019

4. Restoration of hearing in the VGLUT3 knockout mouse using virally mediated gene therapy;Akil;Neuron,2012

5. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene;Alagramam;Nat. Genet.,2001

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