Gene editing in a Myo6 semi-dominant mouse model rescues auditory function-Reference-Cited by-同舟云学术

Gene editing in a Myo6 semi-dominant mouse model rescues auditory function

Published:2022-01 Issue:1 Volume:30 Page:105-118
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Xue Yuanyuan,Hu Xinde,Wang Daqi,Li Di,Li Yige,Wang Fang,Huang Mingqian,Gu Xi,Xu Zhijiao,Zhou Jinan,Wang Jinghan,Chai Renjie,Shen Jun,Chen Zheng-Yi,Li Geng-Lin,Yang Hui,Li Huawei,Zuo Erwei,Shu Yilai

Funder

National Key Research and Development Program of China

Central Public-interest Scientific Institution Basal Research Fund, Chinese Academy of Fishery Sciences

National Institutes of Health

National Key Research and Development Program of China Stem Cell and Translational Research

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Science and Technology Commission of Shanghai Municipality

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

Reference54 articles.

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2. Long single α-helical tail domains bridge the gap between structure and function of myosin VI;Spink;Nat. Struct. Mol. Biol.,2008

3. Mutations of MYO6 are associated with recessive deafness, DFNB37;Ahmed;Am. J. Hum. Genet.,2003

4. Unconventional myosins in inner-ear sensory epithelia;Hasson;J. Cell Biol.,1997

5. MYO6, the human homologue of the gene responsible for deafness in Snell’s waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss;Melchionda;Am. J. Hum. Genet.,2001

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