A small molecule mitigates hearing loss in a mouse model of Usher syndrome III

Usher syndrome type III (USH3) characterized by progressive deafness, variable balance disorder, and blindness is caused by destabilizing mutations in the gene encoding the clarin-1 protein (CLRN1). Here we report a novel strategy to mitigate hearing loss associated with a common USH3 mutation CLRN1...

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Publicado no:Nat Chem Biol
Main Authors: Alagramam, Kumar N., Gopal, Suhasini R., Geng, Ruishuang, Chen, Daniel H.-C., Nemet, Ina, Lee, Richard, Tian, Guilian, Miyagi, Masaru, Malagu, Karine F., Lock, Christopher J., Esmieu, William R. K., Owens, Andrew P., Lindsay, Nicola A., Ouwehand, Krista, Albertus, Faywell, Fischer, David F., Bürli, Roland W., MacLeod, Angus M., Harte, William E., Palczewski, Krzysztof, Imanishi, Yoshikazu
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4871731/
https://ncbi.nlm.nih.gov/pubmed/27110679
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nchembio.2069
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