Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.

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Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

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Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年學術文章

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name

Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.

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Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.

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Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.

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Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.

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Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.

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Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.

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P1476

Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III

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P2093

Akil Omar

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Astra Dinculescu

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Daniel H-C Chen

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David N Furness

http://www.w3.org/2001/XMLSchema#string

David Saperstein

http://www.w3.org/2001/XMLSchema#string

Kumar N Alagramam

http://www.w3.org/2001/XMLSchema#string

Lawrence R Lustig

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Martin L Basch

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Ruben Stepanyan

http://www.w3.org/2001/XMLSchema#string

Ruishuang Geng

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P2860

Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton

Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle.

Serial audiometry and speech recognition findings in Finnish Usher syndrome type III patients

Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3.

Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type III

CLRN1 is nonessential in the mouse retina but is required for cochlear hair cell development

Tetraspanin functions and associated microdomains

Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation

The role of Math1 in inner ear development: Uncoupling the establishment of the sensory primordium from hair cell fate determination

Interactions in the network of Usher syndrome type 1 proteins

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s41598-017-13620-9

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scholarly article

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10.1038/S41598-017-13620-9

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English

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Suhasini R Gopal

William W Hauswirth

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2017-10-18T00:00:00Z

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29044151

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Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.

about

P2860

P2860

Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.

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