Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

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Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

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wetenschappelijk artikel

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наукова стаття, опублікована у 2018

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Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

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Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

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Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

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Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

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Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

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Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

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P1476

Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

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P2093

J Beth Kempton

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John V Brigande

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Lingyan Wang

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P2860

Notch signalling pathway mediates hair cell development in mammalian cochlea

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

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

TMC1 and TMC2 are components of the mechanotransduction channel in hair cells of the mammalian inner ear

The lncRNA Malat1 is dispensable for mouse development but its transcription plays a cis-regulatory role in the adult

Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes.

Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice.

Methionine oxidation and reduction in proteins

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300

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P31

scholarly article

P356

10.3389/FNMOL.2018.00300

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English

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P577

2018-01-01T00:00:00Z

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30210291

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P921

molecular biology

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6123355

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