Biochemical characterization of native Usher protein complexes from a vesicular subfraction of tracheal epithelial cells. - Wikidata - wikimedia - TriplyDB

Biochemical characterization of native Usher protein complexes from a vesicular subfraction of tracheal epithelial cells.

Biochemical characterization of native Usher protein complexes from a vesicular subfraction of tracheal epithelial cells.

http://www.wikidata.org/entity/Q33745351

about

Clarin-1 acts as a modulator of mechanotransduction activity and presynaptic ribbon assembly.Role for a novel Usher protein complex in hair cell synaptic maturation.Current understanding of usher syndrome type II.Regulated vesicular trafficking of specific PCDH15 and VLGR1 variants in auditory hair cells.The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically Usher protein functions in hair cells and photoreceptors.Impact of the Usher syndrome on olfaction.Accelerated age-related olfactory decline among type 1 Usher patients.

P2860

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P2860

Biochemical characterization of native Usher protein complexes from a vesicular subfraction of tracheal epithelial cells.

http://www.wikidata.org/entity/Q33745351

description

2010 nî lūn-bûn

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2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի փետրվարին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Biochemical characterization o ...... of tracheal epithelial cells.

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Biochemical characterization o ...... of tracheal epithelial cells.

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Biochemical characterization o ...... of tracheal epithelial cells.

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Biochemical characterization o ...... of tracheal epithelial cells.

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Dominic Cosgrove

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Joseph H Sisson

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Marisa Zallocchi

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P2860

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system

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

A domain-specific usherin/collagen IV interaction may be required for stable integration into the basement membrane superstructure

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

The unconventional myosin-VIIa associates with lysosomes

The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP

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1236-1247

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scholarly article

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10.1021/BI9020617

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6

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49

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20058854

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