Structures of usher syndrome 1 proteins and their complexes - Test2 - elhamkhani - TriplyDB

Structures of usher syndrome 1 proteins and their complexes

Structures of usher syndrome 1 proteins and their complexes

http://www.wikidata.org/entity/Q27023615

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Intestinal brush border assembly driven by protocadherin-based intermicrovillar adhesion.ANKS4B Is Essential for Intermicrovillar Adhesion Complex Formation Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.Compound heterozygosity of the functionally null Cdh23(v-ngt) and hypomorphic Cdh23(ahl) alleles leads to early-onset progressive hearing loss in mice.Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice.Localization of PDZD7 to the stereocilia ankle-link associates this scaffolding protein with the Usher syndrome protein network Structures and target recognition modes of PDZ domains: recurring themes and emerging pictures.Structural Basis of Cargo Recognition by Unconventional Myosins in Cellular Trafficking.Hearing lessons from flies.Myosin-7b Promotes Distal Tip Localization of the Intermicrovillar Adhesion Complex.Structure of Myo7b/USH1C complex suggests a general PDZ domain binding mode by MyTH4-FERM myosins.Targeted next generation sequencing in Italian patients with Usher syndrome: phenotype-genotype correlations.Beyond Cell-Cell Adhesion: Sensational Cadherins for Hearing and Balance.Usher's Syndrome Type II: A Comparative Study of Genetic Mutations and Vestibular System Evaluation.Proteostasis: Chaperoning for hearing loss.Using Drosophila to study mechanisms of hereditary hearing loss.Structure and function of the guanylate kinase-like domain of the MAGUK family scaffold proteins

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Structures of usher syndrome 1 proteins and their complexes

http://www.wikidata.org/entity/Q27023615

description

2012 nî lūn-bûn

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2012 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2012 թվականի փետրվարին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Structures of usher syndrome 1 proteins and their complexes

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Structures of usher syndrome 1 proteins and their complexes

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Structures of usher syndrome 1 proteins and their complexes

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Structures of usher syndrome 1 proteins and their complexes

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Structures of usher syndrome 1 proteins and their complexes

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Structures of usher syndrome 1 proteins and their complexes

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Structures of usher syndrome 1 proteins and their complexes

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Structures of usher syndrome 1 proteins and their complexes

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Structures of usher syndrome 1 proteins and their complexes

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Structures of usher syndrome 1 proteins and their complexes

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L. Pan

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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

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

PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

Structural basis of cargo recognition by the myosin-X MyTH4-FERM domain

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II

Defective myosin VIIA gene responsible for Usher syndrome type 1B

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

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25-42

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scholarly article

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10.1152/PHYSIOL.00037.2011

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