Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle.
about
Proteomic analysis of the enterocyte brush borderA functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafnessIntestinal brush border assembly driven by protocadherin-based intermicrovillar adhesion.A new role for the architecture of microvillar actin bundles in apical retention of membrane proteinsFERM domain-containing unconventional myosin VIIA interacts with integrin β5 subunit and regulates αvβ5-mediated cell adhesion and migrationThe DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type IIConsortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexinsDigenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humansClarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeletonIdentification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type IIReview series: The cell biology of hearingAutosomal recessive nonsyndromic deafness genes: a reviewUsher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapyCadherins and mechanotransduction by hair cellsUncovering quantitative protein interaction networks for mouse PDZ domains using protein microarraysUsherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cellsAn actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewalThe dynamic architecture of photoreceptor ribbon synapses: cytoskeletal, extracellular matrix, and intramembrane proteinsSensing sound: molecules that orchestrate mechanotransduction by hair cellsMyosins in cell junctionsStructures of usher syndrome 1 proteins and their complexesClass III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth.The Stereociliary Paracrystal Is a Dynamic Cytoskeletal Scaffold In VivoAssembling stable hair cell tip link complex via multidentate interactions between harmonin and cadherin 23The structure of the harmonin/sans complex reveals an unexpected interaction mode of the two Usher syndrome proteinsStructure of MyTH4-FERM domains in myosin VIIa tail bound to cargoCargo recognition mechanism of myosin X revealed by the structure of its tail MyTH4-FERM tandem in complex with the DCC P3 domainA mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene.Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activationLocalization and expression of clarin-1, the Clrn1 gene product, in auditory hair cells and photoreceptorsHarp (harmonin-interacting, ankyrin repeat-containing protein), a novel protein that interacts with harmonin in epithelial tissuesMyosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransductionCyclic nucleotide-gated channel α-3 (CNGA3) interacts with stereocilia tip-link cadherin 23 + exon 68 or alternatively with myosin VIIa, two proteins required for hair cell mechanotransductionPostnatal developmental expression of the PDZ scaffolds Na+ -H+ exchanger regulatory factors 1 and 2 in the rat cochleaMyosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directlyPhysical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cellsInteractions in the network of Usher syndrome type 1 proteinsRole of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes
P2860
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P248
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P2860
Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle.
description
2002 nî lūn-bûn
@nan
2002 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Myosin VIIa, harmonin and cadh ...... e the sensory hair cell bundle
@nl
Myosin VIIa, harmonin and cadh ...... the sensory hair cell bundle.
@ast
Myosin VIIa, harmonin and cadh ...... the sensory hair cell bundle.
@en
Myosin VIIa, harmonin and cadh ...... the sensory hair cell bundle.
@en-gb
type
label
Myosin VIIa, harmonin and cadh ...... e the sensory hair cell bundle
@nl
Myosin VIIa, harmonin and cadh ...... the sensory hair cell bundle.
@ast
Myosin VIIa, harmonin and cadh ...... the sensory hair cell bundle.
@en
Myosin VIIa, harmonin and cadh ...... the sensory hair cell bundle.
@en-gb
prefLabel
Myosin VIIa, harmonin and cadh ...... e the sensory hair cell bundle
@nl
Myosin VIIa, harmonin and cadh ...... the sensory hair cell bundle.
@ast
Myosin VIIa, harmonin and cadh ...... the sensory hair cell bundle.
@en
Myosin VIIa, harmonin and cadh ...... the sensory hair cell bundle.
@en-gb
P2093
P2860
P50
P921
P3181
P356
P1433
P1476
Myosin VIIa, harmonin and cadh ...... the sensory hair cell bundle.
@en
P2093
Anne Houdusse
Batiste Boëda
Guy Richardson
Isabelle Perfettini
Jan Reiners
Laurent Daviet
Pierre Legrain
Richard Goodyear
Stéphane Blanchard
Uwe Wolfrum
P2860
P304
P3181
P356
10.1093/EMBOJ/CDF689
P407
P50
P577
2002-12-01T00:00:00Z