Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning
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Integrating the biophysical and molecular mechanisms of auditory hair cell mechanotransductionTargeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeletonDevelopment and regeneration of sensory transduction in auditory hair cells requires functional interaction between cadherin-23 and protocadherin-15.Review series: The cell biology of hearingCadherins and mechanotransduction by hair cellsGenetics of Nonsyndromic Congenital Hearing LossClass III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth.Conserved expression of vertebrate microvillar gene homologs in choanocytes of freshwater sponges.Harmonin (Ush1c) is required in zebrafish Müller glial cells for photoreceptor synaptic development and functionInternational Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptorsSticky signaling--adhesion class G protein-coupled receptors take the stageDeletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in mice.Hair bundle defects and loss of function in the vestibular end organs of mice lacking the receptor-like inositol lipid phosphatase PTPRQStereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane.A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cellsLocalization and expression of clarin-1, the Clrn1 gene product, in auditory hair cells and photoreceptorsDiversity of the Genes Implicated in Algerian Patients Affected by Usher SyndromeAlternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia.Whirlin and PDZ domain-containing 7 (PDZD7) proteins are both required to form the quaternary protein complex associated with Usher syndrome type 2Very large G protein-coupled receptor 1 regulates myelin-associated glycoprotein via Gαs/Gαq-mediated protein kinases A/C.Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish.Murine Fam65b forms ring-like structures at the base of stereocilia critical for mechanosensory hair cell function.Gene Therapy Restores Hair Cell Stereocilia Morphology in Inner Ears of Deaf Whirler Mice.A study of whirlin isoforms in the mouse vestibular system suggests potential vestibular dysfunction in DFNB31-deficient patientsUsher syndrome: Hearing loss, retinal degeneration and associated abnormalities.The physiology of mechanoelectrical transduction channels in hearing.USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptoms.TMC function in hair cell transductionGenetics of auditory mechano-electrical transduction.Sensory transduction and adaptation in inner and outer hair cells of the mouse auditory system.Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells.Linking genes underlying deafness to hair-bundle development and function.MicroRNAs in hair cell development and deafness.Function and expression pattern of nonsyndromic deafness genesInheritance patterns of progressive hearing loss in laboratory strains of miceMyosin VIIA, important for human auditory function, is necessary for Drosophila auditory organ development.Control of exocytosis by synaptotagmins and otoferlin in auditory hair cells.Subunit determination of the conductance of hair-cell mechanotransducer channelsDistinct expression and function of whirlin isoforms in the inner ear and retina: an insight into pathogenesis of USH2D and DFNB31.
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P2860
Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning
description
2007 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հունիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2007
@ast
im Juni 2007 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2007/06/13)
@sk
vědecký článek publikovaný v roce 2007
@cs
wetenschappelijk artikel (gepubliceerd op 2007/06/13)
@nl
наукова стаття, опублікована в червні 2007
@uk
مقالة علمية (نشرت في 13-6-2007)
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name
Molecular characterization of ...... in the hair bundle functioning
@ast
Molecular characterization of ...... in the hair bundle functioning
@en
Molecular characterization of ...... in the hair bundle functioning
@nl
type
label
Molecular characterization of ...... in the hair bundle functioning
@ast
Molecular characterization of ...... in the hair bundle functioning
@en
Molecular characterization of ...... in the hair bundle functioning
@nl
prefLabel
Molecular characterization of ...... in the hair bundle functioning
@ast
Molecular characterization of ...... in the hair bundle functioning
@en
Molecular characterization of ...... in the hair bundle functioning
@nl
P2093
P50
P921
P3181
P1476
Molecular characterization of ...... in the hair bundle functioning
@en
P2093
Dominique Weil
Gaëlle Lefèvre
Jean-Pierre Hardelin
Makoto Sato
Pascal Martin
Sébastien Chardenoux
Vincent Michel
P304
P3181
P356
10.1523/JNEUROSCI.0342-07.2007
P407
P577
2007-06-01T00:00:00Z