Identification of the hair cell soma-1 antigen, HCS-1, as otoferlin. - Wikidata - wikimedia - TriplyDB

Identification of the hair cell soma-1 antigen, HCS-1, as otoferlin.

Identification of the hair cell soma-1 antigen, HCS-1, as otoferlin.

http://www.wikidata.org/entity/Q30434073

about

Catecholaminergic connectivity to the inner ear, central auditory, and vocal motor circuitry in the plainfin midshipman fish porichthys notatus.Otoferlin deficiency in zebrafish results in defects in balance and hearing: rescue of the balance and hearing phenotype with full-length and truncated forms of mouse otoferlin.Expression and Misexpression of the miR-183 Family in the Developing Hearing Organ of the Chicken.A simple method for purification of vestibular hair cells and non-sensory cells, and application for proteomic analysis.Balancing cell numbers during organogenesis: Six1a differentially affects neurons and sensory hair cells in the inner ear.Developmental acquisition of a rapid calcium-regulated vesicle supply allows sustained high rates of exocytosis in auditory hair cells.Epigenetic influences on sensory regeneration: histone deacetylases regulate supporting cell proliferation in the avian utricle.Supporting cells eliminate dying sensory hair cells to maintain epithelial integrity in the avian inner ear.Cisplatin ototoxicity blocks sensory regeneration in the avian inner ear A prestin motor in chicken auditory hair cells: active force generation in a nonmammalian species Expression of the Pax2 transcription factor is associated with vestibular phenotype in the avian inner ear Exocytosis in the frog amphibian papilla.Numb is not a critical regulator of Notch-mediated cell fate decisions in the developing chick inner ear.The SNARE complex in neuronal and sensory cells.Activation of canonical Wnt/β-catenin signaling stimulates proliferation in neuromasts in the zebrafish posterior lateral line.Artificial induction of Sox21 regulates sensory cell formation in the embryonic chicken inner ear Ribbon synapses in zebrafish hair cells.Pseudo-immortalization of postnatal cochlear progenitor cells yields a scalable cell line capable of transcriptionally regulating mature hair cell genes.Zebrafish crypt neurons project to a single, identified mediodorsal glomerulus.Two cell populations participate in clearance of damaged hair cells from the sensory epithelia of the inner ear.Activity-Dependent Phosphorylation by CaMKIIδ Alters the Ca2+ Affinity of the Multi-C2-Domain Protein Otoferlin.Molecular cloning and functional characterisation of chicken Atonal homologue 1: a comparison with human Atoh1.Tryptophan-rich basic protein (WRB) mediates insertion of the tail-anchored protein otoferlin and is required for hair cell exocytosis and hearing.Delayed Otolith Development Does Not Impair Vestibular Circuit Formation in Zebrafish.Wnt9a Can Influence Cell Fates and Neural Connectivity across the Radial Axis of the Developing Cochlea.Transmission Disrupted: Modeling Auditory Synaptopathy in Zebrafish Ectopic otoconial formation in the lagena of the pigeon inner ear

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P2860

Identification of the hair cell soma-1 antigen, HCS-1, as otoferlin.

http://www.wikidata.org/entity/Q30434073

description

2010 nî lūn-bûn

@nan

2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Identification of the hair cell soma-1 antigen, HCS-1, as otoferlin.

@ast

Identification of the hair cell soma-1 antigen, HCS-1, as otoferlin.

@en

type

label

Identification of the hair cell soma-1 antigen, HCS-1, as otoferlin.

@ast

Identification of the hair cell soma-1 antigen, HCS-1, as otoferlin.

@en

prefLabel

Identification of the hair cell soma-1 antigen, HCS-1, as otoferlin.

@ast

Identification of the hair cell soma-1 antigen, HCS-1, as otoferlin.

@en

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P1476

Identification of the hair cell soma-1 antigen, HCS-1, as otoferlin

@en

P2093

Bei Xia

http://www.w3.org/2001/XMLSchema#string

Guy P Richardson

http://www.w3.org/2001/XMLSchema#string

Jeffrey R Christiansen

http://www.w3.org/2001/XMLSchema#string

Jeffrey T Corwin

http://www.w3.org/2001/XMLSchema#string

Julia Korchagina

http://www.w3.org/2001/XMLSchema#string

Mark E Warchol

http://www.w3.org/2001/XMLSchema#string

P Kevin Legan

http://www.w3.org/2001/XMLSchema#string

Richard J Goodyear

http://www.w3.org/2001/XMLSchema#string

P2860

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene

Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss.

RIBEYE, a component of synaptic ribbons: a protein's journey through evolution provides insight into synaptic ribbon function

Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness

Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse

How the ear's works work

A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function

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573-586

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Jonathan E Gale

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2010-08-31T00:00:00Z

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46109108

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