Prestin is the motor protein of cochlear outer hair cells - Wikidata - wikimedia - TriplyDB

Prestin is the motor protein of cochlear outer hair cells

Prestin is the motor protein of cochlear outer hair cells

http://www.wikidata.org/entity/Q28144919

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Expression pattern of oxidative stress and antioxidant defense-related genes in the aging Fischer 344/NHsd rat cochlea Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9 Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).SLC26A9 is expressed in gastric surface epithelial cells, mediates Cl-/HCO3- exchange, and is inhibited by NH4+Identification of a basolateral Cl-/HCO3- exchanger specific to gastric parietal cells Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domains Thyroid hormone is a critical determinant for the regulation of the cochlear motor protein prestin.Tension sensitivity of prestin: comparison with the membrane motor in outer hair cells Essential role of retinoblastoma protein in mammalian hair cell development and hearing.Evidence that prestin has at least two voltage-dependent steps.Review series: The cell biology of hearing Mechanical amplification by hair cells in the semicircular canals The ultrastructural distribution of prestin in outer hair cells: a post-embedding immunogold investigation of low-frequency and high-frequency regions of the rat cochlea.Prestin's anion transport and voltage-sensing capabilities are independent A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis Anion control of voltage sensing by the motor protein prestin in outer hair cells Essential helix interactions in the anion transporter domain of prestin revealed by evolutionary trace analysis Acute regulation of the SLC26A3 congenital chloride diarrhoea anion exchanger (DRA) expressed in Xenopus oocytes Prestin and the cochlear amplifier Regulation of electromotility in the cochlear outer hair cell Ca2+ current-driven nonlinear amplification by the mammalian cochlea in vitro.Assessment of potential effects of the electromagnetic fields of mobile phones on hearing A faster way to make GFP-based biosensors: two new transposons for creating multicolored libraries of fluorescent fusion proteins High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss.STAS domain structure and function Genetics of hearing and deafness Modeling auditory coding: from sound to spikes Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness.Consequences of Location-Dependent Organ of Corti Micro-Mechanics.Stemness of the organ of Corti relates to the epigenetic status of Sox2 enhancers Glutamate transporter homolog-based model predicts that anion-π interaction is the mechanism for the voltage-dependent response of prestin.Transcription Factors Expressed in Mouse Cochlear Inner and Outer Hair Cells Cytoarchitecture of the mouse organ of corti from base to apex, determined using in situ two-photon imaging Susceptibility of outer hair cells to cholesterol chelator 2-hydroxypropyl-β-cyclodextrine is prestin-dependent Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier SLC26A2 (diastrophic dysplasia sulfate transporter) is expressed in developing and mature cartilage but also in other tissues and cell types Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea N-linked glycosylation sites of the motor protein prestin: effects on membrane targeting and electrophysiological function Action of 2,3-butanedione monoxime on capacitance and electromotility of guinea-pig cochlear outer hair cells Salicylate toxicity model of tinnitus.

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Prestin is the motor protein of cochlear outer hair cells

http://www.wikidata.org/entity/Q28144919

description

2000 nî lūn-bûn

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2000 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի մայիսին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年论文

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name

Prestin is the motor protein of cochlear outer hair cells

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Prestin is the motor protein of cochlear outer hair cells

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Prestin is the motor protein of cochlear outer hair cells

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type

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Prestin is the motor protein of cochlear outer hair cells

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Prestin is the motor protein of cochlear outer hair cells

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Prestin is the motor protein of cochlear outer hair cells

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prefLabel

Prestin is the motor protein of cochlear outer hair cells

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Prestin is the motor protein of cochlear outer hair cells

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Prestin is the motor protein of cochlear outer hair cells

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Prestin is the motor protein of cochlear outer hair cells

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D Z He

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J Zheng

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K B Long

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L D Madison

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P Dallos

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An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

Charge movement associated with the opening and closing of the activation gates of the Na channels

Similarities between a soybean nodulin, Neurospora crassa sulphate permease II and a putative human tumour suppressor

Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries

Limiting dynamics of high-frequency electromechanical transduction of outer hair cells.

Motility voltage sensor of the outer hair cell resides within the lateral plasma membrane.

A membrane-based force generation mechanism in auditory sensory cells.

Force generation in the outer hair cell of the cochlea.

Mapping the distribution of the outer hair cell motility voltage sensor by electrical amputation.

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10.1038/35012009

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1011988004

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