The micromachinery of mechanotransduction in hair cells. - Test2 - elhamkhani - TriplyDB

The micromachinery of mechanotransduction in hair cells.

The micromachinery of mechanotransduction in hair cells.

http://www.wikidata.org/entity/Q30481576

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Functional auditory hair cells produced in the mammalian cochlea by in utero gene transfer.Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes.Cadherins and mechanotransduction by hair cells Touch sense: functional organization and molecular determinants of mechanosensitive receptors ASICs and cardiovascular homeostasis Structures of usher syndrome 1 proteins and their complexes The Stereociliary Paracrystal Is a Dynamic Cytoskeletal Scaffold In Vivo Ankyrin Repeats Convey Force to Gate the NOMPC Mechanotransduction Channel Mechanical overstimulation of hair bundles: suppression and recovery of active motility Structural determinants of cadherin-23 function in hearing and deafness In Vitro Bone Cell Models: Impact of Fluid Shear Stress on Bone Formation Differential Contribution of TRPA1, TRPV4 and TRPM8 to Colonic Nociception in Mice Cyclic 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 mechanotransduction Mechanotransduction as an Adaptation to Gravity.ATP8B1 is essential for maintaining normal hearing High-order synchronization of hair cell bundles.From Biological Cilia to Artificial Flow Sensors: Biomimetic Soft Polymer Nanosensors with High Sensing Performance Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.The physiology of mechanoelectrical transduction channels in hearing.Tumor Necrosis Factor-α-Induced Ototoxicity in Mouse Cochlear Organotypic Culture.Identification of a gene set to evaluate the potential effects of loud sounds from seismic surveys on the ears of fishes: a study with Salmo salar.Disruption of intracellular calcium regulation is integral to aminoglycoside-induced hair cell death Time course of dynamic range adaptation in the auditory nerve.A mutation in the cdh23 gene causes age-related hearing loss in Cdh23(nmf308/nmf308) mice The stat3/socs3a pathway is a key regulator of hair cell regeneration in zebrafish. [corrected].Molecular biology of hearing.Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia.Coupling and elastic loading affect the active response by the inner ear hair cell bundles.Roles of the espin actin-bundling proteins in the morphogenesis and stabilization of hair cell stereocilia revealed in CBA/CaJ congenic jerker mice.The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in mice.Interactions between hair cells shape spontaneous otoacoustic emissions in a model of the tokay gecko's cochlea.Distribution of frequencies of spontaneous oscillations in hair cells of the bullfrog sacculus.Harmonin mutations cause mechanotransduction defects in cochlear hair cells.PR65, the HEAT-repeat scaffold of phosphatase PP2A, is an elastic connector that links force and catalysis Ion-dependent polymerization differences between mammalian beta- and gamma-nonmuscle actin isoforms A doublecortin containing microtubule-associated protein is implicated in mechanotransduction in Drosophila sensory cilia.Tissue engineering the mechanosensory circuit of the stretch reflex arc: sensory neuron innervation of intrafusal muscle fibers.Mode-locking dynamics of hair cells of the inner ear Characterization and regulation of an additional actin-filament-binding site in large isoforms of the stereocilia actin-bundling protein espin Interaction with phosphoinositides confers adaptation onto the TRPV1 pain receptor.

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The micromachinery of mechanotransduction in hair cells.

http://www.wikidata.org/entity/Q30481576

description

2007 nî lūn-bûn

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2007 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2007 թվականի հունվարին հրատարակված գիտական հոդված

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2007年の論文

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年學術文章

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The micromachinery of mechanotransduction in hair cells.

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The micromachinery of mechanotransduction in hair cells.

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The micromachinery of mechanotransduction in hair cells.

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The micromachinery of mechanotransduction in hair cells.

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The micromachinery of mechanotransduction in hair cells.

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The micromachinery of mechanotransduction in hair cells.

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ANNUREV.NEURO.29.051605.112917

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Annual Review of Neuroscience

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The micromachinery of mechanotransduction in hair cells.

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David P Corey

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Kelvin Y Kwan

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Melissa A Vollrath

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P2860

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells

Identification and overlapping expression of multiple unconventional myosin genes in vertebrate cell types

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.

A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice

Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice.

Vanilloid receptor-related osmotically activated channel (VR-OAC), a candidate vertebrate osmoreceptor

Regeneration of broken tip links and restoration of mechanical transduction in hair cells.

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Mechanotransduction

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