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A quantitative survey of gravity receptor function in mutant mouse strains.

A quantitative survey of gravity receptor function in mutant mouse strains.

http://www.wikidata.org/entity/Q30492589

about

Stereocilia-staircase spacing is influenced by myosin III motors and their cargos espin-1 and espin-like.Annexin A5 is the Most Abundant Membrane-Associated Protein in Stereocilia but is Dispensable for Hair-Bundle Development and Function Application of Mouse Models to Research in Hearing and Balance Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation Jxc1/Sobp, encoding a nuclear zinc finger protein, is critical for cochlear growth, cell fate, and patterning of the organ of corti Plastin 1 widens stereocilia by transforming actin filament packing from hexagonal to liquid.Genetics of peripheral vestibular dysfunction: lessons from mutant mouse strains.The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction.The adequate stimulus for mammalian linear vestibular evoked potentials (VsEPs).Gravity receptor aging in the CBA/CaJ strain: a comparison to auditory aging.A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9 Otoconin-90 deletion leads to imbalance but normal hearing: a comparison with other otoconia mutants A comparison of vestibular and auditory phenotypes in inbred mouse strains.Preserved otolith organ function in caspase-3-deficient mice with impaired horizontal semicircular canal function Characterization of the 3D angular vestibulo-ocular reflex in C57BL6 mice Differential effects of Cdh23(753A) on auditory and vestibular functional aging in C57BL/6J mice Consequences of chromsome18q deletions.Genome-Wide Association Analysis Identifies Dcc as an Essential Factor in the Innervation of the Peripheral Vestibular System in Inbred Mice.Molecular characterization of an allelic series of mutations in the mouse Nox3 gene Effect of M-current modulation on mammalian vestibular responses to transient head motion.Rescue of peripheral vestibular function in Usher syndrome mice using a splice-switching antisense oligonucleotide.

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P2860

A quantitative survey of gravity receptor function in mutant mouse strains.

http://www.wikidata.org/entity/Q30492589

description

2005 nî lūn-bûn

@nan

2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2005年の論文

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2005年論文

@yue

2005年論文

@zh-hant

2005年論文

@zh-hk

2005年論文

@zh-mo

2005年論文

@zh-tw

2005年论文

@wuu

name

A quantitative survey of gravity receptor function in mutant mouse strains.

@ast

A quantitative survey of gravity receptor function in mutant mouse strains.

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type

label

A quantitative survey of gravity receptor function in mutant mouse strains.

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A quantitative survey of gravity receptor function in mutant mouse strains.

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A quantitative survey of gravity receptor function in mutant mouse strains.

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A quantitative survey of gravity receptor function in mutant mouse strains.

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A quantitative survey of gravity receptor function in mutant mouse strains.

@en

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Heping Yu

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Kenneth R Johnson

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Kumar N Alagramam

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Lawrence C Erway

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Natasha Pollak

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Sherri M Jones

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Timothy A Jones

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P2860

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

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

Focusing on the genetics of hearing: you ain't heard nothin' yet.

KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells

Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2

Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice

Degenerative hairlets on the vestibular sensory cells in mutant bustling (BUS/Idr) mice

Circling behavior exhibited by a transgenic insertional mutant

Genetic and age related models of neurodegeneration in mice: dystrophic axons

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