Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation.
about
Audiologic impairment associated with bilirubin-induced neurologic damageWhere hearing starts: the development of the mammalian cochleaMechanisms of hearing loss after blast injury to the ear.The candidate splicing factor Sfswap regulates growth and patterning of inner ear sensory organsA point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus).A mouse model for human deafness DFNB22 reveals that hearing impairment is due to a loss of inner hair cell stimulation.Two-Dimensional Cochlear Micromechanics Measured In Vivo Demonstrate Radial Tuning within the Mouse Organ of Corti.Hair cell force generation does not amplify or tune vibrations within the chicken basilar papilla.Activity-dependent regulation of prestin expression in mouse outer hair cellsReverse transduction measured in the living cochlea by low-coherence heterodyne interferometry.Modified protein expression in the tectorial membrane of the cochlea reveals roles for the striated sheet matrix.Noninvasive in vivo imaging reveals differences between tectorial membrane and basilar membrane traveling waves in the mouse cochlea.Vibration of the organ of Corti within the cochlear apex in mice.Porosity controls spread of excitation in tectorial membrane traveling waves.Loss of the tectorial membrane protein CEACAM16 enhances spontaneous, stimulus-frequency, and transiently evoked otoacoustic emissions.Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membraneFrequency-dependent properties of the tectorial membrane facilitate energy transmission and amplification in the cochlea.Prestin regulation and function in residual outer hair cells after noise-induced hearing loss.Imaging high-frequency periodic motion in the mouse ear with coherently interleaved optical coherence tomographyAn allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.Auditory mechanics of the tectorial membrane and the cochlear spiral.Biophysical mechanisms underlying outer hair cell loss associated with a shortened tectorial membrane.Tectorial membrane material properties in Tecta(Y)(1870C/+) heterozygous mice.Structural and mechanical analysis of tectorial membrane Tecta mutantsA rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian familyDFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.In vivo vibrometry inside the apex of the mouse cochlea using spectral domain optical coherence tomography.Neuroplastin Isoform Np55 Is Expressed in the Stereocilia of Outer Hair Cells and Required for Normal Outer Hair Cell Function.Bilirubin-Induced Audiologic Injury in Preterm Infants.Mechanical tuning and amplification within the apex of the guinea pig cochlea.Quantitative imaging of cochlear soft tissues in wild-type and hearing-impaired transgenic mice by spectral domain optical coherence tomographyPrevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss.Using Drosophila to study mechanisms of hereditary hearing loss.
P2860
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P2860
Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation.
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին 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
Deficient forward transduction ...... G human hearing loss mutation.
@ast
Deficient forward transduction ...... G human hearing loss mutation.
@en
type
label
Deficient forward transduction ...... G human hearing loss mutation.
@ast
Deficient forward transduction ...... G human hearing loss mutation.
@en
prefLabel
Deficient forward transduction ...... G human hearing loss mutation.
@ast
Deficient forward transduction ...... G human hearing loss mutation.
@en
P2093
P2860
P356
P1476
Deficient forward transduction ...... G human hearing loss mutation.
@en
P2093
Alexander Osborn
Andreas Bress
Anping Xia
Fred A Pereira
John S Oghalai
Markus Pfister
Simon S Gao
Stephen M Maricich
P2860
P304
P356
10.1242/DMM.004135
P577
2010-02-08T00:00:00Z