Altered traveling wave propagation and reduced endocochlear potential associated with cochlear dysplasia in the BETA2/NeuroD1 null mouse
about
Audiologic impairment associated with bilirubin-induced neurologic damageHeparin binding-epidermal growth factor-like growth factor for the regeneration of chronic tympanic membrane perforations in mice.A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus).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 cellsNoninvasive 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.Prestin regulation and function in residual outer hair cells after noise-induced hearing loss.Perilymph osmolality modulates cochlear functionBiophysical mechanisms underlying outer hair cell loss associated with a shortened tectorial membrane.Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation.Calcium imaging of inner ear hair cells within the cochlear epithelium of mice using two-photon microscopy.Atoh1-lineal neurons are required for hearing and for the survival of neurons in the spiral ganglion and brainstem accessory auditory nuclei.Designer aminoglycosides prevent cochlear hair cell loss and hearing lossA lack of immune system genes causes loss in high frequency hearing but does not disrupt cochlear synapse maturation in mice.Neurod1 suppresses hair cell differentiation in ear ganglia and regulates hair cell subtype development in the cochlea.Functional Outcomes of Heparin-Binding Epidermal Growth Factor-Like Growth Factor for Regeneration of Chronic Tympanic Membrane Perforations in Mice.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.Neurod1 regulates survival and formation of connections in mouse ear and brain.
P2860
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P2860
Altered traveling wave propagation and reduced endocochlear potential associated with cochlear dysplasia in the BETA2/NeuroD1 null mouse
description
2007 nî lūn-bûn
@nan
2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Altered traveling wave propaga ...... n the BETA2/NeuroD1 null mouse
@ast
Altered traveling wave propaga ...... n the BETA2/NeuroD1 null mouse
@en
type
label
Altered traveling wave propaga ...... n the BETA2/NeuroD1 null mouse
@ast
Altered traveling wave propaga ...... n the BETA2/NeuroD1 null mouse
@en
prefLabel
Altered traveling wave propaga ...... n the BETA2/NeuroD1 null mouse
@ast
Altered traveling wave propaga ...... n the BETA2/NeuroD1 null mouse
@en
P2093
P2860
P1433
P1476
Altered traveling wave propaga ...... n the BETA2/NeuroD1 null mouse
@en
P2093
Ann Marie B Visosky
Anping Xia
Fred A Pereira
Jang-Hyeon Cho
John S Oghalai
Ming-Jer Tsai
P2860
P2888
P304
P356
10.1007/S10162-007-0092-9
P577
2007-08-15T00:00:00Z
P5875
P6179
1052720015