Altered traveling wave propagation and reduced endocochlear potential associated with cochlear dysplasia in the BETA2/NeuroD1 null mouse - Wikidata - wikimedia - TriplyDB

Altered traveling wave propagation and reduced endocochlear potential associated with cochlear dysplasia in the BETA2/NeuroD1 null mouse

Altered traveling wave propagation and reduced endocochlear potential associated with cochlear dysplasia in the BETA2/NeuroD1 null mouse

http://www.wikidata.org/entity/Q30492370

about

Audiologic impairment associated with bilirubin-induced neurologic damage Heparin 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 cells 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.Prestin regulation and function in residual outer hair cells after noise-induced hearing loss.Perilymph osmolality modulates cochlear function Biophysical 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 loss A 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.

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P2860

Altered traveling wave propagation and reduced endocochlear potential associated with cochlear dysplasia in the BETA2/NeuroD1 null mouse

http://www.wikidata.org/entity/Q30492370

description

2007 nî lūn-bûn

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2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2007 թվականի օգոստոսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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Altered traveling wave propaga ...... n the BETA2/NeuroD1 null mouse

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Altered traveling wave propaga ...... n the BETA2/NeuroD1 null mouse

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Altered traveling wave propaga ...... n the BETA2/NeuroD1 null mouse

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Altered traveling wave propaga ...... n the BETA2/NeuroD1 null mouse

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Ann Marie B Visosky

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Anping Xia

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Fred A Pereira

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Jang-Hyeon Cho

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John S Oghalai

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Ming-Jer Tsai

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P2860

Ca2+ current-driven nonlinear amplification by the mammalian cochlea in vitro.

Prestin is the motor protein of cochlear outer hair cells

Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier

Loss of BETA2/NeuroD leads to malformation of the dentate gyrus and epilepsy

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

NeuroD-null mice are deaf due to a severe loss of the inner ear sensory neurons during development

Essential role of BETA2/NeuroD1 in development of the vestibular and auditory systems

Conversion of Xenopus ectoderm into neurons by NeuroD, a basic helix-loop-helix protein

Lighting up the senses: FM1-43 loading of sensory cells through nonselective ion channels.

Mechanics of the mammalian cochlea.

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