نتایج جستجو برای: cochlea

تعداد نتایج: 4625  

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2010
Chandrakala Puligilla Alain Dabdoub Stephan D Brenowitz Matthew W Kelley

In the cochlea, spiral ganglion neurons play a critical role in hearing as they form the relay between mechanosensory hair cells in the inner ear and cochlear nuclei in the brainstem. The proneural basic helix-loop-helix transcription factors Neurogenin1 (Neurog1) and NeuroD1 have been shown to be essential for the development of otocyst-derived inner ear sensory neurons. Here, we show neural c...

2001
ANDRÉ VAN SCHAIK

This paper presents an electronic system that extracts the periodicity of a sound. It uses three analog VLSI building blocks: a silicon cochlea, two Inner Hair Cell circuits and two spiking neuron chips. The silicon cochlea consists of a cascade of filters which delays (and filters) the input sound as it passes along the cascade. The time delay added by each individual filter in the cochlea inc...

Journal: :SIAM Journal of Applied Mathematics 2015
William Ko John M. Stockie

The cochlea or inner ear has a remarkable ability to amplify sound signals. This is understood to derive at least in part from some active process that magnifies vibrations of the basilar membrane (BM) and the cochlear partition in which it is embedded, to the extent that it overcomes the effect of viscous damping from the surrounding cochlear fluid. Many authors have associated this amplificat...

Journal: :Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2015
S A Likhachev I P Maryenko

AIM To study the state of statokinetic stability in patients with recurrent vestibular dysfunction caused by the vascular compression of the cochlea-vestibular nerve. MATERIAL AND METHODS Authors examined 30 patients with recurrent vestibular dysfunction in which neuroimaging studies revealed the vessel adjacent to the cochlea-vestibular nerve. Statokinetic stability evaluation was selected a...

Journal: :Journal of visualized experiments : JoVE 2016
Scott C Montgomery Brandon C Cox

The organ of Corti, housed in the cochlea of the inner ear, contains mechanosensory hair cells and surrounding supporting cells which are organized in a spiral shape and have a tonotopic gradient for sound detection. The mouse cochlea is approximately 6 mm long and often divided into three turns (apex, middle, and base) for analysis. To investigate cell loss, cell division, or mosaic gene expre...

Journal: :Hearing research 2008
Glen H MacDonald Edwin W Rubel

The complex anatomy of the mammalian cochlea is most readily understood by representation in three-dimensions. However, the cochlea is often sectioned to minimize the effects of its anatomic complexity and optical properties on image acquisition by light microscopy. We have found that optical aberrations present in the decalcified cochlea can be greatly reduced by dehydration through graded eth...

Journal: :AJNR. American journal of neuroradiology 2016
M N Pakdaman G Ishiyama A Ishiyama K A Peng H J Kim W B Pope A R Sepahdari

BACKGROUND AND PURPOSE Menière disease and idiopathic sudden sensorineural hearing loss can have overlapping clinical presentation and may have similar pathophysiology. Prior studies using postcontrast 3D-FLAIR MR imaging suggest abnormal blood-labyrinth barrier permeability in both conditions, but the 2 diseases have not been directly compared by using the same imaging techniques. We hypothesi...

Journal: :The Journal of laryngology and otology 1967
L Naftalin

EVIDENCE concerning frequency analysis which was drawn together from several sources allowed the suggestion to be made that the design of the cochlea—i.e. its internal geometry—was itself a frequency analyser to a first approximation (Naftalin, 1965). Two sets of biological observations which seem to be of fundamental importance from the physical (acoustic) point of view may be cited as offerin...

Journal: :PLoS ONE 2008
Qing Chang Wenxue Tang Shoeb Ahmad Binfei Zhou Xi Lin

Connexin26 (Cx26) and connexin30 (Cx30) are two major protein subunits that co-assemble to form gap junctions (GJs) in the cochlea. Mutations in either one of them are the major cause of non-syndromic prelingual deafness in humans. Because the mechanisms of cochlear pathogenesis caused by Cx mutations are unclear, we investigated effects of Cx30 null mutation on GJ-mediated ionic and metabolic ...

Journal: :Hearing research 1991
G Zajic T S Nair M Ptok C Van Waes R A Altschuler J Schacht T E Carey

Murine monoclonal antibodies against guinea pig cochlear epithelium were generated with the goal of identifying cochlea-specific antigens and elucidating their function. To compensate for the limited amount of cochlear tissue, intrasplenic immunization was used. Hybridoma supernatants were screened by ELISA for antibody production and for binding to homogenates from cochlea, liver, lung, kidney...

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