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Timing of cochlear feedback: spatial and temporal representation of a tone across the basilar membrane
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0169(1998)41:2<138::aid-cm5>3.0.co;2-aopenalex-snapshot
Keratin filament deployment and cytoskeletal networking in a sensory epithelium that vibrates during hearing
inferredcites →https://doi.org/10.1002/lary.5540680314openalex-snapshot
Transmission and transduction in the cochlea
inferredcites →https://doi.org/10.1007/bf00386170openalex-snapshot
Patch clamped responses from outer hair cells in the intact adult organ of Corti
inferredcites →https://doi.org/10.1016/0166-2236(95)90091-8openalex-snapshot
A faster transduction mechanism for the cochlear amplifier?
inferredcites →https://doi.org/10.1016/0378-5955(88)90113-xopenalex-snapshot
Whole cell currents and mechanical responses of isolated outer hair cells
inferredcites →https://doi.org/10.1016/0378-5955(91)90037-aopenalex-snapshot
Laser Doppler velocimetry of basilar membrane vibration
inferredcites →https://doi.org/10.1016/0378-5955(92)90083-yopenalex-snapshot
Basilar membrane mechanics in the hook region of cat and guinea-pig cochleae: Sharp tuning and nonlinearity in the absence of baseline position shifts
inferredcites →https://doi.org/10.1016/0378-5955(92)90084-zopenalex-snapshot
Basilar membrane tonotopicity in the hook region of the cat cochlea
inferredcites →https://doi.org/10.1016/0378-5955(92)90182-mopenalex-snapshot
Acoustic lesions in the mammalian cochlea: Implications for the spatial distribution of the ‘active process’
inferredcites →https://doi.org/10.1016/0378-5955(95)00064-bopenalex-snapshot
A cochlear model using feed-forward outer-hair-cell forces
inferredcites →https://doi.org/10.1016/s0006-3495(95)79883-6openalex-snapshot
Modeling the active process of the cochlea: phase relations, amplification, and spontaneous oscillation
inferredcites →https://doi.org/10.1016/s0006-3495(97)78255-9openalex-snapshot
Mechanics of microtubule bundles in pillar cells from the inner ear
inferredcites →https://doi.org/10.1016/s0378-5955(98)00079-3openalex-snapshot
Development of the base of the cochlea: place code shift in the gerbil
inferredcites →https://doi.org/10.1038/350155a0openalex-snapshot
Nature of the motor element in electrokinetic shape changes of cochlear outer hair cells
inferredcites →https://doi.org/10.1038/365838a0openalex-snapshot
Reverse transduction measured in the isolated cochlea by laser Michelson interferometry
inferredcites →https://doi.org/10.1073/pnas.93.16.8727openalex-snapshot
Resonant tectorial membrane motion in the inner ear: its crucial role in frequency tuning.
inferredcites →https://doi.org/10.1073/pnas.94.6.2660openalex-snapshot
The location of the cochlear amplifier: Spatial representation of a single tone on the guinea pig basilar membrane
inferredcites →https://doi.org/10.1073/pnas.96.7.3676openalex-snapshot
Comparing in vitro , in situ , and in vivo experimental data in a three-dimensional model of mammalian cochlear mechanics
inferredcites →https://doi.org/10.1073/pnas.96.8.4420openalex-snapshot
Limiting dynamics of high-frequency electromechanical transduction of outer hair cells
inferredcites →https://doi.org/10.1098/rspb.1992.0126openalex-snapshot
Mechanical filtering of sound in the inner ear
inferredcites →https://doi.org/10.1113/jphysiol.1983.sp014668openalex-snapshot
Low‐frequency characteristics of intracellularly recorded receptor potentials in guinea‐pig cochlear hair cells.
inferredcites →https://doi.org/10.1113/jphysiol.1987.sp016617openalex-snapshot
A fast motile response in guinea‐pig outer hair cells: the cellular basis of the cochlear amplifier.
inferredcites →https://doi.org/10.1121/1.385198openalex-snapshot
Cochlear micromechanics—A physical model of transduction
inferredcites →https://doi.org/10.1121/1.387996openalex-snapshot
Measurement of basilar membrane motion in the guinea pig using the Mössbauer technique
inferredcites →https://doi.org/10.1121/1.394389openalex-snapshot
Basilar membrane mechanics at the base of the chinchilla cochlea. I. Input–output functions, tuning curves, and response phases
inferredcites →https://doi.org/10.1121/1.399052openalex-snapshot
A cochlear frequency-position function for several species—29 years later
inferredcites →https://doi.org/10.1121/1.404281openalex-snapshot
Using acoustic distortion products to measure the cochlear amplifier gain on the basilar membrane
inferredcites →https://doi.org/10.1121/1.414732openalex-snapshot
Steady-state sinusoidal velocity responses of the basilar membrane in guinea pig
inferredcites →https://doi.org/10.1121/1.418265openalex-snapshot
Basilar-membrane responses to tones at the base of the chinchilla cochlea
inferredcites →https://doi.org/10.1121/1.420083openalex-snapshot
Medial efferent inhibition suppresses basilar membrane responses to near characteristic frequency tones of moderate to high intensities
inferredcites →https://doi.org/10.1126/science.3966153openalex-snapshot
Evoked Mechanical Responses of Isolated Cochlear Outer Hair Cells
inferredcites →https://doi.org/10.1126/science.7701325openalex-snapshot
High-Frequency Motility of Outer Hair Cells and the Cochlear Amplifier
inferredcites →https://doi.org/10.1142/9789814531023openalex-snapshot
Diversity in Auditory Mechanics
inferredcites →https://doi.org/10.1152/jn.1995.74.6.2319openalex-snapshot
Passive compliance and active force generation in the guinea pig outer hair cell
inferredcites →https://doi.org/10.1523/jneurosci.11-04-01057.1991openalex-snapshot
Furosemide alters organ of corti mechanics: evidence for feedback of outer hair cells upon the basilar membrane
inferredcites →https://doi.org/10.1523/jneurosci.12-05-01906.1992openalex-snapshot
On the frequency limit and phase of outer hair cell motility: effects of the membrane filter
inferredcites →https://doi.org/10.1523/jneurosci.16-01-00325.1996openalex-snapshot
The effect of efferent stimulation on basilar membrane displacement in the basal turn of the guinea pig cochlea
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.3076111openalex-extracted
Helmholtz's Piano Strings: Reverberation of Ripples on the Tectorial Membrane
inferred← citeshttps://doi.org/10.1007/2506_2013_23openalex-snapshot
Roles for Prestin in Harnessing the Basilar Membrane to the Organ of Corti
inferred← citeshttps://doi.org/10.1007/s00422-006-0134-0openalex-snapshot
Tuning the cochlea: wave-mediated positive feedback between cells
inferred← citeshttps://doi.org/10.1007/s10162-008-0151-xopenalex-snapshot
Variation in the Phase of Response to Low-Frequency Pure Tones in the Guinea Pig Auditory Nerve as Functions of Stimulus Level and Frequency
inferred← citeshttps://doi.org/10.1016/j.bpj.2024.07.015openalex-snapshot
Local cochlear mechanical responses revealed through outer hair cell receptor potential measurements
inferred← citeshttps://doi.org/10.1016/j.devcel.2005.02.009openalex-snapshot
Sprouty2, a Mouse Deafness Gene, Regulates Cell Fate Decisions in the Auditory Sensory Epithelium by Antagonizing FGF Signaling
inferred← citeshttps://doi.org/10.1016/j.heares.2020.108094openalex-snapshot
Cochlear microphonic latency predicts outer hair cell function in animal models and clinical populations
inferred← citeshttps://doi.org/10.1016/j.heares.2021.108407openalex-snapshot
An outer hair cell-powered global hydromechanical mechanism for cochlear amplification
inferred← citeshttps://doi.org/10.1016/j.neuron.2012.09.031openalex-snapshot
The Spatial Pattern of Cochlear Amplification
inferred← citeshttps://doi.org/10.1016/j.neuron.2012.11.016openalex-snapshot
Probing the Cochlear Amplifier by Immobilizing Molecular Motors of Sensory Hair Cells
inferred← citeshttps://doi.org/10.1016/s0006-3495(04)74132-6openalex-snapshot
Measuring Hearing Organ Vibration Patterns with Confocal Microscopy and Optical Flow
inferred← citeshttps://doi.org/10.1038/ncomms10282openalex-snapshot
Reverse transduction measured in the living cochlea by low-coherence heterodyne interferometry
inferred← citeshttps://doi.org/10.1038/ncomms1226openalex-snapshot
Measurement of cochlear power gain in the sensitive gerbil ear
inferred← citeshttps://doi.org/10.1038/nn0205-132openalex-snapshot
The cochlear amplifier and Ca2+ current–driven active stereocilia motion
inferred← citeshttps://doi.org/10.1038/nn1047openalex-snapshot
Sound-induced differential motion within the hearing organ
inferred← citeshttps://doi.org/10.1038/s41598-022-23525-xopenalex-snapshot
Cochlear motion across the reticular lamina implies that it is not a stiff plate
inferred← citeshttps://doi.org/10.1038/s42003-024-06293-4openalex-snapshot
Asymmetric vibrations in the organ of Corti by outer hair cells measured from excised gerbil cochlea
inferred← citeshttps://doi.org/10.1063/1.3658127openalex-snapshot
Acoustically Evoked Different Vibration Pattern Across the Width of the Cochlea Partition
inferred← citeshttps://doi.org/10.1063/1.5038485openalex-snapshot
Spatial profiles of sound-evoked vibration in the gerbil cochlea
inferred← citeshttps://doi.org/10.1063/5.0010802openalex-snapshot
Balance in the feedback loop components of the mammalian cochlear amplifier
inferred← citeshttps://doi.org/10.1073/pnas.0401395101openalex-snapshot
Evidence of tectorial membrane radial motion in a propagating mode of a complex cochlear model
inferred← citeshttps://doi.org/10.1073/pnas.0511125103openalex-snapshot
Nanomechanics of the subtectorial space caused by electromechanics of cochlear outer hair cells
inferred← citeshttps://doi.org/10.1073/pnas.1110036108openalex-snapshot
Piezoelectric materials mimic the function of the cochlear sensory epithelium
inferred← citeshttps://doi.org/10.1073/pnas.97.22.11744openalex-snapshot
Mechanical bases of frequency tuning and neural excitation at the base of the cochlea: Comparison of basilar-membrane vibrations and auditory-nerve-fiber responses in chinchilla
inferred← citeshttps://doi.org/10.1073/pnas.97.22.11751openalex-snapshot
The spatial and temporal representation of a tone on the guinea pig basilar membrane
inferred← citeshttps://doi.org/10.1093/bmb/63.1.59openalex-snapshot
Biophysics of the cochlea – biomechanics and ion channelopathies
inferred← citeshttps://doi.org/10.1098/rsif.2015.0913openalex-snapshot
Finite-element model of the active organ of Corti
inferred← citeshttps://doi.org/10.1098/rsta.2000.0548openalex-snapshot
Finite-element modelling: a new tool for the biologist
inferred← citeshttps://doi.org/10.1101/2023.02.24.529908openalex-snapshot
Outer hair cell receptor potentials reveal a local resonance in the mammalian cochlea
inferred← citeshttps://doi.org/10.1121/1.1369098openalex-snapshot
Intracochlear pressure measurements related to cochlear tuning
inferred← citeshttps://doi.org/10.1121/1.1766053openalex-snapshot
The cochlear amplifier as a standing wave: “Squirting” waves between rows of outer hair cells?
inferred← citeshttps://doi.org/10.1121/1.1771571openalex-snapshot
Mathematical modeling of the radial profile of basilar membrane vibrations in the inner ear
inferred← citeshttps://doi.org/10.1121/1.1880812openalex-snapshot
Two-tone distortion in intracochlear pressure
inferred← citeshttps://doi.org/10.1121/1.1993147openalex-snapshot
Two modes of motion of the alligator lizard cochlea: Measurements and model predictions
inferred← citeshttps://doi.org/10.1121/1.2017899openalex-snapshot
Medial-olivocochlear-efferent inhibition of the first peak of auditory-nerve responses: Evidence for a new motion within the cochlea
inferred← citeshttps://doi.org/10.1121/1.2776154openalex-snapshot
Outer hair cell active force generation in the cochlear environment
inferred← citeshttps://doi.org/10.1121/1.428648openalex-snapshot
Auditory-nerve-fiber responses to high-level clicks: Interference patterns indicate that excitation is due to the combination of multiple drives
inferred← citeshttps://doi.org/10.1121/1.429404openalex-snapshot
Study of mechanical motions in the basal region of the chinchilla cochlea
inferred← citeshttps://doi.org/10.1121/1.5132711openalex-snapshot
Use of the guinea pig in studies on the development and prevention of acquired sensorineural hearing loss, with an emphasis on noise
inferred← citeshttps://doi.org/10.1121/10.0014794openalex-snapshot
Overturning the mechanisms of cochlear amplification via area deformations of the organ of Corti
inferred← citeshttps://doi.org/10.1152/jn.00680.2003openalex-snapshot
Role of the Tectorial Membrane Revealed by Otoacoustic Emissions Recorded From Wild-Type and Transgenic TectaΔENT/ΔENT Mice
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Mechanics of the Mammalian Cochlea
inferred← citeshttps://doi.org/10.1155/2020/8856159openalex-snapshot
An Analytical Mechanical Model of Corti in the Cochlea
inferred← citeshttps://doi.org/10.1159/000046856openalex-snapshot
Mechanical Transduction in Outer Hair Cells
inferred← citeshttps://doi.org/10.1159/000046858openalex-snapshot
In vivo Micromechanical Measurements of the Organ of Corti in the Basal Cochlear Turn
inferred← citeshttps://doi.org/10.1371/journal.pone.0086090openalex-snapshot
Lateralization of Travelling Wave Response in the Hearing Organ of Bushcrickets
inferred← citeshttps://doi.org/10.1515/jbcpp.2010.21.3.231openalex-snapshot
How are the Inner Hair Cells and Auditory Nerve Fibers Activated without the Mediation of the Outer Hair Cells and the Cochlear Amplifier?
inferred← citeshttps://doi.org/10.1523/jneurosci.0722-14.2014openalex-snapshot
Filtering of Acoustic Signals within the Hearing Organ
inferred← citeshttps://doi.org/10.1523/jneurosci.2241-21.2022openalex-snapshot
A Gap-Junction Mutation Reveals That Outer Hair Cell Extracellular Receptor Potentials Drive High-Frequency Cochlear Amplification
inferred← citeshttps://doi.org/10.1523/jneurosci.23-29-09508.2003openalex-snapshot
Synchronization of a Nonlinear Oscillator: Processing the Cf Component of the Echo-Response Signal in the Cochlea of the Mustached Bat
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The Development of a Single Frequency Place in the Mammalian Cochlea: The Cochlear Resonance in the Mustached BatPteronotus parnellii
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Mechanical Responses of the Organ of Corti to Acoustic and Electrical Stimulation In Vitro
inferred← citeshttps://doi.org/10.1529/biophysj.106.083634openalex-snapshot
Imaging Electrically Evoked Micromechanical Motion within the Organ of Corti of the Excised Gerbil Cochlea
inferred← citeshttps://doi.org/10.1529/biophysj.106.084087openalex-snapshot
Evidence for Outer Hair Cell Driven Oscillatory Fluid Flow in the Tunnel of Corti
inferred← citeshttps://doi.org/10.21037/qims.2019.05.10openalex-snapshot
Revealing the morphology and function of the cochlea and middle ear with optical coherence tomography
inferred← citeshttps://doi.org/10.3410/f.733951373.793550658openalex-snapshot
Faculty Opinions recommendation of Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae.
inferred← citeshttps://doi.org/10.7554/elife.37625openalex-snapshot
Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae
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