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Active outer hair cell motility can suppress vibrations in the organ of Corti
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s10162-015-0529-5openalex-snapshot
Energy Flux in the Cochlea: Evidence Against Power Amplification of the Traveling Wave
inferredcites →https://doi.org/10.1016/0378-5955(95)00089-mopenalex-snapshot
The osmotic response of the isolated, unfixed mouse tectorial membrane to isosmotic solutions: effect of Na+, K+, and Ca2+ concentration
inferredcites →https://doi.org/10.1016/j.bpj.2016.08.048openalex-snapshot
Two-Tone Suppression of Simultaneous Electrical and Mechanical Responses in the Cochlea
inferredcites →https://doi.org/10.1016/j.heares.2012.04.017openalex-snapshot
Von Békésy and cochlear mechanics
inferredcites →https://doi.org/10.1016/j.heares.2017.10.013openalex-snapshot
An elemental approach to modelling the mechanics of the cochlea
inferredcites →https://doi.org/10.1016/j.heares.2019.04.001openalex-snapshot
Nonlinearity and amplification in cochlear responses to single and multi-tone stimuli
inferredcites →https://doi.org/10.1016/j.neuron.2008.07.012openalex-snapshot
Making an Effort to Listen: Mechanical Amplification in the Ear
inferredcites →https://doi.org/10.1016/j.neuron.2012.09.031openalex-snapshot
The Spatial Pattern of Cochlear Amplification
inferredcites →https://doi.org/10.1016/s0006-3495(02)75481-7openalex-snapshot
Piezoelectric Reciprocal Relationship of the Membrane Motor in the Cochlear Outer Hair Cell
inferredcites →https://doi.org/10.1016/s0378-5955(98)00133-6openalex-snapshot
Measurements of the stiffness map challenge a basic tenet of cochlear theories
inferredcites →https://doi.org/10.1038/365838a0openalex-snapshot
Reverse transduction measured in the isolated cochlea by laser Michelson interferometry
inferredcites →https://doi.org/10.1038/nn.2827openalex-snapshot
A differentially amplified motion in the ear for near-threshold sound detection
inferredcites →https://doi.org/10.1038/nn1385openalex-snapshot
Ca2+ current–driven nonlinear amplification by the mammalian cochlea in vitro
inferredcites →https://doi.org/10.1038/nrn1828openalex-snapshot
The sensory and motor roles of auditory hair cells
inferredcites →https://doi.org/10.1038/s41467-018-05483-zopenalex-snapshot
Vibration hotspots reveal longitudinal funneling of sound-evoked motion in the mammalian cochlea
inferredcites →https://doi.org/10.1038/s41598-019-41112-5openalex-snapshot
Probing hair cell’s mechano-transduction using two-tone suppression measurements
inferredcites →https://doi.org/10.1038/s41598-019-43970-5openalex-snapshot
Reducing tectorial membrane viscoelasticity enhances spontaneous otoacoustic emissions and compromises the detection of low level sound
inferredcites →https://doi.org/10.1073/pnas.0511125103openalex-snapshot
Nanomechanics of the subtectorial space caused by electromechanics of cochlear outer hair cells
inferredcites →https://doi.org/10.1073/pnas.1500038112openalex-snapshot
Noninvasive in vivo imaging reveals differences between tectorial membrane and basilar membrane traveling waves in the mouse cochlea
inferredcites →https://doi.org/10.1073/pnas.1606317113openalex-snapshot
Minimal basilar membrane motion in low-frequency hearing
inferredcites →https://doi.org/10.1073/pnas.1607428113openalex-snapshot
Reticular lamina and basilar membrane vibrations in living mouse cochleae
inferredcites →https://doi.org/10.1073/pnas.1720979115openalex-snapshot
Cochlear amplification and tuning depend on the cellular arrangement within the organ of Corti
inferredcites →https://doi.org/10.1073/pnas.1900695116openalex-snapshot
Unified cochlear model for low- and high-frequency mammalian hearing
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/10.1121/1.1910547openalex-snapshot
Model of the Displacement between Opposing Points on the Tectorial Membrane and Reticular Lamina
inferredcites →https://doi.org/10.1121/1.1914361openalex-snapshot
Transmission of radial shear forces to cochlear hair cells
inferredcites →https://doi.org/10.1121/1.385198openalex-snapshot
Cochlear micromechanics—A physical model of transduction
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/10.1142/9789812793980_0016openalex-snapshot
RADIAL VARIATION IN THE VIBRATIONS OF THE COCHLEAR PARTITION
inferredcites →https://doi.org/10.1152/jn.00446.2003openalex-snapshot
Stiffness of the Gerbil Basilar Membrane: Radial and Longitudinal Variations
inferredcites →https://doi.org/10.1152/jn.00702.2017openalex-snapshot
Organ of Corti vibration within the intact gerbil cochlea measured by volumetric optical coherence tomography and vibrometry
inferredcites →https://doi.org/10.1152/physrev.00044.2006openalex-snapshot
Cochlear Outer Hair Cell Motility
inferredcites →https://doi.org/10.1371/journal.pone.0032757openalex-snapshot
In Vivo Outer Hair Cell Length Changes Expose the Active Process in the Cochlea
inferredcites →https://doi.org/10.1523/jneurosci.0425-18.2018openalex-snapshot
The Frequency Response of Outer Hair Cell Voltage-Dependent Motility Is Limited by Kinetics of Prestin
inferredcites →https://doi.org/10.1523/jneurosci.09-08-02954.1989openalex-snapshot
Asymmetry in voltage-dependent movements of isolated outer hair cells from the organ of Corti
inferredcites →https://doi.org/10.1523/jneurosci.1127-05.2005openalex-snapshot
The Transduction Channel Filter in Auditory Hair Cells
inferredcites →https://doi.org/10.1523/jneurosci.1157-16.2016openalex-snapshot
Two-Dimensional Cochlear Micromechanics Measured In Vivo Demonstrate Radial Tuning within the Mouse Organ of Corti
inferredcites →https://doi.org/10.1523/jneurosci.2608-18.2019openalex-snapshot
Amplification and Suppression of Traveling Waves along the Mouse Organ of Corti: Evidence for Spatial Variation in the Longitudinal Coupling of Outer Hair Cell-Generated Forces
inferredcites →https://doi.org/10.1523/jneurosci.3011-15.2016openalex-snapshot
Adaptation Independent Modulation of Auditory Hair Cell Mechanotransduction Channel Open Probability Implicates a Role for the Lipid Bilayer
inferredcites →https://doi.org/10.1529/biophysj.106.083634openalex-snapshot
Imaging Electrically Evoked Micromechanical Motion within the Organ of Corti of the Excised Gerbil Cochlea
inferredcites →https://doi.org/10.1529/biophysj.106.084087openalex-snapshot
Evidence for Outer Hair Cell Driven Oscillatory Fluid Flow in the Tunnel of Corti
inferredcites →https://doi.org/10.3109/00016489109138403openalex-snapshot
Effects of Salicylate on Shape, Electromotility and Membrane Characteristics of Isolated Outer Hair Cells from Guinea Pig Cochlea
inferredcites →https://doi.org/10.7554/elife.37625openalex-snapshot
Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.cophys.2020.08.022openalex-snapshot
Cochlear mechanics: new insights from vibrometry and optical coherence tomography
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