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High-Frequency Motility of Outer Hair Cells and the Cochlear Amplifier
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4613-3970-0openalex-snapshot
Analysis of Physiological Systems
inferredcites →https://doi.org/10.1007/bf00340870openalex-snapshot
Structural features of the lateral walls in mammalian cochlear outer hair cells
inferredcites →https://doi.org/10.1016/0378-5955(83)90120-xopenalex-snapshot
Some electrical circuit properties of the organ of Corti. I. Analysis without reactive elements
inferredcites →https://doi.org/10.1016/0378-5955(83)90136-3openalex-snapshot
An active process in cochlear mechanics
inferredcites →https://doi.org/10.1016/0378-5955(86)90082-1openalex-snapshot
Motile responses in outer hair cells
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(90)90084-3openalex-snapshot
Saturation of outer hair cell receptor currents causes two-tone suppression
inferredcites →https://doi.org/10.1016/0378-5955(91)90019-6openalex-snapshot
Outer hair cell electromotility: The sensitivity and vulnerability of the DC component
inferredcites →https://doi.org/10.1016/0378-5955(92)90018-iopenalex-snapshot
High frequency distortion products from the ears of two bat species, Megaderma lyra and Carollia perspicillata
inferredcites →https://doi.org/10.1016/s0196-0709(81)80034-8openalex-snapshot
The second filter is real, but how does it work?
inferredcites →https://doi.org/10.1037/h0023953openalex-snapshot
Development of cochlear function in the ear of the infant rat.
inferredcites →https://doi.org/10.1038/322365a0openalex-snapshot
Electrokinetic shape changes of cochlear outer hair cells
inferredcites →https://doi.org/10.1038/322368a0openalex-snapshot
Ionic basis of membrane potential in outer hair cells of guinea pig cochlea
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.74.6.2407openalex-snapshot
Sensitivity, polarity, and conductance change in the response of vertebrate hair cells to controlled mechanical stimuli.
inferredcites →https://doi.org/10.1073/pnas.89.18.8671openalex-snapshot
A membrane-based force generation mechanism in auditory sensory cells.
inferredcites →https://doi.org/10.1073/pnas.90.18.8347openalex-snapshot
Stereocilia displacement induced somatic motility of cochlear outer hair cells.
inferredcites →https://doi.org/10.1093/icb/21.1.211openalex-snapshot
On the Diversity of Electric Signals in a Community of Mormyrid Electric Fish in West Africa
inferredcites →https://doi.org/10.1098/rspb.1992.0014openalex-snapshot
Voltage responses to tones of outer hair cells in the basal turn of the guinea-pig cochlea: significance for electromotility and desensitization
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/10.1113/jphysiol.1992.sp019030openalex-snapshot
Ionic currents of outer hair cells isolated from the guinea‐pig cochlea.
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/10.1126/science.176.4030.66openalex-snapshot
Cochlear Microphonic Audiograms in the "Pure Tone" Bat Chilonycteris parnellii parnellii
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.6623090openalex-snapshot
Alternating Current Delivered into the Scala Media Alters Sound Pressure at the Eardrum
inferredcites →https://doi.org/10.1152/jn.1993.70.1.299openalex-snapshot
Theory of electrically driven shape changes of cochlear outer hair cells
inferredcites →https://doi.org/10.1523/jneurosci.05-06-01591.1985openalex-snapshot
Response characteristics of mammalian cochlear hair cells
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.11-10-03096.1991openalex-snapshot
Reversible inhibition of voltage-dependent outer hair cell motility and capacitance
inferredcites →https://doi.org/10.1523/jneurosci.12-05-01575.1992openalex-snapshot
The phase and magnitude of hair cell receptor potentials and frequency tuning in the guinea pig cochlea
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.12-12-04575.1992openalex-snapshot
The active 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/10.1002/(sici)1097-0185(199805)251:1<97::aid-ar15>3.0.co;2-6openalex-snapshot
Cytologic evidence for mechanisms of K+ transport and genesis of Hensen bodies and subsurface cisternae in outer hair cells
inferred← citeshttps://doi.org/10.1002/1097-0029(20001115)51:4<364::aid-jemt6>3.0.co;2-eopenalex-snapshot
Plasticity of the superior olivary complex
inferred← citeshttps://doi.org/10.1002/aur.70152openalex-snapshot
Altered Auditory Maturation in Fragile X Syndrome and Its Involvement in Audiogenic Seizure Susceptibility
inferred← citeshttps://doi.org/10.1002/cne.20180openalex-snapshot
Superior olivary contributions to auditory system plasticity: Medial but not lateral olivocochlear neurons are the source of cochleotomy‐induced GAP‐43 expression in the ventral cochlear nucleus
inferred← citeshttps://doi.org/10.1002/cne.20311openalex-snapshot
Low density of membrane particles in auditory hair cells of lizards and birds suggests an absence of somatic motility
inferred← citeshttps://doi.org/10.1002/humu.22023openalex-snapshot
Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss
inferred← citeshttps://doi.org/10.1007/0-387-31706-6_2openalex-snapshot
The Development of Hair Cells in the Inner Ear
inferred← citeshttps://doi.org/10.1007/0-387-31706-6_7openalex-snapshot
The Piezoelectric Outer Hair Cell
inferred← citeshttps://doi.org/10.1007/978-0-387-30374-1_4openalex-snapshot
Cellular and Molecular Mechanisms of Mechanical Amplification in the Mammalian Cochlea
inferred← citeshttps://doi.org/10.1007/978-0-387-71469-1_10openalex-snapshot
Cellular and Molecular Mechanisms in the Efferent Control of Cochlear Nonlinearities
inferred← citeshttps://doi.org/10.1007/978-0-387-71469-1_2openalex-snapshot
Traveling Waves, Second Filters, and Physiological Vulnerability: A Short History of the Discovery of Active Processes in Hearing
inferred← citeshttps://doi.org/10.1007/978-0-387-71469-1_5openalex-snapshot
The Morphological Specializations and Electromotility of the Mammalian Outer Hair Cell
inferred← citeshttps://doi.org/10.1007/978-1-4419-8957-4_1openalex-snapshot
An Outline of the Evolution of Vertebrate Hearing Organs
inferred← citeshttps://doi.org/10.1007/978-1-4612-0757-3_1openalex-snapshot
Overview: Cochlear Neurobiology
inferred← citeshttps://doi.org/10.1007/978-1-4612-0757-3_8openalex-snapshot
Physiology of Olivocochlear Efferents
inferred← citeshttps://doi.org/10.1007/978-3-319-52073-5_4openalex-snapshot
Mechanical Transduction Processes in the Hair Cell
inferred← citeshttps://doi.org/10.1007/978-3-319-52073-5_5openalex-snapshot
Prestin: Molecular Mechanisms Underlying Outer Hair Cell Electromotility
inferred← citeshttps://doi.org/10.1007/978-3-662-09604-8_12openalex-snapshot
Nucleoside and Nucleotide Transmission in Sensory Systems
inferred← citeshttps://doi.org/10.1007/978-3-7091-6025-1_6openalex-snapshot
The Outer Hair Cell: A Mechanoelectrical and Electromechanical Sensor/Actuator
inferred← citeshttps://doi.org/10.1007/bf02740601openalex-snapshot
Extracellular nucleotide signaling in the inner ear
inferred← citeshttps://doi.org/10.1007/s00106-019-0615-9openalex-snapshot
The speed limit of outer hair cell electromechanical activity
inferred← citeshttps://doi.org/10.1007/s00232-005-0833-9openalex-snapshot
Tuning in to the Amazing Outer Hair Cell: Membrane Wizardry with a Twist and Shout
inferred← citeshttps://doi.org/10.1007/s00232-005-0843-7openalex-snapshot
Electromechanical Models of the Outer Hair Cell Composite Membrane
inferred← citeshttps://doi.org/10.1007/s00232-007-9004-5openalex-snapshot
Developmental Expression of the Outer Hair Cell Motor Prestin in the Mouse
inferred← citeshttps://doi.org/10.1007/s00335-002-2227-yopenalex-snapshot
Genomic characterization and expression of mouse prestin, the motor protein of outer hair cells
inferred← citeshttps://doi.org/10.1007/s00405-004-0817-xopenalex-snapshot
Cochlear implantation in patients with MELAS syndrome
inferred← citeshttps://doi.org/10.1007/s00405-008-0663-3openalex-snapshot
Complex level alterations of the 2f 1−f 2 distortion product due to hypoxia in the guinea pig
inferred← citeshttps://doi.org/10.1007/s00405-009-1052-2openalex-snapshot
Level alterations of the 2f 1–f 2 distortion product due to hypoxia in the guinea pig depend on the stimulus frequency
inferred← citeshttps://doi.org/10.1007/s00405-013-2754-zopenalex-snapshot
A longitudinal study of changes in distortion-product otoacoustic emissions and pure-tone thresholds in an industrial setting
inferred← citeshttps://doi.org/10.1007/s00424-005-0038-1openalex-snapshot
Differential expression of potassium currents in Deiters cells of the guinea pig cochlea
inferred← citeshttps://doi.org/10.1007/s004240050395openalex-snapshot
The outer hair cell motor in membrane patches
inferred← citeshttps://doi.org/10.1007/s004240050464openalex-snapshot
Sodium current expression during postnatal development of rat outer hair cells
inferred← citeshttps://doi.org/10.1007/s00441-001-0483-xopenalex-snapshot
Microtubule cold stability in supporting cells of the gerbil auditory sensory epithelium: correlation with tubulin post-translational modifications
inferred← citeshttps://doi.org/10.1007/s10162-004-4025-6openalex-snapshot
Linopirdine Blocks α9α10-Containing Nicotinic Cholinergic Receptors of Cochlear Hair Cells
inferred← citeshttps://doi.org/10.1007/s10162-005-0015-6openalex-snapshot
High-Frequency Force Generation in the Constrained Cochlear Outer Hair Cell: A Model Study
inferred← citeshttps://doi.org/10.1007/s10162-022-00884-wopenalex-snapshot
The Long Outer-Hair-Cell RC Time Constant: A Feature, Not a Bug, of the Mammalian Cochlea
inferred← citeshttps://doi.org/10.1007/s101620010006openalex-snapshot
Properties of Voltage-Dependent Somatic Stiffness of Cochlear Outer Hair Cells
inferred← citeshttps://doi.org/10.1007/s10439-005-5749-0openalex-snapshot
Mechanosensitive Channels in the Lateral Wall Can Enhance the Cochlear Outer Hair Cell Frequency Response
inferred← citeshttps://doi.org/10.1007/s12264-022-00839-4openalex-snapshot
Prestin-Mediated Frequency Selectivity Does not Cover Ultrahigh Frequencies in Mice
inferred← citeshttps://doi.org/10.1016/0304-3940(96)12524-6openalex-snapshot
Acoustic modulation of electrically evoked distortion product otoacoustic emissions in gerbil cochlea
inferred← citeshttps://doi.org/10.1016/0378-5955(95)00216-2openalex-snapshot
Electromotile hearing: evidence from basilar membrane motion and otoacoustic emissions
inferred← citeshttps://doi.org/10.1016/0378-5955(95)00217-0openalex-snapshot
Extracochlear electrically evoked otoacoustic emissions: a model for in vivo assessment of outer hair cell electromotility
inferred← citeshttps://doi.org/10.1016/0378-5955(96)00026-3openalex-snapshot
Effect of acetylcholine and GABA on the transfer function of electromotility in isolated outer hair cells
inferred← citeshttps://doi.org/10.1016/0378-5955(96)00070-6openalex-snapshot
Time-varying alterations in the f2-f1 DPOAE response to continuous primary stimulation II. Influence of local calcium-dependent mechanisms
inferred← citeshttps://doi.org/10.1016/0378-5955(96)00082-2openalex-snapshot
Frequency response for electromotility of isolated outer hair cells of the guinea pig
inferred← citeshttps://doi.org/10.1016/b978-0-08-057455-4.50062-1openalex-snapshot
Acoustic Transduction
inferred← citeshttps://doi.org/10.1016/b978-0-12-387738-3.00037-8openalex-snapshot
Acoustic Transduction
inferred← citeshttps://doi.org/10.1016/b978-0-12-804042-3.00010-5openalex-snapshot
Evolutionary Trends in Land Vertebrate Hearing Organs
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.24192-8openalex-snapshot
Genetics of Mechanoreceptor Evolution and Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.24221-1openalex-snapshot
Anatomy and Biophysics of Sensory Cells
inferred← citeshttps://doi.org/10.1016/b978-0-323-05283-2.00147-6openalex-snapshot
Cochlear Transduction and the Molecular Basis of Auditory Pathology
inferred← citeshttps://doi.org/10.1016/b978-012370880-9.00006-2openalex-snapshot
Genetics of Mechanoreceptor Evolution and Development
inferred← citeshttps://doi.org/10.1016/b978-012370880-9.00012-8openalex-snapshot
Molecular Anatomy of Receptor Cells and Organ of Corti
inferred← citeshttps://doi.org/10.1016/b978-012656976-6/50138-4openalex-snapshot
Acoustic Transduction
inferred← citeshttps://doi.org/10.1016/b978-1-4557-4696-5.00146-9openalex-snapshot
10.1016/b978-1-4557-4696-5.00146-9
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.05.014openalex-snapshot
Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 gene
inferred← citeshttps://doi.org/10.1016/j.bpj.2009.12.4097openalex-snapshot
Structural Rearrangements of the Motor Protein Prestin Revealed by Fluorescence Resonance Energy Transfer
inferred← citeshttps://doi.org/10.1016/j.bpj.2011.12.040openalex-snapshot
Outer Hair Cell Somatic Electromotility In Vivo and Power Transfer to the Organ of Corti
inferred← citeshttps://doi.org/10.1016/j.bpj.2013.06.049openalex-snapshot
Detection of Cochlear Amplification and Its Activation
inferred← citeshttps://doi.org/10.1016/j.bpj.2013.11.021openalex-snapshot
Non-uniform Distribution of Outer Hair Cell Transmembrane Potential Induced by Extracellular Electric Field
inferred← citeshttps://doi.org/10.1016/j.bpj.2014.05.018openalex-snapshot
Chloride-driven Electromechanical Phase Lags at Acoustic Frequencies Are Generated by SLC26a5, the Outer Hair Cell Motor Protein
inferred← citeshttps://doi.org/10.1016/j.bpj.2016.05.002openalex-snapshot
Chloride Anions Regulate Kinetics but Not Voltage-Sensor Q max of the Solute Carrier SLC26a5
inferred← citeshttps://doi.org/10.1016/j.bpj.2017.12.005openalex-snapshot
Forward and Reverse Waves: Modeling Distortion Products in the Intracochlear Fluid Pressure
inferred← citeshttps://doi.org/10.1016/j.bpj.2020.06.011openalex-snapshot
Interactions between Passive and Active Vibrations in the Organ of Corti In Vitro
inferred← citeshttps://doi.org/10.1016/j.compbiomed.2009.06.010openalex-snapshot
An adaptive model simulating the somatic motility and the active hair bundle motion of the OHC
inferred← citeshttps://doi.org/10.1016/j.compbiomed.2021.104756openalex-snapshot
Time-domain analysis of a three-dimensional numerical model of the human spiral cochlea at medium intensity
inferred← citeshttps://doi.org/10.1016/j.compstruc.2007.01.003openalex-snapshot
A coupled boundary element/finite difference method for fluid–structure interaction with application to dynamic analysis of outer hair cells
inferred← citeshttps://doi.org/10.1016/j.heares.2004.08.016openalex-snapshot
Mechanisms of noise-induced hearing loss potentiation by hypoxia
inferred← citeshttps://doi.org/10.1016/j.heares.2004.11.002openalex-snapshot
Spatial distribution of electrically induced high frequency vibration on basilar membrane
inferred← citeshttps://doi.org/10.1016/j.heares.2006.01.018openalex-snapshot
Fast cochlear amplification with slow outer hair cells
inferred← citeshttps://doi.org/10.1016/j.heares.2007.05.012openalex-snapshot
Contribution of outer hair cell bending to stereocilium deflection in the cochlea
inferred← citeshttps://doi.org/10.1016/j.heares.2009.05.001openalex-snapshot
Central auditory plasticity after carboplatin-induced unilateral inner ear damage in the chinchilla: Up-regulation of GAP-43 in the ventral cochlear nucleus
inferred← citeshttps://doi.org/10.1016/j.heares.2009.10.005openalex-snapshot
Multiple roles for the tectorial membrane in the active cochlea
inferred← citeshttps://doi.org/10.1016/j.heares.2010.03.094openalex-snapshot
Somatic motility and hair bundle mechanics, are both necessary for cochlear amplification?
inferred← citeshttps://doi.org/10.1016/j.heares.2010.05.001openalex-snapshot
The remarkable cochlear amplifier
inferred← citeshttps://doi.org/10.1016/j.heares.2011.05.013openalex-snapshot
Motile responses of cochlear outer hair cells stimulated with an alternating electrical field
inferred← citeshttps://doi.org/10.1016/j.heares.2012.04.017openalex-snapshot
Von Békésy and cochlear mechanics
inferred← citeshttps://doi.org/10.1016/j.heares.2013.05.002openalex-snapshot
Up-regulation of GAP-43 in the chinchilla ventral cochlear nucleus after carboplatin-induced hearing loss: Correlations with inner hair cell loss and outer hair cell loss
inferred← citeshttps://doi.org/10.1016/j.heares.2013.12.002openalex-snapshot
Prestin at year 14: Progress and prospect
inferred← citeshttps://doi.org/10.1016/j.heares.2026.109578openalex-snapshot
Recovery patterns and influencing factors of temporary threshold shifts in occupational noise-exposed workers
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2006.05.009openalex-snapshot
A two-layer outer hair cell model with orthotropic piezoelectric properties: Correlation of cell resonant frequencies with tuning in the cochlea
inferred← citeshttps://doi.org/10.1016/j.mcn.2022.103732openalex-snapshot
Signatures of cochlear processing in neuronal coding of auditory information
inferred← citeshttps://doi.org/10.1016/j.medengphy.2007.03.002openalex-snapshot
Physiologically inspired signal preprocessing for auditory prostheses: Insights from the electro-motility of the OHC
inferred← citeshttps://doi.org/10.1016/j.medengphy.2011.07.009openalex-snapshot
An adaptive panoramic filter bank as a qualitative model of the filtering system of the cochlea: The peculiarities in linear and nonlinear mode
inferred← citeshttps://doi.org/10.1016/j.neulet.2006.05.059openalex-snapshot
Effects of tarantula toxin GsMTx4 on the membrane motor of outer hair cells
inferred← citeshttps://doi.org/10.1016/j.neulet.2015.09.001openalex-snapshot
Metabolomic profiling in inner ear fluid by gas chromatography/mass spectrometry in guinea pig cochlea
inferred← citeshttps://doi.org/10.1016/j.neuron.2005.10.017openalex-snapshot
Hair-Cell Mechanotransduction and Cochlear Amplification
inferred← citeshttps://doi.org/10.1016/j.neuron.2008.07.012openalex-snapshot
Making an Effort to Listen: Mechanical Amplification in the Ear
inferred← citeshttps://doi.org/10.1016/j.neuron.2011.06.002openalex-snapshot
Pushing the Envelope of Sound
inferred← citeshttps://doi.org/10.1016/s0006-3495(00)76437-xopenalex-snapshot
Fluctuation of Motor Charge in the Lateral Membrane of the Cochlear Outer Hair Cell
inferred← citeshttps://doi.org/10.1016/s0006-3495(00)76775-0openalex-snapshot
Three-Dimensional Motion of the Organ of Corti
inferred← citeshttps://doi.org/10.1016/s0006-3495(01)75895-xopenalex-snapshot
A Two-State Piezoelectric Model for Outer Hair Cell Motility
inferred← citeshttps://doi.org/10.1016/s0006-3495(97)78174-8openalex-snapshot
Mapping the distribution of outer hair cell voltage-dependent conductances by electrical amputation
inferred← citeshttps://doi.org/10.1016/s0006-3495(97)78198-0openalex-snapshot
Cochlear outer hair cell bending in an external electric field
inferred← citeshttps://doi.org/10.1016/s0006-3495(97)78325-5openalex-snapshot
Current noise spectrum and capacitance due to the membrane motor of the outer hair cell: theory
inferred← citeshttps://doi.org/10.1016/s0006-8993(01)02806-2openalex-snapshot
Tetraethylammonium ions block the nicotinic cholinergic receptors of cochlear outer hair cells
inferred← citeshttps://doi.org/10.1016/s0006-8993(99)02227-1openalex-snapshot
Olivocochlear efferent vs. middle-ear contributions to the alteration of otoacoustic emissions by contralateral noise
inferred← citeshttps://doi.org/10.1016/s0026-895x(24)23062-5openalex-snapshot
Memantine Inhibits Efferent Cholinergic Transmission in the Cochlea by Blocking Nicotinic Acetylcholine Receptors of Outer Hair Cells
inferred← citeshttps://doi.org/10.1016/s0165-0173(99)00077-6openalex-snapshot
Cell coupling in Corti's organ
inferred← citeshttps://doi.org/10.1016/s0165-0270(00)00322-8openalex-snapshot
A technique for slicing the rat cochlea around the onset of hearing
inferred← citeshttps://doi.org/10.1016/s0166-2236(97)01192-2openalex-snapshot
How well do we understand the cochlea?
inferred← citeshttps://doi.org/10.1016/s0194-5998(98)70167-6openalex-snapshot
Contribution of membrane cholesterol to outer hair cell lateral wall stiffness
inferred← citeshttps://doi.org/10.1016/s0306-4522(97)00163-2openalex-snapshot
Localization of proteins associated with the outer hair cell plasma membrane in the gerbil cochlea
inferred← citeshttps://doi.org/10.1016/s0378-5955(00)00012-5openalex-snapshot
Evidence for active, nonlinear, negative feedback in the vibration response of the apical region of the in-vivo guinea-pig cochlea
inferred← citeshttps://doi.org/10.1016/s0378-5955(00)00238-0openalex-snapshot
Electrically evoked otoacoustic emissions from apical and basal perilymphatic electrode positions in the guinea pig cochlea
inferred← citeshttps://doi.org/10.1016/s0378-5955(01)00355-0openalex-snapshot
Distribution of protein motors along the lateral wall of the outer hair cell
inferred← citeshttps://doi.org/10.1016/s0378-5955(01)00363-xopenalex-snapshot
Effects of 4-aminopyridine on electrically evoked cochlear emissions and mechano-transduction in guinea pig outer hair cells
inferred← citeshttps://doi.org/10.1016/s0378-5955(01)00425-7openalex-snapshot
Partial recovery of cisplatin-induced hearing loss in the albino guinea pig in relation to cisplatin dose
inferred← citeshttps://doi.org/10.1016/s0378-5955(02)00745-1openalex-snapshot
Effect of click intensity on click-evoked otoacoustic emission waveforms: implications for the origin of emissions
inferred← citeshttps://doi.org/10.1016/s0378-5955(03)00192-8openalex-snapshot
Expression of prestin, a membrane motor protein, in the mammalian auditory and vestibular periphery
inferred← citeshttps://doi.org/10.1016/s0378-5955(96)00087-1openalex-snapshot
The early postnatal development of F-actin patterns in the organ of Corti of the gerbil (Meriones unguiculatus) and the horseshoe bat (Rhinolophus rouxi)
inferred← citeshttps://doi.org/10.1016/s0378-5955(96)00154-2openalex-snapshot
Effects of aging on potassium homeostasis and the endocochlear potential in the gerbil cochlea
inferred← citeshttps://doi.org/10.1016/s0378-5955(97)00011-7openalex-snapshot
Acoustic and electric forward-masking of the auditory nerve compound action potential: evidence for linearity of electro-mechanical transduction
inferred← citeshttps://doi.org/10.1016/s0378-5955(97)00070-1openalex-snapshot
Spontaneous otoacoustic emissions in the barn owl
inferred← citeshttps://doi.org/10.1016/s0378-5955(97)00086-5openalex-snapshot
Calmodulin-dependent protein kinases mediate calcium-induced slow motility of mammalian outer hair cells
inferred← citeshttps://doi.org/10.1016/s0378-5955(99)00029-5openalex-snapshot
Responses of auditory nerve fibers innervating regenerated hair cells after local application of gentamicin at the round window of the cochlea in the pigeon
inferred← citeshttps://doi.org/10.1016/s0378-5955(99)00031-3openalex-snapshot
The effect of quinine on outer hair cell shape, compliance and force
inferred← citeshttps://doi.org/10.1016/s0959-4388(03)00100-4openalex-snapshot
New tunes from Corti’s organ: the outer hair cell boogie rules
inferred← citeshttps://doi.org/10.1016/s0959-4388(97)80026-8openalex-snapshot
Mechanical amplification of stimuli by hair cells
inferred← citeshttps://doi.org/10.1016/s0959-4388(98)80033-0openalex-snapshot
Phylogenetic development of the cochlea and its innervation
inferred← citeshttps://doi.org/10.1016/s0960-9822(99)80358-3openalex-snapshot
Cochlear function: Hearing in the fast lane
inferred← citeshttps://doi.org/10.1016/s1672-2930(14)50017-7openalex-snapshot
The Cochlear Amplifier: Is it Hair Bundle Motion of Outer Hair Cells?
inferred← citeshttps://doi.org/10.1021/jm000493iopenalex-snapshot
Molecular Modeling Studies of the Akt PH Domain and Its Interaction with Phosphoinositides
inferred← citeshttps://doi.org/10.1023/a:1007002916772openalex-snapshot
Molecular characterization of anion exchangers in the cochlea
inferred← citeshttps://doi.org/10.1023/a:1007076007642openalex-snapshot
Phosphate activated glutaminase is concentrated in mitochondria of sensory hair cells in rat inner ear: a high resolution immunogold study
inferred← citeshttps://doi.org/10.1038/10197openalex-snapshot
Timing of cochlear feedback: spatial and temporal representation of a tone across the basilar membrane
inferred← citeshttps://doi.org/10.1038/11174openalex-snapshot
A sugar transporter as a candidate for the outer hair cell motor
inferred← citeshttps://doi.org/10.1038/12230openalex-snapshot
Erratum: Timing of cochlear feedback: spatial and temporal representation of a tone across the basilar membrane
inferred← citeshttps://doi.org/10.1038/20686openalex-snapshot
Auditory collusion and a coupled couple of outer hair cells
inferred← citeshttps://doi.org/10.1038/35012009openalex-snapshot
Prestin is the motor protein of cochlear outer hair cells
inferred← citeshttps://doi.org/10.1038/37968openalex-snapshot
An intrinsic frequency limit to the cochlear amplifier
inferred← citeshttps://doi.org/10.1038/ncomms14530openalex-snapshot
A connexin30 mutation rescues hearing and reveals roles for gap junctions in cochlear amplification and micromechanics
inferred← citeshttps://doi.org/10.1038/nn1509openalex-snapshot
Motility-associated hair-bundle motion in mammalian outer hair cells
inferred← citeshttps://doi.org/10.1038/s41598-017-12411-6openalex-snapshot
Negative membrane capacitance of outer hair cells: electromechanical coupling near resonance
inferred← citeshttps://doi.org/10.1038/s41598-018-28958-xopenalex-snapshot
Transgenic Tmc2 expression preserves inner ear hair cells and vestibular function in mice lacking Tmc1
inferred← citeshttps://doi.org/10.1038/s41598-020-73873-9openalex-snapshot
A role for tectorial membrane mechanics in activating the cochlear amplifier
inferred← citeshttps://doi.org/10.1038/srep17792openalex-snapshot
Pseudo-immortalization of postnatal cochlear progenitor cells yields a scalable cell line capable of transcriptionally regulating mature hair cell genes
inferred← citeshttps://doi.org/10.1038/srep39116openalex-snapshot
High-order synchronization of hair cell bundles
inferred← citeshttps://doi.org/10.1039/c1sm05120bopenalex-snapshot
Hair cell inspired mechanotransduction with a gel-supported, artificial lipid membrane
inferred← citeshttps://doi.org/10.1044/hhdc12.2.11openalex-snapshot
Outer Hair Cells, Cochlear Mechanical Amplification, Otoacoustic Emissions, and the Cochlear Microphonic
inferred← citeshttps://doi.org/10.1046/j.0953-816x.2001.01826.xopenalex-snapshot
The voltage‐sensitive motor protein and the Ca2+‐sensitive cytoskeleton in developing rat cochlear outer hair cells
inferred← citeshttps://doi.org/10.1063/1.3658082openalex-snapshot
Outer Hair Cell Electromotility in vivo
inferred← citeshttps://doi.org/10.1063/1.4939340openalex-snapshot
The basilar membrane acts as a passive support structure at the cochlear apex
inferred← citeshttps://doi.org/10.1063/1.5038450openalex-snapshot
Cochlear partition tuning within the 2nd apical turn of the intact gerbil cochlea
inferred← citeshttps://doi.org/10.1063/1.5038499openalex-snapshot
Roles for gap-junctions in cochlear amplification and micromechanics exposed by a conexin 30 mutation
inferred← citeshttps://doi.org/10.1063/5.0010802openalex-snapshot
Balance in the feedback loop components of the mammalian cochlear amplifier
inferred← citeshttps://doi.org/10.1063/5.0189846openalex-snapshot
Two operating modes for outer hair cells and implications for cochlear tuning
inferred← citeshttps://doi.org/10.1073/pnas.0408232101openalex-snapshot
Vibration pattern of the organ of Corti up to 50 kHz: Evidence for resonant electromechanical force
inferred← citeshttps://doi.org/10.1073/pnas.041604998openalex-snapshot
In vivo evidence for a cochlear amplifier in the hair-cell bundle of lizards
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.052609899openalex-snapshot
Thyroid hormone is a critical determinant for the regulation of the cochlear motor protein prestin
inferred← citeshttps://doi.org/10.1073/pnas.0700356104openalex-snapshot
Prestin-based outer hair cell electromotility in knockin mice does not appear to adjust the operating point of a cilia-based amplifier
inferred← citeshttps://doi.org/10.1073/pnas.071613498openalex-snapshot
Reciprocal electromechanical properties of rat prestin: The motor molecule from rat outer hair cells
inferred← citeshttps://doi.org/10.1073/pnas.1302911110openalex-snapshot
Effects of cochlear loading on the motility of active outer hair cells
inferred← citeshttps://doi.org/10.1073/pnas.2025206118openalex-snapshot
Cochlear outer hair cell electromotility enhances organ of Corti motion on a cycle-by-cycle basis at high frequencies in vivo
inferred← citeshttps://doi.org/10.1073/pnas.210389497openalex-snapshot
Negative hair-bundle stiffness betrays a mechanism for mechanical amplification by the hair cell
inferred← citeshttps://doi.org/10.1073/pnas.2217891120openalex-snapshot
Prestin’s fast motor kinetics is essential for mammalian cochlear amplification
inferred← citeshttps://doi.org/10.1073/pnas.93.16.8727openalex-snapshot
Resonant tectorial membrane motion in the inner ear: its crucial role in frequency tuning.
inferred← citeshttps://doi.org/10.1073/pnas.94.26.14450openalex-snapshot
Otogelin: A glycoprotein specific to the acellular membranes of the inner ear
inferred← citeshttps://doi.org/10.1073/pnas.96.13.7244openalex-snapshot
Electrically driven motor in the outer hair cell: Effect of a mechanical constraint
inferred← citeshttps://doi.org/10.1073/pnas.96.14.8223openalex-snapshot
Somatic stiffness of cochlear outer hair cells is voltage-dependent
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1073/pnas.96.8.4420openalex-snapshot
Limiting dynamics of high-frequency electromechanical transduction of outer hair cells
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/10.1073/pnas.97.22.11759openalex-snapshot
Molecular mechanisms of sound amplification in the mammalian cochlea
inferred← citeshttps://doi.org/10.1080/14992020500190201openalex-snapshot
The effect of impulse noise on distortion product otoacoustic emissions
inferred← citeshttps://doi.org/10.1080/14992027.2018.1534010openalex-snapshot
Effects of noise exposure on auditory brainstem response and speech-in-noise tasks: a review of the literature
inferred← citeshttps://doi.org/10.1085/jgp.201812280openalex-snapshot
Outer hair cell electromotility is low-pass filtered relative to the molecular conformational changes that produce nonlinear capacitance
inferred← citeshttps://doi.org/10.1086/377052openalex-snapshot
Snake Bioacoustics: Toward a Richer Understanding of the Behavioral Ecology of Snakes
inferred← citeshttps://doi.org/10.1088/1748-3182/2/4/s05openalex-snapshot
Micromachined biomimetic artificial haircell sensors
inferred← citeshttps://doi.org/10.1088/1748-3190/11/3/036008openalex-snapshot
Toward cell-inspired materials that feel: measurements and modeling of mechanotransduction in droplet-based, multi-membrane arrays
inferred← citeshttps://doi.org/10.1091/mbc.9.8.1961openalex-snapshot
The Membrane-based Mechanism of Cell Motility in Cochlear Outer Hair Cells
inferred← citeshttps://doi.org/10.1093/brain/123.1.82openalex-snapshot
The spectrum of hearing loss due to mitochondrial DNA defects
inferred← citeshttps://doi.org/10.1093/hmg/12.6.631openalex-snapshot
LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice
inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190849061.013.3openalex-snapshot
Efferent Innervation to the Cochlea
inferred← citeshttps://doi.org/10.1097/00003446-200202000-00004openalex-snapshot
What Drives Mechanical Amplification in the Mammalian Cochlea?
inferred← citeshttps://doi.org/10.1097/01.gim.0000237781.10594.d1openalex-snapshot
Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy
inferred← citeshttps://doi.org/10.1097/aud.0000000000000947openalex-snapshot
Effective Masking Levels for Bone Conduction Auditory Brainstem Response Stimuli in Infants and Adults with Normal Hearing
inferred← citeshttps://doi.org/10.1097/wnr.0b013e3282ff84e8openalex-snapshot
Voltage-dependent outer hair cell stereocilia stiffness at acoustic frequencies
inferred← citeshttps://doi.org/10.1098/rsif.2008.0201openalex-snapshot
Three-dimensional current flow in a large-scale model of the cochlea and the mechanism of amplification of sound
inferred← citeshttps://doi.org/10.1101/2020.01.03.893933openalex-snapshot
Active outer hair cell motility can suppress vibrations in the organ of Corti
inferred← citeshttps://doi.org/10.1101/2022.02.02.478769openalex-snapshot
The outer-hair-cell RC time constant: A feature, not a bug, of the mammalian cochlea
inferred← citeshttps://doi.org/10.1109/jmems.2010.2076778openalex-snapshot
Bioinspired 3-D Tactile Sensor for Minimally Invasive Surgery
inferred← citeshttps://doi.org/10.1109/jssc.2009.2020465openalex-snapshot
A Bio-Inspired Active Radio-Frequency Silicon Cochlea
inferred← citeshttps://doi.org/10.1109/spawda.2019.8681789openalex-snapshot
Simulation of Outer Hair Cell Electromotility due to Flexoelectricity
inferred← citeshttps://doi.org/10.1111/ejn.13209openalex-snapshot
The chloride‐channel blocker 9‐anthracenecarboxylic acid reduces the nonlinear capacitance of prestin‐associated charge movement
inferred← citeshttps://doi.org/10.1111/j.1365-2273.2004.00769.xopenalex-snapshot
The MELAS syndrome. Review of the literature: the role of the otologist
inferred← citeshttps://doi.org/10.1111/j.1460-9568.2006.04796.xopenalex-snapshot
Membrane traffic in outer hair cells of the adult mammalian cochlea
inferred← citeshttps://doi.org/10.1111/j.1469-7793.1999.0791n.xopenalex-snapshot
Expression density and functional characteristics of the outer hair cell motor protein are regulated during postnatal development in rat
inferred← citeshttps://doi.org/10.1111/j.1749-6632.1996.tb15703.xopenalex-snapshot
Determinants of Semicircular Canal Afferent Response Dynamics in Fisha
inferred← citeshttps://doi.org/10.1113/jp288299openalex-snapshot
High‐frequency electrical tuning and linear filter properties of Knollenorgan electroreceptors of mormyrid electric fish
inferred← citeshttps://doi.org/10.1113/jphysiol.1996.sp021715openalex-snapshot
Differential expression of outer hair cell potassium currents in the isolated cochlea of the guinea‐pig.
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