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Helmholtz's Piano Strings: Reverberation of Ripples on the Tectorial Membrane

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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DIPLACUSIS: A LOCALIZING SYMPTOM OF DISEASE OF THE ORGAN OF CORTI: THEORETIC CONSIDERATIONS, CLINICAL OBSERVATIONS AND PRACTICAL APPLICATION

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Cellular Pattern and Nerve Supply of the Human Organ of Corti: A Preliminary Report

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Lehrbuch der Ohrenheilkunde.

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On the nature of the tectorial membrane and its probable role in the anatomy of hearing

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Theory of phase transition in polymer gels

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Physiology of Olivocochlear Efferents

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Analysis and Synthesis of Cochlear Mechanical Function Using Models

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The Curious Half-Octave Shift: Evidence for a Basalward Migration of the Traveling-Wave Envelope with Increasing Intensity

inferredcites →https://doi.org/10.1007/978-1-4684-5640-0_34openalex-extracted

Historical Background to the Proposal, 40 Years Ago, of an Active Model for Cochlear Frequency Analysis

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Modelling Cochlear Echoes: The Influence of Irregularities in Frequency Mapping on Summed Cochlear Activity

inferredcites →https://doi.org/10.1007/bf00375096openalex-extracted

Forces involved in length changes of cochlear outer hair cells

inferredcites →https://doi.org/10.1007/bfb0024050openalex-extracted

Rubber elasticity of polymer networks: Theories

inferredcites →https://doi.org/10.1016/0024-3205(63)90016-xopenalex-extracted

The transmission of acoustic energy from air to the receptor organ in the cochlea

inferredcites →https://doi.org/10.1016/0304-3940(83)90051-4openalex-extracted

Sound emission from the ear triggered by single molecules?

inferredcites →https://doi.org/10.1016/0370-1573(80)90100-3openalex-extracted

Auditory physics. Physical principles in hearing theory. I

inferredcites →https://doi.org/10.1016/0370-1573(84)90108-xopenalex-extracted

Auditory physics. Physical principles in hearing theory. II

inferredcites →https://doi.org/10.1016/0370-1573(91)90068-wopenalex-extracted

Auditory physics. Physical principles in hearing theory. III

inferredcites →https://doi.org/10.1016/0375-9601(84)90371-2openalex-extracted

Quantum limits to oscillator stability: Theory and experiments on acoustic emissions from the human ear

inferredcites →https://doi.org/10.1016/0378-5955(80)90057-xopenalex-extracted

Intracochlear sound pressure measurements in guinea pigs

inferredcites →https://doi.org/10.1016/0378-5955(80)90060-xopenalex-extracted

Evidence for a cochlear origin for acoustic re-emissions, threshold fine-structure and tonal tinnitus

inferredcites →https://doi.org/10.1016/0378-5955(80)90061-1openalex-extracted

Evoked acoustical responses from the human ear: Some experimental results

inferredcites →https://doi.org/10.1016/0378-5955(80)90090-8openalex-extracted

Model for cochlear echoes and tinnitus based on an observed electrical correlate

inferredcites →https://doi.org/10.1016/0378-5955(81)90054-xopenalex-extracted

Energy transduction in the cochlea

inferredcites →https://doi.org/10.1016/0378-5955(83)90035-7openalex-extracted

The tectorial membrane of mammals

inferredcites →https://doi.org/10.1016/0378-5955(83)90136-3openalex-extracted

An active process in cochlear mechanics

inferredcites →https://doi.org/10.1016/0378-5955(84)90116-3openalex-extracted

Interactions among spontaneous otoacoustic emissions. I. Distortion products and linked emissions

inferredcites →https://doi.org/10.1016/0378-5955(85)90138-8openalex-extracted

Intermodulation distortion in the cochlea: could basal vibration be the major cause of round window CM distortion?

inferredcites →https://doi.org/10.1016/0378-5955(88)90021-4openalex-extracted

Spontaneous otoacoustic emissions in a nonhuman primate. II. Cochlear anatomy

inferredcites →https://doi.org/10.1016/0378-5955(94)90048-5openalex-extracted

Tuned hair cells for hearing, but tuned basilar membrane for overload protection: Evidence from dolphins, bats, and desert rodents

inferredcites →https://doi.org/10.1016/0378-5955(94)90166-xopenalex-extracted

On the shape of (evoked) otoacoustic emission spectra

inferredcites →https://doi.org/10.1016/0378-5955(96)00006-8openalex-extracted

Further studies on the mechanics of the cochlear partition in the mustached bat. II. A second cochlear frequency map derived from acoustic distortion products

inferredcites →https://doi.org/10.1016/0378-5955(96)00056-1openalex-extracted

Distortion product otoacoustic emission suppression tuning curves in human adults and neonates

inferredcites →https://doi.org/10.1016/0378-5955(96)00117-7openalex-extracted

Postnatal changes in the reticular lamina of the guinea pig organ of Corti

inferredcites →https://doi.org/10.1016/b978-0-08-041847-6.50011-3openalex-extracted

Correlation Between the Length of Outer Hair Cells and the Frequency Coding of the Cochlea

inferredcites →https://doi.org/10.1016/b978-0-12-504250-5.50006-0openalex-extracted

COCHLEAR NONLINEARITIES

inferredcites →https://doi.org/10.1016/s0079-6123(08)63028-9openalex-extracted

Chapter 34 Do sensory cells in the ear have a motile function?

inferredcites →https://doi.org/10.1016/s0166-2236(97)01192-2openalex-extracted

How well do we understand the cochlea?

inferredcites →https://doi.org/10.1016/s0378-5955(00)00041-1openalex-extracted

Deformations of the isolated mouse tectorial membrane produced by oscillatory forces

inferredcites →https://doi.org/10.1016/s0378-5955(97)00147-0openalex-extracted

Basilar membrane velocity noise

inferredcites →https://doi.org/10.1016/s0378-5955(97)00160-3openalex-extracted

Frequency spacing of multiple spontaneous otoacoustic emissions shows relation to critical bands: a large-scale cumulative study

inferredcites →https://doi.org/10.1016/s0378-5955(98)00133-6openalex-extracted

Measurements of the stiffness map challenge a basic tenet of cochlear theories

inferredcites →https://doi.org/10.1016/s0378-5955(99)00009-xopenalex-extracted

The radial pattern of basilar membrane motion evoked by electric stimulation of the cochlea

inferredcites →https://doi.org/10.1017/s0033291700021735openalex-extracted

Handbook of Psychopharmacology. Edited by L. L. Iversen, S. D. Iversen and S. H. Snyder. Plenum Press: New York. 1978. - Volume 7Principles of Behavioral Pharmacology. (Pp. 453; illustrated; $34.50.) Plenum Press: New York. 1978. - Volume 8Drugs, Neurotransmitters, and Behavior. (Pp. 590;…

inferredcites →https://doi.org/10.1021/la00013a009openalex-extracted

Rheological study of ternary cubic phases

inferredcites →https://doi.org/10.1038/10197openalex-extracted

Timing of cochlear feedback: spatial and temporal representation of a tone across the basilar membrane

inferredcites →https://doi.org/10.1038/221935a0openalex-extracted

Is Resonance Possible in the Cochlea After All?

inferredcites →https://doi.org/10.1038/322365a0openalex-extracted

Electrokinetic shape changes of cochlear outer hair cells

inferredcites →https://doi.org/10.1038/335635a0openalex-extracted

A cytoskeletal spring in cochlear outer hair cells

inferredcites →https://doi.org/10.1038/375585a0openalex-extracted

Elevation of auditory thresholds by spontaneous cochlear oscillations

inferredcites →https://doi.org/10.1038/990092openalex-extracted

Direct measurement of intra-cochlear pressure waves

inferredcites →https://doi.org/10.1046/j.1460-9568.1998.00188.xopenalex-extracted

Direct evidence of cubic difference tone propagation by intracochlear acoustic pressure measurements in the guinea‐pig

inferredcites →https://doi.org/10.1073/pnas.90.18.8347openalex-extracted

Stereocilia displacement induced somatic motility of cochlear outer hair cells.

inferredcites →https://doi.org/10.1073/pnas.94.6.2660openalex-extracted

The location of the cochlear amplifier: Spatial representation of a single tone on the guinea pig basilar membrane

inferredcites →https://doi.org/10.1080/00016489.1992.11665413openalex-extracted

Stiffness, Compliance, Elasticity and Force Generation of Outer Hair Cells

inferredcites →https://doi.org/10.1093/oso/9780195069402.001.0001openalex-extracted

Acoustic Systems In Biology

inferredcites →https://doi.org/10.1098/rspb.1948.0024openalex-extracted

Hearing. I. The cochlea as a frequency analyzer

inferredcites →https://doi.org/10.1098/rspb.1948.0025openalex-extracted

Hearing. II. The physical basis of the action of the cochlea

inferredcites →https://doi.org/10.1098/rspb.1992.0126openalex-extracted

Mechanical filtering of sound in the inner ear

inferredcites →https://doi.org/10.1101/sqb.1965.030.01.019openalex-extracted

Some New Proposals Regarding Acoustic Transmission and Transduction

inferredcites →https://doi.org/10.1103/physrevlett.54.725openalex-extracted

Quantum Noise and the Threshold of Hearing

inferredcites →https://doi.org/10.1109/proc.1976.10200openalex-extracted

Surface-acoustic-wave resonators

inferredcites →https://doi.org/10.1109/proc.1976.10202openalex-extracted

Acoustoelectric interactions in acoustic-surface-wave devices

inferredcites →https://doi.org/10.1115/1.2930149openalex-extracted

Biomechanics of Hearing Sensitivity

inferredcites →https://doi.org/10.1121/1.1314396openalex-extracted

Effect of turgor pressure on outer hair cell motility

inferredcites →https://doi.org/10.1121/1.1906615openalex-extracted

A Dynamical Theory of the Cochlea

inferredcites →https://doi.org/10.1121/1.1906628openalex-extracted

The Acoustic Pathways to the Cochlea

inferredcites →https://doi.org/10.1121/1.1910396openalex-extracted

Auditory Nonlinearity

inferredcites →https://doi.org/10.1121/1.1912163openalex-extracted

Low-Frequency Auditory Characteristics: Species Dependence

inferredcites →https://doi.org/10.1121/1.382104openalex-extracted

Stimulated acoustic emissions from within the human auditory system

inferredcites →https://doi.org/10.1121/1.383064openalex-extracted

Cochlear macromechanics: Time domain solutions

inferredcites →https://doi.org/10.1121/1.385198openalex-extracted

Cochlear micromechanics—A physical model of transduction

inferredcites →https://doi.org/10.1121/1.394389openalex-extracted

Basilar membrane mechanics at the base of the chinchilla cochlea. I. Input–output functions, tuning curves, and response phases

inferredcites →https://doi.org/10.1121/1.396515openalex-extracted

Suppression tuning curves for spontaneous otoacoustic emissions in infants and adults

inferredcites →https://doi.org/10.1121/1.397728openalex-extracted

Acoustic distortion products in humans: Systematic changes in amplitude as a function of f2/f1 ratio

inferredcites →https://doi.org/10.1121/1.400897openalex-extracted

A review of otoacoustic emissions

inferredcites →https://doi.org/10.1121/1.403931openalex-extracted

An empirical bound on the compressibility of the cochlea

inferredcites →https://doi.org/10.1121/1.412994openalex-extracted

Distortion product otoacoustic emission delay measurement in human ears

inferredcites →https://doi.org/10.1121/1.413746openalex-extracted

The equality of volume displacements in the inner ear windows

inferredcites →https://doi.org/10.1121/1.414680openalex-extracted

Spontaneous otoacoustic emissions in two gecko species, Gekko gecko and Eublepharis macularius

inferredcites →https://doi.org/10.1121/1.416062openalex-extracted

Is the pressure difference between the oval and round windows the effective acoustic stimulus for the cochlea?

inferredcites →https://doi.org/10.1121/1.420389openalex-extracted

Surface wave formation at an impedance discontinuity

inferredcites →https://doi.org/10.1121/1.421377openalex-extracted

Basilar-membrane responses to clicks at the base of the chinchilla cochlea

inferredcites →https://doi.org/10.1121/1.423083openalex-extracted

Observing middle and inner ear mechanics with novel intracochlear pressure sensors

inferredcites →https://doi.org/10.1121/1.428648openalex-extracted

Auditory-nerve-fiber responses to high-level clicks: Interference patterns indicate that excitation is due to the combination of multiple drives

inferredcites →https://doi.org/10.1121/1.429404openalex-extracted

Study of mechanical motions in the basal region of the chinchilla cochlea

inferredcites →https://doi.org/10.1126/science.282.5395.1882openalex-extracted

Frequency Tuning of Basilar Membrane and Auditory Nerve Fibers in the Same Cochleae

inferredcites →https://doi.org/10.1126/science.7701325openalex-extracted

High-Frequency Motility of Outer Hair Cells and the Cochlear Amplifier

inferredcites →https://doi.org/10.1152/jn.1999.82.2.676openalex-extracted

Micromechanical Responses to Tones in the Auditory Fovea of the Greater Mustached Bat’s Cochlea

inferredcites →https://doi.org/10.1159/000013830openalex-extracted

Intracochlear Acoustic Pressure Measurements: Transfer Functions of the Middle Ear and Cochlear Mechanics

inferredcites →https://doi.org/10.21236/ada109430openalex-extracted

Potential for Interaction of Low-Level Impulse and Continuous Noise

inferredcites →https://doi.org/10.2307/3363877openalex-extracted

On the Sensations of Tone, as a Physiological Basis for the Theory of Music

inferredcites →https://doi.org/10.3109/00016485909129180openalex-extracted

The Transfer of Energy Across the Cochlea

inferredcites →https://doi.org/10.3109/00016486609127043openalex-extracted

Hairs of the Cochlear Sensory Cells and Their Attachment to the Tectorial Membrane

inferredcites →https://doi.org/10.3109/05384916309101762openalex-extracted

Clinical Observations Concerning the Question on Diplacusis and Echoacusis

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inferred← citeshttps://doi.org/10.1057/9781137027252_13openalex-snapshot

Deleted Expletives: Vibration and the Modernist Vocal Imaginary

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