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Noise-induced and age-related hearing loss: new perspectives and potential therapies

https://doi.org/10.12688/f1000research.11310.1

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What this work says

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

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Intracellular labeling of auditory nerve fibers in guinea pig: central and peripheral projections

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Resprouting and survival of guinea pig cochlear neurons in response to the administration of the neurotrophins brain-derived neurotrophic factor and neurotrophin-3

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The central projections of intracellularly labeled auditory nerve fibers in cats

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Afferent innervation of outer hair cells in adult cats: I. Light microscopic analysis of fibers labeled with horseradish peroxidase

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Afferent and efferent innervation of the cat cochlea: Quantitative analysis with light and electron microscopy

inferredcites →https://doi.org/10.1002/cne.903130205openalex-snapshot

Central projections of auditory‐nerve fibers of differing spontaneous rate. I. Anteroventral cochlear nucleus

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Serial Section Reconstruction of the Neural Poles of Hair Cells in the Human Organ Of Corti. I. Inner Hair Cells

inferredcites →https://doi.org/10.1007/s10162-015-0510-3openalex-snapshot

Dynamics of cochlear synaptopathy after acoustic overexposure

inferredcites →https://doi.org/10.1007/s101620020028openalex-snapshot

Dynamics of Noise-Induced Cellular Injury and Repair in the Mouse Cochlea

inferredcites →https://doi.org/10.1016/0378-5955(80)90007-6openalex-snapshot

Morphological differences among radial afferent fibers in the cat cochlea: An electron-microscopic study of serial sections

inferredcites →https://doi.org/10.1016/0378-5955(83)90031-xopenalex-snapshot

Functional significance of dendritic swelling after loud sounds in the guinea pig cochlea

inferredcites →https://doi.org/10.1016/0378-5955(84)90025-xopenalex-snapshot

Single-neuron labeling and chronic cochlear pathology. III. Stereocilia damage and alterations of threshold tuning curves

inferredcites →https://doi.org/10.1016/0378-5955(85)90006-1openalex-snapshot

Kainic acid selectively alters auditory dendrites connected with cochlear inner hair cells

inferredcites →https://doi.org/10.1016/0378-5955(90)90120-eopenalex-snapshot

Diversity of characteristic frequency rate-intensity functions in guinea pig auditory nerve fibres

inferredcites →https://doi.org/10.1016/0378-5955(95)00158-1openalex-snapshot

Quantitative evaluation of myelinated nerve fibres and hair cells in cochleae of humans with age-related high-tone hearing loss

inferredcites →https://doi.org/10.1016/0959-4388(92)90179-oopenalex-snapshot

Responses to sound of the basilar membrane of the mammalian cochlea

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Calcium, ischemia and excitotoxicity

inferredcites →https://doi.org/10.1016/j.conb.2008.08.016openalex-snapshot

Cochlear amplification, outer hair cells and prestin

inferredcites →https://doi.org/10.1016/j.cub.2015.01.009openalex-snapshot

A Non-canonical Pathway from Cochlea to Brain Signals Tissue-Damaging Noise

inferredcites →https://doi.org/10.1016/j.heares.2006.07.014openalex-snapshot

Synaptic alterations at inner hair cells precede spiral ganglion cell loss in aging C57BL/6J mice

inferredcites →https://doi.org/10.1016/j.heares.2011.05.010openalex-snapshot

Anti-epileptic drugs delay age-related loss of spiral ganglion neurons via T-type calcium channel

inferredcites →https://doi.org/10.1016/j.heares.2013.03.012openalex-snapshot

Insensitivity of the audiogram to carboplatin induced inner hair cell loss in chinchillas

inferredcites →https://doi.org/10.1016/j.heares.2014.09.009openalex-snapshot

Importance of cochlear health for implant function

inferredcites →https://doi.org/10.1016/j.heares.2015.04.014openalex-snapshot

Cochlear neuropathy in human presbycusis: Confocal analysis of hidden hearing loss in post-mortem tissue

inferredcites →https://doi.org/10.1016/j.heares.2016.10.028openalex-snapshot

Effects of noise exposure on young adults with normal audiograms I: Electrophysiology

inferredcites →https://doi.org/10.1016/j.heares.2016.12.010openalex-snapshot

Translational issues in cochlear synaptopathy

inferredcites →https://doi.org/10.1016/j.neuro.2013.11.002openalex-snapshot

Topographic and quantitative evaluation of gentamicin-induced damage to peripheral innervation of mouse cochleae

inferredcites →https://doi.org/10.1016/j.neuron.2012.10.032openalex-snapshot

Notch Inhibition Induces Cochlear Hair Cell Regeneration and Recovery of Hearing after Acoustic Trauma

inferredcites →https://doi.org/10.1017/s0022215100050465openalex-snapshot

An Experimental and Clinical Study of Deafness from Lesions of the Cochlear Nerve

inferredcites →https://doi.org/10.1038/nature03418openalex-snapshot

Hair cell synaptic ribbons are essential for synchronous auditory signalling

inferredcites →https://doi.org/10.1038/srep24907openalex-snapshot

Round-window delivery of neurotrophin 3 regenerates cochlear synapses after acoustic overexposure

inferredcites →https://doi.org/10.1038/srep31754openalex-snapshot

Pathophysiology of the inner ear after blast injury caused by laser-induced shock wave

inferredcites →https://doi.org/10.1073/pnas.1515228112openalex-snapshot

Unmyelinated type II afferent neurons report cochlear damage

inferredcites →https://doi.org/10.1073/pnas.1605737113openalex-snapshot

Hair cells use active zones with different voltage dependence of Ca 2+ influx to decompose sounds into complementary neural codes

inferredcites →https://doi.org/10.1080/14992027.2016.1255359openalex-snapshot

Commentary on the regulatory implications of noise-induced cochlear neuropathy

inferredcites →https://doi.org/10.1093/oxfordjournals.aje.a009713openalex-snapshot

Prevalence of Hearing Loss in Older Adults in Beaver Dam, Wisconsin: The Epidemiology of Hearing Loss Study

inferredcites →https://doi.org/10.1097/aud.0000000000000370openalex-snapshot

Auditory Brainstem Response Altered in Humans With Noise Exposure Despite Normal Outer Hair Cell Function

inferredcites →https://doi.org/10.1097/mao.0000000000000616openalex-snapshot

Otologic Outcomes After Blast Injury

inferredcites →https://doi.org/10.1097/mao.0000000000001191openalex-snapshot

Applying Neurotrophins to the Round Window Rescues Auditory Function and Reduces Inner Hair Cell Synaptopathy After Noise-induced Hearing Loss

inferredcites →https://doi.org/10.1111/j.1749-6632.1999.tb08646.xopenalex-snapshot

Excitotoxicity, Synaptic Repair, and Functional Recovery in the Mammalian Cochlea: A Review of Recent Findings

inferredcites →https://doi.org/10.1121/1.1903482openalex-snapshot

Hearing loss due to continuous exposure to steady-state broad-band noise

inferredcites →https://doi.org/10.1121/1.1903521openalex-snapshot

Rate versus level functions for auditory-nerve fibers in cats: tone-burst stimuli

inferredcites →https://doi.org/10.1121/1.381736openalex-snapshot

Auditory-nerve response from cats raised in a low-noise chamber

inferredcites →https://doi.org/10.1121/1.388677openalex-snapshot

The cochlear frequency map for the cat: Labeling auditory-nerve fibers of known characteristic frequency

inferredcites →https://doi.org/10.1126/science.7079757openalex-snapshot

Single-Neuron Labeling in the Cat Auditory Nerve

inferredcites →https://doi.org/10.1126/science.7089553openalex-snapshot

Hair-Cell Innervation by Spiral Ganglion Cells in Adult Cats

inferredcites →https://doi.org/10.1152/jn.00164.2013openalex-snapshot

Noise-induced cochlear neuropathy is selective for fibers with low spontaneous rates

inferredcites →https://doi.org/10.1152/jn.00574.2004openalex-snapshot

Response Properties of Single Auditory Nerve Fibers in the Mouse

inferredcites →https://doi.org/10.1152/jn.00738.2013openalex-snapshot

Contribution of auditory nerve fibers to compound action potential of the auditory nerve

inferredcites →https://doi.org/10.1152/jn.1978.41.2.365openalex-snapshot

Properties of auditory nerve responses in absence of outer hair cells

inferredcites →https://doi.org/10.1152/jn.1984.51.6.1326openalex-snapshot

Effects of continuous noise backgrounds on rate response of auditory nerve fibers in cat

inferredcites →https://doi.org/10.1152/jn.1996.76.4.2799openalex-snapshot

Age-related loss of activity of auditory-nerve fibers

inferredcites →https://doi.org/10.1177/000348946207100313openalex-snapshot

LXII Presbycusis Study of a Relatively Noise-Free Population in the Sudan

inferredcites →https://doi.org/10.1177/000348947208100203openalex-snapshot

Sensory and Neural Degeneration with Aging, as Seen in Microdissections of the Human Inner Ear

inferredcites →https://doi.org/10.1177/000348947408300303openalex-snapshot

Sequence of Degeneration of Corti's Organ and its First-Order Neurons

inferredcites →https://doi.org/10.1177/00034894931020s101openalex-snapshot

Cochlear Pathology in Presbycusis

inferredcites →https://doi.org/10.1258/ebm.2009.009281openalex-snapshot

The challenge of hair cell regeneration

inferredcites →https://doi.org/10.1288/00005537-197609000-00001openalex-snapshot

Human cochlear changes in noise induced hearing loss

inferredcites →https://doi.org/10.1288/00005537-198306000-00015openalex-snapshot

Serial section reconstruction of the neural poles of hair cells in the human organ of corti. II. outer hair cells

inferredcites →https://doi.org/10.1371/journal.pone.0162726openalex-snapshot

Toward a Differential Diagnosis of Hidden Hearing Loss in Humans

inferredcites →https://doi.org/10.1523/jneurosci.2156-11.2011openalex-snapshot

Tinnitus with a Normal Audiogram: Physiological Evidence for Hidden Hearing Loss and Computational Model

inferredcites →https://doi.org/10.1523/jneurosci.2845-09.2009openalex-snapshot

Adding Insult to Injury: Cochlear Nerve Degeneration after “Temporary” Noise-Induced Hearing Loss

inferredcites →https://doi.org/10.1523/jneurosci.3389-10.2011openalex-snapshot

Opposing Gradients of Ribbon Size and AMPA Receptor Expression Underlie Sensitivity Differences among Cochlear-Nerve/Hair-Cell Synapses

inferredcites →https://doi.org/10.1523/jneurosci.4460-15.2016openalex-snapshot

Auditory Brainstem Response Latency in Noise as a Marker of Cochlear Synaptopathy

inferredcites →https://doi.org/10.1523/jneurosci.4985-05.2006openalex-snapshot

Acceleration of Age-Related Hearing Loss by Early Noise Exposure: Evidence of a Misspent Youth

inferredcites →https://doi.org/10.1523/jneurosci.5138-14.2015openalex-snapshot

Aging after Noise Exposure: Acceleration of Cochlear Synaptopathy in “Recovered” Ears

inferredcites →https://doi.org/10.2307/1416497openalex-snapshot

Hearing: Its Psychology and Physiology

inferredcites →https://doi.org/10.3109/00016486909125448openalex-snapshot

Innervation Patterns in the Organ of Corti of the Cat

inferredcites →https://doi.org/10.3109/00016487209138937openalex-snapshot

Innervation Densities of the Cochlea

inferredcites →https://doi.org/10.3109/00016489309135819openalex-snapshot

Pathophysiology of the Glutamatergic Synapses in the Cochlea

inferredcites →https://doi.org/10.3389/fnins.2016.00231openalex-snapshot

Coding Deficits in Noise-Induced Hidden Hearing Loss May Stem from Incomplete Repair of Ribbon Synapses in the Cochlea

inferredcites →https://doi.org/10.3766/jaaa.23.10.4openalex-snapshot

The Relationship between High-Frequency Pure-Tone Hearing Loss, Hearing in Noise Test (HINT) Thresholds, and the Articulation Index

inferredcites →https://doi.org/10.4103/1463-1741.140511openalex-snapshot

Comparison of occupational noise legislation in the Americas: An overview and analysis

inferredcites →https://doi.org/10.7554/elife.03564openalex-snapshot

Neurotrophin-3 regulates ribbon synapse density in the cochlea and induces synapse regeneration after acoustic trauma

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Turnover and activity-dependent transcriptional control of NompC in the Drosophila ear

inferred← citeshttps://doi.org/10.1016/j.isci.2024.108825openalex-snapshot

Spatial patterns of noise-induced inner hair cell ribbon loss in the mouse mid-cochlea

inferred← citeshttps://doi.org/10.1016/j.mcpro.2023.100704openalex-snapshot

Proteomic Analysis Reveals the Composition of Glutamatergic Organelles of Auditory Inner Hair Cells

inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2019.04.007openalex-snapshot

GABAergic and glutamatergic cells in the inferior colliculus dynamically express the GABAAR γ1 subunit during aging

inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2021.04.001openalex-snapshot

Inferior collicular cells that project to the auditory thalamus are increasingly surrounded by perineuronal nets with age

inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2025.06.002openalex-snapshot

Age-related differences in GABAergic synapses across the central inferior colliculus in the Fischer Brown Norway rat

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2018.07.053openalex-snapshot

Primary Neural Degeneration in the Human Cochlea: Evidence for Hidden Hearing Loss in the Aging Ear

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2018.09.026openalex-snapshot

Noise-induced Cochlear Synaptopathy and Signal Processing Disorders

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2018.12.048openalex-snapshot

Coding-in-Noise Deficits are Not Seen in Responses to Amplitude Modulation in Subjects with cochlear Synaptopathy Induced by a Single Noise Exposure

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2019.05.012openalex-snapshot

Inner Hair Cell and Neuron Degeneration Contribute to Hearing Loss in a DFNA2-Like Mouse Model

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2019.12.049openalex-snapshot

Repeated Moderate Sound Exposure Causes Accumulated Trauma to Cochlear Ribbon Synapses in Mice

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2020.02.038openalex-snapshot

Temporary Versus Permanent Synaptic Loss from Repeated Noise Exposure in Guinea Pigs and C57 Mice

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2023.01.037openalex-snapshot

Dendritic Degeneration and Altered Synaptic Innervation of a Central Auditory Neuron During Age-related Hearing Loss

inferred← citeshttps://doi.org/10.1016/j.nicl.2021.102823openalex-snapshot

Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2019.05.003openalex-snapshot

New molecular therapies for the treatment of hearing loss

inferred← citeshttps://doi.org/10.1016/j.ssci.2025.106942openalex-snapshot

Hearing loss in miners exposed to high noise levels: A systematic review and meta-analysis of the last 10 years

inferred← citeshttps://doi.org/10.1016/j.tins.2019.03.006openalex-snapshot

Mechanisms of Hair Cell Damage and Repair

inferred← citeshttps://doi.org/10.1016/j.tins.2020.07.005openalex-snapshot

The Effects of Age-Related Hearing Loss on the Brain and Cognitive Function

inferred← citeshttps://doi.org/10.1038/s41434-020-0177-1openalex-snapshot

Gene therapy development in hearing research in China

inferred← citeshttps://doi.org/10.1038/s41467-018-06033-3openalex-snapshot

Neuronal heterogeneity and stereotyped connectivity in the auditory afferent system

inferred← citeshttps://doi.org/10.1038/s41467-020-19521-2openalex-snapshot

Neuronal processes and glial precursors form a scaffold for wiring the developing mouse cochlea

inferred← citeshttps://doi.org/10.1038/s41598-019-39119-zopenalex-snapshot

Sodium-activated potassium channels shape peripheral auditory function and activity of the primary auditory neurons in mice

inferred← citeshttps://doi.org/10.1038/s41598-022-05657-2openalex-snapshot

Targeted deletion of the RNA-binding protein Caprin1 leads to progressive hearing loss and impairs recovery from noise exposure in mice

inferred← citeshttps://doi.org/10.1038/s41598-024-76892-yopenalex-snapshot

A primate model animal revealed the inter-species differences and similarities in the subtype specifications of the spiral ganglion neurons

inferred← citeshttps://doi.org/10.1038/s41598-025-10263-zopenalex-snapshot

Individual differences in auditory scene analysis abilities in music and speech

inferred← citeshttps://doi.org/10.1038/s42003-022-03408-7openalex-snapshot

Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

inferred← citeshttps://doi.org/10.1044/2022_aja-21-00233openalex-snapshot

Factors Affecting the Use of Speech Testing in Adult Audiology

inferred← citeshttps://doi.org/10.1044/2024_jslhr-24-00487openalex-snapshot

Postural Control in Adults With Age-Related Hearing Loss

inferred← citeshttps://doi.org/10.1044/2025_aja-25-00124openalex-snapshot

The Impact of Age, Sex, and Hearing Thresholds on Speech Recognition in Quiet and Noise

inferred← citeshttps://doi.org/10.1044/2025_jslhr-24-00472openalex-snapshot

The Effect of Dialect and Accent on Digit Perception in Noise in Young Listeners With Normal Hearing

inferred← citeshttps://doi.org/10.1055/a-1506-0701openalex-snapshot

Bei der Begutachtung oft nicht bedacht: Unfallpatienten und Patienten nach einem Lärmtrauma – Eine patientenzugewandte, komplementäre Sichtweise

inferred← citeshttps://doi.org/10.1055/s-0038-1641744openalex-snapshot

Effects of Including Information about Hidden Hearing Loss in an Adopt-A-Band Program on College Band Members' Attitudes toward Healthy Hearing Behaviors

inferred← citeshttps://doi.org/10.1055/s-0043-121595openalex-snapshot

Molekulares Verstehen des Hörens – Was ändert sich für den Patienten?

inferred← citeshttps://doi.org/10.1073/pnas.1903315116openalex-snapshot

Extended high-frequency hearing enhances speech perception in noise

inferred← citeshttps://doi.org/10.1073/pnas.2000760117openalex-snapshot

Preventing presbycusis in mice with enhanced medial olivocochlear feedback

inferred← citeshttps://doi.org/10.1073/pnas.2217033120openalex-snapshot

Molecular signatures define subtypes of auditory afferents with distinct peripheral projection patterns and physiological properties

inferred← citeshttps://doi.org/10.1073/pnas.2315599121openalex-snapshot

Auditory hair cells and spiral ganglion neurons regenerate synapses with refined release properties in vitro

inferred← citeshttps://doi.org/10.1080/00016489.2022.2086706openalex-snapshot

Morphology changes in the cochlea of impulse noise-induced hidden hearing loss

inferred← citeshttps://doi.org/10.1080/10803548.2020.1772546openalex-snapshot

A critical review of the literature on comfort of hearing protection devices: analysis of the comfort measurement variability

inferred← citeshttps://doi.org/10.1080/13543784.2023.2242253openalex-snapshot

Experimental drugs for the prevention or treatment of sensorineural hearing loss

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/10.1093/cercor/bhab518openalex-snapshot

Cortical tracking of formant modulations derived from silently presented lip movements and its decline with age

inferred← citeshttps://doi.org/10.1093/med/9780198834380.003.0009openalex-snapshot

I am a neurologist, what otology do I need to know?

inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190849061.013.16openalex-snapshot

Aging Processes in the Subcortical Auditory System

inferred← citeshttps://doi.org/10.1097/aud.0000000000000787openalex-snapshot

Chronic Conductive Hearing Loss Is Associated With Speech Intelligibility Deficits in Patients With Normal Bone Conduction Thresholds

inferred← citeshttps://doi.org/10.1097/aud.0000000000000804openalex-snapshot

Middle Ear Muscle Reflex and Word Recognition in “Normal-Hearing” Adults: Evidence for Cochlear Synaptopathy?

inferred← citeshttps://doi.org/10.1097/aud.0000000000000956openalex-snapshot

Improved Sensitivity of Digits-in-Noise Test to High-Frequency Hearing Loss

inferred← citeshttps://doi.org/10.1097/aud.0000000000001457openalex-snapshot

A Guinea Pig Model Suggests That Objective Assessment of Acoustic Hearing Preservation in Human Ears With Cochlear Implants Is Confounded by Shifts in the Spatial Origin of Acoustically Evoked Potential Measurements Along the Cochlear Length

inferred← citeshttps://doi.org/10.1097/jcma.0000000000001005openalex-snapshot

GRAIL gene knockout mice protect against aging-related and noise-induced hearing loss

inferred← citeshttps://doi.org/10.1097/mao.0000000000002848openalex-snapshot

Noise Damage Accelerates Auditory Aging and Tinnitus: A Canadian Population-Based Study

inferred← citeshttps://doi.org/10.1097/mao.0000000000004577openalex-snapshot

Serum Testosterone and Dehydroepiandrosterone Sulfate Levels and Hearing Loss in Older Males: The Hitachi Health Study II

inferred← citeshttps://doi.org/10.1097/moo.0000000000000829openalex-snapshot

Auditory neuropathy: from etiology to management

inferred← citeshttps://doi.org/10.1098/rsos.230644openalex-snapshot

Recent advances and future challenges in gene therapy for hearing loss

inferred← citeshttps://doi.org/10.1101/2020.07.31.20165225openalex-snapshot

Improved Sensitivity of Digits-in-Noise Test to High-Frequency Hearing Loss

inferred← citeshttps://doi.org/10.1101/2023.02.27.530354openalex-snapshot

Noise-Induced Synaptopathy Impacts the Long and Short Sensory Hair Cells Differently in the Mammalian Cochlea

inferred← citeshttps://doi.org/10.1101/2023.05.19.541526openalex-snapshot

Frequency-dependent Distribution of Different Subtypes of Spiral Ganglion Neurons in the Cochlea and the Changes During Aging

inferred← citeshttps://doi.org/10.1101/2024.02.14.580267openalex-snapshot

Presynaptic Nrxn3 is essential for ribbon-synapse assembly in hair cells

inferred← citeshttps://doi.org/10.1101/2024.08.27.609839openalex-snapshot

Auditory perception and neural representation of temporal features are altered by age but not by cochlear synaptopathy

inferred← citeshttps://doi.org/10.1101/2024.09.25.615093openalex-snapshot

Evaluating the Effects of Aircraft Noise on Hearing and Physiological Indicators: A Study of Military Personnel Using iTRAQ Proteomics and Cognitive Assessments

inferred← citeshttps://doi.org/10.1101/311407openalex-snapshot

Genome-wide Association Study for Noise-induced Cochlear Synaptopathy

inferred← citeshttps://doi.org/10.1101/754416openalex-snapshot

Early neuronal processes interact with glia to establish a scaffold for orderly innervation of the cochlea

inferred← citeshttps://doi.org/10.1101/cshperspect.a033555openalex-snapshot

Interactions between Macrophages and the Sensory Cells of the Inner Ear

inferred← citeshttps://doi.org/10.1109/dph70309.2026.11650091openalex-snapshot

Fine-Tuning YOLO26 for Outer and Inner Cochlear Hair Cell Detection

inferred← citeshttps://doi.org/10.1109/ijcnn48605.2020.9206731openalex-snapshot

Multivariate Models for Decoding Hearing Impairment using EEG Gamma-Band Power Spectral Density

inferred← citeshttps://doi.org/10.1111/coa.13927openalex-snapshot

Hearing preservation in cochlear implant recipients: A cross‐sectional cohort study

inferred← citeshttps://doi.org/10.1111/cpr.13775openalex-snapshot

Direct reprogramming of fibroblasts into spiral ganglion neurons by defined transcription factors

inferred← citeshttps://doi.org/10.1113/jp279795openalex-snapshot

Age‐related changes in the biophysical and morphological characteristics of mouse cochlear outer hair cells

inferred← citeshttps://doi.org/10.1113/jp281014openalex-snapshot

Biased auditory nerve central synaptopathy is associated with age‐related hearing loss

inferred← citeshttps://doi.org/10.1113/jp284980openalex-snapshot

Age‐related changes in P2Y receptor signalling in mouse cochlear supporting cells

inferred← citeshttps://doi.org/10.1121/1.5009603openalex-snapshot

Subcortical amplitude modulation encoding deficits suggest evidence of cochlear synaptopathy in normal-hearing 18–19 year olds with higher lifetime noise exposure

inferred← citeshttps://doi.org/10.1121/1.5134465openalex-snapshot

Occupational noise exposure: A review of its effects, epidemiology, and impact with recommendations for reducing its burden

inferred← citeshttps://doi.org/10.1121/10.0009802openalex-snapshot

Adaptation to noise in normal and impaired hearing

inferred← citeshttps://doi.org/10.1121/10.0024614openalex-snapshot

The perception of ultrasonic vocalizations by laboratory mice following intense noise exposures

inferred← citeshttps://doi.org/10.1121/10.0028583openalex-snapshot

Individual differences in the perception of phonetic category structure predict speech-in-noise performance

inferred← citeshttps://doi.org/10.1136/bmjopen-2020-041290openalex-snapshot

Natural history of tinnitus in adults: a cross-sectional and longitudinal analysis

inferred← citeshttps://doi.org/10.1152/jn.00016.2020openalex-snapshot

Electrophysiological markers of cochlear function correlate with hearing-in-noise performance among audiometrically normal subjects

inferred← citeshttps://doi.org/10.1152/jn.00039.2021openalex-snapshot

Longitudinal auditory pathophysiology following mild blast-induced trauma

inferred← citeshttps://doi.org/10.1152/jn.00233.2020openalex-snapshot

Can auditory brain stem response accurately reflect the cochlear function?

inferred← citeshttps://doi.org/10.1152/jn.00677.2018openalex-snapshot

Cochlear compound action potentials from high-level tone bursts originate from wide cochlear regions that are offset toward the most sensitive cochlear region

inferred← citeshttps://doi.org/10.1152/physrev.00053.2017openalex-snapshot

Toward Cochlear Therapies

inferred← citeshttps://doi.org/10.1155/2018/3989201openalex-snapshot

N-Methyl-D-Aspartate Receptors Involvement in the Gentamicin-Induced Hearing Loss and Pathological Changes of Ribbon Synapse in the Mouse Cochlear Inner Hair Cells

inferred← citeshttps://doi.org/10.1159/000514143openalex-snapshot

Noise Exposure and Distortion Product Otoacoustic Emission Suprathreshold Amplitudes: A Genome-Wide Association Study

inferred← citeshttps://doi.org/10.1159/000539359openalex-snapshot

Early Loss of Spiral Ganglion Neurons in the Auditory System after Noise Trauma

inferred← citeshttps://doi.org/10.1177/2331216519872378openalex-snapshot

FreeHear: A New Sound-Field Speech-in-Babble Hearing Assessment Tool

inferred← citeshttps://doi.org/10.1242/dev.176750openalex-snapshot

Neurogenesis in the inner ear: the zebrafish statoacoustic ganglion provides new neurons from a Neurod/Nestin-positive progenitor pool well into adulthood

inferred← citeshttps://doi.org/10.1242/dev.202723openalex-snapshot

Presynaptic Nrxn3 is essential for ribbon-synapse maturation in hair cells

inferred← citeshttps://doi.org/10.1242/dev.205054openalex-snapshot

Axonal defasciculation is restricted to specific branching points during regeneration of the lateral line nerve in zebrafish

inferred← citeshttps://doi.org/10.1242/jcs.259912openalex-snapshot

FCHSD2 is required for stereocilia maintenance in mouse cochlear hair cells

inferred← citeshttps://doi.org/10.12688/f1000research.141954.1openalex-snapshot

A study of hearing acuity and health of the external auditory canal in earphone users

inferred← citeshttps://doi.org/10.12688/f1000research.17717.1openalex-snapshot

Primary sensory map formations reflect unique needs and molecular cues specific to each sensory system

inferred← citeshttps://doi.org/10.12703/r/10-47openalex-snapshot

Neurog1, Neurod1, and Atoh1 are essential for spiral ganglia, cochlear nuclei, and cochlear hair cell development

inferred← citeshttps://doi.org/10.13201/j.issn.2096-7993.2021.06.018openalex-snapshot

[Hyperacusis: a mini review].

inferred← citeshttps://doi.org/10.1371/journal.pbio.3002257openalex-snapshot

Phytosterols reverse antiretroviral-induced hearing loss, with potential implications for cochlear aging

inferred← citeshttps://doi.org/10.1371/journal.pgen.1008826openalex-snapshot

Congenital hearing impairment associated with peripheral cochlear nerve dysmyelination in glycosylation-deficient muscular dystrophy

inferred← citeshttps://doi.org/10.1371/journal.pone.0224022openalex-snapshot

BDNF, NT-3 and Trk receptor agonist monoclonal antibodies promote neuron survival, neurite extension, and synapse restoration in rat cochlea ex vivo models relevant for hidden hearing loss

inferred← citeshttps://doi.org/10.1371/journal.pone.0255356openalex-snapshot

Workplace noise exposure and the prevalence and 10-year incidence of age-related hearing loss

inferred← citeshttps://doi.org/10.1371/journal.pone.0292676openalex-snapshot

Apical-basal distribution of different subtypes of spiral ganglion neurons in the cochlea and the changes during aging

inferred← citeshttps://doi.org/10.1523/jneurosci.0253-22.2022openalex-snapshot

Peripheral Auditory Nerve Impairment in a Mouse Model of Syndromic Autism

inferred← citeshttps://doi.org/10.1523/jneurosci.1550-18.2018openalex-snapshot

Viral transfer of mini-otoferlins partially restores the fast component of exocytosis and uncovers ultrafast endocytosis in auditory hair cells of otoferlin knock-out mice

inferred← citeshttps://doi.org/10.1523/jneurosci.1747-21.2021openalex-snapshot

Neural Presbyacusis in Humans Inferred from Age-Related Differences in Auditory Nerve Function and Structure

inferred← citeshttps://doi.org/10.1523/jneurosci.1773-21.2022openalex-snapshot

Calretinin-Expressing Synapses Show Improved Synaptic Efficacy with Reduced Asynchronous Release during High-Rate Activity

inferred← citeshttps://doi.org/10.1523/jneurosci.2784-18.2019openalex-snapshot

Temporal Coding of Single Auditory Nerve Fibers Is Not Degraded in Aging Gerbils

inferred← citeshttps://doi.org/10.1523/jneurosci.3368-17.2018openalex-snapshot

Codeficiency of Lysosomal Mucolipins 3 and 1 in Cochlear Hair Cells Diminishes Outer Hair Cell Longevity and Accelerates Age-Related Hearing Loss

inferred← citeshttps://doi.org/10.15252/emmm.202215798openalex-snapshot

Is there an unmet medical need for improved hearing restoration?

inferred← citeshttps://doi.org/10.1620/tjem.2023.j031openalex-snapshot

Effects of Ndufs4 Deletion on Hearing after Various Acoustic Exposures

inferred← citeshttps://doi.org/10.18632/aging.202936openalex-snapshot

Neural presbycusis at ultra-high frequency in aged common marmosets and rhesus monkeys

inferred← citeshttps://doi.org/10.19080/gjo.2018.17.555969openalex-snapshot

Auditory Synaptopathy and Masking Psychometric Function Slope: A Conjecture

inferred← citeshttps://doi.org/10.20492/aeahtd.1312952openalex-snapshot

Normal İşiten Tinnitus Hastalarında Yüksek Frekans Odyometrinin Rolü

inferred← citeshttps://doi.org/10.20868/upm.thesis.72026openalex-snapshot

Validación de la Terapia de Ambiente Acústicamente Enriquecido EAE para el tratamiento de pacientes con Tinnitus

inferred← citeshttps://doi.org/10.21203/rs.3.rs-1616459/v1openalex-snapshot

Hoveyzeh ear cohort study in southwest Iran: Objectives and design

inferred← citeshttps://doi.org/10.2139/ssrn.5111668openalex-snapshot

Age-Related Changes to Gabaergic Synapses Across the Central Inferior Colliculus

inferred← citeshttps://doi.org/10.2147/ijgm.s546037openalex-snapshot

Unravelling the Silence: Exploring Tinnitus Pathophysiology and the Promise of Traditional Chinese Medicine

inferred← citeshttps://doi.org/10.22038/ijbms.2020.41007.9693openalex-snapshot

Effect of myricetin on the gene expressions of NOX3, TGF-β1, prestin, and HSP-70 and anti-oxidant activity in the cochlea of noise-exposed rats.

inferred← citeshttps://doi.org/10.31234/osf.io/yptfropenalex-snapshot

Immediate ambiguity resolution in speech perception based on prior acoustic experience

inferred← citeshttps://doi.org/10.33540/1628openalex-snapshot

Structure and hearing preservation in cochlear implant surgery

inferred← citeshttps://doi.org/10.3389/fcell.2021.728352openalex-snapshot

Cochlear Sox2+ Glial Cells Are Potent Progenitors for Spiral Ganglion Neuron Reprogramming Induced by Small Molecules

inferred← citeshttps://doi.org/10.3389/fimmu.2025.1470625openalex-snapshot

Role of RGS17 in cisplatin-induced cochlear inflammation and ototoxicity via caspase-3 activation

inferred← citeshttps://doi.org/10.3389/fnagi.2020.00027openalex-snapshot

The Density of Perineuronal Nets Increases With Age in the Inferior Colliculus in the Fischer Brown Norway Rat

inferred← citeshttps://doi.org/10.3389/fnagi.2022.803973openalex-snapshot

Early Noise-Induced Hearing Loss Accelerates Presbycusis Altering Aging Processes in the Cochlea

inferred← citeshttps://doi.org/10.3389/fnagi.2022.846804openalex-snapshot

Age-Related Hearing Loss Is Accompanied by Chronic Inflammation in the Cochlea and the Cochlear Nucleus

inferred← citeshttps://doi.org/10.3389/fnagi.2023.1271008openalex-snapshot

Age-related upregulation of perineuronal nets on inferior collicular cells that project to the cochlear nucleus

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