ReviewFundamental research2026
Molecular identity of the mechanotransduction machinery in inner ear hair cells and mechanotransduction-linked hearing loss.
Review in Fundamental research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Noncoding RNA Transcripts Based Molecular Phenotyping of MASLD and MASH Patients.Liver international communications · 2026Article
- Subtype-Specific Vulnerability of Spiral Ganglion Neurons in Sensorineural Hearing Loss Across the Lifespan.Brain sciences · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hearing is among the most sensitive sensory modalities in vertebrates, and its dysfunction can lead to hearing loss. Auditory perception within the inner ear relies on mechanosensitive hair cells and a sophisticated network of molecules that comprise the machinery responsible for mechanotransduction. The mechanosensory hair cells exhibit distinct structural features that enable them to transform sound vibrations into electrical signals, which are then relayed to the spiral ganglion neurons (SGNs) that are connecting between the cochlear hair cells and the cochlear nuclei with high accuracy and fidelity. Despite over 40 years of research, the precise molecular composition and assembly of the mechanotransduction channel complex within cochlear hair cells remains elusive. This review presents recent findings that provide new perspectives on the molecular components and assembly of the mechanotransduction apparatus in cochlear hair cells, as well as genetic mutations related to mechanotransduction dysfunction and hearing loss.
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Registered trials
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