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MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss

MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_nrf_kci_oai_kci_go_kr_ARTI_10650548

MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss

About this item

Full title

MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss

Publisher

London: Nature Publishing Group UK

Journal title

Experimental and Molecular Medicine, 2024, 56(0), , pp.2423-2435

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Myh1
is a mouse deafness gene with an unknown function in the auditory system. Hearing loss in
Myh1
-knockout mice is characterized by an elevated threshold for the auditory brainstem response and the absence of a threshold for distortion product otoacoustic emission. Here, we investigated the role of MYH1 in outer hair cells (OHCs), cruci...

Alternative Titles

Full title

MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_nrf_kci_oai_kci_go_kr_ARTI_10650548

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_nrf_kci_oai_kci_go_kr_ARTI_10650548

Other Identifiers

ISSN

2092-6413,1226-3613

E-ISSN

2092-6413

DOI

10.1038/s12276-024-01338-4

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