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The Journal of Physiology|July 2, 2020
Age-related changes in the biophysical and morphological characteristics of mouse cochlear outer hair cellsJing-Yi Jeng, Stuart L Johnson, Adam J Carlton, et al.
JCI Insight|December 22, 2017
Identification of ion-channel modulators that protect against aminoglycoside-induced hair cell deathEmma J Kenyon, Nerissa K Kirkwood, Siân R Kitcher, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2011
Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)Jing Zheng, Katharine K Miller, Tao Yang, et al.
Medrxiv : the Preprint Server for Health Sciences|August 20, 2025
The TECTB-C225Y Variant Causing Autosomal Dominant Deafness in a Nicaraguan Family Enhances Sensitivity to Noise-Induced Hearing Loss in MiceEvan B Hale, Barbara Vona, Richard J Goodyear, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 7, 2013
Progressive hearing loss and gradual deterioration of sensory hair bundles in the ears of mice lacking the actin-binding protein Eps8L2David N Furness, Stuart L Johnson, Uri Manor, et al.
Cell|June 1, 2010
Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearingShin-ichiro Kitajiri, Takeshi Sakamoto, Inna A Belyantseva, et al.
JCI Insight|March 18, 2021
Identification of a series of hair-cell MET channel blockers that protect against aminoglycoside-induced ototoxicityEmma J Kenyon, Nerissa K Kirkwood, Siân R Kitcher, et al.
American Journal of Human Genetics|October 23, 2012
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing lossSimon von Ameln, Geng Wang, Redouane Boulouiz, et al.
The Journal of Cell Biology|June 5, 2025
Taperin bundles F-actin at stereocilia pivot points enabling optimal lifelong mechanosensitivityInna A Belyantseva, Chang Liu, Abigail K Dragich, et al.
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