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Frontiers in Veterinary Science|August 28, 2020
Echolocating Whales and Bats Express the Motor Protein Prestin in the Inner Ear: A Potential Marker for Hearing LossMaria Morell, A Wayne Vogl, Lonneke L IJsseldijk, et al.
Communications Biology|April 18, 2026
Ferritin light-chain contributes to hair cells function and survivalChloé P Petit, Sahia Mahaman Bachir Dodo, Lina María Jaime Tobón, et al.
The Journal of Comparative Neurology|October 2, 2014
Ultrastructure of the Odontocete organ of Corti: scanning and transmission electron microscopyMaria Morell, Marc Lenoir, Robert E Shadwick, et al.
The Journal of Biological Chemistry|April 2, 2011
Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearingLydie Fasquelle, Hamish S Scott, Marc Lenoir, et al.
Brain : a Journal of Neurology|December 20, 2012
The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouseEmmanuelle Sarzi, Claire Angebault, Marie Seveno, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 20, 2024
Dysfunction of specific auditory fibers impacts cortical oscillations, driving an autism phenotype despite near-normal hearingPhiline Marchetta, Konrad Dapper, Morgan Hess, et al.
Annals of Neurology|October 22, 2005
OPA1 R445H mutation in optic atrophy associated with sensorineural deafnessPatrizia Amati-Bonneau, Agnès Guichet, Aurélien Olichon, et al.
American Journal of Human Genetics|August 5, 2008
Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null miceJérôme Ruel, Sarah Emery, Régis Nouvian, et al.
Neuropharmacology|December 8, 2019
LSP5-2157 a new inhibitor of vesicular glutamate transportersOdile Poirel, Lauren E Mamer, Melissa A Herman, et al.
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