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Journal of Neurophysiology|March 4, 2003
Contribution of BK Ca2+-activated K+ channels to auditory neurotransmission in the Guinea pig cochleaLiam J Skinner, Veronique Enée, Maryline Beurg, et al.
The European Journal of Neuroscience|September 24, 2005
Ryanodine receptors and BK channels act as a presynaptic depressor of neurotransmission in cochlear inner hair cellsMaryline Beurg, Aziz Hafidi, Liam J Skinner, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 20, 2024
Clarin-2 gene supplementation durably preserves hearing in a model of progressive hearing lossClara Mendia, Thibault Peineau, Mina Zamani, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|January 23, 2026
Compensatory Interplay Between Clarin-1 and Clarin-2 Deafness-Associated Proteins Governs Phenotypic Variability in HearingMaureen Wentling, Aïda Yakhlef Sanchez, Nicolas Thelen, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 25, 2017
Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1GAlice Emptoz, Vincent Michel, Andrea Lelli, et al.
Iscience|December 9, 2022
The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapsesCharlotte Calvet, Thibault Peineau, Najate Benamer, et al.
The Journal of Clinical Investigation|July 10, 2018
Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndromeDidier Dulon, Samantha Papal, Pranav Patni, et al.
Cell|November 7, 2015
Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of PeroxisomesSedigheh Delmaghani, Jean Defourny, Asadollah Aghaie, et al.
EMBO Molecular Medicine|August 27, 2019
Clarin-2 is essential for hearing by maintaining stereocilia integrity and functionLucy A Dunbar, Pranav Patni, Carlos Aguilar, et al.
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