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Paul Avan

Showing results (91-100 of 98) with videos related to

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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.
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.
Elife|November 8, 2017
Otoferlin acts as a Ca<sup>2+</sup> sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapsesNicolas Michalski, Juan D Goutman, Sarah Marie Auclair, et al.
EMBO Molecular Medicine|November 1, 2017
CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survivalVincent Michel, Kevin T Booth, Pranav Patni, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 18, 2025
Deciphering Auditory Hyperexcitability in Otogl Mutant Mice Unravels an Auditory Neuropathy MechanismMathilde Gagliardini, Sabrina Mechaussier, Carolina Campos Pina, et al.
Science Translational Medicine|October 5, 2022
<i>NOS1</i> mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile miceKonstantina Chachlaki, Andrea Messina, Virginia Delli, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 24, 2020
Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusisSophie Boucher, Fabienne Wong Jun Tai, Sedigheh Delmaghani, et al.
Pageof 10

Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
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.
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.
Elife|November 8, 2017
Otoferlin acts as a Ca<sup>2+</sup> sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapsesNicolas Michalski, Juan D Goutman, Sarah Marie Auclair, et al.
EMBO Molecular Medicine|November 1, 2017
CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survivalVincent Michel, Kevin T Booth, Pranav Patni, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 18, 2025
Deciphering Auditory Hyperexcitability in Otogl Mutant Mice Unravels an Auditory Neuropathy MechanismMathilde Gagliardini, Sabrina Mechaussier, Carolina Campos Pina, et al.
Science Translational Medicine|October 5, 2022
<i>NOS1</i> mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile miceKonstantina Chachlaki, Andrea Messina, Virginia Delli, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 24, 2020
Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusisSophie Boucher, Fabienne Wong Jun Tai, Sedigheh Delmaghani, et al.
Pageof 10