Publications by authors named "Sebastien Chardenoux"

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Mice humanized for MHC and hACE2 with high permissiveness to SARS-CoV-2 omicron replication.
Fabien Le Chevalier, Pierre Authié, Sébastien Chardenoux, Maryline Bourgine, Benjamin Vesin

Microbes Infect· November 2023

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Brain cross-protection against SARS-CoV-2 variants by a lentiviral vaccine in new transgenic mice.
Min-Wen Ku, Pierre Authié, Maryline Bourgine, François Anna, Amandine Noirat, Sébastien Chardenoux

EMBO Mol Med· December 2021

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Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness.
Sedigheh Delmaghani, Asadollah Aghaie, Yosra Bouyacoub, Hala El Hachmi, Crystel Bonnet, Sebastien Chardenoux

Am J Hum Genet· June 2016

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Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia.
Elisa Caberlotto, Vincent Michel, Isabelle Foucher, Amel Bahloul, Richard J Goodyear, Sébastien Chardenoux

Proc Natl Acad Sci U S A· April 2011

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Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning.
Nicolas Michalski, Vincent Michel, Amel Bahloul, Gaëlle Lefèvre, Jérémie Barral, Sébastien Chardenoux

J Neurosci· June 2007

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Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells.
Avital Adato, Gaëlle Lefèvre, Benjamin Delprat, Vincent Michel, Nicolas Michalski, Sébastien Chardenoux

Hum Mol Genet· December 2005

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Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.
Saber Masmoudi, Abdelaziz Tlili, Marja Majava, Abdel Monem Ghorbel, Sébastien Chardenoux

Eur J Hum Genet· February 2003

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DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.
Mirna Mustapha, Eliane Chouery, Sébastien Chardenoux, Mohamed Naboulsi, Joël Paronnaud

Eur J Hum Genet· March 2002

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