Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes von Delmaghani, Sedigheh, Defourny, Jean, Aghaie, Asadollah, Beurg, Maryline, Dulon, Didier, Thelen, Nicolas, Perfettini, Isabelle, Zelles, Tibor, Aller, Mate, Meyer, Anaïs, Emptoz, Alice, Giraudet, Fabrice, Leibovici, Michel, Dartevelle, Sylvie, Soubigou, Guillaume, Thiry, Marc, Vizi, E. Sylvester, Safieddine, Saaid, Hardelin, Jean-Pierre, Avan, Paul, Petit, Christine

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Usher syndrome type 1-associated cadherins shape the photoreceptor outer segment von Schietroma, Cataldo, Parain, Karine, Estivalet, Amrit, Aghaie, Asadollah, Boutet de Monvel, Jacques, Picaud, Serge, Sahel, José-Alain, Perron, Muriel, El-Amraoui, Aziz, Petit, Christine

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Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice von Sahly, Iman, Dufour, Eric, Schietroma, Cataldo, Michel, Vincent, Bahloul, Amel, Perfettini, Isabelle, Pepermans, Elise, Estivalet, Amrit, Carette, Diane, Aghaie, Asadollah, Ebermann, Inga, Lelli, Andrea, Iribarne, Maria, Hardelin, Jean-Pierre, Weil, Dominique, Sahel, José-Alain, El-Amraoui, Aziz, Petit, Christine

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Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth von Lelli, Andrea, Michel, Vincent, Boutet de Monvel, Jacques, Cortese, Matteo, Bosch-Grau, Montserrat, Aghaie, Asadollah, Perfettini, Isabelle, Dupont, Typhaine, Avan, Paul, El-Amraoui, Aziz, Petit, Christine

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Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness von DELMAGHANI, Sedigheh, AGHAIE, Asadollah, MICHALSKI, Nicolas, BONNET, Crystel, WEIL, Dominique, PETIT, Christine

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CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival von Michel, Vincent, Booth, Kevin T, Patni, Pranav, Cortese, Matteo, Azaiez, Hela, Bahloul, Amel, Kahrizi, Kimia, Labbé, Ménélik, Emptoz, Alice, Lelli, Andrea, Dégardin, Julie, Dupont, Typhaine, Aghaie, Asadollah, Oficjalska‐Pham, Danuta, Picaud, Serge, Najmabadi, Hossein, Smith, Richard J, Bowl, Michael R, Brown, Steven DM, Avan, Paul, Petit, Christine, El‐Amraoui, Aziz

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Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy von Lathrop, Mark, Van Camp, Guy, Michel, Vincent, del Castillo, Francisco J, Leibovici, Michel, Delmaghani, Sedigheh, Ron, Uri, Petit, Christine, Langa, Francina, Weil, Dominique, Ben-Tal, Nir, Aghaie, Asadollah, Van Laer, Lut, Avan, Paul

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New Insights into the Alternative d-Glucarate Degradation Pathway von Aghaie, Asadollah, Lechaplais, Christophe, Sirven, Peggy, Tricot, Sabine, Besnard-Gonnet, Marielle, Muselet, Delphine, de Berardinis, Véronique, Kreimeyer, Annett, Gyapay, Gabor, Salanoubat, Marcel, Perret, Alain

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Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness von Delmaghani, Sedigheh, Aghaie, Asadollah, Bouyacoub, Yosra, El Hachmi, Hala, Bonnet, Crystel, Riahi, Zied, Chardenoux, Sebastien, Perfettini, Isabelle, Hardelin, Jean-Pierre, Houmeida, Ahmed, Herbomel, Philippe, Petit, Christine

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DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1 von DELMAGHANI, Sedigheh, AGHAIE, Asadollah, COMPAIN-NOUAILLE, Sylvie, ATAIE, Afsaneh, LEMAINQUE, Arnaud, ZEINALI, Sirous, LATHROP, Mark, WEIL, Dominique, PETIT, Christine

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The Mitochondrial Protease AFG3L2 Is Essential for Axonal Development von Maltecca, Francesca, Aghaie, Asadollah, Schroeder, David G, Cassina, Laura, Taylor, Benjamin A, Phillips, Sandra J, Malaguti, Mariachiara, Previtali, Stefano, Guenet, Jean-Louis, Quattrini, Angelo, Cox, Gregory A, Casari, Giorgio

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Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth von Lelli, Andrea, Michel, Vincent, Boutet de Monvel, Jacques, Cortese, Matteo, Bosch-Grau, Montserrat, Aghaie, Asadollah, Perfettini, Isabelle, Dupont, Typhaine, Avan, Paul, El-Amraoui, Aziz, Petit, Christine

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The paralysé (par) mouse neurological mutation maps to a 9 Mbp (4 cM) interval of mouse chromosome 18 von Silva Neto, Lino, Aghaie, Asadollah, Guénet, Jean-Louis, Godard, Ana Lúcia Brunialti

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Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice: Usher 1 retinal pathogenesis von Sahly, Iman, Dufour, Eric, Schietroma, Cataldo, Michel, Vincent, Bahloul, Amel, Perfettini, Isabelle, Pepermans, Elise, Estivalet, Amrit, Carette, Diane, Aghaie, Asadollah, Ebermann, Inga, Lelli, Andrea, Iribarne, Maria, Hardelin, Jean-Pierre, Weil, Dominique, Sahel, José-Alain, El-Amraoui, Aziz, Petit, Christine

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crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1) von Conti, Valerio, Aghaie, Asadollah, Cilli, Michele, Martin, Natalia, Caridi, Gianluca, Musante, Luca, Candiano, Giovanni, Castagna, Maura, Fairen, Alfonso, Ravazzolo, Roberto, Guenet, Jean-Louis, Puliti, Aldamaria

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New Insights into the Alternative d-Glucarate Degradation PathwayS von Aghaie, Asadollah, Lechaplais, Christophe, Sirven, Peggy, Tricot, Sabine, Besnard-Gonnet, Marielle, Muselet, Delphine, de Berardinis, Véronique, Kreimeyer, Annett, Gyapay, Gabor, Salanoubat, Marcel, Perret, Alain

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PREVENTION AND/OR TREATMENT OF HEARING LOSS OR IMPAIRMENT von PETIT, Christine, DELMAGHANI, Sedigheh, DEFOURNY, Jean, SAFIEDDINE, Saaid, EMPTOZ, Alice, AGHAIE, Asadollah, AVAN, Paul

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Prevention and/or treatment of hearing loss or impairment von Defourny, Jean, Avan, Paul, Safieddine, Saaid, Emptoz, Alice, Petit, Christine, Delmaghani, Sedigheh, Aghaie, Asadollah

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PREVENTION AND/OR TREATMENT OF HEARING LOSS OR IMPAIRMENT von PETIT, Christine, DELMAGHANI, Sedigheh, DEFOURNY, Jean, SAFIEDDINE, Saaid, EMPTOZ, Alice, AGHAIE, Asadollah, AVAN, Paul

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Prevention and/or treatment of hearing loss or impairment von Defourny, Jean, Avan, Paul, Safieddine, Saaid, Emptoz, Alice, Petit, Christine, Delmaghani, Sedigheh, Aghaie, Asadollah

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