Search Results - Bonnet, Crystel

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  1. 1
    A mitotically inheritable unit containing a MAP kinase module

    A mitotically inheritable unit containing a MAP kinase module by Kicka, Sébastien, Bonnet, Crystel, Sobering, Andrew K., Ganesan, Latha P., Silar, Philippe

    Published 2006
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  2. 2
    Contributions of Age-Related and Audibility-Related Deficits to Aided Consonant Identification in Presbycusis: A Causal-Inference Analysis

    Contributions of Age-Related and Audibility-Related Deficits to Aided Consonant Identification in Presbycusis: A Causal-Inference Analysis by Varnet, Léo, Léger, Agnès C., Boucher, Sophie, Bonnet, Crystel, Petit, Christine, Lorenzi, Christian

    Published 2021
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  3. 3
    mRNA localization to the mitochondrial surface allows the efficient translocation inside the organelle of a nuclear recoded ATP6 protein

    mRNA localization to the mitochondrial surface allows the efficient translocation inside the organelle of a nuclear recoded ATP6 protein by Kaltimbacher, Valérie, Bonnet, Crystel, Lecoeuvre, Gaëlle, Forster, Valérie, Sahel, José-Alain, Corral-Debrinski, Marisol

    Published 2006
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  4. 4
    Phylogenetic analysis of Harmonin homology domains

    Phylogenetic analysis of Harmonin homology domains by Colcombet-Cazenave, Baptiste, Druart, Karen, Bonnet, Crystel, Petit, Christine, Spérandio, Olivier, Guglielmini, Julien, Wolff, Nicolas

    Published 2021
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  5. 5
    Clinical and Haplotypic Variability of Slovenian USH2A Patients Homozygous for the c. 11864G>A Nonsense Mutation

    Clinical and Haplotypic Variability of Slovenian USH2A Patients Homozygous for the c. 11864G>A Nonsense Mutation by Zupan, Andrej, Fakin, Ana, Battelino, Saba, Jarc-Vidmar, Martina, Hawlina, Marko, Bonnet, Crystel, Petit, Christine, Glavač, Damjan

    Published 2019
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  6. 6
    A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders

    A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders by Bousfiha, Amale, Bakhchane, Amina, Charoute, Hicham, Riahi, Zied, Snoussi, Khalid, Rouba, Hassan, Bonnet, Crystel, Petit, Christine, Barakat, Abdelhamid

    Published 2017
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  7. 7
    EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss

    EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss by Dahmani, Malika, Ammar-Khodja, Fatima, Bonnet, Crystel, Lefèvre, Gaelle M., Hardelin, Jean-Pierre, Ibrahim, Hassina, Mallek, Zahia, Petit, Christine

    Published 2015
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  8. 8
    Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis

    Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis by Ben-Rebeh, Imen, Grati, Mhamed, Bonnet, Crystel, Bouassida, Walid, Hadjamor, Imen, Ayadi, Hammadi, Ghorbel, Abdelmonem, Petit, Christine, Masmoudi, Saber

    Published 2016
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  9. 9
    Optimized Allotopic Expression of the Human Mitochondrial ND4 Prevents Blindness in a Rat Model of Mitochondrial Dysfunction

    Optimized Allotopic Expression of the Human Mitochondrial ND4 Prevents Blindness in a Rat Model of Mitochondrial Dysfunction by Ellouze, Sami, Augustin, Sébastien, Bouaita, Aicha, Bonnet, Crystel, Simonutti, Manuel, Forster, Valérie, Picaud, Serge, Sahel, Jose-Alain, Corral-Debrinski, Marisol

    Published 2008
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  10. 10
    Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy

    Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy by Fakin, Ana, Šuštar, Maja, Brecelj, Jelka, Bonnet, Crystel, Petit, Christine, Zupan, Andrej, Glavač, Damjan, Jarc-Vidmar, Martina, Battelino, Saba, Hawlina, Marko

    Published 2019
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  11. 11
    Screening of BRCA1/2 variants in Mauritanian breast cancer patients

    Screening of BRCA1/2 variants in Mauritanian breast cancer patients by Brahim, Selma Mohamed, Zein, Ekht Elbenina, Bonnet, Crystel, Hamed, Cheikh Tijani, Salame, Malak, Zein, Mohamed Vall, Khyatti, Meriem, Tolba, Ahmedou, Houmeida, Ahmed

    Published 2022
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  12. 12
    Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing

    Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing by Ammar-Khodja, Fatima, Bonnet, Crystel, Dahmani, Malika, Ouhab, Sofiane, Lefèvre, Gaelle M, Ibrahim, Hassina, Hardelin, Jean-Pierre, Weil, Dominique, Louha, Malek, Petit, Christine

    Published 2015
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  13. 13
    Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness

    Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness by 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

    Published 2016
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  14. 14
    Retinal findings in pediatric patients with Usher syndrome Type 1 due to mutations in MYO7A gene

    Retinal findings in pediatric patients with Usher syndrome Type 1 due to mutations in MYO7A gene by Subirà, Olaia, Català-Mora, Jaume, Díaz-Cascajosa, Jesús, Padrón-Pérez, Noel, Claveria, M. A., Coll-Alsina, Natalia, Bonnet, Crystel, Petit, Christine, Caminal, J. M., Prat, Joan

    Published 2019
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  15. 15
    Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush

    Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush by Fakin, Ana, Bonnet, Crystel, Kurtenbach, Anne, Mohand-Said, Saddek, Zobor, Ditta, Stingl, Katarina, Testa, Francesco, Simonelli, Francesca, Sahel, José-Alain, Audo, Isabelle, Zrenner, Eberhart, Hawlina, Marko, Petit, Christine

    Published 2021
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  16. 16
    Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma

    Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma by Hadrami, Mouna, Bonnet, Crystel, Zeitz, Christina, Veten, Fatimetou, Biya, Med, Hamed, Cheikh T., Condroyer, Christel, Wang, Panfeng, Sidi, Med Mahmoud, Cheikh, Sidi, Zhang, Qingjiong, Audo, Isabelle, Petit, Christine, Houmeida, Ahmed

    Published 2019
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  17. 17
    EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness

    EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness by Behlouli, Asma, Bonnet, Crystel, Abdi, Samia, Bouaita, Aïcha, Lelli, Andrea, Hardelin, Jean-Pierre, Schietroma, Cataldo, Rous, Yahia, Louha, Malek, Cheknane, Ahmed, Lebdi, Hayet, Boudjelida, Kamel, Makrelouf, Mohamed, Zenati, Akila, Petit, Christine

    Published 2014
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  18. 18
    Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort

    Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort by Smirnov, Vasily M., Nassisi, Marco, Mohand-Saïd, Saddek, Bonnet, Crystel, Aubois, Anne, Devisme, Céline, Dib, Thilissa, Zeitz, Christina, Loundon, Natalie, Marlin, Sandrine, Petit, Christine, Bodaghi, Bahram, Sahel, José-Alain, Audo, Isabelle

    Published 2022
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  19. 19
    The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells

    The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells by Pepermans, Elise, Michel, Vincent, Goodyear, Richard, Bonnet, Crystel, Abdi, Samia, Dupont, Typhaine, Gherbi, Souad, Holder, Muriel, Makrelouf, Mohamed, Hardelin, Jean-Pierre, Marlin, Sandrine, Zenati, Akila, Richardson, Guy, Avan, Paul, Bahloul, Amel, Petit, Christine

    Published 2014
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  20. 20
    Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome

    Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome by Abdi, Samia, Bahloul, Amel, Behlouli, Asma, Hardelin, Jean-Pierre, Makrelouf, Mohamed, Boudjelida, Kamel, Louha, Malek, Cheknene, Ahmed, Belouni, Rachid, Rous, Yahia, Merad, Zahida, Selmane, Djamel, Hasbelaoui, Mokhtar, Bonnet, Crystel, Zenati, Akila, Petit, Christine

    Published 2016
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