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Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids

Amel Bahloul , Vincent Michel , Jean-Pierre Hardelin , Sylvie Nouaille , Sylviane Hoos , et al.
Human Molecular Genetics, 2010, 19 (18), pp.3557 - 3565. ⟨10.1093/hmg/ddq271⟩
Article dans une revue pasteur-03525648v1
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SCRIB controls apical contractility during epithelial differentiation

Batiste Boëda , Vincent Michel , Raphael Etournay , Patrick England , Stéphane Rigaud , et al.
Journal of Cell Biology, 2023, 222 (12), pp.e202211113. ⟨10.1083/jcb.202211113⟩
Article dans une revue pasteur-04284391v1
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Synchronization of inspiratory burst onset along the ventral respiratory column in the neonate mouse is mediated by electrotonic coupling

Boris Gourévitch , Teresa Pitts , Kimberly Iceman , Mitchell Reed , Jun Cai , et al.
BMC Biology, 2023, 21 (1), pp.108. ⟨10.1186/s12915-023-01575-5⟩
Article dans une revue hal-04290157v1
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Temporal alterations to central auditory processing without synaptopathy after lifetime exposure to environmental noise

Florian Occelli , Florian Hasselmann , Jérôme Bourien , Jean-Luc Puel , Nathalie Desvignes , et al.
Cerebral Cortex, 2021, pp.bhab310. ⟨10.1093/cercor/bhab310⟩
Article dans une revue hal-03325048v1

Myosin VI is required for the proper maturation and function of inner hair cell ribbon synapses

Isabelle Roux , Suzanne Hosie , Stuart Johnson , Amel Bahloul , Nadège Cayet , et al.
Human Molecular Genetics, 2009, 18 (23), pp.4615-4628. ⟨10.1093/hmg/ddp429⟩
Article dans une revue hal-04159601v1
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Hearing Is Normal without Connexin30

Anne-Cécile Boulay , Francisco J. Del Castillo , Fabrice Giraudet , Ghislaine Hamard , Christian Giaume , et al.
Journal of Neuroscience, 2013, 33 (2), pp.430-434. ⟨10.1523/JNEUROSCI.4240-12.2013⟩
Article dans une revue hal-04027322v1
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Reduction in sound discrimination in noise is related to envelope similarity and not to a decrease in envelope tracking abilities

Samira Souffi , Léo Varnet , Meryem Zaidi , Brice Bathellier , Chloé Huetz , et al.
The Journal of Physiology, 2023, 601 (1), pp.123-149. ⟨10.1113/JP283526⟩
Article dans une revue hal-03853055v1
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Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness.

Veronique Pingault , Virginie Bodereau , Viviane Baral , Severine Marcos , Yuli Watanabe , et al.
American Journal of Human Genetics, 2013, 92 (5), pp.707-24. ⟨10.1016/j.ajhg.2013.03.024⟩
Article dans une revue inserm-00836181v1

Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis

Sophie Boucher , Fabienne Wong Jun Tai , Sedigheh Delmaghani , Andrea Lelli , Amrit Singh-Estivalet , et al.
Proceedings of the National Academy of Sciences of the United States of America, 2020, 117 (49), pp.31278-31289. ⟨10.1073/pnas.2010782117⟩
Article dans une revue pasteur-03215054v1
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Vestibular impairment in cochlear implanted children presenting enlarged vestibular aqueduct and enlarged endolymphatic sac

P. Reynard , E. Ionescu , C.A. Joly , A. Ltaief-Boudrigua , A. Coudert , et al.
International Journal of Pediatric Otorhinolaryngology, 2021, 141, pp.110557. ⟨10.1016/j.ijporl.2020.110557⟩
Article dans une revue hal-03493153v1
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Implication of Vestibular Hair Cell Loss of Planar Polarity for the Canal and Otolith-Dependent Vestibulo-Ocular Reflexes in Celsr1–/– Mice

François Simon , Fadel Tissir , Vincent Michel , Ghizlene Lahlou , Michael Deans , et al.
Frontiers in Neuroscience, 2021, 15, pp.750596. ⟨10.3389/fnins.2021.750596⟩
Article dans une revue hal-03451916v1
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Cochlear Implant: Effect of the Number of Channel and Frequency Selectivity on Speech Understanding in Noise Preliminary Results in Simulation with Normal-Hearing Subjects

Pierre-Antoine Cucis , Christian Berger-Vachon , Ruben Hermann , Hung Thai-Van , Stéphane Gallego , et al.
Modelling, measurement and control C, 2020, 81 (1-4), pp 17-23. ⟨10.18280/mmc_c.811-404⟩
Article dans une revue hal-03160348v1
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Awake perception is associated with dedicated neuronal assemblies in the cerebral cortex

Anton Filipchuk , Joanna Schwenkgrub , Alain Destexhe , Brice Bathellier
Nature Neuroscience, 2022, 25 (10), pp.1327-1338. ⟨10.1038/s41593-022-01168-5⟩
Article dans une revue hal-03814483v2
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Nanocarriers for drug delivery to the inner ear: Physicochemical key parameters, biodistribution, safety and efficacy

Céline Jaudoin , Florence Agnely , Yann Nguyen , Evelyne Ferrary , Amélie Bochot
International Journal of Pharmaceutics, 2021, 592, pp.120038. ⟨10.1016/j.ijpharm.2020.120038⟩
Article dans une revue hal-03493235v1
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Thérapie génique des surdités humaines

Anaïs Meyer , Christine Petit , Saaid Safieddine
Médecine/Sciences, 2013, 29 (10), pp.883 - 889. ⟨10.1051/medsci/20132910016⟩
Article dans une revue hal-04159599v1
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Benefits of a contralateral routing of signal device for unilateral Naída CI cochlear implant recipients

Isabelle Mosnier , Ghizlene Lahlou , Jonathan Flament , Nathalie Mathias , Evelyne Ferrary , et al.
European Archives of Oto-Rhino-Laryngology, 2019, 276 (8), pp.2205-2213. ⟨10.1007/s00405-019-05467-9⟩
Article dans une revue hal-02385205v1
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Best Fit 3D Basilar Membrane Reconstruction to Routinely Assess the Scalar Position of the Electrode Array after Cochlear Implantation

Renato Torres , Hannah Daoudi , Ghizlene Lahlou , Neil Grislain , Eugénie Breil , et al.
Journal of Clinical Medicine, 2022, 11 (8), pp.2075. ⟨10.3390/jcm11082075⟩
Article dans une revue pasteur-03691543v1
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COVID-19-related anosmia is associated with viral persistence and inflammation in human olfactory epithelium and brain infection in hamsters

Guilherme Dias de Melo , Françoise Lazarini , Sylvain Levallois , Charlotte Hautefort , Vincent Michel , et al.
Science Translational Medicine, 2021, pp.eabf8396. ⟨10.1126/scitranslmed.abf8396⟩
Article dans une revue pasteur-03242618v1
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Paradoxical and labile medial olivocochlear functioning as a potential marker of auditory processing disorder in a child with learning disabilities

P. Reynard , E. Veuillet , H. Thai-Van
European Annals of Otorhinolaryngology, Head and Neck Diseases, 2020, 137 (4), pp.339 - 342. ⟨10.1016/j.anorl.2020.03.005⟩
Article dans une revue hal-03492283v1
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Signatures of cochlear processing in neuronal coding of auditory information

Nadège Marin , Fernando Lobo Cerna , Jérémie Barral
Molecular and Cellular Neuroscience, 2022, 120, pp.103732. ⟨10.1016/j.mcn.2022.103732⟩
Article dans une revue hal-03656874v1
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Inner Ear Gene Therapies Take Off: Current Promises and Future Challenges

Sedigheh Delmaghani , Aziz El-Amraoui
Journal of Clinical Medicine, 2020, 9 (7), pp.2309. ⟨10.3390/jcm9072309⟩
Article dans une revue pasteur-03261812v1
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Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush

Ana Fakin , Crystel Bonnet , Anne Kurtenbach , Saddek Mohand-Said , Ditta Zobor , et al.
International Journal of Molecular Sciences, 2021, 22 (19), pp.10352. ⟨10.3390/ijms221910352⟩
Article dans une revue hal-03417248v1
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How sacculo-collic function assessed by cervical vestibular evoked myogenic Potentials correlates with the quality of postural control in hearing impaired children?

Eugen Ionescu , Pierre Reynard , Nathalie Goulème , Cécile Becaud , Karen Spruyt , et al.
International Journal of Pediatric Otorhinolaryngology, 2020, 130, pp.109840. ⟨10.1016/j.ijporl.2019.109840⟩
Article dans une revue hal-03489667v1
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Un système olivocochléaire médian instable et paradoxal chez un enfant en difficulté scolaire

P. Reynard , E. Veuillet , H. Thai-Van
Annales françaises d'Oto-rhino-laryngologie et de Pathologie Cervico-faciale, 2020, 137 (4), pp.313 - 316. ⟨10.1016/j.aforl.2019.11.005⟩
Article dans une revue hal-03491586v1
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Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G

Alice Emptoz , Vincent Michel , Andrea Lelli , Omar Akil , Jacques Boutet de Monvel , et al.
Proceedings of the National Academy of Sciences of the United States of America, 2017, 114 (36), pp.9695 - 9700. ⟨10.1073/pnas.1708894114⟩
Article dans une revue hal-01661148v1
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Viral transfer of mini-otoferlins partially restores the fast component of exocytosis and uncovers ultrafast endocytosis in auditory hair cells of otoferlin knock-out mice

Margot Tertrais , Yohan Bouleau , Alice Emptoz , Séverin Belleudy , R Bryan Sutton , et al.
Journal of Neuroscience, 2019, 39 (18), pp.3394-3411. ⟨10.1523/JNEUROSCI.1550-18.2018⟩
Article dans une revue hal-04159459v1
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A Novel Heterozygous Missense Variant (c.667G>T;p.Gly223Cys) in USH1C That Interferes With Cadherin-Related 23 and Harmonin Interaction Causes Autosomal Dominant Nonsyndromic Hearing Loss

Ju Sun Song , Amel Bahloul , Christine Petit , Sang Jin Kim , Il Joon Moon , et al.
Annals of Laboratory Medicine, 2020, 40 (3), pp.224-231. ⟨10.3343/alm.2020.40.3.224⟩
Article dans une revue hal-02433812v1

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco

Imane Aitraise , Ghita Amalou , Amale Bousfiha , Hicham Charoute , Hassan Rouba , et al.
Molecular Biology Reports, 2022, 49 (5), pp.3949-3954. ⟨10.1007/s11033-022-07245-z⟩
Article dans une revue pasteur-03985530v1
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A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders

Amale Bousfiha , Amina Bakhchane , Hicham Charoute , Zied Riahi , Khalid Snoussi , et al.
Human Genome Variation, 2017, 4 (1), pp.17009. ⟨10.1038/hgv.2017.9⟩
Article dans une revue pasteur-03219646v1
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Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy

Christina Zeitz , Cécile Méjécase , Christelle Michiels , Christel Condroyer , Juliette Wohlschlegel , et al.
International Journal of Molecular Sciences, 2021, 22 (15), pp.7875. ⟨10.3390/ijms22157875⟩
Article dans une revue inserm-03841438v1