|
|
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.
Article dans une revue
pasteur-03525648v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
SCRIB controls apical contractility during epithelial differentiation
Batiste Boëda
,
Vincent Michel
,
Raphael Etournay
,
Patrick England
,
Stéphane Rigaud
,
et al.
Article dans une revue
pasteur-04284391v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-04290157v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-03325048v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-04159601v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
Hearing Is Normal without Connexin30
Anne-Cécile Boulay
,
Francisco J. Del Castillo
,
Fabrice Giraudet
,
Ghislaine Hamard
,
Christian Giaume
,
et al.
Article dans une revue
hal-04027322v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-03853055v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness.
Veronique Pingault
,
Virginie Bodereau
,
Viviane Baral
,
Severine Marcos
,
Yuli Watanabe
,
et al.
Article dans une revue
inserm-00836181v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-03493153v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-03451916v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-03160348v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
Awake perception is associated with dedicated neuronal assemblies in the cerebral cortex
Anton Filipchuk
,
Joanna Schwenkgrub
,
Alain Destexhe
,
Brice Bathellier
Article dans une revue
hal-03814483v2
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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
Article dans une revue
hal-03493235v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
Thérapie génique des surdités humaines
Anaïs Meyer
,
Christine Petit
,
Saaid Safieddine
Article dans une revue
hal-04159599v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-02385205v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
pasteur-03691543v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
pasteur-03242618v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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
Article dans une revue
hal-03492283v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
Signatures of cochlear processing in neuronal coding of auditory information
Nadège Marin
,
Fernando Lobo Cerna
,
Jérémie Barral
Article dans une revue
hal-03656874v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
Inner Ear Gene Therapies Take Off: Current Promises and Future Challenges
Sedigheh Delmaghani
,
Aziz El-Amraoui
Article dans une revue
pasteur-03261812v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-03417248v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-03489667v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
Un système olivocochléaire médian instable et paradoxal chez un enfant en difficulté scolaire
P. Reynard
,
E. Veuillet
,
H. Thai-Van
Article dans une revue
hal-03491586v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-04159459v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
hal-02433812v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
pasteur-03985530v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders
Amale Bousfiha
,
Amina Bakhchane
,
Hicham Charoute
,
Zied Riahi
,
Khalid Snoussi
,
et al.
Article dans une revue
pasteur-03219646v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|
|
|
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.
Article dans une revue
inserm-03841438v1
|
Partager
Gmail
Facebook
X
LinkedIn
More
|