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Molecular Characterization of the Ankle-Link Complex in Cochlear Hair Cells and Its Role in the Hair Bundle Functioning
N. Michalski
,
V. Michel
,
A. Bahloul
,
G. Lefevre
,
J. Barral
,
et al.
Journal articles
hal-03771502v1
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Conditional knock-out reveals that zygotic vezatin-null mouse embryos die at implantation
Vincent Hyenne
,
Céline Souilhol
,
Michel Cohen-Tannoudji
,
Silvia Cereghini
,
Christine Petit
,
et al.
Journal articles
pasteur-02075502v1
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Connexins Responsible for Hereditary Deafness — The Tale Unfolds
Martine Cohen-Salmon
,
Francisco del Castillo
,
Christine Petit
Book sections
hal-04028261v1
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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
,
et al.
Journal articles
pasteur-03926831v1
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Connexin30 deficiency causes instrastrial fluid–blood barrier disruption within the cochlear stria vascularis
Martine Cohen-Salmon
,
Béatrice Regnault
,
Nadège Cayet
,
Dorothée Caille
,
Karine Demuth
,
et al.
Proceedings of the National Academy of Sciences of the United States of America, 2007, 104 (15), pp.6229-6234. ⟨10.1073/pnas.0605108104⟩
Journal articles
hal-04027329v1
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SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.
Sébastien Albert
,
Hélène Blons
,
Laurence Jonard
,
Delphine Feldmann
,
Pierre Chauvin
,
et al.
Journal articles
inserm-00102388v1
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Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse.
Isabelle Roux
,
Saaid Safieddine
,
Régis Nouvian
,
M'Hamed Grati
,
Marie-Christine Simmler
,
et al.
Journal articles
hal-00111976v1
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