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Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31
Philomena Mburu
,
Mirna Mustapha
,
Anabel Varela
,
Dominique Weil
,
Aziz El-Amraoui
,
et al.
Journal articles
pasteur-03926895v1
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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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Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly
Benjamin Delprat
,
Vincent Michel
,
Richard Goodyear
,
Yasuhiro Yamasaki
,
Nicolas Michalski
,
et al.
Journal articles
istex
pasteur-03926836v1
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Interactions in the network of Usher syndrome type 1 proteins
Avital Adato
,
Vincent Michel
,
Yoshiaki Kikkawa
,
Jan Reiners
,
Kumar N Alagramam
,
et al.
Journal articles
istex
pasteur-03926828v1
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