Roux, Isabelle, Hosie, Suzanne, Johnson, Stuart L., Bahloul, Amel, Cayet, Nadège, Nouaille, Sylvie, ...
The ribbon synapses of auditory inner hair cells (IHCs) undergo morphological and electrophysiological transitions during cochlear development. Here we report that myosin VI (Myo6), an actin-based...
Boëda, Batiste, El-Amraoui, Aziz, Bahloul, Amel, Goodyear, Richard, Daviet, Laurent, Blanchard, Stéphane, ...
Deaf-blindness in three distinct genetic forms of Usher type I syndrome (USH1) is caused by defects in myosin VIIa, harmonin and cadherin 23. Despite being critical for hearing, the functions of...
The unique insert in myosin VI is a structural calcium–calmodulin binding site
Bahloul, Amel, Chevreux, Guillaume, Wells, Amber L., Martin, Davy, Nolt, Jocelyn, Yang, Zhaohui, ...
Myosin VI contains an inserted sequence that is unique among myosin superfamily members and has been suggested to be a determinant of the reverse directionality and unusual motility of the motor. It...
Boëda, Batiste, El-Amraoui, Aziz, Bahloul, Amel, Goodyear, Richard, Daviet, Laurent, Blanchard, Stéphane, ...
Deaf-blindness in three distinct genetic forms of Usher type I syndrome (USH1) is caused by defects in myosin VIIa, harmonin and cadherin 23. Despite being critical for hearing, the functions of...
The unique insert in myosin VI is a structural calcium–calmodulin binding site
Bahloul, Amel, Chevreux, Guillaume, Wells, Amber L., Martin, Davy, Nolt, Jocelyn, Yang, Zhaohui, ...
Myosin VI contains an inserted sequence that is unique among myosin superfamily members and has been suggested to be a determinant of the reverse directionality and unusual motility of the motor. It...