Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Nature|October 14, 2008
Stereocilin-deficient mice reveal the origin of cochlear waveform distortionsElisabeth Verpy, Dominique Weil, Michel Leibovici, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2012
A mouse model for human deafness DFNB22 reveals that hearing impairment is due to a loss of inner hair cell stimulationAndrei N Lukashkin, P Kevin Legan, Thomas D Weddell, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2004
Hearing loss and retarded cochlear development in mice lacking type 2 iodothyronine deiodinaseLily Ng, Richard J Goodyear, Chad A Woods, et al.
Human Molecular Genetics|December 24, 2013
Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membraneP Kevin Legan, Richard J Goodyear, Matías Morín, et al.
Developmental Cell|March 16, 2017
Cell-Cell Contact Area Affects Notch Signaling and Notch-Dependent PatterningOren Shaya, Udi Binshtok, Micha Hersch, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 16, 2006
The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundlesJoann McGee, Richard J Goodyear, D Randy McMillan, et al.
Molecular Therapy. Methods & Clinical Development|August 29, 2022
AAV-mediated rescue of Eps8 expression in vivo restores hair-cell function in a mouse model of recessive deafnessJing-Yi Jeng, Adam J Carlton, Richard J Goodyear, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 26, 2011
Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereociliaElisa Caberlotto, Vincent Michel, Isabelle Foucher, et al.
Pageof 5