Mice with conditional deletion of Cx26 exhibit no vestibular phenotype despite secondary loss of Cx30 in the vestibular end organs

Author:

Lee Min Young,Takada Tomoko,Takada Yohei,Kappy Michelle D.,Beyer Lisa A.,Swiderski Donald L.,Godin Ashley L.,Brewer Shannon,King W. Michael,Raphael Yehoash

Funder

Hirschfield Foundation

R. Jamison and Betty Williams Professorship

NIH/NIDCD

Publisher

Elsevier BV

Subject

Sensory Systems

Reference75 articles.

1. Auditory and vestibular mouse mutants: models for human deafness;Ahituv;J. Basic Clin. Physiol. Pharmacol.,2000

2. Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness;Ahmad;Proc. Natl. Acad. Sci. U. S. A.,2007

3. Restoration of hearing in the VGLUT3 knockout mouse using virally mediated gene therapy;Akil;Neuron,2012

4. The development of sensorimotor reflexes in albino mice; albino rats and black-hooded rats;Allam;Int. J. Dev. Neurosci.,2012

5. Differential vulnerability of outer and inner hair cells during and after oxygen-glucose deprivation in organotypic cultures of newborn rats;Amarjargal;Physiol. Res.,2009

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