Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience
Reference200 articles.
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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. Transfer of biologically important molecules between cells through gap junction channels;Alexander;Curr. Med. Chem.,2003
4. Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems;Altevogt;J. Neurosci.,2002
5. ATP release through connexin hemichannels and gap junction transfer of second messengers propagate Ca2+ signals across the inner ear;Anselmi;Proc. Natl. Acad. Sci. U. S. A.,2008
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1. Cytomembrane Trafficking Pathways of Connexin 26, 30, and 43;International Journal of Molecular Sciences;2023-06-19
2. A Chemical Chaperone Restores Connexin 26 Mutant Activity;ACS Pharmacology & Translational Science;2023-06-01
3. Recent insights into gap junction biogenesis in the cochlea;Developmental Dynamics;2022-09-26
4. Volumetric Analysis of Hearing-Related Structures of Brain in Children with GJB2-Related Congenital Deafness;Children;2022-05-30
5. Tricellular adherens junctions provide a cell surface delivery platform for connexin 26/30 oligomers in the cochlea;Hearing Research;2021-02
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