Molecular composition and distribution of gap junctions in the sensory epithelium of the human cochlea—a super-resolution structured illumination microscopy (SR-SIM) study

BACKGROUND: Mutations in the GJB2 gene, which encodes the Connexin26 (Cx26) protein, are the most common cause of childhood hearing loss in American and European populations. The cochlea contains a gap junction (GJ) network in the sensory epithelium and two connective tissue networks in the lateral...

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Detalhes bibliográficos
Publicado no:Ups J Med Sci
Main Authors: Liu, Wei, Li, Hao, Edin, Fredrik, Brännström, Johan, Glueckert, Rudolf, Schrott-Fischer, Annelies, Molnar, Matyas, Pacholsky, Dirk, Pfaller, Kristian, Rask-Andersen, Helge
Formato: Artigo
Idioma:Inglês
Publicado em: Taylor & Francis 2017
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5649321/
https://ncbi.nlm.nih.gov/pubmed/28513246
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/03009734.2017.1322645
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