Ultrastructural pathological changes in the cochlear cells of connexin 26 conditional knockout mice

Mutations in the gene of connexin 26 (Cx26) are the most common cause of human non-syndromic hereditary deafness. The pathogenesis of deafness caused by Cx26 remains uncertain. To explore the basic mechanism underlying Cx26 null mutations, ultrastructural changes and a number of marker proteins in t...

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Detalles Bibliográficos
Autores principales: LIN, LAN, WANG, YUN-FENG, WANG, SHU-YI, LIU, SHAO-FENG, YU, ZHANG, XI, LIN, LI, HUA-WEI
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981006/
https://www.ncbi.nlm.nih.gov/pubmed/23917463
http://dx.doi.org/10.3892/mmr.2013.1614

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981006/
https://www.ncbi.nlm.nih.gov/pubmed/23917463
http://dx.doi.org/10.3892/mmr.2013.1614

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