EKV mutant connexin 31 associated cell death is mediated by ER stress

The epidermis expresses a number of connexin (Cx) proteins that are implicated in gap junction-mediated cell communication. Distinct dominantly inherited mutations in Cx31 cause the skin disease erythrokeratoderma variabilis (EKV) and hearing loss with or without neuropathy. Functional studies revea...

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Detalles Bibliográficos
Autores principales: Tattersall, Daniel, Scott, Claire A., Gray, Colin, Zicha, Daniel, Kelsell, David P.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778370/
https://www.ncbi.nlm.nih.gov/pubmed/19755382
http://dx.doi.org/10.1093/hmg/ddp436

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778370/
https://www.ncbi.nlm.nih.gov/pubmed/19755382
http://dx.doi.org/10.1093/hmg/ddp436

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