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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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Main Authors: | , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Oxford University Press
2009
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Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2778370/ https://ncbi.nlm.nih.gov/pubmed/19755382 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp436 |
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