The Mechanical Behavior of Mutant K14-R125P Keratin Bundles and Networks in NEB-1 Keratinocytes

Epidermolysis bullosa simplex (EBS) is an inherited skin-blistering disease that is caused by dominant mutations in the genes for keratin K5 or K14 proteins. While the link between keratin mutations and keratinocyte fragility in EBS patients is clear, the exact biophysical mechanisms underlying cell...

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Detalles Bibliográficos
Autores principales: Beriault, Daniel R., Haddad, Oualid, McCuaig, John V., Robinson, Zachary J., Russell, David, Lane, E. Birgitte, Fudge, Douglas S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283645/
https://www.ncbi.nlm.nih.gov/pubmed/22363617
http://dx.doi.org/10.1371/journal.pone.0031320

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283645/
https://www.ncbi.nlm.nih.gov/pubmed/22363617
http://dx.doi.org/10.1371/journal.pone.0031320

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