Kindlin-1 Regulates Keratinocyte Electrotaxis

Kindler syndrome (KS) is an autosomal recessive blistering skin disease resulting from pathogenic mutations in FERMT1. This gene encodes kindlin-1, a focal adhesion protein involved in activation of the integrin family of extracellular matrix receptors. Most cases of KS show a marked reduction or co...

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Detalles Bibliográficos
Autores principales: Zhang, Gaofeng, Gu, Yu, Begum, Rumena, Chen, Hongduo, Gao, Xinghua, McGrath, John A., Parsons, Maddy, Song, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756539/
https://www.ncbi.nlm.nih.gov/pubmed/27427485
http://dx.doi.org/10.1016/j.jid.2016.05.129

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756539/
https://www.ncbi.nlm.nih.gov/pubmed/27427485
http://dx.doi.org/10.1016/j.jid.2016.05.129

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