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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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| Publicat a: | J Invest Dermatol |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5756539/ https://ncbi.nlm.nih.gov/pubmed/27427485 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jid.2016.05.129 |
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