Caricamento...
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...
Salvato in:
| Pubblicato in: | J Invest Dermatol |
|---|---|
| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2016
|
| Soggetti: | |
| Accesso online: | 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 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|