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Kindlin-1 Regulates Epidermal Growth Factor Receptor Signaling
Kindler syndrome is an autosomal recessive genodermatosis that results from mutations in the FERMT1 gene encoding t kindlin-1. Kindlin-1 localizes to focal adhesion and is known to contribute to the activation of integrin receptors. Most cases of Kindler syndrome show a reduction or complete absence...
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| Publicado no: | J Invest Dermatol |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6345584/ https://ncbi.nlm.nih.gov/pubmed/30248333 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jid.2018.08.020 |
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