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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...
Autores principales: | Michael, Magdalene, Begum, Rumena, Chan, Grace K., Whitewood, Austin J., Matthews, Daniel R., Goult, Benjamin T., McGrath, John A., Parsons, Maddy |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345584/ https://www.ncbi.nlm.nih.gov/pubmed/30248333 http://dx.doi.org/10.1016/j.jid.2018.08.020 |
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