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Normal CFTR Inhibits Epidermal Growth Factor Receptor-Dependent Pro-Inflammatory Chemokine Production in Human Airway Epithelial Cells

Mutations in cystic fibrosis transmembrane conductance regulator (CFTR) protein cause cystic fibrosis, a disease characterized by exaggerated airway epithelial production of the neutrophil chemokine interleukin (IL)-8, which results in exuberant neutrophilic inflammation. Because activation of an ep...

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Detalles Bibliográficos
Autores principales:	Kim, Suil, Beyer, Brittney A., Lewis, Courtney, Nadel, Jay A.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2013
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745379/ https://www.ncbi.nlm.nih.gov/pubmed/23977375 http://dx.doi.org/10.1371/journal.pone.0072981

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