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

  • Author(s): Nadel, Jay
  • Kim, S
  • Beyer, BA
  • Lewis, C
  • et al.

Published Web Location

http://europepmc.org/articles/PMC3745379?pdf=render
No data is associated with this publication.
Abstract

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 neutrophil

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