Airway Epithelial Inflammation In Vitro Augments the Rescue of Mutant CFTR by Current CFTR Modulator Therapies

In cystic fibrosis (CF), defective biogenesis and activity of the cystic fibrosis transmembrane conductance regulator (CFTR) leads to airway dehydration and impaired mucociliary clearance, resulting in chronic airway infection and inflammation. The most common CFTR mutation, F508del, results in a pr...

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Main Authors: Martina Gentzsch (Author), Deborah M. Cholon (Author), Nancy L. Quinney (Author), Mary E. B. Martino (Author), John T. Minges (Author), Susan E. Boyles (Author), Tara N. Guhr Lee (Author), Charles R. Esther (Author), Carla M. P. Ribeiro (Author)
Format: Book
Published: Frontiers Media S.A., 2021-03-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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