Challenges Facing Airway Epithelial Cell-Based Therapy for Cystic Fibrosis

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene cause the life-limiting hereditary disease, cystic fibrosis (CF). Decreased or absent functional CFTR protein in airway epithelial cells leads to abnormally viscous mucus and impaired mucociliary transport, resulting in...

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Bibliographic Details
Main Authors: Andrew Berical (Author), Rhianna E. Lee (Author), Scott H. Randell (Author), Finn Hawkins (Author)
Format: Book
Published: Frontiers Media S.A., 2019-02-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
Copy 1 Available