TMEM16A in Cystic Fibrosis: Activating or Inhibiting?

The inflammatory airway disease cystic fibrosis (CF) is characterized by airway obstruction due to mucus hypersecretion, airway plugging, and bronchoconstriction. The cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel is dysfunctional in CF, leading to defects in epithelial...

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Main Authors: Karl Kunzelmann (Author), Jiraporn Ousingsawat (Author), Inês Cabrita (Author), Tereza Doušová (Author), Andrea Bähr (Author), Melanie Janda (Author), Rainer Schreiber (Author), Roberta Benedetto (Author)
Format: Book
Published: Frontiers Media S.A., 2019-01-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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