The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.

Ítems similars

• The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na(+) channel
  per: Schreiber, Rainer, et al.
  Publicat: (1999)
• The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl(–) concentration
  per: König, Jens, et al.
  Publicat: (2001)
• Cl(−) transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na(+) channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC
  per: Briel, M, et al.
  Publicat: (1998)
• Cystic fibrosis transmembrane conductance regulator is involved in airway epithelial wound repair
  per: Schiller, Katherine R., et al.
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• Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections
  per: Hisert, Katherine B., et al.
  Publicat: (2017)