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

Samankaltaisia teoksia

• The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na(+) channel
  Tekijä: Schreiber, Rainer, et al.
  Julkaistu: (1999)
• The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl(–) concentration
  Tekijä: König, Jens, et al.
  Julkaistu: (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
  Tekijä: Briel, M, et al.
  Julkaistu: (1998)
• Cystic fibrosis transmembrane conductance regulator is involved in airway epithelial wound repair
  Tekijä: Schiller, Katherine R., et al.
  Julkaistu: (2010)
• Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections
  Tekijä: Hisert, Katherine B., et al.
  Julkaistu: (2017)