The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl(–) concentration

Gelijkaardige items

• 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
  door: Briel, M, et al.
  Gepubliceerd in: (1998)
• ENaC inhibition in cystic fibrosis: potential role in the new era of CFTR modulator therapies
  door: Mall, Marcus A.
  Gepubliceerd in: (2020)
• The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na(+) channel
  door: Schreiber, Rainer, et al.
  Gepubliceerd in: (1999)
• Direct Sensing of Intracellular pH by the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Cl(−) Channel
  door: Chen, Jeng-Haur, et al.
  Gepubliceerd in: (2009)
• The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.
  door: Mall, M, et al.
  Gepubliceerd in: (1998)