The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na(+) channel

Samankaltaisia teoksia

• The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.
  Tekijä: Mall, M, et al.
  Julkaistu: (1998)
• 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)
• The Cystic Fibrosis Transmembrane Conductance Regulator Impedes Proteolytic Stimulation of the Epithelial Na(+) Channel
  Tekijä: Gentzsch, Martina, et al.
  Julkaistu: (2010)
• Relationship between nucleotide binding and ion channel gating in cystic fibrosis transmembrane conductance regulator
  Tekijä: Aleksandrov, Andrei A, et al.
  Julkaistu: (2009)