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

Lignende værker

• The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl(–) concentration
  af: König, Jens, et al.
  Udgivet: (2001)
• Proteases, ENaCs and cystic fibrosis
  af: Kleyman, Thomas R, et al.
  Udgivet: (2014)
• Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
  af: Giuseppe Fabio Parisi, et al.
  Udgivet: (2022-05-01)
• The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.
  af: Mall, M, et al.
  Udgivet: (1998)
• CFTR fails to inhibit the epithelial sodium channel ENaC expressed in Xenopus laevis oocytes
  af: Nagel, G, et al.
  Udgivet: (2005)