Identification of the Cystic Fibrosis Transmembrane Conductance Regulator Domains That Are Important for Interactions with ROMK2

This publication has 26 references indexed in Scilit:

• Structure and Function of the CFTR Chloride Channel
  Physiological Reviews, 1999
• CFTR Is a Conductance Regulator as well as a Chloride Channel
  Physiological Reviews, 1999
• Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator
  Proceedings of the National Academy of Sciences, 1998
• Mechanisms of renal tubular cell hypertrophy: mitogen-induced suppression of proteolysis
  American Journal of Physiology-Cell Physiology, 1997
• Inhibition of epithelial Na⁺ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator
  FEBS Letters, 1997
• Sensitivity of a renal K+ channel (ROMK2) to the inhibitory sulfonylurea compound glibenclamide is enhanced by coexpression with the ATP-binding cassette transporter cystic fibrosis transmembrane regulator.
  Proceedings of the National Academy of Sciences, 1996
• Wild type but not ΔF508 CFTR inhibits Na⁺ conductance when coexpressed in Xenopus oocytes
  FEBS Letters, 1996
• CFTR as a cAMP-Dependent Regulator of Sodium Channels
  Science, 1995
• Defective regulation of outwardly rectifying Cl− channels by protein kinase A corrected by insertion of CFTR
  Nature, 1992
• Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)
  Cell, 1992