Inhibition of the Cystic Fibrosis Transmembrane Conductance Regulator By ATP‐Sensitive K⁺ Channel Regulators^a

This publication has 40 references indexed in Scilit:

• Effect of ATP-sensitive K+ channel regulators on cystic fibrosis transmembrane conductance regulator chloride currents.
  The Journal of general physiology, 1992
• Regulation by ATP and ADP of CFTR Chloride Channels That Contain Mutant Nucleotide-Binding Domains
  Science, 1992
• Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia.
  Journal of Clinical Investigation, 1992
• Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel.
  Journal of Clinical Investigation, 1991
• Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity
  Science, 1991
• Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells
  Nature, 1990
• Righting the wrong protein
  Nature, 1990
• Bacterial periplasmic permeases belong to a family of transport proteins operating from Escherichia coli to human: Traffic ATPases
  FEMS Microbiology Letters, 1990
• ATP mediates both activation and inhibition of K(ATP) channel activity via cAMP-dependent protein kinase in insulin-secreting cell lines.
  The Journal of general physiology, 1989
• The gating of nucleotide-sensitive K+ channels in insulin-secreting cells can be modulated by changes in the ratio ATP4−/ADP3− and by nonhydrolyzable derivatives of both ATP and ADP
  The Journal of Membrane Biology, 1988