Mutant (δF508) Cystic Fibrosis Transmembrane Conductance Regulator Cl− Channel Is Functional When Retained in Endoplasmic Reticulum of Mammalian Cells

This publication has 30 references indexed in Scilit:

• CFTR displays voltage dependence and two gating modes during stimulation.
  The Journal of general physiology, 1994
• Molecular basis of defective anion transport in L cells expressing recombinant forms of CFTR
  Human Molecular Genetics, 1993
• Identification of revertants for the cystic fibrosis ΔF508 mutation using STE6-CFTR chimeras in yeast
  Cell, 1993
• The Nuclear Membrane
  Science, 1992
• Immunocytochemical analysis reveals differences between the subcellular localization of normal and ΔPhe508 recombinant cystic fibrosis transmembrane conductance regulator
  Experimental Cell Research, 1992
• Cystic fibrosis transmembrane conductance regulator: A chloride channel with novel regulation
  Neuron, 1992
• Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation
  Nature, 1991
• Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene
  Nature, 1991
• Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
  Science, 1989
• Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
  Science, 1989