Cystic Fibrosis-associated Mutations at Arginine 347 Alter the Pore Architecture of CFTR

This publication has 34 references indexed in Scilit:

• Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Anion Binding as a Probe of the Pore
  Biophysical Journal, 1998
• Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment
  Biophysical Journal, 1996
• Novel pore-lining residues in CFTR that govern permeation and open-channel block
  Neuron, 1994
• Multi-ion pore behaviour in the CFTR chloride channel
  Nature, 1993
• The Cystic Fibrosis Transmembrane Conductance Regulator
  Annual Review of Physiology, 1993
• Mutations in CFTR associated with mild-disease-form CI- channels with altered pore properties
  Nature, 1993
• 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 the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance
  Cell, 1991
• Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients
  Cell, 1990