All Stories

  1. High-content assay for CFTR monitoring: simultaneous quantification of channel function and biogenesis
  2. Structure, Gating, and Regulation of the CFTR Anion Channel
  3. CFTR potentiation by VX-770 involves stabilization of the pre-hydrolytic, O1 state
  4. Structure of Transmembrane Helix 8 and Possible Membrane Defects in CFTR
  5. Improved fluorescence assays to measure the defects associated with F508del-CFTR allow identification of new active compounds
  6. Discovery of Multitarget Agents Active as Broad-Spectrum Antivirals and Correctors of Cystic Fibrosis Transmembrane Conductance Regulator for Associated Pulmonary Diseases
  7. Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)
  8. Increased apical Na+permeability in cystic fibrosis is supported by a quantitative model of epithelial ion transport
  9. Conformational changes in the catalytically inactive nucleotide-binding site of CFTR
  10. Mutant cycles at CFTR’s non-canonical ATP-binding site support little interface separation during gating
  11. Electrophysiological, Biochemical, and Bioinformatic Methods for Studying CFTR Channel Gating and Its Regulation
  12. Involvement of F1296 and N1303 of CFTR in induced-fit conformational change in response to ATP binding at NBD2
  13. Strict coupling between CFTR’s catalytic cycle and gating of its Cl − ion pore revealed by distributions of open channel burst durations
  14. ATP hydrolysis-driven gating in cystic fibrosis transmembrane conductance regulator
  15. In vivo phosphorylation of CFTR promotes formation of a nucleotide-binding domain heterodimer
  16. The ABC protein turned chloride channel whose failure causes cystic fibrosis
  17. Control of the CFTR channel's gates
  18. CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains
  19. Prolonged Nonhydrolytic Interaction of Nucleotide with CFTR's NH2-terminal Nucleotide Binding Domain and its Role in Channel Gating
  20. On the Mechanism of MgATP-dependent Gating of CFTR Cl−Channels
  21. Mutations in the yeast two pore K+channel YKC1 identify functional differences between the pore domains
  22. Mutations in the pore regions of the yeast K+ channel YKC1 affect gating by extracellular K+
  23. Extracellular K+and Ba2+mediate voltage-dependent inactivation of the outward-rectifying K+channel encoded by the yeast geneTOK1
  24. Complementation of a yeast Δpkc1mutant by theArabidopsisprotein ANT