All Stories

  1. CFTR in GtoPdb v.2025.3
  2. K978C CFTR restores essential epithelial function with greater efficiency than wildtype CFTR when expressed in CF airway cells
  3. Can two wrongs make a right? F508del-CFTR ion channel rescue by second-site mutations in its transmembrane domains
  4. Can two wrongs make a right? F508del-CFTR ion channel rescue by second-site mutations in its transmembrane domains
  5. Fluorescence assay for simultaneous quantification of CFTR ion-channel function and plasma membrane proximity
  6. Strategies for cystic fibrosis transmembrane conductance regulator inhibition: from molecular mechanisms to treatment for secretory diarrhoeas
  7. Multitarget CFTR Modulators Endowed with Multiple Beneficial Side Effects for Cystic Fibrosis Patients: Toward a Simplified Therapeutic Approach
  8. High-content assay for CFTR monitoring: simultaneous quantification of channel function and biogenesis
  9. Does Disruption of the E873-R933 Salt Bridge in CFTR and Alteration of the Membrane Bilayer Around It Play a Biological Role?
  10. Structure, Gating, and Regulation of the CFTR Anion Channel
  11. CFTR potentiation by VX-770 involves stabilization of the pre-hydrolytic, O1 state
  12. Structure of Transmembrane Helix 8 and Possible Membrane Defects in CFTR
  13. Improved fluorescence assays to measure the defects associated with F508del-CFTR allow identification of new active compounds
  14. Discovery of Multitarget Agents Active as Broad-Spectrum Antivirals and Correctors of Cystic Fibrosis Transmembrane Conductance Regulator for Associated Pulmonary Diseases
  15. Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)
  16. Increased apical Na+permeability in cystic fibrosis is supported by a quantitative model of epithelial ion transport
  17. Conformational changes in the catalytically inactive nucleotide-binding site of CFTR
  18. Mutant cycles at CFTR’s non-canonical ATP-binding site support little interface separation during gating
  19. Electrophysiological, Biochemical, and Bioinformatic Methods for Studying CFTR Channel Gating and Its Regulation
  20. Involvement of F1296 and N1303 of CFTR in induced-fit conformational change in response to ATP binding at NBD2
  21. Strict coupling between CFTR’s catalytic cycle and gating of its Cl − ion pore revealed by distributions of open channel burst durations
  22. ATP hydrolysis-driven gating in cystic fibrosis transmembrane conductance regulator
  23. In vivo phosphorylation of CFTR promotes formation of a nucleotide-binding domain heterodimer
  24. The ABC protein turned chloride channel whose failure causes cystic fibrosis
  25. Control of the CFTR channel's gates
  26. CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains
  27. Prolonged Nonhydrolytic Interaction of Nucleotide with CFTR's NH2-terminal Nucleotide Binding Domain and its Role in Channel Gating
  28. On the Mechanism of MgATP-dependent Gating of CFTR Cl−Channels
  29. Mutations in the yeast two pore K+channel YKC1 identify functional differences between the pore domains
  30. Mutations in the pore regions of the yeast K+ channel YKC1 affect gating by extracellular K+
  31. Extracellular K+and Ba2+mediate voltage-dependent inactivation of the outward-rectifying K+channel encoded by the yeast geneTOK1
  32. Complementation of a yeast Δpkc1mutant by theArabidopsisprotein ANT
  33. Relationship between fusaric acid uptake and its binding to cell structures by leaves of Egeria densa and its toxic effects on membrane permeability and respiration