A functional R domain from cystic fibrosis transmembrane conductance regulator is predominantly unstructured in solution

Eitemau Tebyg

• Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR(−/−) mice
  gan: Ostedgaard, Lynda S., et al.
  Cyhoeddwyd: (2011)
• Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia
  gan: Ostedgaard, Lynda S., et al.
  Cyhoeddwyd: (2003)
• Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia.
  gan: Denning, G M, et al.
  Cyhoeddwyd: (1992)
• Mechanism of dysfunction of two nucleotide binding domain mutations in cystic fibrosis transmembrane conductance regulator that are associated with pancreatic sufficiency.
  gan: Sheppard, D N, et al.
  Cyhoeddwyd: (1995)
• Human–mouse cystic fibrosis transmembrane conductance regulator (CFTR) chimeras identify regions that partially rescue CFTR-ΔF508 processing and alter its gating defect
  gan: Dong, Qian, et al.
  Cyhoeddwyd: (2012)