Human–mouse cystic fibrosis transmembrane conductance regulator (CFTR) chimeras identify regions that partially rescue CFTR-ΔF508 processing and alter its gating defect

Lignende værker

• Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR(−/−) mice
  af: Ostedgaard, Lynda S., et al.
  Udgivet: (2011)
• Processing and function of CFTR-ΔF508 are species-dependent
  af: Ostedgaard, Lynda S., et al.
  Udgivet: (2007)
• A Genomic Signature Approach to Rescue ΔF508-Cystic Fibrosis Transmembrane Conductance Regulator Biosynthesis and Function
  af: Ramachandran, Shyam, et al.
  Udgivet: (2014)
• ΔF508 CFTR interactome remodeling promotes rescue of Cystic Fibrosis
  af: Pankow, Sandra, et al.
  Udgivet: (2015)
• Functional Stability of Rescued ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator in Airway Epithelial Cells
  af: Jurkuvenaite, Asta, et al.
  Udgivet: (2010)