Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia

Ítems similars

• CFTR with a partially deleted R domain corrects the cystic fibrosis chloride transport defect in human airway epithelia in vitro and in mouse nasal mucosa in vivo
  per: Ostedgaard, Lynda S., et al.
  Publicat: (2002)
• Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia.
  per: Denning, G M, et al.
  Publicat: (1992)
• A shortened adeno-associated virus expression cassette for CFTR gene transfer to cystic fibrosis airway epithelia
  per: Ostedgaard, Lynda S., et al.
  Publicat: (2005)
• Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia
  Publicat: (1992)
• A functional R domain from cystic fibrosis transmembrane conductance regulator is predominantly unstructured in solution
  per: Ostedgaard, Lynda S., et al.
  Publicat: (2000)