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Epithelial cell chloride channel activity correlates with improved airway function in cystic fibrosis patients with the major mutant: Delta F508.

AuthorsJacqueline F Kidd, Christine E Bear
JournalPediatric research (Pediatr Res) Vol. 52 Issue 5 Pg. 625-7 (Nov 2002) ISSN: 0031-3998 [Print] United States
PMID12409505 (Publication Type: Comment, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • CFTR protein, human
  • Chlorides
  • Codon
  • Cystic Fibrosis Transmembrane Conductance Regulator
Topics
  • Chlorides (metabolism)
  • Codon (genetics)
  • Cystic Fibrosis (genetics, physiopathology)
  • Cystic Fibrosis Transmembrane Conductance Regulator (genetics, physiology)
  • Epithelial Cells (metabolism)
  • Genotype
  • Glycosylation
  • Humans
  • Ion Transport
  • Nasal Mucosa (metabolism, pathology)
  • Protein Folding
  • Protein Processing, Post-Translational
  • Sequence Deletion

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