Cellular heterogeneity of CFTR expression and function in the lung: Implications for gene therapy of cystic fibrosis

European Journal of Human Genetics

Volumn 6, Issue 1, 1998, Pages 12-31

  Jiang, Q ^a   Engelhardt, J F ^a  

^a UNIVERSITY OF IOWA   (United States)

Author keywords

Airway; CFTR; Cystic fibrosis; Gene therapy; Lung

Indexed keywords

AMILORIDE; CHLORIDE; CHLORIDE CHANNEL; LIPOSOME; SODIUM CHANNEL; TRANSMEMBRANE CONDUCTANCE REGULATOR;

CELL MEMBRANE PERMEABILITY; CELL TYPE; CHLORIDE TRANSPORT; CILIATED EPITHELIUM; CYSTIC FIBROSIS; ELECTROLYTE BALANCE; FLUID BALANCE; GENE TARGETING; GENE THERAPY; GOBLET CELL; HUMAN; INTERSTITIUM; MEMBRANE CONDUCTANCE; PATHOGENESIS; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROTEIN EXPRESSION; RESPIRATORY EPITHELIUM; REVIEW; VIRUS RECOMBINANT;

EID: 0031889465     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200158     Document Type: Review

References (157)