Loss of CFTR chloride channels alters salt absorption by cystic fibrosis airway epithelia in vitro

Molecular Cell

Volumn 2, Issue 3, 1998, Pages 397-403

  Zabner, Joseph ^a   Smith, Jeffrey J ^a   Karp, Philip H ^a   Widdicombe, Jonathan H ^b   Welsh, Michael J ^a  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMILORIDE; BENZAMIL; CFTR PROTEIN, HUMAN; CHLORIDE; CYCLIC AMP; DRUG DERIVATIVE; FORSKOLIN; SODIUM CHLORIDE; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ABSORPTION; ARTICLE; BRONCHUS; CELL CULTURE; DRUG EFFECT; EPITHELIUM CELL; HUMAN; KINETICS; METABOLISM; NOSE MUCOSA; OSMOLARITY; PATHOLOGY; PATHOPHYSIOLOGY; PHYSIOLOGY; REFERENCE VALUE; TRACHEA; TRANSPORT AT THE CELLULAR LEVEL;

ABSORPTION; AMILORIDE; BIOLOGICAL TRANSPORT; BRONCHI; CELLS, CULTURED; CHLORIDES; CYCLIC AMP; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EPITHELIAL CELLS; FORSKOLIN; HUMANS; KINETICS; NASAL MUCOSA; OSMOLAR CONCENTRATION; REFERENCE VALUES; SODIUM CHLORIDE; TRACHEA;

EID: 0032160101     PISSN: 10972765     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1097-2765(00)80284-1     Document Type: Article

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