CFTR is required for cAMP inhibition of intestinal Na+ absorption in a cystic fibrosis mouse model

American Journal of Physiology - Gastrointestinal and Liver Physiology

Volumn 270, Issue 2 33-2, 1996, Pages

  Clarke, Lane L ^a   Harline, Matthew C ^a  

^a UNIVERSITY OF MISSOURI   (United States)

Author keywords

adenosine 3',5' cyclic monophosphate; chloride; cystic fibrosis transmembrane conductance regulator; secretion; sodium

Indexed keywords

BUMETANIDE; CHLORIDE ION; CHLORINE 36; CYCLIC AMP; ISOBUTYLMETHYLXANTHINE; SODIUM 22; SODIUM CHLORIDE; SODIUM ION; TETRODOTOXIN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CHLORIDE TRANSPORT; CONTROLLED STUDY; CYSTIC FIBROSIS; ION TRANSPORT; JEJUNUM; MEMBRANE POTENTIAL; MOUSE; NONHUMAN; PRIORITY JOURNAL; SHORT CIRCUIT CURRENT; SMALL INTESTINE ABSORPTION; SODIUM ABSORPTION;

EID: 0029968716     PISSN: 01931857     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpgi.1996.270.2.g259     Document Type: Article

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