Abnormal passive chloride absorption in cystic fibrosis jejunum functionally opposes the classic chloride secretory defect

Journal of Clinical Investigation

Volumn 112, Issue 1, 2003, Pages 118-125

  Russo, Michael A ^a,b   Högenauer, Christoph ^a,c   Coates Jr , Stephen W ^a   Santa Ana, Carol A ^a   Porter, Jack L ^a   Rosenblatt, Randall L ^b   Emmett, Michael ^a   Fordtran, John S ^a  

^a BAYLOR UNIVERSITY MEDICAL CENTER   (United States)

^b CHILDREN S MEDICAL CENTER   (United States)

^c UNIVERSITY OF GRAZ   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

BICARBONATE; CHLORIDE; SODIUM; TRANSMEMBRANE CONDUCTANCE REGULATOR; WATER; CFTR PROTEIN, HUMAN; UREA; XYLOSE;

ADULT; ARTICLE; CLINICAL ARTICLE; CYSTIC FIBROSIS; DISEASE SEVERITY; FEMALE; GENE MUTATION; HUMAN; INTESTINE ABSORPTION; JEJUNUM; MALE; PRIORITY JOURNAL; WATER ABSORPTION; DIFFUSION; METABOLISM; PHYSIOLOGY;

ADULT; BICARBONATES; CHLORIDES; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DIFFUSION; FEMALE; HUMANS; INTESTINAL ABSORPTION; JEJUNUM; MALE; UREA; XYLOSE;

EID: 0346727280     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI200317667     Document Type: Article

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