UTP inhibits Na+ absorption in wild-type and ΔF508 CFTR-expressing human bronchial epithelia

American Journal of Physiology - Cell Physiology

Volumn 276, Issue 4 45-4, 1999, Pages

  Devor, Daniel C ^a   Pilewski, Joseph M ^a  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

Author keywords

Cystic fibrosis; Cystic fibrosis transmembrane conductance regulator; Epithelial sodium channel; Human airway; Uridine 5' triphosphate

Indexed keywords

AMILORIDE; APYRASE; BRADYKININ; CHLORIDE ION; ETHYLENE GLYCOL 1,2 BIS(2 AMINOPHENYL) ETHER N,N,N',N' TETRAACETIC ACID; HISTAMINE; NYSTATIN; PHORBOL 13 ACETATE 12 MYRISTATE; PHOSPHATASE; PHOSPHOLIPASE A2 INHIBITOR; POTASSIUM ION; PROTEIN KINASE C INHIBITOR; SODIUM ION; THAPSIGARGIN; TRANSMEMBRANE CONDUCTANCE REGULATOR; URIDINE TRIPHOSPHATE;

ARTICLE; BASOLATERAL MEMBRANE; BRONCHUS MUCOSA; CALCIUM TRANSPORT; CHLORIDE TRANSPORT; CONTROLLED STUDY; CYSTIC FIBROSIS; DRUG EFFECT; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; POTASSIUM CONDUCTANCE; POTASSIUM CURRENT; PRIORITY JOURNAL; SHORT CIRCUIT CURRENT; SODIUM ABSORPTION;

BRONCHUS;

EID: 0032899770     PISSN: 03636143     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpcell.1999.276.4.c827     Document Type: Article

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