Cystic fibrosis transmembrane conductance regulator inhibits epithelial Na+ channels carrying Liddle's syndrome mutations

Journal of Biological Chemistry

Volumn 274, Issue 20, 1999, Pages 13894-13899

  Hopf, Anna ^a   Schreiber, Rainer ^a   Mall, Marcus ^a   Greger, Rainer ^a   Kunzelmann, Karl ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIC AMP DEPENDENT PROTEIN KINASE; SODIUM CHANNEL; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ANIMAL CELL; ARTICLE; ENZYME ACTIVITY; GENE EXPRESSION; GENE MUTATION; LIDDLE SYNDROME; NONHUMAN; POINT MUTATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN PROTEIN INTERACTION; REGULATORY MECHANISM; SODIUM CONDUCTANCE; SODIUM CURRENT;

1-METHYL-3-ISOBUTYLXANTHINE; ANIMALS; ANTIBODIES; CALCIUM-BINDING PROTEINS; CYCLIC AMP-DEPENDENT PROTEIN KINASES; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DYNAMINS; EPITHELIAL SODIUM CHANNEL; GTP PHOSPHOHYDROLASES; HUMANS; HYPERTENSION; LIGASES; PHOSPHODIESTERASE INHIBITORS; POINT MUTATION; PROTEIN CONFORMATION; RATS; SERINE ENDOPEPTIDASES; SODIUM CHANNEL BLOCKERS; SODIUM CHANNELS; STRUCTURE-ACTIVITY RELATIONSHIP; SYNDROME; TRYPSIN; UBIQUITIN-PROTEIN LIGASES; UBIQUITINS;

EID: 0033553396     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.274.20.13894     Document Type: Article

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