Turnover of the cystic fibrosis transmembrane conductance regulator (CFTR): Slow degradation of wild-type and ΔF508 CFTR in surface membrane preparations of immortalized airway epithelial cells

Journal of Cellular Physiology

Volumn 168, Issue 2, 1996, Pages 373-384

  Wei, Xiaofang ^b   Eisman, Robin ^b   Xu, Jin ^b   Harsch, Alan D ^b   Mulberg, Andrew E ^b   Bevins, Charles L ^b   Glick, Mary Catherine ^b   Scanlin, Thomas F ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CASTANOSPERMINE; CHLORIDE CHANNEL; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ARTICLE; CELL SURFACE; GENE EXPRESSION; GENE MUTATION; HUMAN; HUMAN CELL; IMMUNOBLOTTING; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN LOCALIZATION; RESPIRATORY TRACT MUCOSA;

ALPHA-GLUCOSIDASES; AMINO ACID SEQUENCE; BLOTTING, WESTERN; CELL LINE; CELL MEMBRANE; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; ELECTROPHORESIS, POLYACRYLAMIDE GEL; EPITHELIAL CELLS; EPITHELIUM; HUMANS; INDOLIZINES; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; PRECIPITIN TESTS; RESPIRATORY SYSTEM;

EID: 0029760291     PISSN: 00219541     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-4652(199608)168:2<373::AID-JCP16>3.0.CO;2-4     Document Type: Article

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