Cystic fibrosis transmembrane conductance regulator (CFTR) functionality is dependent on coatomer protein I (COPI)

Biology of the Cell

Volumn 99, Issue 8, 2007, Pages 433-444

  Yu, Ying ^a,b   Platoshyn, Oleksandr ^a   Safrina, Olga ^b   Tsigelny, Igor ^c   Yuan, Jason X J ^a   Keller, Steven H ^a  

^a UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Coatomer protein; Cystic fibrosis; Endoplasmic reticulum; IdIF cell; Ion channel trafficking

Indexed keywords

CELL PROTEIN; CHLORIDE CHANNEL; COATOMER PROTEIN; COATOMER PROTEIN 1; CYCLIC AMP; EPSILON COATOMER PROTEIN; POLYPEPTIDE; TRANSMEMBRANE CONDUCTANCE REGULATOR; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BIOTINYLATION; CELL SURFACE; CHLORIDE TRANSPORT; CONTROLLED STUDY; ELECTROPHYSIOLOGY; ENDOPLASMIC RETICULUM; GENE MUTATION; GENETIC TRANSFECTION; IMMUNOFLUORESCENCE MICROSCOPY; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN SYNTHESIS; TEMPERATURE SENSITIVITY; WILD TYPE;

ANIMALS; BIOTINYLATION; CHO CELLS; COP-COATED VESICLES; CRICETINAE; CRICETULUS; CYCLIC AMP; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; ENDOPLASMIC RETICULUM; FORSKOLIN; HUMANS; ION CHANNEL GATING; OLIGOSACCHARIDES;

EID: 34547970891     PISSN: 02484900     EISSN: None     Source Type: Journal    
DOI: 10.1042/BC20060114     Document Type: Article

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