Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

Cell

Volumn 63, Issue 4, 1990, Pages 827-834

  Cheng, Seng H ^a   Gregory, Richard J ^a   Marshall, John ^a   Paul, Sucharita ^a   Souza, David W ^a   White, Gary A ^a   O'Riordan, Catherine R ^a   Smith, Alan E ^a  

^a GENZYME CORPORATION   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN;

ANIMAL CELL; ARTICLE; CYSTIC FIBROSIS; INTRACELLULAR TRANSPORT; PRIORITY JOURNAL; PROTEIN PROCESSING;

ANIMAL; CELL LINE; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FLUORESCENT ANTIBODY TECHNIQUE; GLYCOSIDE HYDROLASES; GLYCOSYLATION; HUMAN; KINETICS; MEMBRANE PROTEINS; MUTAGENESIS, SITE-DIRECTED; PLASMIDS; PROTEIN PROCESSING, POST-TRANSLATIONAL; RECOMBINANT PROTEINS; SUPPORT, NON-U.S. GOV'T; TRANSFECTION;

ANIMALIA;

EID: 0025242929     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/0092-8674(90)90148-8     Document Type: Article

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