GFP-tagged CFTR transgene is functional in the G551D cystic fibrosis mouse colon

Journal of Membrane Biology

Volumn 192, Issue 3, 2003, Pages 159-167

  Oceandy, D ^a   McMorran, B ^a   Schreiber, R ^b   Wainwright, B J ^a   Kunzelmann, K ^b  

^a UNIVERSITY OF QUEENSLAND   (Australia)

^b UNIVERSITY OF REGENSBURG   (Germany)

Author keywords

Airways; Bitransgenic mouse; Colon; Cystic fibrosis; Epithelial transport; GFP CFTR

Indexed keywords

CYTOKERATIN; GREEN FLUORESCENT PROTEIN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

AMINO TERMINAL SEQUENCE; ANIMAL TISSUE; ARTICLE; COLON; COLON MUCOSA; CONTROLLED STUDY; CYSTIC FIBROSIS; EPITHELIUM CELL; GENE FUNCTION; GENE MUTATION; MOUSE; NONHUMAN; PROMOTER REGION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN SYNTHESIS; RESPIRATORY EPITHELIUM; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TRANSGENE;

ANIMALS; COLON; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; GENE EXPRESSION REGULATION; GENE THERAPY; INTESTINAL MUCOSA; MICE; MICE, INBRED CFTR; MICE, TRANSGENIC; RECOMBINANT FUSION PROTEINS; RESPIRATORY MUCOSA; TRACHEA;

ANIMALIA; MUS MUSCULUS;

EID: 0042430125     PISSN: 00222631     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00232-002-1072-y     Document Type: Article

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