Pharmacological rescue of the mutant cystic fibrosis transmembrane conductance regulator (CFTR) detected by use of a novel fluorescence platform.

Molecular medicine (Cambridge, Mass.)

Volumn 18, Issue , 2012, Pages 685-696

  Holleran, John P ^a   Glover, Matthew L ^b   Peters, Kathryn W ^b   Bertrand, Carol A ^b   Watkins, Simon C ^b   Jarvik, Jonathan W ^b   Frizzell, Raymond A ^b  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; HYBRID PROTEIN;

ARTICLE; CELL LINE; CELL MEMBRANE; CYSTIC FIBROSIS; DRUG SCREENING; FLUORESCENCE MICROSCOPY; GENE EXPRESSION; GENETICS; HUMAN; METABOLISM; METHODOLOGY; MUTATION; REPORTER GENE; STAINING;

CELL LINE; CELL MEMBRANE; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DRUG EVALUATION, PRECLINICAL; GENE EXPRESSION; GENES, REPORTER; HUMANS; MICROSCOPY, FLUORESCENCE; MUTATION; RECOMBINANT FUSION PROTEINS; STAINING AND LABELING;

EID: 84872098873     PISSN: None     EISSN: 15283658     Source Type: Journal    
DOI: 10.2119/molmed.2012.00001     Document Type: Article

References (0)