Cystic fibrosis transmembrane conductance regulator is expressed in Mucin granules from calu-3 and primary human airway epithelial cells

American Journal of Respiratory Cell and Molecular Biology

Volumn 49, Issue 4, 2013, Pages 511-516

  Le Simple, Pierre ^a   Goepp, Julie ^a   Palmer, Melissa L ^b   Fahrenkrug, Scott C ^b   O'Grady, Scott M ^b   Ferraro, Pasquale ^c   Robert, Renaud ^a   Hanrahan, John W ^a,d  

^a MCGILL UNIVERSITY   (Canada)

^b UNIVERSITY OF MINNESOTA   (United States)

^c CENTRE HOSPITALIER DE L UNIVERSITÉ DE MONTRÉAL   (Canada)

^d MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

Author keywords

CFTR; Cystic fibrosis; Mucus

Indexed keywords

ACRIDINE ORANGE; ADENOSINE TRIPHOSPHATASE; ANION CHANNEL; BICARBONATE; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; MUCIN 5AC;

APICAL MEMBRANE; ARTICLE; CONTROLLED STUDY; DEHYDRATION; ELECTRON MICROSCOPY; EPITHELIUM CELL; GENE SILENCING; HUMAN; HUMAN CELL; HUMAN CELL CULTURE; IMMUNOBLOTTING; IMMUNOHISTOCHEMISTRY; ION CONDUCTANCE; LUNG CYSTIC FIBROSIS; LUNG FIBROSIS; MUCUS; PRIMARY CELL CULTURE; PROTEIN EXPRESSION; RESPIRATORY EPITHELIUM;

CELL LINE; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EPITHELIAL CELLS; HUMANS; MUCIN 5AC; MUCINS; RESPIRATORY MUCOSA;

EID: 84886486316     PISSN: 10441549     EISSN: 15354989     Source Type: Journal    
DOI: 10.1165/rcmb.2012-0419RC     Document Type: Article

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