Measurement of halide efflux from cultured and primary airway epithelial cells using fluorescence indicators

Author:

Munkonge Felix,Alton Eric W.F.W.,Andersson Charlotte,Davidson Heather,Dragomir Anca,Edelman Aleksander,Farley Ray,Hjelte Lena,McLachlan Gerry,Stern Myra,Roomans Godfried M.

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference14 articles.

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2. Functional activation of the cystic fibrosis trafficking mutant ΔF508 CFTR by overexpression;Cheng;Am. J. Physiol.,1995

3. Stoichiometry of recombinant cystic fibrosis transmembrane conductance regulator in epithelial cells and its functional reconstitution into cells in vitro;Marshall;J. Biol. Chem.,1994

4. Quantitative fluorescence measurements of chloride secretion in native airway epithelium from CF and non-CF subjects;Stern;Gene Ther.,1995

5. The introduction of two silent mutations into a CFTR cDNA constructs allows improved detection of exogenous mRNA in gene transfer experiments;Hart;Hum. Mol. Genet.,1995

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