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Wu JV, Krouse ME, Wine JJ. Acinar origin of CFTR-dependent airway submucosal gland fluid secretion. Am J Physiol Lung Cell Mol Physiol 2007; 292(1):L304-11. [More details]

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Ianowski JP, Choi JY, Wine JJ, Hanrahan JW. Mucus secretion by single tracheal submucosal glands from normal and cystic fibrosis transmembrane conductance regulator knockout mice. J Physiol 2007; 580(Pt 1):301-14. [More details]

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Su X, Li Q, Shrestha K, Cormet-Boyaka E, Chen L, Smith PR, et al. Interregulation of proton-gated Na+ channel 3 and cystic fibrosis transmembrane conductance regulator. J Biol Chem 2006; 281(48):36960-8. [More details]

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Vanthanouvong V, Kozlova I, Roomans GM. Ionic composition of rat airway surface liquid determined by X-ray microanalysis. Microsc Res Tech 2005; 68(1):6-12. [More details]

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Scholte BJ, Davidson DJ, Wilke M, De Jonge HR. Animal models of cystic fibrosis. J Cyst Fibros 2004; 3(Suppl 2):183-90. [More details]

2

Irokawa T, Krouse ME, Joo NS, Wu JV, Wine JJ. A 'virtual gland' method for quantifying epithelial fluid secretion. Am J Physiol Lung Cell Mol Physiol 2004; 287(4):L784-93. [More details]

1

Kidd JF, Kogan I, Bear CE. Molecular basis for the chloride channel activity of cystic fibrosis transmembrane conductance regulator and the consequences of disease-causing mutations. Curr Top Dev Biol 2004; 60:215-49. [More details]