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Automated acquisition and analysis of airway surface liquid height by confocal microscopy.
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Identification of the SPLUNC1 ENaC-inhibitory domain yields novel strategies to treat sodium hyperabsorption in cystic fibrosis airway epithelial cultures.
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SPLUNC1 degradation by the cystic fibrosis mucosal environment drives airway surface liquid dehydration.
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Pulmonary Ionocytes Regulate Airway Surface Liquid pH in Primary Human Bronchial Epithelial Cells.
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Non-genomic estrogen regulation of ion transport and airway surface liquid dynamics in cystic fibrosis bronchial epithelium.
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Evaluation of a SPLUNC1-derived peptide for the treatment of cystic fibrosis lung disease.
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Establishment of the deuterium oxide dilution method as a new possibility for determining the transendothelial water permeability.
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Expression of gain-of-function CFTR in cystic fibrosis airway cells restores epithelial function better than wild-type or codon-optimized CFTR.
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Culture with apically applied healthy or disease sputum alters the airway surface liquid proteome and ion transport across human bronchial epithelial cells.
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E-cigarette constituents propylene glycol and vegetable glycerin decrease glucose uptake and its metabolism in airway epithelial cells in vitro.
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Ion channels of the lung and their role in disease pathogenesis.
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1
Linking increased airway hydration, ciliary beating, and mucociliary clearance through ENaC inhibition.
Am J Physiol Lung Cell Mol Physiol. 2015 Jan 1;308(1):L22-32. doi: 10.1152/ajplung.00163.2014. Epub 2014 Oct 31.
2
Identification of the SPLUNC1 ENaC-inhibitory domain yields novel strategies to treat sodium hyperabsorption in cystic fibrosis airway epithelial cultures.
Am J Physiol Lung Cell Mol Physiol. 2013 Dec;305(12):L990-L1001. doi: 10.1152/ajplung.00103.2013. Epub 2013 Oct 11.
3
Molecular basis for pH-dependent mucosal dehydration in cystic fibrosis airways.
Proc Natl Acad Sci U S A. 2013 Oct 1;110(40):15973-8. doi: 10.1073/pnas.1311999110. Epub 2013 Sep 16.
4
Airway inflammation in cystic fibrosis: molecular mechanisms and clinical implications.
Thorax. 2013 Dec;68(12):1157-62. doi: 10.1136/thoraxjnl-2013-203204. Epub 2013 May 23.
5
ENaC inhibitors and airway re-hydration in cystic fibrosis: state of the art.
Curr Mol Pharmacol. 2013 Mar;6(1):3-12. doi: 10.2174/18744672112059990025.
6
Method for quantitative study of airway functional microanatomy using micro-optical coherence tomography.
PLoS One. 2013;8(1):e54473. doi: 10.1371/journal.pone.0054473. Epub 2013 Jan 23.
7
Human nasal and tracheo-bronchial respiratory epithelial cell culture.
Methods Mol Biol. 2013;945:109-21. doi: 10.1007/978-1-62703-125-7_8.
8
Proteases, cystic fibrosis and the epithelial sodium channel (ENaC).
Cell Tissue Res. 2013 Feb;351(2):309-23. doi: 10.1007/s00441-012-1439-z. Epub 2012 May 22.
9
Airway epithelial cells--hyperabsorption in CF?
Int J Biochem Cell Biol. 2012 Aug;44(8):1232-5. doi: 10.1016/j.biocel.2012.04.012. Epub 2012 Apr 21.
10
Correction of the F508del-CFTR protein processing defect in vitro by the investigational drug VX-809.
Proc Natl Acad Sci U S A. 2011 Nov 15;108(46):18843-8. doi: 10.1073/pnas.1105787108. Epub 2011 Oct 5.

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