Found: 17
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Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Substance P stimulates human airway submucosal gland secretion mainly via a CFTR-dependent process.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Combined agonists act synergistically to increase mucociliary clearance in a cystic fibrosis airway model.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98122-5
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- Publication type:
- Article
Disease phenotype of a ferret CFTR-knockout model of cystic fibrosis.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis.
- Published in:
- Journal of Clinical Investigation, 2007, v. 117, n. 10, p. 3118, doi. 10.1172/JCI31992
- By:
- Publication type:
- Article
Marked increases in mucociliary clearance produced by synergistic secretory agonists or inhibition of the epithelial sodium channel.
- Published in:
- Scientific Reports, 2016, p. 36806, doi. 10.1038/srep36806
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- Publication type:
- Article
Inhibition of airway surface fluid absorption by cholinergic stimulation.
- Published in:
- Scientific Reports, 2016, p. 20735, doi. 10.1038/srep20735
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- Publication type:
- Article
QUEST FOR CYSTIC FIBROSIS PHARMACOTHERAPY.
- Published in:
- 2008
- By:
- Publication type:
- Editorial
Proteomic Analysis of Pure Human Airway Gland Mucus Reveals a Large Component of Protective Proteins.
- Published in:
- PLoS ONE, 2015, v. 10, n. 2, p. 1, doi. 10.1371/journal.pone.0116756
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- Publication type:
- Article
<i>In Vivo</i> Readout of CFTR Function: Ratiometric Measurement of CFTR-Dependent Secretion by Individual, Identifiable Human Sweat Glands.
- Published in:
- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0077114
- By:
- Publication type:
- Article
Defective Fluid Secretion from Submucosal Glands of Nasal Turbinates from CFTR-/- and CFTRDF508/DF508 Pigs.
- Published in:
- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0024424
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- Publication type:
- Article
Glandular Proteome Identifies Antiprotease Cystatin C as a Critical Modulator of Airway Hydration and Clearance.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2016, v. 54, n. 4, p. 469, doi. 10.1165/rcmb.2015-0090OC
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- Publication type:
- Article
Glandular Proteome Identifies Antiprotease Cystatin C as a Critical Modulator of Airway Hydration and Clearance.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2016, v. 54, n. 4, p. E1, doi. 10.1165/rcmb.2015-0090oc
- By:
- Publication type:
- Article
Variation in CFTR-dependent 'β-sweating' among healthy adults.
- Published in:
- PLoS ONE, 2022, v. 17, n. 3, p. 1, doi. 10.1371/journal.pone.0265432
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- Publication type:
- Article
Secretion rates of human nasal submucosal glands from patients with chronic rhinosinusitis or cystic fibrosis.
- Published in:
- American Journal of Rhinology & Allergy, 2015, v. 29, n. 5, p. 334, doi. 10.2500/ajra.2015.29.4213
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- Publication type:
- Article
Impaired PGE<sub>2</sub>-stimulated Cl<sup>-</sup> and HCO<sub>3</sub><sup>-</sup> secretion contributes to cystic fibrosis airway disease.
- Published in:
- PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0189894
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- Publication type:
- Article