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Items: 1 to 20 of 173

1.

Substance P stimulates human airway submucosal gland secretion mainly via a CFTR-dependent process.

Choi JY, Khansaheb M, Joo NS, Krouse ME, Robbins RC, Weill D, Wine JJ.

J Clin Invest. 2009 May;119(5):1189-200. doi: 10.1172/JCI37284. Epub 2009 Apr 20. Erratum in: J Clin Invest. 2010 Mar 1;120(3):931-2.

2.

Properties of substance P-stimulated mucus secretion from porcine tracheal submucosal glands.

Khansaheb M, Choi JY, Joo NS, Yang YM, Krouse M, Wine JJ.

Am J Physiol Lung Cell Mol Physiol. 2011 Mar;300(3):L370-9. doi: 10.1152/ajplung.00372.2010. Epub 2010 Dec 3.

3.

Mucus secretion by single tracheal submucosal glands from normal and cystic fibrosis transmembrane conductance regulator knockout mice.

Ianowski JP, Choi JY, Wine JJ, Hanrahan JW.

J Physiol. 2007 Apr 1;580(Pt 1):301-14. Epub 2007 Jan 4.

4.

Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis.

Choi JY, Joo NS, Krouse ME, Wu JV, Robbins RC, Ianowski JP, Hanrahan JW, Wine JJ.

J Clin Invest. 2007 Oct;117(10):3118-27.

5.

Defective fluid secretion from submucosal glands of nasal turbinates from CFTR-/- and CFTR (ΔF508/ΔF508) pigs.

Cho HJ, Joo NS, Wine JJ.

PLoS One. 2011;6(8):e24424. doi: 10.1371/journal.pone.0024424. Epub 2011 Aug 31.

6.

Substance P stimulates CFTR-dependent fluid secretion by mouse tracheal submucosal glands.

Ianowski JP, Choi JY, Wine JJ, Hanrahan JW.

Pflugers Arch. 2008 Nov;457(2):529-37. doi: 10.1007/s00424-008-0527-0. Epub 2008 May 29.

PMID:
18509672
7.

Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs.

Joo NS, Cho HJ, Khansaheb M, Wine JJ.

J Clin Invest. 2010 Sep;120(9):3161-6. doi: 10.1172/JCI43466. Epub 2010 Aug 25.

8.

Mucus secretion from individual submucosal glands of the ferret trachea.

Cho HJ, Joo NS, Wine JJ.

Am J Physiol Lung Cell Mol Physiol. 2010 Jul;299(1):L124-36. doi: 10.1152/ajplung.00049.2010. Epub 2010 Apr 30.

9.

Why mouse airway submucosal gland serous cells do not secrete fluid in response to cAMP stimulation.

Lee RJ, Foskett JK.

J Biol Chem. 2012 Nov 2;287(45):38316-26. doi: 10.1074/jbc.M112.412817. Epub 2012 Sep 18.

10.

HCO3- transport in relation to mucus secretion from submucosal glands.

Joo NS, Krouse ME, Wu JV, Saenz Y, Jayaraman S, Verkman AS, Wine JJ.

JOP. 2001 Jul;2(4 Suppl):280-4. Review.

11.

Hyposecretion, not hyperabsorption, is the basic defect of cystic fibrosis airway glands.

Joo NS, Irokawa T, Robbins RC, Wine JJ.

J Biol Chem. 2006 Mar 17;281(11):7392-8. Epub 2006 Jan 12.

12.

Acinar origin of CFTR-dependent airway submucosal gland fluid secretion.

Wu JV, Krouse ME, Wine JJ.

Am J Physiol Lung Cell Mol Physiol. 2007 Jan;292(1):L304-11. Epub 2006 Sep 22.

13.

cAMP-activated Ca2+ signaling is required for CFTR-mediated serous cell fluid secretion in porcine and human airways.

Lee RJ, Foskett JK.

J Clin Invest. 2010 Sep;120(9):3137-48. doi: 10.1172/JCI42992. Epub 2010 Aug 25.

14.

Mucociliary clearance and submucosal gland secretion in the ex vivo ferret trachea.

Jeong JH, Joo NS, Hwang PH, Wine JJ.

Am J Physiol Lung Cell Mol Physiol. 2014 Jul 1;307(1):L83-93. doi: 10.1152/ajplung.00009.2014. Epub 2014 May 2.

15.

Absent secretion to vasoactive intestinal peptide in cystic fibrosis airway glands.

Joo NS, Irokawa T, Wu JV, Robbins RC, Whyte RI, Wine JJ.

J Biol Chem. 2002 Dec 27;277(52):50710-5. Epub 2002 Oct 3.

16.

Secretion rates of human nasal submucosal glands from patients with chronic rhinosinusitis or cystic fibrosis.

Jeong JH, Hwang PH, Cho DY, Joo NS, Wine JJ.

Am J Rhinol Allergy. 2015 Sep-Oct;29(5):334-8. doi: 10.2500/ajra.2015.29.4213.

PMID:
26358343
17.

Mucus secretion from single submucosal glands of pig. Stimulation by carbachol and vasoactive intestinal peptide.

Joo NS, Saenz Y, Krouse ME, Wine JJ.

J Biol Chem. 2002 Aug 2;277(31):28167-75. Epub 2002 May 13.

18.

Fluid transport across cultures of human tracheal glands is altered in cystic fibrosis.

Jiang C, Finkbeiner WE, Widdicombe JH, Miller SS.

J Physiol. 1997 Jun 15;501 ( Pt 3):637-47.

19.

A small molecule CFTR inhibitor produces cystic fibrosis-like submucosal gland fluid secretions in normal airways.

Thiagarajah JR, Song Y, Haggie PM, Verkman AS.

FASEB J. 2004 May;18(7):875-7. Epub 2004 Mar 4.

PMID:
15001557
20.

Fluid secretion by submucosal glands of the tracheobronchial airways.

Ballard ST, Spadafora D.

Respir Physiol Neurobiol. 2007 Dec 15;159(3):271-7. Epub 2007 Jul 7. Review.

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