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Items: 18

1.

Role of CFTR in epithelial physiology.

Saint-Criq V, Gray MA.

Cell Mol Life Sci. 2017 Jan;74(1):93-115. doi: 10.1007/s00018-016-2391-y. Epub 2016 Oct 6. Review.

2.

PATHOPHYSIOLOGIC EVALUATION OF THE TRANSGENIC CFTR "GUT-CORRECTED" PORCINE MODEL OF CYSTIC FIBROSIS.

Ballard ST, Evans JW, Drag HS, Schuler M.

Am J Physiol Lung Cell Mol Physiol. 2016 Aug 19:ajplung.00242.2016. doi: 10.1152/ajplung.00242.2016. [Epub ahead of print]

3.

A relationship between Pseudomonal growth behaviour and cystic fibrosis patient lung function identified in a metabolomic investigation.

Kozlowska J, Rivett DW, Vermeer LS, Carroll MP, Bruce KD, Mason AJ, Rogers GB.

Metabolomics. 2013 Dec;9(6). doi: 10.1007/s11306-013-0538-5.

4.

Lentiviral vector gene transfer to porcine airways.

Sinn PL, Cooney AL, Oakland M, Dylla DE, Wallen TJ, Pezzulo AA, Chang EH, McCray PB Jr.

Mol Ther Nucleic Acids. 2012 Nov 27;1:e56. doi: 10.1038/mtna.2012.47.

5.

Mechanisms of bicarbonate secretion: lessons from the airways.

Bridges RJ.

Cold Spring Harb Perspect Med. 2012 Aug 1;2(8). pii: a015016. doi: 10.1101/cshperspect.a015016. Review.

6.

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.

7.

Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator-dependent bicarbonate secretion.

Garcia MA, Yang N, Quinton PM.

J Clin Invest. 2009 Sep;119(9):2613-22. doi: 10.1172/JCI38662. Epub 2009 Aug 24. Erratum in: J Clin Invest. 2009 Nov;119(11):3497.

8.

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.

9.

Alcian Blue and Pyronine Y histochemical stains permit assessment of multiple parameters in pulmonary disease models.

Meyerholz DK, Rodgers J, Castilow EM, Varga SM.

Vet Pathol. 2009 Mar;46(2):325-8. doi: 10.1354/vp.46-2-325.

10.

Differential gene expression in human conducting airway surface epithelia and submucosal glands.

Fischer AJ, Goss KL, Scheetz TE, Wohlford-Lenane CL, Snyder JM, McCray PB Jr.

Am J Respir Cell Mol Biol. 2009 Feb;40(2):189-99. doi: 10.1165/rcmb.2008-0240OC. Epub 2008 Aug 14.

11.

HCO3(-) secretion by murine nasal submucosal gland serous acinar cells during Ca2+-stimulated fluid secretion.

Lee RJ, Harlow JM, Limberis MP, Wilson JM, Foskett JK.

J Gen Physiol. 2008 Jul;132(1):161-83. doi: 10.1085/jgp.200810017.

12.

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.

13.

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.

14.

Optical imaging of Ca2+-evoked fluid secretion by murine nasal submucosal gland serous acinar cells.

Lee RJ, Limberis MP, Hennessy MF, Wilson JM, Foskett JK.

J Physiol. 2007 Aug 1;582(Pt 3):1099-124. Epub 2007 May 24.

15.
16.

Disruptive effects of anion secretion inhibitors on airway mucus morphology in isolated perfused pig lung.

Trout L, Townsley MI, Bowden AL, Ballard ST.

J Physiol. 2003 Jun 15;549(Pt 3):845-53. Epub 2003 Apr 17.

17.

Regulation of intracellular pH in Calu-3 human airway cells.

Inglis SK, Finlay L, Ramminger SJ, Richard K, Ward MR, Wilson SM, Olver RE.

J Physiol. 2002 Jan 15;538(Pt 2):527-39.

18.

Submucosal gland secretions in airways from cystic fibrosis patients have normal [Na(+)] and pH but elevated viscosity.

Jayaraman S, Joo NS, Reitz B, Wine JJ, Verkman AS.

Proc Natl Acad Sci U S A. 2001 Jul 3;98(14):8119-23. Epub 2001 Jun 26.

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