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Items: 1 to 20 of 48

1.

Mucus clearance as a primary innate defense mechanism for mammalian airways.

Knowles MR, Boucher RC.

J Clin Invest. 2002 Mar;109(5):571-7. Review. No abstract available.

2.

Innate immune functions of the airway epithelium.

Bartlett JA, Fischer AJ, McCray PB Jr.

Contrib Microbiol. 2008;15:147-63. doi: 10.1159/000136349. Review.

PMID:
18511860
3.

Mucociliary clearance--a critical upper airway host defense mechanism and methods of assessment.

Antunes MB, Cohen NA.

Curr Opin Allergy Clin Immunol. 2007 Feb;7(1):5-10. Review.

PMID:
17218804
4.

Airway mucus function and dysfunction.

Fahy JV, Dickey BF.

N Engl J Med. 2010 Dec 2;363(23):2233-47. doi: 10.1056/NEJMra0910061. Review. No abstract available.

5.

Effective mucus clearance is essential for respiratory health.

Randell SH, Boucher RC; University of North Carolina Virtual Lung Group.

Am J Respir Cell Mol Biol. 2006 Jul;35(1):20-8. Epub 2006 Mar 9. Review. No abstract available.

6.
7.

Cystic fibrosis and other respiratory diseases of impaired mucus clearance.

Livraghi A, Randell SH.

Toxicol Pathol. 2007 Jan;35(1):116-29. Review.

PMID:
17325980
8.

[The significance of muco-ciliary clearance as a defense mechanism in the respiratory tract].

Pietrzyk A, Krasnowska M.

Pneumonol Alergol Pol. 1996;64(11-12):821-8. Review. Polish. No abstract available.

PMID:
9162330
9.

Electron tomography of respiratory cilia.

Shoemark A, Hogg C.

Thorax. 2013 Feb;68(2):190-1. doi: 10.1136/thoraxjnl-2012-202938. Epub 2012 Nov 28. Review.

PMID:
23192883
10.

Congenital problems of mucociliary clearance: primary ciliary dyskinesia.

Rimmer J.

Rhinology. 2012 Dec;50(4):353-9. doi: 10.4193/Rhino12.126. Review.

PMID:
23181248
11.

Regulation of normal and cystic fibrosis airway surface liquid volume by phasic shear stress.

Tarran R, Button B, Boucher RC.

Annu Rev Physiol. 2006;68:543-61. Review.

PMID:
16460283
12.

Primary ciliary dyskinesia: prospects for new therapies, building on the experience in cystic fibrosis.

Amirav I, Cohen-Cymberknoh M, Shoseyov D, Kerem E.

Paediatr Respir Rev. 2009 Jun;10(2):58-62. doi: 10.1016/j.prrv.2008.11.003. Epub 2009 Apr 9. Review.

PMID:
19410203
13.

Innate immunity.

Ooi EH, Psaltis AJ, Witterick IJ, Wormald PJ.

Otolaryngol Clin North Am. 2010 Jun;43(3):473-87, vii. doi: 10.1016/j.otc.2010.02.020. Review.

PMID:
20525504
14.

Regulation of human airway surface liquid.

Widdicombe JH, Widdicombe JG.

Respir Physiol. 1995 Jan;99(1):3-12. Review.

PMID:
7740210
15.

Innate and Adaptive Immunity in Cystic Fibrosis.

Bruscia EM, Bonfield TL.

Clin Chest Med. 2016 Mar;37(1):17-29. doi: 10.1016/j.ccm.2015.11.010. Epub 2015 Dec 28. Review.

PMID:
26857765
16.

Effects of airway surface liquid pH on host defense in cystic fibrosis.

Berkebile AR, McCray PB Jr.

Int J Biochem Cell Biol. 2014 Jul;52:124-9. doi: 10.1016/j.biocel.2014.02.009. Epub 2014 Feb 19. Review.

17.

Mucociliary clearance in cystic fibrosis.

Robinson M, Bye PT.

Pediatr Pulmonol. 2002 Apr;33(4):293-306. Review.

PMID:
11921459
18.

Role of cilia, mucus, and airway surface liquid in mucociliary dysfunction: lessons from mouse models.

Mall MA.

J Aerosol Med Pulm Drug Deliv. 2008 Mar;21(1):13-24. doi: 10.1089/jamp.2007.0659. Review.

PMID:
18518828
19.

[The respiratory system--its self-cleaning system. General mechanisms of clearance].

Mustajbegović J, Zuskin E.

Lijec Vjesn. 1998 Jan-Feb;120(1-2):28-31. Review. Croatian.

PMID:
9650483
20.

Pathogenesis of respiratory infections and host defenses.

Zeiher BG, Hornick DB.

Curr Opin Pulm Med. 1996 May;2(3):166-73. Review.

PMID:
9363135

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