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Similar articles for PubMed (Select 24678594)

1.

Lack of neutrophil elastase reduces inflammation, mucus hypersecretion, and emphysema, but not mucus obstruction, in mice with cystic fibrosis-like lung disease.

Gehrig S, Duerr J, Weitnauer M, Wagner CJ, Graeber SY, Schatterny J, Hirtz S, Belaaouaj A, Dalpke AH, Schultz C, Mall MA.

Am J Respir Crit Care Med. 2014 May 1;189(9):1082-92. doi: 10.1164/rccm.201311-1932OC.

PMID:
24678594
2.

Hypoxic Epithelial Necrosis Triggers Neutrophilic Inflammation via IL-1 Receptor Signaling in Cystic Fibrosis Lung Disease.

Fritzsching B, Zhou-Suckow Z, Trojanek JB, Schubert SC, Schatterny J, Hirtz S, Agrawal R, Muley T, Kahn N, Sticht C, Gunkel N, Welte T, Randell SH, Länger F, Schnabel P, Herth FJ, Mall MA.

Am J Respir Crit Care Med. 2015 Apr 15;191(8):902-13. doi: 10.1164/rccm.201409-1610OC.

PMID:
25607238
3.

Airway mucus obstruction triggers macrophage activation and matrix metalloproteinase 12-dependent emphysema.

Trojanek JB, Cobos-Correa A, Diemer S, Kormann M, Schubert SC, Zhou-Suckow Z, Agrawal R, Duerr J, Wagner CJ, Schatterny J, Hirtz S, Sommerburg O, Hartl D, Schultz C, Mall MA.

Am J Respir Cell Mol Biol. 2014 Nov;51(5):709-20. doi: 10.1165/rcmb.2013-0407OC.

PMID:
24828142
4.

Genetically determined heterogeneity of lung disease in a mouse model of airway mucus obstruction.

Livraghi-Butrico A, Grubb BR, Kelly EJ, Wilkinson KJ, Yang H, Geiser M, Randell SH, Boucher RC, O'Neal WK.

Physiol Genomics. 2012 Apr 15;44(8):470-84. doi: 10.1152/physiolgenomics.00185.2011. Epub 2012 Mar 6.

5.

Preventive but not late amiloride therapy reduces morbidity and mortality of lung disease in betaENaC-overexpressing mice.

Zhou Z, Treis D, Schubert SC, Harm M, Schatterny J, Hirtz S, Duerr J, Boucher RC, Mall MA.

Am J Respir Crit Care Med. 2008 Dec 15;178(12):1245-56. doi: 10.1164/rccm.200803-442OC. Epub 2008 Oct 10.

PMID:
18849497
6.
7.

Early cystic fibrosis lung disease: Role of airway surface dehydration and lessons from preventive rehydration therapies in mice.

Mall MA, Graeber SY, Stahl M, Zhou-Suckow Z.

Int J Biochem Cell Biol. 2014 Jul;52:174-9. doi: 10.1016/j.biocel.2014.02.006. Epub 2014 Feb 20. Review.

PMID:
24561284
8.

Potential role of high-mobility group box 1 in cystic fibrosis airway disease.

Rowe SM, Jackson PL, Liu G, Hardison M, Livraghi A, Solomon GM, McQuaid DB, Noerager BD, Gaggar A, Clancy JP, O'Neal W, Sorscher EJ, Abraham E, Blalock JE.

Am J Respir Crit Care Med. 2008 Oct 15;178(8):822-31. doi: 10.1164/rccm.200712-1894OC. Epub 2008 Jul 24.

9.

Effects of cystic fibrosis airway secretions on rat lung: role of neutrophil elastase.

Rees DD, Brain JD.

Am J Physiol. 1995 Aug;269(2 Pt 1):L195-202.

PMID:
7653580
10.

Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice.

Mall M, Grubb BR, Harkema JR, O'Neal WK, Boucher RC.

Nat Med. 2004 May;10(5):487-93. Epub 2004 Apr 11.

PMID:
15077107
11.

Development of chronic bronchitis and emphysema in beta-epithelial Na+ channel-overexpressing mice.

Mall MA, Harkema JR, Trojanek JB, Treis D, Livraghi A, Schubert S, Zhou Z, Kreda SM, Tilley SL, Hudson EJ, O'Neal WK, Boucher RC.

Am J Respir Crit Care Med. 2008 Apr 1;177(7):730-42. Epub 2007 Dec 13.

12.

Mucus clearance, MyD88-dependent and MyD88-independent immunity modulate lung susceptibility to spontaneous bacterial infection and inflammation.

Livraghi-Butrico A, Kelly EJ, Klem ER, Dang H, Wolfgang MC, Boucher RC, Randell SH, O'Neal WK.

Mucosal Immunol. 2012 Jul;5(4):397-408. doi: 10.1038/mi.2012.17. Epub 2012 Mar 14.

13.

Airway inflammation in cystic fibrosis.

Elizur A, Cannon CL, Ferkol TW.

Chest. 2008 Feb;133(2):489-95. doi: 10.1378/chest.07-1631. Review.

PMID:
18252915
14.

Neutrophil elastase induces mucus cell metaplasia in mouse lung.

Voynow JA, Fischer BM, Malarkey DE, Burch LH, Wong T, Longphre M, Ho SB, Foster WM.

Am J Physiol Lung Cell Mol Physiol. 2004 Dec;287(6):L1293-302. Epub 2004 Jul 23.

15.

2-O, 3-O-desulfated heparin inhibits neutrophil elastase-induced HMGB-1 secretion and airway inflammation.

Griffin KL, Fischer BM, Kummarapurugu AB, Zheng S, Kennedy TP, Rao NV, Foster WM, Voynow JA.

Am J Respir Cell Mol Biol. 2014 Apr;50(4):684-9. doi: 10.1165/rcmb.2013-0338RC.

16.

In vivo monitoring of cystic fibrosis-like lung disease in mice by volumetric computed tomography.

Wielpütz MO, Eichinger M, Zhou Z, Leotta K, Hirtz S, Bartling SH, Semmler W, Kauczor HU, Puderbach M, Mall MA.

Eur Respir J. 2011 Nov;38(5):1060-70. doi: 10.1183/09031936.00149810. Epub 2011 Apr 8.

17.

Hypertonic saline is effective in the prevention and treatment of mucus obstruction, but not airway inflammation, in mice with chronic obstructive lung disease.

Graeber SY, Zhou-Suckow Z, Schatterny J, Hirtz S, Boucher RC, Mall MA.

Am J Respir Cell Mol Biol. 2013 Sep;49(3):410-7. doi: 10.1165/rcmb.2013-0050OC. Erratum in: Am J Respir Cell Mol Biol. 2014 Apr;50(4):838.

18.

The ENaC-overexpressing mouse as a model of cystic fibrosis lung disease.

Zhou Z, Duerr J, Johannesson B, Schubert SC, Treis D, Harm M, Graeber SY, Dalpke A, Schultz C, Mall MA.

J Cyst Fibros. 2011 Jun;10 Suppl 2:S172-82. doi: 10.1016/S1569-1993(11)60021-0. Review.

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