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Items: 1 to 20 of 102

1.

Myeloperoxidase-dependent oxidative metabolism of nitric oxide in the cystic fibrosis airway.

Chapman AL, Morrissey BM, Vasu VT, Juarez MM, Houghton JS, Li CS, Cross CE, Eiserich JP.

J Cyst Fibros. 2010 Mar;9(2):84-92. doi: 10.1016/j.jcf.2009.10.001. Epub 2010 Jan 15.

2.

Myeloperoxidase and protein oxidation in cystic fibrosis.

Van Der Vliet A, Nguyen MN, Shigenaga MK, Eiserich JP, Marelich GP, Cross CE.

Am J Physiol Lung Cell Mol Physiol. 2000 Sep;279(3):L537-46.

3.

Catalase, myeloperoxidase and hydrogen peroxide in cystic fibrosis.

Worlitzsch D, Herberth G, Ulrich M, Döring G.

Eur Respir J. 1998 Feb;11(2):377-83.

4.

Evaluation of thiol-based antioxidant therapeutics in cystic fibrosis sputum: Focus on myeloperoxidase.

Vasu VT, de Cruz SJ, Houghton JS, Hayakawa KA, Morrissey BM, Cross CE, Eiserich JP.

Free Radic Res. 2011 Feb;45(2):165-76. doi: 10.3109/10715762.2010.521154. Epub 2010 Oct 18.

5.

Nitric oxide and protein nitration in the cystic fibrosis airway.

Morrissey BM, Schilling K, Weil JV, Silkoff PE, Rodman DM.

Arch Biochem Biophys. 2002 Oct 1;406(1):33-9.

PMID:
12234487
6.

Nitric oxide production by polymorphonuclear leucocytes in infected cystic fibrosis sputum consumes oxygen.

Kolpen M, Bjarnsholt T, Moser C, Hansen CR, Rickelt LF, Kühl M, Hempel C, Pressler T, Høiby N, Jensen PØ.

Clin Exp Immunol. 2014 Jul;177(1):310-9. doi: 10.1111/cei.12318.

7.

Antioxidant properties of cystic fibrosis sputum.

Dauletbaev N, Rickmann J, Viel K, Diegel H, von Mallinckrodt C, Stein J, Wagner TO, Bargon J.

Am J Physiol Lung Cell Mol Physiol. 2005 May;288(5):L903-9. Epub 2005 Jan 7.

8.

Oral bacteria--the missing link to ambiguous findings of exhaled nitrogen oxides in cystic fibrosis.

Zetterquist W, Marteus H, Kalm-Stephens P, Näs E, Nordvall L, Johannesson M, Alving K.

Respir Med. 2009 Feb;103(2):187-93. doi: 10.1016/j.rmed.2008.09.009. Epub 2008 Nov 9.

9.

Peroxidase activity within circulating neutrophils correlates with pulmonary phenotype in cystic fibrosis.

Garner HP, Phillips JR, Herron JG, Severson SJ, Milla CE, Regelmann WE.

J Lab Clin Med. 2004 Sep;144(3):127-33.

PMID:
15454881
10.

Asymmetric dimethylarginine contributes to airway nitric oxide deficiency in patients with cystic fibrosis.

Grasemann H, Al-Saleh S, Scott JA, Shehnaz D, Mehl A, Amin R, Rafii M, Pencharz P, Belik J, Ratjen F.

Am J Respir Crit Care Med. 2011 May 15;183(10):1363-8. doi: 10.1164/rccm.201012-1995OC. Epub 2011 Jan 28.

PMID:
21278301
11.

Total sputum nitrate plus nitrite is raised during acute pulmonary infection in cystic fibrosis.

Linnane SJ, Keatings VM, Costello CM, Moynihan JB, O'Connor CM, Fitzgerald MX, McLoughlin P.

Am J Respir Crit Care Med. 1998 Jul;158(1):207-12.

PMID:
9655731
12.

Increased arginase activity in cystic fibrosis airways.

Grasemann H, Schwiertz R, Matthiesen S, Racké K, Ratjen F.

Am J Respir Crit Care Med. 2005 Dec 15;172(12):1523-8. Epub 2005 Sep 15.

PMID:
16166623
13.
14.

Nitric oxide metabolites in cystic fibrosis lung disease.

Grasemann H, Ioannidis I, Tomkiewicz RP, de Groot H, Rubin BK, Ratjen F.

Arch Dis Child. 1998 Jan;78(1):49-53.

15.

Exhaled nitric oxide is not reduced in infants with cystic fibrosis.

Franklin PJ, Hall GL, Moeller A, Horak F Jr, Brennan S, Stick SM.

Eur Respir J. 2006 Feb;27(2):350-3.

17.
18.

L-ornithine derived polyamines in cystic fibrosis airways.

Grasemann H, Shehnaz D, Enomoto M, Leadley M, Belik J, Ratjen F.

PLoS One. 2012;7(10):e46618. doi: 10.1371/journal.pone.0046618. Epub 2012 Oct 5.

19.

Exhaled breath condensate pH in patients with cystic fibrosis.

Antus B, Barta I, Csiszer E, Kelemen K.

Inflamm Res. 2012 Oct;61(10):1141-7. doi: 10.1007/s00011-012-0508-9. Epub 2012 Jun 16.

PMID:
22706320
20.

Total sputum nitrate plus nitrite is raised during acute pulmonary infection in cystic fibrosis.

Grasemann H.

Am J Respir Crit Care Med. 1999 Feb;159(2):684-5. No abstract available.

PMID:
10075477

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