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PUBMED FOR HANDHELDS

Journal Abstract Search


211 related items for PubMed ID: 33264072

  • 1. Polysulfated Hyaluronan GlycoMira-1111 Inhibits Elastase and Improves Rheology in Cystic Fibrosis Sputum.
    Kummarapurugu AB, Zheng S, Pulsipher A, Savage JR, Ma J, Rubin BK, Kennedy TP, Voynow JA.
    Am J Respir Cell Mol Biol; 2021 Feb; 64(2):260-267. PubMed ID: 33264072
    [Abstract] [Full Text] [Related]

  • 2. Molecular principles for heparin oligosaccharide-based inhibition of neutrophil elastase in cystic fibrosis.
    Kummarapurugu AB, Afosah DK, Sankaranarayanan NV, Navaz Gangji R, Zheng S, Kennedy T, Rubin BK, Voynow JA, Desai UR.
    J Biol Chem; 2018 Aug 10; 293(32):12480-12490. PubMed ID: 29903912
    [Abstract] [Full Text] [Related]

  • 3. Unfractionated heparin reduces the elasticity of sputum from patients with cystic fibrosis.
    Broughton-Head VJ, Shur J, Carroll MP, Smith JR, Shute JK.
    Am J Physiol Lung Cell Mol Physiol; 2007 Nov 10; 293(5):L1240-9. PubMed ID: 17827252
    [Abstract] [Full Text] [Related]

  • 4. On the Process of Discovering Leads That Target the Heparin-Binding Site of Neutrophil Elastase in the Sputum of Cystic Fibrosis Patients.
    Morla S, Sankaranarayanan NV, Afosah DK, Kumar M, Kummarapurugu AB, Voynow JA, Desai UR.
    J Med Chem; 2019 Jun 13; 62(11):5501-5511. PubMed ID: 31074986
    [Abstract] [Full Text] [Related]

  • 5. Effect of recombinant human DNase on alpha1-proteinase inhibitor function: an experimental approach to the combined clinical use of rhDNase and alpha1-PI in CF patients.
    Hansen G, Hoffjan S, Mosler K, Schuster A.
    Lung; 2001 Jun 13; 179(3):185-94. PubMed ID: 11891608
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  • 7. Dornase alfa. A review of its pharmacological properties and therapeutic potential in cystic fibrosis.
    Bryson HM, Sorkin EM.
    Drugs; 1994 Dec 13; 48(6):894-906. PubMed ID: 7533697
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  • 8. Poly-L-Lysine compacts DNA, kills bacteria, and improves protease inhibition in cystic fibrosis sputum.
    Dubois AV, Midoux P, Gras D, Si-Tahar M, Bréa D, Attucci S, Khelloufi MK, Ramphal R, Diot P, Gauthier F, Hervé V.
    Am J Respir Crit Care Med; 2013 Sep 15; 188(6):703-9. PubMed ID: 23947381
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  • 10. Aerosolized dornase alfa (rhDNase) for therapy of cystic fibrosis.
    Hodson ME.
    Am J Respir Crit Care Med; 1995 Mar 15; 151(3 Pt 2):S70-4. PubMed ID: 7881698
    [Abstract] [Full Text] [Related]

  • 11. The role of DNA and actin polymers on the polymer structure and rheology of cystic fibrosis sputum and depolymerization by gelsolin or thymosin beta 4.
    Kater A, Henke MO, Rubin BK.
    Ann N Y Acad Sci; 2007 Sep 15; 1112():140-53. PubMed ID: 17496063
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  • 13. Dornase alfa. A review of pharmacoeconomic and quality-of-life aspects of its use in cystic fibrosis.
    Goa KL, Lamb H.
    Pharmacoeconomics; 1997 Sep 15; 12(3):409-22. PubMed ID: 10170464
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  • 16. 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 15; 50(4):684-9. PubMed ID: 24325600
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  • 18. Elastase activity on sputum neutrophils correlates with severity of lung disease in cystic fibrosis.
    Dittrich AS, Kühbandner I, Gehrig S, Rickert-Zacharias V, Twigg M, Wege S, Taggart CC, Herth F, Schultz C, Mall MA.
    Eur Respir J; 2018 Mar 15; 51(3):. PubMed ID: 29545279
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  • 20. Inhaled mannitol for cystic fibrosis.
    Nolan SJ, Thornton J, Murray CS, Dwyer T.
    Cochrane Database Syst Rev; 2015 Oct 09; (10):CD008649. PubMed ID: 26451533
    [Abstract] [Full Text] [Related]


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