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Journal Abstract Search

198 related items for PubMed ID: 11069833

  • 1. Cystic fibrosis sputum: a barrier to the transport of nanospheres.
    Sanders NN, De Smedt SC, Van Rompaey E, Simoens P, De Baets F, Demeester J.
    Am J Respir Crit Care Med; 2000 Nov; 162(5):1905-11. PubMed ID: 11069833
    [Abstract] [Full Text] [Related]

  • 2. Actin limits enhancement of nanoparticle diffusion through cystic fibrosis sputum by mucolytics.
    Broughton-Head VJ, Smith JR, Shur J, Shute JK.
    Pulm Pharmacol Ther; 2007 Nov; 20(6):708-17. PubMed ID: 17055310
    [Abstract] [Full Text] [Related]

  • 3. Enhanced viscoelasticity of human cystic fibrotic sputum correlates with increasing microheterogeneity in particle transport.
    Dawson M, Wirtz D, Hanes J.
    J Biol Chem; 2003 Dec 12; 278(50):50393-401. PubMed ID: 13679362
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  • 5. Is cystic fibrosis mucus abnormal?
    King M.
    Pediatr Res; 1981 Feb 12; 15(2):120-2. PubMed ID: 7254936
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  • 8. Improved clearability of cystic fibrosis sputum with dextran treatment in vitro.
    Feng W, Garrett H, Speert DP, King M.
    Am J Respir Crit Care Med; 1998 Mar 12; 157(3 Pt 1):710-4. PubMed ID: 9517580
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  • 12. 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 12; 293(5):L1240-9. PubMed ID: 17827252
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  • 13. Rheological effects of hypertonic saline and sodium bicarbonate solutions on cystic fibrosis sputum in vitro.
    Budai-Szűcs M, Berkó S, Kovács A, Jaikumpun P, Ambrus R, Halász A, Szabó-Révész P, Csányi E, Zsembery Á.
    BMC Pulm Med; 2021 Jul 12; 21(1):225. PubMed ID: 34253193
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  • 14. Drug diffusion through cystic fibrotic mucus: steady-state permeation, rheologic properties, and glycoprotein morphology.
    Bhat PG, Flanagan DR, Donovan MD.
    J Pharm Sci; 1996 Jun 12; 85(6):624-30. PubMed ID: 8773960
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  • 15. Impact of PEGylation on the mucolytic activity of recombinant human deoxyribonuclease I in cystic fibrosis sputum.
    Guichard MJ, Kinoo D, Aubriot AS, Bauwens N, Gougué J, Vermeulen F, Lebecque P, Leal T, Vanbever R.
    Clin Sci (Lond); 2018 Jul 18; 132(13):1439-1452. PubMed ID: 29871879
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  • 16. Mucus structure and properties in cystic fibrosis.
    Rubin BK.
    Paediatr Respir Rev; 2007 Mar 18; 8(1):4-7. PubMed ID: 17419972
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  • 17. Recombinant human DNase I reduces the viscosity of cystic fibrosis sputum.
    Shak S, Capon DJ, Hellmiss R, Marsters SA, Baker CL.
    Proc Natl Acad Sci U S A; 1990 Dec 18; 87(23):9188-92. PubMed ID: 2251263
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  • 18. DNA and actin bind and inhibit interleukin-8 function in cystic fibrosis sputa: in vitro effects of mucolytics.
    Perks B, Shute JK.
    Am J Respir Crit Care Med; 2000 Nov 18; 162(5):1767-72. PubMed ID: 11069810
    [Abstract] [Full Text] [Related]

  • 19. Structural alterations of gene complexes by cystic fibrosis sputum.
    Sanders NN, Van Rompaey E, De Smedt SC, Demeester J.
    Am J Respir Crit Care Med; 2001 Aug 01; 164(3):486-93. PubMed ID: 11500355
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  • 20. Mobility and stability of gene complexes in biogels.
    Sanders NN, De Smedt SC, Demeester J.
    J Control Release; 2003 Feb 21; 87(1-3):117-29. PubMed ID: 12618028
    [Abstract] [Full Text] [Related]

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