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Journal Abstract Search

199 related items for PubMed ID: 33948572

  • 1. Transcriptional firing represses bactericidal activity in cystic fibrosis airway neutrophils.
    Margaroli C, Moncada-Giraldo D, Gulick DA, Dobosh B, Giacalone VD, Forrest OA, Sun F, Gu C, Gaggar A, Kissick H, Wu R, Gibson G, Tirouvanziam R.
    Cell Rep Med; 2021 Apr 20; 2(4):100239. PubMed ID: 33948572
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  • 2. BPI-ANCA is expressed in the airways of cystic fibrosis patients and correlates to platelet numbers and Pseudomonas aeruginosa colonization.
    Hovold G, Lindberg U, Ljungberg JK, Shannon O, Påhlman LI.
    Respir Med; 2020 Apr 20; 170():105994. PubMed ID: 32843162
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  • 5. Neutrophils from F508del cystic fibrosis patients produce IL-17A and express IL-23 - dependent IL-17RC.
    Taylor PR, Bonfield TL, Chmiel JF, Pearlman E.
    Clin Immunol; 2016 Sep 20; 170():53-60. PubMed ID: 27155366
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  • 8. Conditions associated with the cystic fibrosis defect promote chronic Pseudomonas aeruginosa infection.
    Staudinger BJ, Muller JF, Halldórsson S, Boles B, Angermeyer A, Nguyen D, Rosen H, Baldursson O, Gottfreðsson M, Guðmundsson GH, Singh PK.
    Am J Respir Crit Care Med; 2014 Apr 01; 189(7):812-24. PubMed ID: 24467627
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  • 10. Cysteamine re-establishes the clearance of Pseudomonas aeruginosa by macrophages bearing the cystic fibrosis-relevant F508del-CFTR mutation.
    Ferrari E, Monzani R, Villella VR, Esposito S, Saluzzo F, Rossin F, D'Eletto M, Tosco A, De Gregorio F, Izzo V, Maiuri MC, Kroemer G, Raia V, Maiuri L.
    Cell Death Dis; 2017 Jan 12; 8(1):e2544. PubMed ID: 28079883
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  • 12. Expression and antimicrobial function of bactericidal permeability-increasing protein in cystic fibrosis patients.
    Aichele D, Schnare M, Saake M, Röllinghoff M, Gessner A.
    Infect Immun; 2006 Aug 12; 74(8):4708-14. PubMed ID: 16861658
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  • 13. The role of the CFTR in susceptibility to Pseudomonas aeruginosa infections in cystic fibrosis.
    Goldberg JB, Pier GB.
    Trends Microbiol; 2000 Nov 12; 8(11):514-20. PubMed ID: 11121762
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  • 14. Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections.
    Hisert KB, Heltshe SL, Pope C, Jorth P, Wu X, Edwards RM, Radey M, Accurso FJ, Wolter DJ, Cooke G, Adam RJ, Carter S, Grogan B, Launspach JL, Donnelly SC, Gallagher CG, Bruce JE, Stoltz DA, Welsh MJ, Hoffman LR, McKone EF, Singh PK.
    Am J Respir Crit Care Med; 2017 Jun 15; 195(12):1617-1628. PubMed ID: 28222269
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  • 15. Changes in Airway Microbiome and Inflammation with Ivacaftor Treatment in Patients with Cystic Fibrosis and the G551D Mutation.
    Harris JK, Wagner BD, Zemanick ET, Robertson CE, Stevens MJ, Heltshe SL, Rowe SM, Sagel SD.
    Ann Am Thorac Soc; 2020 Feb 15; 17(2):212-220. PubMed ID: 31604026
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  • 16. Hyperinflammation in airways of cystic fibrosis patients: what's new?
    Jacquot J, Tabary O, Clement A.
    Expert Rev Mol Diagn; 2008 Jul 15; 8(4):359-63. PubMed ID: 18598217
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  • 17. High expression of midkine in the airways of patients with cystic fibrosis.
    Nordin SL, Jovic S, Kurut A, Andersson C, Gela A, Bjartell A, Mörgelin M, Olin AI, Lund M, Egesten A.
    Am J Respir Cell Mol Biol; 2013 Dec 15; 49(6):935-42. PubMed ID: 23815177
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  • 19. High Nuclease Activity of Long Persisting Staphylococcus aureus Isolates Within the Airways of Cystic Fibrosis Patients Protects Against NET-Mediated Killing.
    Herzog S, Dach F, de Buhr N, Niemann S, Schlagowski J, Chaves-Moreno D, Neumann C, Goretzko J, Schwierzeck V, Mellmann A, Dübbers A, Küster P, Schültingkemper H, Rescher U, Pieper DH, von Köckritz-Blickwede M, Kahl BC.
    Front Immunol; 2019 Dec 15; 10():2552. PubMed ID: 31772562
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