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Journal Abstract Search

563 related items for PubMed ID: 26709821

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  • 2. Lung pathology in response to repeated exposure to Staphylococcus aureus in congenic residual function cystic fibrosis mice does not increase in response to decreased CFTR levels or increased bacterial load.
    Davidson DJ, Webb S, Teague P, Govan JR, Dorin JR.
    Pathobiology; 2004; 71(3):152-8. PubMed ID: 15051928
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  • 4. Ceramide accumulation mediates inflammation, cell death and infection susceptibility in cystic fibrosis.
    Teichgräber V, Ulrich M, Endlich N, Riethmüller J, Wilker B, De Oliveira-Munding CC, van Heeckeren AM, Barr ML, von Kürthy G, Schmid KW, Weller M, Tümmler B, Lang F, Grassme H, Döring G, Gulbins E.
    Nat Med; 2008 Apr; 14(4):382-91. PubMed ID: 18376404
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  • 7. Increased susceptibility of Cftr-/- mice to LPS-induced lung remodeling.
    Bruscia EM, Zhang PX, Barone C, Scholte BJ, Homer R, Krause DS, Egan ME.
    Am J Physiol Lung Cell Mol Physiol; 2016 Apr 15; 310(8):L711-9. PubMed ID: 26851259
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  • 9. Strain-dependent pulmonary gene expression profiles of a cystic fibrosis mouse model.
    Haston CK, Cory S, Lafontaine L, Dorion G, Hallett MT.
    Physiol Genomics; 2006 Apr 13; 25(2):336-45. PubMed ID: 16614460
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  • 10. Regulation of cystic fibrosis transmembrane conductance regulator by microRNA-145, -223, and -494 is altered in ΔF508 cystic fibrosis airway epithelium.
    Oglesby IK, Chotirmall SH, McElvaney NG, Greene CM.
    J Immunol; 2013 Apr 01; 190(7):3354-62. PubMed ID: 23436935
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  • 20. Acquired Cystic Fibrosis Transmembrane Conductance Regulator Deficiency.
    Cho DY, Woodworth BA.
    Adv Otorhinolaryngol; 2016 Apr 01; 79():78-85. PubMed ID: 27466849
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