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PUBMED FOR HANDHELDS

Journal Abstract Search


336 related items for PubMed ID: 20423679

  • 1. The NF-kappaB signaling in cystic fibrosis lung disease: pathophysiology and therapeutic potential.
    Bodas M, Vij N.
    Discov Med; 2010 Apr; 9(47):346-56. PubMed ID: 20423679
    [Abstract] [Full Text] [Related]

  • 2. Protein processing and inflammatory signaling in Cystic Fibrosis: challenges and therapeutic strategies.
    Belcher CN, Vij N.
    Curr Mol Med; 2010 Feb; 10(1):82-94. PubMed ID: 20205681
    [Abstract] [Full Text] [Related]

  • 3. Selective inhibition of endoplasmic reticulum-associated degradation rescues DeltaF508-cystic fibrosis transmembrane regulator and suppresses interleukin-8 levels: therapeutic implications.
    Vij N, Fang S, Zeitlin PL.
    J Biol Chem; 2006 Jun 23; 281(25):17369-17378. PubMed ID: 16621797
    [Abstract] [Full Text] [Related]

  • 4. Effects of cystic fibrosis transmembrane conductance regulator and DeltaF508CFTR on inflammatory response, ER stress, and Ca2+ of airway epithelia.
    Hybiske K, Fu Z, Schwarzer C, Tseng J, Do J, Huang N, Machen TE.
    Am J Physiol Lung Cell Mol Physiol; 2007 Nov 23; 293(5):L1250-60. PubMed ID: 17827250
    [Abstract] [Full Text] [Related]

  • 5. Defective CFTR- β-catenin interaction promotes NF-κB nuclear translocation and intestinal inflammation in cystic fibrosis.
    Liu K, Zhang X, Zhang JT, Tsang LL, Jiang X, Chan HC.
    Oncotarget; 2016 Sep 27; 7(39):64030-64042. PubMed ID: 27588407
    [Abstract] [Full Text] [Related]

  • 6. Localization of cystic fibrosis transmembrane conductance regulator to lipid rafts of epithelial cells is required for Pseudomonas aeruginosa-induced cellular activation.
    Kowalski MP, Pier GB.
    J Immunol; 2004 Jan 01; 172(1):418-25. PubMed ID: 14688350
    [Abstract] [Full Text] [Related]

  • 7. Resistance to Pseudomonas aeruginosa chronic lung infection requires cystic fibrosis transmembrane conductance regulator-modulated interleukin-1 (IL-1) release and signaling through the IL-1 receptor.
    Reiniger N, Lee MM, Coleman FT, Ray C, Golan DE, Pier GB.
    Infect Immun; 2007 Apr 01; 75(4):1598-608. PubMed ID: 17283089
    [Abstract] [Full Text] [Related]

  • 8. Inflammation in cystic fibrosis airways: relationship to increased bacterial adherence.
    Scheid P, Kempster L, Griesenbach U, Davies JC, Dewar A, Weber PP, Colledge WH, Evans MJ, Geddes DM, Alton EW.
    Eur Respir J; 2001 Jan 01; 17(1):27-35. PubMed ID: 11307750
    [Abstract] [Full Text] [Related]

  • 9. Regulation of gap junctional communication by a pro-inflammatory cytokine in cystic fibrosis transmembrane conductance regulator-expressing but not cystic fibrosis airway cells.
    Chanson M, Berclaz PY, Scerri I, Dudez T, Wernke-Dollries K, Pizurki L, Pavirani A, Fiedler MA, Suter S.
    Am J Pathol; 2001 May 01; 158(5):1775-84. PubMed ID: 11337375
    [Abstract] [Full Text] [Related]

  • 10. Activation of NF-kappaB in airway epithelial cells is dependent on CFTR trafficking and Cl- channel function.
    Weber AJ, Soong G, Bryan R, Saba S, Prince A.
    Am J Physiol Lung Cell Mol Physiol; 2001 Jul 01; 281(1):L71-8. PubMed ID: 11404248
    [Abstract] [Full Text] [Related]

  • 11. Expression of wild-type CFTR suppresses NF-kappaB-driven inflammatory signalling.
    Hunter MJ, Treharne KJ, Winter AK, Cassidy DM, Land S, Mehta A.
    PLoS One; 2010 Jul 14; 5(7):e11598. PubMed ID: 20644644
    [Abstract] [Full Text] [Related]

  • 12. Cystic fibrosis and the innate immune system: therapeutic implications.
    Conese M.
    Endocr Metab Immune Disord Drug Targets; 2011 Mar 14; 11(1):8-22. PubMed ID: 21348822
    [Abstract] [Full Text] [Related]

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  • 14. DeltaF508-CFTR causes constitutive NF-kappaB activation through an ER-overload response in cystic fibrosis lungs.
    Knorre A, Wagner M, Schaefer HE, Colledge WH, Pahl HL.
    Biol Chem; 2002 Feb 14; 383(2):271-82. PubMed ID: 11934265
    [Abstract] [Full Text] [Related]

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  • 16. Infection of polarized airway epithelial cells by normal and small-colony variant strains of Staphylococcus aureus is increased in cells with abnormal cystic fibrosis transmembrane conductance regulator function and is influenced by NF-κB.
    Mitchell G, Grondin G, Bilodeau G, Cantin AM, Malouin F.
    Infect Immun; 2011 Sep 14; 79(9):3541-51. PubMed ID: 21708986
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  • 19. Cystic fibrosis transmembrane conductance regulator controls lung proteasomal degradation and nuclear factor-kappaB activity in conditions of oxidative stress.
    Boncoeur E, Roque T, Bonvin E, Saint-Criq V, Bonora M, Clement A, Tabary O, Henrion-Caude A, Jacquot J.
    Am J Pathol; 2008 May 14; 172(5):1184-94. PubMed ID: 18372427
    [Abstract] [Full Text] [Related]

  • 20. CFTR negatively regulates cyclooxygenase-2-PGE(2) positive feedback loop in inflammation.
    Chen J, Jiang XH, Chen H, Guo JH, Tsang LL, Yu MK, Xu WM, Chan HC.
    J Cell Physiol; 2012 Jun 14; 227(6):2759-66. PubMed ID: 21913191
    [Abstract] [Full Text] [Related]


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