These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

293 related articles for article (PubMed ID: 18776130)

  • 21. Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function.
    Zhang S; Shrestha CL; Kopp BT
    Sci Rep; 2018 Nov; 8(1):17066. PubMed ID: 30459435
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Pulmonary T(H)2 response in Pseudomonas aeruginosa-infected patients with cystic fibrosis.
    Hartl D; Griese M; Kappler M; Zissel G; Reinhardt D; Rebhan C; Schendel DJ; Krauss-Etschmann S
    J Allergy Clin Immunol; 2006 Jan; 117(1):204-11. PubMed ID: 16387607
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Role for cystic fibrosis transmembrane conductance regulator protein in a glutathione response to bronchopulmonary pseudomonas infection.
    Day BJ; van Heeckeren AM; Min E; Velsor LW
    Infect Immun; 2004 Apr; 72(4):2045-51. PubMed ID: 15039325
    [TBL] [Abstract][Full Text] [Related]  

  • 24. TLR-induced inflammation in cystic fibrosis and non-cystic fibrosis airway epithelial cells.
    Greene CM; Carroll TP; Smith SG; Taggart CC; Devaney J; Griffin S; O'neill SJ; McElvaney NG
    J Immunol; 2005 Feb; 174(3):1638-46. PubMed ID: 15661927
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Liposomes Loaded With Phosphatidylinositol 5-Phosphate Improve the Antimicrobial Response to
    Poerio N; De Santis F; Rossi A; Ranucci S; De Fino I; Henriquez A; D'Andrea MM; Ciciriello F; Lucidi V; Nisini R; Bragonzi A; Fraziano M
    Front Immunol; 2020; 11():532225. PubMed ID: 33117337
    [TBL] [Abstract][Full Text] [Related]  

  • 26. X-Box-Binding Protein 1 and Innate Immune Responses of Human Cystic Fibrosis Alveolar Macrophages.
    Lubamba BA; Jones LC; O'Neal WK; Boucher RC; Ribeiro CM
    Am J Respir Crit Care Med; 2015 Dec; 192(12):1449-61. PubMed ID: 26331676
    [TBL] [Abstract][Full Text] [Related]  

  • 27. HDAC6 depletion improves cystic fibrosis mouse airway responses to bacterial challenge.
    Rosenjack J; Hodges CA; Darrah RJ; Kelley TJ
    Sci Rep; 2019 Jul; 9(1):10282. PubMed ID: 31311988
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Gene complementation of airway epithelium in the cystic fibrosis mouse is necessary and sufficient to correct the pathogen clearance and inflammatory abnormalities.
    Oceandy D; McMorran BJ; Smith SN; Schreiber R; Kunzelmann K; Alton EW; Hume DA; Wainwright BJ
    Hum Mol Genet; 2002 May; 11(9):1059-67. PubMed ID: 11978765
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Inflammatory cytokines in cystic fibrosis lungs.
    Bonfield TL; Panuska JR; Konstan MW; Hilliard KA; Hilliard JB; Ghnaim H; Berger M
    Am J Respir Crit Care Med; 1995 Dec; 152(6 Pt 1):2111-8. PubMed ID: 8520783
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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; 75(4):1598-608. PubMed ID: 17283089
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Linoleic acid supplementation results in increased arachidonic acid and eicosanoid production in CF airway cells and in cftr-/- transgenic mice.
    Zaman MM; Martin CR; Andersson C; Bhutta AQ; Cluette-Brown JE; Laposata M; Freedman SD
    Am J Physiol Lung Cell Mol Physiol; 2010 Nov; 299(5):L599-606. PubMed ID: 20656894
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Granulocyte-macrophage colony stimulatory factor enhances the pro-inflammatory response of interferon-γ-treated macrophages to Pseudomonas aeruginosa infection.
    Singh S; Barr H; Liu YC; Robins A; Heeb S; Williams P; Fogarty A; Cámara M; Martínez-Pomares L
    PLoS One; 2015; 10(2):e0117447. PubMed ID: 25706389
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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; 8(1):e2544. PubMed ID: 28079883
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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; 170():53-60. PubMed ID: 27155366
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Impaired functions of macrophage from cystic fibrosis patients: CD11b, TLR-5 decrease and sCD14, inflammatory cytokines increase.
    Simonin-Le Jeune K; Le Jeune A; Jouneau S; Belleguic C; Roux PF; Jaguin M; Dimanche-Boitre MT; Lecureur V; Leclercq C; Desrues B; Brinchault G; Gangneux JP; Martin-Chouly C
    PLoS One; 2013; 8(9):e75667. PubMed ID: 24098711
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Innate immune response in CF airway epithelia: hyperinflammatory?
    Machen TE
    Am J Physiol Cell Physiol; 2006 Aug; 291(2):C218-30. PubMed ID: 16825601
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Innate lung defenses and compromised Pseudomonas aeruginosa clearance in the malnourished mouse model of respiratory infections in cystic fibrosis.
    Yu H; Nasr SZ; Deretic V
    Infect Immun; 2000 Apr; 68(4):2142-7. PubMed ID: 10722612
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Delivery of CFTR by adenoviral vector to cystic fibrosis mouse lung in a model of chronic Pseudomonas aeruginosa lung infection.
    Van Heeckeren AM; Scaria A; Schluchter MD; Ferkol TW; Wadsworth S; Davis PB
    Am J Physiol Lung Cell Mol Physiol; 2004 Apr; 286(4):L717-26. PubMed ID: 14514520
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Myeloid CFTR loss-of-function causes persistent neutrophilic inflammation in cystic fibrosis.
    Ng HP; Jennings S; Wellems D; Sun F; Xu J; Nauseef WM; Wang G
    J Leukoc Biol; 2020 Dec; 108(6):1777-1785. PubMed ID: 32531843
    [TBL] [Abstract][Full Text] [Related]  

  • 40. In vivo monitoring of lung inflammation in CFTR-deficient mice.
    Stellari F; Bergamini G; Ruscitti F; Sandri A; Ravanetti F; Donofrio G; Boschi F; Villetti G; Sorio C; Assael BM; Melotti P; Lleo MM
    J Transl Med; 2016 Jul; 14(1):226. PubMed ID: 27468800
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.