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Journal Abstract Search

563 related items for PubMed ID: 26709821

  • 21. Regulation of the inflammasome by ceramide in cystic fibrosis lungs.
    Grassmé H, Carpinteiro A, Edwards MJ, Gulbins E, Becker KA.
    Cell Physiol Biochem; 2014; 34(1):45-55. PubMed ID: 24977480
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  • 22. Lung arginase expression and activity is increased in cystic fibrosis mouse models.
    Jaecklin T, Duerr J, Huang H, Rafii M, Bear CE, Ratjen F, Pencharz P, Kavanagh BP, Mall MA, Grasemann H.
    J Appl Physiol (1985); 2014 Aug 01; 117(3):284-8. PubMed ID: 24925982
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  • 23. Generation of a conditional null allele for Cftr in mice.
    Hodges CA, Cotton CU, Palmert MR, Drumm ML.
    Genesis; 2008 Oct 01; 46(10):546-52. PubMed ID: 18802965
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  • 27. Lung disease in mice with cystic fibrosis.
    Kent G, Iles R, Bear CE, Huan LJ, Griesenbach U, McKerlie C, Frndova H, Ackerley C, Gosselin D, Radzioch D, O'Brodovich H, Tsui LC, Buchwald M, Tanswell AK.
    J Clin Invest; 1997 Dec 15; 100(12):3060-9. PubMed ID: 9399953
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  • 30. Invariant natural killer T (iNKT) cells prevent autoimmunity, but induce pulmonary inflammation in cystic fibrosis.
    Siegmann N, Worbs D, Effinger F, Bormann T, Gebhardt M, Ulrich M, Wermeling F, Müller-Hermelink E, Biedermann T, Tighe M, Edwards MJ, Caldwell C, Leadbetter E, Karlsson MC, Becker KA, Gulbins E, Döring G.
    Cell Physiol Biochem; 2014 Dec 15; 34(1):56-70. PubMed ID: 24977481
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  • 31. Toll-like receptor-4 genotype influences the survival of cystic fibrosis mice.
    Canale-Zambrano JC, Auger ML, Haston CK.
    Am J Physiol Gastrointest Liver Physiol; 2010 Aug 15; 299(2):G381-90. PubMed ID: 20522639
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  • 32. Severe osteopenia in CFTR-null mice.
    Dif F, Marty C, Baudoin C, de Vernejoul MC, Levi G.
    Bone; 2004 Sep 15; 35(3):595-603. PubMed ID: 15336594
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  • 35. Novel role of cystic fibrosis transmembrane conductance regulator in maintaining adult mouse olfactory neuronal homeostasis.
    Pfister S, Weber T, Härtig W, Schwerdel C, Elsaesser R, Knuesel I, Fritschy JM.
    J Comp Neurol; 2015 Feb 15; 523(3):406-30. PubMed ID: 25271146
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  • 38. Bacterial overgrowth in the cystic fibrosis transmembrane conductance regulator null mouse small intestine.
    Norkina O, Burnett TG, De Lisle RC.
    Infect Immun; 2004 Oct 15; 72(10):6040-9. PubMed ID: 15385508
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  • 39. 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 15; 383(2):271-82. PubMed ID: 11934265
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