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Journal Abstract Search

911 related items for PubMed ID: 29282053

  • 1. Characterization of pediatric cystic fibrosis airway epithelial cell cultures at the air-liquid interface obtained by non-invasive nasal cytology brush sampling.
    Schögler A, Blank F, Brügger M, Beyeler S, Tschanz SA, Regamey N, Casaulta C, Geiser T, Alves MP.
    Respir Res; 2017 Dec 28; 18(1):215. PubMed ID: 29282053
    [Abstract] [Full Text] [Related]

  • 2. CFTR delivery to 25% of surface epithelial cells restores normal rates of mucus transport to human cystic fibrosis airway epithelium.
    Zhang L, Button B, Gabriel SE, Burkett S, Yan Y, Skiadopoulos MH, Dang YL, Vogel LN, McKay T, Mengos A, Boucher RC, Collins PL, Pickles RJ.
    PLoS Biol; 2009 Jul 28; 7(7):e1000155. PubMed ID: 19621064
    [Abstract] [Full Text] [Related]

  • 3. Cystic fibrosis airway epithelium remodelling: involvement of inflammation.
    Adam D, Roux-Delrieu J, Luczka E, Bonnomet A, Lesage J, Mérol JC, Polette M, Abély M, Coraux C.
    J Pathol; 2015 Feb 28; 235(3):408-19. PubMed ID: 25348090
    [Abstract] [Full Text] [Related]

  • 4. Significant functional differences in differentiated Conditionally Reprogrammed (CRC)- and Feeder-free Dual SMAD inhibited-expanded human nasal epithelial cells.
    Awatade NT, Wong SL, Capraro A, Pandzic E, Slapetova I, Zhong L, Turgutoglu N, Fawcett LK, Whan RM, Jaffe A, Waters SA.
    J Cyst Fibros; 2021 Mar 28; 20(2):364-371. PubMed ID: 33414087
    [Abstract] [Full Text] [Related]

  • 5. In vitro 3D culture lung model from expanded primary cystic fibrosis human airway cells.
    Rayner RE, Wellmerling J, Osman W, Honesty S, Alfaro M, Peeples ME, Cormet-Boyaka E.
    J Cyst Fibros; 2020 Sep 28; 19(5):752-761. PubMed ID: 32565193
    [Abstract] [Full Text] [Related]

  • 6. Interleukin-8 production by cystic fibrosis nasal epithelial cells after tumor necrosis factor-alpha and respiratory syncytial virus stimulation.
    Black HR, Yankaskas JR, Johnson LG, Noah TL.
    Am J Respir Cell Mol Biol; 1998 Aug 28; 19(2):210-5. PubMed ID: 9698592
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  • 7. Apical CFTR expression in human nasal epithelium correlates with lung disease in cystic fibrosis.
    van Meegen MA, Terheggen-Lagro SW, Koymans KJ, van der Ent CK, Beekman JM.
    PLoS One; 2013 Aug 28; 8(3):e57617. PubMed ID: 23483918
    [Abstract] [Full Text] [Related]

  • 8. Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells.
    Carbone A, Castellani S, Favia M, Diana A, Paracchini V, Di Gioia S, Seia M, Casavola V, Colombo C, Conese M.
    J Cell Mol Med; 2014 Aug 28; 18(8):1631-43. PubMed ID: 24894806
    [Abstract] [Full Text] [Related]

  • 9. Choice of Differentiation Media Significantly Impacts Cell Lineage and Response to CFTR Modulators in Fully Differentiated Primary Cultures of Cystic Fibrosis Human Airway Epithelial Cells.
    Saint-Criq V, Delpiano L, Casement J, Onuora JC, Lin J, Gray MA.
    Cells; 2020 Sep 21; 9(9):. PubMed ID: 32967385
    [Abstract] [Full Text] [Related]

  • 10. An immunocytochemical assay to detect human CFTR expression following gene transfer.
    Davidson H, Wilson A, Gray RD, Horsley A, Pringle IA, McLachlan G, Nairn AC, Stearns C, Gibson J, Holder E, Jones L, Doherty A, Coles R, Sumner-Jones SG, Wasowicz M, Manvell M, Griesenbach U, Hyde SC, Gill DR, Davies J, Collie DD, Alton EW, Porteous DJ, Boyd AC.
    Mol Cell Probes; 2009 Dec 21; 23(6):272-80. PubMed ID: 19615439
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  • 12. The HDAC inhibitor SAHA does not rescue CFTR membrane expression in Cystic Fibrosis.
    Bergougnoux A, Petit A, Knabe L, Bribes E, Chiron R, De Sario A, Claustres M, Molinari N, Vachier I, Taulan-Cadars M, Bourdin A.
    Int J Biochem Cell Biol; 2017 Jul 21; 88():124-132. PubMed ID: 28478266
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  • 15. Junctional abnormalities in human airway epithelial cells expressing F508del CFTR.
    Molina SA, Stauffer B, Moriarty HK, Kim AH, McCarty NA, Koval M.
    Am J Physiol Lung Cell Mol Physiol; 2015 Sep 01; 309(5):L475-87. PubMed ID: 26115671
    [Abstract] [Full Text] [Related]

  • 16. Aggregates of mutant CFTR fragments in airway epithelial cells of CF lungs: new pathologic observations.
    Du K, Karp PH, Ackerley C, Zabner J, Keshavjee S, Cutz E, Yeger H.
    J Cyst Fibros; 2015 Mar 01; 14(2):182-93. PubMed ID: 25453871
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  • 18. Akt-driven TGF-β and DKK1 Secretion Impairs F508del Cystic Fibrosis Airway Epithelium Polarity.
    Idris T, Bachmann M, Bacchetta M, Wehrle-Haller B, Chanson M, Badaoui M.
    Am J Respir Cell Mol Biol; 2024 Jul 01; 71(1):81-94. PubMed ID: 38531016
    [Abstract] [Full Text] [Related]

  • 19. Exploring intrinsic variability between cultured nasal and bronchial epithelia in cystic fibrosis.
    Rodenburg LW, Metzemaekers M, van der Windt IS, Smits SMA, den Hertog-Oosterhoff LA, Kruisselbrink E, Brunsveld JE, Michel S, de Winter-de Groot KM, van der Ent CK, Stadhouders R, Beekman JM, Amatngalim GD.
    Sci Rep; 2023 Oct 30; 13(1):18573. PubMed ID: 37903789
    [Abstract] [Full Text] [Related]

  • 20. Decreased expression of the CFTR protein in remodeled human nasal epithelium from non-cystic fibrosis patients.
    Brezillon S, Dupuit F, Hinnrasky J, Marchand V, Kälin N, Tümmler B, Puchelle E.
    Lab Invest; 1995 Feb 30; 72(2):191-200. PubMed ID: 7531792
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