BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

324 related articles for article (PubMed ID: 20156845)

  • 1. Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers.
    LeSimple P; Liao J; Robert R; Gruenert DC; Hanrahan JW
    J Physiol; 2010 Apr; 588(Pt 8):1195-209. PubMed ID: 20156845
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Paracellular permeability of bronchial epithelium is controlled by CFTR.
    Weiser N; Molenda N; Urbanova K; Bähler M; Pieper U; Oberleithner H; Schillers H
    Cell Physiol Biochem; 2011; 28(2):289-96. PubMed ID: 21865736
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CFTR and tight junctions in cultured bronchial epithelial cells.
    Nilsson HE; Dragomir A; Lazorova L; Johannesson M; Roomans GM
    Exp Mol Pathol; 2010 Feb; 88(1):118-27. PubMed ID: 19818767
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Epithelial barrier function properties of the 16HBE14o- human bronchial epithelial cell culture model.
    Callaghan PJ; Ferrick B; Rybakovsky E; Thomas S; Mullin JM
    Biosci Rep; 2020 Oct; 40(10):. PubMed ID: 32985670
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Nanomolar affinity small molecule correctors of defective Delta F508-CFTR chloride channel gating.
    Yang H; Shelat AA; Guy RK; Gopinath VS; Ma T; Du K; Lukacs GL; Taddei A; Folli C; Pedemonte N; Galietta LJ; Verkman AS
    J Biol Chem; 2003 Sep; 278(37):35079-85. PubMed ID: 12832418
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel natural product compound enhances cAMP-regulated chloride conductance of cells expressing CFTR[delta]F508.
    deCarvalho AC; Ndi CP; Tsopmo A; Tane P; Ayafor J; Connolly JD; Teem JL
    Mol Med; 2002 Feb; 8(2):75-87. PubMed ID: 12080183
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Paracellular transport through healthy and cystic fibrosis bronchial epithelial cell lines--do we have a proper model?
    Molenda N; Urbanova K; Weiser N; Kusche-Vihrog K; Günzel D; Schillers H
    PLoS One; 2014; 9(6):e100621. PubMed ID: 24945658
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Organic solutes rescue the functional defect in delta F508 cystic fibrosis transmembrane conductance regulator.
    Zhang XM; Wang XT; Yue H; Leung SW; Thibodeau PH; Thomas PJ; Guggino SE
    J Biol Chem; 2003 Dec; 278(51):51232-42. PubMed ID: 14532265
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The anion transporter SLC26A9 localizes to tight junctions and is degraded by the proteasome when co-expressed with F508del-CFTR.
    Sato Y; Thomas DY; Hanrahan JW
    J Biol Chem; 2019 Nov; 294(48):18269-18284. PubMed ID: 31645438
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Functional activation of the cystic fibrosis trafficking mutant delta F508-CFTR by overexpression.
    Cheng SH; Fang SL; Zabner J; Marshall J; Piraino S; Schiavi SC; Jefferson DM; Welsh MJ; Smith AE
    Am J Physiol; 1995 Apr; 268(4 Pt 1):L615-24. PubMed ID: 7733303
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Functional stability of rescued delta F508 cystic fibrosis transmembrane conductance regulator in airway epithelial cells.
    Jurkuvenaite A; Chen L; Bartoszewski R; Goldstein R; Bebok Z; Matalon S; Collawn JF
    Am J Respir Cell Mol Biol; 2010 Mar; 42(3):363-72. PubMed ID: 19502384
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genistein potentiates wild-type and delta F508-CFTR channel activity.
    Hwang TC; Wang F; Yang IC; Reenstra WW
    Am J Physiol; 1997 Sep; 273(3 Pt 1):C988-98. PubMed ID: 9316420
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Na+/H+ exchanger regulatory factor isoform 1 overexpression modulates cystic fibrosis transmembrane conductance regulator (CFTR) expression and activity in human airway 16HBE14o- cells and rescues DeltaF508 CFTR functional expression in cystic fibrosis cells.
    Guerra L; Fanelli T; Favia M; Riccardi SM; Busco G; Cardone RA; Carrabino S; Weinman EJ; Reshkin SJ; Conese M; Casavola V
    J Biol Chem; 2005 Dec; 280(49):40925-33. PubMed ID: 16203733
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.
    French PJ; van Doorninck JH; Peters RH; Verbeek E; Ameen NA; Marino CR; de Jonge HR; Bijman J; Scholte BJ
    J Clin Invest; 1996 Sep; 98(6):1304-12. PubMed ID: 8823295
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The short apical membrane half-life of rescued {Delta}F508-cystic fibrosis transmembrane conductance regulator (CFTR) results from accelerated endocytosis of {Delta}F508-CFTR in polarized human airway epithelial cells.
    Swiatecka-Urban A; Brown A; Moreau-Marquis S; Renuka J; Coutermarsh B; Barnaby R; Karlson KH; Flotte TR; Fukuda M; Langford GM; Stanton BA
    J Biol Chem; 2005 Nov; 280(44):36762-72. PubMed ID: 16131493
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Protective role of CFTR during fungal infection of cystic fibrosis bronchial epithelial cells with
    Illek B; Fischer H; Machen TE; Hari G; Clemons KV; Sass G; Ferreira JAG; Stevens DA
    Front Cell Infect Microbiol; 2023; 13():1196581. PubMed ID: 37680748
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Augmentation of Cystic Fibrosis Transmembrane Conductance Regulator Function in Human Bronchial Epithelial Cells via SLC6A14-Dependent Amino Acid Uptake. Implications for Treatment of Cystic Fibrosis.
    Ahmadi S; Wu YS; Li M; Ip W; Lloyd-Kuzik A; Di Paola M; Du K; Xia S; Lew A; Bozoky Z; Forman-Kay J; Bear CE; Gonska T
    Am J Respir Cell Mol Biol; 2019 Dec; 61(6):755-764. PubMed ID: 31189070
    [TBL] [Abstract][Full Text] [Related]  

  • 18. In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR.
    Rubenstein RC; Egan ME; Zeitlin PL
    J Clin Invest; 1997 Nov; 100(10):2457-65. PubMed ID: 9366560
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Calcium-pump inhibitors induce functional surface expression of Delta F508-CFTR protein in cystic fibrosis epithelial cells.
    Egan ME; Glöckner-Pagel J; Ambrose C; Cahill PA; Pappoe L; Balamuth N; Cho E; Canny S; Wagner CA; Geibel J; Caplan MJ
    Nat Med; 2002 May; 8(5):485-92. PubMed ID: 11984593
    [TBL] [Abstract][Full Text] [Related]  

  • 20. NHERF1 and CFTR restore tight junction organisation and function in cystic fibrosis airway epithelial cells: role of ezrin and the RhoA/ROCK pathway.
    Castellani S; Guerra L; Favia M; Di Gioia S; Casavola V; Conese M
    Lab Invest; 2012 Nov; 92(11):1527-40. PubMed ID: 22964850
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.