167 related articles for article (PubMed ID: 10498856)
1. Differential sensitivity of normal and cystic fibrosis airway epithelial cells to epinephrine.
Goncz KK; Feeney L; Gruenert DC
Br J Pharmacol; 1999 Sep; 128(1):227-33. PubMed ID: 10498856
[TBL] [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; 7(7):e1000155. PubMed ID: 19621064
[TBL] [Abstract][Full Text] [Related]
3. Purinergic signaling underlies CFTR control of human airway epithelial cell volume.
Braunstein GM; Zsembery A; Tucker TA; Schwiebert EM
J Cyst Fibros; 2004 Jun; 3(2):99-117. PubMed ID: 15463893
[TBL] [Abstract][Full Text] [Related]
4. Phosphodiesterase 8A Regulates CFTR Activity in Airway Epithelial Cells.
Turner MJ; Sato Y; Thomas DY; Abbott-Banner K; Hanrahan JW
Cell Physiol Biochem; 2021 Dec; 55(6):784-804. PubMed ID: 34936285
[TBL] [Abstract][Full Text] [Related]
5. Transient receptor potential canonical channel 6 links Ca2+ mishandling to cystic fibrosis transmembrane conductance regulator channel dysfunction in cystic fibrosis.
Antigny F; Norez C; Dannhoffer L; Bertrand J; Raveau D; Corbi P; Jayle C; Becq F; Vandebrouck C
Am J Respir Cell Mol Biol; 2011 Jan; 44(1):83-90. PubMed ID: 20203293
[TBL] [Abstract][Full Text] [Related]
6. Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis.
Gianotti A; Melani R; Caci E; Sondo E; Ravazzolo R; Galietta LJ; Zegarra-Moran O
Am J Respir Cell Mol Biol; 2013 Sep; 49(3):445-52. PubMed ID: 23600628
[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. A powerful method for in vitro selection of normal versus cystic fibrosis airway epithelial cells.
Vega MA; Goossens M; Besmond C
Gene Ther; 1994 Jan; 1(1):59-63. PubMed ID: 7584061
[TBL] [Abstract][Full Text] [Related]
9. Chronic β2AR stimulation limits CFTR activation in human airway epithelia.
Brewington JJ; Backstrom J; Feldman A; Kramer EL; Moncivaiz JD; Ostmann AJ; Zhu X; Lu LJ; Clancy JP
JCI Insight; 2018 Feb; 3(4):. PubMed ID: 29467332
[TBL] [Abstract][Full Text] [Related]
10. 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; 18(8):1631-43. PubMed ID: 24894806
[TBL] [Abstract][Full Text] [Related]
11. Cystic fibrosis transmembrane conductance regulator is involved in airway epithelial wound repair.
Schiller KR; Maniak PJ; O'Grady SM
Am J Physiol Cell Physiol; 2010 Nov; 299(5):C912-21. PubMed ID: 20686068
[TBL] [Abstract][Full Text] [Related]
12. Control of the proinflammatory state in cystic fibrosis lung epithelial cells by genes from the TNF-alphaR/NFkappaB pathway.
Eidelman O; Srivastava M; Zhang J; Leighton X; Murtie J; Jozwik C; Jacobson K; Weinstein DL; Metcalf EL; Pollard HB
Mol Med; 2001 Aug; 7(8):523-34. PubMed ID: 11591888
[TBL] [Abstract][Full Text] [Related]
13. Regulation of cystic fibrosis transmembrane conductance regulator by microRNA-145, -223, and -494 is altered in ΔF508 cystic fibrosis airway epithelium.
Oglesby IK; Chotirmall SH; McElvaney NG; Greene CM
J Immunol; 2013 Apr; 190(7):3354-62. PubMed ID: 23436935
[TBL] [Abstract][Full Text] [Related]
14. Modeling Cystic Fibrosis Using Pluripotent Stem Cell-Derived Human Pancreatic Ductal Epithelial Cells.
Simsek S; Zhou T; Robinson CL; Tsai SY; Crespo M; Amin S; Lin X; Hon J; Evans T; Chen S
Stem Cells Transl Med; 2016 May; 5(5):572-9. PubMed ID: 27034411
[TBL] [Abstract][Full Text] [Related]
15. Sensitivity of chloride efflux vs. transepithelial measurements in mixed CF and normal airway epithelial cell populations.
Illek B; Lei D; Fischer H; Gruenert DC
Cell Physiol Biochem; 2010; 26(6):983-90. PubMed ID: 21220929
[TBL] [Abstract][Full Text] [Related]
16. Improvement of defective cystic fibrosis airway epithelial wound repair after CFTR rescue.
Trinh NT; Bardou O; Privé A; Maillé E; Adam D; Lingée S; Ferraro P; Desrosiers MY; Coraux C; Brochiero E
Eur Respir J; 2012 Dec; 40(6):1390-400. PubMed ID: 22496330
[TBL] [Abstract][Full Text] [Related]
17. 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; 9(9):. PubMed ID: 32967385
[TBL] [Abstract][Full Text] [Related]
18. The Effect of Sodium Bicarbonate, a Beneficial Adjuvant Molecule in Cystic Fibrosis, on Bronchial Epithelial Cells Expressing a Wild-Type or Mutant CFTR Channel.
Gróf I; Bocsik A; Harazin A; Santa-Maria AR; Vizsnyiczai G; Barna L; Kiss L; Fűr G; Rakonczay Z; Ambrus R; Szabó-Révész P; Gosselet F; Jaikumpun P; Szabó H; Zsembery Á; Deli MA
Int J Mol Sci; 2020 Jun; 21(11):. PubMed ID: 32512832
[TBL] [Abstract][Full Text] [Related]
19. Correction of delF508-CFTR activity with benzo(c)quinolizinium compounds through facilitation of its processing in cystic fibrosis airway cells.
Dormer RL; Dérand R; McNeilly CM; Mettey Y; Bulteau-Pignoux L; Métayé T; Vierfond JM; Gray MA; Galietta LJ; Morris MR; Pereira MM; Doull IJ; Becq F; McPherson MA
J Cell Sci; 2001 Nov; 114(Pt 22):4073-81. PubMed ID: 11739639
[TBL] [Abstract][Full Text] [Related]
20. Generation and phenotype of cell lines derived from CF and non-CF mice that carry the H-2K(b)-tsA58 transgene.
Takacs-Jarrett M; Sweeney WE; Avner ED; Cotton CU
Am J Physiol Cell Physiol; 2001 Jan; 280(1):C228-36. PubMed ID: 11121394
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
