119 related articles for article (PubMed ID: 17237149)
1. NHE-RF1 protein rescues DeltaF508-CFTR function.
Bossard F; Robay A; Toumaniantz G; Dahimene S; Becq F; Merot J; Gauthier C
Am J Physiol Lung Cell Mol Physiol; 2007 May; 292(5):L1085-94. PubMed ID: 17237149
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Functional cystic fibrosis transmembrane conductance regulator tagged with an epitope of the vesicular stomatis virus glycoprotein can be addressed to the apical domain of polarized cells.
Costa de Beauregard MA; Edelman A; Chesnoy-Marchais D; Tondelier D; Lapillonne A; El Marjou F; Robine S; Louvard D
Eur J Cell Biol; 2000 Nov; 79(11):795-802. PubMed ID: 11139142
[TBL] [Abstract][Full Text] [Related]
5. Trafficking of GFP-tagged DeltaF508-CFTR to the plasma membrane in a polarized epithelial cell line.
Loffing-Cueni D; Loffing J; Shaw C; Taplin AM; Govindan M; Stanton CR; Stanton BA
Am J Physiol Cell Physiol; 2001 Dec; 281(6):C1889-97. PubMed ID: 11698247
[TBL] [Abstract][Full Text] [Related]
6. Increased functional cell surface expression of CFTR and DeltaF508-CFTR by the anthracycline doxorubicin.
Maitra R; Shaw CM; Stanton BA; Hamilton JW
Am J Physiol Cell Physiol; 2001 May; 280(5):C1031-7. PubMed ID: 11287314
[TBL] [Abstract][Full Text] [Related]
7. The role of the C terminus and Na+/H+ exchanger regulatory factor in the functional expression of cystic fibrosis transmembrane conductance regulator in nonpolarized cells and epithelia.
Benharouga M; Sharma M; So J; Haardt M; Drzymala L; Popov M; Schwapach B; Grinstein S; Du K; Lukacs GL
J Biol Chem; 2003 Jun; 278(24):22079-89. PubMed ID: 12651858
[TBL] [Abstract][Full Text] [Related]
8. Chaperone displacement from mutant cystic fibrosis transmembrane conductance regulator restores its function in human airway epithelia.
Sun F; Mi Z; Condliffe SB; Bertrand CA; Gong X; Lu X; Zhang R; Latoche JD; Pilewski JM; Robbins PD; Frizzell RA
FASEB J; 2008 Sep; 22(9):3255-63. PubMed ID: 18556464
[TBL] [Abstract][Full Text] [Related]
9. The CFTR-Associated Ligand Arrests the Trafficking of the Mutant ΔF508 CFTR Channel in the ER Contributing to Cystic Fibrosis.
Bergbower E; Boinot C; Sabirzhanova I; Guggino W; Cebotaru L
Cell Physiol Biochem; 2018; 45(2):639-655. PubMed ID: 29402832
[TBL] [Abstract][Full Text] [Related]
10. Activation of DeltaF508 CFTR in an epithelial monolayer.
Bebök Z; Venglarik CJ; Pánczél Z; Jilling T; Kirk KL; Sorscher EJ
Am J Physiol; 1998 Aug; 275(2):C599-607. PubMed ID: 9688615
[TBL] [Abstract][Full Text] [Related]
11. Failure of cAMP agonists to activate rescued deltaF508 CFTR in CFBE41o- airway epithelial monolayers.
Bebok Z; Collawn JF; Wakefield J; Parker W; Li Y; Varga K; Sorscher EJ; Clancy JP
J Physiol; 2005 Dec; 569(Pt 2):601-15. PubMed ID: 16210354
[TBL] [Abstract][Full Text] [Related]
12. RNA Interference Screen to Identify Kinases That Suppress Rescue of ΔF508-CFTR.
Trzcińska-Daneluti AM; Chen A; Nguyen L; Murchie R; Jiang C; Moffat J; Pelletier L; Rotin D
Mol Cell Proteomics; 2015 Jun; 14(6):1569-83. PubMed ID: 25825526
[TBL] [Abstract][Full Text] [Related]
13. Matrine modulates HSC70 levels and rescues ΔF508-CFTR.
Basile A; Pascale M; Franceschelli S; Nieddu E; Mazzei MT; Fossa P; Turco MC; Mazzei M
J Cell Physiol; 2012 Sep; 227(9):3317-23. PubMed ID: 22170045
[TBL] [Abstract][Full Text] [Related]
14. Annexin A5 increases the cell surface expression and the chloride channel function of the DeltaF508-cystic fibrosis transmembrane regulator.
Le Drévo MA; Benz N; Kerbiriou M; Giroux-Metges MA; Pennec JP; Trouvé P; Férec C
Biochim Biophys Acta; 2008 Oct; 1782(10):605-14. PubMed ID: 18773956
[TBL] [Abstract][Full Text] [Related]
15. Beta-oestradiol rescues DeltaF508CFTR functional expression in human cystic fibrosis airway CFBE41o- cells through the up-regulation of NHERF1.
Fanelli T; Cardone RA; Favia M; Guerra L; Zaccolo M; Monterisi S; De Santis T; Riccardi SM; Reshkin SJ; Casavola V
Biol Cell; 2008 Jul; 100(7):399-412. PubMed ID: 18184109
[TBL] [Abstract][Full Text] [Related]
16. SERCA pump inhibitors do not correct biosynthetic arrest of deltaF508 CFTR in cystic fibrosis.
Grubb BR; Gabriel SE; Mengos A; Gentzsch M; Randell SH; Van Heeckeren AM; Knowles MR; Drumm ML; Riordan JR; Boucher RC
Am J Respir Cell Mol Biol; 2006 Mar; 34(3):355-63. PubMed ID: 16284361
[TBL] [Abstract][Full Text] [Related]
17. Functional expression and apical localization of the cystic fibrosis transmembrane conductance regulator in MDCK I cells.
Mohamed A; Ferguson D; Seibert FS; Cai HM; Kartner N; Grinstein S; Riordan JR; Lukacs GL
Biochem J; 1997 Feb; 322 ( Pt 1)(Pt 1):259-65. PubMed ID: 9078271
[TBL] [Abstract][Full Text] [Related]
18. Transcytosis maintains CFTR apical polarity in the face of constitutive and mutation-induced basolateral missorting.
Bidaud-Meynard A; Bossard F; Schnúr A; Fukuda R; Veit G; Xu H; Lukacs GL
J Cell Sci; 2019 May; 132(10):. PubMed ID: 30975917
[TBL] [Abstract][Full Text] [Related]
19. Rescue of DeltaF508-CFTR by the SGK1/Nedd4-2 signaling pathway.
Caohuy H; Jozwik C; Pollard HB
J Biol Chem; 2009 Sep; 284(37):25241-53. PubMed ID: 19617352
[TBL] [Abstract][Full Text] [Related]
20. Rescue of DeltaF508-CFTR trafficking and gating in human cystic fibrosis airway primary cultures by small molecules.
Van Goor F; Straley KS; Cao D; González J; Hadida S; Hazlewood A; Joubran J; Knapp T; Makings LR; Miller M; Neuberger T; Olson E; Panchenko V; Rader J; Singh A; Stack JH; Tung R; Grootenhuis PD; Negulescu P
Am J Physiol Lung Cell Mol Physiol; 2006 Jun; 290(6):L1117-30. PubMed ID: 16443646
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
