98 related articles for article (PubMed ID: 11502568)
1. Proton leak and CFTR in regulation of Golgi pH in respiratory epithelial cells.
Chandy G; Grabe M; Moore HP; Machen TE
Am J Physiol Cell Physiol; 2001 Sep; 281(3):C908-21. PubMed ID: 11502568
[TBL] [Abstract][Full Text] [Related]
2. Cystic fibrosis transmembrane conductance regulator and H+ permeability in regulation of Golgi pH.
Machen TE; Chandy G; Wu M; Grabe M; Moore HP
JOP; 2001 Jul; 2(4 Suppl):229-36. PubMed ID: 11875264
[TBL] [Abstract][Full Text] [Related]
3. Evidence against defective trans-Golgi acidification in cystic fibrosis.
Seksek O; Biwersi J; Verkman AS
J Biol Chem; 1996 Jun; 271(26):15542-8. PubMed ID: 8663158
[TBL] [Abstract][Full Text] [Related]
4. High-affinity activators of cystic fibrosis transmembrane conductance regulator (CFTR) chloride conductance identified by high-throughput screening.
Ma T; Vetrivel L; Yang H; Pedemonte N; Zegarra-Moran O; Galietta LJ; Verkman AS
J Biol Chem; 2002 Oct; 277(40):37235-41. PubMed ID: 12161441
[TBL] [Abstract][Full Text] [Related]
5. Glutathione levels and BAX activation during apoptosis due to oxidative stress in cells expressing wild-type and mutant cystic fibrosis transmembrane conductance regulator.
Jungas T; Motta I; Duffieux F; Fanen P; Stoven V; Ojcius DM
J Biol Chem; 2002 Aug; 277(31):27912-8. PubMed ID: 12023951
[TBL] [Abstract][Full Text] [Related]
6. Revisiting the role of cystic fibrosis transmembrane conductance regulator and counterion permeability in the pH regulation of endocytic organelles.
Barriere H; Bagdany M; Bossard F; Okiyoneda T; Wojewodka G; Gruenert D; Radzioch D; Lukacs GL
Mol Biol Cell; 2009 Jul; 20(13):3125-41. PubMed ID: 19420138
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. In vivo activation of the cystic fibrosis transmembrane conductance regulator mutant deltaF508 in murine nasal epithelium.
Kelley TJ; Thomas K; Milgram LJ; Drumm ML
Proc Natl Acad Sci U S A; 1997 Mar; 94(6):2604-8. PubMed ID: 9122242
[TBL] [Abstract][Full Text] [Related]
9. Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator.
Poulsen JH; Fischer H; Illek B; Machen TE
Proc Natl Acad Sci U S A; 1994 Jun; 91(12):5340-4. PubMed ID: 7515498
[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. 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]
12. 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]
13. Spliceosome-mediated RNA trans-splicing with recombinant adeno-associated virus partially restores cystic fibrosis transmembrane conductance regulator function to polarized human cystic fibrosis airway epithelial cells.
Liu X; Luo M; Zhang LN; Yan Z; Zak R; Ding W; Mansfield SG; Mitchell LG; Engelhardt JF
Hum Gene Ther; 2005 Sep; 16(9):1116-23. PubMed ID: 16149910
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Evidence against the acidification hypothesis in cystic fibrosis.
Gibson GA; Hill WG; Weisz OA
Am J Physiol Cell Physiol; 2000 Oct; 279(4):C1088-99. PubMed ID: 11003589
[TBL] [Abstract][Full Text] [Related]
16. Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels.
Wang F; Zeltwanger S; Hu S; Hwang TC
J Physiol; 2000 May; 524 Pt 3(Pt 3):637-48. PubMed ID: 10790148
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Interaction between calcium-activated chloride channels and the cystic fibrosis transmembrane conductance regulator.
Wei L; Vankeerberghen A; Cuppens H; Eggermont J; Cassiman JJ; Droogmans G; Nilius B
Pflugers Arch; 1999 Oct; 438(5):635-41. PubMed ID: 10555560
[TBL] [Abstract][Full Text] [Related]
19. Cystic fibrosis transmembrane conductance regulator (CFTR) confers glibenclamide sensitivity to outwardly rectifying chloride channel (ORCC) in Hi-5 insect cells.
Julien M; Verrier B; Cerutti M; Chappe V; Gola M; Devauchelle G; Becq F
J Membr Biol; 1999 Apr; 168(3):229-39. PubMed ID: 10191357
[TBL] [Abstract][Full Text] [Related]
20. Base treatment corrects defects due to misfolding of mutant cystic fibrosis transmembrane conductance regulator.
Namkung W; Kim KH; Lee MG
Gastroenterology; 2005 Dec; 129(6):1979-90. PubMed ID: 16344066
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]