133 related articles for article (PubMed ID: 17084917)
1. CFTR surface expression and chloride currents are decreased by inhibitors of N-WASP and actin polymerization.
Ganeshan R; Nowotarski K; Di A; Nelson DJ; Kirk KL
Biochim Biophys Acta; 2007 Feb; 1773(2):192-200. PubMed ID: 17084917
[TBL] [Abstract][Full Text] [Related]
2. Involvement of the Cdc42 pathway in CFTR post-translational turnover and in its plasma membrane stability in airway epithelial cells.
Ferru-Clément R; Fresquet F; Norez C; Métayé T; Becq F; Kitzis A; Thoreau V
PLoS One; 2015; 10(3):e0118943. PubMed ID: 25768293
[TBL] [Abstract][Full Text] [Related]
3. N-WASP inhibitor wiskostatin nonselectively perturbs membrane transport by decreasing cellular ATP levels.
Guerriero CJ; Weisz OA
Am J Physiol Cell Physiol; 2007 Apr; 292(4):C1562-6. PubMed ID: 17092993
[TBL] [Abstract][Full Text] [Related]
4. Inhibition of heterologously expressed cystic fibrosis transmembrane conductance regulator Cl- channels by non-sulphonylurea hypoglycaemic agents.
Cai Z; Lansdell KA; Sheppard DN
Br J Pharmacol; 1999 Sep; 128(1):108-18. PubMed ID: 10498841
[TBL] [Abstract][Full Text] [Related]
5. Constitutive internalization of cystic fibrosis transmembrane conductance regulator occurs via clathrin-dependent endocytosis and is regulated by protein phosphorylation.
Lukacs GL; Segal G; Kartner N; Grinstein S; Zhang F
Biochem J; 1997 Dec; 328 ( Pt 2)(Pt 2):353-61. PubMed ID: 9371688
[TBL] [Abstract][Full Text] [Related]
6. Differential roles for actin polymerization and a myosin II motor in assembly of the epithelial apical junctional complex.
Ivanov AI; Hunt D; Utech M; Nusrat A; Parkos CA
Mol Biol Cell; 2005 Jun; 16(6):2636-50. PubMed ID: 15800060
[TBL] [Abstract][Full Text] [Related]
7. Heterologous regulation of anion transporters by menthol in human airway epithelial cells.
Morise M; Ito Y; Matsuno T; Hibino Y; Mizutani T; Ito S; Hashimoto N; Kondo M; Imaizumi K; Hasegawa Y
Eur J Pharmacol; 2010 Jun; 635(1-3):204-11. PubMed ID: 20362570
[TBL] [Abstract][Full Text] [Related]
8. Effects of chemical inhibition of N-WASP, a critical regulator of actin polymerization on aqueous humor outflow through the conventional pathway.
Inoue T; Pattabiraman PP; Epstein DL; Vasantha Rao P
Exp Eye Res; 2010 Feb; 90(2):360-7. PubMed ID: 19961849
[TBL] [Abstract][Full Text] [Related]
9. Cystic fibrosis transmembrane conductance regulator (CFTR) functionality is dependent on coatomer protein I (COPI).
Yu Y; Platoshyn O; Safrina O; Tsigelny I; Yuan JX; Keller SH
Biol Cell; 2007 Aug; 99(8):433-44. PubMed ID: 17388782
[TBL] [Abstract][Full Text] [Related]
10. Actin filament organization is required for proper cAMP-dependent activation of CFTR.
Prat AG; Cunningham CC; Jackson GR; Borkan SC; Wang Y; Ausiello DA; Cantiello HF
Am J Physiol; 1999 Dec; 277(6):C1160-9. PubMed ID: 10600767
[TBL] [Abstract][Full Text] [Related]
11. Syntaxin 8 impairs trafficking of cystic fibrosis transmembrane conductance regulator (CFTR) and inhibits its channel activity.
Bilan F; Thoreau V; Nacfer M; Dérand R; Norez C; Cantereau A; Garcia M; Becq F; Kitzis A
J Cell Sci; 2004 Apr; 117(Pt 10):1923-35. PubMed ID: 15039462
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. G551D-CFTR needs more bound actin than wild-type CFTR to maintain its presence in plasma membranes.
Trouvé P; Kerbiriou M; Teng L; Benz N; Taiya M; Le Hir S; Férec C
Cell Biol Int; 2015 Aug; 39(8):978-85. PubMed ID: 25712891
[TBL] [Abstract][Full Text] [Related]
14. Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel.
Prince LS; Workman RB; Marchase RB
Proc Natl Acad Sci U S A; 1994 May; 91(11):5192-6. PubMed ID: 7515188
[TBL] [Abstract][Full Text] [Related]
15. Mouse cystic fibrosis transmembrane conductance regulator forms cAMP-PKA-regulated apical chloride channels in cortical collecting duct.
Lu M; Dong K; Egan ME; Giebisch GH; Boulpaep EL; Hebert SC
Proc Natl Acad Sci U S A; 2010 Mar; 107(13):6082-7. PubMed ID: 20231442
[TBL] [Abstract][Full Text] [Related]
16. CFTR is restricted to a small population of high expresser cells that provide a forskolin-sensitive transepithelial Cl- conductance in the proximal colon of the possum, Trichosurus vulpecula.
Fan S; Harfoot N; Bartolo RC; Butt AG
J Exp Biol; 2012 Apr; 215(Pt 7):1218-30. PubMed ID: 22399668
[TBL] [Abstract][Full Text] [Related]
17. Rab4GTPase modulates CFTR function by impairing channel expression at plasma membrane.
Saxena SK; Kaur S; George C
Biochem Biophys Res Commun; 2006 Mar; 341(1):184-91. PubMed ID: 16413502
[TBL] [Abstract][Full Text] [Related]
18. Biochemical properties and inhibitors of (N-)WASP.
Leung DW; Morgan DM; Rosen MK
Methods Enzymol; 2006; 406():281-96. PubMed ID: 16472665
[TBL] [Abstract][Full Text] [Related]
19. General anesthetic octanol and related compounds activate wild-type and delF508 cystic fibrosis chloride channels.
Marcet B; Becq F; Norez C; Delmas P; Verrier B
Br J Pharmacol; 2004 Mar; 141(6):905-14. PubMed ID: 14967738
[TBL] [Abstract][Full Text] [Related]
20. Trafficking of immature DeltaF508-CFTR to the plasma membrane and its detection by biotinylation.
Luo Y; McDonald K; Hanrahan JW
Biochem J; 2009 Apr; 419(1):211-9, 2 p following 219. PubMed ID: 19053947
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
