297 related articles for article (PubMed ID: 16987954)
1. Tracking of quantum dot-labeled CFTR shows near immobilization by C-terminal PDZ interactions.
Haggie PM; Kim JK; Lukacs GL; Verkman AS
Mol Biol Cell; 2006 Dec; 17(12):4937-45. PubMed ID: 16987954
[TBL] [Abstract][Full Text] [Related]
2. Increased diffusional mobility of CFTR at the plasma membrane after deletion of its C-terminal PDZ binding motif.
Haggie PM; Stanton BA; Verkman AS
J Biol Chem; 2004 Feb; 279(7):5494-500. PubMed ID: 14660592
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. A sequence upstream of canonical PDZ-binding motif within CFTR COOH-terminus enhances NHERF1 interaction.
Sharma N; LaRusch J; Sosnay PR; Gottschalk LB; Lopez AP; Pellicore MJ; Evans T; Davis E; Atalar M; Na CH; Rosson GD; Belchis D; Milewski M; Pandey A; Cutting GR
Am J Physiol Lung Cell Mol Physiol; 2016 Dec; 311(6):L1170-L1182. PubMed ID: 27793802
[TBL] [Abstract][Full Text] [Related]
5. A PDZ-interacting domain in CFTR is an apical membrane polarization signal.
Moyer BD; Denton J; Karlson KH; Reynolds D; Wang S; Mickle JE; Milewski M; Cutting GR; Guggino WB; Li M; Stanton BA
J Clin Invest; 1999 Nov; 104(10):1353-61. PubMed ID: 10562297
[TBL] [Abstract][Full Text] [Related]
6. E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells.
Sun F; Hug MJ; Lewarchik CM; Yun CH; Bradbury NA; Frizzell RA
J Biol Chem; 2000 Sep; 275(38):29539-46. PubMed ID: 10893422
[TBL] [Abstract][Full Text] [Related]
7. Na+/H+ exchanger regulatory factor 1 overexpression-dependent increase of cytoskeleton organization is fundamental in the rescue of F508del cystic fibrosis transmembrane conductance regulator in human airway CFBE41o- cells.
Favia M; Guerra L; Fanelli T; Cardone RA; Monterisi S; Di Sole F; Castellani S; Chen M; Seidler U; Reshkin SJ; Conese M; Casavola V
Mol Biol Cell; 2010 Jan; 21(1):73-86. PubMed ID: 19889841
[TBL] [Abstract][Full Text] [Related]
8. Plasma membrane CFTR regulates RANTES expression via its C-terminal PDZ-interacting motif.
Estell K; Braunstein G; Tucker T; Varga K; Collawn JF; Schwiebert LM
Mol Cell Biol; 2003 Jan; 23(2):594-606. PubMed ID: 12509457
[TBL] [Abstract][Full Text] [Related]
9. A molecular switch in the scaffold NHERF1 enables misfolded CFTR to evade the peripheral quality control checkpoint.
Loureiro CA; Matos AM; Dias-Alves Â; Pereira JF; Uliyakina I; Barros P; Amaral MD; Matos P
Sci Signal; 2015 May; 8(377):ra48. PubMed ID: 25990958
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. VIP regulates CFTR membrane expression and function in Calu-3 cells by increasing its interaction with NHERF1 and P-ERM in a VPAC1- and PKCε-dependent manner.
Alshafie W; Chappe FG; Li M; Anini Y; Chappe VM
Am J Physiol Cell Physiol; 2014 Jul; 307(1):C107-19. PubMed ID: 24788249
[TBL] [Abstract][Full Text] [Related]
12. Ezrin controls the macromolecular complexes formed between an adapter protein Na+/H+ exchanger regulatory factor and the cystic fibrosis transmembrane conductance regulator.
Li J; Dai Z; Jana D; Callaway DJ; Bu Z
J Biol Chem; 2005 Nov; 280(45):37634-43. PubMed ID: 16129695
[TBL] [Abstract][Full Text] [Related]
13. Dynamic regulation of cystic fibrosis transmembrane conductance regulator by competitive interactions of molecular adaptors.
Lee JH; Richter W; Namkung W; Kim KH; Kim E; Conti M; Lee MG
J Biol Chem; 2007 Apr; 282(14):10414-22. PubMed ID: 17244609
[TBL] [Abstract][Full Text] [Related]
14. The relative binding affinities of PDZ partners for CFTR: a biochemical basis for efficient endocytic recycling.
Cushing PR; Fellows A; Villone D; Boisguérin P; Madden DR
Biochemistry; 2008 Sep; 47(38):10084-98. PubMed ID: 18754678
[TBL] [Abstract][Full Text] [Related]
15. Role of the scaffold protein RACK1 in apical expression of CFTR.
Auerbach M; Liedtke CM
Am J Physiol Cell Physiol; 2007 Jul; 293(1):C294-304. PubMed ID: 17409124
[TBL] [Abstract][Full Text] [Related]
16. The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane.
Moyer BD; Duhaime M; Shaw C; Denton J; Reynolds D; Karlson KH; Pfeiffer J; Wang S; Mickle JE; Milewski M; Cutting GR; Guggino WB; Li M; Stanton BA
J Biol Chem; 2000 Sep; 275(35):27069-74. PubMed ID: 10852925
[TBL] [Abstract][Full Text] [Related]
17. Yes-associated protein 65 localizes p62(c-Yes) to the apical compartment of airway epithelia by association with EBP50.
Mohler PJ; Kreda SM; Boucher RC; Sudol M; Stutts MJ; Milgram SL
J Cell Biol; 1999 Nov; 147(4):879-90. PubMed ID: 10562288
[TBL] [Abstract][Full Text] [Related]
18. CFTR-NHERF2-LPA₂ Complex in the Airway and Gut Epithelia.
Zhang W; Zhang Z; Zhang Y; Naren AP
Int J Mol Sci; 2017 Sep; 18(9):. PubMed ID: 28869532
[TBL] [Abstract][Full Text] [Related]
19. Membrane lateral diffusion and capture of CFTR within transient confinement zones.
Bates IR; Hébert B; Luo Y; Liao J; Bachir AI; Kolin DL; Wiseman PW; Hanrahan JW
Biophys J; 2006 Aug; 91(3):1046-58. PubMed ID: 16714353
[TBL] [Abstract][Full Text] [Related]
20. In vitro analysis of PDZ-dependent CFTR macromolecular signaling complexes.
Wu Y; Wang S; Li C
J Vis Exp; 2012 Aug; (66):. PubMed ID: 22907480
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
