467 related articles for article (PubMed ID: 22505710)
1. Human heat shock protein 105/110 kDa (Hsp105/110) regulates biogenesis and quality control of misfolded cystic fibrosis transmembrane conductance regulator at multiple levels.
Saxena A; Banasavadi-Siddegowda YK; Fan Y; Bhattacharya S; Roy G; Giovannucci DR; Frizzell RA; Wang X
J Biol Chem; 2012 Jun; 287(23):19158-70. PubMed ID: 22505710
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Silencing of the Hsp70-specific nucleotide-exchange factor BAG3 corrects the F508del-CFTR variant by restoring autophagy.
Hutt DM; Mishra SK; Roth DM; Larsen MB; Angles F; Frizzell RA; Balch WE
J Biol Chem; 2018 Aug; 293(35):13682-13695. PubMed ID: 29986884
[TBL] [Abstract][Full Text] [Related]
4. Control of cystic fibrosis transmembrane conductance regulator membrane trafficking: not just from the endoplasmic reticulum to the Golgi.
Farinha CM; Matos P; Amaral MD
FEBS J; 2013 Sep; 280(18):4396-406. PubMed ID: 23773658
[TBL] [Abstract][Full Text] [Related]
5. AAV exploits subcellular stress associated with inflammation, endoplasmic reticulum expansion, and misfolded proteins in models of cystic fibrosis.
Johnson JS; Gentzsch M; Zhang L; Ribeiro CM; Kantor B; Kafri T; Pickles RJ; Samulski RJ
PLoS Pathog; 2011 May; 7(5):e1002053. PubMed ID: 21625534
[TBL] [Abstract][Full Text] [Related]
6. The human DnaJ homologue (Hdj)-1/heat-shock protein (Hsp) 40 co-chaperone is required for the in vivo stabilization of the cystic fibrosis transmembrane conductance regulator by Hsp70.
Farinha CM; Nogueira P; Mendes F; Penque D; Amaral MD
Biochem J; 2002 Sep; 366(Pt 3):797-806. PubMed ID: 12069690
[TBL] [Abstract][Full Text] [Related]
7. The cochaperone HspBP1 inhibits the CHIP ubiquitin ligase and stimulates the maturation of the cystic fibrosis transmembrane conductance regulator.
Alberti S; Böhse K; Arndt V; Schmitz A; Höhfeld J
Mol Biol Cell; 2004 Sep; 15(9):4003-10. PubMed ID: 15215316
[TBL] [Abstract][Full Text] [Related]
8. ERp29 regulates DeltaF508 and wild-type cystic fibrosis transmembrane conductance regulator (CFTR) trafficking to the plasma membrane in cystic fibrosis (CF) and non-CF epithelial cells.
Suaud L; Miller K; Alvey L; Yan W; Robay A; Kebler C; Kreindler JL; Guttentag S; Hubbard MJ; Rubenstein RC
J Biol Chem; 2011 Jun; 286(24):21239-53. PubMed ID: 21525008
[TBL] [Abstract][Full Text] [Related]
9. Sequential quality-control checkpoints triage misfolded cystic fibrosis transmembrane conductance regulator.
Younger JM; Chen L; Ren HY; Rosser MF; Turnbull EL; Fan CY; Patterson C; Cyr DM
Cell; 2006 Aug; 126(3):571-82. PubMed ID: 16901789
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Hsp90 cochaperone Aha1 downregulation rescues misfolding of CFTR in cystic fibrosis.
Wang X; Venable J; LaPointe P; Hutt DM; Koulov AV; Coppinger J; Gurkan C; Kellner W; Matteson J; Plutner H; Riordan JR; Kelly JW; Yates JR; Balch WE
Cell; 2006 Nov; 127(4):803-15. PubMed ID: 17110338
[TBL] [Abstract][Full Text] [Related]
12. Hsp70 and DNAJA2 limit CFTR levels through degradation.
Kim Chiaw P; Hantouche C; Wong MJH; Matthes E; Robert R; Hanrahan JW; Shrier A; Young JC
PLoS One; 2019; 14(8):e0220984. PubMed ID: 31408507
[TBL] [Abstract][Full Text] [Related]
13. Syntaxin 8 and the Endoplasmic Reticulum Processing of ΔF508-CFTR.
Sabirzhanova I; Boinot C; Guggino WB; Cebotaru L
Cell Physiol Biochem; 2018; 51(3):1489-1499. PubMed ID: 30485852
[TBL] [Abstract][Full Text] [Related]
14. Selective Binding of HSC70 and its Co-Chaperones to Structural Hotspots on CFTR.
Baaklini I; Gonçalves CC; Lukacs GL; Young JC
Sci Rep; 2020 Mar; 10(1):4176. PubMed ID: 32144307
[TBL] [Abstract][Full Text] [Related]
15. Cysteine string protein promotes proteasomal degradation of the cystic fibrosis transmembrane conductance regulator (CFTR) by increasing its interaction with the C terminus of Hsp70-interacting protein and promoting CFTR ubiquitylation.
Schmidt BZ; Watts RJ; Aridor M; Frizzell RA
J Biol Chem; 2009 Feb; 284(7):4168-78. PubMed ID: 19098309
[TBL] [Abstract][Full Text] [Related]
16. Cystic fibrosis transmembrane conductance regulator degradation: cross-talk between the ubiquitylation and SUMOylation pathways.
Ahner A; Gong X; Frizzell RA
FEBS J; 2013 Sep; 280(18):4430-8. PubMed ID: 23809253
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Endoplasmic reticulum protein quality control is determined by cooperative interactions between Hsp/c70 protein and the CHIP E3 ligase.
Matsumura Y; Sakai J; Skach WR
J Biol Chem; 2013 Oct; 288(43):31069-79. PubMed ID: 23990462
[TBL] [Abstract][Full Text] [Related]
19. Sodium 4-phenylbutyrate downregulates Hsc70: implications for intracellular trafficking of DeltaF508-CFTR.
Rubenstein RC; Zeitlin PL
Am J Physiol Cell Physiol; 2000 Feb; 278(2):C259-67. PubMed ID: 10666020
[TBL] [Abstract][Full Text] [Related]
20. Coupling cystic fibrosis to endoplasmic reticulum stress: Differential role of Grp78 and ATF6.
Kerbiriou M; Le Drévo MA; Férec C; Trouvé P
Biochim Biophys Acta; 2007 Dec; 1772(11-12):1236-49. PubMed ID: 18022401
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
