BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

364 related articles for article (PubMed ID: 21884936)

  • 1. Rescue of ΔF508-CFTR trafficking via a GRASP-dependent unconventional secretion pathway.
    Gee HY; Noh SH; Tang BL; Kim KH; Lee MG
    Cell; 2011 Sep; 146(5):746-60. PubMed ID: 21884936
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Monomerization and ER Relocalization of GRASP Is a Requisite for Unconventional Secretion of CFTR.
    Kim J; Noh SH; Piao H; Kim DH; Kim K; Cha JS; Chung WY; Cho HS; Kim JY; Lee MG
    Traffic; 2016 Jul; 17(7):733-53. PubMed ID: 27062250
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sec16A is critical for both conventional and unconventional secretion of CFTR.
    Piao H; Kim J; Noh SH; Kweon HS; Kim JY; Lee MG
    Sci Rep; 2017 Jan; 7():39887. PubMed ID: 28067262
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Rescue of DeltaF508-CFTR (cystic fibrosis transmembrane conductance regulator) by curcumin: involvement of the keratin 18 network.
    Lipecka J; Norez C; Bensalem N; Baudouin-Legros M; Planelles G; Becq F; Edelman A; Davezac N
    J Pharmacol Exp Ther; 2006 May; 317(2):500-5. PubMed ID: 16424149
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Low temperature induces the delivery of mature and immature CFTR to the plasma membrane.
    Rennolds J; Boyaka PN; Bellis SL; Cormet-Boyaka E
    Biochem Biophys Res Commun; 2008 Feb; 366(4):1025-9. PubMed ID: 18096515
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of conventional and unconventional trafficking of CFTR and other membrane proteins.
    Gee HY; Kim JY; Lee MG
    Methods Mol Biol; 2015; 1270():137-54. PubMed ID: 25702115
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. S-nitrosylating agents: a novel class of compounds that increase cystic fibrosis transmembrane conductance regulator expression and maturation in epithelial cells.
    Zaman K; Carraro S; Doherty J; Henderson EM; Lendermon E; Liu L; Verghese G; Zigler M; Ross M; Park E; Palmer LA; Doctor A; Stamler JS; Gaston B
    Mol Pharmacol; 2006 Oct; 70(4):1435-42. PubMed ID: 16857740
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Surface expression of the cystic fibrosis transmembrane conductance regulator mutant DeltaF508 is markedly upregulated by combination treatment with sodium butyrate and low temperature.
    Heda GD; Marino CR
    Biochem Biophys Res Commun; 2000 May; 271(3):659-64. PubMed ID: 10814518
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Specific autophagy and ESCRT components participate in the unconventional secretion of CFTR.
    Noh SH; Gee HY; Kim Y; Piao H; Kim J; Kang CM; Lee G; Mook-Jung I; Lee Y; Cho JW; Lee MG
    Autophagy; 2018; 14(10):1761-1778. PubMed ID: 29969945
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Non-conventional trafficking of the cystic fibrosis transmembrane conductance regulator through the early secretory pathway.
    Yoo JS; Moyer BD; Bannykh S; Yoo HM; Riordan JR; Balch WE
    J Biol Chem; 2002 Mar; 277(13):11401-9. PubMed ID: 11799116
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Improved maturation of CFTR by an ER export signal.
    Wendeler MW; Nufer O; Hauri HP
    FASEB J; 2007 Aug; 21(10):2352-8. PubMed ID: 17392477
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Misassembled mutant DeltaF508 CFTR in the distal secretory pathway alters cellular lipid trafficking.
    Gentzsch M; Choudhury A; Chang XB; Pagano RE; Riordan JR
    J Cell Sci; 2007 Feb; 120(Pt 3):447-55. PubMed ID: 17213331
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of molecular determinants that modulate trafficking of DeltaF508 CFTR, the mutant ABC transporter associated with cystic fibrosis.
    Tsigelny I; Hotchko M; Yuan JX; Keller SH
    Cell Biochem Biophys; 2005; 42(1):41-53. PubMed ID: 15673927
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional rescue of DeltaF508-CFTR by peptides designed to mimic sorting motifs.
    Kim Chiaw P; Huan LJ; Gagnon S; Ly D; Sweezey N; Rotin D; Deber CM; Bear CE
    Chem Biol; 2009 May; 16(5):520-30. PubMed ID: 19477416
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Traffic-independent function of the Sar1p/COPII machinery in proteasomal sorting of the cystic fibrosis transmembrane conductance regulator.
    Fu L; Sztul E
    J Cell Biol; 2003 Jan; 160(2):157-63. PubMed ID: 12538638
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rescue of DeltaF508 and other misprocessed CFTR mutants by a novel quinazoline compound.
    Loo TW; Bartlett MC; Clarke DM
    Mol Pharm; 2005; 2(5):407-13. PubMed ID: 16196493
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Curcumin enhances cystic fibrosis transmembrane regulator expression by down-regulating calreticulin.
    Harada K; Okiyoneda T; Hashimoto Y; Oyokawa K; Nakamura K; Suico MA; Shuto T; Kai H
    Biochem Biophys Res Commun; 2007 Feb; 353(2):351-6. PubMed ID: 17178109
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.