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339 related items for PubMed ID: 29402832

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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 23; 47(38):10084-98. PubMed ID: 18754678
    [Abstract] [Full Text] [Related]

  • 3. 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 17; 286(24):21239-53. PubMed ID: 21525008
    [Abstract] [Full Text] [Related]

  • 4. Sodium 4-phenylbutyrate downregulates Hsc70: implications for intracellular trafficking of DeltaF508-CFTR.
    Rubenstein RC, Zeitlin PL.
    Am J Physiol Cell Physiol; 2000 Feb 17; 278(2):C259-67. PubMed ID: 10666020
    [Abstract] [Full Text] [Related]

  • 5. Diffusional mobility of the cystic fibrosis transmembrane conductance regulator mutant, delta F508-CFTR, in the endoplasmic reticulum measured by photobleaching of GFP-CFTR chimeras.
    Haggie PM, Stanton BA, Verkman AS.
    J Biol Chem; 2002 May 10; 277(19):16419-25. PubMed ID: 11877404
    [Abstract] [Full Text] [Related]

  • 6. 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 01; 287(23):19158-70. PubMed ID: 22505710
    [Abstract] [Full Text] [Related]

  • 7. Knockdown of NHERF1 enhances degradation of temperature rescued DeltaF508 CFTR from the cell surface of human airway cells.
    Kwon SH, Pollard H, Guggino WB.
    Cell Physiol Biochem; 2007 Jun 01; 20(6):763-72. PubMed ID: 17982258
    [Abstract] [Full Text] [Related]

  • 8. 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 17; 127(4):803-15. PubMed ID: 17110338
    [Abstract] [Full Text] [Related]

  • 9. Targeting CAL as a negative regulator of DeltaF508-CFTR cell-surface expression: an RNA interference and structure-based mutagenetic approach.
    Wolde M, Fellows A, Cheng J, Kivenson A, Coutermarsh B, Talebian L, Karlson K, Piserchio A, Mierke DF, Stanton BA, Guggino WB, Madden DR.
    J Biol Chem; 2007 Mar 16; 282(11):8099-109. PubMed ID: 17158866
    [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 16; 22(9):3255-63. PubMed ID: 18556464
    [Abstract] [Full Text] [Related]

  • 11. Combination of Correctors Rescue ΔF508-CFTR by Reducing Its Association with Hsp40 and Hsp27.
    Lopes-Pacheco M, Boinot C, Sabirzhanova I, Morales MM, Guggino WB, Cebotaru L.
    J Biol Chem; 2015 Oct 16; 290(42):25636-45. PubMed ID: 26336106
    [Abstract] [Full Text] [Related]

  • 12. Ubiquitination and degradation of CFTR by the E3 ubiquitin ligase MARCH2 through its association with adaptor proteins CAL and STX6.
    Cheng J, Guggino W.
    PLoS One; 2013 Oct 16; 8(6):e68001. PubMed ID: 23818989
    [Abstract] [Full Text] [Related]

  • 13. 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 16; 280(18):4396-406. PubMed ID: 23773658
    [Abstract] [Full Text] [Related]

  • 14. Hsp 70/Hsp 90 organizing protein as a nitrosylation target in cystic fibrosis therapy.
    Marozkina NV, Yemen S, Borowitz M, Liu L, Plapp M, Sun F, Islam R, Erdmann-Gilmore P, Townsend RR, Lichti CF, Mantri S, Clapp PW, Randell SH, Gaston B, Zaman K.
    Proc Natl Acad Sci U S A; 2010 Jun 22; 107(25):11393-8. PubMed ID: 20534503
    [Abstract] [Full Text] [Related]

  • 15. Syntaxin 6 and CAL mediate the degradation of the cystic fibrosis transmembrane conductance regulator.
    Cheng J, Cebotaru V, Cebotaru L, Guggino WB.
    Mol Biol Cell; 2010 Apr 01; 21(7):1178-87. PubMed ID: 20130090
    [Abstract] [Full Text] [Related]

  • 16. Partial restoration of cAMP-stimulated CFTR chloride channel activity in DeltaF508 cells by deoxyspergualin.
    Jiang C, Fang SL, Xiao YF, O'Connor SP, Nadler SG, Lee DW, Jefferson DM, Kaplan JM, Smith AE, Cheng SH.
    Am J Physiol; 1998 Jul 01; 275(1):C171-8. PubMed ID: 9688848
    [Abstract] [Full Text] [Related]

  • 17. Processing and function of CFTR-DeltaF508 are species-dependent.
    Ostedgaard LS, Rogers CS, Dong Q, Randak CO, Vermeer DW, Rokhlina T, Karp PH, Welsh MJ.
    Proc Natl Acad Sci U S A; 2007 Sep 25; 104(39):15370-5. PubMed ID: 17873061
    [Abstract] [Full Text] [Related]

  • 18. 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 02; 146(5):746-60. PubMed ID: 21884936
    [Abstract] [Full Text] [Related]

  • 19. 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 02; 70(4):1435-42. PubMed ID: 16857740
    [Abstract] [Full Text] [Related]

  • 20. 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 15; 366(Pt 3):797-806. PubMed ID: 12069690
    [Abstract] [Full Text] [Related]

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