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Journal Abstract Search

171 related items for PubMed ID: 23555857

  • 1. Insulin-like growth factor 1 (IGF-1) enhances the protein expression of CFTR.
    Lee HW, Cheng J, Kovbasnjuk O, Donowitz M, Guggino WB.
    PLoS One; 2013; 8(3):e59992. PubMed ID: 23555857
    [Abstract] [Full Text] [Related]

  • 2. Regulation of cystic fibrosis transmembrane regulator trafficking and protein expression by a Rho family small GTPase TC10.
    Cheng J, Wang H, Guggino WB.
    J Biol Chem; 2005 Feb 04; 280(5):3731-9. PubMed ID: 15546864
    [Abstract] [Full Text] [Related]

  • 3. 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 Feb 04; 8(6):e68001. PubMed ID: 23818989
    [Abstract] [Full Text] [Related]

  • 4. Failure of cAMP agonists to activate rescued deltaF508 CFTR in CFBE41o- airway epithelial monolayers.
    Bebok Z, Collawn JF, Wakefield J, Parker W, Li Y, Varga K, Sorscher EJ, Clancy JP.
    J Physiol; 2005 Dec 01; 569(Pt 2):601-15. PubMed ID: 16210354
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. A Golgi-associated PDZ domain protein modulates cystic fibrosis transmembrane regulator plasma membrane expression.
    Cheng J, Moyer BD, Milewski M, Loffing J, Ikeda M, Mickle JE, Cutting GR, Li M, Stanton BA, Guggino WB.
    J Biol Chem; 2002 Feb 01; 277(5):3520-9. PubMed ID: 11707463
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Low temperature and chemical rescue affect molecular proximity of DeltaF508-cystic fibrosis transmembrane conductance regulator (CFTR) and epithelial sodium channel (ENaC).
    Qadri YJ, Cormet-Boyaka E, Rooj AK, Lee W, Parpura V, Fuller CM, Berdiev BK.
    J Biol Chem; 2012 May 11; 287(20):16781-90. PubMed ID: 22442149
    [Abstract] [Full Text] [Related]

  • 9. 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 May 11; 45(2):639-655. PubMed ID: 29402832
    [Abstract] [Full Text] [Related]

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  • 11. 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 11; 280(18):4396-406. PubMed ID: 23773658
    [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 11; 1782(10):605-14. PubMed ID: 18773956
    [Abstract] [Full Text] [Related]

  • 13. Modulation of mature cystic fibrosis transmembrane regulator protein by the PDZ domain protein CAL.
    Cheng J, Wang H, Guggino WB.
    J Biol Chem; 2004 Jan 16; 279(3):1892-8. PubMed ID: 14570915
    [Abstract] [Full Text] [Related]

  • 14. Enhanced cell-surface stability of rescued DeltaF508 cystic fibrosis transmembrane conductance regulator (CFTR) by pharmacological chaperones.
    Varga K, Goldstein RF, Jurkuvenaite A, Chen L, Matalon S, Sorscher EJ, Bebok Z, Collawn JF.
    Biochem J; 2008 Mar 15; 410(3):555-64. PubMed ID: 18052931
    [Abstract] [Full Text] [Related]

  • 15. Targeting autophagy as a novel strategy for facilitating the therapeutic action of potentiators on ΔF508 cystic fibrosis transmembrane conductance regulator.
    Luciani A, Villella VR, Esposito S, Gavina M, Russo I, Silano M, Guido S, Pettoello-Mantovani M, Carnuccio R, Scholte B, De Matteis A, Maiuri MC, Raia V, Luini A, Kroemer G, Maiuri L.
    Autophagy; 2012 Nov 15; 8(11):1657-72. PubMed ID: 22874563
    [Abstract] [Full Text] [Related]

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  • 17. 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]

  • 18. DeltaF508 CFTR processing correction and activity in polarized airway and non-airway cell monolayers.
    Rowe SM, Pyle LC, Jurkevante A, Varga K, Collawn J, Sloane PA, Woodworth B, Mazur M, Fulton J, Fan L, Li Y, Fortenberry J, Sorscher EJ, Clancy JP.
    Pulm Pharmacol Ther; 2010 Aug 17; 23(4):268-78. PubMed ID: 20226262
    [Abstract] [Full Text] [Related]

  • 19. Activation of 3-phosphoinositide-dependent kinase 1 (PDK1) and serum- and glucocorticoid-induced protein kinase 1 (SGK1) by short-chain sphingolipid C4-ceramide rescues the trafficking defect of ΔF508-cystic fibrosis transmembrane conductance regulator (ΔF508-CFTR).
    Caohuy H, Yang Q, Eudy Y, Ha TA, Xu AE, Glover M, Frizzell RA, Jozwik C, Pollard HB.
    J Biol Chem; 2014 Dec 26; 289(52):35953-68. PubMed ID: 25384981
    [Abstract] [Full Text] [Related]

  • 20. 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]

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