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Journal Abstract Search

195 related items for PubMed ID: 17272822

  • 1. VCP/p97 AAA-ATPase does not interact with the endogenous wild-type cystic fibrosis transmembrane conductance regulator.
    Goldstein RF, Niraj A, Sanderson TP, Wilson LS, Rab A, Kim H, Bebok Z, Collawn JF.
    Am J Respir Cell Mol Biol; 2007 Jun; 36(6):706-14. PubMed ID: 17272822
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  • 2. Selective inhibition of endoplasmic reticulum-associated degradation rescues DeltaF508-cystic fibrosis transmembrane regulator and suppresses interleukin-8 levels: therapeutic implications.
    Vij N, Fang S, Zeitlin PL.
    J Biol Chem; 2006 Jun 23; 281(25):17369-17378. PubMed ID: 16621797
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  • 3. 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
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  • 4. Functional cystic fibrosis transmembrane conductance regulator tagged with an epitope of the vesicular stomatis virus glycoprotein can be addressed to the apical domain of polarized cells.
    Costa de Beauregard MA, Edelman A, Chesnoy-Marchais D, Tondelier D, Lapillonne A, El Marjou F, Robine S, Louvard D.
    Eur J Cell Biol; 2000 Nov 10; 79(11):795-802. PubMed ID: 11139142
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  • 8. UBXD1 is a VCP-interacting protein that is involved in ER-associated degradation.
    Nagahama M, Ohnishi M, Kawate Y, Matsui T, Miyake H, Yuasa K, Tani K, Tagaya M, Tsuji A.
    Biochem Biophys Res Commun; 2009 May 01; 382(2):303-8. PubMed ID: 19275885
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  • 11. A small molecule that binds to an ATPase domain of Hsc70 promotes membrane trafficking of mutant cystic fibrosis transmembrane conductance regulator.
    Cho HJ, Gee HY, Baek KH, Ko SK, Park JM, Lee H, Kim ND, Lee MG, Shin I.
    J Am Chem Soc; 2011 Dec 21; 133(50):20267-76. PubMed ID: 22074182
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  • 13. Activation of the unfolded protein response by deltaF508 CFTR.
    Bartoszewski R, Rab A, Jurkuvenaite A, Mazur M, Wakefield J, Collawn JF, Bebok Z.
    Am J Respir Cell Mol Biol; 2008 Oct 21; 39(4):448-57. PubMed ID: 18458236
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  • 15. ATPase activity of p97/valosin-containing protein is regulated by oxidative modification of the evolutionally conserved cysteine 522 residue in Walker A motif.
    Noguchi M, Takata T, Kimura Y, Manno A, Murakami K, Koike M, Ohizumi H, Hori S, Kakizuka A.
    J Biol Chem; 2005 Dec 16; 280(50):41332-41. PubMed ID: 16234241
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  • 17. 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
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  • 19. 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
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  • 20. AAA ATPase p97/valosin-containing protein interacts with gp78, a ubiquitin ligase for endoplasmic reticulum-associated degradation.
    Zhong X, Shen Y, Ballar P, Apostolou A, Agami R, Fang S.
    J Biol Chem; 2004 Oct 29; 279(44):45676-84. PubMed ID: 15331598
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