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PUBMED FOR HANDHELDS

Journal Abstract Search


116 related items for PubMed ID: 19764408

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  • 4. Mannosidase action, independent of glucose trimming, is essential for proteasome-mediated degradation of unassembled glycosylated Ig light chains.
    Chillarón J, Adán C, Haas IG.
    Biol Chem; 2000 Dec; 381(12):1155-64. PubMed ID: 11209750
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  • 7. Overexpression of Man2C1 leads to protein underglycosylation and upregulation of endoplasmic reticulum-associated degradation pathway.
    Bernon C, Carré Y, Kuokkanen E, Slomianny MC, Mir AM, Krzewinski F, Cacan R, Heikinheimo P, Morelle W, Michalski JC, Foulquier F, Duvet S.
    Glycobiology; 2011 Mar; 21(3):363-75. PubMed ID: 20978011
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  • 8. [Molecular mechanisms of protein C deficiency caused by C64W and F139V mutations].
    Zhou RF, Cai XH, Xie S, Wang WB, Dai J, Ding QL, Fang Y, Xie F, Wang XF, Wang H.
    Zhonghua Xue Ye Xue Za Zhi; 2007 Mar; 28(3):156-9. PubMed ID: 17649706
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  • 9. Defective sorting to secretory vesicles in trans-Golgi network is partly responsible for protein C deficiency: molecular mechanisms of impaired secretion of abnormal protein C R169W, R352W, and G376D.
    Naito M, Mimuro J, Endo H, Madoiwa S, Ogata K, Kikuchi J, Sugo T, Yasu T, Kariya Y, Hoshino Y, Sakata Y.
    Circ Res; 2003 May 02; 92(8):865-72. PubMed ID: 12663483
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  • 10. Mannose trimming targets mutant alpha(2)-plasmin inhibitor for degradation by the proteasome.
    Chung DH, Ohashi K, Watanabe M, Miyasaka N, Hirosawa S.
    J Biol Chem; 2000 Feb 18; 275(7):4981-7. PubMed ID: 10671537
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  • 11. Ubiquitylation-independent ER-associated degradation of an AE1 mutant associated with dominant hereditary spherocytosis in cattle.
    Ito D, Koshino I, Arashiki N, Adachi H, Tomihari M, Tamahara S, Kurogi K, Amano T, Ono K, Inaba M.
    J Cell Sci; 2006 Sep 01; 119(Pt 17):3602-12. PubMed ID: 16912075
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  • 12. Protein misfolding and degradation in genetic diseases.
    Bross P, Corydon TJ, Andresen BS, Jørgensen MM, Bolund L, Gregersen N.
    Hum Mutat; 1999 Sep 01; 14(3):186-98. PubMed ID: 10477427
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  • 13. Differential role of mannose and glucose trimming in the ER degradation of asialoglycoprotein receptor subunits.
    Ayalon-Soffer M, Shenkman M, Lederkremer GZ.
    J Cell Sci; 1999 Oct 01; 112 ( Pt 19)():3309-18. PubMed ID: 10504336
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  • 14. Stimulation of ERAD of misfolded null Hong Kong alpha1-antitrypsin by Golgi alpha1,2-mannosidases.
    Hosokawa N, You Z, Tremblay LO, Nagata K, Herscovics A.
    Biochem Biophys Res Commun; 2007 Oct 26; 362(3):626-32. PubMed ID: 17727818
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  • 15. Analysis of ER-associated glycoprotein degradation using synthetic glycopeptide probes.
    Hagihara S, Goda K, Matsuo I, Ito Y.
    Biochem Biophys Res Commun; 2007 Aug 24; 360(2):357-62. PubMed ID: 17592722
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  • 16. Distinguishing between retention signals and degrons acting in ERAD.
    Shapira I, Charuvi D, Elkabetz Y, Hirschberg K, Bar-Nun S.
    J Cell Sci; 2007 Dec 15; 120(Pt 24):4377-87. PubMed ID: 18042626
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  • 17. Missense mutations as a cause of metachromatic leukodystrophy. Degradation of arylsulfatase A in the endoplasmic reticulum.
    Poeppel P, Habetha M, Marcão A, Büssow H, Berna L, Gieselmann V.
    FEBS J; 2005 Mar 15; 272(5):1179-88. PubMed ID: 15720392
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  • 18. Role of the aggresome pathway in cancer: targeting histone deacetylase 6-dependent protein degradation.
    Rodriguez-Gonzalez A, Lin T, Ikeda AK, Simms-Waldrip T, Fu C, Sakamoto KM.
    Cancer Res; 2008 Apr 15; 68(8):2557-60. PubMed ID: 18413721
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  • 19. Inactivation of the 20S proteasome maturase, Ump1p, leads to the instability of mtDNA in Saccharomyces cerevisiae.
    Malc E, Dzierzbicki P, Kaniak A, Skoneczna A, Ciesla Z.
    Mutat Res; 2009 Oct 02; 669(1-2):95-103. PubMed ID: 19467248
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  • 20. Thrombomodulin-mediated catabolism of protein C by pleural mesothelial and vascular endothelial cells.
    Iakhiaev AV, Rezaie AR, Idell S.
    Thromb Haemost; 2007 Sep 02; 98(3):627-34. PubMed ID: 17849052
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