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118 related items for PubMed ID: 15583735
1. Gradually glycosylated protein C mutants (Arg178Gln and Cys331Arg) are degraded by proteasome after mannose trimming. Nakahara M, Koyama T, Nakazawa F, Nishio M, Shibamiya A, Hirosawa S. Thromb Haemost; 2004 Dec; 92(6):1284-90. PubMed ID: 15583735 [Abstract] [Full Text] [Related]
2. [Proteasome degradation of protein C and plasmin inhibitor mutants: molecular mechanism of congenital protein deficiency]. Nishio M, Koyama T, Hirosawa S. Rinsho Byori; 2009 Aug; 57(8):737-45. PubMed ID: 19764408 [Abstract] [Full Text] [Related]
3. Proteasome degradation of protein C and plasmin inhibitor mutants. Nishio M, Koyama T, Nakahara M, Egawa N, Hirosawa S. Thromb Haemost; 2008 Sep; 100(3):405-12. PubMed ID: 18766255 [Abstract] [Full Text] [Related]
4. Degradation of trafficking-defective long QT syndrome type II mutant channels by the ubiquitin-proteasome pathway. Gong Q, Keeney DR, Molinari M, Zhou Z. J Biol Chem; 2005 May 13; 280(19):19419-25. PubMed ID: 15760896 [Abstract] [Full Text] [Related]
5. N-glycosylation is crucial for folding, trafficking, and stability of human tripeptidyl-peptidase I. Wujek P, Kida E, Walus M, Wisniewski KE, Golabek AA. J Biol Chem; 2004 Mar 26; 279(13):12827-39. PubMed ID: 14702339 [Abstract] [Full Text] [Related]
6. 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 [Abstract] [Full Text] [Related]
7. N-glycan structure of a short-lived variant of ribophorin I expressed in the MadIA214 glycosylation-defective cell line reveals the role of a mannosidase that is not ER mannosidase I in the process of glycoprotein degradation. Ermonval M, Kitzmüller C, Mir AM, Cacan R, Ivessa NE. Glycobiology; 2001 Jul 18; 11(7):565-76. PubMed ID: 11447136 [Abstract] [Full Text] [Related]
8. 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 18; 381(12):1155-64. PubMed ID: 11209750 [Abstract] [Full Text] [Related]
9. 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 18; 112 ( Pt 19)():3309-18. PubMed ID: 10504336 [Abstract] [Full Text] [Related]
10. Characterization of endoplasmic reticulum-associated degradation of a protein S mutant identified in a family of quantitative protein S deficiency. Tsuda H, Tokunaga F, Nagamitsu H, Koide T. Thromb Res; 2006 Oct 18; 117(3):323-31. PubMed ID: 15893367 [Abstract] [Full Text] [Related]
11. 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 18; 21(3):363-75. PubMed ID: 20978011 [Abstract] [Full Text] [Related]
12. In vitro mannose trimming property of human ER α-1,2 mannosidase I. Aikawa J, Matsuo I, Ito Y. Glycoconj J; 2012 Jan 18; 29(1):35-45. PubMed ID: 22160784 [Abstract] [Full Text] [Related]
14. Discrimination between lumenal and cytosolic sites of deglycosylation in endoplasmic reticulum-associated degradation of glycoproteins by using benzyl mannose in CHO cell lines. Duvet S, Foulquier F, Mir AM, Chirat F, Cacan R. Glycobiology; 2004 Sep 05; 14(9):841-9. PubMed ID: 15175254 [Abstract] [Full Text] [Related]
15. DPM1, the catalytic subunit of dolichol-phosphate mannose synthase, is tethered to and stabilized on the endoplasmic reticulum membrane by DPM3. Ashida H, Maeda Y, Kinoshita T. J Biol Chem; 2006 Jan 13; 281(2):896-904. PubMed ID: 16280320 [Abstract] [Full Text] [Related]
17. Processing of N-linked glycans during endoplasmic-reticulum-associated degradation of a short-lived variant of ribophorin I. Kitzmüller C, Caprini A, Moore SE, Frénoy JP, Schwaiger E, Kellermann O, Ivessa NE, Ermonval M. Biochem J; 2003 Dec 15; 376(Pt 3):687-96. PubMed ID: 12952521 [Abstract] [Full Text] [Related]
20. 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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]