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Journal Abstract Search


214 related items for PubMed ID: 8871612

  • 1.
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  • 2. Antigen presentation enhanced by the alternatively spliced invariant chain gene product p41.
    Peterson M, Miller J.
    Nature; 1992 Jun 18; 357(6379):596-8. PubMed ID: 1608470
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  • 3. The p41 isoform of invariant chain is a chaperone for cathepsin L.
    Lennon-Duménil AM, Roberts RA, Valentijn K, Driessen C, Overkleeft HS, Erickson A, Peters PJ, Bikoff E, Ploegh HL, Wolf Bryant P.
    EMBO J; 2001 Aug 01; 20(15):4055-64. PubMed ID: 11483509
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  • 4. Major histocompatibility complex class II-associated p41 invariant chain fragment is a strong inhibitor of lysosomal cathepsin L.
    Bevec T, Stoka V, Pungercic G, Dolenc I, Turk V.
    J Exp Med; 1996 Apr 01; 183(4):1331-8. PubMed ID: 8666891
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  • 5. Modulation of antigen presentation and class II expression by a class II-associated invariant chain peptide.
    Zechel MA, Chaturvedi P, Lee-Chan EC, Rider BJ, Singh B.
    J Immunol; 1996 Jun 01; 156(11):4232-9. PubMed ID: 8666792
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  • 6. DM-mediated release of a naturally occurring invariant chain degradation intermediate from MHC class II molecules.
    Stebbins CC, Peterson ME, Suh WM, Sant AJ.
    J Immunol; 1996 Dec 01; 157(11):4892-8. PubMed ID: 8943393
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  • 7. Invariant chain processing is independent of cathepsin variation between primary human B cells/dendritic cells and B-lymphoblastoid cells.
    Reich M, Zou F, Sieńczyk M, Oleksyszyn J, Boehm BO, Burster T.
    Cell Immunol; 2011 Dec 01; 269(2):96-103. PubMed ID: 21543057
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  • 13. Deletion of a C-terminal sequence of the class II-associated invariant chain abrogates invariant chains oligomer formation and class II antigen presentation.
    Bertolino P, Staschewski M, Trescol-Biémont MC, Freisewinkel IM, Schenck K, Chrétien I, Forquet F, Gerlier D, Rabourdin-Combe C, Koch N.
    J Immunol; 1995 Jun 01; 154(11):5620-9. PubMed ID: 7751615
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  • 14. MHC class II antigen processing in B cells: accelerated intracellular targeting of antigens.
    Cheng PC, Steele CR, Gu L, Song W, Pierce SK.
    J Immunol; 1999 Jun 15; 162(12):7171-80. PubMed ID: 10358163
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  • 17. Identification of residues in the class II-associated Ii peptide (CLIP) region of invariant chain that affect efficiency of MHC class II-mediated antigen presentation in an allele-dependent manner.
    Gautam AM, Yang M, Milburn PJ, Baker R, Bhatnagar A, McCluskey J, Boston T.
    J Immunol; 1997 Sep 15; 159(6):2782-8. PubMed ID: 9300699
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  • 18. Asparagine endopeptidase is not essential for class II MHC antigen presentation but is required for processing of cathepsin L in mice.
    Maehr R, Hang HC, Mintern JD, Kim YM, Cuvillier A, Nishimura M, Yamada K, Shirahama-Noda K, Hara-Nishimura I, Ploegh HL.
    J Immunol; 2005 Jun 01; 174(11):7066-74. PubMed ID: 15905550
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  • 19. Proteolysis of major histocompatibility complex class II-associated invariant chain is regulated by the alternatively spliced gene product, p41.
    Fineschi B, Arneson LS, Naujokas MF, Miller J.
    Proc Natl Acad Sci U S A; 1995 Oct 24; 92(22):10257-61. PubMed ID: 7479763
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  • 20. Crystal structure of MHC class II-associated p41 Ii fragment bound to cathepsin L reveals the structural basis for differentiation between cathepsins L and S.
    Guncar G, Pungercic G, Klemencic I, Turk V, Turk D.
    EMBO J; 1999 Feb 15; 18(4):793-803. PubMed ID: 10022822
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