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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]