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Journal Abstract Search

356 related items for PubMed ID: 2786533

  • 1. I-Ak polymorphisms define a functionally dominant region for the presentation of hen egg lysozyme peptides.
    Rosloniec EF, Vitez LJ, Beck BN, Buerstedde JM, McKean DJ, Landais D, Benoist C, Mathis D, Freed JH.
    J Immunol; 1989 Jul 01; 143(1):50-8. PubMed ID: 2786533
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  • 2. Functional mapping of MHC class II polymorphic residues. The alpha-chain controls the specificity for binding an Ad-versus an A k-restricted peptide and the beta-chain region 65-67 controls T cell recognition but not peptide binding.
    Lee JM, McKean DJ, Watts TH.
    J Immunol; 1991 May 01; 146(9):2952-9. PubMed ID: 1849939
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  • 3. Functional sites on the A alpha-chain. Polymorphic residues involved in antigen presentation to insulin-specific, Ab alpha:Ak beta-restricted T cells.
    Reske-Kunz AB, Landais D, Peccoud J, Benoist C, Mathis D.
    J Immunol; 1989 Sep 01; 143(5):1472-81. PubMed ID: 2474599
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  • 4. Epitopic analysis by anti-I-Ak monoclonal antibodies of I-Ak-restricted presentation of lysozyme peptides.
    Rosloniec EF, Gay D, Freed JH.
    J Immunol; 1989 Jun 15; 142(12):4176-83. PubMed ID: 2470818
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  • 6. The extracellular domains of MHC class II molecules determine their processing requirements for antigen presentation.
    Kjer-Nielsen L, Perera JD, Boyd LF, Margulies DH, McCluskey J.
    J Immunol; 1990 Apr 15; 144(8):2915-24. PubMed ID: 1969876
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  • 8. Co-dominant restriction by a mixed-haplotype I-A molecule (alpha k beta b) for the lysozyme peptide 52-61 in H-2k x H-2b F1 mice.
    Moreno J, Adorini L, Hämmerling GJ.
    J Immunol; 1990 May 01; 144(9):3296-304. PubMed ID: 1970351
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  • 9. Analysis of the interaction of peptide hen egg white lysozyme (34-45) with the I-Ak molecule.
    Lambert LE, Unanue ER.
    J Immunol; 1989 Aug 01; 143(3):802-7. PubMed ID: 2787347
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  • 11. Processing of endogenously synthesized hen egg-white lysozyme retained in the endoplasmic reticulum or in secretory form gives rise to a similar but not identical set of epitopes recognized by class II-restricted T cells.
    Adorini L, Guéry JC, Fuchs S, Ortiz-Navarrete V, Hämmerling GJ, Momburg F.
    J Immunol; 1993 Oct 01; 151(7):3576-86. PubMed ID: 7690807
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  • 15. The importance of dominant negative effects of amino acid side chain substitution in peptide-MHC molecule interactions and T cell recognition.
    Boehncke WH, Takeshita T, Pendleton CD, Houghten RA, Sadegh-Nasseri S, Racioppi L, Berzofsky JA, Germain RN.
    J Immunol; 1993 Jan 15; 150(2):331-41. PubMed ID: 8093457
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  • 16. Functional analysis of the antigen binding region of an MHC class II molecule.
    Rosloniec EF, Beard KS, Freed JH.
    Mol Immunol; 1993 Apr 15; 30(5):491-501. PubMed ID: 7681933
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  • 18. Structural analysis of the interaction of apamin with Ia and its recognition by Ad- or Ab-restricted mouse T cells.
    Regnier-Vigouroux A, Ceard B, Van Rietschoten J, Granier C, Pierres M.
    J Immunol; 1989 Nov 15; 143(10):3167-74. PubMed ID: 2478620
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  • 19. Presentation of antigens internalized through the B cell receptor requires newly synthesized MHC class II molecules.
    Forquet F, Barois N, Machy P, Trucy J, Zimmermann VS, Leserman L, Davoust J.
    J Immunol; 1999 Mar 15; 162(6):3408-16. PubMed ID: 10092796
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