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Dissection of the B10.D2 anti-H-2Kb cytolytic T lymphocyte receptor repertoire.
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Clonal analysis of H-2Kb + TNP recognition by T cells with the use of H-2Kbm mutants and H-2Kb-specific monoclonal antibodies.
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Influence of the major histocompatibility complex on the repertoire of allospecific cytolytic T lymphocytes.
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Interactions between MHC-encoded products and cloned T-cells. I. Fine specificity of induction of proliferation and lysis.
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Restriction fine specificity of long-term, hapten-specific cytotoxic T cell clones: analysis with H-2Kbm-mutant mice and H-2Kb-specific monoclonal antibodies.
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Antigen and MHC restriction specificity of two types of cloned male-specific T cell lines.
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Genetic linkage of the cytolytic T lymphocyte repertoire and immunoglobulin heavy chain genes.
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Alloimmune T cells in transplantation.
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A New Window into the Human Alloresponse.
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Conformational differences in major histocompatibility complex-peptide complexes can result in alloreactivity.
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The peptide p2Ca is immunodominant in allorecognition of Ld by beta chain variable region V beta 8+ but not V beta 8- strains.
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An alloresponse in humans is dominated by cytotoxic T lymphocytes (CTL) cross-reactive with a single Epstein-Barr virus CTL epitope: implications for graft-versus-host disease.
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Natural H-2-specific antibodies in sera of aged mice.
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Capacity of influenza virus-monoclonal antibody mixtures to stimulate memory and cytotoxic T lymphocyte populations.
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Recognition of polymorphic H-2 domains by T lymphocytes. I. Functional role of different H-2 domains for the generation of alloreactive cytotoxic T lymphocytes and determination of precursor frequencies.
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Biochemical studies on the H-2K mutant B6.C-H-2bm10.
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