Effects of different antigenic microenvironments on the course of CD8^+ T cell responses in vivo
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概要
著者
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Tarazona Raquel
Division Of Molecular Immunology National Institute For Medical Research The Ridgeway
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Zhou Min
Immunogenetics Department Institute Of Molecular Medicine And Genetics Medical College Of Georgia
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Mellor Andrew
Immunogenetics Department Institute Of Molecular Medicine And Genetics Medical College Of Georgia
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TOMLINSON Peter
Division of Molecular immunology, National institute for Medical Research
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SPONAAS Anna-marit
Division of Molecular Immunology, National Institute for Medical Research, The Ridgeway
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MAVRIA Georgia
Division of Molecular Immunology, National Institute for Medical Research, The Ridgeway
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SCHULZ Ruth
Division of Molecular Immunology, National Institute for Medical Research, The Ridgeway
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ANTONIOU Jane
Division of Molecular Immunology, National Institute for Medical Research, The Ridgeway
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Schulz Ruth
Division Of Molecular Immunology National Institute For Medical Research The Ridgeway
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Antoniou Jane
Division Of Molecular Immunology National Institute For Medical Research The Ridgeway
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Mavria Georgia
Division Of Molecular Immunology National Institute For Medical Research The Ridgeway
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Sponaas Anna-marit
Division Of Molecular Immunology National Institute For Medical Research The Ridgeway
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Tomlinson Peter
Division Of Molecular Immunology National Institute For Medical Research The Ridgeway
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Tomlinson Peter
Division Of Molecular Immunology National Institute For Medical Research
関連論文
- In vitro positive selection of αβ TCR transgenic thymocytes by a conditionally immortalized cortical epithelial clone
- Unprimed T cells are inefficiently stimulated by glycosylphosphatidylinositol-linked H-2K^b because of its lipid anchor rather than defects in CD8 binding
- Effects of different antigenic microenvironments on the course of CD8^+ T cell responses in vivo
- HLA-G functions as a restriction element and a transplantation antigen in mice
- A minor population of splenic dendritic cells expressing CD19 mediates IDO-dependent T cell suppression via type I IFN signaling following B7 ligation