Critical role of CD81 in cognate T-B cell interactions leading to T_h2 responses
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概要
- 論文の詳細を見る
- 2002-05-01
著者
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Umetsu D
Stanford Univ. Ca Usa
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Freeman G
Harvard Medical School Ma Usa
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Levy Shoshana
Division Of Oncology Department Of Medicine Stanford University School Of Medicine
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DENG Jun
Division of Oncology, Department of Medicine, Stanford University Medical Center
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DEKRUYFF Rosemarie
Division of Immunology and Transplantation Biology, Department of Pediatrics, Stanford University Me
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FREEMAN Gordon
Department of Adult Oncology, Dana-Farber Cancer Institute
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UMETSU Dale
Division of Immunology and Transplantation Biology, Department of Pediatrics, Stanford University Me
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Umetsu Dale
Division Of Immunology & Transplantation Biology Department Of Pediatrics Stanford University
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Freeman Gordon
Department Of Adult Oncology Dana-farber Cancer Institute
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Levy Shoshana
Division Of Oncology Department Of Medicine Stanford University Medical Center
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Dekruyff R
Stanford Univ. Ca Usa
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Dekruyff Rosemarie
Division Of Immunology & Transplantation Biology Department Of Pediatrics Stanford University
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Deng Jun
Division Of Oncology Department Of Medicine Stanford University Medical Center
関連論文
- Critical role of CD81 in cognate T-B cell interactions leading to T_h2 responses
- Enhanced B cell activation in the absence of CD81
- Changes in the strength of co-stimulation through the B7/CD28 pathway alter functional T cell responses to altered peptide ligands
- Differential production of IL-12 in BALB/c and DBA/2 mice controls IL-4 versus IFN-γ synthesis in primed CD4 lymphocytes
- Critical role of B cells in the development of T cell tolerance to aeroallergens