scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1600-065X.2011.01057.X |
P953 | full work available online at | https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1600-065X.2011.01057.x |
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1600-065X.2011.01057.x | ||
P698 | PubMed publication ID | 22017436 |
P50 | author | David R Withers | Q38546237 |
Vasileios Bekiaris | Q56643594 | ||
Graham Anderson | Q56643596 | ||
P2093 | author name string | MiYeon Kim | |
Peter J. L. Lane | |||
Fabrina M. Gaspal | |||
Fiona M. McConnell | |||
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OX40 promotes Bcl-xL and Bcl-2 expression and is essential for long-term survival of CD4 T cells | Q28188488 | ||
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OX40-deficient mice are defective in Th cell proliferation but are competent in generating B cell and CTL Responses after virus infection | Q40907799 | ||
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CD30 is required for CCL21 expression and CD4 T cell recruitment in the absence of lymphotoxin signals | Q51738223 | ||
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Dendritic cells and monocyte/macrophages that create the IL-6/APRIL-rich lymph node microenvironments where plasmablasts mature. | Q51833354 | ||
Early diversification of the TNF superfamily in teleosts: genomic characterization and expression analysis | Q51984110 | ||
The zebrafish retinoid-related orphan receptor (ror) gene family | Q51991174 | ||
Mice deficient in OX40 and CD30 signals lack memory antibody responses because of deficient CD4 T cell memory. | Q51993471 | ||
CD4(+)CD3(-) accessory cells costimulate primed CD4 T cells through OX40 and CD30 at sites where T cells collaborate with B cells | Q52007792 | ||
Neonatal and adult CD4+ CD3- cells share similar gene expression profile, and neonatal cells up-regulate OX40 ligand in response to TL1A (TNFSF15). | Q52009391 | ||
Lymphotoxin-alpha-dependent spleen microenvironment supports the generation of memory B cells and is required for their subsequent antigen-induced activation | Q52028873 | ||
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Memory B cells from human tonsils colonize mucosal epithelium and directly present antigen to T cells by rapid up-regulation of B7-1 and B7-2. | Q52054113 | ||
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Restoration of lymphoid organ integrity through the interaction of lymphoid tissue-inducer cells with stroma of the T cell zone | Q52586488 | ||
The cytokine RANKL produced by positively selected thymocytes fosters medullary thymic epithelial cells that express autoimmune regulator | Q53453365 | ||
Functional dichotomy between OX40 and 4-1BB in modulating effector CD8 T cell responses | Q53588594 | ||
Heterogeneity of lymphoid tissue inducer cell populations present in embryonic and adult mouse lymphoid tissues. | Q54652657 | ||
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Isolated lymphoid follicle formation is inducible and dependent upon lymphotoxin-sufficient B lymphocytes, lymphotoxin beta receptor, and TNF receptor I function | Q73419615 | ||
Developing Lymph Nodes Collect CD4 + CD3 − LTβ + Cells That Can Differentiate to APC, NK Cells, and Follicular Cells but Not T or B Cells | Q73838320 | ||
Regulatory T cells mediate maternal tolerance to the fetus | Q75394803 | ||
OX40 ligand and CD30 ligand are expressed on adult but not neonatal CD4+CD3- inducer cells: evidence that IL-7 signals regulate CD30 ligand but not OX40 ligand expression | Q81767161 | ||
NK cells protect secondary lymphoid tissue from cytomegalovirus via a CD30-dependent mechanism | Q84514962 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | innate immune response | Q428253 |
P304 | page(s) | 134-148 | |
P577 | publication date | 2011-11-01 | |
P1433 | published in | Immunological Reviews | Q15724582 |
P1476 | title | OX40 and CD30 signals in CD4(+) T-cell effector and memory function: a distinct role for lymphoid tissue inducer cells in maintaining CD4(+) T-cell memory but not effector function | |
OX40 and CD30 signals in CD4+ T‐cell effector and memory function: a distinct role for lymphoid tissue inducer cells in maintaining CD4+ T‐cell memory but not effector function | |||
P478 | volume | 244 |
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Q38379448 | Potential role of effector memory T cells in chronic T cell-mediated kidney graft rejection. |
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