Works matching DE "CD8 antigen"
Results: 2039
Kinetics of peripheral blood lymphocyte subpopulations predicts the occurrence of opportunistic infection after kidney transplantation.
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- Transplant International, 2014, v. 27, n. 7, p. 674, doi. 10.1111/tri.12321
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The effect of rabbit antithymocyte globulin on human mesenchymal stem cells.
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- Transplant International, 2013, v. 26, n. 6, p. 651, doi. 10.1111/tri.12109
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P-glycoprotein regulates trafficking of CD8 T cells to the brain parenchyma.
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- Acta Neuropathologica, 2014, v. 127, n. 5, p. 699, doi. 10.1007/s00401-014-1244-8
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Overcoming CD8+ T-Cell Exhaustion in Viral Hepatitis: Lessons from the Mouse Model and Clinical Perspectives.
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- Digestive Diseases, 2017, v. 35, n. 4, p. 334, doi. 10.1159/000456584
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Immune surveillance by CD8αα<sup>+</sup> skin-resident T cells in human herpes virus infection.
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- Nature, 2013, v. 497, n. 7450, p. 494, doi. 10.1038/nature12110
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Vaccine-induced CD8<sup>+</sup> T cells control AIDS virus replication.
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- Nature, 2012, v. 491, n. 7422, p. 129, doi. 10.1038/nature11443
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Multiplexed Immunohistochemistry Reveals Cancer-Reactive Germinal Centers are Enriched with CD8<sup>+</sup> and T<sub>fh</sub> Cells.
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- International Journal of High School Research, 2023, v. 5, n. 4, p. 1, doi. 10.36838/v5i4.1
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Research on the Influence of Exercise on the Immune Function of Middle-aged and Old People.
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- International Journal of Social Science, Innovation, & Educational Technologies, 2021, n. 15, p. 73
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CD8 T Cells Target Antigen Cross-Presented by Bone Marrow Derived Cells to Induce Bystander Rejection of Grafts Lacking the Cognate Peptide-MHC.
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- Cell Transplantation, 2022, v. 31, p. 1, doi. 10.1177/09636897221136149
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K33-linked polyubiquitination of Zap70 by Nrdp1 controls CD8<sup>+</sup> T cell activation.
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- Nature Immunology, 2015, v. 16, n. 12, p. 1253, doi. 10.1038/ni.3258
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Reply to: "CD8<sup>+</sup> T cell diversification by asymmetric cell division".
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- Nature Immunology, 2015, v. 16, n. 9, p. 893, doi. 10.1038/ni.3234
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CD8<sup>+</sup> T cell diversification by asymmetric cell division.
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- Nature Immunology, 2015, v. 16, n. 9, p. 891, doi. 10.1038/ni.3235
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The ubiquitin-specific protease USP8 is critical for the development and homeostasis of T cells.
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- Nature Immunology, 2015, v. 16, n. 9, p. 950, doi. 10.1038/ni.3230
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Batf3 maintains autoactivation of Irf8 for commitment of a CD8α<sup>+</sup> conventional DC clonogenic progenitor.
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- Nature Immunology, 2015, v. 16, n. 7, p. 708, doi. 10.1038/ni.3197
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DNA methylation secures CD4<sup>+</sup> and CD8<sup>+</sup> T cell lineage borders.
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- Nature Immunology, 2015, v. 16, n. 7, p. 681, doi. 10.1038/ni.3207
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Eosinophils orchestrate cancer rejection by normalizing tumor vessels and enhancing infiltration of CD8<sup>+</sup> T cells.
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- Nature Immunology, 2015, v. 16, n. 6, p. 609, doi. 10.1038/ni.3159
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A formidable challenge.
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- Nature Immunology, 2015, v. 16, n. 6, p. 545, doi. 10.1038/ni.3179
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Tissue-specific surveillance.
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- Nature Immunology, 2015, v. 16, n. 6, p. 598, doi. 10.1038/ni.3190
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Proinflammatory microenvironments within the intestine regulate the differentiation of tissue-resident CD8<sup>+</sup> T cells responding to infection.
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- Nature Immunology, 2015, v. 16, n. 4, p. 406, doi. 10.1038/ni.3108
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Thymic IL-7 signaling goes beyond survival.
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- Nature Immunology, 2015, v. 16, n. 4, p. 337, doi. 10.1038/ni.3128
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IL-7 coordinates proliferation, differentiation and Tcra recombination during thymocyte β-selection.
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- Nature Immunology, 2015, v. 16, n. 4, p. 397, doi. 10.1038/ni.3122
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Skin DCs cluster for efficient T cell activation.
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- Nature Immunology, 2014, v. 15, n. 11, p. 1004, doi. 10.1038/ni.3012
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Corrigendum: The transcription factor IRF4 is essential for TCR affinity-mediated metabolic programming and clonal expansion of T cells.
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- Nature Immunology, 2014, v. 15, n. 9, p. 894, doi. 10.1038/ni0914-894b
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c-Myc and AP4: a relay team for metabolic reprogramming of CD8<sup>+</sup> T cells.
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- Nature Immunology, 2014, v. 15, n. 9, p. 828, doi. 10.1038/ni.2962
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c-Myc-induced transcription factor AP4 is required for host protection mediated by CD8<sup>+</sup> T cells.
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- Nature Immunology, 2014, v. 15, n. 9, p. 884, doi. 10.1038/ni.2943
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IL-23 in negative selection.
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- Nature Immunology, 2014, v. 15, n. 9, p. 824, doi. 10.1038/ni.2971
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CD4<sup>+</sup> T cell lineage integrity is controlled by the histone deacetylases HDAC1 and HDAC2.
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- Nature Immunology, 2014, v. 15, n. 5, p. 439, doi. 10.1038/ni.2864
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DC division of labor.
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- Nature Immunology, 2014, v. 15, n. 5, p. 414, doi. 10.1038/ni.2880
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Early specification of CD8<sup>+</sup> T lymphocyte fates during adaptive immunity revealed by single-cell gene-expression analyses.
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- Nature Immunology, 2014, v. 15, n. 4, p. 365, doi. 10.1038/ni.2842
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The unfolded-protein-response sensor IRE-1α regulates the function of CD8α<sup>+</sup> dendritic cells.
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- Nature Immunology, 2014, v. 15, n. 3, p. 248, doi. 10.1038/ni.2808
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Virus-induced autophagy.
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- Nature Immunology, 2014, v. 15, n. 2, p. 142, doi. 10.1038/ni.2817
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A HESitant decision for T cells.
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- Nature Immunology, 2013, v. 14, n. 12, p. 1209, doi. 10.1038/ni.2765
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Transcriptional downregulation of S1pr1 is required for the establishment of resident memory CD8<sup>+</sup> T cells.
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- Nature Immunology, 2013, v. 14, n. 12, p. 1285, doi. 10.1038/ni.2745
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The developmental pathway for CD103<sup>+</sup>CD8<sup>+</sup> tissue-resident memory T cells of skin.
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- Nature Immunology, 2013, v. 14, n. 12, p. 1294, doi. 10.1038/ni.2744
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Hypoxia-inducible factors enhance the effector responses of CD8<sup>+</sup> T cells to persistent antigen.
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- Nature Immunology, 2013, v. 14, n. 11, p. 1173, doi. 10.1038/ni.2714
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Bypassing T cell 'exhaustion'.
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- Nature Immunology, 2013, v. 14, n. 11, p. 1114, doi. 10.1038/ni.2742
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The transcription factor IRF4 is essential for TCR affinity-mediated metabolic programming and clonal expansion of T cells.
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- Nature Immunology, 2013, v. 14, n. 11, p. 1155, doi. 10.1038/ni.2710
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Holding a latent virus at bay.
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- Nature Immunology, 2013, v. 14, n. 10, p. 1023, doi. 10.1038/ni.2721
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Rapid effector function of memory CD8<sup>+</sup> T cells requires an immediate-early glycolytic switch.
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- Nature Immunology, 2013, v. 14, n. 10, p. 1064, doi. 10.1038/ni.2687
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Innate and adaptive immune cells in the tumor microenvironment.
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- Nature Immunology, 2013, v. 14, n. 10, p. 1014, doi. 10.1038/ni.2703
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Sensing and alarm function of resident memory CD8<sup>+</sup> T cells.
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- Nature Immunology, 2013, v. 14, n. 8, p. 876, doi. 10.1038/ni0813-876c
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Killer T cells find meaningful encounters through iMATEs.
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- Nature Immunology, 2013, v. 14, n. 6, p. 533, doi. 10.1038/ni.2620
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Agonist selection.
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- Nature Immunology, 2013, v. 14, n. 6, p. 535, doi. 10.1038/ni.2626
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T cells maintain an exhausted phenotype after antigen withdrawal and population reexpansion.
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- Nature Immunology, 2013, v. 14, n. 6, p. 603, doi. 10.1038/ni.2606
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The microRNA miR-155 controls CD8<sup>+</sup> T cell responses by regulating interferon signaling.
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- Nature Immunology, 2013, v. 14, n. 6, p. 593, doi. 10.1038/ni.2576
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T cell exhaustion: a means or an end?
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- Nature Immunology, 2013, v. 14, n. 6, p. 531, doi. 10.1038/ni.2619
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Intrahepatic myeloid-cell aggregates enable local proliferation of CD8<sup>+</sup> T cells and successful immunotherapy against chronic viral liver infection.
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- Nature Immunology, 2013, v. 14, n. 6, p. 574, doi. 10.1038/ni.2573
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Sensing and alarm function of resident memory CD8<sup>+</sup> T cells.
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- Nature Immunology, 2013, v. 14, n. 5, p. 509, doi. 10.1038/ni.2568
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Sterol regulatory element-binding proteins are essential for the metabolic programming of effector T cells and adaptive immunity.
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- Nature Immunology, 2013, v. 14, n. 5, p. 489, doi. 10.1038/ni.2570
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Transcriptional insights into the CD8<sup>+</sup> T cell response to infection and memory T cell formation.
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- Nature Immunology, 2013, v. 14, n. 4, p. 404, doi. 10.1038/ni.2536
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