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Gene expression changes in multiple sclerosis relapse suggest activation of T and non-T cells.
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MicroRNAs miR-17 and miR-20a inhibit T cell activation genes and are under-expressed in MS whole blood.
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T lymphocyte activation gene identification by coregulated expression on DNA microarrays.
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Macrophages of multiple sclerosis patients display deficient SHP-1 expression and enhanced inflammatory phenotype.
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Glatiramer acetate increases IL-1 receptor antagonist but decreases T cell-induced IL-1beta in human monocytes and multiple sclerosis.
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Abrogation of T cell quiescence characterizes patients at high risk for multiple sclerosis after the initial neurological event.
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