Most other immune subsets, such as MAIT cells, effector memory T cells, and macrophages, showed distributional shifts that failed to reach statistical significance after FDR correction.
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<i>BCL6</i>, <i>DUSP3</i>, and <i>IL6R</i> Are Identified as Shared Druggable Immune-Regulatory Axis in Atrial Fibrillation and Atherosclerosis Through Integrative In Silico and In Vitro Analysis.
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