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CO has been described to suppress the secretion of IL-2, a cytokine required for T-cell entry into the cell cycle (76) and CO-mediated inhibition of CD3-activated T cell proliferation is highly dependent on caspase-3 and -8, which are regulated by p21 Cip1 (77)

Previous in vitro studies showed that DUX4- induced pathology requires both intact homeodomains and a transcription-activating domain (TAD) in the C-terminal region of the protein
