Additional highly significant pathways included “graft-versus-host disease” ( q < 2.10E−15), “antigen processing and presentation” ( q < 2.10E−15), “type I diabetes mellitus” ( q < 2.90E−15), “autoimmune thyroid disease” ( q < 4.75E−14), “viral myocarditis” ( q < 9.44E−14), “phagosome” ( q < 1.27E−10), and “cell adhesion molecules” ( q < 3.37E−09).
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Precision Subtypes of T Cell-Mediated Rejection Identified by Molecular Profiles.
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