“…Specific examples included: in MS (e.g., T‐helper cell differentiation, role of macrophages, fibroblasts, and endothelial cells in RA, B cell receptor signaling, dendritic cell maturation, PI3K signaling in B lymphocytes, CD40 signaling; PKC θ signaling in T lymphocytes, NF‐ κ B activation by viruses); in PD (e.g., dendritic cell maturation – shared with MS, graft‐versus‐host disease signaling, altered T cell and B cell signaling in rheumatoid arthritis); in AD (IL‐8 signaling, IL‐12 signaling and production in macrophages, Fc epsilon RI signaling, Fc γ receptor‐mediated phagocytosis in macrophages and monocytes, role of pattern recognition receptors in recognition of bacteria and viruses, natural killer cell signaling); and in ALS (e.g., NF‐ κ B signaling). The value of the IPA method was also demonstrated in providing significant signals for other pathways previously implicated in the pathogenesis of AD, including CREB signaling in neurons,41 neuregulin signaling, and ErbB signaling 42. For the IPA diseases/biological functions analysis, various cancers came up as most strongly significant for all the disorders.…”