A survey of pathogenic involvement in non-communicable human diseases.

Commun Med (Lond) · 2025 · PMC12181406 · PMID 40542146

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highly significantno p-value reported

Similar to the EBV-SLE results, we again observe highly significant overlap between CMV-altered genes and UC risk loci and insignificant overlap for expressed but unchanged genes (Fig. 5d , purple and gray bars, respectively; Supplementary Data 10 ) in two different cell types (monocytes and dendritic cells).

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