A notable trend of hypomethylation in pro-inflammatory genes (e.g., TLR-2, TLR-4, IL-1β) and hypermethylation in anti-inflammatory genes (e.g., TGF-β, FOXP3) was observed in sepsis groups compared to controls.
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Role of DNA methylation in regulating inflammatory cytokine expression in neonates with late-onset sepsis.
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