Abstract

Human keratinocytes were exposed to continuous wave 900 MHz RF field for 60 minutes. High-throughput RNA sequencing was used to examine global changes in gene expression and differentially expressed genes (DEGs) were defined as having adjusted p value ≤ 0.05 and absolute fold change ≥ 1.3. We used gene enrichment analysis and functional annotation clustering via DAVID Bioinformatics Resources to analyze pathways and gene sets enriched in DEGs. Numerous gene sets related to keratinocyte differentiation and development were enriched in the RF exposed cells.

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