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Simultaneously, the PRMT6/USP7 complex recruits the E3 ubiquitin ligase RNF168 to sites of DNA damage, promoting H2AX monoubiquitination and robust activation of both homologous recombination (HR) and non-homologous end-joining (NHEJ) repair pathways, thereby enhancing DNA damage tolerance

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This co-administration enhances efficiency, reduces injection frequency, and maximizes the pulse and sustain GH release pattern