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The compound's design as a competitive inhibitor fused with HIV-TAT for cellular uptake represents advanced peptide engineering that enables intracellular delivery and specific protein-protein interaction disruption, providing researchers with tools for studying senescence mechanisms that were previously inaccessible

Details of the reaction conditions, CpG sites assayed, and target site primers (Supplementary Table S3) are included in the supplementary methods

Diabetol Int 8(2):218227

The treatment usually starts at a lower dose (2.5 mg) to allow the body to adjust

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