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Description
The project revealed a novel mechanism by which RanBPM regulates p21 protein stability, and plays a critical role in the regulation of DDR, thereby suggesting that it might be a promising therapeutic strategy to develop small molecular compounds destroying the protein interaction between RanBPM and p21
with a shelf life of 956 days
This observed effect could be a significant mechanism in preventing the spread of hepatic cancer and systemic cancer invasion
Despite their extensive application, challenges remain in optimizing bioavailability, understanding absorption mechanisms, and exploring synergistic interactions with other food components
