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Exploring these primary pathways can provide a more comprehensive understanding of the relationship between UA and oxidative stress as well as neuroinflammation in the brain, along with the mechanism underlying the neuroprotective effects of UA in neurodegenerative diseases

10.1016/j.carbpol.2021.118866 110 GatouM.-A.VagenaI

Hepatic first-pass elimination (1 Fractional bioavailability) of Drug A is 60 % while that of Drug B is 40 %

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