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Murine studies regarding the variation of oxidative status in serum, hepatic and brain samples, after administration of some CNS active drugs
reported that the mucosal adherence of bacteriophages increases their in vivo protective efficacy, thereby shielding the murine gut from E
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They do not define a safe PEG-MGF dose, prove therapeutic efficacy, or establish long-term safety in humans [11] [12]
These were accompanied by reductions in signs of oxidative stress
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