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Although its precise mechanisms remain incompletely characterized, BPC157 displays exceptional pharmacodynamic potency at nanomolar doses and remarkable biostabilityresisting hydrolysis, enzymatic degradation, and gastric fluid while maintaining activity at room temperature

Postmortem and magnetic resonance imaging (MRI) studies of progressive MS have revealed chronic active plaques with iron-laden microglia at the edges that are more destructive, expand over time, and are characterized by a ferroptosis signature [252,253,254]

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In summary, straightforward and efficient direct modification of the AON was achieved with 50 equiv