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274 Prion diseases are caused by accumulation of a pathological prion, known as Prion PrP Sc , which are misfolded polypepetides converted form physiologically significant cell-surface glycoprotein PrP C encoded by the PRNP gene

These alterations likely resulted from inflammatory responses and direct cellular damage which resulted in the barrier disruption of the fish intestine (Liu et al

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Current guidelines recommend using the RRR--tocopherol form of vitamin E for MASH treatment, given its antioxidant, anti-inflammatory, and anti-apoptotic properties

Increased prevalence and mortality in undiagnosed celiac disease