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Further investigations are required to understand fully the dynamics of AAT oxidation, and the mechanism of action of oxidized AAT

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Following peripheral administration, exenatide has been shown to suppress food intake via vagal-dependent and vagal-independent pathways that result in the direct activation of GLP-1R in the central nervous system

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Table 3 highlights the predominance of new-onset GD cases, female susceptibility, and a strong association with mRNA vaccines (Pfizer-BioNTech)