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in Frontiers in Endocrinology (2018) suggests this oxidative modification process may contribute to immune recognition and the development of autoimmune thyroid disease, such as Hashimotos thyroiditis and Graves disease (13,13)

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A later study corroborated higher levels of SI in the brain after ad libitum administration to TgCRND8 mice, with reduced A 40 and A 42 brain levels and decreased plaque formation [18]

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