All considered, these data strongly suggest that SAMe depletion contributes to multiple pathophysiological processes observed in the AD brain, including the unsilencing of genes involved in AD development and progression, the depletion of acetylcholine, and the inability to appropriately dephosphorylate tau
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doi: 10.1007/s11033-024-09737-6 109 KhounganianRAudaSAl-ZaqzouqRAl-SemariHShakeelF
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