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- W4308149935 abstract "Genome-wide association studies and functional genomics studies have linked specific cell types, genes, and pathways to Alzheimer's disease (AD) risk. In particular, AD risk alleles primarily affect the abundance or structure, and thus the activity, of genes expressed in macrophages, strongly implicating microglia (the brain-resident macrophages) in the etiology of AD. These genes converge on pathways (endocytosis/phagocytosis, cholesterol metabolism, and immune response) with critical roles in core macrophage functions such as efferocytosis. Here, we review these pathways, highlighting relevant genes identified in the latest AD genetics and genomics studies, and describe how they may contribute to AD pathogenesis. Investigating the functional impact of AD-associated variants and genes in microglia is essential for elucidating disease risk mechanisms and developing effective therapeutic approaches." @default.
- W4308149935 created "2022-11-08" @default.
- W4308149935 creator A5000475810 @default.
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- W4308149935 creator A5017017613 @default.
- W4308149935 creator A5027004714 @default.
- W4308149935 creator A5040692198 @default.
- W4308149935 date "2022-11-01" @default.
- W4308149935 modified "2023-10-16" @default.
- W4308149935 title "Microglial efferocytosis: Diving into the Alzheimer’s disease gene pool" @default.
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