Altered Distribution of the Gangliosides GM1 and GM2 in Alzheimer’s Disease

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Aβ polymerization through interaction with membrane gangliosides

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Lipid Rafts As a Membrane-Organizing Principle

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Late endocytic dysfunction as a putative cause of amyloid fibril formation in Alzheimer’s disease

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Age-dependent high-density clustering of GM1 ganglioside at presynaptic neuritic terminals promotes amyloid β-protein fibrillogenesis

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Up-and-down topological mode of amyloid β-peptide lying on hydrophilic/hydrophobic interface of ganglioside clusters

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Thematic Review Series: Sphingolipids.Role of ganglioside metabolism in the pathogenesis of Alzheimer's disease—a review,

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