Polyunsaturated Fatty Acids Protect Against Prion-Mediated Synapse Damage In Vitro
Journal Article
Bate, C., Tayebi, M., Salmona, M., Diomede, L., & Williams, A. Polyunsaturated Fatty Acids Protect Against Prion-Mediated Synapse Damage In Vitro. Neurotoxicity Research, 17(3), 203-214. https://doi.org/10.1007/s12640-009-9093-2
Outputs (65)
Alpha-synuclein induced synapse damage is enhanced by amyloid-beta
Journal Article
Bate, C., Gentleman, S., & Williams, A. Alpha-synuclein induced synapse damage is enhanced by amyloid-beta. Molecular Neurodegeneration, 5(55), https://doi.org/10.1186/1750-1326-5-55
The cellular prion protein with a monoacylated glycosylphosphatidylinositol anchor modifies cell membranes, inhibits cell signaling and reduces prion formation
Journal Article
Bate, C., & Williams, A. The cellular prion protein with a monoacylated glycosylphosphatidylinositol anchor modifies cell membranes, inhibits cell signaling and reduces prion formation. Prion, 5(2), 65-68. https://doi.org/10.4161/pri.5.2.16095
Monoacylated Cellular Prion Protein Modifies Cell Membranes, Inhibits Cell Signaling, and Reduces Prion Formation
Journal Article
Bate, C., & Williams, A. Monoacylated Cellular Prion Protein Modifies Cell Membranes, Inhibits Cell Signaling, and Reduces Prion Formation. Journal of Biological Chemistry, 286(11), 8752-8758. https://doi.org/10.1074/jbc.M110.186833
Ethanol protects cultured neurons against amyloid-beta and alpha-synuclein-induced synapse damage
Journal Article
Bate, C., & Williams, A. Ethanol protects cultured neurons against amyloid-beta and alpha-synuclein-induced synapse damage. Neuropharmacology, 61(8), 1406-1412. https://doi.org/10.1016/j.neuropharm.2011.08.030
Amyloid-beta-induced Synapse Damage Is Mediated via Cross-linkage of Cellular Prion Proteins
Journal Article
Bate, C., & Williams, A. Amyloid-beta-induced Synapse Damage Is Mediated via Cross-linkage of Cellular Prion Proteins. Journal of Biological Chemistry, 286(44), 37955-37963. https://doi.org/10.1074/jbc.M111.248724
Inhibition of phospholipase A(2) increased the removal of the prion derived peptide PrP82-146 from cultured neurons
Journal Article
Bate, C., Ingham, V., & Williams, A. Inhibition of phospholipase A(2) increased the removal of the prion derived peptide PrP82-146 from cultured neurons. Neuropharmacology, 60(2-3), 365-372. https://doi.org/10.1016/j.neuropharm.2010.10.001
Neurodegeneration Induced by Clustering of Sialylated Glycosylphosphatidylinositols of Prion Proteins
Journal Article
Bate, C., & Williams, A. Neurodegeneration Induced by Clustering of Sialylated Glycosylphosphatidylinositols of Prion Proteins. Journal of Biological Chemistry, 287(11), 7935-7944. https://doi.org/10.1074/jbc.M111.275743
Clustering of sialylated glycosylphosphatidylinositol anchors mediates PrP-induced activation of cytoplasmic phospholipase A(2) and synapse damage
Journal Article
Bate, C., & Williams, A. Clustering of sialylated glycosylphosphatidylinositol anchors mediates PrP-induced activation of cytoplasmic phospholipase A(2) and synapse damage. Prion, 6(4), 350-353. https://doi.org/10.4161/pri.21751
Docosahexaenoic and eicosapentaenoic acids increase neuronal death in response to HuPrP82-146 and A beta 1-42
Journal Article
Bate, C., Marshall, V., Colombo, L., Diomede, L., Salmona, M., & Williams, A. Docosahexaenoic and eicosapentaenoic acids increase neuronal death in response to HuPrP82-146 and A beta 1-42. Neuropharmacology, 54(6), 934-943. https://doi.org/10.1016/j.neuropharm.2008.02.003Dietary supplements containing polyunsaturated fatty acids (PUFA) are frequently taken for their perceived health benefits including a possible reduction in cognitive decline in the elderly. Here we report that pre-treatment with docosahexaenoic acid... Read More about Docosahexaenoic and eicosapentaenoic acids increase neuronal death in response to HuPrP82-146 and A beta 1-42.