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Massimiliano Stagi

Researcher at University of Liverpool

Publications -  25
Citations -  2750

Massimiliano Stagi is an academic researcher from University of Liverpool. The author has contributed to research in topics: Lysosome & Signal transduction. The author has an hindex of 16, co-authored 22 publications receiving 2397 citations. Previous affiliations of Massimiliano Stagi include University of Bonn & Yale University.

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Alzheimer amyloid-β oligomer bound to postsynaptic prion protein activates Fyn to impair neurons

TL;DR: An Aβ oligomer signal transduction pathway that requires PrPC and Fyn to alter synaptic function, with deleterious consequences in Alzheimer's disease is delineated.
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Metabotropic Glutamate Receptor 5 Is a Coreceptor for Alzheimer Aβ Oligomer Bound to Cellular Prion Protein

TL;DR: Transmembrane PSD proteins heterologously screened for the ability to couple Aβo-PrP(C) with Fyn and found coexpression of the metabotropic glutamate receptor, mGluR5, allowed PrP (C)-bound A βo to activate Fyn.
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TREM2-Transduced Myeloid Precursors Mediate Nervous Tissue Debris Clearance and Facilitate Recovery in an Animal Model of Multiple Sclerosis

TL;DR: Intravenous application of TREM2-transduced bone marrow–derived myeloid precursor cells at the EAE peak led to an amelioration of clinical symptoms, reduction in axonal damage, and prevention of further demyelination, indicating a new attractive target for promotion of repair and resolution of inflammation in multiple sclerosis and other neuroinflammatory diseases.
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LPS receptor (CD14): a receptor for phagocytosis of Alzheimer’s amyloid peptide

TL;DR: A direct role of CD14 in Abeta(42) phagocytosis is demonstrated, and a pronounced CD14 immunoreactivity on parenchymal microglia spatially correlated to characteristic Alzheimer's disease lesion sites in brain sections of Alzheimer’s disease patients but not inbrain sections of control subjects are detected.
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SynCAMs organize synapses through heterophilic adhesion

TL;DR: Two immunoglobulin superfamily members, SynCAM 1 and 2, are defined that are expressed in neurons in the developing brain and localize to excitatory and inhibitory synapses and function as components of novel heterophilic transsynaptic adhesion complexes that set up asymmetric interactions.