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  1. Article

    Open Access

    Altered amyloid-β structure markedly reduces gliosis in the brain of mice harboring the Uppsala APP deletion

    Deposition of amyloid beta (Aβ) into plaques is a major hallmark of Alzheimer’s disease (AD). Different amyloid precursor protein (APP) mutations cause early-onset AD by altering the production or aggregation pro...

    María Pagnon de la Vega, Stina Syvänen in Acta Neuropathologica Communications (2024)

  2. Article

    Open Access

    Mutation analysis of disease causing genes in patients with early onset or familial forms of Alzheimer’s disease and frontotemporal dementia

    Most dementia disorders have a clear genetic background and a number of disease genes have been identified. Mutations in the tau gene (MAPT) lead to frontotemporal dementia (FTD), whereas mutations in the genes f...

    María Pagnon de la Vega, Carl Näslund, RoseMarie Brundin, Lars Lannfelt in BMC Genomics (2022)