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Brain and Behavior|March 16, 2018
Early fine motor impairment and behavioral dysfunction in (Thy-1)-h[A30P] alpha-synuclein miceSara Ekmark-Lewén, Veronica Lindström, Astrid Gumucio, et al.Journal of Human Genetics|March 21, 2014
An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalitiesToshiyuki Yamamoto, Anna Wilsdon, Shelagh Joss, et al.Journal of Alzheimer'S Disease : JAD|September 17, 2016
Increased Levels of Extracellular Microvesicle Markers and Decreased Levels of Endocytic/Exocytic Proteins in the Alzheimer's Disease BrainSravani Musunuri, Payam Emami Khoonsari, Maria Mikus, et al.Journal of Neuroinflammation|April 24, 2025
Astrocytic lipid droplets contain MHCII and may act as cogs in the antigen presentation machineryChiara Beretta, Abdulkhalek Dakhel, Khalid Eltom, et al.Cellular and Molecular Neurobiology|October 6, 2018
Secretion and Uptake of α-Synuclein Via Extracellular Vesicles in Cultured CellsGabriel Gustafsson, Camilla Lööv, Emma Persson, et al.Molecular Neurobiology|February 25, 2021
Parkinson's Disease-Associated LRRK2 Interferes with Astrocyte-Mediated Alpha-Synuclein ClearanceLinn Streubel-Gallasch, Veronica Giusti, Michele Sandre, et al.Molecular Therapy. Nucleic Acids|May 4, 2022
CRISPR-Cas9 treatment partially restores amyloid-β 42/40 in human fibroblasts with the Alzheimer's disease PSEN 1 M146L mutationEvangelos Konstantinidis, Agnieszka Molisak, Florian Perrin, et al.Acta Neuropathologica Communications|February 5, 2024
Altered amyloid-β structure markedly reduces gliosis in the brain of mice harboring the Uppsala APP deletionMaría Pagnon de la Vega, Stina Syvänen, Vilmantas Giedraitis, et al.Science Translational Medicine|August 12, 2021
The Uppsala APP deletion causes early onset autosomal dominant Alzheimer's disease by altering APP processing and increasing amyloid β fibril formationMaría Pagnon de la Vega, Vilmantas Giedraitis, Wojciech Michno, et al.Pageof 6