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Neuroserpin and Extracellular Vesicles in Ischemic Stroke: Partners in Neuroprotection?
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- Aging & Disease, 2024, v. 15, n. 5, p. 2191, doi. 10.14336/AD.2024.0518
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- Article
Release of VAMP5‐positive extracellular vesicles by retinal Müller glia in vivo.
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- Journal of Extracellular Vesicles, 2022, v. 11, n. 9, p. 1, doi. 10.1002/jev2.12254
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- Article
Characterization of brain-derived extracellular vesicles reveals changes in cellular origin after stroke and enrichment of the prion protein with a potential role in cellular uptake.
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- Journal of Extracellular Vesicles, 2020, v. 9, n. 1, p. 1, doi. 10.1080/20013078.2020.1809065
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- Article
Characterization of brain‐derived extracellular vesicles reveals changes in cellular origin after stroke and enrichment of the prion protein with a potential role in cellular uptake.
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- Journal of Extracellular Vesicles, 2020, v. 9, n. 1, p. 1, doi. 10.1080/20013078.2020.1809065
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- Article
Lipid Alterations in Lipid Rafts from Alzheimer's Disease Human Brain Cortex.
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- Journal of Alzheimer's Disease, 2010, v. 19, n. 2, p. 489, doi. 10.3233/JAD-2010-1242
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- Article
Ubiquitin-negative mini-pick-like bodies in the dentate gyrus in p301l tauopathy.
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- Journal of Alzheimer's Disease, 2003, v. 5, n. 6, p. 445
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- Article
Brain-Derived Extracellular Vesicles in Health and Disease: A Methodological Perspective.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 3, p. 1365, doi. 10.3390/ijms22031365
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- Article
Molecular Communication of a Dying Neuron in Stroke.
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- International Journal of Molecular Sciences, 2018, v. 19, n. 9, p. 2834, doi. 10.3390/ijms19092834
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- Article
Anchorless risk or released benefit? An updated view on the ADAM10-mediated shedding of the prion protein.
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- Cell & Tissue Research, 2023, v. 392, n. 1, p. 215, doi. 10.1007/s00441-022-03582-4
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- Article
The sheddase ADAM10 is a potent modulator of prion disease.
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- eLife, 2015, p. 1, doi. 10.7554/eLife.04260.001
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CD73-mediated adenosine production by CD8 T cell-derived extracellular vesicles constitutes an intrinsic mechanism of immune suppression.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-26134-w
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P3-305: C-terminal Src kinase (CSK) is diminished in lipid rafts in Alzheimer’s disease
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- 2006
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- Abstract
P3-299: Protein degradation related with post-mortem delay in the study of human neurodegenerative diseases. A proteomics approach
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- 2006
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- Abstract
P3-305: C-terminal Src kinase (CSK) is diminished in lipid rafts in Alzheimer’s disease
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- 2006
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- Abstract
P3-299: Protein degradation related with post-mortem delay in the study of human neurodegenerative diseases. A proteomics approach
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- 2006
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- Abstract
Secretory pathway retention of mutant prion protein induces p38-MAPK activation and lethal disease in mice.
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- Scientific Reports, 2016, p. 24970, doi. 10.1038/srep24970
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- Article
N-Glycans and Glycosylphosphatidylinositol-Anchor Act on Polarized Sorting of Mouse PrP<sup>C</sup> in Madin-Darby Canine Kidney Cells.
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- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0024624
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- Article
Generation and Function of Non-cell-bound CD73 in Inflammation.
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- Frontiers in Immunology, 2019, p. 1, doi. 10.3389/fimmu.2019.01729
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GPI-anchor signal sequence influences PrP<sup>C</sup> sorting, shedding and signalling, and impacts on different pathomechanistic aspects of prion disease in mice.
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- PLoS Pathogens, 2019, v. 15, n. 01, p. 1, doi. 10.1371/journal.ppat.1007520
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- Article
Multiplexed mRNA analysis of brain-derived extracellular vesicles upon experimental stroke in mice reveals increased mRNA content with potential relevance to inflammation and recovery processes.
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- Cellular & Molecular Life Sciences, 2022, v. 79, n. 6, p. 1, doi. 10.1007/s00018-022-04357-4
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- Article
Roles of endoproteolytic α-cleavage and shedding of the prion protein in neurodegeneration.
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- FEBS Journal, 2013, v. 280, n. 18, p. 4338, doi. 10.1111/febs.12196
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- Article
Expression of transcription factors c-Fos, c-Jun, CREB-1 and ATF-2, and caspase-3 in relation with abnormal tau deposits in Pick’s disease.
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- Acta Neuropathologica, 2006, v. 111, n. 4, p. 341, doi. 10.1007/s00401-005-0013-0
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Individual and regional variations of phospho-tau species in progressive supranuclear palsy.
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- Acta Neuropathologica, 2005, v. 110, n. 3, p. 261, doi. 10.1007/s00401-005-1046-0
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Active stress kinase p38 enhances and perpetuates abnormal tau phosphorylation and deposition in Pick’s disease.
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- Acta Neuropathologica, 2004, v. 107, n. 3, p. 185, doi. 10.1007/s00401-003-0793-z
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- Article
Deposition of Hyperphosphorylated Tau in Cerebellum of PS1 E280A Alzheimer's Disease.
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- Brain Pathology, 2011, v. 21, n. 4, p. 452, doi. 10.1111/j.1750-3639.2010.00469.x
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A multifactorial model of pathology for age of onset heterogeneity in familial Alzheimer's disease.
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- Acta Neuropathologica, 2021, v. 141, n. 2, p. 217, doi. 10.1007/s00401-020-02249-0
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Show Me Your Friends and I Tell You Who You Are: The Many Facets of Prion Protein in Stroke.
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- Cells (2073-4409), 2020, v. 9, n. 7, p. 1609, doi. 10.3390/cells9071609
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Structural and mechanistic aspects influencing the ADAM10-mediated shedding of the prion protein.
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- Molecular Neurodegeneration, 2018, v. 13, n. 1, p. 1, doi. 10.1186/s13024-018-0248-6
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- Article
Lack of a-disintegrin-and-metalloproteinase ADAM10 leads to intracellular accumulation and loss of shedding of the cellular prion protein in vivo.
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- Molecular Neurodegeneration, 2011, v. 6, n. 1, p. 36, doi. 10.1186/1750-1326-6-36
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- Article
Retinal regions shape human and murine Müller cell proteome profile and functionality.
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- Glia, 2023, v. 71, n. 2, p. 391, doi. 10.1002/glia.24283
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Inducing prion protein shedding as a neuroprotective and regenerative approach in pathological conditions of the brain: from theory to facts.
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- Neural Regeneration Research, 2023, v. 18, n. 9, p. 1869, doi. 10.4103/1673-5374.366496
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Transgenic Overexpression of the Disordered Prion Protein N1 Fragment in Mice Does Not Protect Against Neurodegenerative Diseases Due to Impaired ER Translocation.
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- Molecular Neurobiology, 2020, v. 57, n. 6, p. 2812, doi. 10.1007/s12035-020-01917-2
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Prion protein oligomers cause neuronal cytoskeletal damage in rapidly progressive Alzheimer's disease.
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- Molecular Neurodegeneration, 2021, v. 16, n. 1, p. 1, doi. 10.1186/s13024-021-00422-x
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- Article