19 Matching Annotations
  1. Last 7 days
  2. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Osmotin-derived 9-amino-acid peptide alleviates α-synuclein and MPTP-induced glial cell activation mediated neuroinflammation, protecting dopaminergic neurons in Parkinson’s disease mice brain
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    pmc.ncbi.nlm.nih.gov/articles/PMC12833940/
  3. Jul 2026
  4. www.biorxiv.org www.biorxiv.org
    Virus-mediated tau aggregate seeding in a cellular model
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    biorxiv.org/content/10.64898/2026.06.25.734433v1
  5. Jun 2026
  6. 54.241.53.176 54.241.53.176
    ssrn-5394581-html.html
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    54.241.53.176/4de15616999ee4e94162457c4e5b4ce5209782b3/ssrn-5394581-html.html
  7. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Mitochondria serve as a holdout compartment for aggregation-prone proteins hindering efficient degradation
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    pmc.ncbi.nlm.nih.gov/articles/PMC13153185/
  8. Jan 2026
  9. www.sciencedirect.com www.sciencedirect.com
    Skin-derived α-synuclein strains from PD, DLB, and MSA induce distinct intracellular pathology and neurodegeneration
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    sciencedirect.com/science/article/pii/S0021925825028571
  10. Sep 2025
  11. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Gangliosides modulate the secretion of extracellular vesicles and their misfolded protein cargo
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    pmc.ncbi.nlm.nih.gov/articles/PMC12442881/
  12. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Integrating artificial intelligence and optogenetics for Parkinson’s disease diagnosis and therapeutics in male mice
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    pmc.ncbi.nlm.nih.gov/articles/PMC12370958/
  13. Aug 2025
  14. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    ANKZF1 helps to eliminate stress-damaged mitochondria by LC3-mediated mitophagy
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    pmc.ncbi.nlm.nih.gov/articles/PMC12307761/
  15. Mar 2025
  16. www.biorxiv.org www.biorxiv.org
    Mitochondria serve as a Holdout Compartment for Aggregation-Prone Proteins hindering Efficient Ubiquitin-Dependent Degradation
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    biorxiv.org/content/10.1101/2025.02.27.640505v1
  17. Apr 2024
  18. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    The SATB1‐MIR22‐GBA axis mediates glucocerebroside accumulation inducing a cellular senescence‐like phenotype in dopaminergic neurons
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    ncbi.nlm.nih.gov/pmc/articles/PMC11019121/
  19. Aug 2023
  20. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    The SATB1-MIR22-GBA axis mediates glucocerebroside accumulation inducing a cellular senescence-like phenotype in dopaminergic neurons
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    ncbi.nlm.nih.gov/pmc/articles/PMC10370136/
  21. May 2023
  22. www.nature.com www.nature.com
    Compounds activating VCP D1 ATPase enhance both autophagic and proteasomal neurotoxic protein clearance
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    nature.com/articles/s41467-022-31905-0
  23. May 2022
  24. www.sciencedirect.com www.sciencedirect.com
    Reduction of phosphorylated α-synuclein through downregulation of casein kinase 2α alleviates dopaminergic-neuronal function
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    sciencedirect.com/science/article/pii/S0006291X22007197
  25. Jan 2022
  26. www.sciencedirect.com www.sciencedirect.com
    Roflupram attenuates α-synuclein-induced cytotoxicity and promotes the mitochondrial translocation of Parkin in SH-SY5Y cells overexpressing A53T mutant α-synuclein
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    sciencedirect.com/science/article/pii/S0041008X21004634
  27. Jun 2021
  28. www.sciencedirect.com www.sciencedirect.com
    LMK235, a small molecule inhibitor of HDAC4/5, protects dopaminergic neurons against neurotoxin- and α-synuclein-induced degeneration in cellular models of Parkinson’s disease
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    sciencedirect.com/science/article/pii/S1044743121000555
  29. May 2021
  30. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    In situ architecture of neuronal α-Synuclein inclusions
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    ncbi.nlm.nih.gov/pmc/articles/PMC8046968/
  31. Feb 2021
  32. www.nature.com www.nature.com
    Endocytic regulation of cellular ion homeostasis controls lysosome biogenesis
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    nature.com/articles/s41556-020-0535-7
  33. Jan 2020
  34. www.frontiersin.org www.frontiersin.org
    Gene Co-expression Analysis Identifies Histone Deacetylase 5 and 9 Expression in Midbrain Dopamine Neurons and as Regulators of Neurite Growth via Bone Morphogenetic Protein Signaling
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    frontiersin.org/articles/10.3389/fcell.2019.00191/full