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Selective neuronal vulnerability in Parkinson disease

Surmeier, D. James, Obeso, José A., Halliday, Glenda M.·2017·Nature Reviews Neuroscience

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  • Oligomeric α-Syn species appear prone to uptake and spread from cell-to-cell in a prion-like manner, leading to templated misfolding of native α-Syn and formation of aggregates throughout the brain.

    “Particularly, the oligomeric α-Syn species appear to be prone to uptake and spread from cell-to-cell in a prion-like manner, leading to the templated misfolding of the native forms of α-Syn and formation of α-Syn aggregates throughout the brain, which are the defining pathological features of Parkinson’s disease (PD) and dementia with Lewy body (DLB) [12–19].”

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Metadata

Authors
Surmeier, D. J., Obeso, J. A., & Halliday, G. M.
Venue
Nature Reviews Neuroscience
Published
2017-01-20
Volume
18
Issue
2
Pages
101-113
ISSN
  • 1471-003X
  • 1471-0048
Cited by
1,116
References
36
Language
en

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