Purinergic Receptors in Basal Ganglia Diseases: Shared Molecular Mechanisms between Huntington’s and Parkinson’s Disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Physiology,General Neuroscience
Link
https://link.springer.com/content/pdf/10.1007/s12264-020-00582-8.pdf
Reference175 articles.
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2. Rikani AA, Choudhry Z, Choudhry AM, Rizvi N, Ikram H, Mobassarah NJ, et al. The mechanism of degeneration of striatal neuronal subtypes in Huntington disease. Ann Neurosci 2014, 21:112–114.
3. Yang W, Xie J, Qiang Q, Li L, Lin X, Ren Y, et al. Gedunin degrades aggregates of mutant huntingtin protein and intranuclear inclusions via the proteasomal pathway in neurons and fibroblasts from patients with Huntington’s disease. Neurosci Bull 2019, 35:1024–1034.
4. Lees AJ, Hardy J, Revesz T, Lila R. Parkinson ’ s disease. Lancet 2009, 373:2055–2066.
5. Jellinger KA. Significance of brain lesions in Parkinson disease dementia and Lewy body dementia. Front Neurol Neurosci 2009, 24:114–125.
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