Article
CK2 alpha prime and alpha-synuclein pathogenic functional interaction mediates synaptic dysregulation in Huntington’s disease
2020-10-29
Abstract excerpt
<h4>Background</h4> Huntington’s Disease (HD) is a neurodegenerative disorder caused by a CAG trinucleotide repeat expansion in the HTT gene for which no therapies are available. This mutation causes HTT protein misfolding and aggregation, preferentially affecting medium spiny neurons (MSNs) of the basal ganglia. Transcriptional perturbations in synaptic genes and neuroinflammation are key processes that precede...
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Identifiers and source
- Literature Corpus work
- b6cdf395-89c0-561b-a3f9-9ee20e7cfb06
- DOI
- 10.1101/2020.10.29.359380
