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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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Literature Corpus work
b6cdf395-89c0-561b-a3f9-9ee20e7cfb06
DOI
10.1101/2020.10.29.359380
Open publication

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CK2 alpha prime and alpha-synuclein pathogenic functional interaction mediates synaptic dysregulation in Huntington’s diseaseDOI 10.1101/2020.10.29.359380
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