Handbook of Neurotoxicity 2022
DOI: 10.1007/978-3-031-15080-7_226
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Huntington’s Disease and Neurodegeneration

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Cited by 2 publications
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“…Gradually, the aggregates may sequester ubiquitin, proteasome subunits, chaperones, transcriptional factors, or wild-type alleles which induce neurotoxic effects, leading to an impairment in the ubiquitin-proteasome system. Indeed, the aggregates show abnormal axonal transport of the autophagosome-lysosome system, contributing to inefficient autophagosome-lysosome fusion and decreased degradation of the aggregates [45].…”
Section: Huntington's Diseasementioning
confidence: 99%
“…Gradually, the aggregates may sequester ubiquitin, proteasome subunits, chaperones, transcriptional factors, or wild-type alleles which induce neurotoxic effects, leading to an impairment in the ubiquitin-proteasome system. Indeed, the aggregates show abnormal axonal transport of the autophagosome-lysosome system, contributing to inefficient autophagosome-lysosome fusion and decreased degradation of the aggregates [45].…”
Section: Huntington's Diseasementioning
confidence: 99%