Article
Anle138b ameliorates pathological phenotypes in mouse and cellular models of Huntington’s disease
2025-03-13
Abstract excerpt
Huntington’s disease (HD) is a debilitating hereditary movement disorder caused by a CAG repeat expansion in the huntingtin gene. HD is characterized by deposition of mutant huntingtin (mHTT) aggregates, and by severe neurodegeneration of the basal ganglia and neocortex. No cure is currently available, and new treatment options are urgently needed. Here, we show that the oligomer modifying molecule anle138b (INN:...
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Identifiers and source
- Literature Corpus work
- 8b5792ff-1204-57ed-b503-7fa55e471791
- DOI
- 10.1101/2025.03.11.642540
