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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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Literature Corpus work
8b5792ff-1204-57ed-b503-7fa55e471791
DOI
10.1101/2025.03.11.642540
Open publication

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Anle138b ameliorates pathological phenotypes in mouse and cellular models of Huntington’s diseaseDOI 10.1101/2025.03.11.642540
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