Neuronal and astrocytic contributions to Huntington’s disease dissected with zinc finger protein transcriptional repressors
Summary: Huntington’s disease (HD) is caused by expanded CAG repeats in the huntingtin gene (HTT) resulting in expression of mutant HTT proteins (mHTT) with extended polyglutamine tracts, including in striatal neurons and astrocytes. It is unknown whether pathophysiology in vivo can be attenuated by...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2023-01-01
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| Col·lecció: | Cell Reports |
| Matèries: | |
| Accés en línia: | http://www.sciencedirect.com/science/article/pii/S221112472201854X |
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