Aggregation of huntingtin in yeast varies with the length of the polyglutamine expansion and the expression of chaperone proteins
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by polyglutamine (polyQ) expansions in the huntingtin (Ht) protein. A hallmark of HD is the proteolytic production of an N-terminal fragment of Ht, containing the polyQ repeat, that forms aggregates in the nucleus and cytopl...
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| Publicado no: | Proc Natl Acad Sci U S A |
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| Principais autores: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2000
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC26479/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10677504/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.97.4.1589 |
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