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Cell-to-cell Transmission of Polyglutamine Aggregates in C. elegans
Huntington disease (HD) is an inherited neurodegenerative disorder characterized by motor and cognitive dysfunction caused by expansion of polyglutamine (polyQ) repeat in exon 1 of huntingtin (HTT). In patients, the number of glutamine residues in polyQ tracts are over 35, and it is correlated with...
Tallennettuna:
| Julkaisussa: | Exp Neurobiol |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
The Korean Society for Brain and Neural Science
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5746497/ https://ncbi.nlm.nih.gov/pubmed/29302199 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5607/en.2017.26.6.321 |
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