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Early activation of microglia and astrocytes in mouse models of Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1 (SCA1) is an incurable, dominantly inherited neurodegenerative disease of the cerebellum caused by a polyglutamine-repeat expansion in the protein ATXN1. While analysis of human autopsy material indicates significant glial pathology in SCA1, previous research has focuse...
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| Publicado no: | Neuroscience |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4344857/ https://ncbi.nlm.nih.gov/pubmed/25595967 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2015.01.003 |
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