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Excess α-synuclein worsens disease in mice lacking ubiquitin carboxy-terminal hydrolase L1
Mutations in α-synuclein (αSN) and ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) have been linked to familial Parkinson's disease (PD). Physical and functional interactions between these two proteins have been described. Whether they act additively in vivo to influence disease has remained c...
Autores principales: | Shimshek, Derya R., Schweizer, Tatjana, Schmid, Peter, van der Putten, P. Herman |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278044/ https://www.ncbi.nlm.nih.gov/pubmed/22355774 http://dx.doi.org/10.1038/srep00262 |
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