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Fbxl18 targets LRRK2 for proteasomal degradation and attenuates cell toxicity
Dominantly inherited mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common cause of familial Parkinson’s disease (PD) and LRRK2 polymorphisms are associated with increased risk for idiopathic PD. However, the molecular mechanisms by which these mutations cause PD remain uncertain. In...
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| Publicado no: | Neurobiol Dis |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5718210/ https://ncbi.nlm.nih.gov/pubmed/27890708 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2016.11.004 |
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