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Dysregulated phosphorylation of Rab GTPases by LRRK2 induces neurodegeneration
BACKGROUND: Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common cause of familial and sporadic Parkinson’s disease (PD). Elevated kinase activity is associated with LRRK2 toxicity, but the substrates that mediate neurodegeneration remain poorly defined. Given the increasing evidenc...
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| Vydáno v: | Mol Neurodegener |
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| Hlavní autoři: | , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5811984/ https://ncbi.nlm.nih.gov/pubmed/29439717 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13024-018-0240-1 |
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