लोड हो रहा है...
LRRK2 and ubiquitination: implications for kinase inhibitor therapy
Pathogenic mutations and risk variants in LRRK2 (leucine-rich repeat kinase 2) represent the most common genetic cause of familial and sporadic PD (Parkinson's disease). LRRK2 protein is widely expressed throughout the brain and the periphery. Structurally, LRRK2 contains several functional dom...
में बचाया:
| में प्रकाशित: | Biochem J |
|---|---|
| मुख्य लेखक: | |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Portland Press Ltd.
2015
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4613699/ https://ncbi.nlm.nih.gov/pubmed/26341487 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20150785 |
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