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Familial Parkinson’s Disease-Associated L166P Mutant DJ-1 is Cleaved by Mitochondrial Serine Protease Omi/HtrA2
Parkinson’s disease (PD) is the most common neurodegenerative movement disorder. Mutations in the DJ-1, including L166P, are responsible for recessive early-onset PD. Many lines of evidence have shown that L166P is not only a loss-of-function mutant, but also a pro-apoptotic-like protein that result...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Neurosci Bull |
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| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Springer Singapore
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5725392/ https://ncbi.nlm.nih.gov/pubmed/29177768 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12264-017-0196-0 |
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