Synphilin-1 attenuates neuronal degeneration in the A53T α-synuclein transgenic mouse model

Genetic alterations in α-synuclein cause autosomal dominant familial Parkinsonism and may contribute to sporadic Parkinson's disease (PD). Synphilin-1 is an α-synuclein-interacting protein, with implications in PD pathogenesis related to protein aggregation. Currently, the in vivo role of synph...

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Bibliografiset tiedot
Päätekijät: Smith, Wanli W., Liu, Zhaohui, Liang, Yideng, Masuda, Naoki, Swing, Debbie A., Jenkins, Nancy A., Copeland, Neal G., Troncoso, Juan C., Pletnikov, Mikhail, Dawson, Ted M., Martin, Lee J., Moran, Timothy H., Lee, Michael K., Borchelt, David R., Ross, Christopher A.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2010
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Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2865369/
https://ncbi.nlm.nih.gov/pubmed/20185556
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq086
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