Selective Enrichment of DJ-1 Protein in Primate Striatal Neuronal Processes: Implications for Parkinson's Disease

Mutations in DJ-1 cause autosomal recessive, early-onset Parkinson's disease (PD). The precise function and distribution of DJ-1 in the central nervous system remain unclear. In this study, we performed a comprehensive analysis of DJ-1 expression in human, monkey, and rat brains using antibodie...

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Detaylı Bibliyografya
Asıl Yazarlar: OLZMANN, JAMES A., BORDELON, JILL R., MULY, E. CHRIS, REES, HOWARD D., LEVEY, ALLAN I., LI, LIAN, CHIN, LIH-SHEN
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2007
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2597443/
https://ncbi.nlm.nih.gov/pubmed/17120294
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cne.21191
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