Neuronal to oligodendroglial alpha-synuclein redistribution in a double transgenic model of MSA

Multiple System Atrophy is a sporadic, progressive, neurodegenerative disease characterized by an oligodendroglial accumulation of α-syn. The mechanisms underlying the oligodendroglial accumulation of α-syn in the brains of patients with Multiple System Atrophy has attracted a great deal of interest...

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Hlavní autoři: Rockenstein, Edward, Ubhi, Kiren, Inglis, Chandra, Mante, Michael, Patrick, Christina, Adame, Anthony, Masliah, Eliezer
Médium: Artigo
Jazyk:Inglês
Vydáno: 2012
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3289254/
https://ncbi.nlm.nih.gov/pubmed/22314685
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WNR.0b013e3283509842
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