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Anle138b modulates α‐synuclein oligomerization and prevents motor decline and neurodegeneration in a mouse model of multiple system atrophy

BACKGROUND: MSA is a fatal neurodegenerative disease characterized by autonomic failure and severe motor impairment. Its main pathological hallmark is the accumulation of α‐synuclein in oligodendrocytes, leading to glial and neuronal dysfunction and neurodegeneration. These features are recapitulate...

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Detalhes bibliográficos
Publicado no:Mov Disord
Main Authors: Heras‐Garvin, Antonio, Weckbecker, Daniel, Ryazanov, Sergey, Leonov, Andrei, Griesinger, Christian, Giese, Armin, Wenning, Gregor K., Stefanova, Nadia
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Inc. 2018
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6492169/
https://ncbi.nlm.nih.gov/pubmed/30452793
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.27562
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