Prion-like propagation as a pathogenic principle in frontotemporal dementia.
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Functional and dynamic polymerization of the ALS-linked protein TDP-43 antagonizes its pathologic aggregation.Split GFP technologies to structurally characterize and quantify functional biomolecular interactions of FTD-related proteinsLet's make microglia great again in neurodegenerative disorders.Frontotemporal dementia: latest evidence and clinical implications.Geschwind Syndrome in frontotemporal lobar degeneration: Neuroanatomical and neuropsychological features over 9 years.Synaptic Paths to Neurodegeneration: The Emerging Role of TDP-43 and FUS in Synaptic Functions.Minimotifs dysfunction is pervasive in neurodegenerative disorders
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Prion-like propagation as a pathogenic principle in frontotemporal dementia.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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2016年学术文章
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2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
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2016年學術文章
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name
Prion-like propagation as a pathogenic principle in frontotemporal dementia.
@en
type
label
Prion-like propagation as a pathogenic principle in frontotemporal dementia.
@en
prefLabel
Prion-like propagation as a pathogenic principle in frontotemporal dementia.
@en
P2860
P356
P1476
Prion-like propagation as a pathogenic principle in frontotemporal dementia
@en
P2093
Eva-Maria Hock
Magdalini Polymenidou
P2860
P304
P356
10.1111/JNC.13668
P407
P478
138 Suppl 1
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2016-08-01T00:00:00Z