Search Results - "Stuart, Erica"
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1
Anti-prion drugs do not improve survival in novel knock-in models of inherited prion disease
Published in PLoS pathogens (01-04-2024)“…Prion diseases uniquely manifest in three distinct forms: inherited, sporadic, and infectious. Wild-type prions are responsible for the sporadic and infectious…”
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Journal Article -
2
Prion-like propagation of β-amyloid aggregates in the absence of APP overexpression
Published in Acta neuropathologica communications (03-04-2018)“…The amyloid cascade hypothesis posits that the initiating event in Alzheimer's disease (AD) is the aggregation and deposition of the β-amyloid (Aβ) peptide,…”
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Journal Article -
3
The G51D SNCA mutation generates a slowly progressive α-synuclein strain in early-onset Parkinson's disease
Published in Acta neuropathologica communications (03-05-2023)“…Unique strains of α-synuclein aggregates have been postulated to underlie the spectrum of clinical and pathological presentations seen across the…”
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Journal Article -
4
Aβ43 aggregates exhibit enhanced prion-like seeding activity in mice
Published in Acta neuropathologica communications (10-05-2021)“…When injected into genetically modified mice, aggregates of the amyloid-β (Aβ) peptide from the brains of Alzheimer's disease (AD) patients or transgenic AD…”
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Journal Article -
5
α-Synuclein strains target distinct brain regions and cell types
Published in Nature neuroscience (01-01-2020)“…The clinical and pathological differences between synucleinopathies such as Parkinson’s disease and multiple system atrophy have been postulated to stem from…”
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6
Synuclein strain propagation is independent of cellular prion protein expression in a transgenic synucleinopathy mouse model
Published in PLoS pathogens (12-09-2024)“…The cellular prion protein, PrP.sup.C, has been postulated to function as a receptor for [alpha]-synuclein, potentially facilitating cell-to-cell spreading…”
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Journal Article -
7
Anti-prion drugs do not improve survival in novel knock-in models of inherited prion disease
Published in PLoS pathogens (01-04-2024)“…Prion diseases uniquely manifest in three distinct forms: inherited, sporadic, and infectious. Wild-type prions are responsible for the sporadic and infectious…”
Get full text
Journal Article -
8
α-Synuclein strain propagation is independent of cellular prion protein expression in a transgenic synucleinopathy mouse model
Published in PLoS pathogens (01-09-2024)“…The cellular prion protein, PrPC, has been postulated to function as a receptor for α-synuclein, potentially facilitating cell-to-cell spreading and/or…”
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Journal Article -
9
Convergent generation of atypical prions in knockin mouse models of genetic prion disease
Published in The Journal of clinical investigation (01-08-2024)“…Most cases of human prion disease arise due to spontaneous misfolding of WT or mutant prion protein, yet recapitulating this event in animal models has proven…”
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Journal Article -
10
Synuclein strains target distinct brain regions and cell types
Published in Nature neuroscience (01-01-2020)“…The clinical and pathological differences between synucleinopathies such as Parkinson's disease and multiple system atrophy have been postulated to stem from…”
Get full text
Journal Article -
11
The G51D SNCA mutation generates a slowly progressive [alpha]-synuclein strain in early-onset Parkinson's disease
Published in Acta neuropathologica communications (03-05-2023)“…Unique strains of [alpha]-synuclein aggregates have been postulated to underlie the spectrum of clinical and pathological presentations seen across the…”
Get full text
Journal Article -
12
A beta 43 aggregates exhibit enhanced prion-like seeding activity in mice
Published in Acta neuropathologica communications (2021)“…When injected into genetically modified mice, aggregates of the amyloid-beta (A beta) peptide from the brains of Alzheimers disease (AD) patients or transgenic…”
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Journal Article -
13
A[beta]43 aggregates exhibit enhanced prion-like seeding activity in mice
Published in Acta neuropathologica communications (10-05-2021)“…When injected into genetically modified mice, aggregates of the amyloid-[beta] (A[beta]) peptide from the brains of Alzheimer's disease (AD) patients or…”
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Journal Article -
14
Prion-like propagation of [beta]-amyloid aggregates in the absence of APP overexpression
Published in Acta neuropathologica communications (03-04-2018)“…The amyloid cascade hypothesis posits that the initiating event in Alzheimer's disease (AD) is the aggregation and deposition of the [beta]-amyloid (A[beta])…”
Get full text
Journal Article