about
Propagation of prions causing synucleinopathies in cultured cellsEvidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonismEvidence that bank vole PrP is a universal acceptor for prionsSpontaneous generation of rapidly transmissible prions in transgenic mice expressing wild-type bank vole prion protein.Convection-enhanced delivery of AAV2-PrPshRNA in prion-infected miceDistinct synthetic Aβ prion strains producing different amyloid deposits in bigenic mice.Serial propagation of distinct strains of Aβ prions from Alzheimer's disease patients.Protease-resistant prions selectively decrease Shadoo protein.White matter involvement in sporadic Creutzfeldt-Jakob disease.Levels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion diseaseSpontaneous generation of anchorless prions in transgenic mice.Use of a 2-aminothiazole to Treat Chronic Wasting Disease in Transgenic MiceIdentification of I137M and other mutations that modulate incubation periods for two human prion strains.Different 2-Aminothiazole Therapeutics Produce Distinct Patterns of Scrapie Prion Neuropathology in Mouse Brains.Purified and synthetic Alzheimer's amyloid beta (Aβ) prions.Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutationConvergent replication of mouse synthetic prion strains.Brain Aggregates: An Effective In Vitro Cell Culture System Modeling Neurodegenerative Diseases.Chimeric elk/mouse prion proteins in transgenic mice.Biaryl amides and hydrazones as therapeutics for prion disease in transgenic mice.Drug resistance confounding prion therapeutics.Guinea Pig Prion Protein Supports Rapid Propagation of Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease Prions.Transmission of multiple system atrophy prions to transgenic micePrion Disease Induces Alzheimer Disease-Like Neuropathologic Changes.Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation casesOligodendroglial deletion of ESCRT-I component TSG101 causes spongiform encephalopathy.Optimization of Aryl Amides that Extend Survival in Prion-Infected Mice.Towards authentic transgenic mouse models of heritable PrP prion diseases.A novel vector for transgenesis in the rat CNS.MSA prions exhibit remarkable stability and resistance to inactivation.Kinetics of Human Mutant Tau Prion Formation in the Brains of 2 Transgenic Mouse Lines.Structural heterogeneity and intersubject variability of Aβ in familial and sporadic Alzheimer's disease.Evidence for sortilin modulating regional accumulation of human tau prions in transgenic mice.Familial Parkinson's point mutation abolishes multiple system atrophy prion replication.
P50
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P50
name
Abby Oehler
@ast
Abby Oehler
@en
Abby Oehler
@nl
type
label
Abby Oehler
@ast
Abby Oehler
@en
Abby Oehler
@nl
prefLabel
Abby Oehler
@ast
Abby Oehler
@en
Abby Oehler
@nl