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A Unifying Role for Prions in Neurodegenerative Diseases

Science (American Association for the Advancement of Science), 2012-06, Vol.336 (6088), p.1511-1513

Prusiner, Stanley B.

2012

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Biology and Genetics of Prions Causing Neurodegeneration

Annual review of genetics, 2013-01, Vol.47 (1), p.601-623

Prusiner, Stanley B

2013

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How an Infection of Sheep Revealed Prion Mechanisms in Alzheimer’s Disease and Other Neurodegenerative Disorders

International journal of molecular sciences, 2021-05, Vol.22 (9), p.4861

2021

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Transmission of multiple system atrophy prions to transgenic mice

Proceedings of the National Academy of Sciences - PNAS, 2013-11, Vol.110 (48), p.19555-19560

2013

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Is Parkinson's disease a prion disorder?

Proceedings of the National Academy of Sciences - PNAS, 2009-08, Vol.106 (31), p.12571-12572

2009

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Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism

Proceedings of the National Academy of Sciences - PNAS, 2015-09, Vol.112 (38), p.E5308-E5317

2015

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Serial propagation of distinct strains of Aβ prions from Alzheimer’s disease patients

Proceedings of the National Academy of Sciences - PNAS, 2014-07, Vol.111 (28), p.10323-10328

2014

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Stacked binding of a PET ligand to Alzheimer’s tau paired helical filaments

Nature communications, 2023-05, Vol.14 (1), p.3048-11, Article 3048

2023

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Purified and synthetic Alzheimer’s amyloid beta (Aβ) prions

Proceedings of the National Academy of Sciences - PNAS, 2012-07, Vol.109 (27), p.11025-11030

2012

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Analysis of proteome dynamics in the mouse brain

Proceedings of the National Academy of Sciences - PNAS, 2010-08, Vol.107 (32), p.14508-14513

2010

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Tau prions from Alzheimer’s disease and chronic traumatic encephalopathy patients propagate in cultured cells

Proceedings of the National Academy of Sciences - PNAS, 2016-12, Vol.113 (50), p.E8187-E8196

2016

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Distinct synthetic Aβ prion strains producing different amyloid deposits in bigenic mice

Proceedings of the National Academy of Sciences - PNAS, 2014-07, Vol.111 (28), p.10329-10334

2014

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Viroids, Satellite RNAs and Prions: Folding of Nucleic Acids and Misfolding of Proteins

Viruses, 2024-02, Vol.16 (3), p.360

2024

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Propagation of prions causing synucleinopathies in cultured cells

Proceedings of the National Academy of Sciences - PNAS, 2015-09, Vol.112 (35), p.E4949-E4958

2015

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Drug resistance confounding prion therapeutics

Proceedings of the National Academy of Sciences - PNAS, 2013-10, Vol.110 (44), p.E4160-E4169

2013

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Multiple system atrophy prions retain strain specificity after serial propagation in two different Tg(SNCAA53T) mouse lines

Acta neuropathologica, 2019-03, Vol.137 (3), p.437-454

2019

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Kinetics of α-synuclein prions preceding neuropathological inclusions in multiple system atrophy

PLoS pathogens, 2020-02, Vol.16 (2), p.e1008222-e1008222

2020

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Prion uptake in the gut: identification of the first uptake and replication sites

PLoS pathogens, 2011-12, Vol.7 (12), p.e1002449-e1002449

2011

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Evidence that bank vole PrP is a universal acceptor for prions

PLoS pathogens, 2014-04, Vol.10 (4), p.e1003990-e1003990

2014

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A Data Processing Pipeline for Mammalian Proteome Dynamics Studies Using Stable Isotope Metabolic Labeling

Molecular & cellular proteomics, 2011-12, Vol.10 (12), p.M111.010728-M111.010728, Article M111.010728

2011

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Evidence for Assembly of Prions with Left-Handed β-Helices into Trimers

Proceedings of the National Academy of Sciences - PNAS, 2004-06, Vol.101 (22), p.8342-8347

2004

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Prions

Proceedings of the National Academy of Sciences - PNAS, 1998-11, Vol.95 (23), p.13363-13383

Prunsiner, S.B. (University of California, San Francisco, CA.)

1998

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Familial Parkinson’s point mutation abolishes multiple system atrophy prion replication

Proceedings of the National Academy of Sciences - PNAS, 2018-01, Vol.115 (2), p.409-414

2018

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Design and construction of diverse mammalian prion strains

Proceedings of the National Academy of Sciences - PNAS, 2009-12, Vol.106 (48), p.20417-20422

2009

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Prion Protein—Antibody Complexes Characterized by Chromatography-Coupled Small-Angle X-Ray Scattering

Biophysical journal, 2015-08, Vol.109 (4), p.793-805

2015

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A Unifying Role for Prions in Neurodegenerative Diseases

Biology and Genetics of Prions Causing Neurodegeneration

How an Infection of Sheep Revealed Prion Mechanisms in Alzheimer’s Disease and Other Neurodegenerative Disorders

Transmission of multiple system atrophy prions to transgenic mice

Is Parkinson's disease a prion disorder?

Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism

Serial propagation of distinct strains of Aβ prions from Alzheimer’s disease patients

Stacked binding of a PET ligand to Alzheimer’s tau paired helical filaments

Purified and synthetic Alzheimer’s amyloid beta (Aβ) prions

Analysis of proteome dynamics in the mouse brain

Tau prions from Alzheimer’s disease and chronic traumatic encephalopathy patients propagate in cultured cells

Distinct synthetic Aβ prion strains producing different amyloid deposits in bigenic mice

Viroids, Satellite RNAs and Prions: Folding of Nucleic Acids and Misfolding of Proteins

Propagation of prions causing synucleinopathies in cultured cells

Drug resistance confounding prion therapeutics

Multiple system atrophy prions retain strain specificity after serial propagation in two different Tg(SNCAA53T) mouse lines

Kinetics of α-synuclein prions preceding neuropathological inclusions in multiple system atrophy

Prion uptake in the gut: identification of the first uptake and replication sites

Evidence that bank vole PrP is a universal acceptor for prions

A Data Processing Pipeline for Mammalian Proteome Dynamics Studies Using Stable Isotope Metabolic Labeling

Evidence for Assembly of Prions with Left-Handed β-Helices into Trimers

Prions

Familial Parkinson’s point mutation abolishes multiple system atrophy prion replication

Design and construction of diverse mammalian prion strains

Prion Protein—Antibody Complexes Characterized by Chromatography-Coupled Small-Angle X-Ray Scattering

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