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Amyloid-β Receptors: The Good, the Bad, and the Prion Protein

The Journal of biological chemistry, 2016-02, Vol.291 (7), p.3174-3183

2016

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Cryo-EM structure of an amyloid fibril formed by full-length human prion protein

Nature structural & molecular biology, 2020-06, Vol.27 (6), p.598-602

2020

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The complex PrP(c)-Fyn couples human oligomeric Aβ with pathological tau changes in Alzheimer's disease

The Journal of neuroscience, 2012-11, Vol.32 (47), p.16857

2012

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Cellular Prion Protein Conformational Shift after Liquid–Liquid Phase Separation Regulated by a Polymeric Antagonist and Mutations

Journal of the American Chemical Society, 2024-10, Vol.146 (40), p.27903-27914

2024

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α-synuclein interacts with PrP C to induce cognitive impairment through mGluR5 and NMDAR2B

Nature neuroscience, 2017-11, Vol.20 (11), p.1569

2017

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An optimized Western blot assay provides a comprehensive assessment of the physiological endoproteolytic processing of the prion protein

The Journal of biological chemistry, 2023-02, Vol.299 (2), p.102823-102823, Article 102823

2023

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Metabotropic Glutamate Receptor 5 Is a Coreceptor for Alzheimer Aβ Oligomer Bound to Cellular Prion Protein

Neuron (Cambridge, Mass.), 2013-09, Vol.79 (5), p.887-902

2013

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Prion-Protein-interacting Amyloid-β Oligomers of High Molecular Weight Are Tightly Correlated with Memory Impairment in Multiple Alzheimer Mouse Models

The Journal of biological chemistry, 2015-07, Vol.290 (28), p.17415-17438

2015

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Alzheimer amyloid-β oligomer bound to postsynaptic prion protein activates Fyn to impair neurons

Nature neuroscience, 2012-09, Vol.15 (9), p.1227-1235

2012

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Interaction between Human Prion Protein and Amyloid-β (Aβ) Oligomers: ROLE OF N-TERMINAL RESIDUES

The Journal of biological chemistry, 2010-08, Vol.285 (34), p.26377-26383

2010

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General Model of Prion Strains and Their Pathogenicity

Science (American Association for the Advancement of Science), 2007-11, Vol.318 (5852), p.930-936

2007

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Divergent prion strain evolution driven by PrP C expression level in transgenic mice

Nature communications, 2017-01, Vol.8, p.14170

2017

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Prion propagation and toxicity in vivo occur in two distinct mechanistic phases

Nature (London), 2011-02, Vol.470 (7335), p.540-542

2011

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A New Paradigm for Enzymatic Control of α-Cleavage and β-Cleavage of the Prion Protein

The Journal of biological chemistry, 2014-01, Vol.289 (2), p.803-813

2014

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The cellular prion protein mediates neurotoxic signalling of β-sheet-rich conformers independent of prion replication

The EMBO journal, 2011-05, Vol.30 (10), p.2057-2070

2011

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Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked

Nature communications, 2014-07, Vol.5 (1), p.4347, Article 4347

2014

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The function of the cellular prion protein in health and disease

Acta neuropathologica, 2018-02, Vol.135 (2), p.159-178

2018

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Deer Prion Proteins Modulate the Emergence and Adaptation of Chronic Wasting Disease Strains

Journal of virology, 2015-12, Vol.89 (24), p.12362-12373

2015

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The cellular prion protein does not affect tau seeding and spreading of sarkosyl-insoluble fractions from Alzheimer’s disease

Scientific reports, 2024-09, Vol.14 (1), p.21622-14

2024

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Intestinal M cells

Journal of biochemistry (Tokyo), 2016-02, Vol.159 (2), p.151-160

Ohno, Hiroshi

2016

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The prion protein as a receptor for amyloid-β

Nature (London), 2010-08, Vol.466 (7308), p.E3-E4

2010

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In Vitro Generation of Infectious Scrapie Prions

Cell, 2005-04, Vol.121 (2), p.195-206

2005

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The uptake of tau amyloid fibrils is facilitated by the cellular prion protein and hampers prion propagation in cultured cells

Journal of neurochemistry, 2020-12, Vol.155 (5), p.577-591

2020

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Recent advances in the histo‐molecular pathology of human prion disease

Brain pathology (Zurich, Switzerland), 2019-03, Vol.29 (2), p.278-300

2019

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Amyloid-β Receptors: The Good, the Bad, and the Prion Protein

Cryo-EM structure of an amyloid fibril formed by full-length human prion protein

The complex PrP(c)-Fyn couples human oligomeric Aβ with pathological tau changes in Alzheimer's disease

Cellular Prion Protein Conformational Shift after Liquid–Liquid Phase Separation Regulated by a Polymeric Antagonist and Mutations

α-synuclein interacts with PrP C to induce cognitive impairment through mGluR5 and NMDAR2B

An optimized Western blot assay provides a comprehensive assessment of the physiological endoproteolytic processing of the prion protein

Metabotropic Glutamate Receptor 5 Is a Coreceptor for Alzheimer Aβ Oligomer Bound to Cellular Prion Protein

Prion-Protein-interacting Amyloid-β Oligomers of High Molecular Weight Are Tightly Correlated with Memory Impairment in Multiple Alzheimer Mouse Models

Alzheimer amyloid-β oligomer bound to postsynaptic prion protein activates Fyn to impair neurons

Interaction between Human Prion Protein and Amyloid-β (Aβ) Oligomers: ROLE OF N-TERMINAL RESIDUES

General Model of Prion Strains and Their Pathogenicity

Divergent prion strain evolution driven by PrP C expression level in transgenic mice

Prion propagation and toxicity in vivo occur in two distinct mechanistic phases

A New Paradigm for Enzymatic Control of α-Cleavage and β-Cleavage of the Prion Protein

The cellular prion protein mediates neurotoxic signalling of β-sheet-rich conformers independent of prion replication

Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked

The function of the cellular prion protein in health and disease

Deer Prion Proteins Modulate the Emergence and Adaptation of Chronic Wasting Disease Strains

The cellular prion protein does not affect tau seeding and spreading of sarkosyl-insoluble fractions from Alzheimer’s disease

Intestinal M cells

The prion protein as a receptor for amyloid-β

In Vitro Generation of Infectious Scrapie Prions

The uptake of tau amyloid fibrils is facilitated by the cellular prion protein and hampers prion propagation in cultured cells

Recent advances in the histo‐molecular pathology of human prion disease

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