Accumulation of cellular prion protein within β‐amyloid oligomer plaques in aged human brains-Reference-Cited by-同舟云学术

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Accumulation of cellular prion protein within β‐amyloid oligomer plaques in aged human brains

Published:2021-02-23 Issue:5 Volume:31 Page:
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:Brain Pathology

Author:

Takahashi Reisuke H.¹²^ORCID,Yokotsuka Mayumi¹,Tobiume Minoru²,Sato Yuko²,Hasegawa Hideki²,Nagao Toshitaka¹,Gouras Gunnar K.³

Affiliation:

1. Department of Anatomic Pathology Tokyo Medical University Tokyo Japan

2. Department of Pathology National Institute of Infectious Diseases Tokyo Japan

3. Experimental Dementia Research Unit Department of Experimental Medical Science Lund University Lund Sweden

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bpa.12941

Reference60 articles.

1. Pre-plaque conformational changes in Alzheimer’s disease-linked Aβ and APP

2. A specific amyloid-β protein assembly in the brain impairs memory

3. Soluble Amyloid β Peptide Concentration as a Predictor of Synaptic Change in Alzheimer's Disease

4. Soluble fibrillar oligomer levels are elevated in Alzheimer's disease brain and correlate with cognitive dysfunction

5. Aβ oligomers trigger and accelerate Aβ seeding

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2. Cleavage site-directed antibodies reveal the prion protein in humans is shed by ADAM10 at Y226 and associates with misfolded protein deposits in neurodegenerative diseases;Acta Neuropathologica;2024-07-09

3. Cannabinoids: Potential for Modulation and Enhancement When Combined with Vitamin B12 in Case of Neurodegenerative Disorders;Pharmaceuticals;2024-06-20

4. Involvement of the cellular prion protein in seeding and spreading of sarkosyl-derived fractions of Alzheimer’s disease inPrnpmutant mice and in the P301S transgenic tauopathy mice model;2024-01-20

5. Cleavage site-directed antibodies reveal the prion protein in humans is shed by ADAM10 at Y226 and associates with misfolded protein deposits in neurodegenerative diseases;2023-12-01

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