Andrew J. Nicoll

London, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 14 publications

Two mouse models of Alzheimer's disease accumulate amyloid at different rates and have distinct Aβ oligomer profiles unaltered by ablation of cellular prion protein.

Two mouse models of Alzheimer's disease accumulate amyloid at different rates and have distinct Aβ oligomer profiles unaltered by ablation of cellular prion protein.

Journal: PloS one

Published: June 05, 2023

Reply to: Intrinsic Toxicity of Antibodies to the Globular Domain of the Prion Protein.

Reply to: Intrinsic Toxicity of Antibodies to the Globular Domain of the Prion Protein.

Journal: Biological psychiatry

Published: March 29, 2018

G-quadruplex-binding small molecules ameliorate C9orf72 FTD/ALS pathology in vitro and in vivo.

G-quadruplex-binding small molecules ameliorate C9orf72 FTD/ALS pathology in vitro and in vivo.

Journal: EMBO molecular medicine

Published: November 09, 2017

Soluble Aβ aggregates can inhibit prion propagation.

Soluble Aβ aggregates can inhibit prion propagation.

Journal: Open biology

Published: June 28, 2017

Prion Protein as a Toxic Acceptor of Amyloid-β Oligomers.

Prion Protein as a Toxic Acceptor of Amyloid-β Oligomers.

Journal: Biological psychiatry

Published: May 31, 2017

Erratum: Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy.

Erratum: Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy.

Journal: Nature

Published: September 17, 2015

Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy.

Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy.

Journal: Nature

Published: April 26, 2015

Identification of a Compound That Disrupts Binding of Amyloid-β to the Prion Protein Using a Novel Fluorescence-based Assay.

Identification of a Compound That Disrupts Binding of Amyloid-β to the Prion Protein Using a Novel Fluorescence-based Assay.

Journal: The Journal of biological chemistry

Published: January 13, 2015

C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins.

C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins.

Journal: Science (New York, N.Y.)

Published: August 09, 2014

N-terminal domain of prion protein directs its oligomeric association.

N-terminal domain of prion protein directs its oligomeric association.

Journal: The Journal of biological chemistry

Published: July 31, 2014

Peripheral administration of a humanized anti-PrP antibody blocks Alzheimer's disease Aβ synaptotoxicity.

Peripheral administration of a humanized anti-PrP antibody blocks Alzheimer's disease Aβ synaptotoxicity.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience

Published: May 03, 2014

mGlu5 receptors and cellular prion protein mediate amyloid-β-facilitated synaptic long-term depression in vivo.

mGlu5 receptors and cellular prion protein mediate amyloid-β-facilitated synaptic long-term depression in vivo.

Journal: Nature communications

Published: October 02, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026