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Brain Communications|May 12, 2026
Methodology for human-induced pluripotent stem cell-derived excitatory and inhibitory neuron coculture with astrocytes for Alzheimer's disease modellingJialin Li, Lucy E Brown, Naiomi Rambarack, et al.
Nature Communications|May 17, 2012
Activin induces cortical interneuron identity and differentiation in embryonic stem cell-derived telencephalic neural precursorsSerafí Cambray, Charles Arber, Graham Little, et al.
Neurochemistry International|May 18, 2021
Abrogation of LRRK2 dependent Rab10 phosphorylation with TLR4 activation and alterations in evoked cytokine release in immune cellsIqra Nazish, Charles Arber, Thomas M Piers, et al.
Development (Cambridge, England)|September 2, 2011
Temporally controlled modulation of FGF/ERK signaling directs midbrain dopaminergic neural progenitor fate in mouse and human pluripotent stem cellsInes Jaeger, Charles Arber, Jessica R Risner-Janiczek, et al.
Brain Communications|May 13, 2020
Amyloid precursor protein processing in human neurons with an allelic series of the PSEN1 intron 4 deletion mutation and total presenilin-1 knockoutCharles Arber, Claudio Villegas-Llerena, Jamie Toombs, et al.
Brain Research|July 29, 2018
Analysis of macroautophagy related proteins in G2019S LRRK2 Parkinson's disease brains with Lewy body pathologyAdamantios Mamais, Claudia Manzoni, Iqra Nazish, et al.
The Journal of Biological Chemistry|April 1, 2017
Mutations in valosin-containing protein (VCP) decrease ADP/ATP translocation across the mitochondrial membrane and impair energy metabolism in human neuronsMarthe H R Ludtmann, Charles Arber, Fernando Bartolome, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|May 22, 2018
Amyloid β peptides are differentially vulnerable to preanalytical surface exposure, an effect incompletely mitigated by the use of ratiosJamie Toombs, Martha S Foiani, Henrietta Wellington, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 8, 2018
Susceptibility of brain atrophy to TRIB3 in Alzheimer's disease, evidence from functional prioritization in imaging geneticsMarco Lorenzi, Andre Altmann, Boris Gutman, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 2, 2024
The presenilin 1 mutation P436S causes familial Alzheimer's disease with elevated Aβ43 and atypical clinical manifestationsCharles Arber, Christopher R S Belder, Filip Tomczuk, et al.
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