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Jakub Scaber
Jakub Scaber
Verified email at ndcn.ox.ac.uk
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Cited by
Year
C9orf72 Hexanucleotide Expansions Are Associated with Altered Endoplasmic Reticulum Calcium Homeostasis and Stress Granule Formation in Induced …
R Dafinca, J Scaber, N Ababneh, T Lalic, G Weir, H Christian, J Vowles, ...
Stem cells 34 (8), 2063-2078, 2016
2342016
C9orf72 and RAB7L1 regulate vesicle trafficking in amyotrophic lateral sclerosis and frontotemporal dementia
Y Aoki, R Manzano, Y Lee, R Dafinca, M Aoki, AGL Douglas, MA Varela, ...
Brain 140 (4), 887-897, 2017
1692017
The diagnostic pathway and prognosis in bulbar-onset amyotrophic lateral sclerosis
MR Turner, J Scaber, JA Goodfellow, ME Lord, R Marsden, K Talbot
Journal of the neurological sciences 294 (1-2), 81-85, 2010
1262010
Impairment of mitochondrial calcium buffering links mutations in C9ORF72 and TARDBP in iPS-derived motor neurons from patients with ALS/FTD
R Dafinca, P Barbagallo, L Farrimond, A Candalija, J Scaber, AA Nida'a, ...
Stem Cell Reports 14 (5), 892-908, 2020
972020
Pattern of spread and prognosis in lower limb-onset ALS
MR Turner, A Brockington, J Scaber, H Hollinger, R Marsden, PJ Shaw, ...
Amyotrophic Lateral Sclerosis 11 (4), 369-373, 2010
822010
TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy
BJ Turner, D Bäumer, NJ Parkinson, J Scaber, O Ansorge, K Talbot
BMC neuroscience 9, 1-11, 2008
762008
Group A streptococcal infections during the seasonal influenza outbreak 2010/11 in South East England
J Scaber, S Saeed, C Ihekweazu, A Efstratiou, N McCarthy, É O’Moore
Euro Surveill 16 (5), 2011
612011
Single-copy expression of an amyotrophic lateral sclerosis-linked TDP-43 mutation (M337V) in BAC transgenic mice leads to altered stress granule dynamics and progressive motor …
D Gordon, R Dafinca, J Scaber, J Alegre-Abarrategui, L Farrimond, ...
Neurobiology of disease 121, 148-162, 2019
602019
Correction of amyotrophic lateral sclerosis related phenotypes in induced pluripotent stem cell-derived motor neurons carrying a hexanucleotide expansion mutation in C9orf72 by …
NA Ababneh, J Scaber, R Flynn, A Douglas, P Barbagallo, A Candalija, ...
Human molecular genetics 29 (13), 2200-2217, 2020
462020
Human stem cell models of neurodegeneration: From basic science of amyotrophic lateral sclerosis to clinical translation
E Giacomelli, BF Vahsen, EL Calder, Y Xu, J Scaber, E Gray, R Dafinca, ...
Cell Stem Cell 29 (1), 11-35, 2022
452022
Multicentre appraisal of amyotrophic lateral sclerosis biofluid biomarkers shows primacy of blood neurofilament light chain
AG Thompson, E Gray, N Verber, Y Bobeva, V Lombardi, SR Shepheard, ...
Brain communications 4 (1), fcac029, 2022
382022
Amyotrophic lateral sclerosis: the complex path to precision medicine
K Talbot, E Feneberg, J Scaber, AG Thompson, MR Turner
Journal of neurology 265, 2454-2462, 2018
382018
Embryonic progenitor pools generate diversity in fine-scale excitatory cortical subnetworks
TJ Ellender, SV Avery, K Mahfooz, J Scaber, A von Klemperer, SL Nixon, ...
Nature Communications 10 (1), 5224, 2019
302019
CGAT-core: a python framework for building scalable, reproducible computational biology workflows
AP Cribbs, S Luna-Valero, C George, IM Sudbery, AJ Berlanga-Taylor, ...
bioRxiv, 581009, 2019
292019
Genetic testing in motor neurone disease
T Dharmadasa, J Scaber, E Edmond, R Marsden, A Thompson, K Talbot, ...
Practical Neurology 22 (2), 107-116, 2022
222022
Initial identification of a blood-based chromosome conformation signature for aiding in the diagnosis of amyotrophic lateral sclerosis
M Salter, E Corfield, A Ramadass, F Grand, J Green, J Westra, CR Lim, ...
EBioMedicine 33, 169-184, 2018
212018
What is the role of TDP-43 in C9orf72-related amyotrophic lateral sclerosis and frontemporal dementia?
J Scaber, K Talbot
Brain 139 (12), 3057-3059, 2016
112016
Human iPSC co-culture model to investigate the interaction between microglia and motor neurons
BF Vahsen, E Gray, A Candalija, KML Cramb, J Scaber, R Dafinca, ...
Scientific Reports 12 (1), 12606, 2022
102022
Modelling amyotrophic lateral sclerosis (ALS) using mutant and CAS9/CRISPR-corrected motor neurons from patients with C9ORF72 mutations reveals disease-specific cellular phenotypes
R Mutihac, N Ababneh, J Scaber, R Wade-Martins, S Cowley, K Talbot
Journal of the Neurological Sciences 357, e48, 2015
62015
C9orf72-ALS human iPSC microglia are pro-inflammatory and toxic to co-cultured motor neurons via MMP9
BF Vahsen, S Nalluru, GR Morgan, L Farrimond, E Carroll, Y Xu, ...
Nature Communications 14 (1), 5898, 2023
22023
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