Artículos con órdenes de acceso público - Ian MackenzieMás información
TotalNIHCIHRMRCDFGNIHREuropean CommissionNHMRCSNSFFWOAlzheimers's UKWellcomeNSERCHelmholtzDoDGovernment of ItalySwedish Research CouncilMichael J Fox FoundationParkinson's UKMSFHRVAGenome CanadaGobierno de EspañaBrain Research, UKARCBMBFParkinson's Foundation, USACCSNSFHHMINSFCVolkswagen FoundationMotor Neurone Disease Association, UKFondazione CariploCZIUSEDFRQSAcademy of FinlandTelethonNWOKnut and Alice Wallenberg FoundationVersus Arthritis, UKDMTNational Centre for the Replacement, Refinement and Reduction of Animals in Research, UKARRSZonMwFNRRCNANRState of CalifoniaNMRCASAPHFSPGobierno de Argentina
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TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia
IRA Mackenzie, R Rademakers, M Neumann
The Lancet Neurology 9 (10), 995-1007, 2010
Órdenes: US National Institutes of Health, Canadian Institutes of Health Research
Phosphorylated TDP-43 in Alzheimer’s disease and dementia with Lewy bodies
T Arai, IRA Mackenzie, M Hasegawa, T Nonoka, K Niizato, K Tsuchiya, ...
Acta neuropathologica 117, 125-136, 2009
Órdenes: Canadian Institutes of Health Research
Quantitative analysis and clinico-pathological correlations of different dipeptide repeat protein pathologies in C9ORF72 mutation carriers
IRA Mackenzie, P Frick, FA Grässer, TF Gendron, L Petrucelli, ...
Acta neuropathologica 130, 845-861, 2015
Órdenes: Canadian Institutes of Health Research
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→ T (Arg493X) mutation: an international initiative
R Rademakers, M Baker, J Gass, J Adamson, ED Huey, P Momeni, ...
The Lancet Neurology 6 (10), 857-868, 2007
Órdenes: Research Foundation (Flanders)
The neuropathology associated with repeat expansions in the C9ORF72 gene
IRA Mackenzie, P Frick, M Neumann
Acta neuropathologica 127, 347-357, 2014
Órdenes: Canadian Institutes of Health Research
Distinct pathological subtypes of FTLD-FUS
IRA Mackenzie, DG Munoz, H Kusaka, O Yokota, K Ishihara, S Roeber, ...
Acta neuropathologica 121, 207-218, 2011
Órdenes: Canadian Institutes of Health Research
Synaptic dysfunction in progranulin-deficient mice
TL Petkau, SJ Neal, A Milnerwood, A Mew, AM Hill, P Orban, J Gregg, ...
Neurobiology of disease 45 (2), 711-722, 2012
Órdenes: Canadian Institutes of Health Research
Progranulin expression in the developing and adult murine brain
TL Petkau, SJ Neal, PC Orban, JL MacDonald, AM Hill, G Lu, ...
Journal of Comparative Neurology 518 (19), 3931-3947, 2010
Órdenes: Canadian Institutes of Health Research
neuropathology of non‐tau frontotemporal lobar degeneration
M Neumann, IRA Mackenzie
Neuropathology and applied neurobiology 45 (1), 19-40, 2019
Órdenes: Canadian Institutes of Health Research, German Research Foundation …
Reappraisal of TDP-43 pathology in FTLD-U subtypes
IR Mackenzie, M Neumann
Acta neuropathologica 134, 79-96, 2017
Órdenes: Canadian Institutes of Health Research, Helmholtz Association
Early dipeptide repeat pathology in a frontotemporal dementia kindred with C9ORF72 mutation and intellectual disability
M Proudfoot, NJ Gutowski, D Edbauer, DA Hilton, M Stephens, J Rankin, ...
Acta neuropathologica 127, 451-458, 2014
Órdenes: Canadian Institutes of Health Research
TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD
S Roeber, IRA Mackenzie, HA Kretzschmar, M Neumann
Acta neuropathologica 116, 147-157, 2008
Órdenes: Canadian Institutes of Health Research
The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments
IRA Mackenzie, R Rademakers
Neurogenetics 8, 237-248, 2007
Órdenes: Research Foundation (Flanders)
eEF2K inhibition blocks Aβ42 neurotoxicity by promoting an NRF2 antioxidant response
A Jan, B Jansonius, A Delaidelli, SP Somasekharan, F Bhanshali, ...
Acta Neuropathologica 133, 101-119, 2017
Órdenes: US National Institutes of Health, Canadian Cancer Society, Canadian …
Subcortical TDP-43 pathology patterns validate cortical FTLD-TDP subtypes and demonstrate unique aspects of C9orf72 mutation cases
IR Mackenzie, M Neumann
Acta neuropathologica 139 (1), 83-98, 2020
Órdenes: Canadian Institutes of Health Research, Helmholtz Association
A novel double mutation in FUS gene causing sporadic ALS
J Robertson, J Bilbao, L Zinman, LN Hazrati, S Tokuhiro, C Sato, ...
Neurobiology of aging 32 (3), 553. e27-553. e30, 2011
Órdenes: Canadian Institutes of Health Research
Accumulation of TMEM106B C-terminal fragments in neurodegenerative disease and aging
J Perneel, M Neumann, B Heeman, S Cheung, M Van den Broeck, ...
Acta neuropathologica 145 (3), 285-302, 2023
Órdenes: US National Institutes of Health, Research Foundation (Flanders), Canadian …
TDP-43 pathology in primary lateral sclerosis
IRA Mackenzie, H Briemberg
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 21 (sup1), 52-58, 2020
Órdenes: Canadian Institutes of Health Research
Drusen in the peripheral retina of the Alzheimer's eye
K Ukalovic, S Cao, S Lee, Q Tang, MF Beg, MV Sarunic, GYR Hsiung, ...
Current Alzheimer Research 15 (8), 743-750, 2018
Órdenes: Canadian Institutes of Health Research, Genome Canada, Michael Smith …
Multiple brain pathologies in dementia are common
M Woodward, IRA Mackenzie, GYR Hsiung, C Jacova, H Feldman
European Geriatric Medicine 1 (5), 259-265, 2010
Órdenes: Canadian Institutes of Health Research
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