Thomas Gillingwater
Thomas Gillingwater
Professor of Anatomy, University of Edinburgh
Verified email at - Homepage
Cited by
Cited by
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis
AL Nishimura, M Mitne-Neto, HCA Silva, A Richieri-Costa, S Middleton, ...
The American Journal of Human Genetics 75 (5), 822-831, 2004
Wallerian degeneration of injured axons and synapses is delayed by a Ube4b/Nmnat chimeric gene
TGA Mack
nature neuroscience 4 (12), 1199-1206, 2001
Selective vulnerability of motor neurons and dissociation of pre-and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy
LM Murray, LH Comley, D Thomson, N Parkinson, K Talbot, ...
Human molecular genetics 17 (7), 949-962, 2008
Total protein analysis as a reliable loading control for quantitative fluorescent Western blotting
SL Eaton, SL Roche, M Llavero Hurtado, KJ Oldknow, C Farquharson, ...
PloS one 8 (8), e72457, 2013
Spinal muscular atrophy: going beyond the motor neuron
G Hamilton, TH Gillingwater
Trends in molecular medicine, 2013
Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy
D Bäumer, S Lee, G Nicholson, JL Davies, NJ Parkinson, LM Murray, ...
PLoS genetics 5 (12), e1000773, 2009
Emerging therapies and challenges in spinal muscular atrophy
MA Farrar, SB Park, S Vucic, KA Carey, BJ Turner, TH Gillingwater, ...
Annals of neurology 81 (3), 355-368, 2017
Synaptic vulnerability in neurodegenerative disease
TM Wishart, SH Parson, TH Gillingwater
Journal of Neuropathology & Experimental Neurology 65 (8), 733-739, 2006
Advances in therapy for spinal muscular atrophy: promises and challenges
EJN Groen, K Talbot, TH Gillingwater
Nature Reviews Neurology 14 (4), 214-224, 2018
Cellular and molecular anatomy of the human neuromuscular junction
RA Jones, C Harrison, SL Eaton, ML Hurtado, LC Graham, L Alkhammash, ...
Cell reports 21 (9), 2348-2356, 2017
Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy
TM Wishart, CA Mutsaers, M Riessland, MM Reimer, G Hunter, ...
The Journal of clinical investigation 124 (4), 1821-1834, 2014
Progressive abnormalities in skeletal muscle and neuromuscular junctions of transgenic mice expressing the Huntington's disease mutation
RR Ribchester, D Thomson, NI Wood, T Hinks, TH Gillingwater, ...
European Journal of Neuroscience 20 (11), 3092-3114, 2004
VAPB interacts with and modulates the activity of ATF6
C Gkogkas, S Middleton, AM Kremer, C Wardrope, M Hannah, ...
Human molecular genetics 17 (11), 1517-1526, 2008
WldS prevents axon degeneration through increased mitochondrial flux and enhanced mitochondrial Ca2+ buffering
MA Avery, TM Rooney, JD Pandya, TM Wishart, TH Gillingwater, ...
Current Biology 22 (7), 596-600, 2012
The role of survival motor neuron protein (SMN) in protein homeostasis
H Chaytow, YT Huang, TH Gillingwater, KME Faller
Cellular and Molecular Life Sciences 75, 3877-3894, 2018
Neuromuscular synaptic vulnerability in motor neurone disease: amyotrophic lateral sclerosis and spinal muscular atrophy
LM Murray, K Talbot, TH Gillingwater
Neuropathology and applied neurobiology 36 (2), 133-156, 2010
The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy
JN Sleigh, TH Gillingwater, K Talbot
Disease models & mechanisms 4 (4), 457-467, 2011
Transcriptional regulation of the AP-1 and Nrf2 target gene sulfiredoxin
FX Soriano, P Baxter, LM Murray, MB Sporn, TH Gillingwater, ...
Molecules and cells 27, 279-282, 2009
UBA1: at the crossroads of ubiquitin homeostasis and neurodegeneration
EJN Groen, TH Gillingwater
Trends in molecular medicine 21 (10), 622-632, 2015
The slow Wallerian degeneration gene, WldS, inhibits axonal spheroid pathology in gracile axonal dystrophy mice
W Mi, B Beirowski, TH Gillingwater, R Adalbert, D Wagner, D Grumme, ...
Brain 128 (2), 405-416, 2005
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