Thomas Gillingwater
Thomas Gillingwater
Professor of Anatomy, University of Edinburgh
Verified email at ed.ac.uk - Homepage
TitleCited byYear
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
8912004
Wallerian degeneration of injured axons and synapses is delayed by a Ube4b/Nmnat chimeric gene
TGA Mack
nature neuroscience 4 (12), 1199-1206, 2001
525*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, 2007
3192007
Spinal muscular atrophy: going beyond the motor neuron
G Hamilton, TH Gillingwater
Trends in molecular medicine, 2013
2282013
Total protein analysis as a reliable loading control for quantitative fluorescent Western blotting
SL Eaton, SL Roche, ML Hurtado, KJ Oldknow, C Farquharson, ...
PloS one 8 (8), e72457, 2013
2242013
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
2202009
Synaptic vulnerability in neurodegenerative disease
TM Wishart, SH Parson, TH Gillingwater
Journal of Neuropathology & Experimental Neurology 65 (8), 733-739, 2006
1642006
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
1482004
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
1282008
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
1262012
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
1172014
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
1162005
Compartmental neurodegeneration and synaptic plasticity in the Wlds mutant mouse
TH Gillingwater, RR Ribchester
The Journal of physiology 534 (3), 627-639, 2001
1152001
Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy
LM Murray, S Lee, D Bäumer, SH Parson, K Talbot, TH Gillingwater
Human molecular genetics 19 (3), 420-433, 2009
1112009
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
1092010
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 (3), 279-282, 2009
1082009
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
1002011
Differential proteomics analysis of synaptic proteins identifies potential cellular targets and protein mediators of synaptic neuroprotection conferred by the slow Wallerian …
TM Wishart, JM Paterson, DM Short, S Meredith, KA Robertson, ...
Molecular & Cellular Proteomics 6 (8), 1318-1330, 2007
912007
SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy
TM Wishart, JPW Huang, LM Murray, DJ Lamont, CA Mutsaers, J Ross, ...
Human molecular genetics 19 (21), 4216-4228, 2010
902010
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
892017
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