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Simon Parson
Simon Parson
Unknown affiliation
Verified email at abdn.ac.uk
Title
Cited by
Cited by
Year
Neuronal P2X7 receptors are targeted to presynaptic terminals in the central and peripheral nervous systems
SA Deuchars, L Atkinson, RE Brooke, H Musa, CJ Milligan, TFC Batten, ...
Journal of Neuroscience 21 (18), 7143-7152, 2001
3522001
Computer three-dimensional reconstruction of the sinoatrial node
H Dobrzynski, J Li, J Tellez, ID Greener, VP Nikolski, SE Wright, ...
Circulation 111 (7), 846-854, 2005
2392005
Synaptic vulnerability in neurodegenerative disease
TM Wishart, SH Parson, TH Gillingwater
Journal of Neuropathology & Experimental Neurology 65 (8), 733-739, 2006
2362006
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
1992014
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
1342010
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, 2010
1282010
Reversible molecular pathology of skeletal muscle in spinal muscular atrophy
CA Mutsaers, TM Wishart, DJ Lamont, M Riessland, J Schreml, ...
Human molecular genetics 20 (22), 4334-4344, 2011
1232011
COVID‐19 and anatomy: Stimulus and initial response
C Brassett, T Cosker, DC Davies, P Dockery, TH Gillingwater, TC Lee, ...
Journal of anatomy 237 (3), 393-403, 2020
1052020
Abnormal fatty acid metabolism is a core component of spinal muscular atrophy
MO Deguise, G Baranello, C Mastella, A Beauvais, J Michaud, A Leone, ...
Annals of clinical and translational neurology 6 (8), 1519-1532, 2019
952019
Vascular D efects and S pinal C ord H ypoxia in S pinal M uscular A trophy
E Somers, RD Lees, K Hoban, JN Sleigh, H Zhou, F Muntoni, K Talbot, ...
Annals of neurology 79 (2), 217-230, 2016
912016
Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophy
RA Powis, E Karyka, P Boyd, J Côme, RA Jones, Y Zheng, E Szunyogova, ...
JCI insight 1 (11), 2016
892016
Survival Motor Neuron (SMN) protein is required for normal mouse liver development
E Szunyogova, H Zhou, GK Maxwell, RA Powis, F Muntoni, ...
Scientific reports 6 (1), 34635, 2016
842016
Severe SMA mice show organ impairment that cannot be rescued by therapy with the HDACi JNJ-26481585
J Schreml, M Riessland, M Paterno, L Garbes, K Roßbach, B Ackermann, ...
European Journal of Human Genetics 21 (6), 643-652, 2013
792013
Density, calibre and ramification of muscle capillaries are altered in a mouse model of severe spinal muscular atrophy
E Somers, Z Stencel, TM Wishart, TH Gillingwater, SH Parson
Neuromuscular Disorders 22 (5), 435-442, 2012
712012
Development of a supported self‐directed learning approach for anatomy education
GS Findlater, F Kristmundsdottir, SH Parson, TH Gillingwater
Anatomical sciences education 5 (2), 114-121, 2012
672012
Survival of motor neurone protein is required for normal postnatal development of the spleen
AK Thomson, E Somers, RA Powis, HK Shorrock, K Murphy, KJ Swoboda, ...
Journal of Anatomy 230 (2), 337-346, 2017
632017
Morphological characteristics of motor neurons do not determine their relative susceptibility to degeneration in a mouse model of severe spinal muscular atrophy
SR Thomson, JE Nahon, CA Mutsaers, D Thomson, G Hamilton, ...
PloS one 7 (12), e52605, 2012
522012
Properties of presynaptic P2X7-like receptors at the neuromuscular junction
TS Moores, B Hasdemir, L Vega-Riveroll, J Deuchars, SH Parson
Brain research 1034 (1-2), 40-50, 2005
522005
Kv3 voltage‐gated potassium channels regulate neurotransmitter release from mouse motor nerve terminals
RE Brooke, TS Moores, NP Morris, SH Parson, J Deuchars
European Journal of Neuroscience 20 (12), 3313-3321, 2004
522004
Histopathological defects in intestine in severe spinal muscular atrophy mice are improved by systemic antisense oligonucleotide treatment
P Sintusek, F Catapano, N Angkathunkayul, E Marrosu, SH Parson, ...
PLoS One 11 (5), e0155032, 2016
462016
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