关注
Simon Parson
Simon Parson
未知所在单位机构
在 abdn.ac.uk 的电子邮件经过验证
标题
引用次数
引用次数
年份
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
3552001
Synaptic vulnerability in neurodegenerative disease
TM Wishart, SH Parson, TH Gillingwater
Journal of Neuropathology & Experimental Neurology 65 (8), 733-739, 2006
2482006
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
2432005
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
2022014
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
1362010
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
1312010
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
1252011
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
1112020
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
1022019
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
922016
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
922016
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
842013
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
692012
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
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
532004
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
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
482016
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