Parson, Simon 照片

Parson, Simon

Prof

所属大学: University of Aberdeen

所属学院: School of Medicine, Medical Sciences and Nutrition

邮箱:
simon.parson@abdn.ac.uk

个人主页:
http://www.abdn.ac.uk/ims/profiles/simon.parson/

个人简介

BSc Zoology, University of Durham, 1987 PhD Neuroscience, University of Edinburgh, 1990 Lecturer in Anatomy, University of Leeds, 1995 Senior Lecturer in Anatomy, University of Edinburgh, 2006 Professor of Anatomy, University of Aberdeen, 2013

研究领域

The Neuromuscular Junction Neurodegenerative diseases of the neuromuscular system Spinal Muscular Atrophy

近期论文

Thomson, AK., Somers, E., Powis, RA., Shorrock, HK., Murphy, K., Swoboda, KJ., Gillingwater, TH. & Parson, SH. (2017). 'Survival of motor neurone protein is required for normal postnatal development of the spleen'. Journal of Anatomy, vol 230, no. 2, pp. 337–346. DOI: [ONLINE] DOI: 10.1111/JOA.12546 Szunyogova, E., Zhou, H., Maxwell, GK., Powis, RA., Muntoni, F., Gillingwater, TH. & Parson, SH. (2016). 'Survival Motor Neuron (SMN) protein is required for normal mouse liver development'. Scientific Reports, vol 6, 34635. DOI: [ONLINE] DOI: 10.1038/SREP3463510.1038/SREP35898 [ONLINE] AURA: SREP34635.PDF Powis, RA., Karyka, E., Boyd, P., Come, J., Jones, RA., Zheng, Y., Szunyogova, E., Groen, EJN., Hunter, G., Thomson, D., Wishart, TM., Becker, CG., Parson, SH., Martinat, C., Azzouz, M. & Gillingwater, TH. (2016). 'Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophy'. JCI Insight, vol 1, no. 11, e87908. DOI: [ONLINE] DOI: 10.1172/JCI.INSIGHT.87908. [ONLINE] AURA: JCI_INSIGHT87908.PDF Sintusek, P., Catapano, F., Angkathunkayul, N., Marrosu, E., Parson, SH., Morgan, JE., Muntoni, F. & Zhou, H. (2016). 'Histopathological Defects in Intestine in Severe Spinal Muscular Atrophy Mice Are Improved by Systemic Antisense Oligonucleotide Treatment'. PLoS ONE, vol 11, no. 5, 0155032. DOI: [ONLINE] DOI: 10.1371/JOURNAL.PONE.0155032 [ONLINE] AURA: JOURNAL.PONE.0155032.PDF Ezzat, A., Parson, S. & Dynes, K. (2016). 'Evolving student–faculty partnerships in medical education through peer-assisted learning'. Medical Education, vol 50, no. 5, pp. 568. DOI: [ONLINE] DOI: 10.1111/MEDU.13015 Somers, E., Lees, RD., Hoban, KH., Sleigh, JN., Zhou, H., Muntoni, F., Talbot, K., Gillingwater, TH. & Parson, SH. (2016). 'Vascular defects and spinal cord hypoxia in spinal muscular atrophy'. Annals of Neurology, vol 79, no. 2, pp. 217-230. DOI: [ONLINE] DOI: 10.1002/ANA.24549 [ONLINE] AURA: REVISED_FINAL_SOMERS_ETAL_ANNNEUROL_RESUBMITTED_3.PDF [ONLINE] AURA: FIGURES_COMBINED.PDF Good, DW., Khan, A., Hammer, S., Scanlan, P., Shu, W., Phipps, S., Parson, SH., Stewart, GD., Reuben, R. & McNeill, SA. (2014). 'Tissue quality assessment using a novel direct elasticity assessment device (the E-finger): a cadaveric study of prostatectomy dissection'. PloS one, vol 9, no. 11, e112872. DOI: [ONLINE] DOI: 10.1371/JOURNAL.PONE.0112872 [ONLINE] AURA: JOURNAL.PONE.0112872.PDF Wishart, TM., Mutsaers, CA., Riessland, M., Reimer, MM., Hunter, G., Hannam, ML., Eaton, SL., Fuller, HR., Roche, SL., Somers, E., Morse, R., Young, PJ., Lamont, DJ., Hammerschmidt, M., Joshi, A., Hohenstein, P., Morris, GE., Parson, SH., Skehel, PA., Becker, T., Robinson, IM., Becker, CG., Wirth, B. & Gillingwater, TH. (2014). 'Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy'. The Journal of Clinical Investigation, vol 124, no. 4, pp. 1821-1834. DOI: [ONLINE] DOI: 10.1172/JCI71318 [ONLINE] AURA: DYSREGULATION_OF_UBIQUITIN_HOMEOSTASIS_AND_CATENIN_SIGNALING... Parson, SH. (2014). 'The singular qualities of motor neurones in health and disease'. Journal of Anatomy, vol 224, no. 1, pp. 1-2. DOI: [ONLINE] DOI: 10.1111/JOA.12110 Somers, E., Riessland, M., Schreml, J., Wirth, B., Gillingwater, TH. & Parson, SH. (2013). 'Increasing SMN levels using the histone deacetylase inhibitor SAHA ameliorates defects in skeletal muscle microvasculature in a mouse model of severe spinal muscular atrophy'. Neuroscience Letters, vol 544, pp. 100-104. DOI: [ONLINE] DOI: 10.1016/J.NEULET.2013.03.052