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Simon Parson - Publications

Affiliations: 
University of Aberdeen, Aberdeen, Scotland, United Kingdom 
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37 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Zhou H, Hong Y, Scoto M, Thomson A, Pead E, MacGillivray T, Hernandez-Gerez E, Catapano F, Meng J, Zhang Q, Hunter G, Shorrock HK, Ng TK, Hamida A, Sanson M, ... ... Parson SH, et al. Microvasculopathy in SMA is driven by a reversible autonomous endothelial cell defect. The Journal of Clinical Investigation. PMID 36099045 DOI: 10.1172/JCI153430  0.555
2022 Gillingwater TH, McWilliam C, Horrocks I, McWilliam K, Hamilton M, Fletcher E, Williams N, Smith S, Parson SH. A call to introduce newborn screening for spinal muscular atrophy (SMA) in Scotland. Scottish Medical Journal. 369330221078994. PMID 35147460 DOI: 10.1177/00369330221078994  0.494
2021 Quondamatteo F, Corzo-Leon DE, Brassett C, Colquhoun I, Davies DC, Dockery P, Grenham S, Guild S, Hunter A, Jones J, Lee TC, Tracey C, Wilkinson T, Munro CA, Gillingwater TH, ... Parson SH, et al. Neutralisation of SARS-CoV-2 by anatomical embalming solutions. Journal of Anatomy. PMID 34633083 DOI: 10.1111/joa.13549  0.436
2021 Deguise MO, Pileggi C, De Repentigny Y, Beauvais A, Tierney A, Chehade L, Michaud J, Llavero-Hurtado M, Lamont D, Atrih A, Wishart TM, Gillingwater TH, Schneider BL, Harper ME, Parson SH, et al. SMN depleted mice offer a robust and rapid onset model of non-alcoholic fatty liver disease. Cellular and Molecular Gastroenterology and Hepatology. PMID 33545428 DOI: 10.1016/j.jcmgh.2021.01.019  0.673
2020 Brassett C, Cosker T, Davies DC, Dockery P, Gillingwater TH, Lee TC, Milz S, Parson SH, Quondamatteo F, Wilkinson T. COVID-19 and anatomy: Stimulus and initial response. Journal of Anatomy. PMID 32628795 DOI: 10.1111/joa.13274  0.447
2020 Allardyce H, Kuhn D, Hernandez-Gerez E, Hensel N, Huang YT, Faller K, Gillingwater TH, Quondamatteo F, Claus P, Parson SH. Renal pathology in a mouse model of severe Spinal Muscular Atrophy is associated with downregulation of Glial Cell-Line Derived Neurotrophic Factor (GDNF). Human Molecular Genetics. PMID 32588893 DOI: 10.1093/hmg/ddaa126  0.589
2019 Deguise MO, Baranello G, Mastella C, Beauvais A, Michaud J, Leone A, De Amicis R, Battezzati A, Dunham C, Selby K, Warman Chardon J, McMillan HJ, Huang YT, Courtney NL, Mole AJ, ... ... Parson SH, et al. Abnormal fatty acid metabolism is a core component of spinal muscular atrophy. Annals of Clinical and Translational Neurology. 6: 1519-1532. PMID 31402618 DOI: 10.1002/Acn3.50855  0.582
2019 Šoltić D, Shorrock HK, Allardyce H, Wilson EL, Holt I, Synowsky SA, Shirran SL, Parson SH, Gillingwater TH, Fuller HR. Lamin A/C dysregulation contributes to cardiac pathology in a mouse model of severe spinal muscular atrophy. Human Molecular Genetics. PMID 31397869 DOI: 10.1093/hmg/ddz195  0.551
2018 Fergusson SJ, Aka JJ, Hennessy CM, Wilson AJ, Parson SH, Harrison EM, Finn GM, Gillingwater TH. Examining the impact of audience response systems on student performance in anatomy education: a randomised controlled trial. Scottish Medical Journal. 36933017741409. PMID 29911503 DOI: 10.1177/0036933017741409  0.448
2018 Maxwell GK, Szunyogova E, Shorrock HK, Gillingwater TH, Parson SH. Developmental and degenerative cardiac defects in the Taiwanese mouse model of severe spinal muscular atrophy. Journal of Anatomy. PMID 29473159 DOI: 10.1111/joa.12793  0.548
2017 Zhou H, Hong Y, Scoto M, Catapano F, Aguti S, Parson S, Brogan P, Muntoni F. Microvascular defects secondary to SMN deficiency in spinal muscular atrophy Neuromuscular Disorders. 27. DOI: 10.1016/S0960-8966(17)30305-X  0.326
2016 Szunyogova E, Zhou H, Maxwell GK, Powis RA, Muntoni F, Gillingwater TH, Parson SH. Corrigendum: Survival Motor Neuron (SMN) protein is required for normal mouse liver development. Scientific Reports. 6: 35898. PMID 27830828 DOI: 10.1038/srep35898  0.584
2016 Thomson AK, Somers E, Powis RA, Shorrock HK, Murphy K, Swoboda KJ, Gillingwater TH, Parson SH. Survival of motor neurone protein is required for normal postnatal development of the spleen. Journal of Anatomy. PMID 27726134 DOI: 10.1111/joa.12546  0.615
2016 Powis RA, Karyka E, Boyd P, Côme J, Jones RA, Zheng Y, Szunyogova E, Groen EJ, Hunter G, Thomson D, Wishart TM, Becker CG, Parson SH, Martinat C, Azzouz M, et al. Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophy. Jci Insight. 1: e87908. PMID 27699224 DOI: 10.1172/jci.insight.87908  0.736
2016 Szunyogova E, Zhou H, Maxwell GK, Powis RA, Francesco M, Gillingwater TH, Parson SH. Survival Motor Neuron (SMN) protein is required for normal mouse liver development. Scientific Reports. 6: 34635. PMID 27698380 DOI: 10.1038/srep34635  0.553
2016 Sintusek P, Catapano F, Angkathunkayul N, Marrosu E, Parson SH, Morgan JE, Muntoni F, Zhou H. Histopathological Defects in Intestine in Severe Spinal Muscular Atrophy Mice Are Improved by Systemic Antisense Oligonucleotide Treatment. Plos One. 11: e0155032. PMID 27163330 DOI: 10.1371/journal.pone.0155032  0.352
2016 Scoto M, Zhou H, Thompson D, Howell K, Hong Y, Imbrigiotta N, Parson S, Brogan P, Muntoni F. Exploring the microvascular abnormalities in a cohort of paediatric patients with spinal muscular atrophy Neuromuscular Disorders. 26. DOI: 10.1016/J.Nmd.2016.06.073  0.308
2015 Somers E, Lees RD, Hoban K, Sleigh JN, Zhou H, Muntoni F, Talbot K, Gillingwater TH, Parson SH. Vascular defects and spinal cord hypoxia in spinal muscular atrophy. Annals of Neurology. PMID 26506088 DOI: 10.1002/Ana.24549  0.588
2014 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, ... ... Parson SH, et al. Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy. The Journal of Clinical Investigation. 124: 1821-34. PMID 24590288 DOI: 10.1172/Jci71318  0.716
2013 Somers E, Riessland M, Schreml J, Wirth B, Gillingwater TH, Parson SH. 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. 544: 100-4. PMID 23583590 DOI: 10.1016/j.neulet.2013.03.052  0.611
2012 Thomson SR, Nahon JE, Mutsaers CA, Thomson D, Hamilton G, Parson SH, Gillingwater TH. Morphological Characteristics of Motor Neurons Do Not Determine Their Relative Susceptibility to Degeneration in a Mouse Model of Severe Spinal Muscular Atrophy Plos One. 7. PMID 23285108 DOI: 10.1371/journal.pone.0052605  0.608
2012 Findlater GS, Kristmundsdottir F, Parson SH, Gillingwater TH. Development of a supported self-directed learning approach for anatomy education. Anatomical Sciences Education. 5: 114-21. PMID 22223487 DOI: 10.1002/ase.1255  0.444
2011 Mutsaers CA, Wishart TM, Lamont DJ, Riessland M, Schreml J, Comley LH, Murray LM, Parson SH, Lochmüller H, Wirth B, Talbot K, Gillingwater TH. Reversible molecular pathology of skeletal muscle in spinal muscular atrophy. Human Molecular Genetics. 20: 4334-44. PMID 21840928 DOI: 10.1093/Hmg/Ddr360  0.725
2011 Comley LH, Fuller HR, Wishart TM, Mutsaers CA, Thomson D, Wright AK, Ribchester RR, Morris GE, Parson SH, Horsburgh K, Gillingwater TH. ApoE isoform-specific regulation of regeneration in the peripheral nervous system. Human Molecular Genetics. 20: 2406-21. PMID 21478199 DOI: 10.1093/Hmg/Ddr147  0.738
2011 Comley LH, Wishart TM, Baxter B, Murray LM, Nimmo A, Thomson D, Parson SH, Gillingwater TH. Induction of cell stress in neurons from transgenic mice expressing yellow fluorescent protein: implications for neurodegeneration research. Plos One. 6: e17639. PMID 21408118 DOI: 10.1371/journal.pone.0017639  0.689
2011 Murray LM, Comley LH, Gillingwater TH, Parson SH. The response of neuromuscular junctions to injury is developmentally regulated. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 25: 1306-13. PMID 21228222 DOI: 10.1096/fj.10-171934  0.613
2010 Wishart TM, Huang JP, Murray LM, Lamont DJ, Mutsaers CA, Ross J, Geldsetzer P, Ansorge O, Talbot K, Parson SH, Gillingwater TH. SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy. Human Molecular Genetics. 19: 4216-28. PMID 20705736 DOI: 10.1093/Hmg/Ddq340  0.727
2010 Murray LM, Gillingwater TH, Parson SH. Using mouse cranial muscles to investigate neuromuscular pathology in vivo Neuromuscular Disorders. 20: 740-743. PMID 20637618 DOI: 10.1016/J.Nmd.2010.06.013  0.587
2010 Murray LM, Lee S, Bäumer D, Parson SH, Talbot K, Gillingwater TH. Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy. Human Molecular Genetics. 19: 420-33. PMID 19884170 DOI: 10.1093/Hmg/Ddp506  0.634
2009 Baxter B, Parsons MJ, Gillingwater T, Parson S. Hypoxia induces rapid and selective injury to alpha-motor nerve terminals Journal of Anatomy. 214: 792-793. DOI: 10.1111/J.1469-7580.2009.01069.X  0.557
2008 Baxter B, Gillingwater TH, Parson SH. Rapid loss of motor nerve terminals following hypoxia-reperfusion injury occurs via mechanisms distinct from classic Wallerian degeneration. Journal of Anatomy. 212: 827-35. PMID 18510509 DOI: 10.1111/j.1469-7580.2008.00909.x  0.579
2008 Findlater GS, Gillingwater TH, Kristmundsdottir F, Parson SH. Eldred Wright Walls, MD, FRCS, FRCSE, FRSE Journal of Anatomy. 213: 230-231. DOI: 10.1111/j.1469-7580.2008.00923.x  0.414
2006 Wishart TM, Parson SH, Gillingwater TH. Synaptic vulnerability in neurodegenerative disease. Journal of Neuropathology and Experimental Neurology. 65: 733-9. PMID 16896307 DOI: 10.1097/01.jnen.0000228202.35163.c4  0.689
2004 Parson SH, Ribchester RR, Davie N, Gandhi NP, Malik RQ, Gillingwater TH, Thomson D. Axotomy-Dependent and -Independent Synapse Elimination in Organ Cultures of WldS Mutant Mouse Skeletal Muscle Journal of Neuroscience Research. 76: 64-75. PMID 15048930 DOI: 10.1002/Jnr.20016  0.707
1997 Parson SH, Mackintosh CL, Ribchester RR. Elimination of motor nerve terminals in neonatal mice expressing a gene for slow Wallerian degeneration (C57Bl/Wld(s)) European Journal of Neuroscience. 9: 1586-1592. PMID 9283813 DOI: 10.1111/j.1460-9568.1997.tb01516.x  0.619
1995 Parson SH, Ribchester RR. Segmental independence and age dependence of neurite outgrowth from embryonic chick sensory neurons Journal of Neurobiology. 26: 1-16. PMID 7714519 DOI: 10.1002/Neu.480260102  0.595
1995 Parson SH, Price JF, Ribchester RR. Cell viability and laminin-induced neurite outgrowth in cultures of embryonic chick neural tube cells: Effects of cytosine-B-D-arabinofuranoside Neurodegeneration. 4: 99-106. PMID 7600190 DOI: 10.1006/neur.1995.0012  0.572
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