Simon Parson - Publications

Affiliations: 
University of Aberdeen, Aberdeen, Scotland, United Kingdom 

25 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, 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
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  0.4
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  0.4
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  0.4
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  0.4
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  0.4
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  0.4
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  0.4
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  0.4
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  0.4
2013 Schreml J, Riessland M, Paterno M, Garbes L, Roßbach K, Ackermann B, Krämer J, Somers E, Parson SH, Heller R, Berkessel A, Sterner-Kock A, Wirth B. Severe SMA mice show organ impairment that cannot be rescued by therapy with the HDACi JNJ-26481585. European Journal of Human Genetics : Ejhg. 21: 643-52. PMID 23073311 DOI: 10.1038/ejhg.2012.222  0.4
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  0.4
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  0.4
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  0.4
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  0.4
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  0.4
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  0.4
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  0.4
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  0.4
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  0.4
2007 Bettini NL, Moores TS, Baxter B, Deuchars J, Parson SH. Dynamic remodelling of synapses can occur in the absence of the parent cell body. Bmc Neuroscience. 8: 79. PMID 17897464 DOI: 10.1186/1471-2202-8-79  0.4
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  0.4
2006 Brooke RE, Atkinson L, Edwards I, Parson SH, Deuchars J. Immunohistochemical localisation of the voltage gated potassium ion channel subunit Kv3.3 in the rat medulla oblongata and thoracic spinal cord. Brain Research. 1070: 101-15. PMID 16403474 DOI: 10.1016/j.brainres.2005.10.102  0.4
2005 Baxter RL, Vega-Riveroll LJ, Deuchars J, Parson SH. A2A adenosine receptors are located on presynaptic motor nerve terminals in the mouse. Synapse (New York, N.Y.). 57: 229-34. PMID 15986392 DOI: 10.1002/syn.20173  0.4
2004 Brooke RE, Moores TS, Morris NP, Parson SH, Deuchars J. Kv3 voltage-gated potassium channels regulate neurotransmitter release from mouse motor nerve terminals. The European Journal of Neuroscience. 20: 3313-21. PMID 15610163 DOI: 10.1111/j.1460-9568.2004.03730.x  0.4
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  0.4
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