Simon Parson

Affiliations: 
University of Aberdeen, Aberdeen, Scotland, United Kingdom 
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"Simon Parson"
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Deguise MO, Baranello G, Mastella C, et al. (2019) Abnormal fatty acid metabolism is a core component of spinal muscular atrophy. Annals of Clinical and Translational Neurology. 6: 1519-1532
Šoltić D, Shorrock HK, Allardyce H, et al. (2019) Lamin A/C dysregulation contributes to cardiac pathology in a mouse model of severe spinal muscular atrophy. Human Molecular Genetics
Fergusson SJ, Aka JJ, Hennessy CM, et al. (2018) Examining the impact of audience response systems on student performance in anatomy education: a randomised controlled trial. Scottish Medical Journal. 36933017741409
Maxwell GK, Szunyogova E, Shorrock HK, et al. (2018) Developmental and degenerative cardiac defects in the Taiwanese mouse model of severe spinal muscular atrophy. Journal of Anatomy
Szunyogova E, Zhou H, Maxwell GK, et al. (2016) Corrigendum: Survival Motor Neuron (SMN) protein is required for normal mouse liver development. Scientific Reports. 6: 35898
Thomson AK, Somers E, Powis RA, et al. (2016) Survival of motor neurone protein is required for normal postnatal development of the spleen. Journal of Anatomy
Powis RA, Karyka E, Boyd P, et al. (2016) Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophy. Jci Insight. 1: e87908
Szunyogova E, Zhou H, Maxwell GK, et al. (2016) Survival Motor Neuron (SMN) protein is required for normal mouse liver development. Scientific Reports. 6: 34635
Somers E, Lees RD, Hoban K, et al. (2015) Vascular defects and spinal cord hypoxia in spinal muscular atrophy. Annals of Neurology
Wishart TM, Mutsaers CA, Riessland M, et al. (2014) Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy. The Journal of Clinical Investigation. 124: 1821-34
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