Simon Parson
Affiliations: | University of Aberdeen, Aberdeen, Scotland, United Kingdom |
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"Simon Parson"
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Publications
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| Leow DM, Ng YK, Wang LC, et al. (2024) Hepatocyte-intrinsic SMN deficiency drives metabolic dysfunction and liver steatosis in spinal muscular atrophy. The Journal of Clinical Investigation |
| Zhou H, Hong Y, Scoto M, et al. (2022) Microvasculopathy in SMA is driven by a reversible autonomous endothelial cell defect. The Journal of Clinical Investigation |
| Gillingwater TH, McWilliam C, Horrocks I, et al. (2022) A call to introduce newborn screening for spinal muscular atrophy (SMA) in Scotland. Scottish Medical Journal. 369330221078994 |
| Quondamatteo F, Corzo-Leon DE, Brassett C, et al. (2021) Neutralisation of SARS-CoV-2 by anatomical embalming solutions. Journal of Anatomy |
| Deguise MO, Pileggi C, De Repentigny Y, et al. (2021) SMN depleted mice offer a robust and rapid onset model of non-alcoholic fatty liver disease. Cellular and Molecular Gastroenterology and Hepatology |
| Brassett C, Cosker T, Davies DC, et al. (2020) COVID-19 and anatomy: Stimulus and initial response. Journal of Anatomy |
| Allardyce H, Kuhn D, Hernandez-Gerez E, et al. (2020) 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 |
| 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 |