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The Institute of Medical Sciences

Professor Simon Parson

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Professor Simon Parson
Professor Simon Parson
Professor Simon Parson

FAS, FRSB

Regius Chair of Anatomy

About
Email Address
simon.parson@abdn.ac.uk
Telephone Number
+44 (0)1224 274328
Office Address

Anatomy Rm 324 Suttie Centre Foresterhill University of Aberdeen Aberdeen AB24 3HF

School/Department
School of Medicine, Medical Sciences and Nutrition

Biography

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

Regius Chair of Anatomy, 2018

Memberships and Affiliations

Internal Memberships

All aspects relating to Home Office legislation of anatomical teaching and research

College Teaching and Learning Committee

Division of Medical and Dental Education Executive Committee

Year 1-3 Medical Executive Committees

Medicine Curriculum Steering Group

External Memberships

Elected Councillor, Anatomical Society: 2010-2016

Meetings Officer, Anatomical Society: 2011- 2016

IFAA Programme Secretary: 2018 - 2019

President, Anatomical Society 2019-2022

Research

Research Overview

Spinal Muscular Atrophy

Systemic involvement in neurodegeneration, especially of the cardiovascular system

Effects of Hypoxia and ischaemia on the nervous system

Current Research

Spinal muscular Atrophy (SMA) is a childhood form of Motor Neurone Disease. It is caused by a defect in a gene which 1:35 of us carry. When two carriers come together there is a 1:4 chance of producing an affected child. SMA is the second most common genetic cause of infant death, affecting between 1:6-10,000 live births Worldwide. The most severely affected children will never sit unaided and will die before their second birthday. The disease is characterised by a loss of motor neurones and resultant muscle weakness and inability to carry out co-ordinated motor tasks including breathing. The genetic defect is well-characterised and attempts to replace or reduce the severe depletion of the key Survival of Motor Neurone (SMN) protein are ongoing. However, even when protein levels in motor neurones are increased and improvements in motor parameters are reported, survival is not increased. 

There is an increasing appreciation that this is not a classical motor neurone disease, but rather a systemic disease in which motor neurones are either most vulnerable or that defects in them are most clinically relevant. 

Our research has pioneered significant pre and early symptomatic defects in the cardiovascular system, where the heart, blood vessels and circulating cells are all defective in SMA. We are now particularly interested to determine how this impacts on SMA disease development and progression. This is particularly relevant in the new post- therapeutic landscape, as these were designed to target neuronal defects.

We are currently exploring the extent to which the non-neuronal pathologies described in animal models are also seen in human post-mortem material and are using cellular models to determine the vulnerabilities of SMA cells to hypoxic environments. These will help us to understand and develop novel combinatorial therapies to treat the entirety of SMA pathology in patients. 

Most recently, we are exploring similar non-motor pathologies in ALS/ MNDs.

Collaborations

Professor Tom Gillingwater: University of Edinburgh

Dr Tom Wishart: Roslin Institute Edinburgh

Dr Lyndsay Murray: University of Edinburgh

Dr's Francesco Muntoni and Haiyan Zhou: UCL, London

Prof Rashmi Kothary: University of Ottawa, Canada

Prof Charlotte Sumner: John Hopkins University, USA

Funding and Grants

SMA Europe 

Anatomical Society 

Tenovus Scotland

Teaching

Teaching Responsibilities

All aspects of Anatomy teaching to Medical and Science students

Publications

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  • A reassessment of spinal cord pathology in severe infantile spinal muscular atrophy

    Allardyce, H., Benjamin, L., Sumner, C. J., Parson, S., Crawford, T. O.
    Neuropathology and Applied Neurobiology, vol. 50, no. 5, e13013
    Contributions to Journals: Articles

  • Hepatocyte-intrinsic SMN deficiency drives metabolic dysfunction and liver steatosis in spinal muscular atrophy

    Leow, D. M., Ng, Y. K., Wang, L. C., Koh, H. W., Zhao, T., Khong, Z. J., Tabaglio, T., Narayanan, G., Giadone, R. M., Sobota, R. M., Ng, S., Teo, A. K., Parson, S. H., Rubin, L. L., Ong, W., Darras, B. T., Yeo, C. J.
    The Journal of Clinical Investigation, vol. 134, no. 12, e173702
    Contributions to Journals: Articles

  • Influencing factors in surgical decision-making: a qualitative analysis of colorectal surgeons' experiences of postoperative complications

    Bisset, C. N., Moug, S. J., Oliphant, R., Dames, N., Parson, S., Cleland, J.
    Colorectal Disease, vol. 26, no. 5, pp. 987-993
    Contributions to Journals: Articles

  • Influencing factors in surgical decision-making: a qualitative analysis of colorectal surgeons’ experiences of post-operative complications

    Bisset, C. N., Moug, S., Oliphant, R., Dames, N., Parson, S., Cleland, J. A.
    Colorectal Disease
    Contributions to Journals: Articles

  • Microvasculopathy in SMA is driven by a reversible autonomous endothelial cell defect

    Zhou, H., Hong, Y., Scoto, M., Thomson, A., Pead, E., MacGillivray, T., Hernandez Gerez, E., Catapano, F., Meng, J., Zhang, Q., Hunter, G., Shorrock, H. K., Ng, T., Hamida, A. M. S., Sanson, M., Baranello, G., Howell, K., Gillingwater, T. H., Brogan, P., Thompson, D., Parson, S., Muntoni, F.
    Journal of Clinical Investigation, vol. 132, no. 21, e153430
    Contributions to Journals: Articles

  • Exploring variation in surgical practice: does the surgeon's personality influence anastomotic decision-making?'

    Bisset, C. N., Ferguson, E., Macdermid, E., Yassin, N., Dames, N., Keller, D., Oliphant, R., Parson, S., Cleland, J., Moug, S. J., Stein, S., Collaborators, P. P. S. G.
    British Journal of Surgery, vol. 109, no. 11, pp. 1156-1163
    Contributions to Journals: Articles

  • Developing research skills with weekly online seminars over the summer

    Gregory, J., Cunningham, C., MacLeod, A., Kiezebrink, K., Martin, K., Morgan, H., Myint, P. K., Parson, S., Poobalan, A., Speirs, V., Turner, S.
    Europhysiology 2022
    Contributions to Journals: Abstracts

  • A call to introduce newborn screening for spinal muscular atrophy (SMA) in Scotland

    Gillingwater, T. H., Parson, S., McWilliam, C., Horrocks, I., McWilliam, K., Hamilton, M., Fletcher, E., Williams, N., Smith, S.
    Scottish Medical Journal, vol. 67, no. 1, pp. 46-57
    Contributions to Journals: Letters

  • Neutralisation of SARS-CoV-2 by anatomical embalming solutions

    Quondamatteo, F., Corzo Leon, D., Brassett, C., Colquhoun, I. J., Davies, D. C., Dockery, P., Sue, G., Guild, S., Hunter, A., Jones, J., Tracey, C., Wilkinson, T., Munro, C., Gillingwater, T. H., Parson, S.
    Journal of Anatomy, vol. 239, no. 5, pp. 1221-1225
    Contributions to Journals: Articles

  • Altered retinal vasculature is a biomarker of disease in Spinal Muscular Atrophy in mouse models and human patients

    Thomson, A., Zhou, H., Scoto, M., Thompson, D., Catapano, F., Pead, E., MacGillivray, T., Shorrock, H., Hunter, G., Gillingwater, T., Muntoni, F., Parson, S.
    Journal of Anatomy, vol. 239, no. 4, pp. 969-970
    Contributions to Journals: Abstracts

  • The Relationship between Body Composition, Fatty Acid Metabolism and Diet in Spinal Muscular Atrophy

    Watson, K. S., Boukhloufi,, I., Bowerman, M., Parson, S. H.
    Brain Sciences, vol. 11, no. 2
    Contributions to Journals: Articles

  • SMN Depleted Mice Offer a Robust and Rapid Onset Model of Nonalcoholic Fatty Liver Disease

    Deguise, M., Pileggi, C., De Repentigny, Y., Beauvais, A., Tierney, A., Chehade, L., Michaud, J., Llavero-Hurtado, M., Lamont, D., Atrih, A., Wishart, T. M., Gillingwater, T. H., Schneider, B. L., Harper, M., Parson, S. H., Kothary, R.
    CMGH Cellular and Molecular Gastroenterology and Hepatology, vol. 12, no. 1, pp. 354-377
    Contributions to Journals: Articles

  • Exploring shared surgical decision-making from the patient’s perspective: is the personality of the surgeon important?

    Bisset, C. N., Dames, N., Oliphant, R., Alasadi, A., Anderson, D., Parson, S., Cleland, J., Moug, S. J.
    Colorectal Disease, vol. 22, no. 12, pp. 2214-2221
    Contributions to Journals: Articles

  • Anatomical Evaluation of a Conventional Pectoralis II Versus a Subserratus Plane Block for Breast Surgery

    Robinson, H., Mishra, S., Davies, L., Craigen, F., Vilcina, V., Parson, S., Shahana, S.
    Anesthesia and Analgesia, vol. 131, no. 3, pp. 928-934
    Contributions to Journals: Articles

  • COVID-19 and Anatomy: Stimulus and Initial Response

    Brassett, C., Cosker, T., Davies, D. C., Dockery, P., Gillingwater, T. H., Lee, T. C., Milz, S., Parson, S. H., Quondamatteo, F., Wilkinson, T.
    Journal of Anatomy, vol. 237, no. 3, pp. 393-403
    Contributions to Journals: Review articles

  • Widespread tissue hypoxia dysregulates cell and metabolic pathways in SMA

    Hernandez Gerez, E., Dall'angelo, S., Collinson, J. M., Fleming, I. N., Parson, S. H.
    Annals of Clinical and Translational Neurology, vol. 7, no. 9, pp. 1580-1593
    Contributions to Journals: Articles

  • Renal pathology in a mouse model of severe Spinal Muscular Atrophy is associated with downregulation of Glial Cell-Line Derived Neurotrophic Factor (GDNF)

    Allardyce, H., Kuhn, D., Hernandez Gerez, E., Hensel, N., Huang, Y., Faller, K., Gillingwater, T. H., Quondamatteo, F., Claus, P., Parson, S. H.
    Human Molecular Genetics, vol. 29, no. 14, pp. 2365-2378
    Contributions to Journals: Articles

  • A role for spinal cord hypoxia in neurodegeneration

    Hernandez Gerez, E., Fleming, I. N., Parson, S. H.
    Cell Death & Disease, vol. 10, 861
    Contributions to Journals: Review articles

  • Lamin A/C dysregulation contributes to cardiac pathology in a mouse model of severe spinal muscular atrophy

    Šoltić, D., Shorrock, H. K., Allardyce, H., Wilson, E. L., Holt, I., Synowsky, S. A., Shirran, S. L., Parson, S. H., Gillingwater, T. H., Fuller, H. R.
    Human Molecular Genetics, vol. 28, no. 21, pp. 3515–3527
    Contributions to Journals: Articles

  • Abnormal fatty acid metabolism is a core component of spinal muscular atrophy

    Deguise, M., Baranello, G., Mastella, C., Beauvais, A., Michaud, J., Leone, A., De Amicis, R., Battezzati, A., Dunham, C., Selby, K., Chardon, J. W., McMillan, H. J., Huang, Y., Courtney, N. L., Mole, A. J., Kubinski, S., Claus, P., Murray, L. M., Bowerman, M., Gillingwater, T. H., Bertoli, S., Parson, S. H., Kothary, R.
    Annals of Clinical and Translational Neurology, vol. 6, no. 8, pp. 1519-1532
    Contributions to Journals: Articles

  • Is the Conventional Ultrasound Guided Pectoralis II or Sub-serratus Plane Superior for Brest Surgery: A Cadaveric Study

    Robinson, H., Mishra, S., Nestor, C., Cragen, F., Davies, L., Parson, S. H., Shahana, S.
    Europian Society of Regional Anesthesia, Congress (ESRA 2018)
    Contributions to Journals: Abstracts

  • Is the Conventional Ultrasound Guided Pectoralis II or Sub-serratus Plane Superior for Brest Surgery: A Cadaveric Study

    Robinson, H., Mishra, S., Nestor, C., Cragen, F., Davies, L., Parson, S. H., Shahana, S.
    Europian Society of Regional Anesthesia, Congress (ESRA 2018)
    Contributions to Conferences: Abstracts

  • Is the Conventional Ultrasound Guided Pectoralis II or Sub-serratus Plane Superior for Brest Surgery: A Cadaveric Study

    Robinson, H., Mishra, S., Nestor, C., Cragen, F., Davies, L., Parson, S. H., Shahana, S.
    Europian Society of Regional Anesthesia, Congress (ESRA 2018)
    Contributions to Conferences: Posters

  • An enhanced fresh cadaveric model for reconstructive microsurgery training

    Chouari, T. A. M., Lindsay, K., Bradshaw, E., Parson, S., Watson, L., Ahmed, J., Curnier, A.
    European Journal of Plastic Surgery, vol. 41, no. 4, pp. 439-446
    Contributions to Journals: Articles

  • Developmental and Degenerative Cardiac Defects in the Taiwanese Mouse Model of Severe Spinal Muscular Atrophy

    Maxwell, G. K., Szunyogova, E., Shorrock, H. K., Gillingwater, T. H., Parson, S. H.
    Journal of Anatomy, vol. 232, no. 6, pp. 965-978
    Contributions to Journals: Articles

  • Examining the impact of audience response systems on student performance in anatomy education: a randomized controlled trial

    Fergusson, S. J., Aka, J. J., Hennessy, C. M., Wilson, A. J., Parson, S. H., Harrison, E. M., Finn, G. M., Gillingwater, T. H.
    Scottish Medical Journal, vol. 63, no. 1, pp. 16-21
    Contributions to Journals: Articles

  • Survival of motor neurone protein is required for normal postnatal development of the spleen

    Thomson, A. K., Somers, E., Powis, R. A., Shorrock, H. K., Murphy, K., Swoboda, K. J., Gillingwater, T. H., Parson, S. H.
    Journal of Anatomy, vol. 230, no. 2, pp. 337–346
    Contributions to Journals: Articles

  • Survival Motor Neuron (SMN) protein is required for normal mouse liver development

    Szunyogova, E., Zhou, H., Maxwell, G. K., Powis, R. A., Muntoni, F., Gillingwater, T. H., Parson, S. H.
    Scientific Reports, vol. 6, 34635
    Contributions to Journals: Articles

  • Exploring the microvascular abnormalities in a cohort of paediatric patients with spinal muscular atrophy: P.51

    Scoto, M., Zhou, H., Thompson, D., Howell, K., Hong, Y., Imbrigiotta, N., Parson, S., Brogan, P., Muntoni, F.
    21st International Congress of the World-Muscle-Society, pp. S105
    Contributions to Journals: Abstracts

  • Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophy

    Powis, R. A., Karyka, E., Boyd, P., Come, J., Jones, R. A., Zheng, Y., Szunyogova, E., Groen, E. J. N., Hunter, G., Thomson, D., Wishart, T. M., Becker, C. G., Parson, S. H., Martinat, C., Azzouz, M., Gillingwater, T. H.
    JCI Insight, vol. 1, no. 11, e87908
    Contributions to Journals: Articles

  • Histopathological Defects in Intestine in Severe Spinal Muscular Atrophy Mice Are Improved by Systemic Antisense Oligonucleotide Treatment

    Sintusek, P., Catapano, F., Angkathunkayul, N., Marrosu, E., Parson, S. H., Morgan, J. E., Muntoni, F., Zhou, H.
    PloS ONE, vol. 11, no. 5, pp. 1-15
    Contributions to Journals: Articles

  • Evolving student–faculty partnerships in medical education through peer-assisted learning

    Ezzat, A., Dynes, K., Parson, S. H.
    Medical Education, vol. 50, no. 5, pp. 568-568
    Contributions to Journals: Articles

  • Histological and Histochemical Methods, Theory and Practice, 5th Ed

    Szunyogova, E., Parson, S. H.
    Journal of Anatomy, vol. 228, no. 5, pp. 887
    Contributions to Journals: Reviews of Books, Films and Articles

  • Vascular Defects and Spinal Cord Hypoxia in Spinal Muscular Atrophy

    Somers, E., Lees, R. D., Hoban, K., Sleigh, J. N., Zhou, H., Muntoni, F., Talbot, K., Gillingwater, T. H., Parson, S. H.
    Annals of Neurology, vol. 79, no. 2, pp. 217-230
    Contributions to Journals: Articles

  • Microvascular abnormality in spinal muscular atrophy and its response to antisense oligonucleotide therapy

    Zhou, H., Ying, H., Scoto, M., Brogan, P., Parson, S., Muntoni, F.
    20th International Congress of the World-Muscle-Society, pp. S193
    Contributions to Journals: Abstracts

  • An anatomical study of the neurovascular anatomy of the web spaces between the fingers

    Kinsella, A., Parson, S., Davidson, D. M.
    Journal of hand surgery-European volume, vol. 40, no. 7, pp. 755-757
    Contributions to Journals: Letters

  • An Investigation Into Student Perceptions of Peer Learning During a Medical Undergraduate Course

    Parson, S., Ezzat, M., Foster, O., Moffat, M., Johnston, P.
    The FASEB Journal, vol. 29, no. Suppl. 1
    Contributions to Journals: Abstracts

  • Tissue quality assessment using a novel direct elasticity assessment device (the E-finger): a cadaveric study of prostatectomy dissection

    Good, D. W., Khan, A., Hammer, S., Scanlan, P., Shu, W., Phipps, S., Parson, S. H., Stewart, G. D., Reuben, R., McNeill, S. A.
    PloS ONE, vol. 9, no. 11, e112872
    Contributions to Journals: Articles

  • Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy

    Wishart, T. M., Mutsaers, C. A., Riessland, M., Reimer, M. M., Hunter, G., Hannam, M. L., Eaton, S. L., Fuller, H. R., Roche, S. L., Somers, E., Morse, R., Young, P. J., Lamont, D. J., Hammerschmidt, M., Joshi, A., Hohenstein, P., Morris, G. E., Parson, S. H., Skehel, P. A., Becker, T., Robinson, I. M., Becker, C. G., Wirth, B., Gillingwater, T. H.
    The Journal of Clinical Investigation, vol. 124, no. 4, pp. 1821-1834
    Contributions to Journals: Articles

  • The singular qualities of motor neurones in health and disease

    Parson, S. H.
    Journal of Anatomy, vol. 224, no. 1, pp. 1-2
    Contributions to Journals: Articles

  • Increasing SMN levels using the histone deacetylase inhibitor SAHA ameliorates defects in skeletal muscle microvasculature in a mouse model of severe spinal muscular atrophy

    Somers, E., Riessland, M., Schreml, J., Wirth, B., Gillingwater, T. H., Parson, S. H.
    Neuroscience Letters, vol. 544, pp. 100-104
    Contributions to Journals: Articles

  • Severe SMA mice show organ impairment that cannot be rescued by therapy with the HDACi JNJ-26481585

    Schreml, J., Riessland, M., Paterno, M., Garbes, L., Roßbach, K., Ackermann, B., Krämer, J., Somers, E., Parson, S. H., Heller, R., Berkessel, A., Sterner-Kock, A., Wirth, B.
    EJHG : European journal of human genetics : the official journal of the European Society of Human Genetics. , vol. 21, no. 6, pp. 643-652
    Contributions to Journals: Articles

  • Morphological characteristics of motor neurons do not determine their relative susceptibility to degeneration in a mouse model of severe spinal muscular atrophy

    Thomson, S. R., Nahon, J. E., Mutsaers, C. A., Thomson, D., Hamilton, G., Parson, S. H., Gillingwater, T. H.
    PloS ONE, vol. 7, no. 12, e52605
    Contributions to Journals: Articles

  • Density, calibre and ramification of muscle capillaries are altered in a mouse model of severe spinal muscular atrophy

    Somers, E., Stencel, Z., Wishart, T. M., Gillingwater, T. H., Parson, S. H.
    Neuromuscular Disorders, vol. 22, no. 5, pp. 435-442
    Contributions to Journals: Articles

  • Development of a supported self-directed learning approach for anatomy education

    Findlater, G. S., Kristmundsdottir, F., Parson, S. H., Gillingwater, T. H.
    Anatomical Sciences Education, vol. 5, no. 2, pp. 114-121
    Contributions to Journals: Articles

  • Reversible molecular pathology of skeletal muscle in spinal muscular atrophy

    Mutsaers, C. A., Wishart, T. M., Lamont, D. J., Riessland, M., Schreml, J., Comley, L. H., Murray, L. M., Parson, S. H., Lochmueller, H., Wirth, B., Talbot, K., Gillingwater, T. H.
    Human Molecular Genetics, vol. 20, no. 22, pp. 4334-4344
    Contributions to Journals: Articles

  • ApoE isoform-specific regulation of regeneration in the peripheral nervous system

    Comley, L. H., Fuller, H. R., Wishart, T. M., Mutsaers, C. A., Thomson, D., Wright, A. K., Ribchester, R. R., Morris, G. E., Parson, S. H., Horsburgh, K., Gillingwater, T. H.
    Human Molecular Genetics, vol. 20, no. 12, pp. 2406-2421
    Contributions to Journals: Articles

  • The response of neuromuscular junctions to injury is developmentally regulated

    Murray, L. M., Comley, L. H., Gillingwater, T. H., Parson, S. H.
    The FASEB Journal, vol. 25, no. 4, pp. 1306-1313
    Contributions to Journals: Articles

  • Induction of cell stress in neurons from transgenic mice expressing yellow fluorescent protein: implications for neurodegeneration research

    Comley, L. H., Wishart, T. M., Baxter, B., Murray, L. M., Nimmo, A., Thomson, D., Parson, S. H., Gillingwater, T. H.
    PloS ONE, vol. 6, no. 3, e17639
    Contributions to Journals: Articles

  • SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy

    Wishart, T. M., Huang, J. P. -., Murray, L. M., Lamont, D. J., Mutsaers, C. A., Ross, J., Geldsetzer, P., Ansorge, O., Talbot, K., Parson, S. H., Gillingwater, T. H.
    Human Molecular Genetics, vol. 19, no. 21, pp. 4216-4228
    Contributions to Journals: Articles

  • Using mouse cranial muscles to investigate neuromuscular pathology in vivo

    Murray, L. M., Gillingwater, T. H., Parson, S. H.
    Neuromuscular Disorders, vol. 20, no. 11, pp. 740-743
    Contributions to Journals: Articles

  • Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy

    Murray, L. M., Lee, S., Baeumer, D., Parson, S. H., Talbot, K., Gillingwater, T. H.
    Human Molecular Genetics, vol. 19, no. 3, pp. 420-433
    Contributions to Journals: Articles

  • Rapid loss of motor nerve terminals following hypoxia-reperfusion injury occurs via mechanisms distinct from classic Wallerian degeneration

    Baxter, B., Gillingwater, T. H., Parson, S. H.
    Journal of Anatomy, vol. 212, no. 6, pp. 827-835
    Contributions to Journals: Articles

  • Dynamic remodelling of synapses can occur in the absence of the parent cell body

    Bettini, N. L., Moores, T. S., Baxter, B., Deuchars, J., Parson, S. H.
    BMC Neuroscience, vol. 8, 79
    Contributions to Journals: Articles

  • Synaptic vulnerability in neurodegenerative disease

    Wishart, T. M., Parson, S. H., Gillingwater, T. H.
    Journal of Neuropathology and Experimental Neurology, vol. 65, no. 8, pp. 733-739
    Contributions to Journals: Articles

  • Immunohistochemical localisation of the voltage gated potassium ion channel subunit Kv3.3 in the rat medulla oblongata and thoracic spinal cord

    Brooke, R. E., Atkinson, L., Edwards, I., Parson, S. H., Deuchars, J.
    Brain Research, vol. 1070, no. 1, pp. 101-15
    Contributions to Journals: Articles

  • A2A adenosine receptors are located on presynaptic motor nerve terminals in the mouse

    Baxter, R. L., Vega-Riveroll, L. J., Deuchars, J., Parson, S. H.
    Synapse, vol. 57, no. 4, pp. 229-34
    Contributions to Journals: Articles

  • Nonmuscle myosins IIA and IIB are present in adult motor nerve terminals

    Vega-Riveroll, L. J., Wylie, S. R., Loughna, P. T., Parson, S. H., Chantler, P. D.
    Neuroreport, vol. 16, no. 11, pp. 1143-6
    Contributions to Journals: Articles

  • Computer three-dimensional reconstruction of the sinoatrial node

    Dobrzynski, H., Li, J., Tellez, J., Greener, I. D., Nikolski, V. P., Wright, S. E., Parson, S. H., Jones, S. A., Lancaster, M. K., Yamamoto, M., Honjo, H., Takagishi, Y., Kodama, I., Efimov, I. R., Billeter, R., Boyett, M. R.
    Circulation, vol. 111, no. 7, pp. 846-54
    Contributions to Journals: Articles

  • Properties of presynaptic P2X7-like receptors at the neuromuscular junction

    Moores, T. S., Hasdemir, B., Vega-Riveroll, L., Deuchars, J., Parson, S. H.
    Brain Research, vol. 1034, no. 1-2, pp. 40-50
    Contributions to Journals: Articles

  • Kv3 voltage-gated potassium channels regulate neurotransmitter release from mouse motor nerve terminals

    Brooke, R. E., Moores, T. S., Morris, N. P., Parson, S. H., Deuchars, J.
    European Journal of Neuroscience, vol. 20, no. 12, pp. 3313-21
    Contributions to Journals: Articles

  • Axotomy-dependent and -independent synapse elimination in organ cultures of Wld(s) mutant mouse skeletal muscle

    Parson, S. H., Ribchester, R. R., Davie, N., Gandhi, N. P., Malik, R. Q., Gillingwater, T. H., Thomson, D.
    Journal of neuroscience research, vol. 76, no. 1, pp. 64-75
    Contributions to Journals: Articles

  • Neuronal P2X7 receptors are targeted to presynaptic terminals in the central and peripheral nervous systems

    Deuchars, S. A., Atkinson, L., Brooke, R. E., Musa, H., Milligan, C. J., Batten, T. F., Buckley, N. J., Parson, S. H., Deuchars, J.
    Journal of Neuroscience, vol. 21, no. 18, pp. 7143-52
    Contributions to Journals: Articles

  • Elimination of motor nerve terminals in neonatal mice expressing a gene for slow wallerian degeneration (C57Bl/Wlds)

    Parson, S. H., Mackintosh, C. L., Ribchester, R. R.
    European Journal of Neuroscience, vol. 9, no. 8, pp. 1586-1592
    Contributions to Journals: Articles

  • Loss of myelinated axons is specific to the central nervous system in a mouse model of the fetal alcohol syndrome

    Parson, S. H., Sojitra, N. M.
    Journal of Anatomy, vol. 187 , no. 3, pp. 739-748
    Contributions to Journals: Articles

  • Optic nerve hypoplasia in the fetal alcohol syndrome: a mouse model

    Parson, S. H., Dhillon, B., Findlater, G. S., Kaufman, M. H.
    Journal of Anatomy, vol. 186 , no. 2, pp. 313-320
    Contributions to Journals: Articles

  • Cell viability and laminin-induced neurite outgrowth in cultures of embryonic chick neural tube cells: effects of cytosine-B-D-arabinofuranoside

    Parson, S. H., Price, J. F., Ribchester, R. R.
    Neurodegeneration : a journal for neurodegenerative disorders, neuroprotection, and neuroregeneration, vol. 4, no. 1, pp. 99-106
    Contributions to Journals: Articles

  • Segmental independence and age dependence of neurite outgrowth from embryonic chick sensory neurons

    Parson, S. H., Ribchester, R. R.
    Journal of Neurobiology, vol. 26, no. 1, pp. 1-16
    Contributions to Journals: Articles

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