Dr Jeffrey Davies

Research Highlights

1. Klionsky, D., Abdel-Aziz, A., Abdelfatah, S., Abdellatif, M., Abdoli, A., Abel, S., Abeliovich, H., Abildgaard, M., Abudu, Y., Acevedo-Arozena, A., Adamopoulos, I., Adeli, K., Adolph, T., Adornetto, A., Aflaki, E., Agam, G., Agarwal, A., Aggarwal, B., Agnello, M...., & Tong, C. (2021). Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1. Autophagy, 17(1), 1-382.

   https://doi.org/10.1080/15548627.2020.1797280, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa57781
2. Lin, Z., Kim, E., Ahmed, M., Han, H., Simmons, C., Redhead, Y., Bartlett, J., Altamira, L., Callaghan, I., White, M., Singh, N., Sawiak, S., Spires-Jones, T., Vernon, A., Coleman, M., Green, J., Henstridge, C., Davies, J., Cash, D., & Sreedharan, J. (2021). MRI-guided histology of TDP-43 knock-in mice implicates parvalbumin interneuron loss, impaired neurogenesis and aberrant neurodevelopment in amyotrophic lateral sclerosis-frontotemporal dementia. Brain Communications, 3(2)

   https://doi.org/10.1093/braincomms/fcab114, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa57779
3. Hornsby, A., Buntwal, L., Carisi, C., Santos, V., Johnston, F., Roberts, L., Sassi, M., Mequinion, M., Stark, R., Reichenbach, A., Lockie, S., Siervo, M., Howell, O., Morgan, A., Wells, T., Andrews, Z., Burn, D., & Davies, J. (2020). Unacylated-Ghrelin Impairs Hippocampal Neurogenesis and Memory in Mice and Is Altered in Parkinson’s Dementia in Humans. Cell Reports Medicine, 1(7), 100120

   https://doi.org/10.1016/j.xcrm.2020.100120, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa55678
4. Rees, D., Roberts, L., Carisi, C., Morgan, A., Brown, R., & Davies, J. (2020). Automated Quantification of Mitochondrial Fragmentation in an In-Vitro Parkinson’s Disease Model (Pre-print version). BioRxiv

   https://doi.org/10.1101/2020.05.15.093369, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa54322
5. Rees, D., Roberts, L., Carisi, C., Morgan, A., Brown, R., & Davies, J. (2020). Automated Quantification of Mitochondrial Fragmentation in an In Vitro Parkinson's Disease Model. Current Protocols in Neuroscience, 94(1)

   https://doi.org/10.1002/cpns.105, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa55596
6. Davies, J., Chung, S., Thomas, R., Robinson, A., Hammond, C., Mullins, J., Carta, E., Pearce, B., Harvey, K., Harvey, R., Rees, M., & Davies, J. (2010). The glycinergic system in human startle disease: a genetic screening approach. Frontiers in Molecular Neuroscience, 3, 8-16.

   https://doi.org/10.3389/fnmol.2010.00008, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa13967
7. Beynon, A., Brown, M., Wright, R., Rees, M., Sheldon, I., Davies, J., Brown, R., & Sheldon, M. (2013). Ghrelin inhibits LPS-induced release of IL-6 from mouse dopaminergic neurones. Journal of Neuroinflammation, 10(1), 40

   https://doi.org/10.1186/1742-2094-10-40, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa14452
8. Johnston, A., Kang, J., Shen, W., Pickrell, W., Cushion, T., Davies, J., Baer, K., Mullins, J., Hammond, C., Chung, S., Thomas, R., White, C., Smith, P., Macdonald, R., Rees, M., & Pickrell, O. (2014). A Novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes. Neurobiology of Disease

   https://doi.org/10.1016/j.nbd.2013.12.013, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa17001
9. Hornsby, A., Redhead, Y., Rees, D., Ratcliff, M., Reichenbach, A., Wells, T., Francis, L., Amstalden, K., Andrews, Z., & Davies, J. (2016). Short-term calorie restriction enhances adult hippocampal neurogenesis and remote fear memory in a Ghsr-dependent manner. Psychoneuroendocrinology, 63, 198-207.

   https://doi.org/10.1016/j.psyneuen.2015.09.023, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa26484
10. Churm, R., Davies, J., Stephens, J., Prior, S., Prior, S., Stephens, J., Davies, J., & Churm, R. (2017). Ghrelin function in human obesity and type 2 diabetes: a concise review. Obesity Reviews, 18(2), 140-148.

    https://doi.org/10.1111/obr.12474, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa29770
11. Churm, R., Caplin, S., Barry, J., Davies, J., Stephens, J., & Prior, S. (2019). Acyl-ghrelin mediated lipid retention and inflammation in obesity-related Type 2 diabetes. Molecular and Cellular Endocrinology, 481, 8-13.

    https://doi.org/10.1016/j.mce.2018.11.004, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa45975
12. Corney, B., Widnall, C., Rees, D., Davies, J., Crunelli, V., Carter, D., Davies, J., & Rees, D. (2018). Regulatory Architecture of the Neuronal Cacng2/Tarpγ2 Gene Promoter: Multiple Repressive Domains, a Polymorphic Regulatory Short Tandem Repeat, and Bidirectional Organization with Co-regulated lncRNAs. Journal of Molecular Neuroscience

    https://doi.org/10.1007/s12031-018-1208-x, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa47951
13. Churm, R., Barry, J., Caplin, S., Davies, J., Stephens, J., & Prior, S. (2017). Effect of increased endogenous glucose levels within Type 2 diabetes on cellular lipid profiles. Endocrine Abstracts, 48(2)

    https://doi.org/10.1530/endoabs.48.p2, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa51491
14. Holter, J., Davies, J., Leresche, N., Crunelli, V., & Carter, D. (2005). Identification of Two Further Splice Variants of GABABR1 Characterizes the Conserved Micro-Exon 4 as a Hot Spot for Regulated Splicing in the Rat Brain. Journal of Molecular Neuroscience, 26(1), 099-108.

    https://doi.org/10.1385/JMN:26:1:099, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa52033
15. Buntwal, L., Sassi, M., Morgan, A., Andrews, Z., & Davies, J. (2019). Ghrelin-Mediated Hippocampal Neurogenesis: Implications for Health and Disease. Trends in Endocrinology & Metabolism, 30(11), 844-859.

    https://doi.org/10.1016/j.tem.2019.07.001, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa52032
16. Ratcliff, M., Rees, D., McGrady, S., Buntwal, L., Hornsby, A., Bayliss, J., Kent, B., Bussey, T., Saksida, L., Beynon, A., Howell, O., Morgan, A., Sun, Y., Andrews, Z., Wells, T., & Davies, J. (2019). Calorie restriction activates new adult born olfactory‐bulb neurones in a ghrelin‐dependent manner but acyl‐ghrelin does not enhance subventricular zone neurogenesis. Journal of Neuroendocrinology, 31(7)

    https://doi.org/10.1111/jne.12755, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa51124
17. Elabi, O., Duskova, K., Davies, J., Lane, E., & Davies, J. (2018). The Impact of Ghrelin on the Survival and Efficacy of Dopaminergic Fetal Grafts in the 6-OHDA-Lesioned Rat. Neuroscience, 395, 13-21.

    https://doi.org/10.1016/j.neuroscience.2018.10.045, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa46112
18. Morgan, A., Rees, D., Andrews, Z., & Davies, J. (2018). Ghrelin mediated neuroprotection - A possible therapy for Parkinson's disease?. Neuropharmacology, 136, 317-326.

    https://doi.org/10.1016/j.neuropharm.2017.12.027, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa38126
19. Morgan, A., Andrews, Z., Davies, J., Davies, J., & Morgan, A. (2017). Less is more: Caloric regulation of neurogenesis and adult brain function. Journal of Neuroendocrinology, 29(10), e12512

    https://doi.org/10.1111/jne.12512, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa38127
20. Santos, V., Stark, R., Rial, D., Silva, H., Bayliss, J., Lemus, M., Davies, J., Cunha, R., Prediger, R., & Andrews, Z. (2017). Acyl ghrelin improves cognition, synaptic plasticity deficits and neuroinflammation following amyloid beta (Aβ1-40) administration in mice. Journal of Neuroendocrinology, 29(5)

    https://doi.org/10.1111/jne.12476, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa33091
21. O'Keeffe, S., Beynon, A., Davies, J., Moynagh, P., Coogan, A., Silver, R., & Davies, J. (2017). NF-κB signalling is involved in immune-modulation, but not basal functioning, of the mouse suprachiasmatic circadian clock. European Journal of Neuroscience, 45(8), 1111-1123.

    https://doi.org/10.1111/ejn.13553, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa33089
22. Hopkins, A., Nelson, T., Guschina, I., Parsons, L., Lewis, C., Brown, R., Christian, H., Davies, J., & Wells, T. (2017). Unacylated ghrelin promotes adipogenesis in rodent bone marrow via ghrelin O-acyl transferase and GHS-R1a activity: evidence for target cell-induced acylation. Scientific Reports, 7(1), 45541

    https://doi.org/10.1038/srep45541, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa33090
23. Golding, D., Rees, D., Davies, J., Relkovic, D., Furby, H., Guschina, I., Hopkins, A., Davies, J., Resnick, J., Isles, A., & Wells, T. (2017). Paradoxical leanness in the imprinting-centre deletion mouse model for Prader–Willi syndrome. Journal of Endocrinology, 232(1), 123-135.

    https://doi.org/10.1530/JOE-16-0367, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa31060
24. Bayliss, J., Lemus, M., Stark, R., Santos, V., Thompson, A., Rees, D., Galic, S., Elsworth, J., Kemp, B., Andrews, Z., Davies, J., & Rees, D. (2016). Ghrelin-AMPK Signaling Mediates the Neuroprotective Effects of Calorie Restriction in Parkinson's Disease. Journal of Neuroscience, 36(10), 3049-3063.

    https://doi.org/10.1523/JNEUROSCI.4373-15.2016, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa26033
25. Alquier, T., Bayliss, J., Lemus, M., Santos, V., Deo, M., Davies, J., Kemp, B., Elsworth, J., & Andrews, Z. (2016). Metformin Prevents Nigrostriatal Dopamine Degeneration Independent of AMPK Activation in Dopamine Neurons. PLOS ONE, 11(7), e0159381

    https://doi.org/10.1371/journal.pone.0159381, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa29599
26. Kent, B., Beynon, A., Hornsby, A., Bekinschtein, P., Bussey, T., Davies, J., & Saksida, L. (2014). The orexigenic hormone acyl-ghrelin increases adult hippocampal neurogenesis and enhances pattern separation. Psychoneuroendocrinology, 51, 431-439.

    https://doi.org/10.1016/j.psyneuen.2014.10.015, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa19690

    http://www.sciencedirect.com/science/article/pii/S0306453014003990
27. Wells, T., Davies, J., Guschina, I., Ball, D., Davies, J., Davies, V., Evans, B., Votruba, M., & Davies, J. (2012). Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome. Human Molecular Genetics, 21(22), 4836-4844.

    https://doi.org/10.1093/hmg/dds315, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa12321
28. Davies, J., Klein, D., Carter, D., & Davies, J. (2011). Selective Genomic Targeting by FRA-2/FOSL2 Transcription Factor: REGULATION OF THE Rgs4 GENE IS MEDIATED BY A VARIANT ACTIVATOR PROTEIN 1 (AP-1) PROMOTER SEQUENCE/CREB-BINDING PROTEIN (CBP) MECHANISM. Journal of Biological Chemistry, 286(17), 15227-39.

    https://doi.org/10.1074/jbc.M110.201996, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa9832
29. Glad, C., Kitchen, E., Russ, G., Harris, S., Davies, J., Gevers, E., Gabrielsson, B., Wells, T., & Davies, J. (2011). Reverse Feeding Suppresses the Activity of the GH Axis in Rats and Induces a Preobesogenic State. Endocrinology, 152(3), 869

    https://doi.org/10.1210/en.2010-0713, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa10231
30. Davies, J., Kotokorpi, P., Eccles, S., Barnes, S., Tokarczuk, P., Allen, S., Whitworth, H., Guschina, I., Evans, B., Mode, A., Zigman, J., Wells, T., & Davies, J. (2009). Ghrelin Induces Abdominal Obesity Via GHS-R-Dependent Lipid Retention. Molecular Endocrinology, 23(6), 914

    https://doi.org/10.1210/me.2008-0432, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa9833
31. El-Kasti, M., Christian, H., Huerta-Ocampo, I., Stolbrink, M., Gill, S., Houston, P., Davies, J., Chilcott, J., Hill, N., Matthews, D., Carter, D., Wells, T., & Davies, J. (2008). The Pregnancy-Induced Increase in Baseline Circulating Growth Hormone in Rats is not Induced by Ghrelin. Journal of Neuroendocrinology, 20(3), 309

    https://doi.org/10.1111/j.1365-2826.2008.01650.x, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa9835
32. Davies, J., Gevers, E., Stevenson, A., Coschigano, K., El-Kasti, M., Bull, M., Elford, C., Evans, B., Kopchick, J., & Wells, T. (2007). Adiposity profile in the dwarf rat: an unusually lean model of profound growth hormone deficiency. American Journal of Physiology-Endocrinology and Metabolism, 292(5), E1483-E1494.

    https://doi.org/10.1152/ajpendo.00417.2006, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa38129
33. Davies, J., Thompson, N., Christian, H., Pinilla, L., Ebling, F., Tena-Sempere, M., Wells, T., & Davies, J. (2006). Hypothalamic Expression of Human Growth Hormone Induces Post-Pubertal Hypergonadotrophism in Male Transgenic Growth Retarded Rats. Journal of Neuroendocrinology, 18(10), 719-731.

    https://doi.org/10.1111/j.1365-2826.2006.01467.x, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa38130
34. Davies, J., Carter, D., & Davies, J. (2006). Protein/DNA interaction profiling reveals novel regulators of the pineal transcriptome. Molecular and Cellular Endocrinology, 252(1-2), 19-26.

    https://doi.org/10.1016/j.mce.2006.03.020, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa38131
35. Martini, A., Fernández-Fernández, R., Tovar, S., Navarro, V., Vigo, E., Vazquez, M., Davies, J., Thompson, N., Aguilar, E., Pinilla, L., Wells, T., Dieguez, C., Tena-Sempere, M., & Davies, J. (2006). Comparative Analysis of the Effects of Ghrelin and Unacylated Ghrelin on Luteinizing Hormone Secretion in Male Rats. Endocrinology, 147(5), 2374-2382.

    https://doi.org/10.1210/en.2005-1422, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa38132
36. Holter, J., Davies, J., Leresche, N., Crunelli, V., & Carter, D. (2005). Identification of Two Further Splice Variants of <I>GABABR1</I> Characterizes the Conserved Micro-Exon 4 as a Hot Spot for Regulated Splicing in the Rat Brain. Journal of Molecular Neuroscience, 26(1), 099-108.

    https://doi.org/10.1385/JMN:26:1:099, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa38133
37. Davies, J. & Davies, J. (2004). Manipulating sorting signals to generate co-expression of somatostatin and eGFP in the regulated secretory pathway from a monocistronic construct. Journal of Molecular Endocrinology, 33(2), 523-532.

    https://doi.org/10.1677/jme.1.01578, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa38134
38. Davies, J., Carter, D., & Wells, T. (2004). Photic Stimulation Inhibits Growth Hormone Secretion in Rats: A Hypothalamic Mechanism for Transient Entrainment. Endocrinology, 145(6), 2950-2958.

    https://doi.org/10.1210/en.2003-1236, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa38135
39. Thompson, N., Davies, J., Mode, A., Houston, P., & Wells, T. (2003). Pattern-Dependent Suppression of Growth Hormone (GH) Pulsatility by Ghrelin and GH-Releasing Peptide-6 in Moderately GH-Deficient Rats. Endocrinology, 144(11), 4859-4867.

    https://doi.org/10.1210/en.2003-0423, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa38136
40. Elabi, O., Davies, J., & Lane, E. (2021). L-dopa-Dependent Effects of GLP-1R Agonists on the Survival of Dopaminergic Cells Transplanted into a Rat Model of Parkinson Disease. International Journal of Molecular Sciences, 22(22), 12346

    https://doi.org/10.3390/ijms222212346, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa58729
41. Rees, D., Johnson, A., Lelos, M., Smith, G., Roberts, L., Phelps, L., Dunnett, S., Morgan, A., Brown, R., Wells, T., & Davies, J. (2022). Acyl-ghrelin attenuates neurochemical and motor deficits in the 6-OHDA model of Parkinson’s disease. bioRxiv

    https://doi.org/10.1101/2022.01.31.478447, SU Repository: https://cronfa.swan.ac.uk/Record/cronfa59475

All Research

• Understanding progressive multiple Sclerosis outcome by integrating genotypic and pathotypic information. (current)

  PhD

  Other supervisor: Dr Jeffrey Davies

  Other supervisor: Dr Owain Howell

• Detection of ghrelin species by Mass Spectrometry, novel biomarkers for diagnosing dementia? (current)

  PhD

  Other supervisor: Dr Alwena Morgan

  Other supervisor: Dr Jeffrey Davies

• Analysis of Adult Hippocampal Neurogenesis in Neurodegenerative disease (current)

  PhD

  Other supervisor: Dr Alwena Morgan

  Other supervisor: Dr Jeffrey Davies

• Characterising the effect of ghrelin-GHS-R signalling on neuronal autophagy (current)

  PhD

  Other supervisor: Dr Alwena Morgan

  Other supervisor: Dr Jeffrey Davies

• An investigation of the complex relationships between different neurological disorders and their associated pathways, using genome-scale bioinformatics platforms. (current)

  MSc

  Other supervisor: Dr Jeffrey Davies

  Other supervisor: Dr Jonathan Mullins

• PM-130 Fundamental Research Skills

  This module is designed to develop the skills required for students of biochemistry and genetics degree programmes. Students meet with their tutors and will be given a series of assignments designed to develop skills in key areas such as essay writing, presentations and general numeracy.

• PM-154 Human Physiology

  Human physiology is the study of how our body works in an integrated way. A central principle of human physiology is homeostasis, the maintenance of a relatively stable internal environment. Failure to maintain homeostasis disrupts normal function that may lead to disease (or pathophysiology). Students will be taught the key concepts of homeostasis in the physiological systems of the body, enabling the student to understand the consequences of pathophysiology to human health. Emphasis will be given to how malfunction of key physiological systems gives rise to disease, using specific examples to enable students to appreciate the relationship between physiology/anatomy and medicine. Fundamental principles of physiology will be illustrated with appropriate clinical examples and during lectures and in practical assignments. Students will gain practical experience in assessing physiological function during four laboratory-based exercises. The impact of pathophysiology of such systems will be assessed through clinical case studies.

• PM-275 Introduction to neuroscience

  In order to help students understand the biological basis for behavioural neuroscience and neurological disorders, this module seeks to integrate cell biology, physiology and biochemistry to understand the founding principles of neuroscience. The aim is to gain a mechanistic and holistic knowledge of the nervous system that builds from the molecular, cellular and developmental, to the systems level. In addition to exploring normal function, this module will introduce common disorders of the central and peripheral nervous systems in an integrated way. Students will be guided in exploring the scientific evidence around what is known and unknown and will be introduced to current research findings in the scientific literature.

• PM-341 Human Biology and the Environment

  This module is intended to provide an understanding of how our environmental factors impact on key aspects of human biology. Various environmental factors such as diet, stress, and pollution will be considered with a focus on their effects on epigenetics, inflammation, gut microbiota, mitochondrial health, and oxidative stress in non-communicable diseases in particular (e.g. chronic respiratory disease, cancer and metabolic disorders). The effect of extreme environments (e.g. altitude, space) and ageing on multiple organ systems will be considered. Students will gain practical experience in communicating these issues to scientific and non-scientific audiences.

• PM-344C Prosiect Capfaen

  Nod y modiwl hwn yw rhoi cyfle i fyfyrwyr gael profiad dysgu capfaen drwy gymryd rhan yn eu prosiect eu hunain yn seiliedig ar gwestiwn ymchwil. Gall y prosiect fod mewn labordy neu heb fod yn labordy ond bydd bob amser yn cynnwys cwestiwn ymchwil sy'n deillio o'r llenyddiaeth, ac sy'n canolbwyntio ar bwnc perthnasol i wyddor feddygol. Bydd yn gofyn cwestiwn ymchwil newydd ac yn cynnwys dadansoddiad beirniadol o ganfyddiadau ymchwil. Bydd myfyrwyr yn mireinio eu sgiliau cyfathrebu llafar ac ysgrifenedig i lefel raddedig, drwy lunio cyflwyniad rhagarweiniol ar gefndir y prosiect, ynghyd â thraethawd estynedig a chyflwyniad llafar ar ganfyddiadau eu hymchwil.

• PM-347 Human Immunopathology

  The module aims to provide students with a greater understanding of the human immune system and the causes of a range of diseases associated with immune dysfunction including autoimmune diseases, metabolic disorders and neurological conditions.

• PM-368C Doctor as a Practitioner 4

  This module enables medical students to consolidate their clinical and communication skills within their clinical practice, building on what they have learned in the previous years and preparing themselves for the foundation year training programme. Focusing on the notion of the Doctor as a practitioner (Tomorrow's Doctors, GMC 2009), this module enables students to further enhance their skills within a safe but clinically-focused environment.

• PM-405 Advanced Research Project Dissertation

  The advanced research project is a key component of the final year of study, providing students with experience of conducting cutting-edge research in the Institute of Life Science and Centre for Nanohealth over an extended period. The projects undertaken will fall into one of the current medically-related research themes. Students will employ a range of advanced analytical procedures to investigate a specific topic. In addition, they will gain experience in preparing a research proposal and presenting their data in various formats. Research topics will be assigned that are appropriate to a specific degree title.

• PM-405C Traethawd Hir Prosiect Ymchwil Uwch

  Mae'r prosiect ymchwil uwch yn elfen allweddol o'r flwyddyn astudio olaf, gan roi cyfle i fyfyrwyr gael profiad o ymchwil arloesol yn y Sefydliad Gwyddor Bywyd a'r Ganolfan NanoIechyd am gyfnod estynedig o amser. Bydd y prosiect yn seiliedig ar un o'r themâu ymchwil sy'n ymwneud â'r gwyddorau meddygol. Bydd myfyrwyr yn defnyddio amrywiaeth o dechnegau dadansoddi uwch i ymchwilio i bwnc penodol. Yn ogystal, cânt brofiad o lunio cynnig ymchwil a chyflwyno eu data mewn amrywiaeth o fformatau. Dynodir pynciau ymchwil sy'n briodol i deitl gradd penodol.

• PMNM17 Neurodegeneration & Repair

  This MSc Medical Neuroscience module will study the processes involved in brain degeneration and repair. We will review disease pathology and diagnosis, the cellular and molecular basis of disease, and possible new therapies aimed at restoring brain function. Content will involve lectures, tutorials, expert guest seminars and workshops.

• Integrated nanoscopy and microscopy in 3-D to study hippocampal neurogenesis at the synaptic and molecular level 2010

  Medical Research Council, £122,545

• Royal Society Research Grant: Ghrelin-mediated hippocampal neurogenesis: a role for GHSR/D1R heterodimerisation 2011

  , £15000

• Weston Brain Institute: Circulating ghrelin as a dementia biomarker. 2020

  , £315,898