Dr Natalie Courtney
- Lecturer in Biomedical Science (Medicine)
email:
Natalie.Courtney@glasgow.ac.uk
pronouns:
She/her/hers
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email:
Natalie.Courtney@glasgow.ac.uk
pronouns:
She/her/hers
Courtney, N., Welsh, M. and Varsou, O. (2021) Hybrid co-teaching using technology: could this be a model for peer-mentoring? In: Tasler, N., O'Brien, R. and Spiers, A. (eds.) Being creative in the face of adversity - Annual #creativeHE collection 2021. Creativity for Learning in Higher Education community (#creativeHE), pp. 65-68. (doi: 10.25416/NTR.17709860.v4)
Deguise, M.-O. et al. (2019) Abnormal fatty acid metabolism is a core component of spinal muscular atrophy. Annals of Clinical and Translational Neurology, 6(8), pp. 1519-1532. (doi: 10.1002/acn3.50855) (PMID:31402618) (PMCID:PMC6689695)
Courtney, N. L., Mole, A. J., Thomson, A. K. and Murray, L. M. (2019) Reduced P53 levels ameliorate neuromuscular junction loss without affecting motor neuron pathology in a mouse model of spinal muscular atrophy. Cell Death and Disease, 10(7), 515. (doi: 10.1038/s41419-019-1727-6) (PMID:31273192) (PMCID:PMC6609617)
Groen, E. J.N., Perenthaler, E., Courtney, N. L., Jordan, C. Y., Shorrock, H. K., van der Hoorn, D., Huang, Y.-T., Murray, L. M., Viero, G. and Gillingwater, T. H. (2018) Temporal and tissue-specific variability of SMN protein levels in mouse models of spinal muscular atrophy. Human Molecular Genetics, 27(16), pp. 2851-2862. (doi: 10.1093/hmg/ddy195) (PMID:29790918) (PMCID:PMC6077828)
Murray, L. M., Beauvais, A., Gibeault, S., Courtney, N. L. and Kothary, R. (2015) Transcriptional profiling of differentially vulnerable motor neurons at pre-symptomatic stage in the Smn (2b/-) mouse model of spinal muscular atrophy. Acta Neuropathologica Communications, 3, 55. (doi: 10.1186/s40478-015-0231-1) (PMID:26374403) (PMCID:PMC4570693)
Deguise, M.-O. et al. (2019) Abnormal fatty acid metabolism is a core component of spinal muscular atrophy. Annals of Clinical and Translational Neurology, 6(8), pp. 1519-1532. (doi: 10.1002/acn3.50855) (PMID:31402618) (PMCID:PMC6689695)
Courtney, N. L., Mole, A. J., Thomson, A. K. and Murray, L. M. (2019) Reduced P53 levels ameliorate neuromuscular junction loss without affecting motor neuron pathology in a mouse model of spinal muscular atrophy. Cell Death and Disease, 10(7), 515. (doi: 10.1038/s41419-019-1727-6) (PMID:31273192) (PMCID:PMC6609617)
Groen, E. J.N., Perenthaler, E., Courtney, N. L., Jordan, C. Y., Shorrock, H. K., van der Hoorn, D., Huang, Y.-T., Murray, L. M., Viero, G. and Gillingwater, T. H. (2018) Temporal and tissue-specific variability of SMN protein levels in mouse models of spinal muscular atrophy. Human Molecular Genetics, 27(16), pp. 2851-2862. (doi: 10.1093/hmg/ddy195) (PMID:29790918) (PMCID:PMC6077828)
Murray, L. M., Beauvais, A., Gibeault, S., Courtney, N. L. and Kothary, R. (2015) Transcriptional profiling of differentially vulnerable motor neurons at pre-symptomatic stage in the Smn (2b/-) mouse model of spinal muscular atrophy. Acta Neuropathologica Communications, 3, 55. (doi: 10.1186/s40478-015-0231-1) (PMID:26374403) (PMCID:PMC4570693)
Courtney, N., Welsh, M. and Varsou, O. (2021) Hybrid co-teaching using technology: could this be a model for peer-mentoring? In: Tasler, N., O'Brien, R. and Spiers, A. (eds.) Being creative in the face of adversity - Annual #creativeHE collection 2021. Creativity for Learning in Higher Education community (#creativeHE), pp. 65-68. (doi: 10.25416/NTR.17709860.v4)