Giles E. Hardingham

University of Edinburgh, Edinburgh, Scotland, United Kingdom 
NMDA receptors
"Giles Hardingham"
Mean distance: 15.85 (cluster 11)


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Hilmar Bading post-doc 1994-2001 MRC-LMB


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Kunal Gupta grad student 2008-2012
BETA: Related publications


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Mehta AR, Gregory JM, Dando O, et al. (2021) Mitochondrial bioenergetic deficits in C9orf72 amyotrophic lateral sclerosis motor neurons cause dysfunctional axonal homeostasis. Acta Neuropathologica
Booker SA, Simões de Oliveira L, Anstey NJ, et al. (2020) Input-Output Relationship of CA1 Pyramidal Neurons Reveals Intact Homeostatic Mechanisms in a Mouse Model of Fragile X Syndrome. Cell Reports. 32: 107988
Elliott E, Bailey O, Waldron FM, et al. (2020) Therapeutic Targeting of Proteostasis in Amyotrophic Lateral Sclerosis-a Systematic Review and Meta-Analysis of Preclinical Research. Frontiers in Neuroscience. 14: 511
Qiu J, Dando O, Febery JA, et al. (2020) Neuronal Activity and Its Role in Controlling Antioxidant Genes. International Journal of Molecular Sciences. 21
Mehta AR, Walters R, Waldron FM, et al. (2019) Targeting mitochondrial dysfunction in amyotrophic lateral sclerosis: a systematic review and meta-analysis. Brain Communications. 1: fcz009
Zhao C, Devlin AC, Chouhan AK, et al. (2019) Mutant C9orf72 human iPSC-derived astrocytes cause non-cell autonomous motor neuron pathophysiology. Glia
Bas-Orth C, Schneider J, Lewen A, et al. (2019) The mitochondrial calcium uniporter is crucial for the generation of fast cortical network rhythms. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 271678X19887777
Vasistha NA, Johnstone M, Barton SK, et al. (2019) Transplanted t(1;11) patient-derived OPCs form shorter myelin internodes in the hypomyelinated shiverer mice. Molecular Psychiatry. 24: 1567
Booker SA, Domanski APF, Dando OR, et al. (2019) Altered dendritic spine function and integration in a mouse model of fragile X syndrome. Nature Communications. 10: 4813
Vasistha NA, Johnstone M, Barton SK, et al. (2019) Familial t(1;11) translocation is associated with disruption of white matter structural integrity and oligodendrocyte-myelin dysfunction. Molecular Psychiatry
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