Giles E. Hardingham

University of Edinburgh, Edinburgh, Scotland, United Kingdom 
NMDA receptors
"Giles Hardingham"
Mean distance: 15.85 (cluster 11)
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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
Qiu J, Dando O, Febery JA, et al. (2020) Neuronal Activity and Its Role in Controlling Antioxidant Genes. International Journal of Molecular Sciences. 21
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
Marwick KFM, Skehel PA, Hardingham GE, et al. (2019) The human NMDA receptor GluN2A variant influences channel blocker potency. Pharmacology Research & Perspectives. 7: e00495
Asiminas A, Jackson AD, Louros SR, et al. (2019) Sustained correction of associative learning deficits after brief, early treatment in a rat model of Fragile X Syndrome. Science Translational Medicine. 11
Marwick KFM, Hansen KB, Skehel PA, et al. (2019) Functional assessment of triheteromeric NMDA receptors containing a human variant associated with epilepsy. The Journal of Physiology
Strehlow V, Heyne HO, Vlaskamp DRM, et al. (2018) GRIN2A-related disorders: genotype and functional consequence predict phenotype. Brain : a Journal of Neurology
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