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Scientific Reports|December 14, 2017
A Bi-fluorescence complementation system to detect associations between the Endoplasmic reticulum and mitochondriaMark Harmon, Philip Larkman, Giles Hardingham, et al.Lancet (London, England)|August 28, 2015
Effect of a GRIN2A de novo mutation associated with epilepsy and intellectual disability on NMDA receptor currents and Mg(2+) block in cultured primary cortical neuronsKatie Marwick, Paul Skehel, Giles Hardingham, et al.Wellcome Open Research|May 2, 2017
Functional assessment of the NMDA receptor variant GluN2A R586KKatie F M Marwick, Peter Parker, Paul Skehel, et al.F1000Research|September 12, 2019
NMDA receptor C-terminal signaling in development, plasticity, and diseaseGiles HardinghamBiochemical Society Transactions|March 20, 2010
Synaptopathy: dysfunction of synaptic function?Nils Brose, Vincent O'Connor, Paul SkehelJournal of Neuroendocrinology|May 15, 2025
Maternal high fat and high sugar diet impacts on key DNA methylation enzymes in offspring brain in a sex-specific mannerKahyee Hor, Laura Dearden, Emily Herzstein, et al.The Journal of Physiology|January 29, 2016
Cerebellar ataxias: β-III spectrin's interactions suggest common pathogenic pathwaysEmma Perkins, Daumante Suminaite, Mandy JacksonJournal of Neurochemistry|February 1, 2011
The ALS8-associated mutant VAPB(P56S) is resistant to proteolysis in neuronsChristos Gkogkas, Caroline Wardrope, Matthew Hannah, et al.Expert Opinion on Investigational Drugs|October 22, 2002
Therapeutic developments in the treatment of amyotrophic lateral sclerosisMandy Jackson, Jerònia Lladó, Jeffrey D RothsteinCurrent Protocols in Neuroscience|April 23, 2008
Models of amyotrophic lateral sclerosisMandy Jackson, Raquelli Ganel, Jeffrey D RothsteinPageof 7