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Biorxiv : the Preprint Server for Biology|April 1, 2024
Enhancer-targeted CRISPR-Activation Rescues Haploinsufficient Autism Susceptibility GenesGeorge T Chen, Gayatri Nair, Aubrey J Osorio, et al.Frontiers in Cellular Neuroscience|April 9, 2020
Paroxysmal Discharges in Tissue Slices From Pediatric Epilepsy Surgery Patients: Critical Role of GABAB Receptors in the Generation of Ictal ActivitySimon Levinson, Conny H Tran, Joshua Barry, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 26, 2013
Multiple sources of striatal inhibition are differentially affected in Huntington's disease mouse modelsCarlos Cepeda, Laurie Galvan, Sandra M Holley, et al.Experimental Neurology|February 20, 2026
Glucose transporter 3 gene deficiency modifies Huntington's disease progression in zQ175 model miceTomoko Daida, Bo-Chul Shin, Joshua Barry, et al.Frontiers in Neural Circuits|November 17, 2022
Dissociable effects of oxycodone on behavior, calcium transient activity, and excitability of dorsolateral striatal neuronsJoshua Barry, Katerina D Oikonomou, Allison Peng, et al.Journal of Neuroscience Research|July 30, 2019
Developmental origins of cortical hyperexcitability in Huntington's disease: Review and new observationsCarlos Cepeda, Katerina D Oikonomou, Damian Cummings, et al.Epilepsia Open|December 20, 2018
Cellular antiseizure mechanisms of everolimus in pediatric tuberous sclerosis complex, cortical dysplasia, and non-mTOR-mediated etiologiesCarlos Cepeda, Simon Levinson, Vannah-Wila Yazon, et al.Science'S STKE : Signal Transduction Knowledge Environment|May 4, 2006
Where do you think you are going? The NMDA-D1 receptor trapCarlos Cepeda, Michael S LevineNeuron|May 15, 2012
2B or not 2B: a tail of two NMDA receptor subunitsCarlos Cepeda, Michael S LevineThe Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry|November 17, 2020
Synaptic Dysfunction in Huntington's Disease: Lessons from Genetic Animal ModelsCarlos Cepeda, Michael S LevinePageof 16