Scott J Myers
Affiliations: | 1999-2008 | Pharmacology | UNC School of Medicine- Chapel Hill |
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Parents
Sign in to add mentor| Ray Dingledine | grad student | 1999-2008 | UNC School of Medicine- Chapel Hill |
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Publications
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| Allen JP, Garber KB, Perszyk R, et al. (2023) Clinical features, functional consequences, and rescue pharmacology of missense GRID1 and GRID2 human variants. Human Molecular Genetics |
| XiangWei W, Perszyk RE, Liu N, et al. (2023) Clinical and functional consequences of GRIA variants in patients with neurological diseases. Cellular and Molecular Life Sciences : Cmls. 80: 345 |
| Lewis SA, Shetty S, Gamble S, et al. (2023) Intrathecal magnesium delivery for Mg++-insensitive NMDA receptor activity due to GRIN1 mutation. Orphanet Journal of Rare Diseases. 18: 225 |
| Myers SJ, Yuan H, Perszyk RE, et al. (2023) Classification of missense variants in the N-methyl-D-aspartate receptor GRIN gene family as gain- or loss-of-function. Human Molecular Genetics |
| Xie L, McDaniel MJ, Perszyk RE, et al. (2023) Functional effects of disease-associated variants reveal that the S1-M1 linker of the NMDA receptor critically controls channel opening. Cellular and Molecular Life Sciences : Cmls. 80: 110 |
| Harris LD, Regan MC, Myers SJ, et al. (2023) Novel GluN2B-Selective NMDA Receptor Negative Allosteric Modulator Possesses Intrinsic Analgesic Properties and Enhances Analgesia of Morphine in a Rodent Tail Flick Pain Model. Acs Chemical Neuroscience |
| Tang W, Beckley JT, Zhang J, et al. (2023) Novel neuroactive steroids as positive allosteric modulators of NMDA receptors: mechanism, site of action, and rescue pharmacology on GRIN variants associated with neurological conditions. Cellular and Molecular Life Sciences : Cmls. 80: 42 |
| Strehlow V, Rieubland C, Gallati S, et al. (2022) Compound-heterozygous GRIN2A null variants associated with severe developmental and epileptic encephalopathy. Epilepsia |
| Brock S, Laquerriere A, Marguet F, et al. (2022) Overlapping cortical malformations in patients with pathogenic variants in and . Journal of Medical Genetics |
| Han W, Yuan H, Allen JP, et al. (2022) . The Journal of Pharmacology and Experimental Therapeutics |