Robert L. Macdonald

Affiliations: 
Vanderbilt University, Nashville, TN 
Area:
GABA, epilepsy
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"Robert Macdonald"
Mean distance: 13.82 (cluster 46)
 
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Publications

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Hernandez CC, Hu N, Shen W, et al. (2023) Epileptic Encephalopathy Structural Variants Share Common Gating and Trafficking Defects. Biomolecules. 13
Hernandez CC, Shen Y, Hu N, et al. (2023) Variants Associated with Febrile Seizures. Biomolecules. 13
Catron MA, Howe RK, Besing GK, et al. (2022) Sleep slow-wave oscillations trigger seizures in a genetic epilepsy model of Dravet syndrome. Brain Communications. 5: fcac332
Qu S, Jackson LG, Zhou C, et al. (2022) Heterozygous GABA receptor β3 subunit N110D knock-in mice have epileptic spasms. Epilepsia
Qu S, Zhou C, Howe R, et al. (2021) The K328M substitution in the human GABA receptor gamma2 subunit causes GEFS+ and premature sudden death in knock-in mice. Neurobiology of Disease. 105296
Shen D, Chen J, Liu D, et al. (2020) The F343L allele causes spontaneous seizures in a novel transgenic zebrafish model that can be treated with suberanilohydroxamic acid (SAHA). Annals of Translational Medicine. 8: 1560
Shen W, Poliquin S, Macdonald RL, et al. (2020) Endoplasmic reticulum stress increases inflammatory cytokines in an epilepsy mouse model Gabrg2 knockin: A link between genetic and acquired epilepsy? Epilepsia
Zhang CQ, Catron MA, Ding L, et al. (2020) Impaired State-Dependent Potentiation of GABAergic Synaptic Currents Triggers Seizures in a Genetic Generalized Epilepsy Model. Cerebral Cortex (New York, N.Y. : 1991)
Qu S, Catron M, Zhou C, et al. (2020) GABA receptor β3 subunit mutation D120N causes Lennox-Gastaut syndrome in knock-in mice. Brain Communications. 2: fcaa028
Shi YW, Zhang Q, Cai K, et al. (2019) Synaptic clustering differences due to different GABRB3 mutations cause variable epilepsy syndromes. Brain : a Journal of Neurology
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