Robert L. Macdonald

Vanderbilt University, Nashville, TN 
GABA, epilepsy
"Robert Macdonald"
Mean distance: 13.82 (cluster 46)
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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
Zhang CQ, McMahon B, Dong H, et al. (2019) Molecular basis for and chemogenetic modulation of comorbidities in GABRG2-deficient epilepsies. Epilepsia
Hernandez CC, XiangWei W, Hu N, et al. (2019) Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies. Brain : a Journal of Neurology
Hernandez CC, Macdonald RL. (2019) A Structural Look at GABA Receptor Mutations Linked to Epilepsy Syndromes. Brain Research
Lagrange AH, Hu N, Macdonald RL. (2018) GABA beyond the synapse-defining the subtype-specific pharmacodynamics of nonsynaptic GABA receptors. The Journal of Physiology
Lin H, Hu N, Zhang Y, et al. (2018) Whole exome sequencing reveals novel NOV and DCAF13 variants in a Chinese pedigree with familial cortical myoclonic tremor with epilepsy. Neuroscience Letters
Wang CH, Hernandez CC, Wu J, et al. (2018) A missense mutation A384P associated with human hyperekplexia reveals a desensitization site of glycine receptors. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Hernandez CC, Zhang Y, Hu N, et al. (2017) GABA A Receptor Coupling Junction and Pore GABRB3 Mutations are Linked to Early-Onset Epileptic Encephalopathy. Scientific Reports. 7: 15903
Huang X, Zhou C, Tian M, et al. (2017) Overexpressing wild-type γ2 subunits rescued the seizure phenotype in Gabrg2(+/Q390X) Dravet syndrome mice. Epilepsia
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