Robert L. Macdonald
Affiliations: | Vanderbilt University, Nashville, TN |
Area:
GABA, epilepsyGoogle:
"Robert Macdonald"Mean distance: 13.82 (cluster 46)
Parents
Sign in to add mentorDavid Harris Cohen | grad student | 1969 | UVA |
Phillip G. Nelson | research scientist | NIH |
Children
Sign in to add traineeKevin Haas | grad student | University of Michigan | |
Linda M. Nowak | grad student | University of Michigan | |
Kate Gurba | grad student | 2007- | Vanderbilt |
Xuan Huang | grad student | 2008- | Vanderbilt |
Naomi Nagaya | grad student | 1996-2002 | University of Michigan |
David J. Hinkle | grad student | 2003 | University of Michigan |
Matt T. Bianchi | grad student | 2004 | University of Michigan |
Dorothy M. Jones-Davis | grad student | 1998-2004 | University of Michigan |
Emily Schwartz Todd | grad student | 2003-2007 | Vanderbilt |
Xin Tang | grad student | 2003-2008 | Vanderbilt |
Emmanuel J. Botzolakis | grad student | 2004-2008 | Vanderbilt |
Mengnan Tian | grad student | 2006-2012 | Vanderbilt |
Janet Fisher | post-doc | University of Michigan Medical School | |
Robert A. Gross | post-doc | University of Rochester Medical Center | |
Aurea Pimenta | post-doc | 2011- | Vanderbilt |
Chengwen Zhou | post-doc | 2011- | Vanderbilt |
Jaideep Kapur | post-doc | 1993-1998 | University of Michigan |
BETA: Related publications
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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 |