| Year |
Citation |
Score |
| 2022 |
Catron MA, Howe RK, Besing GK, St John EK, Potesta CV, Gallagher MJ, Macdonald RL, Zhou C. Sleep slow-wave oscillations trigger seizures in a genetic epilepsy model of Dravet syndrome. Brain Communications. 5: fcac332. PMID 36632186 DOI: 10.1093/braincomms/fcac332 |
0.536 |
|
| 2022 |
Qu S, Jackson LG, Zhou C, Shen D, Shen W, Nwosu G, Howe R, Caltron M, Flamm C, Biven M, Kang JQ, Macdonald RL. Heterozygous GABA receptor β3 subunit N110D knock-in mice have epileptic spasms. Epilepsia. PMID 36495145 DOI: 10.1111/epi.17470 |
0.546 |
|
| 2021 |
Song YJ, Xing B, Barbour AJ, Zhou C, Jensen FE. Dysregulation of GABAA Receptor-Mediated Neurotransmission during the Auditory Cortex Critical Period in the Fragile X Syndrome Mouse Model. Cerebral Cortex (New York, N.Y. : 1991). PMID 34223875 DOI: 10.1093/cercor/bhab203 |
0.48 |
|
| 2021 |
Qu S, Zhou C, Howe R, Shen W, Huang X, Catron M, Hu N, Macdonald RL. The K328M substitution in the human GABA receptor gamma2 subunit causes GEFS+ and premature sudden death in knock-in mice. Neurobiology of Disease. 105296. PMID 33582225 DOI: 10.1016/j.nbd.2021.105296 |
0.574 |
|
| 2020 |
Zhang CQ, Catron MA, Ding L, Hanna CM, Gallagher MJ, Macdonald RL, Zhou C. Impaired State-Dependent Potentiation of GABAergic Synaptic Currents Triggers Seizures in a Genetic Generalized Epilepsy Model. Cerebral Cortex (New York, N.Y. : 1991). PMID 32930324 DOI: 10.1093/Cercor/Bhaa256 |
0.59 |
|
| 2020 |
Qu S, Catron M, Zhou C, Janve V, Shen W, Howe RK, Macdonald RL. GABA receptor β3 subunit mutation D120N causes Lennox-Gastaut syndrome in knock-in mice. Brain Communications. 2: fcaa028. PMID 32467926 DOI: 10.1093/braincomms/fcaa028 |
0.65 |
|
| 2020 |
Klofas LK, Short BP, Zhou C, Carson RP. Prevention of premature death and seizures in a Depdc5 mouse epilepsy model through inhibition of mTORC1. Human Molecular Genetics. PMID 32280987 DOI: 10.1093/Hmg/Ddaa068 |
0.516 |
|
| 2019 |
Ding L, Satish S, Zhou C, Gallagher MJ. Cortical activation in generalized seizures. Epilepsia. PMID 31368118 DOI: 10.1111/Epi.16306 |
0.506 |
|
| 2017 |
Huang X, Zhou C, Tian M, Kang JQ, Shen W, Verdier K, Pimenta A, MacDonald RL. Overexpressing wild-type γ2 subunits rescued the seizure phenotype in Gabrg2(+/Q390X) Dravet syndrome mice. Epilepsia. PMID 28586508 DOI: 10.1111/Epi.13810 |
0.673 |
|
| 2016 |
Lippman-Bell JJ, Zhou C, Sun H, Feske JS, Jensen FE. Early-life seizures alter synaptic calcium-permeable AMPA receptor function and plasticity. Molecular and Cellular Neurosciences. PMID 27521497 DOI: 10.1016/J.Mcn.2016.08.002 |
0.57 |
|
| 2015 |
Zhou C, Sun H, Klein PM, Jensen FE. Neonatal seizures alter NMDA glutamate receptor GluN2A and 3A subunit expression and function in hippocampal CA1 neurons. Frontiers in Cellular Neuroscience. 9: 362. PMID 26441533 DOI: 10.3389/Fncel.2015.00362 |
0.667 |
|
| 2015 |
Arain F, Zhou C, Ding L, Zaidi S, Gallagher MJ. The developmental evolution of the seizure phenotype and cortical inhibition in mouse models of juvenile myoclonic epilepsy. Neurobiology of Disease. 82: 164-175. PMID 26054439 DOI: 10.1016/J.Nbd.2015.05.016 |
0.519 |
|
| 2015 |
Kang JQ, Shen W, Zhou C, Xu D, Macdonald RL. The human epilepsy mutation GABRG2(Q390X) causes chronic subunit accumulation and neurodegeneration. Nature Neuroscience. 18: 988-96. PMID 26005849 DOI: 10.1038/Nn.4024 |
0.619 |
|
| 2014 |
Zhou C, Ding L, Deel ME, Ferrick EA, Emeson RB, Gallagher MJ. Altered intrathalamic GABAA neurotransmission in a mouse model of a human genetic absence epilepsy syndrome. Neurobiology of Disease. 73: 407-417. PMID 25447232 DOI: 10.1016/J.Nbd.2014.10.021 |
0.507 |
|
| 2013 |
Zhou C, Huang Z, Ding L, Deel ME, Arain FM, Murray CR, Patel RS, Flanagan CD, Gallagher MJ. Altered cortical GABAA receptor composition, physiology, and endocytosis in a mouse model of a human genetic absence epilepsy syndrome. The Journal of Biological Chemistry. 288: 21458-72. PMID 23744069 DOI: 10.1074/Jbc.M112.444372 |
0.565 |
|
| 2012 |
Rakhade SN, Fitzgerald EF, Klein PM, Zhou C, Sun H, Huganir RL, Hunganir RL, Jensen FE. Glutamate receptor 1 phosphorylation at serine 831 and 845 modulates seizure susceptibility and hippocampal hyperexcitability after early life seizures. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 17800-12. PMID 23223299 DOI: 10.1523/Jneurosci.6121-11.2012 |
0.659 |
|
| 2011 |
Zhou C, Lippman JJ, Sun H, Jensen FE. Hypoxia-induced neonatal seizures diminish silent synapses and long-term potentiation in hippocampal CA1 neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 18211-22. PMID 22171027 DOI: 10.1523/Jneurosci.4838-11.2011 |
0.616 |
|
| 2009 |
Zhou C, Jensen FE, Sucher NJ. Altered development of glutamatergic synapses in layer V pyramidal neurons in NR3A knockout mice. Molecular and Cellular Neurosciences. 42: 419-26. PMID 19782137 DOI: 10.1016/J.Mcn.2009.09.004 |
0.541 |
|
| 2008 |
Rakhade SN, Zhou C, Aujla PK, Fishman R, Sucher NJ, Jensen FE. Early alterations of AMPA receptors mediate synaptic potentiation induced by neonatal seizures. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 7979-90. PMID 18685023 DOI: 10.1523/Jneurosci.1734-08.2008 |
0.655 |
|
| 2008 |
Manning SM, Talos DM, Zhou C, Selip DB, Park HK, Park CJ, Volpe JJ, Jensen FE. NMDA receptor blockade with memantine attenuates white matter injury in a rat model of periventricular leukomalacia. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 6670-8. PMID 18579741 DOI: 10.1523/Jneurosci.1702-08.2008 |
0.47 |
|
| 2005 |
Zhou C, Dacheux RF. Glycine- and GABA-activated inhibitory currents on axon terminals of rabbit cone bipolar cells. Visual Neuroscience. 22: 759-67. PMID 16469186 DOI: 10.1017/S095252380522607X |
0.313 |
|
| 2004 |
Zhou C, Dacheux RF. All amacrine cells in the rabbit retina possess AMPA-, NMDA-, GABA-, and glycine-activated currents. Visual Neuroscience. 21: 181-8. PMID 15259569 DOI: 10.1017/S0952523804042099 |
0.372 |
|
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