Jonathon Lovelace, B.A.
Affiliations: | Psychology-Systems Neuroscience | University of California, Riverside, Riverside, CA, United States |
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Parents
Sign in to add mentorEdward Korzus | grad student | UC Riverside | |
Khaleel Razak | post-doc | UC Riverside |
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Publications
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Lovelace JW, Ethell IM, Binder DK, et al. (2020) Minocycline Treatment Reverses Sound Evoked EEG Abnormalities in a Mouse Model of Fragile X Syndrome. Frontiers in Neuroscience. 14: 771 |
Pirbhoy PS, Rais M, Lovelace JW, et al. (2020) Acute pharmacological inhibition of matrix metalloproteinase-9 activity during development restores perineuronal net formation and normalizes auditory processing in Fmr1 KO mice. Journal of Neurochemistry |
McCullagh EA, Rotschafer SE, Auerbach BD, et al. (2020) Mechanisms underlying auditory processing deficits in Fragile X syndrome. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology |
Jonak CR, Lovelace JW, Ethell IM, et al. (2020) Multielectrode array analysis of EEG biomarkers in a mouse model of Fragile X Syndrome. Neurobiology of Disease. 104794 |
Lovelace JW, Rais M, Palacios AR, et al. (2019) Deletion of Fmr1 from Forebrain Excitatory Neurons Triggers Abnormal Cellular, EEG, and Behavioral Phenotypes in the Auditory Cortex of a Mouse Model of Fragile X Syndrome. Cerebral Cortex (New York, N.Y. : 1991) |
Wen TH, Lovelace JW, Ethell IM, et al. (2018) Developmental Changes in EEG Phenotypes in a Mouse Model of Fragile X Syndrome. Neuroscience |
Jonak CR, Lovelace JW, Ethell IM, et al. (2018) Reusable Multielectrode Array Technique for Electroencephalography in Awake Freely Moving Mice. Frontiers in Integrative Neuroscience. 12: 53 |
Lovelace JW, Ethell IM, Binder DK, et al. (2018) Translation-relevant EEG phenotypes in a mouse model of Fragile X Syndrome. Neurobiology of Disease |
David CN, Frias ES, Szu JI, et al. (2016) GLT-1-Dependent Disruption of CNS Glutamate Homeostasis and Neuronal Function by the Protozoan Parasite Toxoplasma gondii. Plos Pathogens. 12: e1005643 |
Lovelace JW, Wen TH, Reinhard S, et al. (2016) Matrix metalloproteinase-9 deletion rescues auditory evoked potential habituation deficit in a mouse model of Fragile X Syndrome. Neurobiology of Disease |