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Brain : a Journal of Neurology|December 26, 2023
Increased expression of chondroitin sulfate proteoglycans in dentate gyrus and amygdala causes postinfectious seizuresDipan C Patel, Nathaniel Swift, Bhanu P Tewari, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 2, 2017
Acute Increases in Protein O-GlcNAcylation Dampen Epileptiform Activity in HippocampusLuke T Stewart, Anas U Khan, Kai Wang, et al.
Molecular Autism|November 2, 2017
RNA sequencing and proteomics approaches reveal novel deficits in the cortex of Mecp2-deficient mice, a model for Rett syndromeNatasha L Pacheco, Michael R Heaven, Leanne M Holt, et al.
Molecular & Cellular Proteomics : MCP|November 22, 2021
Metabolic Enzyme Alterations and Astrocyte Dysfunction in a Murine Model of Alexander Disease With Severe Reactive GliosisMichael R Heaven, Anthony W Herren, Daniel L Flint, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
Brain injury contributes to dopaminergic neurodegeneration, Lewy body pathology, and Parkinsonism preclinically with outcomes altered by T cell modulationColin Kelly, Julia P Milner, Brooke A Lester, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 22, 2025
Degradation of perineuronal nets in hippocampal CA2 explains the loss of social cognition memory in Alzheimer's diseaseLata Chaunsali, Jiangtao Li, Erik Fleischel, et al.
Nature Neuroscience|April 2, 2014
Astrocyte Kir4.1 ion channel deficits contribute to neuronal dysfunction in Huntington's disease model miceXiaoping Tong, Yan Ao, Guido C Faas, et al.
Communications Biology|March 29, 2024
Kir4.1 channels contribute to astrocyte CO2/H+-sensitivity and the drive to breatheColin M Cleary, Jack L Browning, Moritz Armbruster, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 15, 2024
STING-Dependent Signaling in Microglia or Peripheral Immune Cells Orchestrates the Early Inflammatory Response and Influences Brain Injury OutcomeLauren E Fritsch, Colin Kelly, John Leonard, et al.
Journal of Medical Genetics|January 9, 2014
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndromeVishnu Anand Cuddapah, Rajesh B Pillai, Kiran V Shekar, et al.
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