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Neurology|March 8, 2013
Hippocampal volume and cell density changes in a mouse model of human genetic epilepsyKay L Richards, Nyoman D Kurniawan, Zhengyi Yang, et al.
Brain : a Journal of Neurology|April 8, 2010
Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsyYunxiang Liao, Liesbet Deprez, Snezana Maljevic, et al.
Brain : a Journal of Neurology|April 6, 2021
Cation leak underlies neuronal excitability in an HCN1 developmental and epileptic encephalopathyLauren E Bleakley, Chaseley E McKenzie, Ming S Soh, et al.
The Journal of Biological Chemistry|November 3, 2005
A Thr357 to Ser polymorphism in homozygous and compound heterozygous subjects causes absent or reduced P2X7 function and impairs ATP-induced mycobacterial killing by macrophagesAnne N Shemon, Ronald Sluyter, Suran L Fernando, et al.
Neuroimage|September 25, 2013
Visualization of mouse barrel cortex using ex-vivo track density imagingNyoman D Kurniawan, Kay L Richards, Zhengyi Yang, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 5, 2018
Selective NaV1.1 activation rescues Dravet syndrome mice from seizures and premature deathKay L Richards, Carol J Milligan, Robert J Richardson, et al.
Communications Biology|May 31, 2022
Functional correlates of clinical phenotype and severity in recurrent SCN2A variantsGéza Berecki, Katherine B Howell, Jacqueline Heighway, et al.
Molecular Neurodegeneration|September 27, 2023
The Q/R editing site of AMPA receptor GluA2 subunit acts as an epigenetic switch regulating dendritic spines, neurodegeneration and cognitive deficits in Alzheimer's diseaseAmanda L Wright, Lyndsey M Konen, Bruce G Mockett, et al.
JCI Insight|September 29, 2022
Antisense oligonucleotide therapy for KCNT1 encephalopathyLisseth Estefania Burbano, Melody Li, Nikola Jancovski, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 20, 2007
Reduced cortical inhibition in a mouse model of familial childhood absence epilepsyHeneu O Tan, Christopher A Reid, Frank N Single, et al.
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