Department of Cellular Biology and Anatomy
Edward Glasscock has not added Biography.
If you are Edward Glasscock and would like to personalize this page please email our Author Liaison for assistance.
Genomic biomarkers of SUDEP in brain and heart.
Epilepsy & behavior : E&B Sep, 2014 | Pubmed ID: 24139807
Spontaneous seizures in Kcna1-null mice lacking voltage-gated Kv1.1 channels activate Fos expression in select limbic circuits.
Journal of neurochemistry Oct, 2015 | Pubmed ID: 26112121
Expression and function of Kv1.1 potassium channels in human atria from patients with atrial fibrillation.
Basic research in cardiology Sep, 2015 | Pubmed ID: 26162324
Gradient Index Microlens Implanted in Prefrontal Cortex of Mouse Does Not Affect Behavioral Test Performance over Time.
PloS one , 2016 | Pubmed ID: 26799938
Severe respiratory changes at end stage in a FUS-induced disease state in adult rats.
BMC neuroscience Oct, 2016 | Pubmed ID: 27793099
Scn2a deletion improves survival and brain-heart dynamics in the Kcna1-null mouse model of sudden unexpected death in epilepsy (SUDEP).
Human molecular genetics 06, 2017 | Pubmed ID: 28334922
Pharmacogenetics of KCNQ channel activation in 2 potassium channelopathy mouse models of epilepsy.
Epilepsia Dec, 2017 | Pubmed ID: 29265344
Kv1.1 channel subunits in the control of neurocardiac function.
Channels (Austin, Tex.) 12, 2019 | Pubmed ID: 31250689
Neuron-specific Kv1.1 deficiency is sufficient to cause epilepsy, premature death, and cardiorespiratory dysregulation.
Neurobiology of disease 04, 2020 | Pubmed ID: 31978607
Clinical Spectrum of Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity.
International journal of molecular sciences Apr, 2020 | Pubmed ID: 32316562
Decreased bioavailability of hydrogen sulfide links vascular endothelium and atrial remodeling in atrial fibrillation.
Redox biology 01, 2021 | Pubmed ID: 33310503
Kv1.1 potassium channel subunit deficiency alters ventricular arrhythmia susceptibility, contractility, and repolarization.
Physiological reports 01, 2021 | Pubmed ID: 33427415
Kv1.1 deficiency alters repetitive and social behaviors in mice and rescues autistic-like behaviors due to Scn2a haploinsufficiency.
Brain and behavior 04, 2021 | Pubmed ID: 33484493
Kv1.1 subunits localize to cardiorespiratory brain networks in mice where their absence induces astrogliosis and microgliosis.
Molecular and cellular neurosciences Jun, 2021 | Pubmed ID: 33901631
关于 JoVE
版权所属 © 2024 MyJoVE 公司版权所有,本公司不涉及任何医疗业务和医疗服务。