Edward Glasscock

Louisiana State University Health Sciences Center, New Orleans, LA, United States 
ion channels, epilepsy
"Edward Glasscock"
Mean distance: 14.66 (cluster 11)
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Indumathy J, Pruitt A, Gautier NM, et al. (2021) Kv1.1 deficiency alters repetitive and social behaviors in mice and rescues autistic-like behaviors due to Scn2a haploinsufficiency. Brain and Behavior. e02041
Trosclair K, Si M, Watts M, et al. (2021) Kv1.1 potassium channel subunit deficiency alters ventricular arrhythmia susceptibility, contractility, and repolarization. Physiological Reports. 9: e14702
Watts M, Kolluru GK, Dherange P, et al. (2020) Decreased bioavailability of hydrogen sulfide links vascular endothelium and atrial remodeling in atrial fibrillation. Redox Biology. 38: 101817
Trosclair K, Dhaibar HA, Gautier NM, et al. (2020) Neuron-specific Kv1.1 deficiency is sufficient to cause epilepsy, premature death, and cardiorespiratory dysregulation. Neurobiology of Disease. 104759
Cruz-Topete D, Oakley RH, Carroll NG, et al. (2019) Deletion of the Cardiomyocyte Glucocorticoid Receptor Leads to Sexually Dimorphic Changes in Cardiac Gene Expression and Progression to Heart Failure. Journal of the American Heart Association. 8: e011012
Dhaibar H, Gautier NM, Chernyshev OY, et al. (2019) Cardiorespiratory profiling reveals primary breathing dysfunction in Kcna1-null mice: Implications for sudden unexpected death in epilepsy. Neurobiology of Disease. 127: 502-511
Si M, Trosclair K, Hamilton KA, et al. (2018) Genetic ablation or pharmacological inhibition of Kv1.1 potassium channel subunits impairs atrial repolarization in mice. American Journal of Physiology. Cell Physiology
Mishra V, Gautier NM, Glasscock E. (2018) Simultaneous Video-EEG-ECG Monitoring to Identify Neurocardiac Dysfunction in Mouse Models of Epilepsy. Journal of Visualized Experiments : Jove
Vanhoof-Villalba SL, Gautier NM, Mishra V, et al. (2017) Pharmacogenetics of KCNQ channel activation in 2 potassium channelopathy mouse models of epilepsy. Epilepsia
Mishra V, Karumuri BK, Gautier NM, et al. (2017) Scn2a deletion improves survival and brain-heart dynamics in the Kcna1-null mouse model of sudden unexpected death in epilepsy (SUDEP). Human Molecular Genetics
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