Edward Glasscock
Affiliations: | Louisiana State University Health Sciences Center, New Orleans, LA, United States |
Area:
ion channels, epilepsyGoogle:
"Edward Glasscock"Mean distance: 14.66 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentorMark Tanouye | grad student | 2000-2005 | UC Berkeley | |
(Genetic modification of seizure susceptibility in Drosophila.) | ||||
Jeffrey L. Noebels | post-doc | 2005-2012 | Baylor |
Children
Sign in to add traineeNicole Marie Gautier Hall | research assistant | 2013-2019 | Louisiana State University Health Sciences Center - Shreveport |
Kelsey Caryn Paulhus | grad student | ||
Hemangini Dhaibar | grad student | 2014- | LSU Health Sciences Center |
Krystle Trosclair | grad student | 2016- | LSU Health Sciences Center |
Stephanie Villalba | grad student | 2013-2017 | LSU Health Sciences Center |
Vikas Mishra | post-doc | 2014- | LSU Health Sciences Center |
Man Si | post-doc | 2014-2016 | LSU Health Sciences Center |
Collaborators
Sign in to add collaboratorTeresa A. Murray | collaborator | 2015- | Louisiana State University Health Sciences Center - Shreveport |
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Publications
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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 |