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Edward Glasscock, Ph.D.

Affiliations: 
2013-2019 Cellular Biology & Anatomy Louisiana State University Health Sciences Center, New Orleans, LA, United States 
 2019- Biological Sciences Southern Methodist University, Dallas, TX, United States 
Area:
ion channels, epilepsy
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"Edward Glasscock"
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Parents

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Mark Tanouye grad student 2000-2005 UC Berkeley
 (Genetic modification of seizure susceptibility in Drosophila.)
Jeffrey L. Noebels post-doc 2005-2012 Baylor College of Medicine

Children

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Fallon Wenck research assistant 2020- SMU
Nicole 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- LSU Health Sciences Center
Praveen Kumar post-doc 2018- SMU
Indumathy Jagadeeswaran post-doc 2017-2021 SMU

Collaborators

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Teresa A. Murray collaborator 2015- Louisiana State University Health Sciences Center - Shreveport
BETA: Related publications

Publications

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Paulhus K, Glasscock E. (2023) Novel Genetic Variants Expand the Functional, Molecular, and Pathological Diversity of Channelopathy. International Journal of Molecular Sciences. 24
Kumar P, Si M, Paulhus K, et al. (2021) Microelectrode Array Recording of Sinoatrial Node Firing Rate to Identify Intrinsic Cardiac Pacemaking Defects in Mice. Journal of Visualized Experiments : Jove
Kumar P, Si M, Paulhus K, et al. (2021) Microelectrode Array Recording of Sinoatrial Node Firing Rate to Identify Intrinsic Cardiac Pacemaking Defects in Mice. Journal of Visualized Experiments : Jove
Dhaibar HA, Hamilton KA, Glasscock E. (2021) Kv1.1 subunits localize to cardiorespiratory brain networks in mice where their absence induces astrogliosis and microgliosis. Molecular and Cellular Neurosciences. 103615
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
Paulhus K, Ammerman L, Glasscock E. (2020) Clinical Spectrum of Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity. International Journal of Molecular Sciences. 21
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
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