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Edward Glasscock, Ph.D. - Publications

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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30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Si M, Darvish A, Paulhus K, Kumar P, Hamilton KA, Glasscock E. Epilepsy-associated Kv1.1 channel subunits regulate intrinsic cardiac pacemaking in mice. The Journal of General Physiology. 156. PMID 39037413 DOI: 10.1085/jgp.202413578  0.766
2023 Paulhus K, Glasscock E. Novel Genetic Variants Expand the Functional, Molecular, and Pathological Diversity of Channelopathy. International Journal of Molecular Sciences. 24. PMID 37240170 DOI: 10.3390/ijms24108826  0.771
2021 Kumar P, Si M, Paulhus K, Glasscock E. Microelectrode Array Recording of Sinoatrial Node Firing Rate to Identify Intrinsic Cardiac Pacemaking Defects in Mice. Journal of Visualized Experiments : Jove. PMID 34279515 DOI: 10.3791/62735  0.343
2021 Kumar P, Si M, Paulhus K, Glasscock E. Microelectrode Array Recording of Sinoatrial Node Firing Rate to Identify Intrinsic Cardiac Pacemaking Defects in Mice. Journal of Visualized Experiments : Jove. PMID 34279515 DOI: 10.3791/62735  0.738
2021 Dhaibar HA, Hamilton KA, Glasscock E. Kv1.1 subunits localize to cardiorespiratory brain networks in mice where their absence induces astrogliosis and microgliosis. Molecular and Cellular Neurosciences. 103615. PMID 33901631 DOI: 10.1016/j.mcn.2021.103615  0.792
2021 Indumathy J, Pruitt A, Gautier NM, Crane K, Glasscock E. Kv1.1 deficiency alters repetitive and social behaviors in mice and rescues autistic-like behaviors due to Scn2a haploinsufficiency. Brain and Behavior. e02041. PMID 33484493 DOI: 10.1002/brb3.2041  0.353
2021 Trosclair K, Si M, Watts M, Gautier NM, Voigt N, Traylor J, Bitay M, Baczko I, Dobrev D, Hamilton KA, Bhuiyan MS, Dominic P, Glasscock E. Kv1.1 potassium channel subunit deficiency alters ventricular arrhythmia susceptibility, contractility, and repolarization. Physiological Reports. 9: e14702. PMID 33427415 DOI: 10.14814/phy2.14702  0.804
2020 Watts M, Kolluru GK, Dherange P, Pardue S, Si M, Shen X, Trosclair K, Glawe J, Al-Yafeai Z, Iqbal M, Pearson BH, Hamilton KA, Orr AW, Glasscock E, Kevil CG, et al. Decreased bioavailability of hydrogen sulfide links vascular endothelium and atrial remodeling in atrial fibrillation. Redox Biology. 38: 101817. PMID 33310503 DOI: 10.1016/j.redox.2020.101817  0.75
2020 Paulhus K, Ammerman L, Glasscock E. Clinical Spectrum of Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity. International Journal of Molecular Sciences. 21. PMID 32316562 DOI: 10.3390/Ijms21082802  0.765
2020 Trosclair K, Dhaibar HA, Gautier NM, Mishra V, Glasscock E. Neuron-specific Kv1.1 deficiency is sufficient to cause epilepsy, premature death, and cardiorespiratory dysregulation. Neurobiology of Disease. 104759. PMID 31978607 DOI: 10.1016/J.Nbd.2020.104759  0.784
2019 Cruz-Topete D, Oakley RH, Carroll NG, He B, Myers PH, Xu X, Watts MN, Trosclair K, Glasscock E, Dominic P, Cidlowski JA. 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. PMID 31311395 DOI: 10.1161/Jaha.118.011012  0.787
2019 Glasscock E. Kv1.1 channel subunits in the control of neurocardiac function. Channels (Austin, Tex.). 13: 299-307. PMID 31250689 DOI: 10.1080/19336950.2019.1635864  0.531
2019 Dhaibar H, Gautier NM, Chernyshev OY, Dominic P, Glasscock E. Cardiorespiratory profiling reveals primary breathing dysfunction in Kcna1-null mice: Implications for sudden unexpected death in epilepsy. Neurobiology of Disease. 127: 502-511. PMID 30974168 DOI: 10.1016/J.Nbd.2019.04.006  0.818
2018 Si M, Trosclair K, Hamilton KA, Glasscock E. Genetic ablation or pharmacological inhibition of Kv1.1 potassium channel subunits impairs atrial repolarization in mice. American Journal of Physiology. Cell Physiology. PMID 30427720 DOI: 10.1152/Ajpcell.00335.2018  0.785
2018 Mishra V, Gautier NM, Glasscock E. Simultaneous Video-EEG-ECG Monitoring to Identify Neurocardiac Dysfunction in Mouse Models of Epilepsy. Journal of Visualized Experiments : Jove. PMID 29443088 DOI: 10.3791/57300  0.705
2017 Vanhoof-Villalba SL, Gautier NM, Mishra V, Glasscock E. Pharmacogenetics of KCNQ channel activation in 2 potassium channelopathy mouse models of epilepsy. Epilepsia. PMID 29265344 DOI: 10.1111/Epi.13978  0.663
2017 Mishra V, Karumuri BK, Gautier NM, Liu R, Hutson TN, Vanhoof-Villalba SL, Vlachos I, Iasemidis L, Glasscock E. Scn2a deletion improves survival and brain-heart dynamics in the Kcna1-null mouse model of sudden unexpected death in epilepsy (SUDEP). Human Molecular Genetics. PMID 28334922 DOI: 10.1093/Hmg/Ddx104  0.747
2016 Jackson KL, Dhaibar HA, Dayton RD, Cananzi SG, Mayhan WG, Glasscock E, Klein RL. Severe respiratory changes at end stage in a FUS-induced disease state in adult rats. Bmc Neuroscience. 17: 69. PMID 27793099 DOI: 10.1186/S12868-016-0304-5  0.747
2016 Lee SA, Holly KS, Voziyanov V, Villalba SL, Tong R, Grigsby HE, Glasscock E, Szele FG, Vlachos I, Murray TA. Gradient Index Microlens Implanted in Prefrontal Cortex of Mouse Does Not Affect Behavioral Test Performance over Time. Plos One. 11: e0146533. PMID 26799938 DOI: 10.1371/Journal.Pone.0146533  0.704
2015 Glasscock E, Voigt N, McCauley MD, Sun Q, Li N, Chiang DY, Zhou XB, Molina CE, Thomas D, Schmidt C, Skapura DG, Noebels JL, Dobrev D, Wehrens XH. Expression and function of Kv1.1 potassium channels in human atria from patients with atrial fibrillation. Basic Research in Cardiology. 110: 505. PMID 26162324 DOI: 10.1007/S00395-015-0505-6  0.675
2015 Gautier NM, Glasscock E. Spontaneous seizures in Kcna1-null mice lacking voltage-gated Kv1.1 channels activate Fos expression in select limbic circuits. Journal of Neurochemistry. 135: 157-64. PMID 26112121 DOI: 10.1111/Jnc.13206  0.476
2014 Glasscock E. Genomic biomarkers of SUDEP in brain and heart. Epilepsy & Behavior : E&B. 38: 172-9. PMID 24139807 DOI: 10.1016/J.Yebeh.2013.09.019  0.44
2012 Glasscock E, Qian J, Kole MJ, Noebels JL. Transcompartmental reversal of single fibre hyperexcitability in juxtaparanodal Kv1.1-deficient vagus nerve axons by activation of nodal KCNQ channels. The Journal of Physiology. 590: 3913-26. PMID 22641786 DOI: 10.1113/Jphysiol.2012.235606  0.636
2010 Glasscock E, Yoo JW, Chen TT, Klassen TL, Noebels JL. Kv1.1 potassium channel deficiency reveals brain-driven cardiac dysfunction as a candidate mechanism for sudden unexplained death in epilepsy. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 5167-75. PMID 20392939 DOI: 10.1523/Jneurosci.5591-09.2010  0.707
2009 Goldman AM, Glasscock E, Yoo J, Chen TT, Klassen TL, Noebels JL. Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death. Science Translational Medicine. 1: 2ra6. PMID 20368164 DOI: 10.1126/Scitranslmed.3000289  0.675
2008 Glasscock E, Noebels JL. When a disease gene is not really a disease gene Future Neurology. 3: 103-106. DOI: 10.2217/14796708.3.2.103  0.58
2007 Glasscock E, Qian J, Yoo JW, Noebels JL. Masking epilepsy by combining two epilepsy genes. Nature Neuroscience. 10: 1554-8. PMID 17982453 DOI: 10.1038/Nn1999  0.701
2005 Glasscock E, Singhania A, Tanouye MA. The mei-P26 gene encodes a RING finger B-box coiled-coil-NHL protein that regulates seizure susceptibility in Drosophilia. Genetics. 170: 1677-89. PMID 15937125 DOI: 10.1534/Genetics.105.043174  0.687
2005 Glasscock E, Tanouye MA. Drosophila couch potato mutants exhibit complex neurological abnormalities including epilepsy phenotypes. Genetics. 169: 2137-49. PMID 15687283 DOI: 10.1534/Genetics.104.028357  0.687
2001 Benavides F, Venables A, Poetschke Klug H, Glasscock E, Rudensky A, Gómez M, Martin Palenzuela N, Guénet JL, Richie ER, Conti CJ. The CD4 T cell-deficient mouse mutation nackt (nkt) involves a deletion in the cathepsin L (CtsI) gene. Immunogenetics. 53: 233-42. PMID 11398968 DOI: 10.1007/S002510100320  0.305
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