Edward Glasscock - Publications

Affiliations: 
Louisiana State University Health Sciences Center, New Orleans, LA, United States 
Area:
ion channels, epilepsy

17 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, 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
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  1
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  0.68
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  1
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  1
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  1
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  0.36
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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