Year |
Citation |
Score |
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 |
0.76 |
|
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 |
0.337 |
|
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 |
0.716 |
|
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 |
0.355 |
|
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 |
0.788 |
|
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 |
0.741 |
|
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 |
0.755 |
|
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 |
0.779 |
|
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 |
0.785 |
|
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 |
0.505 |
|
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 |
0.815 |
|
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 |
0.764 |
|
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 |
0.706 |
|
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 |
0.662 |
|
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 |
0.741 |
|
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 |
0.7 |
|
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 |
0.656 |
|
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 |
0.471 |
|
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 |
0.444 |
|
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 |
0.63 |
|
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 |
0.695 |
|
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 |
0.676 |
|
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 |
0.586 |
|
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 |
0.699 |
|
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 |
0.689 |
|
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 |
0.689 |
|
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 |
0.312 |
|
Low-probability matches (unlikely to be authored by this person) |
2020 |
Hutson TN, Rezaei F, Gautier NM, Indumathy J, Glasscock E, Iasemidis L. Directed Connectivity Analysis of the Neuro-Cardio- and Respiratory Systems Reveals Novel Biomarkers of Susceptibility to SUDEP. Ieee Open Journal of Engineering in Medicine and Biology. 1: 301-311. PMID 34223181 DOI: 10.1109/ojemb.2020.3036544 |
0.289 |
|
2020 |
Hutson TN, Rezaei F, Gautier NM, Indumathy J, Glasscock E, Iasemidis L. Directed Connectivity Analysis of the Neuro-Cardio- and Respiratory Systems Reveals Novel Biomarkers of Susceptibility to SUDEP. Ieee Open Journal of Engineering in Medicine and Biology. 1: 301-311. PMID 34223181 DOI: 10.1109/ojemb.2020.3036544 |
0.289 |
|
2000 |
Benavides F, Stern MC, Glasscock E, DiGiovanni J, Coghlan LG, Conti CJ. Microsatellite DNA variants between the inbred SENCAR mouse strains. Molecular Carcinogenesis. 28: 191-5. PMID 10972988 DOI: 10.1002/1098-2744(200008)28:4<191::Aid-Mc1>3.0.Co;2-K |
0.258 |
|
2003 |
Benavides F, Conti CJ, LaCava M, Flores M, Glasscock E, Sternik G, Gimenez-Conti IB, Johnston DA, Dunsford HA, Goldstein LS, Rodriguez LV. Loss of heterozygosity analysis of mouse pulmonary adenomas induced by coal tar. Environmental and Molecular Mutagenesis. 41: 300-8. PMID 12717785 DOI: 10.1002/Em.10155 |
0.253 |
|
2001 |
Benavides F, Glasscock E, Coghlan LG, Stern MC, Weiss DA, Conti CJ. PCR-based microsatellite analysis for differentiation and genetic monitoring of nine inbred SENCAR mouse strains. Laboratory Animals. 35: 157-62. PMID 11315165 DOI: 10.1258/0023677011911534 |
0.243 |
|
2022 |
Lin King YH, Chen C, Lin King JV, Simms J, Glasscock E, Yang SB, Jan YN, Jan LY. K1.1 preserves the neural stem cell pool and facilitates neuron maturation during adult hippocampal neurogenesis. Proceedings of the National Academy of Sciences of the United States of America. 119: e2118240119. PMID 35613055 DOI: 10.1073/pnas.2118240119 |
0.121 |
|
1953 |
GLASSCOCK E, BRUEGGEMAN JM, ULETT G, SASLOW G. Teaching comprehensive nursing care. Nursing Outlook. 1: 268-71. PMID 13055176 |
0.01 |
|
1953 |
MCARTHUR JW, JOY FB, GLASSCOCK EL. Adolescent girl and her menstrual problems. Pediatrics. 11: 70-8. PMID 13026352 |
0.01 |
|
Hide low-probability matches. |