日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Cardiac-specific Kv1.1 deficiency alters cardiomyocyte electrophysiology without modifying overall cardiac function or arrhythmia susceptibility

心脏特异性Kv1.1缺陷会改变心肌细胞电生理,但不会改变整体心脏功能或心律失常易感性。

Halvorson, Kelsey; Si, Man; Trosclair, Krystle; Aughenbaugh, Ellen; Parkinson, Maxine; Gautier-Hall, Nicole M; Watts, Megan; Kizek, Frederica; Bhuiyan, Md Shenuarin; Dominic, Paari; Hamilton, Kathryn A; Glasscock, Edward

Translational Research Symposium: Current State of SUDEP Research

转化研究研讨会:SUDEP研究现状

Ryan, Justin M; Donner, Elizabeth J; Zulfiqar-Ali, Quratulain; Auerbach, David S; Glasscock, Edward; Maganti, Rama; Sivathamboo, Shobi; Liu, Anli L

Artificial Intelligence Reveals Subtle Mouse Seizure Behaviors That Predict Fatal Outcomes

人工智能揭示小鼠癫痫发作的细微行为,这些行为可预测致命后果

Glasscock, Edward

Seizures and premature death in mice with targeted Kv1.1 deficiency in corticolimbic circuits

皮质边缘回路中Kv1.1靶向缺陷的小鼠出现癫痫发作和过早死亡

Paulhus, Kelsey; Glasscock, Edward

From General Anesthetic to Designer Antiepileptic: Propofol's Mechanism of Action Reveals Hope for Precision Treatment of HCN1-Related Epilepsy

从全身麻醉剂到定制抗癫痫药:丙泊酚的作用机制揭示了精准治疗HCN1相关癫痫的希望

Glasscock, Edward

EGR3 Deletion Rescues Developmental and Epileptic Encephalopathy in Kcna1-null Mice

EGR3 缺失可挽救 Kcna1 基因敲除小鼠的发育性和癫痫性脑病

Mazumder, Arindam Ghosh; Karedia, Saifina; Adhyapak, Nandani; Schimer, Catharina; Bass, John Samuel; Kamen, Jessica L; Jankovic, Miranda J; Miao, Qinglong; Gallitano, Amelia L; Saltzman, Alexander B; Jain, Antrix; Malovannaya, Anna; Glasscock, Edward; Aiba, Isamu; Noebels, Jeffrey L; Krishnan, Vaishnav

Resistance is not Futile: Common Genetic Factor Identified for Drug-Resistant Focal Epilepsy

抵抗并非徒劳:耐药性局灶性癫痫的常见遗传因素已被确定

Glasscock, Edward

Adapt or Die: Seizures Weaken Chemosensory Responses of Retrotrapezoid Nucleus Neurons to Hypercapnia

适应或死亡:癫痫发作会减弱后梯形核神经元对高碳酸血症的化学感觉反应

Glasscock, Edward

Newly Identified KCNA3 Gene Variants Put the "Excite"-ment Back in Kv1.3 Channelopathy

新发现的KCNA3基因变异体让Kv1.3通道病重新焕发活力

Glasscock, Edward

Novel Genetic Variants Expand the Functional, Molecular, and Pathological Diversity of KCNA1 Channelopathy

新型基因变异扩展了KCNA1通道病的功能、分子和病理多样性

Paulhus, Kelsey; Glasscock, Edward