Molecular and cellular basis: Insights from experimental models of Dravet syndrome
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2011.03006.x/fullpdf
Reference15 articles.
1. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001
2. Mutations of SCN1A encoding a neuronal sodium channel, in two families with GEFS+2;Escayg;Nat Genet,2000
3. Mutations of sodium channel alpha type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures;Fujiwara;Brain,2003
4. Type I and type II Na+ channel α-subunit polypeptides exhibit distinct spatial and temporal patterning, and association with auxiliary subunits in rat brain;Gong;J Comp Neurol,1999
5. Molecular basis of an inherited epilepsy;Lossin;Neuron,2002
Cited by 15 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Clocking Epilepsies: A Chronomodulated Strategy-Based Therapy for Rhythmic Seizures;International Journal of Molecular Sciences;2023-02-20
2. Parvalbumin Role in Epilepsy and Psychiatric Comorbidities: From Mechanism to Intervention;Frontiers in Integrative Neuroscience;2022-02-17
3. Chronic partial TrkB activation reduces seizures and mortality in a mouse model of Dravet syndrome;Proceedings of the National Academy of Sciences;2022-02-14
4. Transfer of SCN1A to the brain of adolescent mouse model of Dravet syndrome improves epileptic, motor, and behavioral manifestations;Molecular Therapy - Nucleic Acids;2021-09
5. A systematic review of adults with Dravet syndrome;Seizure;2021-04
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3