Cacna1gis a genetic modifier of epilepsy caused by mutation of voltage-gated sodium channelScn2a-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Cacna1gis a genetic modifier of epilepsy caused by mutation of voltage-gated sodium channelScn2a

Published:2016-04-25 Issue:6 Volume:57 Page:e103-e107
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Calhoun Jeffrey D.¹²,Hawkins Nicole A.¹³,Zachwieja Nicole J.¹,Kearney Jennifer A.¹²

Affiliation:

1. Department of Pharmacology; Northwestern University Feinberg School of Medicine; Chicago Illinois U.S.A.

2. Department of Medicine; Vanderbilt University; Nashville Tennessee U.S.A.

3. Neuroscience Program; Vanderbilt University; Nashville Tennessee U.S.A.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.13390/fullpdf

Reference14 articles.

1. A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities;Kearney;Neuroscience,2001

2. Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a;Bergren;Mamm Genome,2005

3. Voltage-gated potassium channel KCNV2 (Kv8.2) contributes to epilepsy susceptibility;Jorge;Proc Natl Acad Sci U S A,2011

4. Confirmation of an epilepsy modifier locus on mouse chromosome 11 and candidate gene analysis by RNA-Seq;Hawkins;Genes Brain Behav,2012

5. Hlf is a genetic modifier of epilepsy caused by voltage-gated sodium channel mutations;Hawkins;Epilepsy Res,2016

Cited by 47 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. Integrative analysis of epilepsy-associated genes reveals expression-phenotype correlations;Scientific Reports;2024-02-13

2. Tracing topics and trends in drug‐resistant epilepsy research using a natural language processing–based topic modeling approach;Epilepsia;2024-02-05

3. Voltage‐gated calcium channels in genetic epilepsies;Journal of Neurochemistry;2023-10-11

4. KAT6Amutations drive transcriptional dysregulation of cell cycle and Autism risk genes in an Arboleda-Tham Syndrome cerebral organoid model;2023-06-18

5. Integrative Analysis of Epilepsy-Associated Genes Reveals Expression-Phenotype Correlations;2023-06-11

同舟云学术

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