Ion channel genes and human neurological disease: Recent progress, prospects, and challenges
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference98 articles.
1. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
2. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
3. A Potassium Channel Mutation in Neonatal Human Epilepsy
4. Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes
5. Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B
Cited by 126 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. Naphthalene Diimide‐Based Metallacage as an Artificial Ion Channel for Chloride Ion Transport;Advanced Science;2024-03-08
2. Oxidative stress and ion channels in neurodegenerative diseases;Frontiers in Physiology;2024-01-29
3. Mechanistic basis for potassium efflux–driven activation of the human NLRP1 inflammasome;Proceedings of the National Academy of Sciences;2024-01-04
4. Mechanistic basis for nigericin-induced NLRP1 inflammasome activation in human epithelial cells;2023-06-25
5. Machine learning in computational modelling of membrane protein sequences and structures: From methodologies to applications;Computational and Structural Biotechnology Journal;2023
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