Research Highlights: Highlights from the latest articles focusing on a new gene set for better drug response prediction of epilepsy patients
Author:
Affiliation:
1. Genomics & Molecular Medicine Unit, Institute of Genomics & Integrative Biology (IGIB), Council of Scientific & Industrial Research (CSIR), Mall Road, Delhi 110 007, India
Publisher
Future Medicine Ltd
Subject
Pharmacology,Genetics,Molecular Medicine
Link
https://www.futuremedicine.com/doi/pdf/10.2217/pgs.14.11
Reference45 articles.
1. Mechanisms of human inherited epilepsies
2. Genetics of Idiopathic Generalized Epilepsies
3. Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy
4. De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy
5. Amino-termini isoforms of the Slack K+channel, regulated by alternative promoters, differentially modulate rhythmic firing and adaptation
Cited by 4 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. Dysfunction of the SNARE complex in neurological and psychiatric disorders;Pharmacological Research;2021-03
2. Integration of epigenomics and metabolomics: From biomarkers discovery to personalized medicine;Epigenetics and Metabolomics;2021
3. Synergistic association of STX 1A and VAMP 2 with cryptogenic epilepsy in North Indian population;Brain and Behavior;2016-06-14
4. Evaluating the Role of Genetic Variants on first-line antiepileptic drug response in North India: Significance ofSCN1AandGABRA1Gene Variants in Phenytoin Monotherapy and its Serum Drug Levels;CNS Neuroscience & Therapeutics;2016-06-01
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