Gain of function of sporadic/familial hemiplegic migraine-causing SCN1A mutations: Use of an optimized cDNA
出版年份 2018 全文链接
标题
Gain of function of sporadic/familial hemiplegic migraine-causing SCN1A mutations: Use of an optimized cDNA
作者
关键词
-
出版物
CEPHALALGIA
Volume -, Issue -, Pages 033310241878833
出版商
SAGE Publications
发表日期
2018-07-10
DOI
10.1177/0333102418788336
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Codon optimality, bias and usage in translation and mRNA decay
- (2017) Gavin Hanson et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Structure of a eukaryotic voltage-gated sodium channel at near-atomic resolution
- (2017) Huaizong Shen et al. SCIENCE
- Early-onset familial hemiplegic migraine due to a novel SCN1A mutation
- (2016) Chunxiang Fan et al. CEPHALALGIA
- A novel SCN1A mutation identified in a Chinese family with familial hemiplegic migraine: A case report
- (2016) Yang Zhang et al. CEPHALALGIA
- Clinical and electroencephalographic abnormalities during the full duration of a sporadic hemiplegic migraine attack
- (2016) Nathalie Chastan et al. NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY
- Roles for Synonymous Codon Usage in Protein Biogenesis
- (2015) Julie L. Chaney et al. Annual Review of Biophysics
- The hitchhiker’s guide to the voltage-gated sodium channel galaxy
- (2015) Christopher A. Ahern et al. JOURNAL OF GENERAL PHYSIOLOGY
- Two novel SCN1A mutations identified in families with familial hemiplegic migraine
- (2014) Claudia M Weller et al. CEPHALALGIA
- Familial hemiplegic migraine due to L263V SCN1A mutation: Discordance for epilepsy between two kindreds from Douro Valley
- (2014) José Barros et al. CEPHALALGIA
- A supercritical density of Na+ channels ensures fast signaling in GABAergic interneuron axons
- (2014) Hua Hu et al. NATURE NEUROSCIENCE
- Divergent effects of the T1174SSCN1Amutation associated with seizures and hemiplegic migraine
- (2013) Sandrine Cestèle et al. EPILEPSIA
- Sequence and structure-specific elements of HERG mRNA determine channel synthesis and trafficking efficiency
- (2013) Jakub Sroubek et al. FASEB JOURNAL
- Febrile temperatures unmask biophysical defects in Nav1.1 epilepsy mutations supportive of seizure initiation
- (2013) Linda Volkers et al. JOURNAL OF GENERAL PHYSIOLOGY
- Nonfunctional NaV1.1 familial hemiplegic migraine mutant transformed into gain of function by partial rescue of folding defects
- (2013) S. Cestele et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Pathophysiology of Migraine
- (2012) Daniela Pietrobon et al. Annual Review of Physiology
- GENETIC CODE REDUNDANCY AND ITS INFLUENCE ON THE ENCODED POLYPEPTIDES
- (2012) Paige S. Spencer et al. Computational and Structural Biotechnology Journal
- Sodium channel SCN1A and epilepsy: Mutations and mechanisms
- (2010) Andrew Escayg et al. EPILEPSIA
- High cortical spreading depression susceptibility and migraine-associated symptoms in Cav2.1 S218L mice
- (2009) Arn M. J. M. van den Maagdenberg et al. ANNALS OF NEUROLOGY
- Molecular genetics of migraine
- (2009) Boukje de Vries et al. HUMAN GENETICS
- Elicited repetitive daily blindness: A new phenotype associated with hemiplegic migraine and SCN1A mutations
- (2009) K. Vahedi et al. NEUROLOGY
- Rare Codons Cluster
- (2008) Thomas F. Clarke et al. PLoS One
- Divergent sodium channel defects in familial hemiplegic migraine
- (2008) K. M. Kahlig et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started