Gain of function of sporadic/familial hemiplegic migraine-causing SCN1A mutations: Use of an optimized cDNA

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