(Q36652537)

15 August 2017

1 reference

title

Voltage-gated sodium channels: action players with many faces (English)

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15 August 2017

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3

Arthur A M Wilde

1 reference

15 August 2017

Tamara T Koopmann

1

1 reference

PubMed ID

17101538

15 August 2017

Connie R Bezzina

series ordinal

2

1 reference

PubMed ID

17101538

15 August 2017

language of work or name

English

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publication date

1 January 2006

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15 August 2017

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15 August 2017

38

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15 August 2017

7

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15 August 2017

472-482

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Evolution and diversity of mammalian sodium channel genes

15 August 2017

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Molecular cloning of an atypical voltage-gated sodium channel expressed in human heart and uterus: evidence for a distinct gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

NaX sodium channel is expressed in non-myelinating Schwann cells and alveolar type II cells in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Resurgence of sodium channel research

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

The subfornical organ is the primary locus of sodium-level sensing by Na(x) sodium channels for the control of salt-intake behavior.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Alternative splicing of the sodium channel SCN8A predicts a truncated two-domain protein in fetal brain and non-neuronal cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Expression of alternatively spliced sodium channel alpha-subunit genes. Unique splicing patterns are observed in dorsal root ganglia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Distribution and functional characterization of human Nav1.3 splice variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Functional analysis of a voltage-gated sodium channel and its splice variant from rat dorsal root ganglia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Sodium-channel defects in benign familial neonatal-infantile seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Isolation of a human-brain sodium-channel gene encoding two isoforms of the subtype III alpha-subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Multiple transcripts of sodium channel SCN8A (Na(V)1.6) with alternative 5'- and 3'-untranslated regions and initial characterization of the SCN8A promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

A neutral amino acid change in segment IIS4 dramatically alters the gating properties of the voltage-dependent sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Structure and function of the beta 2 subunit of brain sodium channels, a transmembrane glycoprotein with a CAM motif

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

beta 3: an additional auxiliary subunit of the voltage-sensitive sodium channel that modulates channel gating with distinct kinetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Characterization of sodium channel alpha- and beta-subunits in rat and mouse cardiac myocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

The sodium channel -subunit SCN3b modulates the kinetics of SCN5a and is expressed heterogeneously in sheep heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Primary structure and functional expression of the beta 1 subunit of the rat brain sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Cloning, localization, and functional expression of sodium channel beta1A subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Molecular cloning and functional expression of the human sodium channel β1B subunit, a novel splicing variant of the β1 subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Molecular localization of an ion-binding site within the pore of mammalian sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Calcium channel characteristics conferred on the sodium channel by single mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Mechanisms of sodium/calcium selectivity in sodium channels probed by cysteine mutagenesis and sulfhydryl modification

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Kinetic analysis of block of open sodium channels by a peptide containing the isoleucine, phenylalanine, and methionine (IFM) motif from the inactivation gate

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

The Na+ channel inactivation gate is a molecular complex: a novel role of the COOH-terminal domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Na+ channel subunits and Ig domains.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Accessory subunits and sodium channel inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Sodium channel beta subunits: anything but auxiliary

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Genetic control of sodium channel function

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Cardiac conduction defects associate with mutations in SCN5A

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Cardiac sodium channel and inherited arrhythmia syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

In vivo human demonstration of phase 2 reentry

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Molecular mechanism for an inherited cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Sodium channel mutations in epilepsy and other neurological disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Increase in mRNAs encoding neonatal II and III sodium channel alpha-isoforms during kainate-induced seizures in adult rat hippocampus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Changes in the mRNAs encoding voltage-gated sodium channel types II and III in human epileptic hippocampus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Suicide attempt and basic mechanisms in neural conduction: relationships to the SCN8A and VAMP4 genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Mice lacking sodium channel beta1 subunits display defects in neuronal excitability, sodium channel expression, and nodal architecture

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Electrophysiological properties of mutant Nav1.7 sodium channels in a painful inherited neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Neuropathic pain develops normally in mice lacking both Na(v)1.7 and Na(v)1.8.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

A tetrodotoxin-resistant voltage-gated sodium channel from human dorsal root ganglia, hPN3/SCN10A

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Inhibition of neuropathic pain by decreased expression of the tetrodotoxin-resistant sodium channel, NaV1.8.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

NaN, a novel voltage-gated Na channel, is expressed preferentially in peripheral sensory neurons and down-regulated after axotomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Two sodium channels contribute to the TTX-R sodium current in primary sensory neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Contribution of the tetrodotoxin-resistant voltage-gated sodium channel NaV1.9 to sensory transmission and nociceptive behavior

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Linkage of atypical myotonia congenita to a sodium channel locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Different effects on gating of three myotonia-causing mutations in the inactivation gate of the human muscle sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Ion-channel defects and aberrant excitability in myotonia and periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Functional expression of sodium channel mutations identified in families with periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Sodium channel inactivation defects are associated with acetazolamide-exacerbated hypokalemic periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Generalized epilepsy with febrile seizures plus: further heterogeneity in a large family

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

SCNM1, a putative RNA splicing factor that modifies disease severity in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890600969072

10.1080/07853890600969072

21 January 2018

Identifiers

DOI

1 reference

15 August 2017

1 reference

PubMed ID

17101538