(Q37073177)

18 August 2017

1 reference

title

Nervous system KV7 disorders: breakdown of a subthreshold brake (English)

1 reference

18 August 2017

0 references

Snezana Maljevic

1

1 reference

18 August 2017

Thomas V Wuttke

series ordinal

2

1 reference

18 August 2017

Holger Lerche

series ordinal

3

1 reference

18 August 2017

language of work or name

English

0 references

publication date

31 January 2008

1 reference

18 August 2017

11

1 reference

inferred from page(s)

published in

Journal of Physiology

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18 August 2017

586

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18 August 2017

7

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18 August 2017

1791-1801

1 reference

Bilateral tonic-clonic epileptic seizures in non-benign familial neonatal convulsions.

18 August 2017

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

A potassium channel mutation in neonatal human epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Pathways modulating neural KCNQ/M (Kv7) potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

KCNQ2 is a nodal K+ channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Activation of KCNQ5 channels stably expressed in HEK293 cells by BMS-204352.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Immunohistochemical analysis of KCNQ3 potassium channels in mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Phenotypic variants of autoimmune peripheral nerve hyperexcitability

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

A novel mutation ofKCNQ3 (c.925T?C) in a Japanese family with benign familial neonatal convulsions

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Structural insight into KCNQ (Kv7) channel assembly and channelopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Subthreshold changes of voltage-dependent activation of the K(V)7.2 channel in neonatal epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Neuronal KCNQ potassium channels: physiology and role in disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

The open pore conformation of potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Ion channel defects in idiopathic epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Crystal structure of a mammalian voltage-dependent Shaker family K+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensor

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Age-dependent modulation of hippocampal excitability by KCNQ-channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Effects of the anticonvulsant retigabine on cultured cortical neurons: changes in electroresponsive properties and synaptic transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

The novel anticonvulsant retigabine activates M-currents in Chinese hamster ovary-cells tranfected with human KCNQ2/3 subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Molecular determinants of KCNQ (Kv7) K+ channel sensitivity to the anticonvulsant retigabine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Neonatal seizures with tonic clonic sequences and poor developmental outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K+ channels involved in epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Benign familial neonatal convulsions: always benign?

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

The KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Immunohistochemical analysis of KCNQ2 potassium channels in adult and developing mouse brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Novel anticonvulsant drugs targeting voltage-dependent ion channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Neutralization of a negative charge in the S1-S2 region of the KV7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

The new anticonvulsant retigabine favors voltage-dependent opening of the Kv7.2 (KCNQ2) channel by binding to its activation gate

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Stoichiometry of expressed KCNQ2/KCNQ3 potassium channels and subunit composition of native ganglionic M channels deduced from block by tetraethylammonium

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375730

C-terminal interaction of KCNQ2 and KCNQ3 K+ channels.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375730

Benign familial neonatal convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375730

Activation of expressed KCNQ potassium currents and native neuronal M-type potassium currents by the anti-convulsant drug retigabine.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375730

Differential expression of kcnq2 splice variants: implications to m current function during neuronal development

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375730

Retigabine, a novel anti-convulsant, enhances activation of KCNQ2/Q3 potassium channels

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375730

Modulation of KCNQ2/3 potassium channels by the novel anticonvulsant retigabine

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375730

A novel mutation of KCNQ3 (c.925T-->C) in a Japanese family with benign familial neonatal convulsions

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375730

Muscarinic suppression of a novel voltage-sensitive K+ current in a vertebrate neurone

4 September 2018

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2008.150656

Self-assembly of the isolated KCNQ2 subunit interaction domain

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18238816

12 December 2020

inferred from PubMed ID database lookup

Contribution of persistent Na+ current and M-type K+ current to somatic bursting in CA1 pyramidal cells: combined experimental and modeling study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18238816

12 December 2020

inferred from PubMed ID database lookup

Calmodulin regulates the trafficking of KCNQ2 potassium channels

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18238816

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1113/JPHYSIOL.2008.150656

1 reference

18 August 2017

0 references

1 reference