(Q46593538)

English

Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization.

scientific article published on 15 May 2008

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scholarly article

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Europe PubMed Central

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7 January 2020

Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization (English)

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7 January 2020

neuroplasticity

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based on heuristic

inferred from title

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Jonathan Leslie

5

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7 January 2020

Jeffrey L. Noebels

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7 January 2020

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Nanda A Singh

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7 January 2020

James F Otto

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7 January 2020

E Jill Dahle

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7 January 2020

Chris Pappas

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7 January 2020

Alex Vilaythong

6

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7 January 2020

H Steve White

8

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7 January 2020

Karen S Wilcox

9

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7 January 2020

Mark F Leppert

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7 January 2020

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15 May 2008

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7 January 2020

Journal of Physiology

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7 January 2020

586

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7 January 2020

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7 January 2020

3405-3423

1 reference

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7 January 2020

Genetic polymorphisms and idiopathic generalized epilepsies.

1 reference

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29 September 2018

Effects of seizures on developmental processes in the immature brain

1 reference

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The progression of epilepsy

1 reference

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29 September 2018

Polarized axonal surface expression of neuronal KCNQ channels is mediated by multiple signals in the KCNQ2 and KCNQ3 C-terminal domains

1 reference

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29 September 2018

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

1 reference

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29 September 2018

Immunohistochemical analysis of KCNQ3 potassium channels in mouse brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538806

29 September 2018

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

1 reference

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29 September 2018

A spontaneous mutation involving Kcnq2 (Kv7.2) reduces M-current density and spike frequency adaptation in mouse CA1 neurons.

1 reference

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29 September 2018

Plasticity of neuropeptide Y in the dentate gyrus after seizures, and its relevance to seizure-induced neurogenesis

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29 September 2018

NKCC1 transporter facilitates seizures in the developing brain

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29 September 2018

Conditional transgenic suppression of M channels in mouse brain reveals functions in neuronal excitability, resonance and behavior.

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29 September 2018

Mice carrying the szt1 mutation exhibit increased seizure susceptibility and altered sensitivity to compounds acting at the m-channel

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Expression of apoptosis inhibitor protein Mcl1 linked to neuroprotection in CNS neurons.

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Genetic control of sensitivity to hippocampal cell death induced by kainic acid: a quantitative trait loci analysis

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29 September 2018

KCNQ/M channels control spike afterdepolarization and burst generation in hippocampal neurons.

1 reference

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29 September 2018

KCNQ2 is a nodal K+ channel.

1 reference

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29 September 2018

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

1 reference

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29 September 2018

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

1 reference

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29 September 2018

Spontaneous deletion of epilepsy gene orthologs in a mutant mouse with a low electroconvulsive threshold

1 reference

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29 September 2018

Animal models of epileptogenesis

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Molecular correlates of the M-current in cultured rat hippocampal neurons

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29 September 2018

Electroconvulsive thresholds of inbred mouse strains.

1 reference

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Disruption of the epilepsy KCNQ2 gene results in neural hyperexcitability

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Targeting genes for self-excision in the germ line

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

1 reference

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29 September 2018

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

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29 September 2018

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

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Development of spontaneous seizures over extended electrical kindling. I. Electrographic, behavioral, and transfer kindling correlates.

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A potassium channel mutation in neonatal human epilepsy

1 reference

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29 September 2018

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

1 reference

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29 September 2018

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

1 reference

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Derivation of completely cell culture-derived mice from early-passage embryonic stem cells

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Benign familial neonatal convulsions: Evidence for clinical and genetic heterogeneity

1 reference

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Stimulus parameters for electroshock seizures in rats

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Seizure characteristics in chromosome 20 benign familial neonatal convulsions

1 reference

https://pubmed.ncbi.nlm.nih.gov/18483067

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative genetic study of maximal electroshock seizure threshold in mice: evidence for a major seizure susceptibility locus on distal chromosome 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/18483067

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1113/JPHYSIOL.2008.154971

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7 January 2020

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7 January 2020

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