(Q45030223)

8 December 2017

title

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

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8 December 2017

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James F Otto

1

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8 December 2017

Yan Yang

2

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8 December 2017

Wayne N Frankel

3

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8 December 2017

Karen S Wilcox

4

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8 December 2017

H Steve White

5

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8 December 2017

publication date

1 September 2004

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8 December 2017

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8 December 2017

volume

45

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8 December 2017

issue

9

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8 December 2017

page(s)

1009-1016

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

8 December 2017

cites work

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https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.65703.X

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21 January 2018

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The anticonvulsant retigabine potently suppresses epileptiform discharges in the low Ca ++ and low Mg++ model in the hippocampal slice preparation.

21 January 2018

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Effects of retigabine (D-23129) on different patterns of epileptiform activity induced by 4-aminopyridine in rat entorhinal cortex hippocampal slices.

21 January 2018

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

21 January 2018

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Nicotinic receptors in the rat prefrontal cortex: increase in glutamate release and facilitation of mediodorsal thalamo-cortical transmission.

21 January 2018

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Anticholinergic and antiglutamatergic agents protect against soman-induced brain damage and cognitive dysfunction

21 January 2018

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A new Chrna4 mutation with low penetrance in nocturnal frontal lobe epilepsy

21 January 2018

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Disruption of the epilepsy KCNQ2 gene results in neural hyperexcitability

21 January 2018

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

21 January 2018

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Pharmacological characterization of the 6 Hz psychomotor seizure model of partial epilepsy

21 January 2018

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Electroconvulsive thresholds of inbred mouse strains.

21 January 2018

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Genetic influences on electrical seizure threshold.

21 January 2018

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Complete loss of the cytoplasmic carboxyl terminus of the KCNQ2 potassium channel: a novel mutation in a large Czech pedigree with benign neonatal convulsions or other epileptic phenotypes

21 January 2018

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ARFGAP1 promotes the formation of COPI vesicles, suggesting function as a component of the coat

21 January 2018

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Disease modification in partial epilepsy

21 January 2018

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10.1111/J.0013-9580.2004.65703.X

21 January 2018

Identifiers

DOI

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8 December 2017

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