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Quantitative trait locus on distal chromosome 1 regulates the occurrence of spontaneous spike-wave discharges in DBA/2 mice.

author

Thomas Bessaih

1980 -

published in: Epilepsia

date of publication: 2012-05-21

main subject: quantitative trait locus

Cites articles 42

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Potassium channel activity and glutamate uptake are impaired in astrocytes of seizure-susceptible DBA/2 mice
2010-09-01

A mutation in PEX19 causes a severe clinical phenotype in a patient with peroxisomal biogenesis disorder

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2010-11-26

Abnormalities in GABAergic synaptic transmission of intralaminar thalamic neurons in a genetic rat model of absence epilepsy
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Enhanced tonic GABAA inhibition in typical absence epilepsy

Giuseppe Di Giovanni, Gergely Orbán, Adam Errington, Magor L Lőrincz, David A Carter, Vincenzo Crunelli
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Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations

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Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.

Sheldon W. Tobe
2009-03-02

Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice

Sergio Tufik
2009-02-01

Genetic enhancement of thalamocortical network activity by elevating alpha 1g-mediated low-voltage-activated calcium current induces pure absence epilepsy

Jeffrey L. Noebels
2009-01-01

A Cav3.2 T-type calcium channel point mutation has splice-variant-specific effects on function and segregates with seizure expression in a polygenic rat model of absence epilepsy

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2009-10-28

Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy.

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2008-11-14

Dissection of a QTL hotspot on mouse distal chromosome 1 that modulates neurobehavioral phenotypes and gene expression

Thomas Schikorski, Robert W. Williams
2008-08-06

T current potentiation increases the occurrence and temporal fidelity of synaptically evoked burst firing in sensory thalamic neurons

Thomas Bessaih, Nathalie Leresche
2008-03-03

Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4
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Increased thalamic inhibition in the absence seizure prone DBA/2J mouse
2007-10-01

Conditional knock-out of Kir4.1 leads to glial membrane depolarization, inhibition of potassium and glutamate uptake, and enhanced short-term synaptic potentiation

Lih-Shen Chin
2007-02-01

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Levetiracetam attenuates spontaneous spike-and-wave discharges in DBA/2J mice

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Beta and gamma range EEG power-spectrum correlation with spiking discharges in DBA/2J mice absence model: role of GABA receptors

Federico A Santoni, Mauro Fà, Luigi Barberini, Roberto Frau
2006-09-13

Nucleus-specific abnormalities of GABAergic synaptic transmission in a genetic model of absence seizures

Diego Ruano, Nathalie Leresche, Thomas Bessaih, Bertrand Lambolez, Vincenzo Crunelli
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Consciousness and epilepsy: why are patients with absence seizures absent?
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Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy
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Elevated thalamic low-voltage-activated currents precede the onset of absence epilepsy in the SNAP25-deficient mouse mutant coloboma

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Mutations in high-voltage-activated calcium channel genes stimulate low-voltage-activated currents in mouse thalamic relay neurons

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Vincenzo Crunelli, Nathalie Leresche
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Article - wd:Q42274838

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