Childhood absence epilepsy: Genes, channels, neurons and networks

No abstract is available for this paper.

• Publication year

  2002

• Venue

  Nature Reviews Neuroscience

• Publication date

  2002-05-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/nrn811PMID 11988776
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• Tandem pore domain K(+)-channel TASK-3 (KCNK9) and idiopathic absence epilepsies.

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• Activity of Thalamic Reticular Neurons during Spontaneous Genetically Determined Spike and Wave Discharges

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• Optimisation of methods for selecting candidate genes from cDNA array screens: application to rat brain punches and pineal.

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• A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.

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• Genome scan of idiopathic generalized epilepsy: Evidence for major susceptibility gene and modifying genes influencing the seizure type

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• Differences in quantal amplitude reflect GluR4- subunit number at corticothalamic synapses on two populations of thalamic neurons

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• Lack of the burst firing of thalamocortical relay neurons and resistance to absence seizures in mice lacking alpha(1G) T-type Ca(2+) channels.

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• Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.

  2001influential reference
• Ducky Mouse Phenotype of Epilepsy and Ataxia Is Associated with Mutations in the Cacna2d2 Gene and Decreased Calcium Channel Current in Cerebellar Purkinje Cells

  2001cited by this paper
• Genetic engineering of neural function in transgenic rodents: towards a comprehensive strategy?

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• Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity

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• Contribution of intralaminar thalamic nuclei to spike‐and‐wave‐discharges during spontaneous seizures in a genetic rat model of absence epilepsy

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• Electrophysiological and pharmacological characteristics of two types of spike-wave discharges in WAG/Rij rats.

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• Generalized Epileptic Disorders: An Update

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• Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME.

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• Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures.

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• T-STAR gene: fine mapping in the candidate region for childhood absence epilepsy on 8q24 and mutational analysis in patients.

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• Ictal Single Photon Emission Computed Tomography in Absence Seizures: Apparent Implication of Different Neuronal Mechanisms

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• Role of T-type calcium channels in the genesis of absence seizure in the mutant mice for α 1A, the pore-forming subunit of the P/Q-type calcium channel

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• Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizures

  2001influential reference
• Lack of the burst firing of thalamocortical relay neurons and resistance to absence seizures in mice lacking α1G T-type Ca2+ channels

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• Contribution of GABAA and GABAB Receptors to Thalamic Neuronal Activity during Spontaneous Absence Seizures in Rats

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• Epileptic seizures and sleep–wake rhythm

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• Treatment of Typical Absence Seizures and Related Epileptic Syndromes

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• First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene

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• Failure to replicate association between the gene for the neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) and IGE.

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• Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.

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• Low-voltage-activated calcium channel subunit expression in a genetic model of absence epilepsy in the rat.

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• Stargazin regulates synaptic targeting of AMPA receptors by two distinct mechanisms

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• Genetics of childhood epilepsy

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• KCNQ2/KCNQ3 K+ channels and the molecular pathogenesis of epilepsy: implications for therapy.

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• Ictal and interictal SPECT findings in childhood absence epilepsy.

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• Corticothalamic Inputs Control the Pattern of Activity Generated in Thalamocortical Networks

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• Glial glutamate transporter mRNAs in the genetically absence epilepsy rat from Strasbourg.

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• Genome search for susceptibility loci of common idiopathic generalised epilepsies.

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• No association found between polymorphisms in genes encoding mGluR7 and mGluR8 and idiopathic generalised epilepsy in a case control study.

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• Variation of the genes encoding the human glutamate EAAT2, serotonin and dopamine transporters and Susceptibility to idiopathic generalized epilepsy.

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• Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy.

  2000cited by this paper
• Ion channels and epilepsy in man and mouse.

  2000cited by this paper
• Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy.

  1999cited by this paper
• Reciprocal inhibitory connections and network synchrony in the mammalian thalamus.

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• Exclusion of the JRK/JH8 gene as a candidate for human childhood absence epilepsy mapped on 8q24.

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• Neocortical Synchronized Oscillations Induced by Thalamic Disinhibition In Vivo

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• On the putative contribution of GABA(B) receptors to the electrical events occurring during spontaneous spike and wave discharges.

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• An ultrastructural study of granule cell/Purkinje cell synapses in tottering (tg/tg), leaner (tg(la)/tg(la)) and compound heterozygous tottering/leaner (tg/tg(la)) mice.

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• Single gene defects in mice: the role of voltage-dependent calcium channels in absence models.

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• Evidence for linkage of adolescent-onset idiopathic generalized epilepsies to chromosome 8-and genetic heterogeneity.

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• Ataxic mouse mutants and molecular mechanisms of absence epilepsy.

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• Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit.

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• Spike-wave complexes and fast components of cortically generated seizures. II. Extra- and intracellular patterns.

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• Cortical versus thalamic mechanisms underlying spike and wave discharges in GAERS.

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• Absence epilepsy in tottering mutant mice is associated with calcium channel defects.

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