about
BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsyThe GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizuresUsing Patient-Derived Induced Pluripotent Stem Cells to Model and Treat EpilepsiesThe neurogenetics of alternative splicingRegulation of hippocampal and behavioral excitability by cyclin-dependent kinase 5.Integrative biological analysis for neuropsychopharmacologyProtein Phosphatase 2a and glycogen synthase kinase 3 signaling modulate prepulse inhibition of the acoustic startle response by altering cortical M-Type potassium channel activityControl of neuronal ion channel function by glycogen synthase kinase-3: new prospective for an old kinase.Kv4.2 knockout mice demonstrate increased susceptibility to convulsant stimulationMechanisms of prickle1a function in zebrafish epilepsy and retinal neurogenesisExtracting a needle from a haystack: reanalysis of whole genome data reveals a readily translatable finding.Epilepsy genetics--past, present, and futureAn Etiological Model for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons.Emerging drugs for epilepsy.The splicing regulator Rbfox1 (A2BP1) controls neuronal excitation in the mammalian brain.Optogenetic photochemical control of designer K+ channels in mammalian neurons.Biophysical properties of Na(v) 1.8/Na(v) 1.2 chimeras and inhibition by µO-conotoxin MrVIB.Drug resistance in epilepsy: putative neurobiologic and clinical mechanisms.Epi4K: gene discovery in 4,000 genomes.Susceptibility genes for complex epilepsy.Analysis of genetically complex epilepsies.Genetics of drug resistance.Refractory epilepsy: mechanisms and solutions.Voltage-gated calcium channels and idiopathic generalized epilepsies.Familial cortical myoclonic tremor with epilepsy and cerebellar changes: description of a new pathology case and review of the literature.Multiplex families with epilepsy: Success of clinical and molecular genetic characterization.Genetics of epilepsies.A seizure-induced gain-of-function in BK channels is associated with elevated firing activity in neocortical pyramidal neurons.Computer modelling of epilepsyForty years from markers to genes.Effects of neuronal nicotinic acetylcholine receptor allosteric modulators in animal behavior studies.SNAP-25 in neuropsychiatric disorders.Double Trouble? Potential for Hyperexcitability Following Both Channelopathic up- and Downregulation of I(h) in Epilepsy.Levetiracetam: a comprehensive review.Mutations in GABAA receptor subunits associated with genetic epilepsies.Origins of temporal lobe epilepsy: febrile seizures and febrile status epilepticus.Calcium dysregulation and homeostasis of neural calcium in the molecular mechanisms of neurodegenerative diseases provide multiple targets for neuroprotection.Advances in functional assays for high-throughput screening of ion channels targets.Potassium Channels in Epilepsy.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Channelopathies as a genetic cause of epilepsy
@ast
Channelopathies as a genetic cause of epilepsy
@en
Channelopathies as a genetic cause of epilepsy
@nl
type
label
Channelopathies as a genetic cause of epilepsy
@ast
Channelopathies as a genetic cause of epilepsy
@en
Channelopathies as a genetic cause of epilepsy
@nl
prefLabel
Channelopathies as a genetic cause of epilepsy
@ast
Channelopathies as a genetic cause of epilepsy
@en
Channelopathies as a genetic cause of epilepsy
@nl
P2093
P1476
Channelopathies as a genetic cause of epilepsy
@en
P2093
Ingrid E Scheffer
John C Mulley
Steven Petrou
P356
10.1097/00019052-200304000-00009
P407
P577
2003-04-01T00:00:00Z