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Altered cardiac electrophysiology and SUDEP in a model of Dravet syndromeInhibitory interneuron deficit links altered network activity and cognitive dysfunction in Alzheimer model.Functional implications of axon initial segment cytoskeletal disruption in strokeMolecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channelsTrafficking mechanisms underlying neuronal voltage-gated ion channel localization at the axon initial segmentTowards a Unified Theory of Calmodulin Regulation (Calmodulation) of Voltage-Gated Calcium and Sodium ChannelsIssues related to symptomatic and disease-modifying treatments affecting cognitive and neuropsychiatric comorbidities of epilepsyGenetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndromeExaggerated Nighttime Sleep and Defective Sleep Homeostasis in a Drosophila Knock-In Model of Human EpilepsyThe C-terminal helical bundle of the tetrameric prokaryotic sodium channel accelerates the inactivation rateCrystal Structure of the Ternary Complex of a NaV C-Terminal Domain, a Fibroblast Growth Factor Homologous Factor, and CalmodulinNav1.1 modulation by a novel triazole compound attenuates epileptic seizures in rodentsMajor channels involved in neuropsychiatric disorders and therapeutic perspectivesSelective spider toxins reveal a role for the Nav1.1 channel in mechanical painOpposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile SeizuresCellular mechanisms of desynchronizing effects of hypothermia in an in vitro epilepsy model.Sudden unexpected death in a mouse model of Dravet syndrome.Preferential inactivation of Scn1a in parvalbumin interneurons increases seizure susceptibilityKnock-in model of Dravet syndrome reveals a constitutive and conditional reduction in sodium current.Calcium channels and synaptic transmission in familial hemiplegic migraine type 1 animal models.Structure-based assessment of disease-related mutations in human voltage-gated sodium channels.Generation of the SCN1A epilepsy mutation in hiPS cells using the TALEN technique.Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism.Molecular identity of axonal sodium channels in human cortical pyramidal cellsVoltage-gated sodium channels at 60: structure, function and pathophysiology.Reduced sodium channel Na(v)1.1 levels in BACE1-null miceTau reduction prevents disease in a mouse model of Dravet syndromeNav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome.Alternative splicing modulates inactivation of type 1 voltage-gated sodium channels by toggling an amino acid in the first S3-S4 linker.Sleep impairment and reduced interneuron excitability in a mouse model of Dravet Syndrome.The treatment of autism with low-dose phenytoin: a case report.Clinical utility of neuronal cells directly converted from fibroblasts of patients for neuropsychiatric disorders: studies of lysosomal storage diseases and channelopathyNa(V)1.1 channels are critical for intercellular communication in the suprachiasmatic nucleus and for normal circadian rhythmsFrom Squid to Mammals with the HH Model through the Nav Channels' Half-Activation-Voltage Parameter.Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes.Benchmarking the stability of human detergent-solubilised voltage-gated sodium channels for structural studies using eel as a referencePathophysiological role of omega pore current in channelopathiesThe genetic variants in 3' untranslated region of voltage-gated sodium channel alpha 1 subunit gene affect the mRNA-microRNA interactions and associate with epilepsy.Conotoxins that confer therapeutic possibilities.Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on March 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
NaV1.1 channels and epilepsy.
@en
NaV1.1 channels and epilepsy.
@nl
type
label
NaV1.1 channels and epilepsy.
@en
NaV1.1 channels and epilepsy.
@nl
prefLabel
NaV1.1 channels and epilepsy.
@en
NaV1.1 channels and epilepsy.
@nl
P2093
P2860
P1476
NaV1.1 channels and epilepsy.
@en
P2093
Franck Kalume
John C Oakley
William A Catterall
P2860
P304
P356
10.1113/JPHYSIOL.2010.187484
P407
P577
2010-03-01T00:00:00Z