Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.
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Exaggerated Nighttime Sleep and Defective Sleep Homeostasis in a Drosophila Knock-In Model of Human EpilepsyIon channels in genetic and acquired forms of epilepsy.Mechanisms of sudden unexplained death in epilepsyAn Scn1a epilepsy mutation in Scn8a alters seizure susceptibility and behavior.Convulsive seizures and SUDEP in a mouse model of SCN8A epileptic encephalopathy.Risk factors for febrile status epilepticus: a case-control study.Role of the hippocampus in Nav1.6 (Scn8a) mediated seizure resistance.Unraveling genetic modifiers in the gria4 mouse model of absence epilepsyRare variants of small effect size in neuronal excitability genes influence clinical outcome in Japanese cases of SCN1A truncation-positive Dravet syndrome.Divergent whole-genome methylation maps of human and chimpanzee brains reveal epigenetic basis of human regulatory evolutionmRNA surveillance and endoplasmic reticulum quality control processes alter biogenesis of mutant GABAA receptor subunits associated with genetic epilepsies.Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry.Novel HCN2 mutation contributes to febrile seizures by shifting the channel's kinetics in a temperature-dependent mannerGenetic forms of epilepsies and other paroxysmal disordersSudden unexpected death in epilepsy genetics: Molecular diagnostics and preventionMechanistic insights into hypothermic ventricular fibrillation: the role of temperature and tissue size.Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice.A common susceptibility factor of both autism and epilepsy: functional deficiency of GABA A receptors.The intrinsic severity hypothesis of pharmacoresistance to antiepileptic drugs.The SCN1A gene variants and epileptic encephalopathies.Dravet syndrome--from epileptic encephalopathy to channelopathy.Precision physiology and rescue of brain ion channel disorders.Protective effect of the ketogenic diet in Scn1a mutant mice.Trafficking-deficient mutant GABRG2 subunit amount may modify epilepsy phenotype.Neurobiological bases of autism-epilepsy comorbidity: a focus on excitation/inhibition imbalance.Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy.Cacna1g is a genetic modifier of epilepsy in a mouse model of Dravet syndrome.Hlf is a genetic modifier of epilepsy caused by voltage-gated sodium channel mutations.Monoterpenoid terpinen-4-ol exhibits anticonvulsant activity in behavioural and electrophysiological studies.Role of temperature on nonlinear cardiac dynamics.Regulation of Thalamic and Cortical Network Synchrony by Scn8a.Understanding Network Connections Connects Genotype to Epilepsy Phenotype.Selective targeting of Scn8a prevents seizure development in a mouse model of mesial temporal lobe epilepsy.Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes
P2860
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P2860
Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.
description
2010 nî lūn-bûn
@nan
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Neuronal voltage-gated ion cha ...... sy with febrile seizures plus.
@ast
Neuronal voltage-gated ion cha ...... sy with febrile seizures plus.
@en
type
label
Neuronal voltage-gated ion cha ...... sy with febrile seizures plus.
@ast
Neuronal voltage-gated ion cha ...... sy with febrile seizures plus.
@en
prefLabel
Neuronal voltage-gated ion cha ...... sy with febrile seizures plus.
@ast
Neuronal voltage-gated ion cha ...... sy with febrile seizures plus.
@en
P2093
P2860
P1476
Neuronal voltage-gated ion cha ...... sy with febrile seizures plus.
@en
P2093
Andrew Escayg
Jennifer A Kearney
Melinda S Martin
Nicole A Hawkins
Wayne N Frankel
P2860
P304
P356
10.1016/J.NBD.2010.11.016
P577
2010-12-13T00:00:00Z