about
New ether-à-go-go K(+) channel family members localized in human telencephalonCloning, characterization, and chromosomal location of a novel human K+-Cl- cotransporterMolecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversityCloning of a human ether-a-go-go potassium channel expressed in myoblasts at the onset of fusionFunctional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsyA carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly.Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.Polarized axonal surface expression of neuronal KCNQ channels is mediated by multiple signals in the KCNQ2 and KCNQ3 C-terminal domainsMyokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channelInhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptorsColocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsyInactivation as a new regulatory mechanism for neuronal Kv7 channelsDisruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and miceMolecular targets for antiepileptic drug developmentKCNQ potassium channels in sensory system and neural circuitsGenetic neurological channelopathies: molecular genetics and clinical phenotypes.Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channelsScorpion toxins specific for potassium (K+) channels: a historical overview of peptide bioengineeringGenetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental modelsDriving with no brakes: molecular pathophysiology of Kv7 potassium channelsThe riluzole derivative 2-amino-6-trifluoromethylthio-benzothiazole (SKA-19), a mixed KCa2 activator and NaV blocker, is a potent novel anticonvulsant.Understanding Genotypes and Phenotypes in Epileptic EncephalopathiesHomeostasis or channelopathy? Acquired cell type-specific ion channel changes in temporal lobe epilepsy and their antiepileptic potentialEpileptic syndromes: From clinic to geneticA reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsionsKCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currentsA locus for febrile seizures (FEB3) maps to chromosome 2q23-24A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigreeIon channels and epilepsySevere myoclonic epilepsy of infancy: extended spectrum of GEFS+?A novel splicing mutation in KCNQ2 in a multigenerational family with BFNC followed for 25 yearsComplete loss of the cytoplasmic carboxyl terminus of the KCNQ2 potassium channel: a novel mutation in a large Czech pedigree with benign neonatal convulsions or other epileptic phenotypesFunctional coassembly of KCNQ4 with KCNE-beta- subunits in Xenopus oocytesThe KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3Differential tetraethylammonium sensitivity of KCNQ1-4 potassium channelsVariable K(+) channel subunit dysfunction in inherited mutations of KCNA1From pan-reactive KV7 channel opener to subtype selective opener/inhibitor by addition of a methyl groupK(V)7/KCNQ channels are functionally expressed in oligodendrocyte progenitor cellsKCNE1 induces fenestration in the Kv7.1/KCNE1 channel complex that allows for highly specific pharmacological targeting
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
A potassium channel mutation in neonatal human epilepsy
@ast
A potassium channel mutation in neonatal human epilepsy
@en
A potassium channel mutation in neonatal human epilepsy
@en-gb
A potassium channel mutation in neonatal human epilepsy
@nl
type
label
A potassium channel mutation in neonatal human epilepsy
@ast
A potassium channel mutation in neonatal human epilepsy
@en
A potassium channel mutation in neonatal human epilepsy
@en-gb
A potassium channel mutation in neonatal human epilepsy
@nl
prefLabel
A potassium channel mutation in neonatal human epilepsy
@ast
A potassium channel mutation in neonatal human epilepsy
@en
A potassium channel mutation in neonatal human epilepsy
@en-gb
A potassium channel mutation in neonatal human epilepsy
@nl
P2093
P3181
P1433
P1476
A potassium channel mutation in neonatal human epilepsy
@en
P2093
B C Schroeder
C Biervert
O K Steinlein
P Propping
S F Berkovic
T J Jentsch
P3181
P356
10.1126/SCIENCE.279.5349.403
P407
P577
1998-01-16T00:00:00Z