Electrophysiological and pharmacological properties of the human brain type IIA Na+ channel expressed in a stable mammalian cell line.
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Ion channels as drug targets in central nervous system disordersNav1.1 modulation by a novel triazole compound attenuates epileptic seizures in rodentsThe neurobiology of antiepileptic drugsEffect of lamotrigine and carbamazepine on corticotropin-releasing factor-associated serotonergic transmission in rat dorsal raphe nucleusModulation of sodium channel inactivation gating by a novel lactam: implications for seizure suppression in chronic limbic epilepsyA pharmacophore derived phenytoin analogue with increased affinity for slow inactivated sodium channels exhibits a desired anticonvulsant profileExcitability constraints on voltage-gated sodium channelsMolecular model of anticonvulsant drug binding to the voltage-gated sodium channel inner pore.Binding specificity of sea anemone toxins to Nav 1.1-1.6 sodium channels: unexpected contributions from differences in the IV/S3-S4 outer loop.Differential role of sodium channels SCN1A and SCN2A gene polymorphisms with epilepsy and multiple drug resistance in the north Indian population.Effects of various antiepileptics used to alleviate neuropathic pain on compound action potential in frog sciatic nerves: comparison with those of local anesthetics.Anticonvulsant pharmacology of voltage-gated Na+ channels in hippocampal neurons of control and chronically epileptic rats.N-salicyloyltryptamine, a new anticonvulsant drug, acts on voltage-dependent Na+, Ca2+, and K+ ion channels.Effects of anti-epileptic drugs on spreading depolarization-induced epileptiform activity in mouse hippocampal slices.Effect of systemic and intracortical administration of phenytoin in two genetic models of absence epilepsy.Effect of acute and chronic lamotrigine on basal and stimulated extracellular 5-hydroxytryptamine and dopamine in the hippocampus of the freely moving rat.Preferential action of gabapentin and pregabalin at P/Q-type voltage-sensitive calcium channels: inhibition of K+-evoked [3H]-norepinephrine release from rat neocortical slices.Dual effects of gabapentin and pregabalin on glutamate release at rat entorhinal synapses in vitro.Differential targeting and functional specialization of sodium channels in cultured cerebellar granule cells.
P2860
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P2860
Electrophysiological and pharmacological properties of the human brain type IIA Na+ channel expressed in a stable mammalian cell line.
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Electrophysiological and pharm ...... a stable mammalian cell line.
@ast
Electrophysiological and pharm ...... a stable mammalian cell line.
@en
type
label
Electrophysiological and pharm ...... a stable mammalian cell line.
@ast
Electrophysiological and pharm ...... a stable mammalian cell line.
@en
prefLabel
Electrophysiological and pharm ...... a stable mammalian cell line.
@ast
Electrophysiological and pharm ...... a stable mammalian cell line.
@en
P2093
P356
P1433
P1476
Electrophysiological and pharm ...... a stable mammalian cell line.
@en
P2093
P2888
P304
P356
10.1007/S004240000448
P577
2001-01-01T00:00:00Z
P5875
P6179
1052655039