Voltage-dependent calcium channel mutations in neurological disease.
about
Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.Facilitation versus depression in cultured hippocampal neurons determined by targeting of Ca2+ channel Cavbeta4 versus Cavbeta2 subunits to synaptic terminalsGene expression in cortical interneuron precursors is prescient of their mature function.Pregabalin modulation of neurotransmitter release is mediated by change in intrinsic activation/inactivation properties of ca(v)2.1 calcium channels.Genome-wide gene expression profiling in GluR1 knockout mice: key role of the calcium signaling pathway in glutamatergically mediated hippocampal transmissionElevated NMDA receptor levels and enhanced postsynaptic long-term potentiation induced by prenatal exposure to valproic acid.Developmental febrile seizures modulate hippocampal gene expression of hyperpolarization-activated channels in an isoform- and cell-specific manner.Molecular biology of channelopathies: impact on diagnosis and treatment.Disruption of polycystin-L causes hippocampal and thalamocortical hyperexcitabilityThe role of T-type calcium channel genes in absence seizures.Upregulation of L-type calcium channels in colonic inhibitory motoneurons of P/Q-type calcium channel-deficient mice.N-type and L-type calcium channels mediate glycinergic synaptic inputs to retinal ganglion cells of tiger salamanders.Loss of the calcium channel β4 subunit impairs parallel fibre volley and Purkinje cell firing in cerebellum of adult ataxic mice.Structural consequences of Kcna1 gene deletion and transfer in the mouse hippocampus.Enhanced G protein-dependent modulation of excitatory synaptic transmission in the cerebellum of the Ca2+ channel-mutant mouse, tottering.Energetics of discrete selectivity bands and mutation-induced transitions in the calcium-sodium ion channels family.Modeling human epilepsies in mice.Family MRX9 revisited: further evidence for locus heterogeneity in MRX.
P2860
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P2860
Voltage-dependent calcium channel mutations in neurological disease.
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Voltage-dependent calcium channel mutations in neurological disease.
@ast
Voltage-dependent calcium channel mutations in neurological disease.
@en
type
label
Voltage-dependent calcium channel mutations in neurological disease.
@ast
Voltage-dependent calcium channel mutations in neurological disease.
@en
prefLabel
Voltage-dependent calcium channel mutations in neurological disease.
@ast
Voltage-dependent calcium channel mutations in neurological disease.
@en
P2860
P1476
Voltage-dependent calcium channel mutations in neurological disease
@en
P2093
D L Burgess
P2860
P304
P356
10.1111/J.1749-6632.1999.TB11287.X
P407
P577
1999-04-01T00:00:00Z