Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. Online.
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High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate geneA Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar AtaxiaCooperative activation of the T-type CaV3.2 channel: interaction between Domains II and III.Role of voltage-gated calcium channels in epilepsy.I-II loop structural determinants in the gating and surface expression of low voltage-activated calcium channels.Genetic enhancement of thalamocortical network activity by elevating alpha 1g-mediated low-voltage-activated calcium current induces pure absence epilepsy.Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice.Confirmation of an epilepsy modifier locus on mouse chromosome 11 and candidate gene analysis by RNA-Seq.Calcium Channel CaVα₁ Splice Isoforms - Tissue Specificity and Drug Action.Novel β-catenin target genes identified in thalamic neurons encode modulators of neuronal excitability.Neurochemical and behavioral features in genetic absence epilepsy and in acutely induced absence seizures.Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats.How voltage-gated calcium channels gate forms of homeostatic synaptic plasticityInhibitory peptidergic modulation of C. elegans serotonin neurons is gated by T-type calcium channels.Low threshold T-type calcium channels as targets for novel epilepsy treatments.Development of individualized medicine for epilepsy based on genetic information.The relationship between genes affecting the development of epilepsy and approaches to epilepsy therapy.Calcium signaling and epilepsy.The role of T-type calcium channel genes in absence seizures.The Role of Calcium Channels in Epilepsy.Tapping the Brakes: Cellular and Synaptic Mechanisms that Regulate Thalamic Oscillations.T-type calcium channel blockers that attenuate thalamic burst firing and suppress absence seizures.Deep sequencing reveals 50 novel genes for recessive cognitive disorders.Calcium channel antibodies in patients with absence epilepsy.Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy.
P2860
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P2860
Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. Online.
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2007 nî lūn-bûn
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2007年の論文
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2007年学术文章
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2007年学术文章
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2007年学术文章
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name
Mutational analysis of CACNA1G ...... utation in brief #962. Online.
@en
Mutational analysis of CACNA1G ...... utation in brief #962. Online.
@nl
type
label
Mutational analysis of CACNA1G ...... utation in brief #962. Online.
@en
Mutational analysis of CACNA1G ...... utation in brief #962. Online.
@nl
prefLabel
Mutational analysis of CACNA1G ...... utation in brief #962. Online.
@en
Mutational analysis of CACNA1G ...... utation in brief #962. Online.
@nl
P2093
P356
P1433
P1476
Mutational analysis of CACNA1G ...... utation in brief #962. Online.
@en
P2093
Antonio V Delgado-Escueta
Arnaud Monteil
Baljinder Singh
Hirokazu Oguni
Isabelle Bidaud
Kazuhiro Yamakawa
Makiko Osawa
Maria E Alonso
Norio Yasui-Furukori
Philippe Lory
P304
P356
10.1002/HUMU.9491
P577
2007-05-01T00:00:00Z