Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy - Wikidata - wikimedia - TriplyDB

Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy

Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy

http://www.wikidata.org/entity/Q28239380

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Caveolin-3 regulates protein kinase A modulation of the Ca(V)3.2 (alpha1H) T-type Ca2+ channels The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia Neuronal T-type calcium channels: what's new? Iftinca: T-type channel regulation The neurobiology of antiepileptic drugs Contrasting the roles of the I-II loop gating brake in CaV3.1 and CaV3.3 calcium channels.The voltage dependence of gating currents of the neuronal CA(v)3.3 channel is determined by the gating brake in the I-II loop Genetic enhancement of thalamocortical network activity by elevating alpha 1g-mediated low-voltage-activated calcium current induces pure absence epilepsy.Neurological channelopathies.Characterization of novel cannabinoid based T-type calcium channel blockers with analgesic effects.1,4-Dihydropyridine derivatives with T-type calcium channel blocking activity attenuate inflammatory and neuropathic pain.Genetics and function of neocortical GABAergic interneurons in neurodevelopmental disorders Cellular and network mechanisms of genetically-determined absence seizures.Sacred disease secrets revealed: the genetics of human epilepsy.Susceptibility genes for complex epilepsy.Molecular basis of inherited calcium channelopathies: role of mutations in pore-forming subunits.Voltage-gated calcium channels and idiopathic generalized epilepsies.Channelopathies in idiopathic epilepsy.A polygenic heterogeneity model for common epilepsies with complex genetics.Gene expression, genetics, and genomics in epilepsy: some answers, more questions.Neurochemical and behavioral features in genetic absence epilepsy and in acutely induced absence seizures.Genetic variations and associated pathophysiology in the management of epilepsy.An acquired channelopathy involving thalamic T-type Ca2+ channels after status epilepticus.CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism.Axon initial segment dysfunction in epilepsy.Trafficking and stability of voltage-gated calcium channels.T-type Ca2+ channels in normal and abnormal brain functions.The molecular biology of genetic-based epilepsies.T-type Ca2+ channels in absence epilepsy.T-type calcium channels in chronic pain: mouse models and specific blockers.The role of T-type calcium channel genes in absence seizures.Targeting voltage-gated calcium channels in neurological and psychiatric diseases.The Role of Calcium Channels in Epilepsy.CACNA1H missense mutations associated with amyotrophic lateral sclerosis alter Cav3.2 T-type calcium channel activity and reticular thalamic neuron firing.Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy.Transcriptional regulation of T-type calcium channel CaV3.2: bi-directionality by early growth response 1 (Egr1) and repressor element 1 (RE-1) protein-silencing transcription factor (REST).Zn(2+) slows down Ca(V)3.3 gating kinetics: implications for thalamocortical activity.Selective inhibition of Cav3.3 T-type calcium channels by Galphaq/11-coupled muscarinic acetylcholine receptors.Modulation of Cav3.2 T-type calcium channel permeability by asparagine-linked glycosylation.

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P2860

Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy

http://www.wikidata.org/entity/Q28239380

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2004 nî lūn-bûn

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2004 թուականի Մարտին հրատարակուած գիտական յօդուած

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2004 թվականի մարտին հրատարակված գիտական հոդված

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2004年の論文

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Gating effects of mutations in ...... ith childhood absence epilepsy

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Gating effects of mutations in ...... ith childhood absence epilepsy

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Gating effects of mutations in ...... ith childhood absence epilepsy

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P2093

Brett Simms

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Christophe Altier

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Houman Khosravani

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Janette Mezeyova

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John E McRory

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Kevin S Hamming

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Terrance P Snutch

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P2860

Molecular characterization of a neuronal low-voltage-activated T-type calcium channel

Specific contribution of human T-type calcium channel isotypes (alpha(1G), alpha(1H) and alpha(1I)) to neuronal excitability

The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells

Association between genetic variation of CACNA1H and childhood absence epilepsy

The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution

Different action of ethosuximide on low- and high-threshold calcium currents in rat sensory neurons

Characterization of ethosuximide reduction of low-threshold calcium current in thalamic neurons

The amino side of the C-terminus determines fast inactivation of the T-type calcium channel alpha1G

Inactivation determinants in segment IIIS6 of Ca(v)3.1

Molecular and functional characterization of a family of rat brain T-type calcium channels

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