Sudden unexpected death in a mouse model of Dravet syndrome. - Wikidata - awgldk - TriplyDB

Sudden unexpected death in a mouse model of Dravet syndrome.

Sudden unexpected death in a mouse model of Dravet syndrome.

http://www.wikidata.org/entity/Q30538288

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Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome Sudden unexpected death in epilepsy: fatal post-ictal respiratory and arousal mechanisms Dissecting the phenotypes of Dravet syndrome by gene deletion Pathogenesis and new candidate treatments for infantile spasms and early life epileptic encephalopathies: A view from preclinical studies Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome The human epilepsy mutation GABRG2(Q390X) causes chronic subunit accumulation and neurodegeneration Spreading depolarization in the brainstem mediates sudden cardiorespiratory arrest in mouse SUDEP models Mechanisms of sudden unexplained death in epilepsy Sodium channel β subunits: emerging targets in channelopathies De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy Abnormalities of serotonergic neurotransmission in animal models of SUDEP.Mapping genetic modifiers of survival in a mouse model of Dravet syndrome.Leaky RyR2 channels unleash a brainstem spreading depolarization mechanism of sudden cardiac death.Screening of conventional anticonvulsants in a genetic mouse model of epilepsy.Correlations in timing of sodium channel expression, epilepsy, and sudden death in Dravet syndrome.Impaired excitability of somatostatin- and parvalbumin-expressing cortical interneurons in a mouse model of Dravet syndrome ABHD6 blockade exerts antiepileptic activity in PTZ-induced seizures and in spontaneous seizures in R6/2 mice.High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile.Epilepsy-induced electrocardiographic alterations following cardiac ischemia and reperfusion in rats.Tau reduction prevents disease in a mouse model of Dravet syndrome Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs.Sleep impairment and reduced interneuron excitability in a mouse model of Dravet Syndrome.The genetic basis for inherited forms of sinoatrial dysfunction and atrioventricular node dysfunction Fine Mapping of a Dravet Syndrome Modifier Locus on Mouse Chromosome 5 and Candidate Gene Analysis by RNA-Seq Influence of vigilance state on physiological consequences of seizures and seizure-induced death in mice.Upregulation of Haploinsufficient Gene Expression in the Brain by Targeting a Long Non-coding RNA Improves Seizure Phenotype in a Model of Dravet Syndrome.Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention Cardiac arrhythmia in a mouse model of sodium channel SCN8A epileptic encephalopathy Overexpression of KCNN3 results in sudden cardiac death.Mouse models of arrhythmogenic cardiovascular disease: challenges and opportunities.The SCN1A gene variants and epileptic encephalopathies.Sudden unexpected death in epilepsy or voodoo heart: analysis of heart/brain connections.Mechanisms of sudden unexpected death in epilepsy: the pathway to prevention.Dravet syndrome--from epileptic encephalopathy to channelopathy.The genetics of the epilepsies.The effect of atomoxetine, a selective norepinephrine reuptake inhibitor, on respiratory arrest and cardiorespiratory function in the DBA/1 mouse model of SUDEP.Time of day influences on respiratory sequelae following maximal electroshock induced seizures in mice.Neonatal and Infantile Epilepsy: Acquired and Genetic Models.Sudden unexpected death in epilepsy: basic mechanisms and clinical implications for prevention.Furthering our understanding of SUDEP: the role of animal models.

P2860

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P2860

Sudden unexpected death in a mouse model of Dravet syndrome.

http://www.wikidata.org/entity/Q30538288

description

2013 nî lūn-bûn

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2013 թուականի Մարտին հրատարակուած գիտական յօդուած

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2013 թվականի մարտին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Sudden unexpected death in a mouse model of Dravet syndrome.

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Sudden unexpected death in a mouse model of Dravet syndrome.

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Sudden unexpected death in a mouse model of Dravet syndrome.

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Sudden unexpected death in a mouse model of Dravet syndrome.

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Sudden unexpected death in a mouse model of Dravet syndrome.

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Journal of Clinical Investigation

P1476

Sudden unexpected death in a mouse model of Dravet syndrome.

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P2093

Christine S Cheah

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Franck Kalume

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Frank H Yu

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John C Oakley

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Ruth E Westenbroek

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Todd Scheuer

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William A Catterall

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P2860

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

Modification of seizure activity by electrical stimulation. II. Motor seizure

Sudden unexpected death in epilepsy

Sudden unexpected death in epilepsy: risk factors and potential pathomechanisms

Unifying the definitions of sudden unexpected death in epilepsy

Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death.

Sudden unexpected death in epilepsy (SUDEP) and sleep

Reduced sodium current in Purkinje neurons from Nav1.1 mutant mice: implications for ataxia in severe myoclonic epilepsy in infancy

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

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1798-1808

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23524966

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3613924

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