Drosophila as a model for epilepsy: bss is a gain-of-function mutation in the para sodium channel gene that leads to seizures.
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Drosophila tools and assays for the study of human diseasesDrosophila sodium channel mutations: Contributions to seizure-susceptibilitySeizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinaseCalcium Imaging of Neuronal Activity in Drosophila Can Identify Anticonvulsive CompoundsMutations of the Calcium Channel Gene cacophony Suppress Seizures in DrosophilaLithium-Responsive Seizure-Like Hyperexcitability Is Caused by a Mutation in the Drosophila Voltage-Gated Sodium Channel Gene paralytic.Mutation of orthologous prickle genes causes a similar epilepsy syndrome in flies and humans.Rescue of easily shocked mutant seizure sensitivity in Drosophila adults.Phenotypic rescue of a Drosophila model of mitochondrial ANT1 disease.Molecular Chaperone Calnexin Regulates the Function of Drosophila Sodium Channel Paralytic.Effects of oxygen concentration and pressure on Drosophila melanogaster: oxidative stress, mitochondrial activity, and survivorship.prickle modulates microtubule polarity and axonal transport to ameliorate seizures in flies.The alternative oxidase AOX does not rescue the phenotype of tko25t mutant fliesδ/ω-Plectoxin-Pt1a: an excitatory spider toxin with actions on both Ca(2+) and Na(+) channels.Regulation of membrane excitability: a convergence on voltage-gated sodium conductance.A new model to study sleep deprivation-induced seizure.Mechanical and temperature stressor-induced seizure-and-paralysis behaviors in Drosophila bang-sensitive mutantsThe kdr-bearing haplotype and susceptibility to Plasmodium falciparum in Anopheles gambiae: genetic correlation and functional testing.A novel Drosophila SOD2 mutant demonstrates a role for mitochondrial ROS in neurodevelopment and diseaseSeizure control through genetic and pharmacological manipulation of Pumilio in Drosophila: a key component of neuronal homeostasisDisruption of Endocytosis with the Dynamin Mutant shibirets1 Suppresses Seizures in DrosophilaInappropriate Neural Activity during a Sensitive Period in Embryogenesis Results in Persistent Seizure-like Behavior.A roadmap for precision medicine in the epilepsies.A knock-in model of human epilepsy in Drosophila reveals a novel cellular mechanism associated with heat-induced seizure.Model systems for studying cellular mechanisms of SCN1A-related epilepsy.Drosophila as a model for intractable epilepsy: gilgamesh suppresses seizures in para(bss1) heterozygote flies.Seizure Suppression by High Temperature via cAMP Modulation in Drosophila.Seizure and epilepsy: studies of seizure disorders in Drosophila.Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders.Seizure suppression through manipulating splicing of a voltage-gated sodium channelGenome-wide screen for modifiers of Na (+) /K (+) ATPase alleles identifies critical genetic loci.A low-cost method for analyzing seizure-like activity and movement in Drosophila.Mutations in Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands of Dendritic Growth and Synaptic IntegrityInvestigation of Seizure-Susceptibility in a Drosophila melanogaster Model of Human Epilepsy with Optogenetic Stimulation.The ATP-sensitive K channel is seizure protective and required for effective dietary therapy in a model of mitochondrial encephalomyopathy.Seizure-sensitivity in Drosophila is ameliorated by dorsal vessel injection of the antiepileptic drug valproate.Extending julius seizure, a bang-sensitive gene, as a model for studying epileptogenesis: Cold shock, and a new insertional mutation.Ras-dependent and Ras-independent effects of PI3K in Drosophila motor neurons.Unraveling Synaptic GCaMP Signals: Differential Excitability and Clearance Mechanisms Underlying Distinct Ca2+ Dynamics in Tonic and Phasic Excitatory, and Aminergic Modulatory Motor Terminals in Drosophila.julius seizure, a Drosophila Mutant, Defines a Neuronal Population Underlying Epileptogenesis.
P2860
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P2860
Drosophila as a model for epilepsy: bss is a gain-of-function mutation in the para sodium channel gene that leads to seizures.
description
2010 nî lūn-bûn
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2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Drosophila as a model for epil ...... l gene that leads to seizures.
@ast
Drosophila as a model for epil ...... l gene that leads to seizures.
@en
Drosophila as a model for epil ...... l gene that leads to seizures.
@nl
type
label
Drosophila as a model for epil ...... l gene that leads to seizures.
@ast
Drosophila as a model for epil ...... l gene that leads to seizures.
@en
Drosophila as a model for epil ...... l gene that leads to seizures.
@nl
prefLabel
Drosophila as a model for epil ...... l gene that leads to seizures.
@ast
Drosophila as a model for epil ...... l gene that leads to seizures.
@en
Drosophila as a model for epil ...... l gene that leads to seizures.
@nl
P2093
P2860
P1433
P1476
Drosophila as a model for epil ...... l gene that leads to seizures.
@en
P2093
Louise Parker
Mark A Tanouye
Miguel Padilla
P2860
P304
P356
10.1534/GENETICS.110.123299
P407
P577
2010-11-29T00:00:00Z