Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism. - Wikidata - thesis-toulmin - TriplyDB

Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.

Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.

http://www.wikidata.org/entity/Q34311667

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The neural substrates of rapid-onset Dystonia-Parkinsonism.Insights into the Pathology of the α3 Na(+)/K(+)-ATPase Ion Pump in Neurological Disorders; Lessons from Animal Models The Influence of Na(+), K(+)-ATPase on Glutamate Signaling in Neurodegenerative Diseases and Senescence Cognitive deficits caused by a disease-mutation in the α3 Na(+)/K(+)-ATPase isoform.Alternating hemiplegia of childhood-related neural and behavioural phenotypes in Na+,K+-ATPase α3 missense mutant mice.Methamphetamine and inflammatory cytokines increase neuronal Na+/K+-ATPase isoform 3: relevance for HIV associated neurocognitive disorders Motor restlessness, sleep disturbances, thermal sensory alterations and elevated serum iron levels in Btbd9 mutant mice.Deficits in social behavioral tests in a mouse model of alternating hemiplegia of childhood.Cholinergic dysregulation produced by selective inactivation of the dystonia-associated protein torsinA.Motor deficits and decreased striatal dopamine receptor 2 binding activity in the striatum-specific Dyt1 conditional knockout mice Abnormal nuclear envelope in the cerebellar Purkinje cells and impaired motor learning in DYT11 myoclonus-dystonia mouse models Distinct neurological disorders with ATP1A3 mutations Behavioral and electrophysiological characterization of Dyt1 heterozygous knockout mice.Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models Improved motor performance in Dyt1 ΔGAG heterozygous knock-in mice by cerebellar Purkinje-cell specific Dyt1 conditional knocking-out Alternative approaches to modeling hereditary dystonias.Aberrant Purkinje cell activity is the cause of dystonia in a shRNA-based mouse model of Rapid Onset Dystonia-Parkinsonism.Recent advances in the molecular pathogenesis of dystonia-plus syndromes and heredodegenerative dystonias.α3Na+/K+-ATPase deficiency causes brain ventricle dilation and abrupt embryonic motility in zebrafish.Engineering animal models of dystonia A role for cerebellum in the hereditary dystonia DYT1.The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.CAOS-Episodic Cerebellar Ataxia, Areflexia, Optic Atrophy, and Sensorineural Hearing Loss: A Third Allelic Disorder of the ATP1A3 Gene.Sodium pump regulation of locomotor control circuits.Mouse model of rare TOR1A variant found in sporadic focal dystonia impairs domains affected in DYT1 dystonia patients and animal models Sodium Pumps Mediate Activity-Dependent Changes in Mammalian Motor Networks.Enhanced inhibitory neurotransmission in the cerebellar cortex of Atp1a3-deficient heterozygous mice.Electromyographic evidence in support of a knock-in mouse model of DYT1 Dystonia.Loss of Na(+)/K(+)-ATPase in Drosophila photoreceptors leads to blindness and age-dependent neurodegeneration.Ionic leakage underlies a gain-of-function effect of dominant disease mutations affecting diverse P-type ATPases.Atp1a3-deficient heterozygous mice show lower rank in the hierarchy and altered social behavior.Knock-in mouse model of alternating hemiplegia of childhood: behavioral and electrophysiologic characterization.Novel pregnancy-triggered episodes of CAPOS syndrome.

P2860

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Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.

http://www.wikidata.org/entity/Q34311667

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2010 nî lūn-bûn

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2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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Characterization of Atp1a3 mut ...... et dystonia with parkinsonism.

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Characterization of Atp1a3 mut ...... et dystonia with parkinsonism.

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Characterization of Atp1a3 mut ...... et dystonia with parkinsonism.

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Characterization of Atp1a3 mut ...... et dystonia with parkinsonism.

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Characterization of Atp1a3 mut ...... et dystonia with parkinsonism.

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Characterization of Atp1a3 mut ...... et dystonia with parkinsonism.

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Characterization of Atp1a3 mut ...... et dystonia with parkinsonism.

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Characterization of Atp1a3 mut ...... et dystonia with parkinsonism.

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Characterization of Atp1a3 mut ...... et dystonia with parkinsonism.

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J.BBR.2010.09.009

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Behavioural Brain Research

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Characterization of Atp1a3 mut ...... set dystonia with parkinsonism

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Fumiaki Yokoi

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Jerry B Lingrel

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Thomas van Groen

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P2860

Parkinson's disease: clinical features and diagnosis

Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism

The early onset dystonia protein torsinA interacts with kinesin light chain 1

Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia

Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia

Mutation I810N in the alpha3 isoform of Na+,K+-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS.

Pathomechanisms in channelopathies of skeletal muscle and brain

DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene

Deficiency in Na,K-ATPase alpha isoform genes alters spatial learning, motor activity, and anxiety in mice

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