Rodent models for dystonia research: characteristics, evaluation, and utility.
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The neural substrates of rapid-onset Dystonia-Parkinsonism.The basal ganglia and cerebellum interact in the expression of dystonic movementA rat model of hemidystonia induced by 3-nitropropionic acidProtein mutated in paroxysmal dyskinesia interacts with the active zone protein RIM and suppresses synaptic vesicle exocytosisResearch priorities in spasmodic dysphoniaTetrahydrobiopterin in the prevention of hypertonia in hypoxic fetal brain.KCa channels as therapeutic targets in episodic ataxia type-2The therapeutic mode of action of 4-aminopyridine in cerebellar ataxia.The anatomical basis of dystonia: current view using neuroimaging.Tor1a+/- mice develop dystonia-like movements via a striatal dopaminergic dysregulation triggered by peripheral nerve injury.Tiagabine treatment in kainic acid induced cerebellar lesion of dystonia rat model.Cholinergic dysregulation produced by selective inactivation of the dystonia-associated protein torsinA.Update on blepharospasm: report from the BEBRF International WorkshopAnimal models of dystonia: Lessons from a mutant rat.Caytaxin deficiency disrupts signaling pathways in cerebellar cortex.Pathogenic chaperone-like RNA induces congophilic aggregates and facilitates neurodegeneration in DrosophilaAlternative 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.The functional neuroanatomy of dystonia.Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.Experimental therapeutics for dystonia.Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia.A commentary on the utility of a new L-DOPA-responsive dystonia mouse modelThe focal dystonias: current views and challenges for future researchGain control of synaptic response function in cerebellar nuclear neurons by a calcium-activated potassium conductanceThe mechanisms of movement control and time estimation in cervical dystonia patients.Dystonia as a network disorder: what is the role of the cerebellum?A role for cerebellum in the hereditary dystonia DYT1.Animal models for drug discovery in dystonia.Cerebellum: An explanation for dystonia?Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia.Impairment of bidirectional synaptic plasticity in the striatum of a mouse model of DYT1 dystonia: role of endogenous acetylcholine.Lesch-Nyhan disease: from mechanism to model and back again.New hypotheses about postural control support the notion that all dystonias are manifestations of excessive brain postural function.The Anatomical Basis for Dystonia: The Motor Network Model.A Novel Ataxic Mutant Mouse Line Having Sensory Neuropathy Shows Heavy Iron Deposition in Kidney.
P2860
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P2860
Rodent models for dystonia research: characteristics, evaluation, and utility.
description
2005 nî lūn-bûn
@nan
2005 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մարտին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Rodent models for dystonia research: characteristics, evaluation, and utility.
@ast
Rodent models for dystonia research: characteristics, evaluation, and utility.
@en
type
label
Rodent models for dystonia research: characteristics, evaluation, and utility.
@ast
Rodent models for dystonia research: characteristics, evaluation, and utility.
@en
prefLabel
Rodent models for dystonia research: characteristics, evaluation, and utility.
@ast
Rodent models for dystonia research: characteristics, evaluation, and utility.
@en
P2093
P2860
P356
P1433
P1476
Rodent models for dystonia research: characteristics, evaluation, and utility.
@en
P2093
Ellen J Hess
H A Jinnah
Mahlon R Delong
Mark G Baxter
Mark S Ledoux
Nutan Sharma
P2860
P304
P356
10.1002/MDS.20364
P407
P577
2005-03-01T00:00:00Z