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Manganese-Induced Parkinsonism Is Not Idiopathic Parkinson's Disease: Environmental and Genetic EvidenceDtorsin, the Drosophila ortholog of the early-onset dystonia TOR1A (DYT1), plays a novel role in dopamine metabolismDevelopmental profile of the aberrant dopamine D2 receptor response in striatal cholinergic interneurons in DYT1 dystoniaMutations in PNKD causing paroxysmal dyskinesia alters protein cleavage and stabilityProtein mutated in paroxysmal dyskinesia interacts with the active zone protein RIM and suppresses synaptic vesicle exocytosisStriatal cholinergic dysfunction as a unifying theme in the pathophysiology of dystoniaCell-autonomous alteration of dopaminergic transmission by wild type and mutant (DeltaE) TorsinA in transgenic mice.Mutant torsinA interacts with tyrosine hydroxylase in cultured cells.Convergent evidence for abnormal striatal synaptic plasticity in dystonia.Dysregulation of striatal dopamine release in a mouse model of dystonia.A unique redox-sensing sensor II motif in TorsinA plays a critical role in nucleotide and partner binding.Direct interaction between causative genes of DYT1 and DYT6 primary dystonia.Genetic and clinical features of primary torsion dystonia.Spatial reorganization of putaminal dopamine D2-like receptors in cranial and hand dystoniaDeep-Brain Stimulation for Basal Ganglia Disorders.Pathological basal ganglia activity in movement disorders.A new knock-in mouse model of l-DOPA-responsive dystonia.Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia.Neuropathology of cervical dystonia.Invertebrate models of dystonia.Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia.Deep Brain Stimulation for Movement Disorders of Basal Ganglia Origin: Restoring Function or Functionality?Subtle microstructural changes of the cerebellum in a knock-in mouse model of DYT1 dystoniaA Dynamic Circuit Hypothesis for the Pathogenesis of Blepharospasm.Molecular pathways in dystonia.Loss of specificity in Basal Ganglia related movement disorders.Dopamine D2 receptor dysfunction is rescued by adenosine A2A receptor antagonism in a model of DYT1 dystonia.Function of dopamine transporter is compromised in DYT1 transgenic animal model in vivoManganese- and 1-methyl-4-phenylpyridinium-induced neurotoxicity display differences in morphological, electrophysiological and genome-wide alterations: implications for idiopathic Parkinson's disease.
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P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Commentary: Dopaminergic dysfunction in DYT1 dystonia.
@ast
Commentary: Dopaminergic dysfunction in DYT1 dystonia.
@en
type
label
Commentary: Dopaminergic dysfunction in DYT1 dystonia.
@ast
Commentary: Dopaminergic dysfunction in DYT1 dystonia.
@en
prefLabel
Commentary: Dopaminergic dysfunction in DYT1 dystonia.
@ast
Commentary: Dopaminergic dysfunction in DYT1 dystonia.
@en
P2860
P1476
Commentary: Dopaminergic dysfunction in DYT1 dystonia.
@en
P2093
Thomas Wichmann
P2860
P304
P356
10.1016/J.EXPNEUROL.2008.04.020
P407
P577
2008-04-26T00:00:00Z