Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.
about
Striatal cholinergic dysfunction as a unifying theme in the pathophysiology of dystoniaAbnormal striatal dopaminergic neurotransmission during rest and task production in spasmodic dysphonia.Evaluation of AZD1446 as a Therapeutic in DYT1 Dystonia.The relationship between the dopaminergic system and depressive symptoms in cervical dystoniaIncreased vesicular monoamine transporter enhances dopamine release and opposes Parkinson disease-related neurodegeneration in vivoMinimal Change in the cytoplasmic calcium dynamics in striatal GABAergic neurons of a DYT1 dystonia knock-in mouse model.Analysis of gait in rats with olivocerebellar lesions and ability of the nicotinic acetylcholine receptor agonist varenicline to attenuate impairmentsA new knock-in mouse model of l-DOPA-responsive dystonia.The ubiquitin ligase F-box/G-domain protein 1 promotes the degradation of the disease-linked protein torsinA through the ubiquitin-proteasome pathway and macroautophagy.Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia.Neuropathology of cervical dystonia.Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia.Animal models for dystonia.The focal dystonias: current views and challenges for future researchEngineering animal models of dystoniaStriatal dopaminergic dysfunction at rest and during task performance in writer's cramp.Subtle microstructural changes of the cerebellum in a knock-in mouse model of DYT1 dystoniaUnderstanding the anatomy of dystonia: determinants of penetrance and phenotype.Dystonia as a network disorder: what is the role of the cerebellum?The genetics of dystonia: new twists in an old tale.Emerging common molecular pathways for primary dystonia.The vesicular monoamine transporter 2: an underexplored pharmacological target.Motor phenotypes and molecular networks associated with germline deficiency of Ciz1.Electromyographic evidence in support of a knock-in mouse model of DYT1 Dystonia.The Anatomical Basis for Dystonia: The Motor Network Model.Effects of disulfiram on choice behavior in a rodent gambling task: association with catecholamine levels.Chemogenetic locus coeruleus activation restores reversal learning in a rat model of Alzheimer's disease.Immunochemical localization of vesicular monoamine transporter 2 (VMAT2) in mouse brain.Dopamine receptor agonist treatment for idiopathic dystonia: A reappraisal in humans and mice.Parkinsonism without dopamine neuron degeneration in aged l-dopa-responsive dystonia knockin mice.
P2860
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P2860
Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.
@ast
Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.
@en
type
label
Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.
@ast
Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.
@en
prefLabel
Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.
@ast
Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.
@en
P2093
P2860
P1476
Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.
@en
P2093
Chang-Hyun Song
Cicely J Exeter
Ellen J Hess
H A Jinnah
Xueliang Fan
P2860
P356
10.1016/J.NBD.2012.05.009
P577
2012-05-31T00:00:00Z