Altered dendritic morphology of Purkinje cells in Dyt1 ΔGAG knock-in and purkinje cell-specific Dyt1 conditional knockout mice.
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TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegenerationA novel conditional knock-in approach defines molecular and circuit effects of the DYT1 dystonia mutation.Genetic silencing of olivocerebellar synapses causes dystonia-like behaviour in miceIn vivo imaging reveals impaired connectivity across cortical and subcortical networks in a mouse model of DYT1 dystonia.Motor deficits and decreased striatal dopamine receptor 2 binding activity in the striatum-specific Dyt1 conditional knockout miceAbnormal nuclear envelope in the cerebellar Purkinje cells and impaired motor learning in DYT11 myoclonus-dystonia mouse modelsUntethering the nuclear envelope and cytoskeleton: biologically distinct dystonias arising from a common cellular dysfunctionTorsin A Localization in the Mouse Cerebellar Synaptic Circuitry.Pre-synaptic release deficits in a DYT1 dystonia mouse model.Dopamine receptor and Gα(olf) expression in DYT1 dystonia mouse models during postnatal development.Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons.Selective and sustained α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor activation in cerebellum induces dystonia in mice.Improved motor performance in Dyt1 ΔGAG heterozygous knock-in mice by cerebellar Purkinje-cell specific Dyt1 conditional knocking-outMutations in CIZ1 cause adult onset primary cervical dystonia.Mouse models of neurodevelopmental disease of the basal ganglia and associated circuits.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.Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia.The focal dystonias: current views and challenges for future researchEngineering animal models of dystoniaSubtle microstructural changes of the cerebellum in a knock-in mouse model of DYT1 dystoniaA role for cerebellum in the hereditary dystonia DYT1.Primary dystonia: moribund or viable.Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia.Motor phenotypes and molecular networks associated with germline deficiency of Ciz1.Microfluidic platform to evaluate migration of cells from patients with DYT1 dystonia.Human TorsinA can function in the yeast cytosol as a molecular chaperone.Electromyographic evidence in support of a knock-in mouse model of DYT1 Dystonia.Loss of inhibition in sensorimotor networks in focal hand dystonia.The Anatomical Basis for Dystonia: The Motor Network Model.An aberrant cerebellar development in mice lacking matrix metalloproteinase-3.
P2860
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P2860
Altered dendritic morphology of Purkinje cells in Dyt1 ΔGAG knock-in and purkinje cell-specific Dyt1 conditional knockout mice.
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Altered dendritic morphology o ...... yt1 conditional knockout mice.
@ast
Altered dendritic morphology o ...... yt1 conditional knockout mice.
@en
type
label
Altered dendritic morphology o ...... yt1 conditional knockout mice.
@ast
Altered dendritic morphology o ...... yt1 conditional knockout mice.
@en
prefLabel
Altered dendritic morphology o ...... yt1 conditional knockout mice.
@ast
Altered dendritic morphology o ...... yt1 conditional knockout mice.
@en
P2093
P2860
P50
P1433
P1476
Altered dendritic morphology o ...... Dyt1 conditional knockout mice
@en
P2093
Fumiaki Yokoi
Yuan-Hu Jin
P2860
P304
P356
10.1371/JOURNAL.PONE.0018357
P407
P577
2011-03-29T00:00:00Z