| scholarly article | Q13442814 |
| P50 | author | Mark P DeAndrade | Q58202709 |
| P2093 | author name string | Fumiaki Yokoi | |
| Yuqing Li | |||
| Mingzhou Ding | |||
| Amy Trongnetrpunya | |||
| J Michael Wyss | |||
| Ning Peng | |||
| Chad C Cheetham | |||
| P2860 | cites work | The neural substrates of rapid-onset Dystonia-Parkinsonism | Q24609728 |
| Cerebellothalamocortical connectivity regulates penetrance in dystonia | Q24652781 | ||
| Deficiency in Na,K-ATPase alpha isoform genes alters spatial learning, motor activity, and anxiety in mice | Q28510410 | ||
| Motor restlessness, sleep disturbances, thermal sensory alterations and elevated serum iron levels in Btbd9 mutant mice | Q28585548 | ||
| Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelope | Q28589351 | ||
| Increased c-fos expression in the central nucleus of the amygdala and enhancement of cued fear memory in Dyt1 DeltaGAG knock-in mice | Q30478968 | ||
| Earlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce. | Q30497374 | ||
| TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration | Q30581663 | ||
| Exclusive paternal expression and novel alternatively spliced variants of epsilon-sarcoglycan mRNA in mouse brain. | Q30999843 | ||
| Cholinergic dysregulation produced by selective inactivation of the dystonia-associated protein torsinA. | Q31061478 | ||
| Chemical enhancement of torsinA function in cell and animal models of torsion dystonia | Q33540113 | ||
| Altered dendritic morphology of Purkinje cells in Dyt1 ΔGAG knock-in and purkinje cell-specific Dyt1 conditional knockout mice. | Q33867544 | ||
| Motor deficits and decreased striatal dopamine receptor 2 binding activity in the striatum-specific Dyt1 conditional knockout mice | Q34023627 | ||
| Abnormal nuclear envelope in the cerebellar Purkinje cells and impaired motor learning in DYT11 myoclonus-dystonia mouse models | Q34063055 | ||
| Kinematic and electromyographic tools for characterizing movement disorders in mice | Q34077700 | ||
| Abnormal high-frequency burst firing of cerebellar neurons in rapid-onset dystonia-parkinsonism | Q34091178 | ||
| Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism. | Q34311667 | ||
| Phenomenology and classification of dystonia: a consensus update | Q34343247 | ||
| The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein | Q34438326 | ||
| Cerebellothalamocortical pathway abnormalities in torsinA DYT1 knock-in mice. | Q34836384 | ||
| Pre-synaptic release deficits in a DYT1 dystonia mouse model. | Q34965241 | ||
| Changes in sensitivity of reward and motor behavior to dopaminergic, glutamatergic, and cholinergic drugs in a mouse model of fragile X syndrome | Q35035766 | ||
| Electromyogram recordings from freely moving animals | Q35119309 | ||
| Behavioral and electrophysiological characterization of Dyt1 heterozygous knockout mice. | Q35208664 | ||
| An anticholinergic reverses motor control and corticostriatal LTD deficits in Dyt1 ΔGAG knock-in mice | Q35576523 | ||
| Motor deficits and hyperactivity in Dyt1 knockdown mice. | Q35629540 | ||
| Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models | Q35688598 | ||
| Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons | Q35759092 | ||
| Improved motor performance in Dyt1 ΔGAG heterozygous knock-in mice by cerebellar Purkinje-cell specific Dyt1 conditional knocking-out | Q35878028 | ||
| Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia | Q36400471 | ||
| Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia. | Q36591812 | ||
| The pathophysiological basis of dystonias. | Q37088920 | ||
| IP3R1 deficiency in the cerebellum/brainstem causes basal ganglia-independent dystonia by triggering tonic Purkinje cell firings in mice | Q37214087 | ||
| Engineering animal models of dystonia | Q37239952 | ||
| Electromyographic characterization in an animal model of dystonia | Q42435388 | ||
| Enhanced inhibitory neurotransmission in the cerebellar cortex of Atp1a3-deficient heterozygous mice. | Q42438187 | ||
| Generation and characterization of Dyt1 DeltaGAG knock-in mouse as a model for early-onset dystonia | Q42671584 | ||
| Abnormal cytoplasmic calcium dynamics in central neurons of a dystonia mouse model. | Q44250762 | ||
| Support vector machine-based classification scheme for myoelectric control applied to upper limb | Q44679314 | ||
| Motor deficits and hyperactivity in cerebral cortex-specific Dyt1 conditional knockout mice | Q46935059 | ||
| Suppression of polyglutamine-induced protein aggregation in Caenorhabditis elegans by torsin proteins | Q47069026 | ||
| Myoclonus, motor deficits, alterations in emotional responses and monoamine metabolism in epsilon-sarcoglycan deficient mice | Q48481174 | ||
| Heterozygous mice deficient in Atp1a3 exhibit motor deficits by chronic restraint stress | Q48684102 | ||
| Dose-response curves and time-course effects of selected anticholinergics on locomotor activity in rats | Q73365919 | ||
| Treatment of dystonia | Q80304443 | ||
| Synaptic vesicle recycling is enhanced by torsinA that harbors the DYT1 dystonia mutation | Q83166918 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1633-1639 | |
| P577 | publication date | 2016-05-31 | |
| P1433 | published in | Movement Disorders | Q1486418 |
| P1476 | title | Electromyographic evidence in support of a knock-in mouse model of DYT1 Dystonia | |
| P478 | volume | 31 |
| Q42622103 | A Role for Dystonia-Associated Genes in Spinal GABAergic Interneuron Circuitry |
| Q37684995 | A role for cerebellum in the hereditary dystonia DYT1. |
| Q90747980 | Decreased number of striatal cholinergic interneurons and motor deficits in dopamine receptor 2-expressing-cell-specific Dyt1 conditional knockout mice |
| Q31114074 | In vivo imaging reveals impaired connectivity across cortical and subcortical networks in a mouse model of DYT1 dystonia |
| Q99723276 | The abnormal firing of Purkinje cells in the knockin mouse model of DYT1 dystonia |
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