| scholarly article | Q13442814 |
| P2093 | author name string | H A Jinnah | |
| Ellen J Hess | |||
| Xueliang Fan | |||
| Chang-Hyun Song | |||
| Cicely J Exeter | |||
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| P433 | issue | 1 | |
| P921 | main subject | dopamine | Q170304 |
| P304 | page(s) | 66-78 | |
| P577 | publication date | 2012-05-31 | |
| P1433 | published in | Neurobiology of Disease | Q15716606 |
| P1476 | title | Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia | |
| P478 | volume | 48 |
| Q36232197 | A new knock-in mouse model of l-DOPA-responsive dystonia |
| Q30441885 | Abnormal striatal dopaminergic neurotransmission during rest and task production in spasmodic dysphonia. |
| Q36591812 | Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia. |
| Q35836503 | Analysis of gait in rats with olivocerebellar lesions and ability of the nicotinic acetylcholine receptor agonist varenicline to attenuate impairments |
| Q37058173 | Animal models for dystonia |
| Q47623854 | Chemogenetic locus coeruleus activation restores reversal learning in a rat model of Alzheimer's disease |
| Q90747980 | Decreased number of striatal cholinergic interneurons and motor deficits in dopamine receptor 2-expressing-cell-specific Dyt1 conditional knockout mice |
| Q92000933 | Diverse Mechanisms Lead to Common Dysfunction of Striatal Cholinergic Interneurons in Distinct Genetic Mouse Models of Dystonia |
| Q48531888 | Dopamine receptor agonist treatment for idiopathic dystonia: A reappraisal in humans and mice |
| Q37592345 | Dystonia as a network disorder: what is the role of the cerebellum? |
| Q89633692 | Dystonia: Sparse Synapses for D2 Receptors in Striatum of a DYT1 Knock-out Mouse Model |
| Q47585471 | Effects of disulfiram on choice behavior in a rodent gambling task: association with catecholamine levels. |
| Q42755733 | Electromyographic evidence in support of a knock-in mouse model of DYT1 Dystonia |
| Q38124786 | Emerging common molecular pathways for primary dystonia. |
| Q37239952 | Engineering animal models of dystonia |
| Q33790163 | Evaluation of AZD1446 as a Therapeutic in DYT1 Dystonia. |
| Q91676683 | Freezing of Gait can persist after an acute levodopa challenge in Parkinson's disease |
| Q48433008 | Immunochemical localization of vesicular monoamine transporter 2 (VMAT2) in mouse brain. |
| Q89595744 | Increased endogenous dopamine prevents myopia in mice |
| Q33919548 | Increased vesicular monoamine transporter enhances dopamine release and opposes Parkinson disease-related neurodegeneration in vivo |
| Q64786603 | Loss of the dystonia gene Thap1 leads to transcriptional deficits that converge on common pathogenic pathways in dystonic syndromes |
| Q35049257 | Minimal Change in the cytoplasmic calcium dynamics in striatal GABAergic neurons of a DYT1 dystonia knock-in mouse model |
| Q39779374 | Motor phenotypes and molecular networks associated with germline deficiency of Ciz1. |
| Q36605114 | Neuropathology of cervical dystonia |
| Q48585249 | Parkinsonism without dopamine neuron degeneration in aged l-dopa-responsive dystonia knockin mice |
| Q61809637 | Retracted: Mouse models of GNAO1-associated movement disorder: Allele- and sex-specific differences in phenotypes |
| Q89675943 | Short-Wavelength (Violet) Light Protects Mice From Myopia Through Cone Signaling |
| Q28648007 | Striatal cholinergic dysfunction as a unifying theme in the pathophysiology of dystonia |
| Q37383467 | Striatal dopaminergic dysfunction at rest and during task performance in writer's cramp |
| Q37424519 | Subtle microstructural changes of the cerebellum in a knock-in mouse model of DYT1 dystonia |
| Q36774120 | Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia |
| Q46481280 | The Anatomical Basis for Dystonia: The Motor Network Model |
| Q37070290 | The focal dystonias: current views and challenges for future research |
| Q38115272 | The genetics of dystonia: new twists in an old tale |
| Q33841496 | The relationship between the dopaminergic system and depressive symptoms in cervical dystonia |
| Q36331007 | 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. |
| Q38176494 | The vesicular monoamine transporter 2: an underexplored pharmacological target |
| Q37444067 | Understanding the anatomy of dystonia: determinants of penetrance and phenotype |
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