| scholarly article | Q13442814 |
| P50 | author | William T Dauer | Q56496446 |
| Samuel S Pappas | Q56909383 | ||
| Daniel Leventhal | Q57567369 | ||
| P2093 | author name string | Roger L Albin | |
| P2860 | cites work | Heterogeneity and diversity of striatal GABAergic interneurons | Q21090474 |
| Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 | Q22337290 | ||
| Genome-wide association study of Tourette's syndrome | Q23936582 | ||
| The dystonia-associated protein torsinA modulates synaptic vesicle recycling | Q24305325 | ||
| Effect of torsinA on membrane proteins reveals a loss of function and a dominant-negative phenotype of the dystonia-associated DeltaE-torsinA mutant | Q24308930 | ||
| Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex | Q24324026 | ||
| Regulation of Torsin ATPases by LAP1 and LULL1 | Q24338125 | ||
| Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome | Q24530286 | ||
| Hematopoietic origin of pathological grooming in Hoxb8 mutant mice | Q24624921 | ||
| Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry | Q24630976 | ||
| Canceling actions involves a race between basal ganglia pathways. | Q24633908 | ||
| Trichotillomania and its treatment: a review and recommendations | Q24635126 | ||
| MeCP2, a key contributor to neurological disease, activates and represses transcription | Q24647533 | ||
| Increased putamen and callosal motor subregion in treatment-naïve boys with Tourette syndrome indicates changes in the bihemispheric motor network | Q63988624 | ||
| Decreased [18F]spiperone binding in putamen in idiopathic focal dystonia | Q67217660 | ||
| H-reflex recovery curve and reciprocal inhibition of H-reflex in different kinds of dystonia | Q68762761 | ||
| Disturbance of sequential movements in patients with Parkinson's disease | Q68984575 | ||
| Extrapyramidal involvement in Rett's syndrome | Q70235869 | ||
| Dopaminergic D2 receptor SPECT imaging in Rett syndrome: increase of specific binding in striatum | Q70506102 | ||
| Auctioneer's jaw: a case of occupational oromandibular hemidystonia | Q71758641 | ||
| Preliminary evidence for neurodegenerative changes in the substantia nigra of Rett syndrome | Q71760080 | ||
| Meige syndrome in the spectrum of Lewy body disease | Q72124094 | ||
| Cerebral morphometric abnormalities in Tourette's syndrome: a quantitative MRI study of monozygotic twins | Q72319662 | ||
| High dosage anticholinergic therapy in dystonia | Q72560936 | ||
| Clonidine ameliorates Gilles de la Tourette syndrome | Q72874697 | ||
| Behavior-related changes in the activity of substantia nigra pars reticulata neurons in freely moving rats | Q73101705 | ||
| Two affected boys in a Rett syndrome family: clinical and molecular findings | Q73172439 | ||
| Psychopharmacological distinction between novel full-efficacy "D1-like" dopamine receptor agonists | Q73705431 | ||
| Cortical inputs to m2-immunoreactive striatal interneurons in rat and monkey | Q73986052 | ||
| Glutamatergic drugs exacerbate symptomatic behavior in a transgenic model of comorbid Tourette's syndrome and obsessive-compulsive disorder | Q74296989 | ||
| Classic Rett syndrome in a boy as a result of somatic mosaicism for a MECP2 mutation | Q77165289 | ||
| TorsinA immunoreactivity in brains of patients with DYT1 and non-DYT1 dystonia | Q77462037 | ||
| An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome Clinical Criteria Consensus Panel Satellite to European Paediatric Neurology Society Meeting, Baden Baden, Germany, 11 September 2001 | Q78369107 | ||
| Basal ganglia activity remains elevated after movement in focal hand dystonia | Q80040787 | ||
| Neuropathology of primary adult-onset dystonia | Q80771643 | ||
| Antipsychotic-induced extrapyramidal symptoms and their management | Q81383731 | ||
| Synaptic vesicle recycling is enhanced by torsinA that harbors the DYT1 dystonia mutation | Q83166918 | ||
| The genetics of Tourette syndrome | Q83629652 | ||
| Deep brain stimulation for dystonia | Q85446619 | ||
| Tourette's syndrome | Q87287270 | ||
| Serum trihexyphenidyl levels in the treatment of torsion dystonia | Q93581508 | ||
| Pharmacokinetics of trihexyphenidyl after short-term and long-term administration to dystonic patients | Q93604771 | ||
| Cortico-striatal synaptic defects and OCD-like behaviours in Sapap3-mutant mice. | Q24648260 | ||
| Cerebellothalamocortical connectivity regulates penetrance in dystonia | Q24652781 | ||
| The basal ganglia and cerebellum interact in the expression of dystonic movement | Q24653882 | ||
| Two types of dopamine neuron distinctly convey positive and negative motivational signals | Q24658285 | ||
| The AAA+ protein torsinA interacts with a conserved domain present in LAP1 and a novel ER protein | Q24678547 | ||
| GKAP, a novel synaptic protein that interacts with the guanylate kinase-like domain of the PSD-95/SAP90 family of channel clustering molecules | Q24681609 | ||
| Sequential super-stereotypy of an instinctive fixed action pattern in hyper-dopaminergic mutant mice: a model of obsessive compulsive disorder and Tourette's | Q24797858 | ||
| Clinical assessment of Tourette syndrome and tic disorders | Q26825003 | ||
| Genetic background modulates the phenotype of a mouse model of DYT1 dystonia | Q27308647 | ||
| Developmental profile of the aberrant dopamine D2 receptor response in striatal cholinergic interneurons in DYT1 dystonia | Q27321884 | ||
| A neural substrate of prediction and reward | Q27860851 | ||
| AAA+: A class of chaperone-like ATPases associated with the assembly, operation, and disassembly of protein complexes | Q28131706 | ||
| Super-stereotypy I: enhancement of a complex movement sequence by systemic dopamine D1 agonists | Q28139960 | ||
| SAPAPs. A family of PSD-95/SAP90-associated proteins localized at postsynaptic density | Q28235849 | ||
| Modulation of neurotransmitter release via histamine H3 heteroreceptors | Q28244199 | ||
| Neurobiology of tourette syndrome: current status and need for further investigation | Q28246791 | ||
| GABAergic circuits mediate the reinforcement-related signals of striatal cholinergic interneurons | Q28255137 | ||
| Neural correlates of encoding and expression in implicit sequence learning | Q28257516 | ||
| Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA | Q28265233 | ||
| Cocaine seeking habits depend upon dopamine-dependent serial connectivity linking the ventral with the dorsal striatum | Q28267577 | ||
| Basal ganglia activity patterns in parkinsonism and computational modeling of their downstream effects | Q28271277 | ||
| Sequence variants in SLITRK1 are associated with Tourette's syndrome | Q28276961 | ||
| A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome | Q28504458 | ||
| Differential mRNA expression and protein localization of the SAP90/PSD-95-associated proteins (SAPAPs) in the nervous system of the mouse | Q28506673 | ||
| MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number | Q28507266 | ||
| Identification and characterization of Slitrk, a novel neuronal transmembrane protein family controlling neurite outgrowth | Q28507516 | ||
| Targeted inactivation of Hoxb8 affects survival of a spinal ganglion and causes aberrant limb reflexes | Q28508096 | ||
| Hoxb8 is required for normal grooming behavior in mice | Q28509145 | ||
| Slitrk1-deficient mice display elevated anxiety-like behavior and noradrenergic abnormalities | Q28510280 | ||
| Action sequencing is impaired in D1A-deficient mutant mice | Q28588198 | ||
| Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelope | Q28589351 | ||
| Gene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndrome | Q28592510 | ||
| Loss of Hoxb8 alters spinal dorsal laminae and sensory responses in mice | Q28594361 | ||
| Enhanced anxiety and stress-induced corticosterone release are associated with increased Crh expression in a mouse model of Rett syndrome | Q28595032 | ||
| MeCP2 is required for normal development of GABAergic circuits in the thalamus | Q33841359 | ||
| Tourette syndrome, associated conditions and the complexities of treatment | Q33844355 | ||
| Inhibitory control of neostriatal projection neurons by GABAergic interneurons | Q33861738 | ||
| Striatal dopamine D1-like receptor binding is unchanged in primary focal dystonia | Q33863502 | ||
| Altered dendritic morphology of Purkinje cells in Dyt1 ΔGAG knock-in and purkinje cell-specific Dyt1 conditional knockout mice. | Q33867544 | ||
| Torsin A and its torsion dystonia-associated mutant forms are lumenal glycoproteins that exhibit distinct subcellular localizations | Q33907326 | ||
| Methyl-CpG-binding protein 2 mutations in Rett syndrome | Q33927087 | ||
| Altered parvalbumin-positive neuron distribution in basal ganglia of individuals with Tourette syndrome | Q33947856 | ||
| L-histidine decarboxylase and Tourette's syndrome | Q33951417 | ||
| Motor sequences and the basal ganglia: kinematics, not habits | Q34004243 | ||
| Motor deficits and decreased striatal dopamine receptor 2 binding activity in the striatum-specific Dyt1 conditional knockout mice | Q34023627 | ||
| The early-onset torsion dystonia-associated protein, torsinA, is a homeostatic regulator of endoplasmic reticulum stress response | Q34083670 | ||
| Toward a neurobiology of obsessive-compulsive disorder | Q34122154 | ||
| Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots | Q34146268 | ||
| Impaired sequence learning in dystonia mutation carriers: a genotypic effect | Q34180210 | ||
| Evidence for altered basal ganglia-brainstem connections in cervical dystonia | Q34181828 | ||
| Deep brain stimulation for dystonia in adults. Overview and developments | Q34185485 | ||
| Cell-autonomous alterations in dendritic arbor morphology and connectivity induced by overexpression of MeCP2 in Xenopus central neurons in vivo | Q34200572 | ||
| Dynamic regulation of midbrain dopamine neuron activity: intrinsic, synaptic, and plasticity mechanisms | Q34211245 | ||
| Spontaneous firing and evoked pauses in the tonically active cholinergic interneurons of the striatum. | Q34217067 | ||
| A mouse model for MeCP2 duplication syndrome: MeCP2 overexpression impairs learning and memory and synaptic transmission | Q34257833 | ||
| Influence of globus pallidus on arm movements in monkeys. I. Effects of kainic acid-induced lesions | Q34261812 | ||
| Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows | Q34278418 | ||
| The organization of the human striatum estimated by intrinsic functional connectivity | Q34290294 | ||
| The evolutionary origin of the vertebrate basal ganglia and its role in action selection | Q34322529 | ||
| Coincident but distinct messages of midbrain dopamine and striatal tonically active neurons | Q34331030 | ||
| Phenomenology and classification of dystonia: a consensus update | Q34343247 | ||
| Rett syndrome and associated movement disorders | Q34359822 | ||
| Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain | Q34387585 | ||
| Tardive tourettism after exposure to neuroleptic therapy | Q34391767 | ||
| Differential roles of monkey striatum in learning of sequential hand movement | Q34432708 | ||
| The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein | Q34438326 | ||
| Neurophysiology of dystonia: The role of inhibition | Q34468828 | ||
| The primate centromedian-parafascicular complex: anatomical organization with a note on neuromodulation | Q37310585 | ||
| Control of basal ganglia output by direct and indirect pathway projection neurons. | Q37325384 | ||
| Loss of muscarinic autoreceptor function impairs long-term depression but not long-term potentiation in the striatum. | Q37361261 | ||
| Dendritic arborization and spine dynamics are abnormal in the mouse model of MECP2 duplication syndrome | Q37381808 | ||
| Updating dopamine reward signals | Q37400352 | ||
| Deep brain stimulation for refractory obsessive-compulsive disorder | Q37410212 | ||
| Dopamine-modulated dynamic cell assemblies generated by the GABAergic striatal microcircuit. | Q37568414 | ||
| Dystonia as a network disorder: what is the role of the cerebellum? | Q37592345 | ||
| Primary dystonia: molecules and mechanisms. | Q37614200 | ||
| The international prevalence, epidemiology, and clinical phenomenology of Tourette syndrome: a cross-cultural perspective | Q37632893 | ||
| Basal ganglia subcircuits distinctively encode the parsing and concatenation of action sequences | Q37638852 | ||
| Consensus paper: use of transcranial magnetic stimulation to probe motor cortex plasticity in dystonia and levodopa-induced dyskinesia. | Q37773019 | ||
| Clinical practice. Tourette's Syndrome | Q37818192 | ||
| Abnormal plasticity in dystonia: Disruption of synaptic homeostasis | Q37822135 | ||
| Impulse control and related disorders in Parkinson's disease patients treated with bilateral subthalamic nucleus stimulation: a review | Q37850587 | ||
| Animal models of obsessive-compulsive disorder: exploring pharmacology and neural substrates | Q37869974 | ||
| Functional properties of the basal ganglia's re-entrant loop architecture: selection and reinforcement | Q37912711 | ||
| Amphetamine stereotypy, the basal ganglia, and the "selection problem". | Q37958589 | ||
| Tic disorders: what happens in the basal ganglia? | Q38011002 | ||
| Surgery for Tourette syndrome | Q38020656 | ||
| Review: genetics and neuropathology of primary pure dystonia | Q38035007 | ||
| Deep brain stimulation in the treatment of obsessive-compulsive disorder | Q38050223 | ||
| Pause and rebound: sensory control of cholinergic signaling in the striatum | Q38052768 | ||
| The psychopathological spectrum of Gilles de la Tourette syndrome | Q38058162 | ||
| Childhood obsessive-compulsive disorder | Q38071064 | ||
| Using optogenetics to study habits | Q38073517 | ||
| Tourette Syndrome and comorbid ADHD: current pharmacological treatment options | Q38087727 | ||
| Rett syndrome and epilepsy: an update for child neurologists | Q38098730 | ||
| Movement disorders in cerebrovascular disease | Q38100484 | ||
| Recognition and treatment of neurologic Wilson's disease | Q38107161 | ||
| Review: electrophysiology of basal ganglia and cortex in models of Parkinson disease | Q38129241 | ||
| Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification. | Q38295937 | ||
| The sensorimotor striatum is necessary for serial order learning | Q38571574 | ||
| Age-dependent decline of nigrostriatal dopaminergic function: a positron emission tomographic study of grandparents and their grandchildren | Q39111862 | ||
| A role for dopamine-mediated learning in the pathophysiology and treatment of Parkinson's disease. | Q39502291 | ||
| Clonidine in Tourette's syndrome | Q39560651 | ||
| Investigating SAPAP3 variants in the etiology of obsessive-compulsive disorder and trichotillomania in the South African white population | Q39786257 | ||
| Lesions of dorsolateral striatum preserve outcome expectancy but disrupt habit formation in instrumental learning | Q44747862 | ||
| Brainstem pathology in DYT1 primary torsion dystonia | Q45083991 | ||
| Altered corticostriatal functional connectivity in obsessive-compulsive disorder | Q45127542 | ||
| By carrot or by stick: cognitive reinforcement learning in parkinsonism | Q45140702 | ||
| Tourettism associated with Huntington's disease | Q45288922 | ||
| Reciprocal inhibition between forearm muscles in patients with writer's cramp and other occupational cramps, symptomatic hemidystonia and hemiparesis due to stroke | Q45634274 | ||
| Deep brain electrophysiological recordings provide clues to the pathophysiology of Tourette syndrome. | Q45769004 | ||
| Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families | Q45771551 | ||
| Local dopamine production in the dorsal striatum restores goal-directed behavior in dopamine-deficient mice | Q45856275 | ||
| Dopaminergic activity in Tourette syndrome and obsessive-compulsive disorder | Q45866616 | ||
| The sz mutant hamster: a genetic model of epilepsy or of paroxysmal dystonia? | Q45923764 | ||
| Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients | Q46068727 | ||
| Striatal denervation pattern predicts levodopa effects on sequence learning in Parkinson's disease | Q46077398 | ||
| Network architecture of gap junction-coupled neuronal linkage in the striatum | Q46142218 | ||
| Sapap3 and pathological grooming in humans: Results from the OCD collaborative genetics study. | Q46217993 | ||
| Transgenic mouse model of early-onset DYT1 dystonia | Q46232270 | ||
| Functional mapping of sequence learning in normal humans. | Q46269044 | ||
| The role of the dorsomedial striatum in instrumental conditioning | Q46306217 | ||
| Inactivation of dorsolateral striatum enhances sensitivity to changes in the action-outcome contingency in instrumental conditioning. | Q46695444 | ||
| Morphine reward in dopamine-deficient mice | Q46845126 | ||
| Motor deficits and hyperactivity in cerebral cortex-specific Dyt1 conditional knockout mice | Q46935059 | ||
| Stereotypic behaviour in the deer mouse: pharmacological validation and relevance for obsessive compulsive disorder | Q46987238 | ||
| Suppression of polyglutamine-induced protein aggregation in Caenorhabditis elegans by torsin proteins | Q47069026 | ||
| Dependence of GABAergic synaptic areas on the interneuron type and target size. | Q47249614 | ||
| “Motor circuit” gray matter changes in idiopathic cervical dystonia | Q47392987 | ||
| Large aspiny cells in the matrix of the rat neostriatum in vitro: physiological identification, relation to the compartments and excitatory postsynaptic currents | Q47932630 | ||
| Basal ganglia motor control. III. Pallidal ablation: normal reaction time, muscle cocontraction, and slow movement | Q47937495 | ||
| Structural abnormalities in the cerebellum and sensorimotor circuit in writer's cramp | Q48097572 | ||
| Overexpression of human wildtype torsinA and human DeltaGAG torsinA in a transgenic mouse model causes phenotypic abnormalities. | Q48120915 | ||
| Voxel based morphometry reveals specific gray matter changes in primary dystonia | Q48127862 | ||
| Role of [corrected] nigrostriatal dopamine system in learning to perform sequential motor tasks in a predictive manner | Q48137648 | ||
| Altered corticostriatal neurotransmission and modulation in dopamine transporter knock-down mice | Q48158205 | ||
| Miniature release events of glutamate from hippocampal neurons are influenced by the dystonia-associated protein torsinA. | Q48161931 | ||
| A bone to pick with compulsive behavior | Q48181721 | ||
| OCD-Like behaviors caused by a neuropotentiating transgene targeted to cortical and limbic D1+ neurons | Q48188537 | ||
| A rodent model of spontaneous stereotypy: initial characterization of developmental, environmental, and neurobiological factors | Q48205607 | ||
| Altered development of glutamate and GABA receptors in the basal ganglia of girls with Rett syndrome | Q48210067 | ||
| Neurochemical alterations in Rett syndrome | Q48248216 | ||
| Stereotactic treatment of Gilles de la Tourette syndrome by high frequency stimulation of thalamus | Q48266108 | ||
| The effects of posteroventral pallidotomy on the preparation and execution of voluntary hand and arm movements in Parkinson's disease | Q48267620 | ||
| Cholinergic neuropil of the striatum observes striosomal boundaries | Q48287562 | ||
| Saccade suppression by electrical microstimulation in monkey caudate nucleus. | Q48302999 | ||
| Responses of monkey dopamine neurons to reward and conditioned stimuli during successive steps of learning a delayed response task | Q48323891 | ||
| Basal Ganglia volumes in patients with Gilles de la Tourette syndrome | Q48335400 | ||
| Abnormalities in motor cortical plasticity differentiate manifesting and nonmanifesting DYT1 carriers | Q48381491 | ||
| Changes in blink reflex excitability after globus pallidus internus stimulation for dystonia | Q48389756 | ||
| Pallidotomy and incidental sequence learning in Parkinson's disease | Q48402336 | ||
| Differential expression of Slitrk family members in the mouse nervous system | Q48403573 | ||
| The pathophysiology of primary dystonia | Q48423358 | ||
| Altered responses to dopaminergic D2 receptor activation and N-type calcium currents in striatal cholinergic interneurons in a mouse model of DYT1 dystonia. | Q48436385 | ||
| Abnormal somatosensory homunculus in dystonia of the hand | Q34480294 | ||
| Striatonigrostriatal pathways in primates form an ascending spiral from the shell to the dorsolateral striatum | Q34507515 | ||
| The DYT1 phenotype and guidelines for diagnostic testing | Q34508690 | ||
| Basal ganglia contributions to motor control: a vigorous tutor | Q34511125 | ||
| Decreased striatal dopamine receptor binding in primary focal dystonia: a D2 or D3 defect? | Q34512173 | ||
| Results of deep brain stimulation for dystonia: a critical reappraisal | Q34522374 | ||
| Decreased striatal D2 receptor binding in non-manifesting carriers of the DYT1 dystonia mutation | Q34554476 | ||
| Bilateral deep-brain stimulation of the globus pallidus in primary generalized dystonia | Q34554762 | ||
| Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses | Q34573373 | ||
| Mutant torsinA interferes with protein processing through the secretory pathway in DYT1 dystonia cells | Q34578567 | ||
| Physiology and pharmacology of striatal neurons | Q34607026 | ||
| A selective role for dopamine in stimulus-reward learning | Q34680325 | ||
| Primary dystonia: conceptualizing the disorder through a structural brain imaging lens | Q34682292 | ||
| Torsion dystonia: a double-blind, prospective trial of high-dosage trihexyphenidyl | Q34689310 | ||
| Increased cerebellar activation during sequence learning in DYT1 carriers: an equiperformance study | Q34703465 | ||
| Family-based genetic association study of DLGAP3 in Tourette Syndrome | Q34733335 | ||
| The basal ganglia and chunking of action repertoires | Q34753448 | ||
| Histaminergic transmission in the mammalian brain | Q34776368 | ||
| Deep brain stimulation of the ventral internal capsule/ventral striatum for obsessive-compulsive disorder: worldwide experience. | Q34779794 | ||
| Cerebellothalamocortical pathway abnormalities in torsinA DYT1 knock-in mice. | Q34836384 | ||
| Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndrome | Q34910081 | ||
| Functional properties of striatal fast-spiking interneurons | Q35062124 | ||
| Decreased firing of striatal neurons related to licking during acquisition and overtraining of a licking task | Q35092311 | ||
| Rett Syndrome -- an update | Q35136636 | ||
| The corticostriatal and corticosubthalamic pathways: two entries, one target. So what? | Q35146020 | ||
| Basal Ganglia disorders associated with imbalances in the striatal striosome and matrix compartments | Q35208420 | ||
| Understanding dopamine and reinforcement learning: the dopamine reward prediction error hypothesis. | Q35222930 | ||
| Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging study | Q35492515 | ||
| Abnormal brain networks in primary torsion dystonia. | Q35543717 | ||
| Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation. | Q35554495 | ||
| The Basal Ganglia and involuntary movements: impaired inhibition of competing motor patterns | Q35564115 | ||
| Selective inhibition of striatal fast-spiking interneurons causes dyskinesias | Q35580745 | ||
| Primary food reward and reward-predictive stimuli evoke different patterns of phasic dopamine signaling throughout the striatum | Q35613463 | ||
| Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2. | Q35629499 | ||
| Motor deficits and hyperactivity in Dyt1 knockdown mice. | Q35629540 | ||
| Neuron-type-specific signals for reward and punishment in the ventral tegmental area | Q35729983 | ||
| Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism | Q35764564 | ||
| Melanocortin 4 receptor signaling in dopamine 1 receptor neurons is required for procedural memory learning. | Q35856900 | ||
| MeCP2 is critical for maintaining mature neuronal networks and global brain anatomy during late stages of postnatal brain development and in the mature adult brain | Q36288388 | ||
| Sapap3 deletion causes mGluR5-dependent silencing of AMPAR synapses | Q36329526 | ||
| Correlation of the vesicular acetylcholine transporter densities in the striata to the clinical abilities of women with Rett syndrome | Q36344561 | ||
| Modulation of striatal projection systems by dopamine | Q36367283 | ||
| Meaningful silences: how dopamine listens to the ACh pause | Q36380354 | ||
| Attention deficit hyperactivity disorder, tics and Tourette's syndrome: the relationship and treatment implications. A commentary | Q36412423 | ||
| TorsinA participates in endoplasmic reticulum-associated degradation | Q36487761 | ||
| The frequency and distribution of medium-sized neurons with indented nuclei in the primate and rodent neostriatum | Q36494620 | ||
| Adulthood outcome of tic and obsessive-compulsive symptom severity in children with Tourette syndrome | Q36536128 | ||
| Deep brain stimulation entrains local neuronal firing in human globus pallidus internus | Q36600722 | ||
| Deep brain stimulation for neurologic and neuropsychiatric disorders | Q36610382 | ||
| Caudate volumes in childhood predict symptom severity in adults with Tourette syndrome | Q36632056 | ||
| Abnormal motor function and dopamine neurotransmission in DYT1 DeltaGAG transgenic mice | Q36666604 | ||
| Synaptic input and output of parvalbumin-immunoreactive neurons in the neostriatum of the rat. | Q36717442 | ||
| MECP2 mutations in males. | Q36757032 | ||
| Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia | Q36774120 | ||
| Deep brain stimulation for treatment-refractory obsessive-compulsive disorder: the search for a valid target | Q36875160 | ||
| Recurrent inhibitory network among striatal cholinergic interneurons | Q36922170 | ||
| Re-emergence of striatal cholinergic interneurons in movement disorders | Q36955354 | ||
| Double deletion of melanocortin 4 receptors and SAPAP3 corrects compulsive behavior and obesity in mice | Q36967624 | ||
| Uncoordinated firing rate changes of striatal fast-spiking interneurons during behavioral task performance | Q37036872 | ||
| Animal models for dystonia | Q37058173 | ||
| Superior colliculus mediates cervical dystonia evoked by inhibition of the substantia nigra pars reticulata | Q37117374 | ||
| The genetics of obsessive compulsive disorder: a review of the evidence | Q37138393 | ||
| Different correlation patterns of cholinergic and GABAergic interneurons with striatal projection neurons | Q37139604 | ||
| Striatal [11C]dihydrotetrabenazine and [11C]methylphenidate binding in Tourette syndrome | Q37180505 | ||
| Motor sequence learning and movement disorders | Q37209418 | ||
| Loss of MeCP2 function is associated with distinct gene expression changes in the striatum | Q37215581 | ||
| Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus | Q37223275 | ||
| Thalamic inputs to striatal interneurons in monkeys: synaptic organization and co-localization of calcium binding proteins | Q31318059 | ||
| Neurons in the thalamic CM-Pf complex supply striatal neurons with information about behaviorally significant sensory events | Q31841603 | ||
| Behavior-related alterations of striatal neurochemistry in a mouse model of stereotyped movement disorder | Q33199027 | ||
| Task-specific hand dystonia: can too much plasticity be bad for you? | Q33235618 | ||
| Multiple rare SAPAP3 missense variants in trichotillomania and OCD. | Q33578270 | ||
| Repetitive behaviours in patients with Gilles de la Tourette syndrome: tics, compulsions, or both? | Q33707542 | ||
| Distinct roles of GABAergic interneurons in the regulation of striatal output pathways | Q33720464 | ||
| Cell-autonomous alteration of dopaminergic transmission by wild type and mutant (DeltaE) TorsinA in transgenic mice. | Q33723034 | ||
| Indirect basal ganglia pathway mediation of repetitive behavior: attenuation by adenosine receptor agonists | Q33749330 | ||
| Convergent evidence for abnormal striatal synaptic plasticity in dystonia | Q33756951 | ||
| Decreased number of parvalbumin and cholinergic interneurons in the striatum of individuals with Tourette syndrome | Q33758561 | ||
| Dissociable effects of dopamine on learning and performance within sensorimotor striatum | Q33760125 | ||
| The role of MeCP2 in brain development and neurodevelopmental disorders | Q33762214 | ||
| Changes in brain anatomy in focal hand dystonia | Q60042446 | ||
| Somatosensory temporal discrimination in patients with primary focal dystonia | Q60730404 | ||
| Generation of a novel rodent model for DYT1 dystonia | Q61163034 | ||
| Striatal dopamine release is triggered by synchronized activity in cholinergic interneurons | Q48441601 | ||
| Pathophysiology of blepharospasm and oromandibular dystonia | Q48456063 | ||
| Cerebellar and cerebral abnormalities in Rett syndrome: a quantitative MR analysis | Q48459708 | ||
| MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother | Q48470303 | ||
| The anatomical basis of symptomatic hemidystonia | Q48482387 | ||
| Tourettism and dystonia after subcortical stroke | Q48494015 | ||
| Interneurons in the rat striatum: relationships between parvalbumin neurons and cholinergic neurons | Q48509611 | ||
| Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey | Q48518059 | ||
| Depletion of unilateral striatal dopamine impairs initiation of contralateral actions and not sensory attention | Q48520680 | ||
| Impaired reaching and grasping after focal inactivation of globus pallidus pars interna in the monkey | Q48569535 | ||
| Cortex, striatum and cerebellum: control of serial order in a grooming sequence | Q48587672 | ||
| Dopamine transporter changes in neuropsychiatric disorders | Q48609533 | ||
| A neural correlate of oculomotor sequences in supplementary eye field | Q48624028 | ||
| Characterization of the rat mutant dystonic (dt): a new animal model of dystonia musculorum deformans. | Q48638937 | ||
| Reinforcement-based decision making in corticostriatal circuits: mutual constraints by neurocomputational and diffusion models | Q48681581 | ||
| Caytaxin deficiency causes generalized dystonia in rats | Q48718509 | ||
| Quantitative recording of rotational behavior in rats after 6-hydroxy-dopamine lesions of the nigrostriatal dopamine system. | Q48876521 | ||
| Tourette syndrome: prediction of phenotypic variation in monozygotic twins by caudate nucleus D2 receptor binding | Q48939331 | ||
| The cortico-striate projection in the monkey | Q48952447 | ||
| Obsessive-compulsive disorder associated with brain lesions: clinical phenomenology, cognitive function, and anatomic correlates | Q48958313 | ||
| Reappraisal of spontaneous stereotypy in the deer mouse as an animal model of obsessive-compulsive disorder (OCD): response to escitalopram treatment and basal serotonin transporter (SERT) density | Q49061911 | ||
| Quantitative magnetic resonance imaging in Rett syndrome | Q50306365 | ||
| Impact of age of onset of illness on clinical phenotype in OCD. | Q50761666 | ||
| The role of cognitive and affective processing in a transgenic mouse model of cortical-limbic neuropotentiated compulsive behavior. | Q51083447 | ||
| CLINICAL AND PATHOLOGICAL STUDIES OF AN HEREDITARY NEUROPATHY IN MICE (DYSTONIA MUSCULORUM) | Q51273841 | ||
| Classic Rett syndrome in a boy with R133C mutation of MECP2. | Q51843571 | ||
| Effect of subthalamic nucleus stimulation on obsessive-compulsive disorder in a patient with Parkinson disease. Case report. | Q51999947 | ||
| Building neural representations of habits. | Q52030807 | ||
| Alterations in dopaminergic function in Rett syndrome. | Q52053727 | ||
| Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. | Q52087714 | ||
| Cognitive processes in idiopathic dystonia treated with high-dose anticholinergic therapy: implications for treatment strategies. | Q52100624 | ||
| Striatal recruitment during an implicit sequence learning task as measured by functional magnetic resonance imaging. | Q52196923 | ||
| The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse. | Q52202965 | ||
| Electrochemical monitoring of extracellular dopamine in nucleus accumbens of rats lever-pressing for food. | Q52215423 | ||
| Elementary processes of response selection mediated by distinct regions of the striatum. | Q52244477 | ||
| Natural syntax rules control action sequence of rats. | Q52258037 | ||
| Decortication abolishes place but not cue learning in rats. | Q52276174 | ||
| Striatal dopamine in early-onset primary torsion dystonia with the DYT1 mutation. | Q52278152 | ||
| Super-stereotypy II: enhancement of a complex movement sequence by intraventricular dopamine D1 agonists. | Q52890857 | ||
| The organization of the projection from the cerebral cortex to the striatum in the rat. | Q53799354 | ||
| Quantitative morphological analysis of striatal cholinergic neurons in perinatal asphyxia. | Q54333921 | ||
| Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families. | Q55055207 | ||
| Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamo-cortical loop | Q56093340 | ||
| Neuropathology of Rett syndrome | Q56909448 | ||
| Translating birdsong: songbirds as a model for basic and applied medical research | Q28654604 | ||
| Emerging concepts in the physiological basis of dystonia | Q28655888 | ||
| Basal ganglia output to the thalamus: still a paradox | Q28661247 | ||
| A cortical motor nucleus drives the basal ganglia-recipient thalamus in singing birds | Q28730710 | ||
| A basal ganglia-forebrain circuit in the songbird biases motor output to avoid vocal errors | Q28752278 | ||
| Characterization of SLITRK1 variation in obsessive-compulsive disorder | Q28854579 | ||
| Parallel Organization of Functionally Segregated Circuits Linking Basal Ganglia and Cortex | Q29391304 | ||
| Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription | Q29547568 | ||
| Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes | Q29616326 | ||
| Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice | Q29616328 | ||
| Reversal of neurological defects in a mouse model of Rett syndrome | Q29616452 | ||
| Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3 | Q29616516 | ||
| The functional anatomy of basal ganglia disorders | Q29617461 | ||
| Phasic firing in dopaminergic neurons is sufficient for behavioral conditioning | Q29618165 | ||
| Primate models of movement disorders of basal ganglia origin | Q29618489 | ||
| What is the role of dopamine in reward: hedonic impact, reward learning, or incentive salience? | Q29618655 | ||
| The debate over dopamine's role in reward: the case for incentive salience | Q29618738 | ||
| The role of the basal ganglia in habit formation | Q29619829 | ||
| Histidine decarboxylase deficiency causes tourette syndrome: parallel findings in humans and mice | Q30421144 | ||
| A behavioral genetics approach to understanding D1 receptor involvement in phasic dopamine signaling | Q30474975 | ||
| Distinct basal ganglia territories are engaged in early and advanced motor sequence learning | Q30476097 | ||
| Dichotomous dopaminergic control of striatal synaptic plasticity | Q30493521 | ||
| Dopamine receptor modulation of repetitive grooming actions in the rat: potential relevance for Tourette syndrome | Q30494205 | ||
| Selective activation of striatal fast-spiking interneurons during choice execution | Q30496027 | ||
| Hyperactivity and impaired response habituation in hyperdopaminergic mice | Q30496538 | ||
| Start/stop signals emerge in nigrostriatal circuits during sequence learning | Q30525757 | ||
| Reversible online control of habitual behavior by optogenetic perturbation of medial prefrontal cortex | Q30528540 | ||
| Focal task-specific dystonia in musicians | Q30540609 | ||
| Impaired striatal D2 receptor function leads to enhanced GABA transmission in a mouse model of DYT1 dystonia. | Q30547556 | ||
| Optogenetic stimulation of lateral orbitofronto-striatal pathway suppresses compulsive behaviors | Q30561087 | ||
| A dual operator view of habitual behavior reflecting cortical and striatal dynamics | Q30573983 | ||
| Repeated cortico-striatal stimulation generates persistent OCD-like behavior | Q30574071 | ||
| Concurrent activation of striatal direct and indirect pathways during action initiation. | Q30579307 | ||
| Thalamic gating of corticostriatal signaling by cholinergic interneurons. | Q30583147 | ||
| Rett syndrome: review of biological abnormalities. | Q30639662 | ||
| Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome). | Q30738155 | ||
| Cholinergic dysregulation produced by selective inactivation of the dystonia-associated protein torsinA. | Q31061478 | ||
| Striatal opioid peptide content in an animal model of spontaneous stereotypic behavior | Q44347720 | ||
| Selective blockade of spontaneous motor stereotypy via intrastriatal pharmacological manipulation | Q44384952 | ||
| Impaired sequence learning in carriers of the DYT1 dystonia mutation | Q44499886 | ||
| Increased ventral striatal monoaminergic innervation in Tourette syndrome | Q44545765 | ||
| Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse. | Q44615423 | ||
| Inactivation of the infralimbic prefrontal cortex reinstates goal-directed responding in overtrained rats | Q44672527 | ||
| Reward without dopamine. | Q44674159 | ||
| Striatal dopaminergic system in dopa-responsive dystonia: a multi-tracer PET study shows increased D2 receptors | Q44721392 | ||
| Effects of intrastriatal administration of selective dopaminergic ligands on spontaneous stereotypy in mice | Q44740585 | ||
| Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome. | Q40151344 | ||
| The organization of the basal ganglia-thalamocortical circuits: open interconnected rather than closed segregated | Q40613269 | ||
| Striatal interneurones: chemical, physiological and morphological characterization | Q40991491 | ||
| Basal ganglia motor control. II. Late pallidal timing relative to movement onset and inconsistent pallidal coding of movement parameters | Q41182209 | ||
| Cortico-striate projections in the rhesus monkey: The organization of certain cortico-caudate connections | Q41353089 | ||
| Cholinergic dysfunction alters synaptic integration between thalamostriatal and corticostriatal inputs in DYT1 dystonia | Q41785434 | ||
| Distinct roles for direct and indirect pathway striatal neurons in reinforcement. | Q41894840 | ||
| Dopamine D2 receptor dysfunction is rescued by adenosine A2A receptor antagonism in a model of DYT1 dystonia. | Q41899842 | ||
| Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa | Q41927308 | ||
| Neuroanatomy of Rett syndrome: a volumetric imaging study | Q41929671 | ||
| Adult neural function requires MeCP2. | Q42083934 | ||
| Dichotomous organization of the external globus pallidus. | Q42108476 | ||
| Modeling the short- and long-duration responses to exogenous levodopa and to endogenous levodopa production in Parkinson's disease | Q42167789 | ||
| Rett syndrome: biogenic amines and metabolites in postmortem brain | Q42192835 | ||
| An Australian study of telegraphists' cramp | Q42209675 | ||
| Anhedonia requires MC4R-mediated synaptic adaptations in nucleus accumbens. | Q42237758 | ||
| Chlorpromazine methiodide acts at the vestibular nuclear complex to induce barrel rotation in the rat. | Q42254466 | ||
| Behavioral and movement disorders induced by local inhibitory dysfunction in primate striatum | Q42446221 | ||
| Gap junctions between striatal fast-spiking interneurons regulate spiking activity and synchronization as a function of cortical activity | Q42452596 | ||
| Selective innervation of neostriatal interneurons by a subclass of neuron in the globus pallidus of the rat. | Q42463448 | ||
| Activity in the caudate nucleus of monkey during spatial sequencing | Q42475140 | ||
| Fast-spiking interneurons of the rat ventral striatum: temporal coordination of activity with principal cells and responsiveness to reward. | Q42475660 | ||
| Activity of striatal neurons reflects dynamic encoding and recoding of procedural memories | Q42485542 | ||
| Cortico-basal ganglia circuit mechanism for a decision threshold in reaction time tasks | Q42496683 | ||
| Responses of tonically active neurons in the primate's striatum undergo systematic changes during behavioral sensorimotor conditioning. | Q42501704 | ||
| Dopamine release is impaired in a mouse model of DYT1 dystonia | Q42513622 | ||
| Pathological report of four patients presenting with cranial dystonias | Q42514366 | ||
| Meige syndrome: neuropathology of a case | Q42515020 | ||
| Implementation of action sequences by a neostriatal site: a lesion mapping study of grooming syntax. | Q42517454 | ||
| Pathology in brainstem regions of individuals with primary dystonia | Q42518439 | ||
| The MeCP2-null mouse hippocampus displays altered basal inhibitory rhythms and is prone to hyperexcitability. | Q42522168 | ||
| Choline acetyltransferase activity and vesamicol binding in Rett syndrome and in rats with nucleus basalis lesions | Q42522455 | ||
| Changes in the control of arm position, movement, and thalamic discharge during local inactivation in the globus pallidus of the monkey | Q42525326 | ||
| Synaptic convergence of motor and somatosensory cortical afferents onto GABAergic interneurons in the rat striatum. | Q42525827 | ||
| Rett syndrome: investigation of nine patients, including PET scan | Q42528390 | ||
| Impairment of bidirectional synaptic plasticity in the striatum of a mouse model of DYT1 dystonia: role of endogenous acetylcholine. | Q42590497 | ||
| Function of dopamine transporter is compromised in DYT1 transgenic animal model in vivo | Q42593925 | ||
| Analysis of open-label trials in torsion dystonia using high dosages of anticholinergics and other drugs | Q42652856 | ||
| Impaired motor learning in mice expressing torsinA with the DYT1 dystonia mutation. | Q42658331 | ||
| Generation and characterization of Dyt1 DeltaGAG knock-in mouse as a model for early-onset dystonia | Q42671584 | ||
| Three-year outcomes in deep brain stimulation for highly resistant obsessive-compulsive disorder | Q42692078 | ||
| Development of repetitive behavior in a mouse model: roles of indirect and striosomal basal ganglia pathways | Q42744117 | ||
| Influence of phasic and tonic dopamine release on receptor activation. | Q42852523 | ||
| Dynamics of action potential firing in electrically connected striatal fast-spiking interneurons. | Q42907695 | ||
| Circuit-selective striatal synaptic dysfunction in the Sapap3 knockout mouse model of obsessive-compulsive disorder | Q43121614 | ||
| What can man do without basal ganglia motor output? The effect of combined unilateral subthalamotomy and pallidotomy in a patient with Parkinson's disease. | Q43278477 | ||
| Positron emission tomographic study of D2 dopamine receptor binding and CSF biogenic amine metabolites in Rett syndrome | Q43407231 | ||
| GABA promotes survival but not proliferation of parvalbumin-immunoreactive interneurons in rodent neostriatum: an in vivo study with stereology | Q43581068 | ||
| Parvalbumin-immunoreactive neurons in the rat neostriatum: a light and electron microscopic study | Q43752203 | ||
| Dissociation between spontaneously emitted and apomorphine-induced stereotypy in Peromyscus maniculatus bairdii | Q43919639 | ||
| Elevated intrasynaptic dopamine release in Tourette's syndrome measured by PET. | Q44086829 | ||
| The production of 53-55-kDa isoforms is not required for rat L-histidine decarboxylase activity | Q44203891 | ||
| Mild overexpression of Mecp2 in mice causes a higher susceptibility toward seizures | Q44244429 | ||
| Abnormal cytoplasmic calcium dynamics in central neurons of a dystonia mouse model. | Q44250762 | ||
| P921 | main subject | neurodevelopmental disorder | Q3450985 |
| P304 | page(s) | 97-169 | |
| P577 | publication date | 2014-01-01 | |
| P1433 | published in | Current Topics in Developmental Biology | Q15745419 |
| P1476 | title | Mouse models of neurodevelopmental disease of the basal ganglia and associated circuits | |
| P478 | volume | 109 |
| Q42247782 | A Rapid Pipeline to Model Rare Neurodevelopmental Disorders with Simultaneous CRISPR/Cas9 Gene Editing |
| Q56529555 | A cell autonomous torsinA requirement for cholinergic neuron survival and motor control |
| Q30670034 | A novel conditional knock-in approach defines molecular and circuit effects of the DYT1 dystonia mutation |
| Q38630519 | A review of animal models of obsessive-compulsive disorder: a focus on developmental, immune, endocrine and behavioral models |
| Q45305006 | A survey-based study identifies common but unrecognized symptoms in a large series of juvenile Huntington's disease |
| Q55631009 | Centella asiatica increases hippocampal synaptic density and improves memory and executive function in aged mice. |
| Q52341984 | Comprehensive Characterization of the Pyroglutamate Amyloid-β Induced Motor Neurodegenerative Phenotype of TBA2.1 Mice. |
| Q50420863 | Early structural and functional plasticity alterations in a susceptibility period of DYT1 dystonia mouse striatum. |
| Q35759092 | Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons |
| Q35340179 | Inherited isolated dystonia: clinical genetics and gene function. |
| Q92748839 | Marble-burying behavior test as a murine model of compulsive-like behavior |
| Q50045831 | Serum levels of 25-hydroxyvitamin D in children with tic disorders |
| Q98513674 | Systems biology reveals reprogramming of the S-nitroso-proteome in the cortical and striatal regions of mice during aging process |
| Q50432878 | The DYT6 Dystonia Protein THAP1 Regulates Myelination within the Oligodendrocyte Lineage. |
| Q99723276 | The abnormal firing of Purkinje cells in the knockin mouse model of DYT1 dystonia |
| Q35865117 | The presence of cortical neurons in striatal-cortical co-cultures alters the effects of dopamine and BDNF on medium spiny neuron dendritic development |
| Q47351833 | TorsinA dysfunction causes persistent neuronal nuclear pore defects. |
| Q38618988 | Tourette Syndrome research highlights 2014 |
| Q92217378 | Understanding Parkinson's disease and deep brain stimulation: Role of monkey models |
Search more.