The external globus pallidus: progress and perspectives
暂无分享,去创建一个
Vivian M. Hernández | C. S. Chan | C Savio Chan | Daniel J Hegeman | Ellie S Hong | Vivian M Hernández | Daniel J. Hegeman | Ellie S. Hong
[1] M. Kelland,et al. In vivo characterization of two cell types in the rat globus pallidus which have opposite responses to dopamine receptor stimulation: Comparison of electrophysiological properties and responses to apomorphine, dizocilpine, and ketamine anesthesia , 1995, Synapse.
[2] C. Kellendonk,et al. Balancing the basal ganglia circuitry: A possible new role for dopamine D2 receptors in health and disease , 2015, Movement disorders : official journal of the Movement Disorder Society.
[3] P. Molinoff,et al. Ontogeny of dopamine D1 and D2 receptor subtypes in rat basal ganglia: a quantitative autoradiographic study. , 1991, Brain research. Developmental brain research.
[4] Martin Lévesque,et al. Extrastriatal dopaminergic innervation of human basal ganglia , 1999, Neuroscience Research.
[5] Clifford B. Saper,et al. Projections of the pedunculopontine tegmental nucleus in the rat: evidence for additional extrapyramidal circuitry , 1982, Brain Research.
[6] Kaye. Zolpidem improves akinesia , dystonia and dyskinesia in advanced Parkinson ’ s disease , 2008 .
[7] F. Windels,et al. Effects of high frequency stimulation of subthalamic nucleus on extracellular glutamate and GABA in substantia nigra and globus pallidus in the normal rat , 2000, The European journal of neuroscience.
[8] M. Deschenes,et al. A Single‐cell Study of the Axonal Projections Arising from the Posterior Intralaminar Thalamic Nuclei in the Rat , 1996, The European journal of neuroscience.
[9] S. A. Wilson. PROGRESSIVE LENTICULAR DEGENERATION : A FAMILIAL NERVOUS DISEASE ASSOCIATED WITH CIRRHOSIS OF THE LIVER. , 1912 .
[10] G. E. Alexander,et al. Functional architecture of basal ganglia circuits: neural substrates of parallel processing , 1990, Trends in Neurosciences.
[11] H. Bergman,et al. Goal-directed and habitual control in the basal ganglia: implications for Parkinson's disease , 2010, Nature Reviews Neuroscience.
[12] A. Dolphin,et al. Inhibition of calcium currents in cultured rat dorsal root ganglion neurones by (−)‐baclofen , 1986, British journal of pharmacology.
[13] L. Heimer,et al. Efferent connections of the caudal part of the globus pallidus in the rat , 1996, The Journal of comparative neurology.
[14] D James Surmeier,et al. Autonomous pacemakers in the basal ganglia: who needs excitatory synapses anyway? , 2005, Current Opinion in Neurobiology.
[15] Xin Jin,et al. Basal Ganglia Subcircuits Distinctively Encode the Parsing and Concatenation of Action Sequences , 2014, Nature Neuroscience.
[16] A. Parent,et al. Evidence for a distinct nigropallidal dopaminergic projection in the squirrel monkey , 1989, Brain Research.
[17] Pavel Osten,et al. HCN Channelopathy in External Globus Pallidus Neurons in Models of Parkinson’s Disease , 2010, Nature Neuroscience.
[18] Y. Smith,et al. The thalamostriatal system: a highly specific network of the basal ganglia circuitry , 2004, Trends in Neurosciences.
[19] J. Tepper,et al. Gabaergic control of rat substantia nigra dopaminergic neurons: role of globus pallidus and substantia nigra pars reticulata , 1999, Neuroscience.
[20] Yan Ao,et al. Astrocyte Kir4.1 ion channel deficits contribute to neuronal dysfunction in Huntington's disease model mice , 2014, Nature Neuroscience.
[21] M. Kimura,et al. Physiological properties of projection neurons in the monkey striatum to the globus pallidus , 2004, Experimental Brain Research.
[22] F. Luo,et al. Neural responses in multiple basal ganglia regions during spontaneous and treadmill locomotion tasks in rats , 2004, Experimental Brain Research.
[23] Elena Cattaneo,et al. Molecular mechanisms and potential therapeutical targets in Huntington's disease. , 2010, Physiological reviews.
[24] Matthew E. Larkum,et al. The GABAB1b Isoform Mediates Long-Lasting Inhibition of Dendritic Ca2+ Spikes in Layer 5 Somatosensory Pyramidal Neurons , 2006, Neuron.
[25] L. Defebvre,et al. External Globus Pallidus Stimulation Modulates Brain Connectivity in Huntington's Disease , 2011, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[26] R. Nicoll,et al. Direct hyperpolarizing action of baclofen on hippocampal pyramidal cells , 1984, Nature.
[27] M. Delong,et al. Putamen: Activity of Single Units during Slow and Rapid Arm Movements , 1973, Science.
[28] Charles J. Wilson,et al. The origins of two-state spontaneous membrane potential fluctuations of neostriatal spiny neurons , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[29] S. Haber,et al. Evidence for interconnections between the two segments of the globus pallidus in primates: a PHA-L anterograde tracing study , 1990, Brain Research.
[30] Shlomo Elias,et al. Statistical Properties of Pauses of the High-Frequency Discharge Neurons in the External Segment of the Globus Pallidus , 2007, The Journal of Neuroscience.
[31] Daniel K. Leventhal,et al. Canceling actions involves a race between basal ganglia pathways , 2013, Nature Neuroscience.
[32] M. Savasta,et al. Autoradiographic distribution of the D1 agonist [3H]SKF 38393, in the rat brain and spinal cord. Comparison with the distribution of D2 dopamine receptors , 1986, Neuroscience.
[33] N. Belluardo,et al. Expression of Cx36 in mammalian neurons , 2000, Brain Research Reviews.
[34] F. Bloom,et al. Distribution of neurons expressing immunoreactivity for the 5HT3 receptor subtype in the rat brain and spinal cord , 1998, The Journal of comparative neurology.
[35] S. A. Wilson. AN EXPERIMENTAL RESEARCH INTO THE ANATOMY AND PHYSIOLOGY OF THE CORPUS STRIATUM , 1914 .
[36] K. Willecke,et al. Differential expression of three gap junction proteins in developing and mature brain tissues. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[37] H. Kita,et al. Parvalbumin-immunopositive neurons in rat globus pallidus: a light and electron microscopic study , 1994, Brain Research.
[38] A. Parent,et al. Functional anatomy of the basal ganglia. II. The place of subthalamic nucleus and external pallidium in basal ganglia circuitry , 1995, Brain Research Reviews.
[39] Hitoshi Kita,et al. Subthalamo‐pallidal interactions underlying parkinsonian neuronal oscillations in the primate basal ganglia , 2011, The European journal of neuroscience.
[40] A. Parent,et al. Differential connections of caudate nucleus and putamen in the squirrel monkey (Saimiri sciureus) , 1986, Neuroscience.
[41] Charles J. Wilson,et al. Active decorrelation in the basal ganglia , 2013, Neuroscience.
[42] Paul J. Harrison,et al. Messenger RNA encoding the D2 dopaminergic receptor detected by in situ hybridization histochemistry in rat brain , 1989, FEBS letters.
[43] R. Shigemoto,et al. Immunohistochemical localization of metabotropic glutamate receptors, mGluR7a and mGluR7b, in the central nervous system of the adult rat and mouse: A light and electron microscopic study , 1998, The Journal of comparative neurology.
[44] Robert W. Williams,et al. Complex trait analysis of the mouse striatum: independent QTLs modulate volume and neuron number , 2001, BMC Neuroscience.
[45] A. Parent,et al. Efferent projections of the subthalamic nucleus in the squirrel monkey as studied by the PHA‐L anterograde tracing method , 1990, The Journal of comparative neurology.
[46] Philip A. Starr,et al. Pallidal neuronal discharge in Huntington's disease: Support for selective loss of striatal cells originating the indirect pathway , 2008, Experimental Neurology.
[47] J. Schipper,et al. Species differences in the distribution of central 5-HT1 binding sites: a comparative autoradiographic study between rat and guinea pig , 1991, Brain Research.
[48] Á. Pazos,et al. Autoradiographic distribution of 5‐HT7 receptors in the human brain using [3H]mesulergine: comparison to other mammalian species , 2004, British journal of pharmacology.
[49] H. Bergman,et al. Neurons in both pallidal segments change their firing properties similarly prior to closure of the eyes. , 2010, Journal of neurophysiology.
[50] R. Seite,et al. Study of the rat neostriatum using a combined Golgi-electron microscope technique and serial sections , 1980, Neuroscience.
[51] J. Golowasch,et al. Adult mouse basal forebrain harbors two distinct cholinergic populations defined by their electrophysiology , 2012, Front. Behav. Neurosci..
[52] Bruno Giros,et al. Localization of dopamine D3 receptor mRNA in the rat brain using in situ hybridization histochemistry: comparison with dopamine D2 receptor mRNA , 1991, Brain Research.
[53] J. Schneider,et al. Alterations in pallidal neuronal responses to peripheral sensory and striatal stimulation in symptomatic and recovered Parkinsonian cats , 1995, Brain Research.
[54] S. Haber,et al. Immunocytochemical localization of the dopamine transporter in human brain , 1999, The Journal of comparative neurology.
[55] P. Somogyi,et al. Distribution and synaptic localisation of the metabotropic glutamate receptor 4 (mGluR4) in the rodent CNS , 2002, Neuroscience.
[56] I. Stanford,et al. Dopamine D2 receptor mediated presynaptic inhibition of striatopallidal GABA(A) IPSCs in vitro. , 2001, Neuropharmacology.
[57] J. Palacios,et al. Serotoninergic terminal transporters are differentially affected in Parkinson's disease and progressive supranuclear palsy: An autoradiographic study with [3H]citalopram , 1993, Neuroscience.
[58] Kenji F. Tanaka,et al. Functional Connectome of the Striatal Medium Spiny Neuron , 2011, The Journal of Neuroscience.
[59] G. Arbuthnott,et al. Electrophysiological and anatomical observations concerning the pallidostriatal pathway in the rat , 2004, Experimental Brain Research.
[60] I. Stanford,et al. Electrophysiological and morphological characteristics of three subtypes of rat globus pallidus neurone in vitro , 2000, The Journal of physiology.
[61] S. Johnson,et al. Presynaptic dopamine D2 and muscarine M3 receptors inhibit excitatory and inhibitory transmission to rat subthalamic neurones in vitro , 2000, The Journal of physiology.
[62] J. Neumaier,et al. Localization of 5-HT7 receptors in rat brain by immunocytochemistry, in situ hybridization, and agonist stimulated cFos expression , 2001, Journal of Chemical Neuroanatomy.
[63] J. Sergeant,et al. Differential distribution, affinity and plasticity of dopamine D-1 and D-2 receptors in the target sites of the mesolimbic system in an animal model of ADHD , 1998, Behavioural Brain Research.
[64] M. Delong,et al. Basal Ganglia Circuits as Targets for Neuromodulation in Parkinson Disease. , 2015, JAMA neurology.
[65] M. Merello,et al. [Functional anatomy of the basal ganglia]. , 2000, Revista de neurologia.
[66] L. Tremblay,et al. Abnormal spontaneous activity of globus pallidus neurons in monkeys with MPTP-induced parkinsonism , 1991, Brain Research.
[67] J. Bolam,et al. Selective Innervation of Neostriatal Interneurons by a Subclass of Neuron in the Globus Pallidus of the Rat , 1998, The Journal of Neuroscience.
[68] A. Priori,et al. Cerebellar and Motor Cortical Transcranial Stimulation Decrease Levodopa-Induced Dyskinesias in Parkinson’s Disease , 2015, The Cerebellum.
[69] G. Dawson,et al. Evidence for a Significant Role of α3-Containing GABAA Receptors in Mediating the Anxiolytic Effects of Benzodiazepines , 2005, The Journal of Neuroscience.
[70] C. Petersen,et al. Cell-Type-Specific Sensorimotor Processing in Striatal Projection Neurons during Goal-Directed Behavior , 2015, Neuron.
[71] R. Marotta,et al. Motor Cortex Stimulation in Parkinson's Disease , 2012, Neurology research international.
[72] C. Marsden,et al. Regional distribution of monoamines in the corpus striatum of the rat. , 1972, Brain research.
[73] J. Rafols,et al. The primate globus pallidus: a Golgi and electron microscopic study. , 1974, Journal fur Hirnforschung.
[74] Joshua L. Plotkin,et al. Corticostriatal synaptic adaptations in Huntington’s disease , 2015, Current Opinion in Neurobiology.
[75] G. Silberberg,et al. A Whole-Brain Atlas of Inputs to Serotonergic Neurons of the Dorsal and Median Raphe Nuclei , 2014, Neuron.
[76] H. Kita,et al. Intracellular study of rat globus pallidus neurons: membrane properties and responses to neostriatal, subthalamic and nigral stimulation , 1991, Brain Research.
[77] W. Yung,et al. 5-HT excites globus pallidus neurons by multiple receptor mechanisms , 2008, Neuroscience.
[78] Cortically evoked responses of human pallidal neurons recorded during stereotactic neurosurgery , 2011 .
[79] E. Vaadia,et al. Physiological aspects of information processing in the basal ganglia of normal and parkinsonian primates , 1998, Trends in Neurosciences.
[80] J. Tepper,et al. Heterogeneity and Diversity of Striatal GABAergic Interneurons , 2010, Front. Neuroanat..
[81] Christian Lüscher,et al. G Protein-Coupled Inwardly Rectifying K+ Channels (GIRKs) Mediate Postsynaptic but Not Presynaptic Transmitter Actions in Hippocampal Neurons , 1997, Neuron.
[82] G. Perea,et al. Tripartite synapses: astrocytes process and control synaptic information , 2009, Trends in Neurosciences.
[83] D. Sibley,et al. Cellular distribution of the rat D4 dopamine receptor protein in the CNS using anti-receptor antisera , 1997, Brain Research.
[84] B. Bean,et al. GABAB Receptor Inhibition of P-type Ca2+ Channels in Central Neurons , 1993, Neuron.
[85] Allan R. Jones,et al. A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing , 2012, Nature Neuroscience.
[86] A. Nambu,et al. Cortically Evoked Long-Lasting Inhibition of Pallidal Neurons in a Transgenic Mouse Model of Dystonia , 2008, The Journal of Neuroscience.
[87] D. Grigoriadis,et al. [3H]quinpirole binding to putative D2 and D3 dopamine receptors in rat brain and pituitary gland: a quantitative autoradiographic study. , 1993, The Journal of pharmacology and experimental therapeutics.
[88] L. Tremblay,et al. Behavioural disorders induced by external globus pallidus dysfunction in primates II. Anatomical study. , 2004, Brain : a journal of neurology.
[89] T. Morera-Herreras,et al. Interaction between the 5-HT system and the basal ganglia: functional implication and therapeutic perspective in Parkinson's disease , 2014, Front. Neural Circuits.
[90] H. Akil,et al. A comparison of D1 receptor binding and mRNA in rat brain using receptor autoradiographic and in situ hybridization techniques , 1991, Neuroscience.
[91] Martin Lévesque,et al. The axonal arborization of single nigrostriatal neurons in rats , 1999, Brain Research.
[92] S. Dymecki,et al. Projections and interconnections of genetically defined serotonin neurons in mice , 2012, The European journal of neuroscience.
[93] H. Kita,et al. Monkey globus pallidus external segment neurons projecting to the neostriatum. , 1999, Neuroreport.
[94] W. Vogel,et al. Activities of enzymes involved in the formation and destruction of biogenic amines in various areas of human brain. , 1969, The Journal of pharmacology and experimental therapeutics.
[95] Erwan Bezard,et al. Phenotype of Striatofugal Medium Spiny Neurons in Parkinsonian and Dyskinetic Nonhuman Primates: A Call for a Reappraisal of the Functional Organization of the Basal Ganglia , 2006, The Journal of Neuroscience.
[96] D. Plenz,et al. A basal ganglia pacemaker formed by the subthalamic nucleus and external globus pallidus , 1999, Nature.
[97] G. Percheron,et al. A Golgi analysis of the primate globus pallidus. II. Quantitative morphology and spatial orientation of dendritic arborizations , 1984, The Journal of comparative neurology.
[98] M. Gelabert-González,et al. [Deep brain stimulation in Parkinson's disease]. , 2013, Revista de neurologia.
[99] B. Pakkenberg,et al. Changes in total cell numbers of the basal ganglia in patients with multiple system atrophy — A stereological study , 2015, Neurobiology of Disease.
[100] P. Blanchet,et al. Opposite rotation induced by dopamine agonists in rats with unilateral lesions of the globus pallidus or substantia nigra Research report , 1998, Behavioural Brain Research.
[101] A. Oliviero,et al. Dopamine Dependency of Oscillations between Subthalamic Nucleus and Pallidum in Parkinson's Disease , 2001, The Journal of Neuroscience.
[102] Philip J. Hahn,et al. Network perspectives on the mechanisms of deep brain stimulation , 2010, Neurobiology of Disease.
[103] M. Parent,et al. Morphological evidence for dopamine interactions with pallidal neurons in primates , 2015, Front. Neuroanat..
[104] Thomas Wichmann,et al. Neuronal firing before and after burst discharges in the monkey basal ganglia is predictably patterned in the normal state and altered in parkinsonism. , 2006, Journal of neurophysiology.
[105] U. Rudolph,et al. GABA-based therapeutic approaches: GABAA receptor subtype functions. , 2006, Current opinion in pharmacology.
[106] R. Vertes. A PHA‐L analysis of ascending projections of the dorsal raphe nucleus in the rat , 1991, The Journal of comparative neurology.
[107] J. H. Carlson,et al. Stimulation of both D1 and D2 dopamine receptors appears necessary for full expression of postsynaptic effects of dopamine agonists: a neurophysiological study , 1987, Brain Research.
[108] E. Rosengren,et al. Detection of 5-S-cysteinyldopamine in human brain , 2005, Journal of Neural Transmission.
[109] Charles J. Wilson,et al. Move to the rhythm: oscillations in the subthalamic nucleus–external globus pallidus network , 2002, Trends in Neurosciences.
[110] Charles J. Wilson,et al. Activity Patterns in a Model for the Subthalamopallidal Network of the Basal Ganglia , 2002, The Journal of Neuroscience.
[111] T. Sharp,et al. Functional Mapping of Dorsal and Median Raphe 5‐Hydroxytryptamine Pathways in Forebrain of the Rat Using Microdialysis , 1997, Journal of neurochemistry.
[112] J. Fritschy,et al. GABAA‐receptor heterogeneity in the adult rat brain: Differential regional and cellular distribution of seven major subunits , 1995, The Journal of comparative neurology.
[113] Danny C. W. Chan,et al. Therapeutic Deep Brain Stimulation in Parkinsonian Rats Directly Influences Motor Cortex , 2012, Neuron.
[114] P. Groves. A theory of the functional organization of the neostriatum and the neostriatal control of voluntary movement , 1983, Brain Research Reviews.
[115] M. Anderson,et al. A horseradish peroxidase study of afferent connections of the globus pallidus in Macaca mulatta , 2004, Experimental Brain Research.
[116] A. Levey,et al. D 1 and D 2 dopamine receptor mRNA in rat brain ( striatum / substantia nigra / amygdala / septum / in situ hybridization ) , 2022 .
[117] P. Demoly,et al. [Transgenic mice]. , 1992, Annales de dermatologie et de venereologie.
[118] N. Severs,et al. CONNEXIN EXPRESSION IN HUNTINGTON'S DISEASED HUMAN BRAIN , 1998, Cell biology international.
[119] Suzanne N Haber,et al. Dopamine Replacement Therapy Does Not Restore the Full Spectrum of Normal Pallidal Activity in the 1-Methyl-4-Phenyl-1,2,3,6-Tetra-Hydropyridine Primate Model of Parkinsonism , 2006, The Journal of Neuroscience.
[120] Maxime Levesque,et al. Motor sequence learning in primate: Role of the D2 receptor in movement chunking during consolidation , 2009, Behavioural Brain Research.
[121] Shigetada Nakanishi,et al. Metabotropic glutamate receptors: Synaptic transmission, modulation, and plasticity , 1994, Neuron.
[122] O. Hornykiewicz. Dopamine (3-hydroxytyramine) and brain function. , 1966, Pharmacological reviews.
[123] Maxime J Parent,et al. Movement chunking during sequence learning is a dopamine-dependant process: a study conducted in Parkinson’s disease , 2010, Experimental Brain Research.
[124] Tzong-Shiue Yu,et al. Changes in the Gene Expression of GABAA Receptor α1 and α2 Subunits and Metabotropic Glutamate Receptor 5 in the Basal Ganglia of the Rats with Unilateral 6-Hydroxydopamine Lesion and Embryonic Mesencephalic Grafts , 2001, Experimental Neurology.
[125] G. Lur,et al. Glutamate Receptor Modulation Is Restricted to Synaptic Microdomains. , 2015, Cell reports.
[126] M. Sambrook,et al. Experimental hemichorea/hemiballismus in the monkey. Studies on the intracerebral site of action in a drug-induced dyskinesia. , 1984, Brain : a journal of neurology.
[127] J. Penney,et al. Expression of N‐Methyl‐D‐Aspartate receptor subunit mRNAs in the human brain: Striatum and globus pallidus , 1998, The Journal of comparative neurology.
[128] Coinciding Decreases in Discharge Rate Suggest That Spontaneous Pauses in Firing of External Pallidum Neurons Are Network Driven , 2015, The Journal of Neuroscience.
[129] R. Kaji,et al. [Diagnosis and treatment of dystonia]. , 2008, Rinsho shinkeigaku = Clinical neurology.
[130] M. D. Crutcher,et al. Relations between parameters of step-tracking movements and single cell discharge in the globus pallidus and subthalamic nucleus of the behaving monkey , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[131] A. Parent,et al. Dopaminergic innervation of human basal ganglia , 2000, Journal of Chemical Neuroanatomy.
[132] R. Duvoisin,et al. The metabotropic glutamate receptors: Structure and functions , 1995, Neuropharmacology.
[133] Matthew D. Johnson,et al. Neural targets for relieving parkinsonian rigidity and bradykinesia with pallidal deep brain stimulation. , 2012, Journal of neurophysiology.
[134] A. Graybiel,et al. Output architecture of the primate putamen , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[135] D. Pinault,et al. Single striatofugal axons arborizing in both pallidal segments and in the substantia nigra in primates , 1995, Brain Research.
[136] J. Penney,et al. The globus pallidus receives a projection from the parafascicular nucleus in the rat , 1991, Brain Research.
[137] E. Richfield,et al. Anatomical and affinity state comparisons between dopamine D1 and D2 receptors in the rat central nervous system , 1989, Neuroscience.
[138] C. Tsai,et al. Zolpidem improves neuropsychiatric symptoms and motor dysfunction in a patient with Parkinson's disease after deep brain stimulation. , 2012, Acta neurologica Taiwanica.
[139] A. Parent,et al. The striatofugal fiber system in primates: a reevaluation of its organization based on single-axon tracing studies. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[140] J. Tepper,et al. GABAergic Afferents Activate Both GABAA and GABAB Receptors in Mouse Substantia Nigra Dopaminergic Neurons In Vivo , 2008, The Journal of Neuroscience.
[141] J. Paysan,et al. Heterogeneity of GABAA-receptors: cell-specific expression, pharmacology, and regulation , 1995, Neurochemical Research.
[142] A. Parent,et al. Dopaminergic innervation of the basal ganglia in the squirrel monkey as revealed by tyrosine hydroxylase immunohistochemistry , 1989, The Journal of comparative neurology.
[143] Y. Smith,et al. Neuronal circuitry and synaptic connectivity of the basal ganglia. , 1998, Neurosurgery clinics of North America.
[144] J. Tepper,et al. Striatal, pallidal, and pars reticulata evoked inhibition of nigrostriatal dopaminergic neurons is mediated by GABAA receptors in vivo , 1999, Neuroscience.
[145] D. A. Brown,et al. GABAB-receptor-activated K+ current in voltage-clamped CA3 pyramidal cells in hippocampal cultures. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[146] R. Shigemoto,et al. GABAB-receptor subtypes assemble into functional heteromeric complexes , 1998, Nature.
[147] A. Charara,et al. Synaptic and extrasynaptic GABA-A and GABA-B receptors in the globus pallidus: An electron microscopic immunogold analysis in monkeys , 2005, Neuroscience.
[148] D. Wright,et al. Comparative localization of serotonin1A, 1C, and 2 receptor subtype mRNAs in rat brain , 1995, The Journal of comparative neurology.
[149] Anatol C. Kreitzer,et al. Physiology and pharmacology of striatal neurons. , 2009, Annual review of neuroscience.
[150] A. Nambu. A new dynamic model of the cortico-basal ganglia loop. , 2004, Progress in brain research.
[151] A. Björklund,et al. Dopaminergic innervation of the globus pallidus by collaterals from the nigrostriatal pathway , 1979, Brain Research.
[152] W. Dauer,et al. Primary dystonia: molecules and mechanisms , 2009, Nature Reviews Neurology.
[153] M. Mesulam,et al. Cortical projections arising from the basal forebrain: A study of cholinergic and noncholinergic components employing combined retrograde tracing and immunohistochemical localization of choline acetyltransferase , 1984, Neuroscience.
[154] Alice Nieuwboer,et al. Transcranial direct current stimulation in Parkinson's disease: Neurophysiological mechanisms and behavioral effects , 2015, Neuroscience & Biobehavioral Reviews.
[155] A. Parent,et al. The organization of the striatal output system: a single-cell juxtacellular labeling study in the rat , 2000, Neuroscience Research.
[156] M. Scanziani,et al. How Inhibition Shapes Cortical Activity , 2011, Neuron.
[157] I. Bar-Gad,et al. Continuous Modulation of Action Potential Firing by a Unitary GABAergic Connection in the Globus Pallidus In Vitro , 2013, The Journal of Neuroscience.
[158] Matthew D. Johnson,et al. Mechanisms and targets of deep brain stimulation in movement disorders , 2008, Neurotherapeutics.
[159] Hitoshi Kita,et al. Role of Striatum in the Pause and Burst Generation in the Globus Pallidus of 6-OHDA-Treated Rats , 2011, Front. Syst. Neurosci..
[160] P. Lavallée,et al. Single-axon tracing study of neurons of the external segment of the globus pallidus in primate. , 2000, The Journal of comparative neurology.
[161] J. Palacios,et al. Localization of 5-HT4 receptor mRNA in rat brain by in situ hybridization histochemistry. , 1996, Brain research. Molecular brain research.
[162] C. Pfister,et al. [The cytoarchitecture of the rat globus pallidus]. , 1981, Journal fur Hirnforschung.
[163] A. Nieoullon,et al. Regional distribution and ontogeny of 5-HT4 binding sites in rodent brain , 1994, Neuropharmacology.
[164] Eric H Kim,et al. The Neuropathology of Huntington's Disease. , 2015, Current topics in behavioral neurosciences.
[165] M. Delong,et al. Deep-Brain Stimulation for Basal Ganglia Disorders. , 2011, Basal ganglia.
[166] M. Delong,et al. Activity of pallidal neurons during movement. , 1971, Journal of neurophysiology.
[167] Shlomo Elias,et al. Complex Locking Rather Than Complete Cessation of Neuronal Activity in the Globus Pallidus of a 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine-Treated Primate in Response to Pallidal Microstimulation , 2004, The Journal of Neuroscience.
[168] M. Ragozzino,et al. The Parafascicular Thalamic Nucleus Concomitantly Influences Behavioral Flexibility and Dorsomedial Striatal Acetylcholine Output in Rats , 2010, The Journal of Neuroscience.
[169] Y. Smith,et al. Distinct Functional Roles of the Metabotropic Glutamate Receptors 1 and 5 in the Rat Globus Pallidus , 2003, The Journal of Neuroscience.
[170] M. Desmurget,et al. Basal ganglia contributions to motor control: a vigorous tutor , 2010, Current Opinion in Neurobiology.
[171] Jérôme Baufreton,et al. Sparse but selective and potent synaptic transmission from the globus pallidus to the subthalamic nucleus. , 2009, Journal of neurophysiology.
[172] J. Lanciego,et al. Differential organization of cortical inputs to striatal projection neurons of the matrix compartment in rats , 2015, Front. Syst. Neurosci..
[173] H. Bergman,et al. The primate subthalamic nucleus. II. Neuronal activity in the MPTP model of parkinsonism. , 1994, Journal of neurophysiology.
[174] J. Penney,et al. The functional anatomy of basal ganglia disorders , 1989, Trends in Neurosciences.
[175] A. Graybiel. Habits, rituals, and the evaluative brain. , 2008, Annual review of neuroscience.
[176] Mark Farrant,et al. NMDA receptor subunits: diversity, development and disease , 2001, Current Opinion in Neurobiology.
[177] T. Kita,et al. Number, origins, and chemical types of rat pallidostriatal projection neurons , 2001, The Journal of comparative neurology.
[178] Y. Smith,et al. Microcircuitry of the direct and indirect pathways of the basal ganglia. , 1998, Neuroscience.
[179] R. Costa. A selectionist account of de novo action learning , 2011, Current Opinion in Neurobiology.
[180] P. Emson,et al. Comparative cellular distribution of GABAA and GABAB receptors in the human basal ganglia: Immunohistochemical colocalization of the α1 subunit of the GABAA receptor, and the GABABR1 and GABABR2 receptor subunits , 2004, The Journal of comparative neurology.
[181] H. Bergman,et al. Neurons in the globus pallidus do not show correlated activity in the normal monkey, but phase-locked oscillations appear in the MPTP model of parkinsonism. , 1995, Journal of neurophysiology.
[182] V. Bigl,et al. Regional and cellular expression sites of theα1 subunit of GABAA receptors in the rat basal forebrain: a cytochemical study with glutamic acid decarboxylase, choline acetyltransferase, calcium-binding proteins and nitric oxide synthase as second markers , 1995, Brain Research.
[183] M. Delong,et al. Deep Brain Stimulation for Neurologic and Neuropsychiatric Disorders , 2006, Neuron.
[184] Chantal François,et al. Behavioural disorders induced by external globus pallidus dysfunction in primates: I. Behavioural study. , 2004, Brain : a journal of neurology.
[185] A. Reiner,et al. Genetics and neuropathology of Huntington's disease. , 2011, International review of neurobiology.
[186] K. Neve,et al. Characterization and distribution of [125I]epidepride binding to dopamine D2 receptors in basal ganglia and cortex of human brain. , 1991, The Journal of pharmacology and experimental therapeutics.
[187] Y. Smith,et al. Topographical and Synaptic Organization of the GABA‐Containing Pallidosubthalamic Projection in the Rat , 1990, The European journal of neuroscience.
[188] T. Klockgether,et al. Functional characterization and expression of thalamic GABAB receptors in a rodent model of Parkinson’s disease , 1999, Neuropharmacology.
[189] F. Chollet,et al. Cortical motor reorganization in akinetic patients with Parkinson's disease: a functional MRI study. , 2000, Brain : a journal of neurology.
[190] R. Martínez-Murillo,et al. Distribution of catecholaminergic afferent fibres in the rat globus pallidus and their relations with cholinergic neurons , 1998, Journal of Chemical Neuroanatomy.
[191] J. Tepper,et al. Pallidal control of substantia nigra dopaminergic neuron firing pattern and its relation to extracellular neostriatal dopamine levels , 2004, Neuroscience.
[192] E. Richfield,et al. Comparative distribution of dopamine D‐1 and D‐2 receptors in the basal ganglia of turtles, pigeons, rats, cats, and monkeys , 1987, The Journal of comparative neurology.
[193] J. Atack,et al. The 5HT1B receptor agonist, CP‐93129, inhibits [3H]‐GABA release from rat globus pallidus slices and reverses akinesia following intrapallidal injection in the reserpine‐treated rat , 2000, British journal of pharmacology.
[194] A. Scimemi. Structure, function, and plasticity of GABA transporters , 2014, Front. Cell. Neurosci..
[195] R. Gaykema,et al. Direct catecholaminergic‐cholinergic interactions in the basal forebrain. II. Substantia nigra‐ventral tegmental area projections to cholinergic neurons , 1996, The Journal of comparative neurology.
[196] B. Costall,et al. On the involvement of the caudate-putamen, globus pallidus and substantia nigra with neuroleptic and cholinergic modification of locomotor activity. , 1972, Neuropharmacology.
[197] K. Sakimura,et al. Molecular diversity of the NMDA receptor channel , 1992, Nature.
[198] T. Chase,et al. D1 dopamine receptor activation required for postsynaptic expression of D2 agonist effects. , 1987, Science.
[199] George R. Marshall,et al. Afferents to the rat substantia nigra studied with horseradish peroxidase, with special reference to fibres from the subthalamic nucleus , 1976, Brain Research.
[200] M. Amalric,et al. Targeting Group III Metabotropic Glutamate Receptors Produces Complex Behavioral Effects in Rodent Models of Parkinson's Disease , 2007, The Journal of Neuroscience.
[201] A. Nambu. Somatotopic Organization of the Primate Basal Ganglia , 2011, Front. Neuroanat..
[202] Peter Redgrave,et al. Basal Ganglia , 2020, Encyclopedia of Autism Spectrum Disorders.
[203] O. Hassani,et al. Increased subthalamic neuronal activity after nigral dopaminergic lesion independent of disinhibition via the globus pallidus , 1996, Neuroscience.
[204] A. Galván,et al. Intrapallidal dopamine restores motor deficits induced by 6-hydroxydopamine in the rat , 2009, Journal of Neural Transmission.
[205] R. Dingledine,et al. Glutamate Receptor Ion Channels: Structure, Regulation, and Function , 2010, Pharmacological Reviews.
[206] F. Horak,et al. Deep brain stimulation for Parkinson disease: an expert consensus and review of key issues. , 2011, Archives of neurology.
[207] J. Rubenstein,et al. The Progenitor Zone of the Ventral Medial Ganglionic Eminence Requires Nkx2-1 to Generate Most of the Globus Pallidus But Few Neocortical Interneurons , 2010, The Journal of Neuroscience.
[208] A. Gittis,et al. Transgenic Mouse Lines Subdivide External Segment of the Globus Pallidus (GPe) Neurons and Reveal Distinct GPe Output Pathways , 2014, The Journal of Neuroscience.
[209] A. Charara,et al. Brainstem dopaminergic, cholinergic and serotoninergic afferents to the pallidum in the squirrel monkey , 1994, Brain Research.
[210] O. Hobert,et al. Maintenance of postmitotic neuronal cell identity , 2014, Nature Neuroscience.
[211] A. Morel,et al. Single-unit analysis of the pallidum, thalamus and subthalamic nucleus in parkinsonian patients , 2000, Neuroscience.
[212] H. Kita. Globus pallidus external segment. , 2007, Progress in brain research.
[213] R. Mckernan,et al. Which GABAA-receptor subtypes really occur in the brain? , 1996, Trends in Neurosciences.
[214] W. Regehr,et al. The Substantia Nigra Conveys Target-Dependent Excitatory and Inhibitory Outputs from the Basal Ganglia to the Thalamus , 2014, The Journal of Neuroscience.
[215] C. S. Chan,et al. Electrophysiological and behavioral effects of zolpidem in rat globus pallidus , 2004, Experimental Neurology.
[216] H. Fibiger,et al. Collateral projections of neurons of the rat globus pallidus to the striatum and substantia nigra , 2004, Experimental Brain Research.
[217] A. Parent,et al. Pedunculopontine nucleus in the squirrel monkey: Projections to the basal ganglia as revealed by anterograde tract‐tracing methods , 1994, The Journal of comparative neurology.
[218] A. Parent,et al. Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamo-cortical loop , 1995, Brain Research Reviews.
[219] T. Kita,et al. Repetitive activation of glutamatergic inputs evokes a long-lasting excitation in rat globus pallidus neurons in vitro. , 2007, Journal of neurophysiology.
[220] Charles J. Wilson. GABAergic inhibition in the neostriatum. , 2007, Progress in brain research.
[221] D. Surmeier,et al. Dichotomous Anatomical Properties of Adult Striatal Medium Spiny Neurons , 2008, The Journal of Neuroscience.
[222] Y. Sari. Serotonin1B receptors: from protein to physiological function and behavior , 2004, Neuroscience & Biobehavioral Reviews.
[223] J. Bolam,et al. Differential localization of GABAA receptor subunits in relation to rat striatopallidal and pallidopallidal synapses , 2011, The European journal of neuroscience.
[224] A. Björklund,et al. Long-Term rAAV-Mediated Gene Transfer of GDNF in the Rat Parkinson's Model: Intrastriatal But Not Intranigral Transduction Promotes Functional Regeneration in the Lesioned Nigrostriatal System , 2000, The Journal of Neuroscience.
[225] T. Wichmann,et al. Localization and pharmacological modulation of GABA-B receptors in the globus pallidus of parkinsonian monkeys , 2011, Experimental Neurology.
[226] Thomas Wichmann,et al. Role of External Pallidal Segment in Primate Parkinsonism: Comparison of the Effects of 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine-Induced Parkinsonism and Lesions of the External Pallidal Segment , 2004, The Journal of Neuroscience.
[227] J. Pin,et al. Pharmacology and functions of metabotropic glutamate receptors. , 1997, Annual review of pharmacology and toxicology.
[228] T. Chase,et al. The D1 dopamine receptor in the rat brain: Quantitative autoradiographic localization using an iodinated ligand , 1988, Neuroscience.
[229] T. Chase,et al. Antiparkinsonian and antidyskinetic activity of drugs targeting central glutamatergic mechanisms , 2000, Journal of Neurology.
[230] M. Caron,et al. Localization of D1 dopamine receptor mRNA in brain supports a role in cognitive, affective, and neuroendocrine aspects of dopaminergic neurotransmission. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[231] M. Bevan,et al. Short-term Depression of External Globus Pallidus-Subthalamic Nucleus Synaptic Transmission and Implications for Patterning Subthalamic Activity , 2013, The Journal of Neuroscience.
[232] F. Cicchetti,et al. Defining midbrain dopaminergic neuron diversity by single-cell gene expression profiling. , 2014, Cell reports.
[233] Adam G. Carter,et al. GABAB receptor modulation of synaptic function , 2011, Current Opinion in Neurobiology.
[234] M. Hallett,et al. Phenomenology and classification of dystonia: A consensus update , 2013, Movement disorders : official journal of the Movement Disorder Society.
[235] F. Gonon,et al. Nigrostriatal lesion induces D2‐modulated phase‐locked activity in the basal ganglia of rats , 2007, The European journal of neuroscience.
[236] T. Kita,et al. Rat intralaminar thalamic nuclei projections to the globus pallidus: A biotinylated dextran amine anterograde tracing study , 2004, The Journal of comparative neurology.
[237] R. M. Beckstead. Association of dopamine d, and d2 receptors with specific cellular elements in the basal ganglia of the cat: The uneven topography of dopamine receptors in the striatum is determined by intrinsic striatal cells, not nigrostriatal axons , 1988, Neuroscience.
[238] M. A. Ariano,et al. D3 and D2 dopamine receptors: Visualization of cellular expression patterns in motor and limbic structures , 1995, Synapse.
[239] J. Penney,et al. Organization of N‐methyl‐D‐aspartate glutamate receptor gene expression in the basal ganglia of the rat , 1994, The Journal of comparative neurology.
[240] Y. Smith,et al. GABA transporter subtype 1 and GABA transporter subtype 3 modulate glutamatergic transmission via activation of presynaptic GABAB receptors in the rat globus pallidus , 2012, The European journal of neuroscience.
[241] Masahiko Watanabe,et al. Behavioral/systems/cognitive Selective Neural Pathway Targeting Reveals Key Roles of Thalamostriatal Projection in the Control of Visual Discrimination , 2022 .
[242] G. Sperk,et al. Distribution of the major γ‐aminobutyric acidA receptor subunits in the basal ganglia and associated limbic brain areas of the adult rat , 2001, The Journal of comparative neurology.
[243] Y. Yanagawa,et al. Distribution and intrinsic membrane properties of basal forebrain GABAergic and parvalbumin neurons in the mouse , 2013, The Journal of comparative neurology.
[244] D. Feldmeyer,et al. Identification of a native low‐conductance NMDA channel with reduced sensitivity to Mg2+ in rat central neurones. , 1996, The Journal of physiology.
[245] Robert M. Beckstead,et al. A pallidostriatal projection in the cat and monkey , 1983, Brain Research Bulletin.
[246] H. V. Van Tol,et al. Distribution of D2 dopamine receptor mRNA in rat brain. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[247] A. Nambu,et al. Discharge patterns of pallidal neurons with input from various cortical areas during movement in the monkey , 1990, Brain Research.
[248] G. Arbuthnott,et al. Plasticity of striatopallidal terminals following unilateral lesion of the dopaminergic nigrostriatal pathway: a morphological study , 1997, Experimental Brain Research.
[249] Hagai Bergman,et al. Temporal Convergence of Dynamic Cell Assemblies in the Striato-Pallidal Network , 2012, The Journal of Neuroscience.
[250] J. Fritschy,et al. Comparison of the rat dorsal and ventral striatopallidal system A study using the GABAA-receptor α1-subunit and parvalbumin immunolabeling , 1998, Experimental Brain Research.
[251] T. Baumann,et al. Characteristics and somatotopic organization of kinesthetic cells in the globus pallidus of patients with Parkinson's disease. , 1996, Journal of neurosurgery.
[252] A Golgi study on the globus pallidus of the mouse , 1979, Neuroscience Letters.
[253] M. Martres,et al. Widespread distribution of brain dopamine receptors evidenced with [125I]iodosulpride, a highly selective ligand. , 1985, Science.
[254] J L Gallant,et al. Sparse coding and decorrelation in primary visual cortex during natural vision. , 2000, Science.
[255] Bente Pakkenberg,et al. Total numbers of neurons and glial cells in cortex and basal ganglia of aged brains with Down syndrome--a stereological study. , 2011, Cerebral cortex.
[256] T. Wichmann,et al. The cortico‐pallidal projection: An additional route for cortical regulation of the basal ganglia circuitry , 2015, Movement disorders : official journal of the Movement Disorder Society.
[257] I. Gotlib,et al. Identification of a direct GABAergic pallidocortical pathway in rodents , 2015, The European journal of neuroscience.
[258] Peter Brown,et al. Effects of dopamine depletion on information flow between the subthalamic nucleus and external globus pallidus. , 2011, Journal of neurophysiology.
[259] P. Gubellini,et al. Distinct effects of mGlu4 receptor positive allosteric modulators at corticostriatal vs. striatopallidal synapses may differentially contribute to their antiparkinsonian action , 2014, Neuropharmacology.
[260] Robert S Turner,et al. Context-Dependent Modulation of Movement-Related Discharge in the Primate Globus Pallidus , 2005, The Journal of Neuroscience.
[261] R. Traub,et al. Neuronal networks for induced ‘40 Hz’ rhythms , 1996, Trends in Neurosciences.
[262] M. Hallett,et al. The pathophysiological basis of dystonias , 2008, Nature Reviews Neuroscience.
[263] M. Mesulam,et al. Central cholinergic pathways in the rat: An overview based on an alternative nomenclature (Ch1–Ch6) , 1983, Neuroscience.
[264] Laura A. Bradfield,et al. The Thalamostriatal Pathway and Cholinergic Control of Goal-Directed Action: Interlacing New with Existing Learning in the Striatum , 2013, Neuron.
[265] J. Penney,et al. Localization of metabotropic glutamate receptor 7 mRNA and mGluR7a protein in the rat basal ganglia , 1999, The Journal of comparative neurology.
[266] C. Waeber,et al. [3H]sumatriptan labels both 5-HT1D and 5-HT1F receptor binding sites in the guinea pig brain: an autoradiographic study , 1995, Naunyn-Schmiedeberg's Archives of Pharmacology.
[267] D James Surmeier,et al. Proliferation of External Globus Pallidus-Subthalamic Nucleus Synapses following Degeneration of Midbrain Dopamine Neurons , 2012, The Journal of Neuroscience.
[268] W. Hauber,et al. The effects of globus pallidus lesions on dopamine-dependent motor behaviour in rats , 1998, Neuroscience.
[269] I. Stanford,et al. Calbindin D-28k positive projection neurones and calretinin positive interneurones of the rat globus pallidus , 2002, Brain Research.
[270] Cengiz Günay,et al. Channel Density Distributions Explain Spiking Variability in the Globus Pallidus: A Combined Physiology and Computer Simulation Database Approach , 2008, The Journal of Neuroscience.
[271] E A Barnard,et al. International Union of Pharmacology. XV. Subtypes of gamma-aminobutyric acidA receptors: classification on the basis of subunit structure and receptor function. , 1998, Pharmacological reviews.
[272] R. Faull,et al. GABAA receptors in the primate basal ganglia: An autoradiographic and a light and electron microscopic immunohistochemical study of the α1 and β2,3 subunits in the baboon brain , 1998, The Journal of comparative neurology.
[273] H. Kita,et al. Serotonin activates presynaptic and postsynaptic receptors in rat globus pallidus. , 2008, Journal of neurophysiology.
[274] Hitoshi Kita,et al. Presynaptic actions of D2-like receptors in the rat cortico-striato-globus pallidus disynaptic connection in vitro. , 2009, Journal of neurophysiology.
[275] H. Kita,et al. Serotonin Modulates Pallidal Neuronal Activity in the Awake Monkey , 2007, The Journal of Neuroscience.
[276] A. Wenzel,et al. Distribution of NMDA receptor subunit proteins NR2A, 2B, 2C and 2D in rat brain , 1995, Neuroreport.
[277] S. Alford,et al. G protein betagamma subunit-mediated presynaptic inhibition: regulation of exocytotic fusion downstream of Ca2+ entry. , 2001, Science.
[278] D. Standaert,et al. Metabotropic glutamate receptor mRNA expression in the basal ganglia of the rat , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[279] R. Nicoll,et al. A bicuculline‐resistant inhibitory post‐synaptic potential in rat hippocampal pyramidal cells in vitro. , 1984, The Journal of physiology.
[280] D James Surmeier,et al. HCN2 and HCN1 Channels Govern the Regularity of Autonomous Pacemaking and Synaptic Resetting in Globus Pallidus Neurons , 2004, The Journal of Neuroscience.
[281] K. Deisseroth. Optogenetics: 10 years of microbial opsins in neuroscience , 2015, Nature Neuroscience.
[282] I. Bar-Gad,et al. Globus Pallidus External Segment Neuron Classification in Freely Moving Rats: A Comparison to Primates , 2012, PloS one.
[283] R. Awatramani,et al. Molecular heterogeneity of midbrain dopaminergic neurons – Moving toward single cell resolution , 2015, FEBS letters.
[284] M. Ishida,et al. The COUP-TFII/Neuropilin-2 is a molecular switch steering diencephalon-derived GABAergic neurons in the developing mouse brain , 2015, Proceedings of the National Academy of Sciences.
[285] Y. Smith,et al. Anatomy of the dopamine system in the basal ganglia , 2000, Trends in Neurosciences.
[286] S. Duty,et al. Activation of group III metabotropic glutamate receptors in selected regions of the basal ganglia alleviates akinesia in the reserpine‐treated rat , 2004, British journal of pharmacology.
[287] E. Vaadia,et al. Encoding of probabilistic rewarding and aversive events by pallidal and nigral neurons. , 2009, Journal of neurophysiology.
[288] J. Vitek,et al. Stimulation of the Subthalamic Nucleus Changes the Firing Pattern of Pallidal Neurons , 2003, The Journal of Neuroscience.
[289] C. Parsons,et al. Glycine and N-methyl-D-aspartate receptors: physiological significance and possible therapeutic applications. , 1998, Pharmacological reviews.
[290] Daniel K. Leventhal,et al. Arkypallidal Cells Send a Stop Signal to Striatum , 2016, Neuron.
[291] K Watanabe,et al. Neural information transferred from the putamen to the globus pallidus during learned movement in the monkey. , 1996, Journal of neurophysiology.
[292] G. Sperk,et al. GABA(A) receptors: immunocytochemical distribution of 13 subunits in the adult rat brain. , 2000, Neuroscience.
[293] A. Parent,et al. Differential dopaminergic innervation of the two pallidal segments in the squirrel monkey (Saimiri sciureus) , 1987, Brain Research.
[294] O. Valenti,et al. Modulation of Inhibitory Transmission in the Rat Globus Pallidus by Activation of mGluR4 , 2003, Annals of the New York Academy of Sciences.
[295] S. T. Kitai,et al. Medium spiny neuron projection from the rat striatum: An intracellular horseradish peroxidase study , 1980, Brain Research.
[296] Luis E. Gonzalez-Reyes,et al. Sonic Hedgehog Maintains Cellular and Neurochemical Homeostasis in the Adult Nigrostriatal Circuit , 2012, Neuron.
[297] F. Fujiyama,et al. Exclusive and common targets of neostriatofugal projections of rat striosome neurons: a single neuron‐tracing study using a viral vector , 2011, The European journal of neuroscience.
[298] P. Schofield. The GABAA receptor: molecular biology reveals a complex picture. , 1989, Trends in pharmacological sciences.
[299] W. T. Thach,et al. Basal ganglia motor control. I. Nonexclusive relation of pallidal discharge to five movement modes. , 1991, Journal of neurophysiology.
[300] H. Kita,et al. The cortico-pallidal projection in the rat: an anterograde tracing study with biotinylated dextran amine , 1994, Brain Research.
[301] Dieter Jaeger,et al. Neuronal activity in the striatum and pallidum of primates related to the execution of externally cued reaching movements , 1995, Brain Research.
[302] Martin Parent,et al. Quantitative and ultrastructural study of serotonin innervation of the globus pallidus in squirrel monkeys , 2013, The European journal of neuroscience.
[303] Werner Sieghart,et al. International Union of Pharmacology. LXX. Subtypes of γ-Aminobutyric AcidA Receptors: Classification on the Basis of Subunit Composition, Pharmacology, and Function. Update , 2008, Pharmacological Reviews.
[304] Anatol C. Kreitzer,et al. Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry , 2010, Nature.
[305] Ling Fu,et al. Whole-Brain Mapping of Inputs to Projection Neurons and Cholinergic Interneurons in the Dorsal Striatum , 2015, PloS one.
[306] A. Charara,et al. GABAB and group I metabotropic glutamate receptors in the striatopallidal complex in primates , 2000, Journal of anatomy.
[307] Anatol C. Kreitzer,et al. Differential Innervation of Direct- and Indirect-Pathway Striatal Projection Neurons , 2013, Neuron.
[308] G. Köhr,et al. Role of heteromer formation in GABAB receptor function. , 1999, Science.
[309] U. Rudolph,et al. Analysis of GABAA receptor function and dissection of the pharmacology of benzodiazepines and general anesthetics through mouse genetics. , 2004, Annual review of pharmacology and toxicology.
[310] E. Boyden. Optogenetics and the future of neuroscience , 2015, Nature Neuroscience.
[311] M. Farrant,et al. Variations on an inhibitory theme: phasic and tonic activation of GABAA receptors , 2005, Nature Reviews Neuroscience.
[312] Atsushi Nambu,et al. Morphology of globus pallidus neurons: Its correlation with electrophysiology in guinea pig brain slices , 1997, The Journal of comparative neurology.
[313] P. Osborne,et al. Electrophysiological properties of cholinergic and noncholinergic neurons in the ventral pallidal region of the nucleus basalis in rat brain slices. , 2000, Journal of neurophysiology.
[314] Alexander B. Wiltschko,et al. Selective Activation of Striatal Fast-Spiking Interneurons during Choice Execution , 2010, Neuron.
[315] C. Gerfen,et al. GENSAT BAC Cre-Recombinase Driver Lines to Study the Functional Organization of Cerebral Cortical and Basal Ganglia Circuits , 2013, Neuron.
[316] Christer Halldin,et al. Autoradiographic localization of extrastriatal D2‐dopamine receptors in the human brain using [125I]epidepride , 1996, Synapse.
[317] G. Perea,et al. Circuit-specific signaling in astrocyte-neuron networks in basal ganglia pathways , 2015, Science.
[318] Alan Wise,et al. Heterodimerization is required for the formation of a functional GABAB receptor , 1998, Nature.
[319] Gavin L. Woodhall,et al. Functional characterization of GABAergic pallidopallidal and striatopallidal synapses in the rat globus pallidus in vitro , 2008, The European journal of neuroscience.
[320] C. Hammond,et al. High-frequency stimulation produces a transient blockade of voltage-gated currents in subthalamic neurons. , 2001, Journal of neurophysiology.
[321] A. Parent,et al. Morphological changes in serotoninergic neurites in the striatum and globus pallidus in levodopa primed MPTP treated common marmosets with dyskinesia , 2010, Neurobiology of Disease.
[322] A. Jayaraman. Topographic organization and morphology of peripallidal and pallidal cells projecting to the striatum in cats , 1983, Brain Research.
[323] J. Schipper,et al. Eltoprazine, a drug which reduces aggressive behaviour, binds selectively to 5-HT1 receptor sites in the rat brain: an autoradiographic study. , 1990, European journal of pharmacology.
[324] B. Averbeck,et al. Effects of Dopamine Depletion on Network Entropy in the External Globus Pallidus , 2009, Journal of neurophysiology.
[325] S. Alford,et al. G Protein βγ Subunit-Mediated Presynaptic Inhibition: Regulation of Exocytotic Fusion Downstream of Ca2+ Entry , 2001, Science.
[326] T. Heida,et al. Pallidal gap junctions-triggers of synchrony in Parkinson's disease? , 2014, Movement disorders : official journal of the Movement Disorder Society.
[327] Jean-Michel Deniau,et al. Striatal Medium-Sized Spiny Neurons: Identification by Nuclear Staining and Study of Neuronal Subpopulations in BAC Transgenic Mice , 2009, PloS one.
[328] P. Goldman-Rakic,et al. Localization of dopamine D4 receptors in GABAergic neurons of the primate brain , 1996, Nature.
[329] M. Hamon,et al. Cellular and subcellular localization of 5-hydroxytryptamine1B receptors in the rat central nervous system: immunocytochemical, autoradiographic and lesion studies , 1999, Neuroscience.
[330] H. Fibiger,et al. Demonstration of a pallido‐nigral projection innervating dopaminergic neurons , 1975, The Journal of comparative neurology.
[331] A. Parent,et al. The striatopallidal projection displays a high degree of anatomical specificity in the primate , 1992, Brain Research.
[332] M. Chen,et al. Glutamate-Dependent Neuroglial Calcium Signaling Differs Between Young and Adult Brain , 2013, Science.
[333] J. Féger,et al. Identification of different subpopulations of neostriatal neurones projecting to globus pallidus or substantia nigra in the monkey: A retrograde fluorescence double-labelling study , 1984, Neuroscience Letters.
[334] Hagai Bergman,et al. Functional Correlations between Neighboring Neurons in the Primate Globus Pallidus Are Weak or Nonexistent , 2003, The Journal of Neuroscience.
[335] P. Brotchie,et al. Motor function of the monkey globus pallidus. 1. Neuronal discharge and parameters of movement. , 1991, Brain : a journal of neurology.
[336] A. Parent,et al. Efferent connections of the centromedian and parafascicular thalamic nuclei in the squirrel monkey: A PHA‐L study of subcortical projections , 1992, The Journal of comparative neurology.
[337] L. Descarries,et al. Somatodendritic localization of 5‐HT1A and preterminal axonal localization of 5‐HT1B serotonin receptors in adult rat brain , 2000, The Journal of comparative neurology.
[338] V. Murthy,et al. Synaptic gain control and homeostasis , 2003, Current Opinion in Neurobiology.
[339] H. Akil,et al. Localization of dopamine D2 receptor mRNA and D1 and D2 receptor binding in the rat brain and pituitary: an in situ hybridization- receptor autoradiographic analysis , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[340] J. Palacios,et al. Serotonin 5‐HT1D Receptors , 1990, Annals of the New York Academy of Sciences.
[341] Oscar Marín,et al. Origin and Molecular Specification of Globus Pallidus Neurons , 2010, The Journal of Neuroscience.
[342] J. Joyce,et al. Localization of dopamine D3 receptors to mesolimbic and D2 receptors to mesostriatal regions of human forebrain. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[343] M. Sofroniew,et al. Astrocytes: biology and pathology , 2009, Acta Neuropathologica.
[344] C. François,et al. Effect of intrastriatal 6-OHDA lesion on dopaminergic innervation of the rat cortex and globus pallidus , 2005, Experimental Neurology.
[345] KouichiC . Nakamura,et al. Prototypic and Arkypallidal Neurons in the Dopamine-Intact External Globus Pallidus , 2015, The Journal of Neuroscience.
[346] B. Scatton,et al. Autoradiographic localization of D1 dopamine receptors in the rat brain with [3H]SKF 38393. , 1985, European journal of pharmacology.
[347] B. Givens,et al. Dopamine electrophysiology of ventral pallidal/substantia innominata neurons: comparison with the dorsal globus pallidus. , 1991, The Journal of pharmacology and experimental therapeutics.
[348] N. Rajakumar,et al. The pallidostriatal projection in the rat: a recurrent inhibitory loop? , 1994, Brain Research.
[349] P. Bonaventure,et al. Mapping of serotonin 5‐HT4 receptor mRNA and ligand binding sites in the post‐mortem human brain , 2000, Synapse.
[350] P. Redgrave,et al. High-frequency electrical stimulation of the subthalamic nucleus excites target structures in a model using c-fos immunohistochemistry , 2014, Neuroscience.
[351] C. Wilson,et al. Projection subtypes of rat neostriatal matrix cells revealed by intracellular injection of biocytin , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[352] R. Bogacz,et al. Effective connectivity of the subthalamic nucleus–globus pallidus network during Parkinsonian oscillations , 2014, The Journal of physiology.
[353] D. James Surmeier,et al. Heterosynaptic Regulation of External Globus Pallidus Inputs to the Subthalamic Nucleus by the Motor Cortex , 2015, Neuron.
[354] Dagoberto Tapia,et al. Control of the subthalamic innervation of the rat globus pallidus by D2/3 and D4 dopamine receptors. , 2006, Journal of neurophysiology.
[355] T. Kuner,et al. Multiple Structural Elements Determine Subunit Specificity of Mg2+ Block in NMDA Receptor Channels , 1996, The Journal of Neuroscience.
[356] H. Kita,et al. Reduced Pallidal Output Causes Dystonia , 2011, Front. Syst. Neurosci..
[357] KouichiC . Nakamura,et al. Dichotomous Organization of the External Globus Pallidus , 2012, Neuron.
[358] R. Faull,et al. The diversity of GABA(A) receptor subunit distribution in the normal and Huntington's disease human brain. , 2015, Advances in pharmacology.
[359] G. Percheron,et al. Spatial relationships between striatal axonal endings and pallidal neurons in macaque monkeys. , 1997, Advances in neurology.
[360] G. Bernardi,et al. Group I mGluRs modulate calcium currents in rat GP: Functional implications , 1998, Synapse.
[361] Anatol C. Kreitzer,et al. Distinct roles for direct and indirect pathway striatal neurons in reinforcement , 2012, Nature Neuroscience.
[362] Bernhard Haslinger,et al. Frequency-correlated decreases of motor cortex activity associated with subthalamic nucleus stimulation in Parkinson's disease , 2005, NeuroImage.
[363] E. Yoon,et al. Gβγ Interferes with Ca2+-Dependent Binding of Synaptotagmin to the Soluble N-Ethylmaleimide-Sensitive Factor Attachment Protein Receptor (SNARE) Complex , 2007, Molecular Pharmacology.
[364] J. Morys,et al. Distribution of the parvalbumin, calbindin-D28K and calretinin immunoreactivity in globus pallidus of the Brazilian short-tailed opossum (Monodelphis domestica). , 2007, Acta neurobiologiae experimentalis.
[365] T. Moriizumi,et al. Electron microscopic analysis of the synaptic organization of the globus pallidus in the cat , 1987, The Journal of comparative neurology.
[366] J. Greenamyre,et al. Polysynaptic regulation of glutamate receptors and mitochondrial enzyme activities in the basal ganglia of rats with unilateral dopamine depletion , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[367] M. Masu,et al. Signal transduction, pharmacological properties, and expression patterns of two rat metabotropic glutamate receptors, mGluR3 and mGluR4 , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[368] Jeanne T Paz,et al. Microcircuits and their interactions in epilepsy: is the focus out of focus? , 2015, Nature Neuroscience.
[369] R. M. Beckstead,et al. Distribution of D1 and D2 dopamine receptors in the basal ganglia of the cat determined by quantitative autoradiography , 1988, The Journal of comparative neurology.
[370] E. Abercrombie,et al. Relative involvement of globus pallidus and subthalamic nucleus in the regulation of somatodendritic dopamine release in substantia nigra is dopamine-dependent , 2003, Neuroscience.
[371] E. Vaadia,et al. Firing Patterns and Correlations of Spontaneous Discharge of Pallidal Neurons in the Normal and the Tremulous 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine Vervet Model of Parkinsonism , 2000, The Journal of Neuroscience.
[372] J. Bolam,et al. Subcellular and subsynaptic distribution of the NR1 subunit of the NMDA receptor in the neostriatum and globus pallidus of the rat: co‐localization at synapses with the GluR2/3 subunit of the AMPA receptor , 1998, The European journal of neuroscience.
[373] W. Staines,et al. Immunogold evidence that neuronal gap junctions in adult rat brain and spinal cord contain connexin-36 but not connexin-32 or connexin-43. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[374] K. F. Schroeder,et al. Morphometric studies of the neuropathological changes in choreatic diseases , 1976, Journal of the Neurological Sciences.
[375] J. Palacios,et al. Dopamine D2 receptors in the rat brain: autoradiographic visualization using a high-affinity selective agonist ligand , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[376] E. Esposito,et al. Serotonin modulation of the basal ganglia circuitry: therapeutic implication for Parkinson's disease and other motor disorders. , 2008, Progress in brain research.
[377] L. Tremblay,et al. Effects of dopamine agonists on the spontaneous activity of globus pallidus neurons in monkeys with MPTP-induced parkinsonism , 1991, Brain Research.
[378] M. Brecht,et al. Sparse and powerful cortical spikes , 2010, Current Opinion in Neurobiology.
[379] Bruno A Olshausen,et al. Sparse coding of sensory inputs , 2004, Current Opinion in Neurobiology.
[380] H. Bergman,et al. Different correlation patterns of cholinergic and GABAergic interneurons with striatal projection neurons , 2013, Front. Syst. Neurosci..
[381] Charles J. Wilson,et al. Intrinsic dynamics and synaptic inputs control the activity patterns of subthalamic nucleus neurons in health and in Parkinson's disease , 2011, Neuroscience.
[382] R. Porter,et al. GluR1 Glutamate Receptor Subunit Is Regulated Differentially in the Primate Basal Ganglia Following Nigrostriatal Dopamine Denervation , 2000, Journal of neurochemistry.
[383] T. Wichmann,et al. The thalamostriatal system in normal and diseased states , 2014, Front. Syst. Neurosci..
[384] S. Mague,et al. NMDA receptor antagonists ameliorate the stepping deficits produced by unilateral medial forebrain bundle injections of 6-OHDA in rats , 2004, Psychopharmacology.
[385] Abdelhamid Benazzouz,et al. Dopaminergic Control of the Globus Pallidus through Activation of D2 Receptors and Its Impact on the Electrical Activity of Subthalamic Nucleus and Substantia Nigra Reticulata Neurons , 2015, PloS one.
[386] Pierre Payoux,et al. Subthalamic nucleus stimulation reduces abnormal motor cortical overactivity in Parkinson disease. , 2004, Archives of neurology.
[387] F. Fujiyama,et al. Quantitative analysis of axon bouton distribution of subthalamic nucleus neurons in the rat by single neuron visualization with a viral vector , 2013, The Journal of comparative neurology.
[388] A. Nambu,et al. The distribution of the globus pallidus neurons with input from various cortical areas in the monkeys , 1993, Brain Research.
[389] Y. Kubota,et al. Regional and cellular localisation of GABAA receptor subunits in the human basal ganglia: An autoradiographic and immunohistochemical study , 1999, The Journal of comparative neurology.
[390] M. Śmiałowska,et al. A biphasic influence of globus pallidus lesions: Spontaneous catalepsy followed by anticataleptic effect , 1983, Pharmacology Biochemistry and Behavior.
[391] A. Parent,et al. Asynaptic feature and heterogeneous distribution of the cholinergic innervation of the globus pallidus in primates , 2014, Brain Structure and Function.
[392] A. Charara,et al. Pre- and postsynaptic localization of GABAB receptors in the basal ganglia in monkeys , 1999, Neuroscience.
[393] L. Riquelme,et al. Distinct changes in evoked and resting globus pallidus activity in early and late Parkinson's disease experimental models , 2007, The European journal of neuroscience.
[394] J. Paysan,et al. Switch in the expression of rat GABAA-receptor subtypes during postnatal development: an immunohistochemical study , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[395] W. Koller,et al. Pharmacologic treatment of parkinsonian tremor. , 1986, Archives of neurology.
[396] Jérôme Baufreton,et al. D2‐like dopamine receptor‐mediated modulation of activity‐dependent plasticity at GABAergic synapses in the subthalamic nucleus , 2008, The Journal of physiology.
[397] B. Bunney,et al. The precise localization of nigral afferents in the rat as determined by a retrograde tracing technique , 1976, Brain Research.
[398] Anatol C. Kreitzer,et al. Control of Basal Ganglia Output by Direct and Indirect Pathway Projection Neurons , 2013, The Journal of Neuroscience.
[399] H. Kita,et al. Efferent projections of the subthalamic nucleus in the rat: Light and electron microscopic analysis with the PHA‐L method , 1987, The Journal of comparative neurology.
[400] K. Jellinger,et al. New developments in the pathology of Parkinson's disease. , 1990, Advances in neurology.
[401] D. Joel,et al. The connections of the primate subthalamic nucleus: indirect pathways and the open-interconnected scheme of basal ganglia-thalamocortical circuitry , 1997, Brain Research Reviews.
[402] Y Agid,et al. Dopaminergic innervation of the pallidum in the normal state, in MPTP‐treated monkeys and in parkinsonian patients , 2000, The European journal of neuroscience.
[403] H. Kita,et al. Excitatory Cortical Inputs to Pallidal Neurons Via the Subthalamic Nucleus in the Monkey , 2000 .
[404] Murtaza Z Mogri,et al. Optical Deconstruction of Parkinsonian Neural Circuitry , 2009, Science.
[405] Allan R. Jones,et al. A robust and high-throughput Cre reporting and characterization system for the whole mouse brain , 2009, Nature Neuroscience.
[406] J. Bolam,et al. Relationship of Activity in the Subthalamic Nucleus–Globus Pallidus Network to Cortical Electroencephalogram , 2000, The Journal of Neuroscience.
[407] S. Charpier,et al. Rhythmic Bursting in the Cortico-Subthalamo-Pallidal Network during Spontaneous Genetically Determined Spike and Wave Discharges , 2005, The Journal of Neuroscience.
[408] Gilles Laurent,et al. Olfactory network dynamics and the coding of multidimensional signals , 2002, Nature Reviews Neuroscience.
[409] J. Bolam,et al. Synaptic Integration of Functionally Diverse Pallidal Information in the Entopeduncular Nucleus and Subthalamic Nucleus in the Rat , 1997, The Journal of Neuroscience.
[410] F. Stephenson,et al. The GABAA receptors. , 1995, The Biochemical journal.
[411] Naoshige Uchida,et al. Organization of monosynaptic inputs to the serotonin and dopamine neuromodulatory systems. , 2014, Cell reports.
[412] J. Schneider,et al. Behaviorally specific limb use deficits following globus pallidus lesions in rats , 1984, Brain Research.
[413] Hagai Bergman,et al. Comparison of MPTP-induced changes in spontaneous neuronal discharge in the internal pallidal segment and in the substantia nigra pars reticulata in primates , 1999, Experimental Brain Research.
[414] J. Penney,et al. The functional anatomy of disorders of the basal ganglia , 1995, Trends in Neurosciences.
[415] Kyle S. Smith,et al. Investigating habits: strategies, technologies and models , 2014, Front. Behav. Neurosci..
[416] S. Nakanishi,et al. Distribution of the mRNA for a metabotropic glutamate receptor (mGluR3) in the rat brain: An in situ hybridization study , 1993, The Journal of comparative neurology.
[417] B. Costall,et al. Catalepsy and circling behaviour after intracerebral injections of neuroleptic, cholinergic and anticholinergic agents into the caudate-putamen, globus pallidus and substantia nigra of rat brain. , 1972, Neuropharmacology.
[418] Adam Ponzi,et al. Sequentially Switching Cell Assemblies in Random Inhibitory Networks of Spiking Neurons in the Striatum , 2010, The Journal of Neuroscience.
[419] G. M. Halliday,et al. Loss of brainstem serotonin- and substance P-containing neurons in Parkinson's disease , 1990, Brain Research.
[420] A. Flaherty,et al. Input-output organization of the sensorimotor striatum in the squirrel monkey , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[421] Robert C. Thompson,et al. The distribution of dopamine D2 receptor heteronuclear RNA (hnRNA) in the rat brain , 1993, Journal of Chemical Neuroanatomy.
[422] J. Marshall,et al. The role of the globus pallidus D2 subfamily of dopamine receptors in pallidal immediate early gene expression , 2001, Neuroscience.
[423] M R Park,et al. An intracellular HRP study of the rat globus pallidus. I. Responses and light microscopic analysis , 1982, The Journal of comparative neurology.
[424] Nathan C. Klapoetke,et al. Transgenic Mice for Intersectional Targeting of Neural Sensors and Effectors with High Specificity and Performance , 2015, Neuron.
[425] T. Blackburn,et al. Immunohistochemical localisation of the 5-HT2C receptor protein in the rat CNS , 2000, Neuropharmacology.
[426] C. Gerfen,et al. Modulation of striatal projection systems by dopamine. , 2011, Annual review of neuroscience.
[427] D. A. Bergstrom,et al. Apomorphine increases the activity of rat globus pallidus neurons , 1982, Brain Research.
[428] W. Yung,et al. Behavioral and electrophysiological effects of 5‐HT in globus pallidus of 6‐hydroxydopamine lesioned rats , 2009, Journal of neuroscience research.
[429] P Jeffrey Conn,et al. Group III Metabotropic Glutamate Receptor-Mediated Modulation of the Striatopallidal Synapse , 2003, The Journal of Neuroscience.
[430] Adam G. Carter,et al. GABAB Receptors Modulate NMDA Receptor Calcium Signals in Dendritic Spines , 2010, Neuron.
[431] Jérôme Baufreton,et al. GABAergic control of the subthalamic nucleus. , 2007, Progress in brain research.
[432] E. Vaadia,et al. Independent Coding of Movement Direction and Reward Prediction by Single Pallidal Neurons , 2004, The Journal of Neuroscience.
[433] S. Marino,et al. Basal ganglia network by constrained spherical deconvolution: A possible cortico‐pallidal pathway? , 2015, Movement disorders : official journal of the Movement Disorder Society.
[434] W. T. Thach,et al. Basal ganglia motor control. II. Late pallidal timing relative to movement onset and inconsistent pallidal coding of movement parameters. , 1991, Journal of neurophysiology.
[435] S. T. Kitai,et al. Single neostriatal efferent axons in the globus pallidus: a light and electron microscopic study. , 1981, Science.
[436] M. Pangalos,et al. GABAB Receptors: A New Paradigm in G Protein Signaling , 2000, Molecular and Cellular Neuroscience.
[437] R. Mcquade,et al. CNS distribution of D1 receptors: Use of a new specific D1 receptor antagonist, [3H]SCH39166 , 1992, Neurochemistry International.
[438] J. Marshall,et al. Further characterization of preproenkephalin mRNA-containing cells in the rodent globus pallidus , 2002, Neuroscience.
[439] W Wisden,et al. The distribution of 13 GABAA receptor subunit mRNAs in the rat brain. I. Telencephalon, diencephalon, mesencephalon , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[440] G. Vauquelin,et al. Autoradiographic distribution of D3-type dopamine receptors in human brain using [3H]7-hydroxy-N,N-di-n-propyl-2-aminotetralin , 1994, Brain Research.
[441] Steven S. Vogel,et al. Concurrent Activation of Striatal Direct and Indirect Pathways During Action Initiation , 2013, Nature.
[442] S. Kish. Biochemistry of Parkinson's disease: is a brain serotonergic deficiency a characteristic of idiopathic Parkinson's disease? , 2003, Advances in neurology.
[443] K. Rhodes,et al. Immunohistochemical localization of subtype 4a metabotropic glutamate receptors in the rat and mouse basal ganglia , 1999, The Journal of comparative neurology.
[444] P. Somogyi,et al. The γ2 Subunit of the GABAA Receptor is Concentrated in Synaptic Junctions Containing the α1 and β 2 3 Subunits in Hippocampus, Cerebellum and Globus Pallidus , 1996, Neuropharmacology.
[445] Hitoshi Kita,et al. Cortical Stimulation Evokes Abnormal Responses in the Dopamine-Depleted Rat Basal Ganglia , 2011, The Journal of Neuroscience.
[446] M. Lévesque,et al. Raclopride-induced motor consolidation impairment in primates: role of the dopamine type-2 receptor in movement chunking into integrated sequences , 2007, Experimental Brain Research.
[447] L. Tremblay,et al. Abnormal influences of passive limb movement on the activity of globus pallidus neurons in parkinsonian monkeys , 1988, Brain Research.
[448] Christian Rosenmund,et al. Activation of metabotropic GABA receptors increases the energy barrier for vesicle fusion , 2011, Journal of Cell Science.
[449] T. Chase,et al. Quantitative autoradiographic localization of D-1 dopamine receptors in the rat brain: Use of the iodinated ligand [125I]SCH 23982 , 1986, Neuroscience Letters.
[450] Astrocytes go awry in Huntington's disease , 2014, Nature Neuroscience.
[451] T. Hattori,et al. Separate neuronal populations of the rat globus pallidus projecting to the subthalamic nucleus, auditory cortex and pedunculopontine tegmental area , 1992, Neuroscience.
[452] P. Salin,et al. Lesion Study of the Distribution of Serotonin 5‐HT4 Receptors in Rat Basal Ganglia and Hippocampus , 1996, The European journal of neuroscience.
[453] Charles J. Wilson,et al. Membrane potential synchrony of simultaneously recorded striatal spiny neurons in vivo , 1998, Nature.
[454] Charles J. Wilson,et al. Spontaneous firing patterns of identified spiny neurons in the rat neostriatum , 1981, Brain Research.
[455] H. Kita,et al. Synaptically released GABA activates both pre- and postsynaptic GABA(B) receptors in the rat globus pallidus. , 2005, Journal of neurophysiology.
[456] S. Oliet,et al. Activity-dependent structural and functional plasticity of astrocyte-neuron interactions. , 2008, Physiological reviews.
[457] M. Savasta,et al. Autoradiographic localization of D1 dopamine receptors in the rat brain with [3H]SCH 23390 , 1986, Brain Research.
[458] W. Hauber,et al. Dopamine D1 or D2 receptor blockade in the globus pallidus produces akinesia in the rat , 1999, Behavioural Brain Research.
[459] Caroline A. Johnson,et al. A direct GABAergic output from the basal ganglia to frontal cortex , 2014, Nature.
[460] Jerrold L. Vitek,et al. External pallidal stimulation improves parkinsonian motor signs and modulates neuronal activity throughout the basal ganglia thalamic network , 2012, Experimental Neurology.
[461] H. Nauta. Projections of the pallidal complex: An autoradiographic study in the cat , 1979, Neuroscience.
[462] O. E. Millhouse. Pallidal neurons in the rat , 1986, The Journal of comparative neurology.
[463] W. Sieghart,et al. Structure and pharmacology of gamma-aminobutyric acidA receptor subtypes. , 1995, Pharmacological reviews.
[464] K. Moriyoshi,et al. Molecular characterization of the family of the N-methyl-D-aspartate receptor subunits. , 1993, The Journal of biological chemistry.
[465] H. Kita. Responses of globus pallidus neurons to cortical stimulation: intracellular study in the rat , 1992, Brain Research.
[466] A. Parent,et al. Compartmental distribution of parvalbumin and calbindin D-28k in rat globus pallidus. , 1994, NeuroReport.
[467] A. D. Smith,et al. A correlated light and electron microscopic study of identified cholinergic basal forebrain neurons that project to the cortex in the rat , 1985, The Journal of comparative neurology.
[468] T. Yasuhara,et al. Intrapallidal metabotropic glutamate receptor activation in a rat model of Parkinson's disease: Behavioral and histological analyses , 2008, Brain Research.
[469] J. Rothstein,et al. Mechanisms of Disease: astrocytes in neurodegenerative disease , 2006, Nature Clinical Practice Neurology.
[470] M. Delong,et al. Acute stimulation in the external segment of the globus pallidus improves parkinsonian motor signs , 2004, Movement disorders : official journal of the Movement Disorder Society.
[471] A. Carlsson,et al. The occurrence, distribution and physiological role of catecholamines in the nervous system. , 1959, Pharmacological reviews.
[472] R. Turner,et al. Spontaneous pallidal neuronal activity in human dystonia: comparison with Parkinson's disease and normal macaque. , 2005, Journal of neurophysiology.
[473] H Mushiake,et al. Pallidal neuron activity during sequential arm movements. , 1995, Journal of neurophysiology.
[474] H. Kita,et al. Role of ionotropic glutamatergic and GABAergic inputs on the firing activity of neurons in the external pallidum in awake monkeys. , 2004, Journal of neurophysiology.
[475] J. Rothstein,et al. Glutamate Transporter Protein Subtypes Are Expressed Differentially during Rat CNS Development , 1997, The Journal of Neuroscience.
[476] Charles J. Wilson,et al. Spontaneous subthreshold membrane potential fluctuations and action potential variability of rat corticostriatal and striatal neurons in vivo. , 1997, Journal of neurophysiology.
[477] P. Haydon,et al. Gephyrin Regulates the Cell Surface Dynamics of Synaptic GABAA Receptors , 2005, The Journal of Neuroscience.
[478] Joshua L. Plotkin,et al. Synaptically driven state transitions in distal dendrites of striatal spiny neurons , 2011, Nature Neuroscience.
[479] L. Tremblay,et al. Activity of pallidal neurons in the monkey during dyskinesia induced by injection of bicuculline in the external pallidum , 1995, Neuroscience.
[480] J. Bolam,et al. Synaptic organisation of the basal ganglia , 2000, Journal of anatomy.
[481] S. Nagel,et al. Preserving cortico-striatal function: deep brain stimulation in Huntington’s disease , 2015, Front. Syst. Neurosci..
[482] J. Pilitsis,et al. Gap junction blockers attenuate beta oscillations and improve forelimb function in hemiparkinsonian rats , 2015, Experimental Neurology.
[483] Vivian M. Hernández,et al. Parvalbumin+ Neurons and Npas1+ Neurons Are Distinct Neuron Classes in the Mouse External Globus Pallidus , 2015, The Journal of Neuroscience.
[484] Charles J. Wilson,et al. Regulation of the timing and pattern of action potential generation in rat subthalamic neurons in vitro by GABA-A IPSPs. , 2002, Journal of neurophysiology.
[485] T. Klockgether,et al. Functional characterization and expression of thalamic GABAB receptors in a rodent model of Parkinson’s disease , 1999, Neuropharmacology.
[486] A. Panatier,et al. Astrocytic mGluR5 and the tripartite synapse , 2016, Neuroscience.
[487] Ian R. Wickersham,et al. Convergent cortical innervation of striatal projection neurons , 2013, Nature Neuroscience.
[488] R. Faull,et al. The distribution of GABAA-benzodiazepine receptors in the basal ganglia in Huntington's disease and in the quinolinic acid-lesioned rat. , 1993, Progress in brain research.
[489] J. Penney,et al. Evidence for a projection from the globus pallidus to the entopeduncular nucleus in the rat , 1991, Neuroscience Letters.
[490] A. Sahs,et al. Amantadine in Parkinson's disease , 1975, Neurology.
[491] Bert Sakmann,et al. Heteromeric NMDA Receptors: Molecular and Functional Distinction of Subtypes , 1992, Science.
[492] J. Dostrovsky,et al. Neuronal firing rates and patterns in the globus pallidus internus of patients with cervical dystonia differ from those with Parkinson's disease. , 2007, Journal of neurophysiology.
[493] Erwan Bezard,et al. Altered pallido‐pallidal synaptic transmission leads to aberrant firing of globus pallidus neurons in a rat model of Parkinson's disease , 2012, The Journal of physiology.
[494] N. Heintz. Gene Expression Nervous System Atlas (GENSAT) , 2004, Nature Neuroscience.
[495] O. Hornykiewicz,et al. Globus pallidus dopamine and Parkinson motor subtypes , 2008, Neurology.
[496] C. McIntyre,et al. Behavioral and neurophysiological evidence for the enhancement of cognitive control under dorsal pallidal deep brain stimulation in Huntington’s disease , 2014, Brain Structure and Function.
[497] W Wisden,et al. The distribution of thirteen GABAA receptor subunit mRNAs in the rat brain. III. Embryonic and postnatal development , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[498] J. Paul Bolam,et al. Pedunculopontine nucleus and basal ganglia: distant relatives or part of the same family? , 2004, Trends in Neurosciences.
[499] H. Kita,et al. Activation of group III metabotropic glutamate receptors presynaptically reduces both GABAergic and glutamatergic transmission in the rat globus pallidus , 2003, Neuroscience.
[500] Yasuyoshi Watanabe,et al. Unique expression patterns of 5‐HT2A and 5‐HT2C receptors in the rat brain during postnatal development: Western blot and immunohistochemical analyses , 2004, The Journal of comparative neurology.
[501] O. Hornykiewicz,et al. Homovanillic acid in different regions of the human brain: attempt at localizing central dopamine fibres. , 1968, Brain research.
[502] T. Hromádka,et al. Sparse Representation of Sounds in the Unanesthetized Auditory Cortex , 2008, PLoS biology.
[503] M. M. Morrow,et al. New Roles for the External Globus Pallidus in Basal Ganglia Circuits and Behavior , 2014, The Journal of Neuroscience.
[504] I. M. Stanford,et al. Dopamine D2 receptor mediated presynaptic inhibition of striatopallidal GABAA IPSCs in vitro , 2001, Neuropharmacology.
[505] N. Canteras,et al. Afferent connections of the subthalamic nucleus: a combined retrograde and anterograde horseradish peroxidase study in the rat , 1990, Brain Research.
[506] A. Triller,et al. Association of gephyrin with synaptic and extrasynaptic GABAa receptors varies during development in cultured hippocampal neurons , 2003, Molecular and Cellular Neuroscience.
[507] J. Bolam,et al. Subcellular localization of GABAB receptor subunits in rat globus pallidus , 2004, The Journal of comparative neurology.
[508] D. Joel,et al. Electrolytic lesion of globus pallidus ameliorates the behavioral and neurodegenerative effects of quinolinic acid lesion of the striatum: a potential novel treatment in a rat model of Huntington's disease , 1998, Brain Research.
[509] C. Gerfen,et al. Distribution of striatonigral and striatopallidal peptidergic neurons in both patch and matrix compartments: an in situ hybridization histochemistry and fluorescent retrograde tracing study , 1988, Brain Research.
[510] R. Shin,et al. Dopamine D4 Receptor-Induced Postsynaptic Inhibition of GABAergic Currents in Mouse Globus Pallidus Neurons , 2003, The Journal of Neuroscience.
[511] G. Sperk,et al. GABAA receptors: immunocytochemical distribution of 13 subunits in the adult rat brain , 2000, Neuroscience.
[512] G. Dawson,et al. Loss of the Major GABAA Receptor Subtype in the Brain Is Not Lethal in Mice , 2001, The Journal of Neuroscience.
[513] R. Llinás,et al. Electrophysiology of globus pallidus neurons in vitro. , 1994, Journal of neurophysiology.
[514] Jilly F. Evans,et al. Identification of a GABAB Receptor Subunit, gb2, Required for Functional GABAB Receptor Activity* , 1999, The Journal of Biological Chemistry.
[515] C. Gall,et al. Dopaminergic neurons in rat ventral midbrain express brain‐derived neurotrophic factor and neurotrophin‐3 mRNAs , 1994, The Journal of comparative neurology.
[516] S. Duty,et al. effect of unilateral 6-hydroxydopamine lesions of the nigrostriatal pathway on GABAA receptor subunit gene expression in the rodent basal ganglia and thalamus , 1999, Neuroscience.
[517] Serotonin in pallidal neuronal circuits: an immunocytochemical study in monkeys. , 1984, Advances in neurology.
[518] Y. Smith,et al. Group I Metabotropic Glutamate Receptors at GABAergic Synapses in Monkeys , 1999, The Journal of Neuroscience.
[519] J. Fallon,et al. Catecholamine innervation of the basal forebrain IV. Topography of the dopamine projection to the basal forebrain and neostriatum , 1978, The Journal of comparative neurology.
[520] N. Mizuno,et al. Direct projections from the globus pallidus to the midbrain and pons in the cat , 1992, Neuroscience Letters.
[521] C. Wilson,et al. Intracellular recording of identified neostriatal patch and matrix spiny cells in a slice preparation preserving cortical inputs. , 1989, Journal of neurophysiology.
[522] F. Mettler,et al. Nigrofugal connections in the primate brain , 1970, The Journal of comparative neurology.
[523] J. Hedreen. Tyrosine hydroxylase‐immunoreactive elements in the human globus pallidus and subthalamic nucleus , 1999, The Journal of comparative neurology.
[524] J. Rothwell,et al. Firing patterns of pallidal cells in Parkinsonian patients correlate with their pre‐pallidotomy clinical scores , 2000, Neuroreport.
[525] J. Marshall,et al. Population characteristics of preproenkephalin mRNA-containing neurons in the globus pallidus of the rat , 1999, Neuroscience Letters.
[526] M. E. Anderson,et al. Pallidal discharge related to the kinematics of reaching movements in two dimensions. , 1997, Journal of neurophysiology.
[527] J. Marshall,et al. Molecular, chemical, and anatomical characterization of globus pallidus dopamine D2 receptor mRNA‐containing neurons , 2004, Synapse.
[528] Y. Smith,et al. Neuroglial Plasticity at Striatal Glutamatergic Synapses in Parkinson's Disease , 2011, Front. Syst. Neurosci..
[529] Sachie K. Ogawa,et al. Whole-Brain Mapping of Direct Inputs to Midbrain Dopamine Neurons , 2012, Neuron.
[530] J. Walters,et al. Unilateral lesion of the nigrostriatal pathway decreases the firing rate and alters the firing pattern of globus pallidus neurons in the rat , 1988, Synapse.
[531] T. Wichmann,et al. Metabotropic glutamate receptor 4 in the basal ganglia of parkinsonian monkeys: Ultrastructural localization and electrophysiological effects of activation in the striatopallidal complex , 2013, Neuropharmacology.
[532] H. Moore,et al. Dopamine D2 Receptors Regulate the Anatomical and Functional Balance of Basal Ganglia Circuitry , 2014, Neuron.
[533] A. Wenzel,et al. Developmental and Regional Expression of NMDA Receptor Subtypes Containing the NR2D Subunit in Rat Brain , 1996, Journal of neurochemistry.
[534] S. Hersch,et al. The dopamine transporter: immunochemical characterization and localization in brain , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[535] M. E. Anderson,et al. An electrophysiological characterization of projections from the pedunculopontine area to entopeduncular nucleus and globus pallidus in the cat , 2004, Experimental Brain Research.
[536] Daniel K. Leventhal,et al. Dissociable effects of dopamine on learning and performance within sensorimotor striatum. , 2014, Basal ganglia.
[537] M. Delong,et al. The primate globus pallidus: neuronal activity related to direction of movement , 2004, Experimental Brain Research.
[538] Michael M. Halassa,et al. The tripartite synapse: roles for gliotransmission in health and disease. , 2007, Trends in molecular medicine.
[539] T. Pasik,et al. A Golgi study of neuronal types in the neostriatum of monkeys , 1976, Brain Research.
[540] Y. Smith,et al. The subthalamic nucleus and the external pallidum: two tightly interconnected structures that control the output of the basal ganglia in the monkey , 1996, Neuroscience.
[541] S. Oliet,et al. Gliotransmitters Travel in Time and Space , 2014, Neuron.
[542] H. Lester,et al. Nicotinic Receptor Subtype-Selective Circuit Patterns in the Subthalamic Nucleus , 2015, The Journal of Neuroscience.
[543] W. Hauber,et al. Dopaminergic innervation of the rat globus pallidus characterized by microdialysis and immunohistochemistry , 2003, Experimental Brain Research.
[544] P. Somogyi,et al. Projection of neostriatal spiny neurons to the substantia nigra. Application of a combined golgi-staining and horse-radish peroxidase transport procedure at both light and electron microscopic levels , 1979, Brain Research.
[545] P. Molinoff,et al. Quantitative autoradiographic localization of the D1 and D2 subtypes of dopamine receptors in rat brain , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[546] G. Percheron,et al. A Golgi analysis of the primate globus pallidus. I. Inconstant processes of large neurons, other neuronal types, and afferent axons , 1984, The Journal of comparative neurology.
[547] J. Bolam,et al. Dopamine regulates the impact of the cerebral cortex on the subthalamic nucleus–globus pallidus network , 2001, Neuroscience.
[548] H. Kita,et al. Down‐regulation of metabotropic glutamate receptor 1α in globus pallidus and substantia nigra of parkinsonian monkeys , 2005, The European journal of neuroscience.
[549] L. Metman,et al. Amantadine as treatment for dyskinesias and motor fluctuations in Parkinson's disease , 1998, Neurology.
[550] Á. Pazos,et al. 5-HT1B receptor binding in degenerative movement disorders , 1998, Brain Research.
[551] S. Bressman,et al. Genetics and treatment of dystonia. , 2009, Neurologic clinics.
[552] K. Clark,et al. The role of the subthalamic nucleus in the response of globus pallidus neurons to stimulation of the prelimbic and agranular frontal cortices in rats , 2004, Experimental Brain Research.
[553] P. Bonaventure,et al. Detailed mapping of serotonin 5-HT1B and 5-HT1D receptor messenger RNA and ligand binding sites in guinea-pig brain and trigeminal ganglion: clues for function , 1997, Neuroscience.
[554] J. Palacios,et al. Visualization of a dopamine D1 receptor mRNA in human and rat brain. , 1991, Brain research. Molecular brain research.
[555] A. MacAskill,et al. Subcellular connectivity underlies pathway-specific signaling in the nucleus accumbens , 2012, Nature Neuroscience.
[556] P. Headley,et al. NMDA receptor antagonists as analgesics: focus on the NR2B subtype. , 2001, Trends in pharmacological sciences.
[557] B Bioulac,et al. Ratio of inhibited-to-activated pallidal neurons decreases dramatically during passive limb movement in the MPTP-treated monkey. , 2000, Journal of neurophysiology.
[558] K. Neve,et al. Extrastriatal dopamine D2 receptors: distribution, pharmacological characterization and region-specific regulation by clozapine. , 1992, The Journal of pharmacology and experimental therapeutics.
[559] H. Bernheimer. Distribution of Homovanillic Acid in the Human Brain , 1964, Nature.
[560] A. Parent,et al. The Nigrostriatal Pathway in the Rat: A Single-Axon Study of the Relationship between Dorsal and Ventral Tier Nigral Neurons and the Striosome/Matrix Striatal Compartments , 2001, The Journal of Neuroscience.
[561] J. Dostrovsky,et al. Differential neuronal activity in segments of globus pallidus in Parkinson's disease patients , 1994, Neuroreport.
[562] Bettina C. Schwab,et al. Synchrony in Parkinson's disease: importance of intrinsic properties of the external globus pallidus , 2013, Front. Syst. Neurosci..
[563] Differential role of GABAA and GABAB receptors in two distinct output stations of the rat striatum: studies on the substantia nigra pars reticulata and the globus pallidus , 2010, Neuroscience.
[564] B. Bean,et al. Subthreshold Sodium Currents and Pacemaking of Subthalamic Neurons Modulation by Slow Inactivation , 2003, Neuron.
[565] T. Wichmann,et al. Localization and function of GABA transporters in the globus pallidus of parkinsonian monkeys , 2010, Experimental Neurology.
[566] J. Thibault,et al. Ultrastructural morphology of dopaminergic nerve terminals and synapses in the striatum of the rat using tyrosine hydroxylase immunocytochemistry: A topographical study , 1984, Brain Research Bulletin.
[567] J. Palacios,et al. Visualization of dopamine D1, D2 and D3 receptor mRNA's in human and rat brain , 1992, Neurochemistry International.
[568] Peter Brown,et al. Parkinsonian Beta Oscillations in the External Globus Pallidus and Their Relationship with Subthalamic Nucleus Activity , 2008, The Journal of Neuroscience.
[569] Todor V. Gerdjikov,et al. A Major External Source of Cholinergic Innervation of the Striatum and Nucleus Accumbens Originates in the Brainstem , 2014, The Journal of Neuroscience.
[570] Philip A. Starr,et al. Single unit “pauser” characteristics of the globus pallidus pars externa distinguish primary dystonia from secondary dystonia and Parkinson's disease , 2009, Experimental Neurology.
[571] T. Powell,et al. The structure of the caudate nucleus of the cat: light and electron microscopy. , 1971, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[572] P. Somogyi,et al. The gamma 2 subunit of the GABAA receptor is concentrated in synaptic junctions containing the alpha 1 and beta 2/3 subunits in hippocampus, cerebellum and globus pallidus. , 1996, Neuropharmacology.
[573] A. Levey,et al. D1 and D2 dopamine receptor mRNA in rat brain. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[574] J. Bolam,et al. A Single-Cell Analysis of Intrinsic Connectivity in the Rat Globus Pallidus , 2007, The Journal of Neuroscience.
[575] M. Nedergaard,et al. Artifact versus reality—How astrocytes contribute to synaptic events , 2012, Glia.
[576] J. Isaacson,et al. Odor representations in mammalian cortical circuits , 2010, Current Opinion in Neurobiology.
[577] J. Benson,et al. The GABAA receptors. From subunits to diverse functions. , 1996, Ion channels.
[578] A. Graybiel. The Basal Ganglia and Chunking of Action Repertoires , 1998, Neurobiology of Learning and Memory.
[579] Thomas Wichmann,et al. Deep brain stimulation for movement and other neurologic disorders , 2012, Annals of the New York Academy of Sciences.
[580] Bernhard A. Kaplan,et al. SYSTEMS NEUROSCIENCE ORIGINAL RESEARCH ARTICLE , 2011 .
[581] J. Marshall,et al. Glutamic Acid Decarboxylase 67 mRNA Regulation in Two Globus Pallidus Neuron Populations by Dopamine and the Subthalamic Nucleus , 2004, The Journal of Neuroscience.
[582] P. Calabresi,et al. Direct and indirect pathways of basal ganglia: a critical reappraisal , 2014, Nature Neuroscience.
[583] Alon Korngreen,et al. Electrophysiological Characteristics of Globus Pallidus Neurons , 2010, PloS one.
[584] W. Yung,et al. Rotational behavior and electrophysiological effects induced by GABAB receptor activation in rat globus pallidus , 2002, Neuroscience.
[585] J. Joyce,et al. Distribution of Dopamine D3 Receptor Expressing Neurons in the Human Forebrain: Comparison with D2 Receptor Expressing Neurons , 1999, Neuropsychopharmacology.
[586] D. Kullmann,et al. Tonically active GABAA receptors: modulating gain and maintaining the tone , 2004, Trends in Neurosciences.
[587] G. M. Peterson,et al. Anterograde and retrograde axonal transport of Phaseolus vulgaris leucoagglutinin (PHA-L) from the globus pallidus to the striatum of the rat , 1988, Journal of Neuroscience Methods.
[588] A. Parent,et al. Projection from the external pallidum to the reticular thalamic nucleus in the squirrel monkey , 1991, Brain Research.
[589] G. Percheron,et al. A Golgi analysis of the primate globus pallidus. III. Spatial organization of the striato‐pallidal complex , 1984, The Journal of comparative neurology.
[590] P Pasik,et al. A Golgi and ultrastructural study of the monkey globus pallidus , 1982, The Journal of comparative neurology.
[591] D. Oorschot. Total number of neurons in the neostriatal, pallidal, subthalamic, and substantia nigral nuclei of the rat basal ganglia: A stereological study using the cavalieri and optical disector methods , 1996, The Journal of comparative neurology.
[592] B Bioulac,et al. Effects of l-DOPA on neuronal activity of the globus pallidus externalis (GPe) and globus pallidus internalis (GPi) in the MPTP-treated monkey , 1998, Brain Research.
[593] H. Steinbusch,et al. Motor and cognitive improvement by deep brain stimulation in a transgenic rat model of Huntington's disease , 2006, Neuroscience Letters.
[594] T. Wichmann,et al. Extrastriatal D2-like receptors modulate basal ganglia pathways in normal and Parkinsonian monkeys. , 2012, Journal of neurophysiology.
[595] M. Starr,et al. Stimulation of basal and l-DOPA-induced motor activity by glutamate antagonists in animal models of Parkinson's disease , 1997, Neuroscience & Biobehavioral Reviews.
[596] Robert M. Kessler,et al. Identification of extrastriatal dopamine D2 receptors in post mortem human brain with [125I]epidepride , 1993, Brain Research.
[597] Rafal Bogacz,et al. Distinct Developmental Origins Manifest in the Specialized Encoding of Movement by Adult Neurons of the External Globus Pallidus , 2015, Neuron.
[598] H. Bergman,et al. Reversal of experimental parkinsonism by lesions of the subthalamic nucleus. , 1990, Science.
[599] H. Kita,et al. The morphology of globus pallidus projection neurons in the rat: an intracellular staining study , 1994, Brain Research.
[600] D James Surmeier,et al. Nav1.6 Sodium Channels Are Critical to Pacemaking and Fast Spiking in Globus Pallidus Neurons , 2007, The Journal of Neuroscience.
[601] D James Surmeier,et al. Enhancement of Excitatory Synaptic Integration by GABAergic Inhibition in the Subthalamic Nucleus , 2005, The Journal of Neuroscience.
[602] D. Standaert,et al. Immunohistochemical localization of metabotropic glutamate receptors mGluR1a and mGluR2/3 in the rat basal ganglia , 1998, The Journal of comparative neurology.
[603] Charles J. Wilson,et al. Calcium-Activated SK Channels Influence Voltage-Gated Ion Channels to Determine the Precision of Firing in Globus Pallidus Neurons , 2009, The Journal of Neuroscience.
[604] Hagai Bergman,et al. Dopamine Replacement Therapy Reverses Abnormal Synchronization of Pallidal Neurons in the 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine Primate Model of Parkinsonism , 2002, The Journal of Neuroscience.
[605] T. Wichmann,et al. Localization and Function of GABA Transporters GAT-1 and GAT-3 in the Basal Ganglia , 2011, Front. Syst. Neurosci..
[606] R. Mostany,et al. Autoradiographic characterisation of [35S]GTPγS binding stimulation mediated by 5-HT1B receptor in postmortem human brain , 2005, Neuropharmacology.
[607] M. Barrot. The ventral tegmentum and dopamine: A new wave of diversity , 2014, Neuroscience.
[608] Anatol C. Kreitzer,et al. Distinct Roles of GABAergic Interneurons in the Regulation of Striatal Output Pathways , 2010, The Journal of Neuroscience.
[609] H. Fibiger,et al. Demonstration of a pallidostriatal pathway by retrograde transport of HRP-labeled lectin , 1981, Brain Research.
[610] F. Horak,et al. Influence of the globus pallidus on arm movements in monkeys. III. Timing of movement-related information. , 1985, Journal of neurophysiology.
[611] Kuldeep Shetty,et al. Deep brain stimulation for movement disorders , 2018, Neurology India.
[612] S. Norton. Hyperactive behavior of rats after lesions of the globus pallidus , 1976, Brain Research Bulletin.
[613] Y. Smith,et al. Metabotropic glutamate receptor 2 modulates excitatory synaptic transmission in the rat globus pallidus , 2005, Neuropharmacology.
[614] R. Glennon,et al. Autoradiographic characterization of (+-)-1-(2,5-dimethoxy-4-[125I] iodophenyl)-2-aminopropane ([125I]DOI) binding to 5-HT2 and 5-HT1c receptors in rat brain. , 1990, The Journal of pharmacology and experimental therapeutics.
[615] R. Dingledine,et al. The glutamate receptor ion channels. , 1999, Pharmacological reviews.