Physiology and Pharmacology of Striatal Neurons

The functional anatomy of basal ganglia disorders

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Primate models of movement disorders of basal ganglia origin

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NEURAL MECHANISMS OF ADDICTION: The Role of Reward-Related Learning and Memory

Hyman, S. E., Malenka, R. C., & Nestler, E. J. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.113009 · Cited by 2,647

The role of the basal ganglia in habit formation

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Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamo-cortical loop

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A gene expression atlas of the central nervous system based on bacterial artificial chromosomes

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The molecular logic of endocannabinoid signalling

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Habits, Rituals, and the Evaluative Brain

Graybiel, A. M. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112851 · Cited by 1,697

Multiple dopamine functions at different time courses

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The organization of the projection from the cerebral cortex to the striatum in the rat

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Morphological changes of glutamatergic synapses in animal models of Parkinson’s disease

Villalba, R. M., Mathai, A., & Smith, Y. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00117 · Cited by 70

Cell type–specific spatial and functional coupling between mammalian brain Kv2.1 K+ channels and ryanodine receptors

Mandikian, D., Bocksteins, E., Parajuli, L. K., Bishop, H. I., Cerda, O., Shigemoto, R., & Trimmer, J. S. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23641 · Cited by 67

Synapse-specific opioid modulation of thalamo-cortico-striatal circuits

Birdsong, W. T., Jongbloets, B. C., Engeln, K. A., Wang, D., Scherrer, G., & Mao, T. (2019) · eLife · doi:10.7554/elife.45146 · Cited by 67

Cerebellar and Striatal Implications in Autism Spectrum Disorders: From Clinical Observations to Animal Models

Thabault, M., Turpin, V., Maïsterrena, A., Jaber, M., Egloff, M., & Galvan, L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042294 · Cited by 74

Spontaneous Synaptic Activation of Muscarinic Receptors by Striatal Cholinergic Neuron Firing

Mamaligas, A. A., & Ford, C. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.021 · Cited by 70

Molecular and cellular mechanisms of dopamine-mediated behavioral plasticity in the striatum

Cerovic, M., d’Isa, R., Tonini, R., & Brambilla, R. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.06.013 · Cited by 77

Singular Location and Signaling Profile of Adenosine A2A-Cannabinoid CB1 Receptor Heteromers in the Dorsal Striatum

Moreno, E., Chiarlone, A., Medrano, M., Puigdellívol, M., Bibič, L., Howell, L. A., Resel, E., Puente, N., Casarejos, M. J., Perucho, J., et al. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.12 · Cited by 66

Dopamine neuron glutamate cotransmission evokes a delayed excitation in lateral dorsal striatal cholinergic interneurons

Chuhma, N., Mingote, S., Yetnikoff, L., Kalmbach, A., Ma, T. C., Ztaou, S., Siena, A.-C., Tepler, S., Poulin, J.-F., Ansorge, M. S., et al. (2018) · eLife · doi:10.7554/elife.39786 · Cited by 66

Dopaminergic Regulation of Striatal Interneurons in Reward and Addiction: Focus on Alcohol

Clarke, R. B. C., & Adermark, L. (2015) · Neural Plasticity · doi:10.1155/2015/814567 · Cited by 68

LRRK2 mouse models: dissecting the behavior, striatal neurochemistry and neurophysiology of PD pathogenesis

Volta, M., & Melrose, H. L. (2017) · Biochemical Society Transactions · doi:10.1042/bst20160238 · Cited by 63

Altered dopaminergic pathways and therapeutic effects of intranasal dopamine in two distinct mouse models of autism

Chao, O. Y.-H., Pathak, S. S., Zhang, H., Dunaway, N., Li, J., Mattern, C., Nikolaus, S., Huston, J. P., & Yang, Y. (2020) · Molecular Brain · doi:10.1186/s13041-020-00649-7 · Cited by 62

A spiking Basal Ganglia model of synchrony, exploration and decision making

Mandali, A., Rengaswamy, M., Chakravarthy, V. S., & Moustafa, A. A. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00191 · Cited by 64

Direct and GABA‐mediated indirect effects of nicotinic ACh receptor agonists on striatal neurones

Luo, R., Janssen, M. J., Partridge, J. G., & Vicini, S. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.241786 · Cited by 62

Differences in social interaction- vs. cocaine reward in mouse vs. rat

Kummer, K. K., Hofhansel, L., Barwitz, C. M., Schardl, A., Prast, J. M., Salti, A., Rawas, R. E., & Zernig, G. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00363 · Cited by 62

Integration and propagation of somatosensory responses in the corticostriatal pathway: an intracellular study in vivo

Pidoux, M., Mahon, S., Deniau, J., & Charpier, S. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.199646 · Cited by 60

Macromolecular Composition Dictates Receptor and G Protein Selectivity of Regulator of G Protein Signaling (RGS) 7 and 9-2 Protein Complexes in Living Cells

Masuho, I., Xie, K., & Martemyanov, K. A. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.462283 · Cited by 60

The disrupted basal ganglia and behavioural control: An integrative cross-domain perspective of spontaneous stereotypy

McBride, S. D., & Parker, M. O. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.05.057 · Cited by 63

Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia

Song, C., Bernhard, D., Bolarinwa, C., Hess, E. J., Smith, Y., & Jinnah, H. A. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2013.01.008 · Cited by 60

The anatomy of the caudal zona incerta in rodents and primates

WATSON, C. R. R., Lind, C. R. P., & Thomas, M. G. (2013) · Journal of Anatomy · doi:10.1111/joa.12132 · Cited by 59

Corticostriatal circuit dysfunction in Huntington‘s disease: intersection of glutamate, dopamine and calcium

Miller, B., & Борисович, Б. И. (2010) · Future Neurology · doi:10.2217/fnl.10.41 · Cited by 61

Review: Electrophysiology of Basal Ganglia and Cortex in Models of Parkinson Disease

Ellens, D. J., & Leventhal, D. (2013) · Journal of Parkinson s Disease · doi:10.3233/jpd-130204 · Cited by 58

Phasic Dopaminergic Activity Exerts Fast Control of Cholinergic Interneuron Firing via Sequential NMDA, D2, and D1 Receptor Activation

Wieland, S., Du, D., Oswald, M. J., Parlato, R., Köhr, G., & Kelsch, W. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1175-14.2014 · Cited by 61

Habit formation: Implications for alcoholism research

O'Tousa, D. S., & Grahame, N. J. (2014) · Alcohol · doi:10.1016/j.alcohol.2014.02.004 · Cited by 58

A brief form of the Affective Neuroscience Personality Scales.

Barrett, F. S., Robins, R. W., & Janata, P. (2013) · Psychological Assessment · doi:10.1037/a0032576 · Cited by 58

Singing-Related Neural Activity Distinguishes Four Classes of Putative Striatal Neurons in the Songbird Basal Ganglia

Goldberg, J. H., & Fee, M. S. (2010) · Journal of Neurophysiology · doi:10.1152/jn.01038.2009 · Cited by 58

Cooperative synaptic and intrinsic plasticity in a disynaptic limbic circuit drive stress-induced anhedonia and passive coping in mice

Pignatelli, M., Tejeda, H. A., Barker, D. J., Bontempi, L., Wu, J., Lopez, A., Ribeiro, S. P., Lucantonio, F., Parise, E. M., Torres‐Berrío, A., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0686-8 · Cited by 60

Synaptic Targets of 9-Tetrahydrocannabinol in the Central Nervous SystemPreprint

Hoffman, A. F., & Lupica, C. R. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a012237 · Cited by 60

Nicotinic and opioid receptor regulation of striatal dopamine D2-receptor mediated transmission

Mamaligas, A. A., Cai, Y., & Ford, C. (2016) · Scientific Reports · doi:10.1038/srep37834 · Cited by 57

Parvalbumin Interneurons of the Mouse Nucleus Accumbens are Required For Amphetamine-Induced Locomotor Sensitization and Conditioned Place Preference

Wang, X., Gallegos, D. A., Pogorelov, V. M., O’Hare, J. K., Calakos, N., Wetsel, W. C., & West, A. E. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.178 · Cited by 56

A synaptomic analysis reveals dopamine hub synapses in the mouse striatum

Paget-Blanc, V., Pfeffer, M. E., Pronot, M., Lapios, P., Angelo, M., Walle, R., Cordelières, F. P., Levet, F., Claverol, S., Lacomme, S., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-30776-9 · Cited by 60

Neurobiological mechanisms associated with antipsychotic drug-induced dystonia

LOONEN, A. J. M., & Ivanova, S. А. (2020) · Journal of Psychopharmacology · doi:10.1177/0269881120944156 · Cited by 55

R7BP Complexes With RGS9-2 and RGS7 in the Striatum Differentially Control Motor Learning and Locomotor Responses to Cocaine

Anderson, G. R., Cao, Y., Davidson, S., Truong, H., Pravetoni, M., Thomas, M. J., Wickman, K., Giesler, G. J., & Martemyanov, K. A. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.212 · Cited by 54

Cannabinoid, melanocortin and opioid receptor expression on DRD1 and DRD2 subpopulations in rat striatum

Ophuis, R. J. A. O., Boender, A. J., van Rozen, A. J., & Adan, R. A. H. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00014 · Cited by 54

Chronic alcohol drinking persistently suppresses thalamostriatal excitation of cholinergic neurons to impair cognitive flexibility

Ma, T., Huang, Z., Xie, X., Cheng, Y., Zhuang, X., Childs, M., Gangal, H., Wang, X., Smith, L., Smith, R., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci154969 · Cited by 53

Hippocampal-Evoked Feedforward Inhibition in the Nucleus Accumbens

Scudder, S. L., Baimel, C., Macdonald, E. E., & Carter, A. G. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1971-18.2018 · Cited by 56

Nucleus accumbens dichotomically controls social dominance in male mice

Shan, Q., Hu, Y., Chen, S., & Tian, Y. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01220-1 · Cited by 50

Deep brain stimulation in the subthalamic nucleus for Parkinson’s disease can restore dynamics of striatal networks

Adam, E. M., Brown, E. N., Kopell, N., & McCarthy, M. M. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2120808119 · Cited by 51

Neurobiologic Rationale for Treatment of Apathy in Alzheimer's Disease With Methylphenidate

van Dyck, C. H., Arnsten, A. F. T., Padala, P. R., Brawman‐Mintzer, O., Lerner, A. J., Porsteinsson, A. P., Scherer, R. W., Levey, A. I., Herrmann, N., Jamil, N., et al. (2020) · American Journal of Geriatric Psychiatry · doi:10.1016/j.jagp.2020.04.026 · Cited by 53

Synergistic Roles for G-protein γ3 and γ7 Subtypes in Seizure Susceptibility as Revealed in Double Knock-out Mice

Schwindinger, W. F., Mirshahi, U. L., Baylor, K. A., Sheridan, K. M., Stauffer, A. M., Usefof, S., Stecker, M. M., Mirshahi, T., & Robishaw, J. D. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.308395 · Cited by 49

Downregulation of cannabinoid receptor 1 from neuropeptide Y interneurons in the basal ganglia of patients with Huntington's disease and mouse models

Horne, E. A., Coy, J. W., Swinney, K., Fung, S., Cherry, A. E., Marrs, W., Naydenov, A. V., Lin, Y. H., Sun, X., Keene, C. D., et al. (2012) · European Journal of Neuroscience · doi:10.1111/ejn.12045 · Cited by 49

Integrated anatomical and physiological mapping of striatal afferent projections

Choi, K., Holly, E. N., Davatolhagh, M. F., Beier, K. T., & Fuccillo, M. V. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13829 · Cited by 51

Phasic Dopamine Modifies Sensory-Driven Output of Striatal Neurons through Synaptic Plasticity

Wieland, S., Schindler, S., Huber, C., Köhr, G., Oswald, M. J., & Kelsch, W. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0127-15.2015 · Cited by 47

Desynchronization of Fast-Spiking Interneurons Reduces β-Band Oscillations and Imbalance in Firing in the Dopamine-Depleted Striatum

Damodaran, S., Cressman, J. R., Jȩdrzejewski-Szmek, Z., & Blackwell, K. T. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3490-14.2015 · Cited by 46

Coordinated Regulation of Synaptic Plasticity at Striatopallidal and Striatonigral Neurons Orchestrates Motor Control

Trusel, M., Cavaccini, A., Gritti, M., Greco, B., Saintot, P., Nazzaro, C., Cerovic, M., Morella, I., Brambilla, R., & Tonini, R. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.10.009 · Cited by 50

Recurrent Implication of Striatal Cholinergic Interneurons in a Range of Neurodevelopmental, Neurodegenerative, and Neuropsychiatric Disorders

Poppi, L. A., Ho-Nguyen, K.-T., Shi, A., Daut, C. T., & Tischfield, M. A. (2021) · Cells · doi:10.3390/cells10040907 · Cited by 47

Cell-type-specific regulation of neuronal intrinsic excitability by macroautophagy

Lieberman, O. J., Frier, M. D., McGuirt, A. F., Griffey, C. J., Rafikian, E. E., Yang, M., Yamamoto, A., Borgkvist, A., Santini, E., & Sulzer, D. (2020) · eLife · doi:10.7554/elife.50843 · Cited by 45

Relationships and Interactions between Ionotropic Glutamate Receptors and Nicotinic Receptors in the CNS

Stone, T. W. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.06.007 · Cited by 49

Astrocyte Gi-GPCR signaling corrects compulsive-like grooming and anxiety-related behaviors in Sapap3 knockout mice

Soto, J. S., Neupane, C., Kaur, M., Pandey, V., Wohlschlegel, J. A., & Khakh, B. S. (2024) · Neuron · doi:10.1016/j.neuron.2024.07.019 · Cited by 43

Consistent Injury to Medium Spiny Neurons and White Matter in the Mouse Striatum after Prolonged Transient Global Cerebral Ischemia

Yoshioka, H., Niizuma, K., Katsu, M., Sakata, H., Okami, N., & Chan, P. H. (2011) · Journal of Neurotrauma · doi:10.1089/neu.2010.1662 · Cited by 43

Endocannabinoids exert CB 1 receptor-mediated neuroprotective effects in models of neuronal damage induced by HIV-1 Tat protein

Xu, C., Hermes, D. J., Nwanguma, B., Jacobs, I. R., Mackie, K., Mukhopadhyay, S., Lichtman, A. H., Ignatowska-Jankowska, B. M., & Fitting, S. (2017) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2017.07.003 · Cited by 43

The subcortical belly of sleep: New possibilities in neuromodulation of basal ganglia?

Hasegawa, H., Selway, R., Gnoni, V., Beniczky, S., Williams, S., Kryger, M. H., Ferini‐Strambi, L., Goadsby, P. J., Leschziner, G. D., Ashkan, K., et al. (2020) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2020.101317 · Cited by 43

Different correlation patterns of cholinergic and GABAergic interneurons with striatal projection neurons

Adler, A., Katabi, S., Finkes, I., Prut, Y., & Bergman, H. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00047 · Cited by 41

Neurobiology of pain, interoception and emotional response: lessons from nerve growth factor‐dependent neurons

Indo, Y. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12448 · Cited by 41

Metaplasticity at the addicted tetrapartite synapse: A common denominator of drug induced adaptations and potential treatment target for addiction

Neuhofer, D., & Kalivas, P. W. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.02.007 · Cited by 41

Differences between Dorsal and Ventral Striatum in the Sensitivity of Tonically Active Neurons to Rewarding Events

Marche, K., Martel, A., & Apicella, P. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00052 · Cited by 39

Complete representation of action space and value in all dorsal striatal pathways

Weglage, M., Wärnberg, E., Lazaridis, I., Calvigioni, D., Tzortzi, O., & Meletis, K. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109437 · Cited by 44

Continuous cholinergic-dopaminergic updating in the nucleus accumbens underlies approaches to reward-predicting cues

Skirzewski, M., Princz‐Lebel, O., German‐Castelan, L., Crooks, A. M., Kim, K., Tarnow, S. H., Reichelt, A. C., Memar, S., Palmer, D. D., Li, Y., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-35601-x · Cited by 41

Applied neurophysiology of the horse; implications for training, husbandry and welfare

McBride, S. D., Parker, M. O., Roberts, K., & Hemmings, A. (2017) · Applied Animal Behaviour Science · doi:10.1016/j.applanim.2017.02.014 · Cited by 43

Mouse Models of Neurodevelopmental Disease of the Basal Ganglia and Associated Circuits

Pappas, S. S., Leventhal, D., Albin, R. L., & Dauer, W. T. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-397920-9.00001-9 · Cited by 41

Exercise-Induced Fatigue Impairs Bidirectional Corticostriatal Synaptic Plasticity

Ma, J., Chen, H., Liu, X., Zhang, L., & Qiao, D. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00014 · Cited by 37

The dopamine neuron synaptic map in the striatum

Chuhma, N., Oh, S. J., & Rayport, S. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112204 · Cited by 37

Isoforms of the neuronal glutamate transporter gene, SLC1A1/EAAC1, negatively modulate glutamate uptake: relevance to obsessive-compulsive disorder

Porton, B., Greenberg, B. D., Askland, K., Serra, L. M., Gesmonde, J., Rudnick, G., Rasmussen, S. A., & Kao, H.-T. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.35 · Cited by 36

Connectivity of the corticostriatal and thalamostriatal systems in normal and parkinsonian states: An update

Martel, A., & Galván, A. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105878 · Cited by 36

Reduced Binding Potential of GABA-A/Benzodiazepine Receptors in Individuals at Ultra-high Risk for Psychosis: An [18F]-Fluoroflumazenil Positron Emission Tomography Study

Kang, J. I., Park, H., Kim, S. J., Kim, K. R., Lee, S., Lee, E. M., An, S. K., Kwon, J. S., & Lee, J. D. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt052 · Cited by 36

The Contribution of NMDA Receptor Signaling in the Corticobasal Ganglia Reward Network to Appetitive Pavlovian Learning

Parker, J. G., Beutler, L. R., & Palmiter, R. D. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2411-11.2011 · Cited by 37

Temporal Learning Among Prefrontal and Striatal Ensembles

Emmons, E. B., Tunes, G. C., Choi, J., Bruce, R. A., Weber, M. A., Kim, Y.-C., & Narayanan, N. (2020) · Cerebral Cortex Communications · doi:10.1093/texcom/tgaa058 · Cited by 35

Quantifying the inverted U: A meta-analysis of prefrontal dopamine, D1 receptors, and working memory.

Weber, M. A., Conlon, M. M., Stutt, H. R., Wendt, L. H., Eyck, P. T., & Narayanan, N. S. (2022) · Behavioral Neuroscience · doi:10.1037/bne0000512 · Cited by 38

Dynorphin and κ-Opioid Receptor Dysregulation in the Dopaminergic Reward System of Human Alcoholics

Bazov, I., Sarkisyan, D., Kononenko, O., Watanabe, H., Yakovleva, T., Hansson, A. C., Sommer, W. H., Spanagel, R., & Bakalkin, G. Y. (2018) · Molecular Neurobiology · doi:10.1007/s12035-017-0844-4 · Cited by 34

The acid-sensing ion channel ASIC1a mediates striatal synapse remodeling and procedural motor learning

Yu, Z., Wu, Y., Wang, Y., Liu, D.-S., Song, X.-L., Jiang, Q., Li, Y., Zhang, S., Xu, N., Zhu, M. X., et al. (2018) · Science Signaling · doi:10.1126/scisignal.aar4481 · Cited by 34

Disentangling the diverse roles of dopamine D2 receptors in striatal function and behavior

Gallo, E. F. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.01.022 · Cited by 38

Dopamine depletion selectively disrupts interactions between striatal neuron subtypes and LFP oscillations

Zemel, D., Gritton, H. J., Cheung, C., Shankar, S., Kramer, M., & Han, X. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110265 · Cited by 34

The percentage of interneurons in the dorsal striatum of the rat, cat, monkey and human: A critique of the evidence

Oorschot, D. E. (2012) · Basal Ganglia · doi:10.1016/j.baga.2012.11.001 · Cited by 34

Mitofusin-2 in nucleus accumbens D2-MSNs regulates social dominance and neuronal function

Ghosal, S., Gebara, E., Ramos‐Fernández, E., Chioino, A., Grosse, J., de Suduiraut, I. G., Zanoletti, O., Schneider, B. L., Antonio Zorzano, A., Astori, S., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112776 · Cited by 33

How Basal Ganglia Outputs Generate Behavior

Yin, H. H. (2014) · Advances in Neuroscience · doi:10.1155/2014/768313 · Cited by 34

A cell autonomous torsinA requirement for cholinergic neuron survival and motor control

Pappas, S. S., Li, J., LeWitt, T. M., Kim, J.-K., Monani, U. R., & Dauer, W. T. (2018) · eLife · doi:10.7554/elife.36691 · Cited by 33

Cholinergic Transmission at Muscarinic Synapses in the Striatum Is Driven Equally by Cortical and Thalamic Inputs

Mamaligas, A. A., Barcomb, K., & Ford, C. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.06.077 · Cited by 33

Striatal cholinergic interneurons regulate cognitive and affective dysfunction in partially dopamine‐depleted mice

Ztaou, S., Lhost, J., Watabe, I., Torromino, G., & Amalric, M. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14153 · Cited by 33

γ-Hydroxybutyric Acid (GHB) Is Not an Agonist of Extrasynaptic GABAA Receptors

Connelly, W. M., Errington, A. C., & Crunelli, V. (2013) · PLoS ONE · doi:10.1371/journal.pone.0079062 · Cited by 32

Striatal GABA ergic interneuron dysfunction in the Q175 mouse model of Huntington's disease

Holley, S. M., Galvan, L., Kamdjou, T., Cepeda, C., & Levine, M. S. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14283 · Cited by 36

Loss of Tsc1 from striatal direct pathway neurons impairs endocannabinoid-LTD and enhances motor routine learning

Benthall, K. N., Cording, K. R., Agopyan-Miu, A. H. C. W., Wong, C. D., Chen, E. Y., & Bateup, H. S. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109511 · Cited by 33

SOX2 is essential for astrocyte maturation and its deletion leads to hyperactive behavior in mice

Wang, Y., Zhang, S., Lan, Z., Doan, V., Kim, B., Liu, S., Zhu, M., Hull, V. L., Rihani, S., Zhang, C., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111842 · Cited by 32

The basal ganglia

Braunlich, K., & Seger, C. A. (2012) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1217 · Cited by 33

An embryonic culture system for the investigation of striatal medium spiny neuron dendritic spine development and plasticity

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Spatial memory, plasticity and nucleus accumbens

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