Physiology and Pharmacology of Striatal Neurons

The functional anatomy of basal ganglia disorders

Albin, R. L., Young, A. B., & Penney, J. B. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90074-x · Cited by 5,353

Primate models of movement disorders of basal ganglia origin

DeLong, M. R. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90110-v · Cited by 3,824

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

Yin, H. H., & Knowlton, B. J. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1919 · Cited by 2,402

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

Parent, A., & Hazrati, L.-N. (1995) · Brain Research Reviews · doi:10.1016/0165-0173(94)00007-c · Cited by 2,161

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

Gong, S., Zheng, C., Doughty, M. L., Losos, K., Didkovsky, N., Schambra, U. B., Nowak, N. J., Joyner, A., Leblanc, G., Hatten, M. E., et al. (2003) · Nature · doi:10.1038/nature02033 · Cited by 2,108

The molecular logic of endocannabinoid signalling

Piomelli, D. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1247 · Cited by 1,957

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

Schultz, W. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135722 · Cited by 1,415

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

McGeorge, A. J., & Faull, R. L. M. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90128-0 · Cited by 1,360

Nicotinic receptor subtypes differentially modulate glutamate release in the dorsal medial striatum

Howe, W. M., Young, D. A., Bekheet, G., & Kozak, R. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.08.009 · Cited by 28

Elevated antibody binding to striatal cholinergic interneurons in patients with pediatric acute-onset neuropsychiatric syndrome

Xu, J., Frankovich, J., Liu, R.-J., Thienemann, M., Silverman, M. A., Farhadian, B., Willett, T. A., Manko, C., Columbo, L. A., Leibold, C. M., et al. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.07.044 · Cited by 28

Pathway-Specific Control of Striatal Neuron Vulnerability by Corticostriatal Cannabinoid CB1 Receptors

Ruiz-Calvo, A., Maroto, I. B., Bajo‐Grañeras, R., Chiarlone, A., Gaudioso, Á., Ferrero, J. J., Resel, E., Sánchez‐Prieto, J., Rodríguez‐Navarro, J. A., Marsicano, G., et al. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx285 · Cited by 28

G‐Protein‐Coupled Receptor Heteromers as Key Players in the Molecular Architecture of the Central Nervous System

Brugarolas, M., Navarro, G., Martínez‐Pinilla, E., Angelats, E., Casadó, V., Lanciego, J. L., & Franco, R. (2014) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12277 · Cited by 27

Astroglial monoacylglycerol lipase controls mutant huntingtin-induced damage of striatal neurons

Ruiz-Calvo, A., Bajo‐Grañeras, R., Maroto, I. B., Zian, D., Grabner, G. F., García-Taboada, E., Resel, E., Zechner, R., Zimmermann, R., Ortega‐Gutiérrez, S., et al. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.03.027 · Cited by 27

A Novel Type of Neuron Within the Dorsal Striatum

Mao, M., Nair, A., & Augustine, G. J. (2019) · Frontiers in Neural Circuits · doi:10.3389/fncir.2019.00032 · Cited by 27

Dynamical changes in neurological diseases and anesthesia

McCarthy, M. M., Ching, S., Whittington, M. A., & Kopell, N. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.02.009 · Cited by 26

Deconstructing value-based decision making via temporally selective manipulation of neural activity: Insights from rodent models

Orsini, C. A., Hernandez, C. M., Bizon, J. L., & Setlow, B. (2018) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-018-00649-0 · Cited by 28

Direct reprogramming into interneurons: potential for brain repair

Pereira, M., Birtele, M., & Ottosson, D. R. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03193-3 · Cited by 26

Multineuromodulator measurements across fronto-striatal network areas of the behaving macaque using solid-phase microextraction

Hassani, S. A., Lendor, S., Boyacı, E., Pawliszyn, J. B., & Womelsdorf, T. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00321.2019 · Cited by 26

Apelin-13 attenuates motor impairments and prevents the changes in synaptic plasticity-related molecules in the striatum of Parkinsonism rats

Haghparast, E., Sheibani, V., Abbasnejad, M., & Esmaeili‐Mahani, S. (2019) · Peptides · doi:10.1016/j.peptides.2019.05.003 · Cited by 25

Mutual activation of glutamatergic mGlu4 and muscarinic M4 receptors reverses schizophrenia-related changes in rodents

Cieślik, P., Woźniak, M., Rook, J. M., Tantawy, M. N., Conn, P. J., Acher, F., Tokarski, K., Kusek, M., Pilc, A., & Wierońska, J. M. (2018) · Psychopharmacology · doi:10.1007/s00213-018-4980-y · Cited by 24

Metabolomics of Neurotransmitters and Related Metabolites in Post-Mortem Tissue from the Dorsal and Ventral Striatum of Alcoholic Human Brain

Kashem, M. A., Ahmed, S., Sultana, N., Ahmed, E. U., Pickford, R., Rae, C. D., Šerý, O., McGregor, I. S., & Balcar, V. J. (2016) · Neurochemical Research · doi:10.1007/s11064-016-1830-3 · Cited by 24

Meta-analytic evidence of elevated choline, reduced N-acetylaspartate, and normal creatine in schizophrenia and their moderation by measurement quality, echo time, and medication status

Yang, Y. S., Smucny, J., Zhang, H., & Maddock, R. J. (2023) · NeuroImage Clinical · doi:10.1016/j.nicl.2023.103461 · Cited by 23

Atlas of transgenic Tet-Off Ca2+/calmodulin-dependent protein kinase II and prion protein promoter activity in the mouse brain

Odeh, F., Leergaard, T. B., Boy, J., Schmidt, T., Rieß, O., & Bjaalie, J. G. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.11.032 · Cited by 24

NCX1 Exchanger Cooperates with Calretinin to Confer Preconditioning-Induced Tolerance Against Cerebral Ischemia in the Striatum

Boscia, F., Casamassa, A., Secondo, A., Esposito, A., Pannaccione, A., Sirabella, R., Pignataro, G., Cuomo, O., Vinciguerra, A., de Rosa, V., et al. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9095-4 · Cited by 23

Synaptosomal Lactate Dehydrogenase Isoenzyme Composition Is Shifted toward Aerobic Forms in Primate Brain Evolution

Duka, T., Anderson, S. M., Collins, Z. M., Raghanti, M. A., Ely, J. J., Hof, P. R., Wildman, D. E., Goodman, M., Grossman, L. I., & Sherwood, C. C. (2014) · Brain Behavior and Evolution · doi:10.1159/000358581 · Cited by 25

Phosphodiesterase 10A inhibitor MP-10 effects in primates: Comparison with risperidone and mechanistic implications

Uthayathas, S., Masilamoni, G. J., Shaffer, C. L., Schmidt, C. J., Menniti, F. S., & Papa, S. M. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.10.015 · Cited by 23

Differential CaMKII regulation by voltage-gated calcium channels in the striatum

Pasek, J. G., Wang, X., & Colbran, R. J. (2015) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2015.08.003 · Cited by 22

BDNF and Huntingtin protein modifications by manganese: implications for striatal medium spiny neuron pathology in manganese neurotoxicity

Stansfield, K. H., Bichell, T. J., Bowman, A. B., & Guilarte, T. R. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12926 · Cited by 22

Fluorescence‐activated sorting of fixed nuclei: a general method for studying nuclei from specific cell populations that preserves post‐translational modifications

Marion‐Poll, L., Montalban, E., Munier, A., Hervé, D., & Girault, J. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12506 · Cited by 23

Differential dopaminergic regulation of inwardly rectifying potassium channel mediated subthreshold dynamics in striatal medium spiny neurons

Zhao, B., Zhu, J.-L., Dai, D., Xing, J.-L., He, J., Fu, Z., Zhang, L., Li, Z., & Wang, W. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.03.037 · Cited by 22

A phase 1 study of the safety, tolerability, pharmacokinetics, and pharmacodynamics of TAK-063, a selective PDE10A inhibitor

Tsai, M. C., Chrones, L., Xie, J., Gevorkyan, H., & Macek, T. A. (2016) · Psychopharmacology · doi:10.1007/s00213-016-4412-9 · Cited by 22

Optogenetic approaches to evaluate striatal function in animal models of Parkinson disease

Parker, K. L., Kim, Y.-C., Alberico, S. L., Emmons, E. B., & Narayanan, N. S. (2016) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2016.18.1/kparker · Cited by 22

Increase in Glutamatergic Terminals in the Striatum Following Dopamine Depletion in a Rat Model of Parkinson’s Disease

Zheng, X., Huang, Z., Zhu, Y., Liu, B., Chen, Z., Chen, T., Jia, L., Li, Y., & Lei, W. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02739-y · Cited by 22

Effect of Selective Serotonin Reuptake Inhibitors via 5-HT1A Receptors on L-DOPA-Induced Rotational Behavior in a Hemiparkinsonian Rat Model

Inden, M., Abe, M., Minamino, H., Takata, K., Yoshimoto, K., Tooyama, I., & Kitamura, Y. (2012) · Journal of Pharmacological Sciences · doi:10.1254/jphs.12003fp · Cited by 21

Erbb4 Deletion from Medium Spiny Neurons of the Nucleus Accumbens Core Induces Schizophrenia-Like Behaviors via Elevated GABAA Receptor α1 Subunit Expression

Geng, H.-Y., Zhang, J., Yang, J., Li, Y., Wang, N., Ye, M., Chen, X.-J., Lian, H., & Li, X. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3948-16.2017 · Cited by 23

Sleep in ADCY5-Related Dyskinesia: Prolonged Awakenings Caused by Abnormal Movements

Méneret, A., Roze, E. F., Maranci, J., Dodet, P., Doummar, D., Riant, F., Tranchant, C., Fraix, V., Anheim, M., Ekmen, A., et al. (2019) · Journal of Clinical Sleep Medicine · doi:10.5664/jcsm.7886 · Cited by 21

Striatal dopamine release in a schizophrenia mouse model measured by electrochemical amperometry in vivo

Xu, H., Zuo, P., Wang, S., Zhou, L., Sun, X., Hu, M., Liu, B., Wu, Q., Dou, H., Liu, B., et al. (2015) · The Analyst · doi:10.1039/c4an02074j · Cited by 21

Chemogenetic Targeting of Dorsomedial Direct-pathway Striatal Projection Neurons Selectively Elicits Rotational Behavior in Mice

Kønig, A. B., Ciriachi, C., Gether, U., & Rickhag, M. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.01.013 · Cited by 20

MeCP2 in cholinergic interneurons of nucleus accumbens regulates fear learning

Zhang, Y., Zhu, Y., Cao, S.-X., Sun, P., Yang, J.-M., Xia, Y., Xie, S., Yu, X.-D., Fu, J., Shen, C.-J., et al. (2020) · eLife · doi:10.7554/elife.55342 · Cited by 21

The Effect of Serotonin Receptor 5-HT1B on Lateral Inhibition between Spiny Projection Neurons in the Mouse Striatum

Pommer, S., Akamine, Y., Schiffmann, S. N., d’Exaerde, A. D. K., & Wickens, J. R. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1037-20.2021 · Cited by 20

Excitatory Projections from the Prefrontal Cortex to Nucleus Accumbens Core D1-MSNs and κ Opioid Receptor Modulate Itch-Related Scratching Behaviors

Wu, X., Zhu, Q., Gao, M.-H., Yan, S.-X., Gu, P.-Y., Zhang, P., Xu, M., & Gao, Y. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1359-22.2023 · Cited by 22

In vitrostudy of the long-term cortisol treatment effects on the growth rate and proliferation of the neural stem/precursor cells

Abdanipour, A., Sagha, M., Noori-Zadeh, A., Pakzad, I., & Tiraihi, T. (2014) · Neurological Research · doi:10.1179/1743132814y.0000000431 · Cited by 20

Chemogenetic selective manipulation of nucleus accumbens medium spiny neurons bidirectionally controls alcohol intake in male and female rats

Strong, C. E., Hagarty, D. P., Guerrero, A. B., Schoepfer, K. J., Cajuste, S., & Kabbaj, M. (2020) · Scientific Reports · doi:10.1038/s41598-020-76183-2 · Cited by 20

Social Interaction and Cocaine Conditioning in Mice Increase Spontaneous Spike Frequency in the Nucleus Accumbens or Septal Nuclei as Revealed by Multielectrode Array Recordings

Kummer, K. K., Rawas, R. E., Kress, M., Saria, A., & Zernig, G. (2015) · Pharmacology · doi:10.1159/000370314 · Cited by 20

Dopamine-Induced Changes in Gαolf Protein Levels in Striatonigral and Striatopallidal Medium Spiny Neurons Underlie the Genesis of l-DOPA-Induced Dyskinesia in Parkinsonian Mice

Morigaki, R., Okita, S., & Goto, S. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00026 · Cited by 20

Putative Role of Pharmacogenetics to Elucidate the Mechanism of Tardive Dyskinesia in Schizophrenia

LOONEN, A. J. M., Wilffert, B., & Ivanova, S. А. (2019) · Pharmacogenomics · doi:10.2217/pgs-2019-0100 · Cited by 21

Chronic stress causes striatal disinhibition mediated by SOM-interneurons in male mice

Rodrigues, D., Jacinto, L., Falcão, M., Castro, A. C., Cruz, A., Santa, C., Manadas, B. J., Marques, F., Sousa, N., & Monteiro, P. (2022) · Nature Communications · doi:10.1038/s41467-022-35028-4 · Cited by 22

Kappa opioid receptor in nucleus accumbens regulates depressive-like behaviors following prolonged morphine withdrawal in mice

Zhang, J., Lu, Y., Jia, M., Bai, Y., Sun, L., Dong, Z., Tian, W., Yin, F., Wei, S., & Wang, Y. (2023) · iScience · doi:10.1016/j.isci.2023.107536 · Cited by 19

Y5 neuropeptide Y receptor overexpression in mice neither affects anxiety- and depression-like behaviours nor seizures but confers moderate hyperactivity

Olesen, M. V., Christiansen, S. H., Gøtzsche, C. R., Holst, B., Kokaia, M., & Woldbye, D. P. D. (2012) · Neuropeptides · doi:10.1016/j.npep.2012.01.002 · Cited by 19

VGLUT 3 gates psychomotor effects induced by amphetamine

Mansouri-Guilani, N., Bernard, V., Vigneault, É., Vialou, V., Daumas, S., Mestikawy, S. E., & Gangarossa, G. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14644 · Cited by 21

Genetic deletion of PDE10A selectively impairs incentive salience attribution and decreases medium spiny neuron excitability

Piccart, E., Backer, J. D., Gall, D., Lambot, L., Raes, A. L., Vanhoof, G., Schiffmann, S. N., & D’Hooge, R. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.03.016 · Cited by 19

Helios expression coordinates the development of a subset of striatopallidal medium spiny neurons

Martín‐Ibáñez, R., Pardo, M., Giralt, A., Miguez, A., Guardia, I., Marion‐Poll, L., Herranz, C., Esgleas, M., Barriga, G. G.-D., Edel, M. J., et al. (2017) · Development · doi:10.1242/dev.138248 · Cited by 20

Putative role of immune reactions in the mechanism of tardive dyskinesia

LOONEN, A. J. M. (2023) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2023.100687 · Cited by 18

Lack or Inhibition of Dopaminergic Stimulation Induces a Development Increase of Striatal Tyrosine Hydroxylase-Positive Interneurons

Busceti, C. L., Bucci, D., Molinaro, G., Pietro, P. D., Zangrandi, L., Gradini, R., Moratalla, R., Battaglia, G., Bruno, V., Nicoletti, F., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044025 · Cited by 19

Evaluation of the LIM homeobox genesLHX6andLHX8as candidates for Tourette syndrome

Paschou, P., Stylianopoulou, E., Karagiannidis, I., Rizzo, R., Tárnok, Z., Wolańczyk, T., Hebebrand, J., Nöthen, M. M., Lehmkuhl, G., Farkas, L., et al. (2012) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2012.00778.x · Cited by 18

Striatal Gαolf/cAMP Signal-Dependent Mechanism to Generate Levodopa-Induced Dyskinesia in Parkinson’s Disease

Goto, S. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00364 · Cited by 18

Allosteric modulation of muscarinic receptors in alcohol and substance use disorders

Walker, L. C., & Lawrence, A. J. (2020) · Advances in pharmacology · doi:10.1016/bs.apha.2020.01.003 · Cited by 18

Overlapping Projections of Neighboring Direct and Indirect Pathway Neostriatal Neurons to Globus Pallidus External Segment

Okamoto, S., Sohn, J., Tanaka, T., Takahashi, M., Ishida, Y., Yamauchi, K., Koike, M., Fujiyama, F., & Hioki, H. (2020) · iScience · doi:10.1016/j.isci.2020.101409 · Cited by 18

Increased Endogenous GDNF in Mice Protects Against Age-Related Decline in Neuronal Cholinergic Markers

Mitra, S., Turconi, G., Darreh‐Shori, T., Mätlik, K., Aquilino, M., Eriksdotter, M., & Andressoo, J. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.714186 · Cited by 18

The Basal Ganglia

Mink, J. W. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-385870-2.00030-5 · Cited by 18

Optical Control of Dopamine D2-like Receptors with Cell-Specific Fast-Relaxing Photoswitches

Hetzler, B. E., Donthamsetti, P., Peitsinis, Z. V., Stanley, C., Trauner, D. H., & Isacoff, E. Y. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c02735 · Cited by 18

Sex differences in the distribution and density of regulatory interneurons in the striatum

Zandt, M. A. V., Flanagan, D., & Pittenger, C. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1415015 · Cited by 18

The Striatal Skeleton: Medium Spiny Projection Neurons and Their Lateral Connections

Plenz, D., & Wickens, J. R. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00006-4 · Cited by 17

Mice carrying a schizophrenia-associated mutation of the Arhgap10 gene are vulnerable to the effects of methamphetamine treatment on cognitive function: association with morphological abnormalities in striatal neurons

Hada, K., Wulaer, B., Nagai, T., Itoh, N., Sawahata, M., Sobue, A., Mizoguchi, H., Mori, D., Kushima, I., Nabeshima, T., et al. (2021) · Molecular Brain · doi:10.1186/s13041-021-00735-4 · Cited by 17

Leveraging VGLUT3 Functions to Untangle Brain Dysfunctions

Favier, M., Pietrancosta, N., Mestikawy, S. E., & Gangarossa, G. (2021) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2021.03.003 · Cited by 17

Consistency and Diversity of Spike Dynamics in the Neurons of Bed Nucleus of Stria Terminalis of the Rat: A Dynamic Clamp Study

Szűcs, A. L., Berton, F., Nowotny, T., Sanna, P. P., & Francesconi, W. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011920 · Cited by 17

Development and validation of a high-throughput calcium mobilization assay for the orphan receptor GPR88

Decker, A. M., Gay, E. A., Mathews, K. M., Rosa, T. C., Langston, T. L., Maitra, R., & Jin, C. (2017) · Journal of Biomedical Science · doi:10.1186/s12929-017-0330-3 · Cited by 17

Functional independence of endogenous μ- and δ-opioid receptors co-expressed in cholinergic interneurons

Arttamangkul, S., Platt, E. J., Carroll, J. R., & Farrens, D. (2021) · eLife · doi:10.7554/elife.69740 · Cited by 16

D2/3Agonist during Learning Potentiates Cued Risky Choice

Mortazavi, L., Hynes, T. J., Chernoff, C. S., Ramaiah, S., Brodie, H. G., Russell, B., Hathaway, B. A., Kaur, S., & Winstanley, C. A. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1459-22.2022 · Cited by 20

Chronic inflammatory pain decreases the glutamate vesicles in presynaptic terminals of the nucleus accumbens

Qi, C., Guo, B., Ren, K., Yao, H., Wang, M., Sun, T., Cai, G., Liu, H., Li, R., Luo, C., et al. (2018) · Molecular Pain · doi:10.1177/1744806918781259 · Cited by 17

Admixing MPTP‐resistant and MPTP‐vulnerable mice enhances striatal field potentials and calbindin‐D28K expression to avert motor behaviour deficits

Vidyadhara, D. J., Sasidharan, A., Kutty, B., Raju, T., & Alladi, P. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.12.015 · Cited by 12

Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome

Pagliaroli, L., Vereczkei, A., Padmanabhuni, S. S., Tárnok, Z., Farkas, L., Nagy, P., Rizzo, R., Wolańczyk, T., Szymańska, U. A., Kapisyzi, M., et al. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00803 · Cited by 16

Evidence that GIRK Channels Mediate the DREADD-hM4Di Receptor Activation-Induced Reduction in Membrane Excitability of Striatal Medium Spiny Neurons

Shan, Q., Fang, Q., & Tian, Y. (2022) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.2c00304 · Cited by 15

Molecular Landscape of Tourette’s Disorder

Widomska, J., Witte, W. D., Buitelaar, J. K., Glennon, J. C., & Poelmans, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021428 · Cited by 15

Neuron type-specific proteomics reveals distinct Shank3 proteoforms in iSPNs and dSPNs lead to striatal synaptopathy in Shank3B–/– mice

Wang, Y., Perez‐Rosello, T., Smukowski, S. N., Surmeier, D. J., & Savas, J. N. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02493-w · Cited by 15

Transcriptomic and metabolomic changes might predict frailty in SAMP8 mice

Dacomo, L., Vitola, P. L., Brunelli, L., Messa, L., Micotti, E., Artioli, L., Sinopoli, E., Cecutti, G., Leva, S., Gagliardi, S., et al. (2024) · Aging Cell · doi:10.1111/acel.14263 · Cited by 15

Inhibition of striatonigral autophagy as a link between cannabinoid intoxication and impairment of motor coordination

Blázquez, C., Ruiz-Calvo, A., Bajo‐Grañeras, R., Baufreton, J., Resel, E., Varilh, M., Zottola, A. C. P., Mariani, Y., Cannich, A., Rodríguez‐Navarro, J. A., et al. (2020) · eLife · doi:10.7554/elife.56811 · Cited by 15

How predictive learning influences choice: Evidence for a GPCR‐based memory process necessary for Pavlovian‐instrumental transfer

Laurent, V., & Balleine, B. W. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15339 · Cited by 15

A model for transforming egocentric views into goal‐directed behavior

LaChance, P. A., & Taube, J. S. (2023) · Hippocampus · doi:10.1002/hipo.23510 · Cited by 15

A Nucleus Accumbens Tac1 Neural Circuit Regulates Avoidance Responses to Aversive Stimuli

He, Z., Xi, K., Liu, K.-J., Yue, M.-H., Wang, Y., Yin, Y.-Y., Liu, L., He, X., Yu, H., Xing, Z., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054346 · Cited by 15

Basal ganglia network dynamics and function: Role of direct, indirect and hyper-direct pathways in action selection

Song, J., Lin, H. Z., & Liu, S. (2023) · Network Computation in Neural Systems · doi:10.1080/0954898x.2023.2173816 · Cited by 16

UBE3A expression during early postnatal brain development is required for proper dorsomedial striatal maturation

Rotaru, D. C., Wallaard, I., de Vries, M., van der Bie, J., & Elgersma, Y. (2023) · JCI Insight · doi:10.1172/jci.insight.166073 · Cited by 15

Striatal Neuropeptides Enhance Selection and Rejection of Sequential Actions

Buxton, D. R., Bracci, E., Overton, P. G., & GURNEY, K. N. (2017) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2017.00062 · Cited by 14

The Potential Role of miRNAs as Predictive Biomarkers in Neurodevelopmental Disorders

Juvale, I. I. A., & Has, A. T. C. (2021) · Journal of Molecular Neuroscience · doi:10.1007/s12031-021-01825-7 · Cited by 14

Somatostatin-Expressing Interneurons Co-Release GABA and Glutamate onto Different Postsynaptic Targets in the StriatumPreprint

Cattaneo, S., Ripamonti, M., Bedogni, F., Sessa, A., & Taverna, S. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/566984 · Cited by 14

Integrative multi-dimensional characterization of striatal projection neuron heterogeneity in adult brainPreprint

Gayden, J. D., Puig, S., Srinivasan, C., Phan, B. N., Abdelhady, G., Buck, S. A., Gamble, M. C., Tejeda, H. A., Dong, Y., Pfenning, A. R., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.04.539488 · Cited by 14

Coupling between GPR143 and dopamine D2 receptor is required for selective potentiation of dopamine D2 receptor function by L‐3,4‐dihydroxyphenylalanine in the dorsal striatum

Masukawa, D., Kitamura, S., Tajika, R., Uchimura, H., Arai, M., Takada, Y., Arisawa, T., Otaki, M., Kanai, K., Kobayashi, K., et al. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15789 · Cited by 13

Modeling the motor striatum under Deep Brain Stimulation in normal and MPTP conditions

Santaniello, S., Gale, J. T., Montgomery, E. B., & Sarma, S. V. (2010) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/iembs.2010.5626354 · Cited by 13

Duration- and sex-dependent neural circuit control of voluntary physical activity

Tanner, M. K., Davis, J. K. P., Jaime, J., Moya, N. A., Hohorst, A. A., Bonar, K., Abrams, K. A., Jamil, N., Han, R., Hubert, T., et al. (2022) · Psychopharmacology · doi:10.1007/s00213-022-06243-0 · Cited by 14

Could theropod dinosaurs have evolved to a human level of intelligence?

Reiner, A. J. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25458 · Cited by 13

Sustained Gq-Protein Signaling Disrupts Striatal Circuits via JNK

Bellocchio, L., Ruiz-Calvo, A., Chiarlone, A., Cabanas, M., Resel, E., Cazalets, J., Blázquez, C., Cho, Y. H., Galve‐Roperh, I., & Guzmán, M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1192-16.2016 · Cited by 15

Bipolar oscillations between positive and negative mood states in a computational model of Basal Ganglia

Balasubramani, P. P., & Chakravarthy, V. S. (2019) · Cognitive Neurodynamics · doi:10.1007/s11571-019-09564-7 · Cited by 13

Discovering the Lost Reward: Critical Locations for Endocannabinoid Modulation of the Cortico–Striatal Loop That Are Implicated in Major Depression

Ferber, S. G., Weller, A., Yadid, G., & Friedman, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041867 · Cited by 14

MiR-142-3p is a Critical Modulator of TNF-mediated Neuronal Toxicity in Multiple Sclerosis

Vito, F. D., Balletta, S., Caioli, S., Musella, A., Guadalupi, L., Vanni, V., Fresegna, D., Bassi, M. S., Gilio, L., Sanna, K., et al. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230404103914 · Cited by 12

Generation and propagation of bursts of activity in the developing basal ganglia

Klavinskis-Whiting, S., Bitzenhofer, S. H., Hanganu‐Opatz, I. L., & Ellender, T. J. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad307 · Cited by 12

Fyn Signaling Is Compartmentalized to Dopamine D1 Receptor Expressing Neurons in the Dorsal Medial Striatum

Phamluong, K., Darcq, E., Wu, S., Sakhai, S. A., & Dorit Ron, A. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00273 · Cited by 12

Inflammation alters AMPA‐stimulated calcium responses in dorsal striatal D2 but not D1 spiny projection neurons

Berger, C., Welsh, N. C., Sepulveda‐Rodriguez, A., Vicini, S., & Maguire‐Zeiss, K. A. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13711 · Cited by 12

Chronic and Acute Manipulation of Cortical Glutamate Transmission Induces Structural and Synaptic Changes in Co-cultured Striatal Neurons

Kuhlmann, N., Valladolid, M. W., Quesada-Ramírez, L., Farrer, M. J., & Milnerwood, A. J. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.569031 · Cited by 14

Mapping whole brain effects of infrared neural stimulation with positron emission tomography

Meneghetti, M., Gudmundsen, F., Jessen, N. S., Sui, K., Baun, C., Palner, M., & Markos, C. (2023) · Imaging Neuroscience · doi:10.1162/imag_a_00052 · Cited by 12

Effects of anisomycin infusions into the dorsal striatum on memory consolidation of intense training and neurotransmitter activity

González-Franco, D. A., Bello-Medina, P. C., Serafín, N., Prado-Alcalá, R. A., & Quirarte, G. L. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.06.005 · Cited by 12

Ablation of striatal somatostatin interneurons affects MSN morphology and electrophysiological properties, and increases cocaine‐induced hyperlocomotion in mice

Gazan, A., Rial, D., & Schiffmann, S. N. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14581 · Cited by 13

Study of the neural basis of striatal modulation of the jaw-opening reflex

Barceló, A. C., Fillipini, B., & Pazo, J. H. (2009) · Journal of Neural Transmission · doi:10.1007/s00702-009-0348-0 · Cited by 12

Altered anterograde axonal transport of mitochondria in cultured striatal neurons of a knock-in mouse model of Huntington's disease

Wu, C., Yin, H., Fu, S., Yoo, H., Zhang, M., & Park, H. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2023.149246 · Cited by 11

Hereditary Patterns and Genetic Associations in Obsessive-Compulsive Disorder (OCD): Neuropsychiatric Insights, Genetic Influences, and Treatment Perspectives

Dhiman, A., Mehan, S., Khan, Z., Tiwari, A., Gupta, G. D., & Narula, A. S. (2024) · Current Gene Therapy · doi:10.2174/0115665232316708240828063527 · Cited by 11

Aging in mice alters regionally enriched striatal astrocytes

Linker, K. E., Durán‐Laforet, V., Ollivier, M., Yu, X., Schafer, D. P., & Khakh, B. S. (2025) · Nature Communications · doi:10.1038/s41467-025-63429-8 · Cited by 11

Circuit and Cell-Specific Contributions to Decision Making Involving Risk of Explicit Punishment in Male and Female Rats

Truckenbrod, L. M., Betzhold, S. M., Wheeler, A.-R., Shallcross, J., Singhal, S. M., Harden, S. W., Schwendt, M., Frazier, C. J., Bizon, J. L., Setlow, B., et al. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0276-23.2023 · Cited by 11

Ivermectin increases striatal cholinergic activity to facilitate dopamine terminal function

Wadsworth, H. A., Warnecke, A. M. P., Barlow, J. C., Robinson, J. K., Steimle, E., Ronström, J. W., Williams, P. E., Galbraith, C., Baldridge, J., Jakowec, M. W., et al. (2024) · Cell & Bioscience · doi:10.1186/s13578-024-01228-2 · Cited by 12

Current Understanding of PDE10A in the Modulation of Basal Ganglia Circuitry

Schülke, J.-P., & Brandon, N. J. (2017) · Advances in neurobiology · doi:10.1007/978-3-319-58811-7_2 · Cited by 11

Local Connectivity Between Striatal Spiny Projection Neurons: A Re-Evaluation

Oorschot, D. E., Tunstall, M. J., & Wickens, J. R. (2002) · Advances in behavioral biology · doi:10.1007/978-1-4615-0715-4_42 · Cited by 25

Intrinsic synaptic connectivity of the nucleus accumbens: Lateral inhibition, functions of fast-spiking interneurons and neuromodulation

Taverna, S., & Pennartz, C. M. A. (2009) · UvA-DARE (University of Amsterdam)

Spike-timing dependent plasticity in striatal interneurons

Fino, É., & Venance, L. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.01.023 · Cited by 80

GABAergic Interneurons of the Striatum

Tepper, J. M., & Koós, T. Z. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00008-8 · Cited by 33

Synaptic regulation of spike firing in interneurons of the striatum in vivo

John, R. (2011) · Frontiers in Computational Neuroscience · doi:10.3389/conf.fncom.2011.53.00176