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

Brain Dopamine and Serotonin Receptors in the Perception of Pain. Positron Emission Tomography Studies in Healthy Subjects

Martikainen, I. K. (2009) · UTUPub (University of Turku) · Cited by 2

Re-emergence of T lymphocyte-mediated synaptopathy in progressive multiple sclerosis

Sanna, K., Bruno, A., Balletta, S., Caioli, S., Nencini, M., Fresegna, D., Guadalupi, L., Dolcetti, E., Azzolini, F., Buttari, F., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1416133 · Cited by 1

Translatome of dorsal striatum parvalbumin interneurons revisited: insights across diverse experimental paradigms

Naon, C., Castell, L., Thirard, S., Moreno, M. P., Rialle, S., Goetz, E., Casals, E., Rogliardo, A., Gut, M. O., Esteve‐Codina, A., et al. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1648461 · Cited by 1

Altered Excitability and Glutamatergic Synaptic Transmission in the Medium Spiny Neurons of the Nucleus Accumbens in Mice Deficient in the Heparan Sulfate Endosulfatase Sulf1

Miya, K., Suzuki, E., Keino‐Masu, K., Okada, T., Kobayashi, K., Momiyama, T., & Masu, M. (2025) · eNeuro · doi:10.1523/eneuro.0088-25.2025 · Cited by 2

Essential Roles of Heparan Sulfate Endosulfatase Sulf1 in Reward and Aversion Learning Through Distinct Dopamine D1 and D2 Receptor Pathways in Male Mice

Miya, K., Ohta, K., Keino‐Masu, K., Okada, T., Mizuno, S., Takahashi, S., Macpherson, T., Hikida, T., & Masu, M. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70338 · Cited by 1

Regional heterogeneity of striatal cholinergic interneurons: setting the stage for diverse behavioral repertoires

Lemos, J. C., Duhne, M., & Chuhma, N. (2026) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2026.1718947 · Cited by 1

Effect of the striatum on $ \beta $-synchronous oscillatory activity

Ji, Q., & Lao, R. (2026) · Electronic Research Archive · doi:10.3934/era.2026110 · Cited by 1

Recent Advances in Dopamine Receptor Ligands as Chemical Biology Tools

Dorogan, M., Krishna, N. H., Patra, S., & Harding, W. W. (2026) · ACS Omega · doi:10.1021/acsomega.6c01474 · Cited by 1

Central Nervous System Injury, Neurocognitive and Quality of Life Outcomes in Children with Brain Tumors Treated with Chemotherapy

Nelson, B., & Christine, M. (2012) · Cited by 1

Short‐term hindlimb unloading negatively affects dopaminergic transmission in the nigrostriatal system of mice

Naumova, A. A., Oleynik, E. A., Khramtsova, A., Nikolaeva, S. D., Chernigovskaya, E. V., & Glazova, M. V. (2023) · Developmental Neurobiology · doi:10.1002/dneu.22924 · Cited by 1

Neurobiology of Tic Disorders and Obsessive–Compulsive Disorder

Pittenger, C. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780197640654.003.0065 · Cited by 1

Regulation of working memory switches from striatal dopamine D2-receptor to D1-receptor neurons under high cognitive load

Chen, X., Li, F. Y., Zhao, X., Chen, L., Xue, J., Yao, Z., Gan, Z., Lian, X., Liu, Z., Tong, L., et al. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003289 · Cited by 1

Comparison of Normal and Parkinsonian Microcircuit Dynamics in the Rodent Striatum

Jáidar, O., Carrillo‐Reid, L., & Bargas, J. (2012) · InTech eBooks · doi:10.5772/21036 · Cited by 1

Investigation of Synaptic Microcircuits Using Patch-Clamp Paired Recordings in Acute Brain Slices

Russo, G., & Taverna, S. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-1096-0_11 · Cited by 1

Basal Ganglia: Acetylcholine Interactions and Behavior☆

Deffains, M., Adler, A. J., Joshua, M., Goldberg, J. A., Morris, G., & Bergman, H. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.02520-7 · Cited by 1

Role of Histone Methylation in Cognition and Effects of Different Durations of Environmental Enrichment on Learning and Memory

Kerimoglu, C. (2012) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3197 · Cited by 1

Neural Coding Strategies in Cortico-Striatal Circuits Subserving Interval Timing

Cheng, R. (2010) · DukeSpace (Duke University) · Cited by 1

Pitx3Null Mutant (Striatal Dopamine-Deficient) Mice Have Exaggerated Spiny Projection Neuron Responses to l-DOPA and D1 Agonism and Lack Baseline Striatonigral Spiking

Sagot, B. (2017) · doi:10.21007/etd.cghs.2017.0442 · Cited by 1

HCN2 in cholinergic interneurons of the nucleus accumbens mediates reward responsePreprint

Lee, J., Weinberger, M., Kawahara, Y., Cheng, J., Umschweif, G., Medrihan, L., Flajolet, M., Nishi, A., & Sagi, Y. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.21.460269 · Cited by 1

Variation in Glutamate and GABA Genes and Their Association with Brain Structure and Chemistry in AutismPreprint

Naaijen, J., Arenella, M., Zöllner, H. J., Puts, N. A. J., Lythgoe, D. J., Brandeis, D., Durston, S., Poelmans, G., Ruisch, I. H., & Buitelaar, J. K. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.25.493390 · Cited by 1

Ventral Striatum Modifies the Activity of Basal Ganglia Circuit: A Computational ModelPreprint

Elibol, R., & Şengör, N. S. (2022) · Research Square · doi:10.21203/rs.3.rs-1594417/v1 · Cited by 1

Complementary cognitive roles for D2-MSNs and D1-MSNs in interval timingPreprint

Bruce, R. A., Weber, M. A., Bova, A. S., Volkman, R. A., Jacobs, C. E., Sivakumar, K., Stutt, H. R., Kim, Y.-C., Curtu, R., & Narayanan, N. S. (2024) · eLife · doi:10.7554/elife.96287.1 · Cited by 1

Predict key biomarkers of Alcohol Dependence in Nucleus accumbens by Weighted gene co-expression network analysisPreprint

Shi, X., Xu, B., He, T., Shi, J., & Zhang, L. (2024) · Research Square · doi:10.21203/rs.3.rs-4201908/v1 · Cited by 1

Translational Evidence for Dopaminergic Alteration of Basal Ganglia Functional Connectivity in Persons with SchizophreniaPreprint

Tubiolo, P. N., Williams, J. C., Gil, R. B., Cassidy, C., Haubold, N. K., Patel, Y., Abeykoon, S. K., Zheng, Z. J., Pham, D. T., Ojeil, N., et al. (2025) · medRxiv · doi:10.1101/2025.03.31.25324962 · Cited by 1

Cellular Mechanism of Obsessive-Compulsive Disorder

Tee, L. Y. (2015) · DukeSpace (Duke University)

A Role for Neuronal Nicotinic Acetylcholine Receptors in Dopamine-Mediated Behaviors and the Hypnotic Response to Anesthetics: A Dissertation

Soll, L. G. (2013) · eScholarship@UMassChan · doi:10.13028/m2ng64

Chronic treatment with simvastatin affects cannabinoid receptor type 1 and muscarinic receptors type 2/4 in different brain regions among sham and 6-hydroxydopamine lesioned rats

Mackovski, N. (2013) · Research Online (University of Wollongong)

Eating too much or too little : an FMRI food reward study of (ab)normal eating behaviour

Siep, N. (2010) · Research Publications (Maastricht University) · doi:10.26481/dis.20101104ns

L-DOPA-induced signaling pathways and neuroepigenetic mechanisms in experimental Parkinsonism and dyskinesia

Feyder, M. T. (2014) · Figshare

Alterations of Thalamostriatal and Corticostriatal Projections in Mouse Models of Huntington’s Disease

Parievsky, A. (2015) · eScholarship (California Digital Library)

La détection centrale des lipides et la régulation du comportement alimentaire : implication dans l’obésité

Cansell, C., & Luquet, S. H. (2014) · Cahiers de Nutrition et de Diététique · doi:10.1016/j.cnd.2013.11.001

A point process model-based framework reveals reinforcement mechanisms in striatum during high frequency STN DBS

Santaniello, S., Gale, J. T., Montgomery, E. B., & Sarma, S. V. (2012) · IEEE Conference on Decision and Control (CDC) · doi:10.1109/cdc.2012.6426098

Modeling receptor induced signaling in MSNs

Nair, A. G. (2014)

Computational Modeling of the Basal Ganglia : Functional Pathways and Reinforcement Learning

Berthet, P. (2015) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

An in vitro analysis of striatal microcircuitry

Elghaba, R. (2015) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)

The Specific Role of Dopamine in the Striatum during Operant Learning

Ivlieva, N. Y., & Ivliev, D. A. (2015) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-015-0200-y

Representation of the body in the lateral striatum of the freely moving rat

Kulik, J. M. (2015) · doi:10.7282/t3f191p8

Striatal Dopamine and Glutamate in Action

Yin, H. H., & Costa, R. M. (2011) · Frontiers in neuroscience · doi:10.1201/b11284-10

Mechanisms underlying dopaminergic modulation of striatal firing and learning

Damodaran, S. (2015) · doi:10.13021/mars/7530

Functional Connectivity of the Rodent Striatum

Albaugh, D. L. (2016) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/jard-1g42

Regulação cerebral e percepção de esforço durante exercício incremental

Bortolotti, H. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.39.2017.tde-13022017-115416

ACTIVITY OF RAT DORSAL STRIATAL MEDIUM SPINY NEURONS DURING ODOUR SAMPLING IN A WORKING MEMORY CAPACITY TASK

Murray, B. G. (2016) · University Library - University of Saskatchewan (University of Saskatchewan)

Targeting muscarinic receptor subtypes as a therapeutic approach in dystonia and Parkinson's disease

Klisko, D. (2017) · Research Portal (King's College London)

Die Wirkungen von akutem Stress auf Erlernen und Abruf erlernter Handlungs-Ergebnis-Beziehungen

Braun, S. (2017) · OPUS Publication Server of the University of Stuttgart (University of Stuttgart) · doi:10.18419/opus-9368

In vivo Observation of the Release of Norepinephrine and In Vivo Optical Studies on the Direct and Indirect Paths of the Striatum

Clark, S. D. (2018) · doi:10.7916/d8fn2pq2

Long-Term Effects of Juvenile NMDAr or DAr Antagonism on Adolescent Reward-Related Neurobehavioral Outcomes

Goheen, K. (2019)

Examination of Cortical/Thalamic-Striatal Circuitry in Modulating Sensitivity to Alcohol and Relapse

Jaramillo, A. A. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/2g98-g192

Dopaminergic Co-transmission with Sonic Hedgehog Inhibits Abnormal Involuntary MovementsPreprint

Malave, L. B., Zuelke, D. R., Uribe‐Cano, S., Starikov, L., Rebholz, H., Friedman, E., Qin, C., Li, Q., Bézard, E., & Kottmann, A. H. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.09.983759

Basic mechanisms of, and treatment planning/targets for, obsessive–compulsive disorder

Burguière, E., & Mallet, L. (2020) · doi:10.1093/med/9780198713005.003.0094

Neural Structures Associated with Music Engagement in Persons with Alzheimer’s Disease

Zaitsev, P. (2020) · UTUPub (University of Turku)

Levodopa-induced dyskinesias in Parkinson's disease

Alberico, S. L., & Narayanan, N. S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-815946-0.00032-6 · Cited by 1

Memory systems of the brainPreprint

Pastor, A. (2020) · OSF Preprints (OSF Preprints) · doi:10.31219/osf.io/w6kn9 · Cited by 2

The Basal Ganglia

Williams, M. R. (2021) · Springer eBooks · doi:10.1007/978-3-030-68308-5_9

Cholinergic Neurons of the Nucleus Accumbens Enhance Cocaine-Induced Dopaminergic Signaling and RewardPreprint

Lee, J., Weinberger, M., Kawahara, Y., Cheng, J., Umscweif, G., Medrihan, L., Flajolet, M., Nishi, A., & Sagi, Y. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3929661

The Role of the Striatum in Organizing Voluntary Behavior

Ivlieva, N. Y. (2021) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-021-01170-7

Interaction between nerve fiber formation and astrocytes

Hashemian, S. (2014) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

Molecular and cellular bases for the protective effects of dopamine D1 receptor antagonist, SCH23390, against methamphetamine-induced neurotoxicity in the rat brain

Beauvais, G. (2012) · theses.fr (ABES) · doi:10.70675/e4fd63d7zc7a0z4ffez880aze37d1bb64c9f

Faculty Opinions recommendation of Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry.

Pandolfo, M. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.4651956.4532054

Results

Pastore, V. P. (2020) · Springer theses · doi:10.1007/978-3-030-59042-0_3

Assessment of Epigenetic profile in Alzheimer's disease

Agbemenyah, H. Y. (2012) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3213

Faculty Opinions recommendation of In vivo reprogramming of astrocytes to neuroblasts in the adult brain.

Berninger, B. (2013) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718116540.793484338

Modulation of Histone Deacetylases Attenuates the Pathogenesis of Alzheimer's disease

Govindarajan, N. (2011) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-449

Long-Term Effects of Juvenile NMDAr or DAr Antagonism on Adolescent Reward-Related Neurobehavioural Outcomes

Goheen, K. (2018) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2018-13451

Faculty Opinions recommendation of Interrogating the Spatiotemporal Landscape of Neuromodulatory GPCR Signaling by Real-Time Imaging of cAMP in Intact Neurons and Circuits.

Dorit Ron, A. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732394172.793544893

[Neural mechanism for modulation of auditory response of the striatum by locomotion].

Huang, W., & Liang, F. (2022) · PubMed Central · doi:10.12122/j.issn.1673-4254.2022.05.20

The Progress of Different Pathways for Shank3 to Cause Autism Spectrum Disorder

Stephanie, L., Song, X., & Lin, Z. (2022) · Highlights in Science Engineering and Technology · doi:10.54097/hset.v2i.584

Basal Ganglia Anatomy, Biochemistry, and Physiology

Singer, H. S., Mink, J. W., Gilbert, D. L., & Jankovic, J. J. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-820552-5.00012-7

[Comparison of electrophysiological properties of parvalbumin neurons in the tail of the striatum and the auditory cortex of mice].

You, J., Song, C., & Liang, F. (2022) · PubMed Central · doi:10.12122/j.issn.1673-4254.2022.12.19

An important new chapter in Neuroscience

Tuckwell, H. C. (2023) · Journal of Multiscale Neuroscience · doi:10.56280/1579486051

Dopamine enhances multisensory responses in the dorsomedial striatumPreprint

Sáez, M., Alegre-Cortés, J., Morgenstern, N. A., Garcı́a-Frigola, C., de la Torre‐Martínez, R., & Reig, R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.25.559270

The Role of Dopamine in Training Automaticity

Lerner, T. N., Miller-Hansen, A. J., & Ambrosi, P. (2024) · Springer eBooks · doi:10.1007/978-3-031-55889-4_9

How can caffeine alleviate the motor symptoms of Parkinson’s disease? – the implications of adenosine 2A receptor antagonism

Wójcik, A., Górny, A., Chwiejczak, J., Młynarska, J., Kościan, J., Szczerkowska, K., Seroka, A., Mitkowska, M., Rybicka, M., & Obrębski, M. (2024) · Journal of Education Health and Sport · doi:10.12775/jehs.2024.71.49808

Enhancement of Haloperidol-Induced Catalepsy by GPR143, an l-DOPA Receptor, in Striatal Cholinergic Interneurons

Hatzipantelis, C. J. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0953-24.2024

The Diencephalon

Armocida, D., Salvati, M., D’Andrea, G., Frati, A., & Ascenzi, B. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-822404-5.00012-7

Synaptic integration of somatosensory and motor cortical inputs onto spiny projection neurons of mice caudoputamen

Sampathkumar, V., Koster, K. P., Carroll, B. J., Sherman, S. M., & Kasthuri, N. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16538

Introduction to stem cell biology and its role in treating neurologic disorders

Parmar, M., & Perrier, A. L. (2024) · Handbook of clinical neurology · doi:10.1016/b978-0-323-90120-8.00005-8

Altérations du sommeil dans les troubles anxio-dépressifs : apports des modèles précliniques

Pujol, M., & Fabre, V. (2025) · Médecine du Sommeil · doi:10.1016/j.msom.2025.05.004

Reward-driven adaptation of movements requires strong recurrent basal ganglia–cortical loops

Leblois, A., Boraud, T., & Hansel, D. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2515994122

Cortico-striatal dynamics across working memory stages

Villet, M., Azoulay, B., Barik, J., Marie, H., & Bethus, I. (2025) · Cerebral Cortex · doi:10.1093/cercor/bhaf334

Additional file 3 of 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) · Figshare · doi:10.6084/m9.figshare.13633089

Additional file 1 of 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. J., Baldridge, J., Jakowec, M. W., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26708354

Additional file 2 of 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) · Figshare · doi:10.6084/m9.figshare.13633086

Proteomic Characterization of Striatal Neurabin Interactome and Its Sex Specific Impact on Motor Behavior

Shah, N. R., Corey, W., Harris, C. N., & Baucum, A. J. (2026) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.5c00802

Animal models of Gilles de la Tourette Syndrome and other tic disorders

Loewenstern, Y., Tahary, O., Bar‐Gad, I., & Belelovsky, K. (2026) · Handbook of clinical neurology · doi:10.1016/b978-0-443-13554-5.00015-8

Dopaminergic regulation of basal ganglia synaptic transmission

Molinari, M. (2026) · doi:10.69622/30801566

Physical exercise modulates T cell activity and mitigates synaptic dysfunction in multiple sclerosis through vagus nerve engagement

Musella, A., Balletta, S., Russo, C., Mariani, F., Tartacca, A., Rosa, G. D., Vito, F. D., Palmerio, F., Fresegna, D., Bruno, A., et al. (2026) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2026.106523 · Cited by 1

Activités développementales et pathologiques des microcircuits GABAergiques du striatum

Dehorter, N. (2010) · theses.fr (ABES) · doi:10.70675/8e547423z1a4ez45ccz86b6z24335d375e05

Implication des interneurones cholinergiques striataux dans la physiopathologie de la maladie de Parkinson : étude optogénétique, pharmacologique et comportementale

Ztaou, S. (2016) · theses.fr (ABES) · doi:10.70675/82c2ea24zaacdz49cfz88e0z86d5151777b4

Conséquences de la délétion conditionnelle du gène Tshz3 dans la circuiterie cortico-striée : implications dans les troubles du spectre autistique

Chabbert, D. (2017) · theses.fr (ABES) · doi:10.70675/6ac224e2z22c7z4bd4zb6dazc3f301e5b758

Modulation of amphetamine-induced behaviors in mice by the atypical vesicular glutamate transporter type 3 (VGLUT3)

Mansouri-Guilani, N. (2017) · theses.fr (ABES) · doi:10.70675/99ced3b5zeac6z4eb2z8e6cz01bcad7cf2d9

The Hippocampal-Prefrontal-Striatal network during successive learning and set-shifting

Oberto, V. J. (2017) · theses.fr (ABES) · doi:10.70675/d64848adzf26az4072zb8e2z0dc40420582c

Rôle du transporteur plasmique des monoamines (PMAT) dans le système nerveux central

Amin, S. R. (2017) · theses.fr (ABES) · doi:10.70675/f562837bz937fz402eza824z24af264eaf90

Rôle de la protéine matricellulaire hevin dans la réponse à la cocaïne

Mongrédien, R. (2018) · theses.fr (ABES) · doi:10.70675/926d644czef3bz4ce3z9fd7z6080a7628079

Long-lasting effects of operant conditioning and cocaine on D1 pyramidal neurons in prefrontal cortex and on the D1 and D2 striatal neurons mRNAs

Montalban, E. (2016) · theses.fr (ABES) · doi:10.70675/7c448b16zc5fdz466az8569z88ff2264863b

Combining a real-time closed-loop system with neuromodulation : an integrative approach to prevent pathological repetitive behaviors

Mondragón-González, S. L. (2019) · theses.fr (ABES) · doi:10.70675/e78705daz18a9z4695zac41zadeb07ee7c37

Role of synaptic zinc in pathophysiology of Parkinson’s disease

Sikora, J. (2020) · theses.fr (ABES) · doi:10.70675/87e4f747zbcf8z45aaz8541z50965800f3c6

Physiopathologie des déficits moteurs dans les troubles du spectre autistique : approche neuroanatomique dans deux modèles environnementaux

Haïda, O. (2018) · theses.fr (ABES) · doi:10.70675/ff06b994z1a54z464cz8830z6a3a9363bee7

Rôle des afférences thalamiques au noyau accumbens dans les comportements motivés chez le rat

Sicre, M. (2021) · theses.fr (ABES) · doi:10.70675/b8ead46dzaf07z4156zb06bzc3755176fcfc

Contribution des interneurones cholinergiques striataux aux déficits cognitifs de la maladie de Parkinson : approches optogénétique et comportementale chez la souris

Lhost, J. (2020) · theses.fr (ABES) · doi:10.70675/f950452bzadb5z4f7ez9635zf0f4496824a0

Mise en lumière des capacités préservées d'apprentissage des personnes malades d'Alzheimer à un stade modéré à sévère à l'aide de l'art : un autre regard pour un autre accompagnement

Coppalle, R. (2020) · theses.fr (ABES) · doi:10.70675/374421dcz7d65z480aza1fcz2a44c1c0f8df

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