Cited by 85Deep Brain Stimulation and Movement DisordersNeurological and metabolic disordersParkinson's Disease Mechanisms and Treatments

The DOI matches its Crossref record; 271 of the 271 references it cites were found in a registry or an index.

Basal Ganglia

Gerfen, Charles R.·2004·The Rat Nervous System

DOI 10.1016/b978-012547638-6/50019-5

Open this paper in CoChat — free account

Integrity signals

Registry

Crossref · 10.1016/b978-012547638-6/50019-5

Cites

271 of 271 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Parallel organization of functionally segregated circuits linking basal ganglia and cortex
Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.09.030186.002041 · Cited by 8,527
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
Handbook of Chemical Neuroanatomy
Stern, C. D. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90021-5 · Cited by 4,160
Functional architecture of basal ganglia circuits: neural substrates of parallel processing
Alexander, G. E., & Crutcher, M. D. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90107-l · Cited by 4,131
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
D 1 and D 2 Dopamine Receptor-regulated Gene Expression of Striatonigral and Striatopallidal Neurons
Gerfen, C. R., Engber, T. M., Mahan, L. C., Susel, Z., Chase, T. N., Monsma, F. J., & Sibley, D. R. (1990) · Science · doi:10.1126/science.2147780 · Cited by 2,967
Self-citation
Basal ganglia-thalamocortical circuits: parallel substrates for motor, oculomotor, "prefrontal" and "limbic" functions.
Alexander, G. E., Crutcher, M. D., & DeLong, M. R. (1990) · PubMed · Cited by 2,422
Characterization and localization of cannabinoid receptors in rat brain: a quantitative in vitro autoradiographic study
Herkenham, M., Lynn, A., Johnson, M., Melvin, L., de Costa, B., & Rice, K. (1991) · The Journal of Neuroscience · doi:10.1523/jneurosci.11-02-00563.1991 · Cited by 2,159
Reversal of experimental parkinsonism by lesions of the subthalamic nucleus.
Bergman, H., Wichmann, T., & Delong, M. (1990) · Science · doi:10.1126/science.2402638 · Cited by 2,003
Chapter 6 Basal ganglia-thalamocortical circuits: Parallel substrates for motor, oculomotor, “prefrontal” and “limbic” functions
(1991) · Progress in Brain Research · doi:10.1016/s0079-6123(08)62678-3 · Cited by 1,961

Show all 271 references

Research works printed but not linked: 7

Bjorklund, 1984, Dopamine-containing systems in the CNS, Vol. 2, 52
Hong, 1978, Rat striatal methionine-enkephalin content after chronic treatment with cataleptogenic and noncataleptogenic drugs, J. Pharmacol. Exp. Ther., 205, 141
Jones, 1984, Laminar distribution of cortical efferent cells, Vol. 1, 521
Mocchetti, 1985, Use of mRNA hybridization and radiommunoassay to study mechanism of drug-induced accumulation of enkaphalins in rat brain structures, Mol. Pharmacol., 28, 86
Ramón, 1911, Histologie du Système Nerveux de l'Homme et des Vertébrés, 2, 504
Royce, 1983, Cortical neurons with collateral projections to both caudate nucleus and the centromedian-parafasciular thalamic complex: A fluorescent retrograde double labeling study in the cat, Exp. Brain Res., 50, 157
Smith, 1998, Microcircuitry of the direct and indirect pathways of the basal ganglia, Neuroscience, 86, 353

Sorted by citations

A mesoscale connectome of the mouse brain
Oh, S. W., Harris, J. A., Ng, L., Winslow, B., Cain, N., Mihalas, S., Wang, Q., Lau, C., Kuan, L., Henry, A. M., et al. (2014) · Nature · doi:10.1038/nature13186 · Cited by 2,612
Self-citation
Putting a spin on the dorsal-ventral divide of the striatum
Voorn, P., Vanderschuren, L. J. M. J., Groenewegen, H. J., Robbins, T. W., & Pennartz, C. M. A. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.06.006 · Cited by 1,188
An Update on the Mechanisms of the Psychostimulant Effects of Caffeine
Ferré, S. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.05196.x · Cited by 440
Cortical activation of accumbens hyperpolarization-active NMDARs mediates aversion-resistant alcohol intake
Seif, T., Chang, S., Simms, J. A., Gibb, S. L., Dadgar, J., Chen, B. T., Harvey, B. K., Dorit Ron, A., Messing, R. O., Bonci, A., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3445 · Cited by 325
Calcium signaling cascade links dopamine D1–D2 receptor heteromer to striatal BDNF production and neuronal growth
Hasbi, A., Fan, T., Alijaniaram, M., Nguyen, T., Perreault, M. L., O’Dowd, B. F., & George, S. R. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903676106 · Cited by 284
Metabotropic glutamate type 5, dopamine D2 and adenosine A2a receptors form higher‐order oligomers in living cells
Cabello, N., Gandía, J., Bertarelli, D. C. G., Watanabe, M., Lluı́s, C., Franco, R., Ferré, S., Luján, R., & Ciruela, F. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06078.x · Cited by 253
Drd1a-tdTomato BAC Transgenic Mice for Simultaneous Visualization of Medium Spiny Neurons in the Direct and Indirect Pathways of the Basal Ganglia
Shuen, J. A., Chen, M., Gloss, B. R., & Calakos, N. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5492-07.2008 · Cited by 231
Distribution of PINK1 and LRRK2 in rat and mouse brain
Taymans, J., den Haute, C. V., & Baekelandt, V. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03919.x · Cited by 184
Marked changes in signal transduction upon heteromerization of dopamine D1 and histamine H3 receptors
Ferrada, C., Moreno, E., Casadó, V., Bongers, G., Cortés, A., Mallol, J., Canela, E. I., Leurs, R., Ferré, S., Lluı́s, C., et al. (2009) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2009.00152.x · Cited by 162
Adenosine–cannabinoid receptor interactions. Implications for striatal function
Ferré, S., Lluı́s, C., Justinová, Z., Quiroz, C., Orrù, M., Navarro, G., Canela, E. I., Franco, R., & Goldberg, S. R. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.00723.x · Cited by 129
Stress responses: the contribution of prostaglandin E2 and its receptors
Furuyashiki, T., & Narumiya, S. (2010) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2010.194 · Cited by 132
Dopamine D1-D2 receptor heteromer signaling pathway in the brain: emerging physiological relevance
Hasbi, A., O’Dowd, B. F., & George, S. R. (2011) · Molecular Brain · doi:10.1186/1756-6606-4-26 · Cited by 121
Differential glutamate‐dependent and glutamate‐independent adenosine A1 receptor‐mediated modulation of dopamine release in different striatal compartments
Borycz, J., Pereira, M. F., Melani, A., Rodrigues, R. J., Köfalvi, A., Panlilio, L. V., Pedata, F., Goldberg, S. R., Cunha, R. A., & Ferré, S. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04386.x · Cited by 118
Pivotal Role of Adenosine Neurotransmission in Restless Legs Syndrome
Ferré, S., Quiroz, C., Guitart, X., Rea, W. P., Seyedian, A., Moreno, E., Casadó-Anguera, V., Díaz‐Ríos, M., Casadó, V., Clemens, S., et al. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00722 · Cited by 102
Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndrome
Stillman, A. A., Krsnik, Ž., Sun, J., Rašin, M., State, M. W., šestan, N., & Louvi, A. (2009) · Journal of Comparative Neurology · doi:10.1002/cne.21919 · Cited by 95
Statistical Properties of Pauses of the High-Frequency Discharge Neurons in the External Segment of the Globus Pallidus
Elias, S., Joshua, M., Goldberg, J. A., Heimer, G., Arkadir, D., Morris, G., & Bergman, H. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4156-06.2007 · Cited by 94
Cellular activation in limbic brain systems during social play behaviour in rats
van Kerkhof, L. W. M., Trezza, V., Mulder, T., Gao, P., Voorn, P., & Vanderschuren, L. J. M. J. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0558-y · Cited by 83
Cellular and subcellular localization of Huntington aggregates in the brain of a rat transgenic for Huntington disease
Petrasch‐Parwez, E., Nguyen, H. P., Löbbecke‐Schumacher, M., Habbes, H., Wieczorek, S., Rieß, O., Andres, K. H., Dermietzel, R., & von Hörsten, S. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21272 · Cited by 86
Targeting hypersensitive corticostriatal terminals in restless legs syndrome
Yepes, G., Guitart, X., Rea, W. P., Newman, A. H., Allen, R. P., Earley, C. J., Quiroz, C., & Ferré, S. (2017) · Annals of Neurology · doi:10.1002/ana.25104 · Cited by 81
The neuroinvasive profiles of H129 (herpes simplex virus type 1) recombinants with putative anterograde-only transneuronal spread properties
Wojaczynski, G. J., Engel, E. A., Steren, K. E., Enquist, L. W., & Card, J. P. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0733-9 · Cited by 76
D-Serine and D-Cycloserine Reduce Compulsive Alcohol Intake in Rats
Seif, T., Simms, J. A., Lei, K., Wegner, S., Bonci, A., Messing, R. O., & Hopf, F. W. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.84 · Cited by 75
Diversity matters – heterogeneity of dopaminergic neurons in the ventral mesencephalon and its relation to Parkinson's Disease
Weisenhorn, D. M. V., Giesert, F., & Wurst, W. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13670 · Cited by 73
Comprehensive Mapping of Regional Expression of the Clock Protein PERIOD2 in Rat Forebrain across the 24-h Day
Harbour, V. L., Weigl, Y., Robinson, B., & Amir, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076391 · Cited by 69
Prostaglandin E2Acts on EP1Receptor and Amplifies Both Dopamine D1and D2Receptor Signaling in the Striatum
Kitaoka, S., Furuyashiki, T., Nishi, A., Shuto, T., Koyasu, S., Matsuoka, T., Miyasaka, M., Greengard, P., & Narumiya, S. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3257-07.2007 · Cited by 63
Quantitative Analyses of the Projection of Individual Neurons from the Midline Thalamic Nuclei to the Striosome and Matrix Compartments of the Rat Striatum
Unzai, T., Kuramoto, E., Kaneko, T., & Fujiyama, F. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv295 · Cited by 61
Untangling dopamine-adenosine receptor assembly in experimental parkinsonism
Fernández‐Dueñas, V., Taura, J. J., Cottet, M., Gómez‐Soler, M., López‐Cano, M., Ledent, C. A., Watanabe, M., Trinquet, E., Pin, J., Luján, R., et al. (2014) · Disease Models & Mechanisms · doi:10.1242/dmm.018143 · Cited by 59
Effects of Exogenous and Endogenous Cannabinoids on GABAergic Neurotransmission between the Caudate-Putamen and the Globus Pallidus in the Mouse
Engler, B., Freiman, I., Urbanski, M. J., & Szabó, B. (2006) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.105.092718 · Cited by 58
Local or Not Local: Investigating the Nature of Striatal Theta Oscillations in Behaving Rats
Lalla, L., Rueda‐Orozco, P. E., Jurado-Parras, M.-T., Brovelli, A., & Robbe, D. (2017) · eNeuro · doi:10.1523/eneuro.0128-17.2017 · Cited by 54
Analysis of the effects of cannabinoids on identified synaptic connections in the caudate‐putamen by paired recordings in transgenic mice
Freiman, I., Anton, A., Monyer, H., Urbanski, M. J., & Szabó, B. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.114272 · Cited by 55
The nigrostriatal DA pathway and Parkinson’s disease
Fuxé, K., Manger, P. R., Genedani, S., & Agnati, L. F. (2006) · Springer eBooks · doi:10.1007/978-3-211-45295-0_13 · Cited by 52
ROLE OF ADENOSINE IN THE CONTROL OF HOMOSYNAPTIC PLASTICITY IN STRIATAL EXCITATORY SYNAPSES
Ferré, S., Borycz, J., Goldberg, S. R., Hope, B. T., Morales, M., Lluı́s, C., Franco, R., Ciruela, F., & Cunha, R. A. (2005) · Journal of Integrative Neuroscience · doi:10.1142/s0219635205000987 · Cited by 50
Basal Ganglia Neuromodulation Over Multiple Temporal and Structural Scales—Simulations of Direct Pathway MSNs Investigate the Fast Onset of Dopaminergic Effects and Predict the Role of Kv4.2
Lindroos, R., Dorst, M. C., Du, K., Filipović, M., Keller, D. X., Ketzef, M., Kozlov, A., Kumar, A., Lindahl, M., Nair, A. G., et al. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00003 · Cited by 44
Noradrenalin and dopamine receptors both control cAMP-PKA signaling throughout the cerebral cortex
Nomura, S., Bouhadana, M., Morel, C., Fauré, P., Cauli, B., Lambolez, B., & Hepp, R. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00247 · Cited by 47
Differential Proteome of the Striatum from Hemiparkinsonian Rats Displays Vivid Structural Remodeling Processes
Lessner, G., Schmitt, O., Haas, S. J.-P., Mikkat, S., Kreutzer, M., Wree, A., & Glocker, M. O. (2010) · Journal of Proteome Research · doi:10.1021/pr100389u · Cited by 46
A cadherin‐based code for the divisions of the mouse basal ganglia
Hertel, N., Krishna‐K, Nuernberger, M., & Redies, C. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21696 · Cited by 46
The Role of Adenosine Tone and Adenosine Receptors in Huntington's Disease
Blum, D. L., Chern, Y., Domenici, M. R., Buée, L., Lin, C., Rea, W. P., Ferré, S., & Popoli, P. (2018) · Journal of Caffeine and Adenosine Research · doi:10.1089/caff.2018.0006 · Cited by 48
Corticofugal GABAergic projection neurons in the mouse frontal cortex
Tomioka, R., Sakimura, K., & Yanagawa, Y. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00133 · Cited by 48
Long-term oral methylphenidate treatment in adolescent and adult rats: differential effects on brain morphology and function
van der Marel, K., Klomp, A., Meerhoff, G. F., Schipper, P., Lucassen, P. J., Homberg, J. R., Dijkhuizen, R. M., & Reneman, L. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2013.169 · Cited by 42
An MRI atlas of the mouse basal ganglia
Ullmann, J. F. P., WATSON, C. R. R., Janke, A. L., Kurniawan, N. D., Paxinos, G., & Reutens, D. C. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0572-0 · Cited by 41
Effect of l‐Dopa on metabotropic glutamate receptor 5 in the brain of parkinsonian monkeys
Ouattara, B., Gasparini, F., Morissette, M., Grégoire, L., Samadi, P., Gomez‐Mancilla, B., & Paolo, T. D. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06635.x · Cited by 43
Neuronal Responses in the Nucleus Accumbens Shell during Sexual Behavior in Male Rats
Matsumoto, J., Urakawa, S., Hori, E., de Araújo, M. F. P., Sakuma, Y., Ono, T., & Nishijo, H. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5140-11.2012 · Cited by 40
GDNF control of the glutamatergic cortico‐striatal pathway requires tonic activation of adenosine A2Areceptors
Gomes, C. A., Simões, P. F., Canas, P. M., Quiroz, C., Sebastião, A. M., Ferré, S., Cunha, R. A., & Ribeiro, J. A. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.05876.x · Cited by 38
The connectome of the basal ganglia
Schmitt, O., Eipert, P., Kettlitz, R., Leßmann, F., & Wree, A. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0936-0 · Cited by 37
The small‐conductance calcium‐activated potassium channel is a key modulator of firing and long‐term depression in the dorsal striatum
Hopf, F. W., Seif, T., Mohamedi, M. L., Chen, B. T., & Bonci, A. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07231.x · Cited by 36
The integrity of cholinergic basal forebrain neurons depends on expression of Nkx2‐1
Magno, L., Kretz, O., Bert, B., Ersözlü, S., Vogt, J., Fink, H., Kimura, S., Vogt, A., Monyer, H., Nitsch, R., et al. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07890.x · Cited by 33
Functional and Neuroprotective Role of Striatal Adenosine A 2A Receptor Heterotetramers
Ferré, S., & Ciruela, F. (2019) · Journal of Caffeine and Adenosine Research · doi:10.1089/caff.2019.0008 · Cited by 35
Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder
Piantadosi, S. C., McClain, L. L., Klei, L., Wang, J., Chamberlain, B. L., Springer, S. A., Lewis, D. A., Devlin, B., & Ahmari, S. E. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01290-1 · Cited by 30
Repeated whisker stimulation evokes invariant neuronal responses in the dorsolateral striatum of anesthetized rats: a potential correlate of sensorimotor habits
Mowery, T. M., Harrold, J. B., & Alloway, K. D. (2011) · Journal of Neurophysiology · doi:10.1152/jn.01018.2010 · Cited by 30
Three-dimensional organization of dendrites and local axon collaterals of shell and core medium-sized spiny projection neurons of the rat nucleus accumbens
van Dongen, Y. C., Mailly, P., Thierry, A. M., Groenewegen, H. J., & Deniau, J. (2008) · Brain Structure and Function · doi:10.1007/s00429-008-0173-5 · Cited by 28
Morphological elucidation of basal ganglia circuits contributing reward prediction
Fujiyama, F., TAKAHASHI, S. Y., & Karube, F. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00006 · Cited by 33
Relation between rotation in the 6-OHDA lesioned rat and dopamine loss in striatal and substantia nigra subregions
OLDS, M. E., Jacques, D., & Kopyov, O. V. (2006) · Synapse · doi:10.1002/syn.20270 · Cited by 26
Selective neuronal expression of the SoxE factor, Sox8, in direct pathway striatal projection neurons of the developing mouse brain
Merchán, P., Nardini, D., Waclaw, R. R., & Campbell, K. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24232 · Cited by 25
Blockade of Adenosine A2AReceptors Prevents Protein Phosphorylation in the Striatum Induced by Cortical Stimulation
Quiroz, C., Gomes, C. A., Pak, A. C., Ribeiro, J. A., Goldberg, S. R., Hope, B. T., & Ferré, S. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1661-06.2006 · Cited by 25
Regulation of the Protocadherin Celsr3 Gene and Its Role in Globus Pallidus Development and Connectivity
Jia, Z., Guo, Y., Tang, Y., Xu, Q., Li, B., & Wu, Q. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.00760-14 · Cited by 24
Evaluation of WGA–Cre-dependent topological transgene expression in the rodent brain
Libbrecht, S., den Haute, C. V., Malinouskaya, L., Gijsbers, R., & Baekelandt, V. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1241-x · Cited by 23
Stimulation of Adenosine Receptors Selectively Activates Gene Expression in Striatal Enkephalinergic Neurons
Karcz‐Kubicha, M., Ferré, S., Dı́az-Ruiz, O., Quiroz-Molina, C., Goldberg, S. R., Hope, B. T., & Morales, M. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301035 · Cited by 22
A Translational Murine Model of Sub-Lethal Intoxication with Shiga Toxin 2 Reveals Novel Ultrastructural Findings in the Brain Striatum
Tironi-Farinati, C., Geoghegan, P. A., Cangelosi, A., Pinto, A., Loidl, C. F., & Goldstein, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055812 · Cited by 19
Decreased parvalbumin immunoreactivity in the cortex and striatum of mice lacking the CB1 receptor
Fitzgerald, M. L., Lupica, C. R., & Pickel, V. M. (2011) · Synapse · doi:10.1002/syn.20911 · Cited by 20
Density gradients of vesicular glutamate‐ and GABA transporter‐immunoreactive boutons in calbindin‐ and μ‐opioid receptor‐defined compartments in the rat striatum
Wouterlood, F. G., Härtig, W., Groenewegen, H. J., & Voorn, P. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.23031 · Cited by 19
Expression pattern of stop lacZ reporter gene in adult and developing mouse brain
Couégnas, A., Schweitzer, A., Andrieux, A., Ghandour, M. S., & Boehm, N. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21278 · Cited by 23
Limb-clasping, cognitive deficit and increased vulnerability to kainic acid-induced seizures in neuronal glycosylphosphatidylinositol deficiency mouse models
Kandasamy, L. C., Tsukamoto, M., Banov, V., Sambuu, T., Nagasawa, Y., Kato, M., Matsumoto, N., Takeda, J., Itohara, S., Ogawa, S., et al. (2021) · Human Molecular Genetics · doi:10.1093/hmg/ddab052 · Cited by 15
Corticofugal projections from medial primary somatosensory cortex avoid EphA7-expressing neurons in striatum and thalamus
Tai, A. X., & Kromer, L. F. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.05.039 · Cited by 13
EphA7 expression identifies a unique neuronal compartment in the rat striatum
Tai, A. X., Cassidy, R. M., & Kromer, L. F. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23308 · Cited by 13
Critical test of the assumption that the hypothalamic entopeduncular nucleus of rodents is homologous with the primate internal pallidum
Puelles, L., Stühmer, T., Rubenstein, J. L. R., & Dı́az, C. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25536 · Cited by 12
Mesencephalic dopamine neurons interfacing the shell of nucleus accumbens and the dorsolateral striatum in the rat
Wouterlood, F. G., Engel, A., Daal, M. R. R., Houwen, G., Meinderts, A., Jordá-Siquier, T., Beliën, J. A. M., van Dongen, Y. C., Scheel‐Krüger, J., Thierry, A. M., et al. (2018) · Journal of Neuroscience Research · doi:10.1002/jnr.24242 · Cited by 12
Restless legs syndrome, neuroleptic-induced akathisia, and opioid-withdrawal restlessness: shared neuronal mechanisms?
Ferré, S., Winkelman, J. W., Garcı́a-Borreguero, D., Belcher, A. M., Chang, J., & Earley, C. J. (2023) · SLEEP · doi:10.1093/sleep/zsad273 · Cited by 10
Detection of Remote Neuronal Reactions in the Thalamus and Hippocampus Induced by Rat Glioma Using the PET Tracer Cis -4-[ 18 F]Fluoro-D-Proline
Geisler, S., Willuweit, A., Schroeter, M., Zilles, K., Hamacher, K., Galldiks, N., Shah, N. J., Coenen, H. H., & Langen, K. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.8 · Cited by 10
Toxic effects of methoxychlor in rat striatum: modifications in several neurotransmitters
Lafuente, A., Cabaleiro, T., Caride, A., Gutiérrez, A. J., & Esquifino, A. I. (2007) · Journal of Physiology and Biochemistry · doi:10.1007/bf03168228 · Cited by 10
The Endocannabinoid System is a Major Player in Schizophrenia
Köfalvi, A., & Fritzsche, M. (2007) · Springer eBooks · doi:10.1007/978-0-387-74349-3_22 · Cited by 10
Targeting the receptor-based interactome of the dopamine D1 receptor: looking for heteromer-selective drugs
Casadó-Anguera, V., Cortés, A., Casadó, V., & Moreno, E. (2019) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2019.1664469 · Cited by 10
Lateral regions of the rodent striatum reveal elevated glutamate decarboxylase 1 mRNA expression in medium‐sized projection neurons
Trifonov, S., Houtani, T., Kase, M., Toida, K., Maruyama, M., Yamashita, Y., Shimizu, J., & Sugimoto, T. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08001.x · Cited by 9
Inducible expression of retrograde transynaptic genetic tracer in mice
Sano, H., Nagai, Y., & Yokoi, M. (2007) · genesis · doi:10.1002/dvg.20273 · Cited by 9
Opposing collicular influences on the parafascicular (Pf) and posteromedial (POm) thalamic nuclei: relationship to POm-induced inhibition in the substantia nigra pars reticulata (SNR)
Watson, G. D. R., & Alloway, K. D. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1534-8 · Cited by 8
Gamma Knife Radiosurgery Targeting Protocols for the Experiments with Small Animals
Tokumaru, O., Hayashi, M., Katayama, Y., Tomida, M., Kawakami, Y., & Kouyama, N. (2007) · Stereotactic and Functional Neurosurgery · doi:10.1159/000099071 · Cited by 7
Effects of superior colliculus ablation on the air-righting reflex in the rat
Yan, X., Okito, K., & Yamaguchi, T. (2010) · The Journal of Physiological Sciences · doi:10.1007/s12576-009-0076-0 · Cited by 6
Striatum-related functional activation during reward- versus punishment-based learning in psychosis risk
Karcher, N. R., Hua, J. P. Y., & Kerns, J. G. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0455-z · Cited by 4
The presence and absence of prosencephalic cell groups relaying striatal information to the medial and lateral thalamus in tenrec
Künzle, H. (2008) · Journal of Anatomy · doi:10.1111/j.1469-7580.2008.00905.x · Cited by 4
Additive Effects of Coadministration of A2A Receptor Agonist CGS-21680and mGluR5 Antagonist MPEP on the Development and Expression of Methamphetamine-Induced Locomotor Sensitization in Rats
Acosta-García, J., Jiménez, J. C., & Miranda, F. (2017) · Journal of Drug and Alcohol Research · doi:10.4303/jdar/236038 · Cited by 3
Temporally and Functionally Distinct Contributions to Value Based Choice Along the Anterior-Posterior Dorsomedial Striatal AxisPreprint
Cifuentes, L. V., Díaz-Hernández, E., Granato, M. M., Tu, W., Choi, K., & Fuccillo, M. V. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.14.643367 · Cited by 3
Optogenetic Dissection of the Striatal Microcircuitry
Silberberg, G., & Planert, H. (2016) · Neuromethods · doi:10.1007/978-1-4939-3411-9_8 · Cited by 1
A Survey of Current Neuroanatomical Tracing Techniques
Wouterlood, F. G. (2014) · Neuromethods · doi:10.1007/978-1-4939-1963-5_1 · Cited by 2
The role of pallidal substance P and neurokinin receptors in the consolidation of spatial memory of rats
Kertes, E., Péczely, L., Ollmann, T., László, K., Berta, B., Kállai, V., Zagorácz, O., Kovács, A., Szabó, Á., Karádi, Z., et al. (2024) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyaf002 · Cited by 1
Signaling of dopamine receptor homo- and heterooligomers
Hasbi, A., O’Dowd, B. F., & George, S. R. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511760334.006
Reward-Modulated Motor Information in Dorsolateral Striatum Neurons
Isomura, Y. (2014) · Advances in cognitive neurodynamics · doi:10.1007/978-94-017-9548-7_65
Imaging of cAMP/PKA dynamics induced by catecholamines in the neocortical network
Nomura, S. (2014) · theses.fr (ABES) · doi:10.70675/362841cbzcc8bz415dzbd43zdfc38b35cdc1

Authors: Gerfen, C. R.
Affiliations: National Institute of Mental Health (US)
Corresponding author: Gerfen, Charles R.
ORCID: Gerfen, Charles R.
Venue: The Rat Nervous System
Publisher: Elsevier
Published: 2004
Pages: 455-508
DOI: 10.1016/b978-012547638-6/50019-5
OpenAlex: W3023504226
Cited by: 85
References: 271
Citations by year: 2025: 1 · 2024: 1 · 2023: 2 · 2021: 2 · 2019: 3 · 2018: 4 · 2017: 5 · 2016: 3 · 2015: 4 · 2014: 10 · 2013: 8 · 2012: 2
FWCI: 19.14
Type: book chapter
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Elsevier eBooks (publishedVersion)
Topics: Health Sciences › Medicine › Clinical Neurology › Deep Brain Stimulation and Movement Disorders
Health Sciences › Medicine › Clinical Neurology › Neurological and metabolic disorders
Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
Keywords: basal ganglia

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Basal Ganglia

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks