Basal Ganglia

Gerfen, Charles R.

doi:10.1016/b978-012547638-6/50019-5

Cited by 85Neurological disorders and treatmentsNeurological and metabolic disordersParkinson's Disease Mechanisms and Treatments

Basal Ganglia

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

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

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The striatum is a cellularly homogeneous structure that can be subdivided into distinct domains selectively targeted by cortical and other inputs.
“Although the striatum is a cellularly homogeneous structure that can be subdivided into distinct domains selectively targeted by cortical and other inputs36 (Fig. 5e), the thalamus is highly heterogeneous, composed of up to 50 discrete nuclei37, receiving and relaying diverse sensory, motor, behavioural state and cognitive information in parallel pathways to and from the isocortex.”
From A mesoscale connectome of the mouse brain (2014) · cites this paper as [36]

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Fine structural studies on a type of somatostatin‐immurioreactive neuron and its synaptic connections in the rat neostriatum: A correlated light and electron microscopic study
Takagi, H., Somogyi, P., Somogyi, J., & Smith, A. D. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902140102 · Cited by 154 · see citing works
Substance P content of substantia nigra after chronic treatment with antischizophrenic drugs
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Distribution of GABA‐immunoreactive neurons in the basal ganglia of the squirrel monkey (Saimiri sciureus)
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Compartmental distribution of striatal cell bodies expressing [Met]enkephalin-like immunoreactivity.
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Synaptic organization of cholinergic neurons in the monkey neostriatum
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Characterization of calretinin-immunoreactive structures in the striatum of the rat
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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 · see citing works
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 · see citing works
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 · see citing works
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 310 · see citing works
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 274 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 128 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 92 · see citing works
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 · see citing works
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 82 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 67 · see citing works
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 66 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 45 · see citing works
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 44 · see citing works
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 · see citing works
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 · see citing works
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 40 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 30 · see citing works
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 29 · see citing works
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 · see citing works
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 · see citing works
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 26 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 20 · see citing works
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 · see citing works
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 · see citing works
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 19 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Effects of superior colliculus ablation on the air-righting reflex in the rat
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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 › Neurology › Neurological disorders and treatments
Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Neurological and metabolic disorders
Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
Keywords: basal ganglia

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