Alexander GE, Crutcher MD. Functional architecture of basal ganglia circuits; neural substrates of
parallel processing. Trends in neurosciences. 1990:266-271. doi:10.1016/0166-2236(90)90107-l
Bayer HM, Glimcher PW. Midbrain dopamine neurons encode a quantitative reward prediction error
signal. Neuron. 2005;47(1):129-141. doi:10.1016/j.neuron.2005.05.020
Bergman H, Feingold A, Nini A, et al. Physiological aspects of information processing in the basal
ganglia of normal and parkinsonian primates. Trends in neurosciences. 1997;21(1):1-7.
Bromberg-Martin ES, Matsumoto M, Hikosaka O. Dopamine in Motivational Control: Rewarding,
Aversive, and Alerting. Neuron. 2010;68(5):815-834. doi:10.1016/j.neuron.2010.11.022
Clark JJ, Hollon NG, Phillips PEM. Pavlovian valuation systems in learning and decision making.
Current Opinion in Neurobiology. 2012;22(6):1054-1061. doi:10.1016/j.conb.2012.06.004
Cohen JY, Haesler S, Vong L, Lowell BB, Uchida N. Neuron-type-specific signals for reward and
punishment in the ventral tegmental area. Nature. 2012;482(7383):85-88. doi:10.1038/nature10754
Cools AR, van Rossum JM. Excitation-mediating and inhibition-mediating dopamine-receptors: A
new concept towards a better understanding of electrophysiological, biochemical, pharmacological,
functional and clinical data. Psychopharmacologia. 1976;45(3):243-254. doi:10.1007/BF00421135
DeLong MR, Crutcher MD, Georgopoulos AP. Primate globus pallidus and subthalamic nucleus:
Functional
organization.
Journal
of
78
Neurophysiology.
1985;53(2):530-543.
doi:10.1152/jn.1985.53.2.530
Deniau JM, Menetrey A, Charpier S. The lamellar organization of the rat substantia nigra pars
reticulata: Segregated patterns of striatal afferents and relationship to the topography of corticostriatal
projections. Neuroscience. 1996;73(3):761-781. doi:10.1016/0306-4522(96)00088-7
Eshel N, Tian J, Bukwich M, Uchida N. Dopamine neurons share common response function for
reward prediction error. Nature Neuroscience. 2016;19(3):479-486. doi:10.1038/nn.4239
Chantal Francois, Gerard Percheron, Jerome Yelnik, Simone Heyner. A histological atlas of the
macaque (Macaca, mulatta) substantia nigra in ventricular coordinates. Brain Research Bulletin.
1985;14(4):349-367. doi:10.1016/0361-9230(85)90196-0
Fu YH, Yuan Y, Halliday G, Rusznák Z, Watson C, Paxinos G. A cytoarchitectonic and
chemoarchitectonic analysis of the dopamine cell groups in the substantia nigra, ventral tegmental
area, and retrorubral field in the mouse. Brain Structure and Function. 2012;217(2):591-612.
doi:10.1007/s00429-011-0349-2
Gangarossa G, Espallergues J, Mailly P, et al. Spatial distribution of D1R- and D2R-expressing
medium-sized spiny neurons differs along the rostro-caudal axis of the mouse dorsal striatum.
Frontiers in Neural Circuits. 2013;7(JUL):1-16. doi:10.3389/fncir.2013.00124
Gerfen CR, Surmeier DJ. Modulation of striatal projection systems by dopamine. Annual Review of
Neuroscience. 2011;34:441-466. doi:10.1146/annurev-neuro-061010-113641
Gerfen CR. The neostriatal mosaic: striatal patch-matrix organization is related to cortical lamination.
Science. 1989;246(4928):385-388. doi:10.1126/science.2799392
García-González D, Khodosevich K, Watanabe Y, Rollenhagen A, Lübke JHR, Monyer H.
79
Serotonergic Projections Govern Postnatal Neuroblast Migration. Neuron. 2017;94(3):534-549.e9.
doi:10.1016/j.neuron.2017.04.013
Griggs WS, Kim HF, Ghazizadeh A, Costello MG, Wall KM, Hikosaka O. Flexible and stable value
coding areas in caudate head and tail receive anatomically distinct cortical and subcortical inputs.
Frontiers in Neuroanatomy. 2017;11(November):1-19. doi:10.3389/fnana.2017.00106
Hintiryan H, Foster NN, Bowman I, et al. The mouse cortico-striatal projectome. Nature
Neuroscience. 2016;19(8):1100-1114. doi:10.1038/nn.4332
Horie M, Tsukano H, Hishida R, Takebayashi H, Shibuki K. Dual compartments of the ventral
division of the medial geniculate body projecting to the core region of the auditory cortex in C57BL/6
mice. Neuroscience Research. 2013;76(4):207-212. doi:10.1016/j.neures.2013.05.004
Hunnicutt BJ, Jongbloets BC, Birdsong WT, Gertz KJ, Zhong H, Mao T. A comprehensive excitatory
input map of the striatum reveals novel functional organization. eLife. 2016;5(November2016):1-32.
doi:10.7554/eLife.19103
Jaeger D, Gilman S, Wayne Aldridge J. Neuronal activity in the striatum and pallidum of primates
related to the execution of externally cued reaching movements. Brain Research. 1995;694(1-2):111127. doi:10.1016/0006-8993(95)00780-T
Jiang H, Kim HF. Anatomical inputs from the sensory and value structures to the tail of the rat
striatum. Frontiers in Neuroanatomy. 2018;12(May):1-17. doi:10.3389/fnana.2018.00030
Kim HF, Hikosaka O. Distinct Basal Ganglia Circuits Controlling Behaviors Guided by Flexible and
Stable Values. Neuron. 2013;79(5):1001-1010. doi:10.1016/j.neuron.2013.06.044
Kim HF, Hikosaka O. Parallel basal ganglia circuits for voluntary and automatic behaviour to reach
80
rewards. Brain. 2015;138(7):1776-1800. doi:10.1093/brain/awv134
Kim HF, Ghazizadeh A, Hikosaka O. Separate groups of dopamine neurons innervate caudate head
and tail encoding flexible and stable value memories. Frontiers in Neuroanatomy. 2014;8(October):112. doi:10.3389/fnana.2014.00120
Kim HF, Ghazizadeh A, Hikosaka O. Dopamine neurons encoding long-term memory of object value
for habitual behavior. Cell. 2015; 163(5):1165-1175. doi.org/10.1016/j.cell.2015.10.063.
Kincaid AE, Penney JB, Young AB, Newman SW. Evidence for a projection from the globus pallidus
to the entopeduncular nucleus in the rat. Neuroscience Letters. 1991;128(1):121-125.
doi:10.1016/0304-3940(91)90774-N
Kita H, Kitai ST. Intracellular study of rat globus pallidus neurons: membrane properties and
responses to neostriatal, subthalamic and nigral stimulation. Brain Res. 1991;564:296–305. doi:
10.1016/0006-8993(91)91466-E
Kreitzer AC. Physiology and pharmacology of striatal neurons. Annual Review of Neuroscience.
2009;32:127-147. doi:10.1146/annurev.neuro.051508.135422
Lança AJ, Boyd S, Kolb B, Kooy DVD. The development of a patchy organization of the rat striatum.
Developmental Brain Research. 1986;27(1):1-10. doi:10.1016/0165-3806(86)90226-9
LeDoux JE, Farb C, Ruggiero DA. Topographic organization of neurons in the acoustic thalamus that
project to the amygdala. Journal of Neuroscience. 1990;10(4):1043-1054. doi:10.1523/jneurosci.1004-01043.1990
Matsuda W, Furuta T, Nakamura KC, et al. Single nigrostriatal dopaminergic neurons form widely
spread and highly dense axonal arborizations in the neostriatum. Journal of Neuroscience.
81
2009;29(2):444-453. doi:10.1523/JNEUROSCI.4029-08.2009
de Mei C, Ramos M, Iitaka C, Borrelli E. Getting specialized: presynaptic and postsynaptic dopamine
D2 receptors. Current Opinion in Pharmacology. 2009;9(1):53-58. doi:10.1016/j.coph.2008.12.002
Menegas W, Bergan JF, Ogawa SK, et al. Dopamine neurons projecting to the posterior striatum form
an anatomically distinct subclass. eLife. 2015;4(AUGUST2015):1-30. doi:10.7554/eLife.10032
Menegas W, Babayan BM, Uchida N, Watabe-Uchida M. Opposite initialization to novel cues in
dopamine
signaling
in
ventral
and
posterior
striatum
in
mice.
eLife.
2017;6:1-26.
doi:10.7554/eLife.21886
Menegas W, Akiti K, Amo R, Uchida N, Watabe-Uchida M. Dopamine neurons projecting to the
posterior
striatum
reinforce
avoidance
of
threatening
stimuli.
Nature
Neuroscience.
2018;21(10):1421-1430. doi:10.1038/s41593-018-0222-1
Mikaelian D.O, Warfield D & Norris Olga. Genetic Progressive Hearing Loss in the C57/M6 Mouse:
Relation
of
Behaviorial
Responses
to
Cochlear
Anatomy.
Acta
Oto-Laryngologica.
1974;77:1(6):327-334. doi:10.3109/00016487409124632
Miyamoto Y, Katayama S, Shigematsu N, Nishi A, Fukuda T. Striosome-based map of the mouse
striatum that is conformable to both cortical afferent topography and uneven distributions of
dopamine D1 and D2 receptor-expressing cells. Brain Structure and Function. 2018;223(9):42754291. doi:10.1007/s00429-018-1749-3
Miyamoto Y, Nagayoshi I, Nishi A, Fukuda T. Three divisions of the mouse caudal striatum differ in
the proportions of dopamine D1 and D2 receptor-expressing cells, distribution of dopaminergic axons,
and composition of cholinergic and GABAergic interneurons. Brain Structure and Function.
82
2019;224(8):2703-2716. doi:10.1007/s00429-019-01928-3
Moriizumi T, Hattori T. Separate neuronal populations of the rat globus pallidus projecting to the
subthalamic nucleus, auditory cortex and pedunculopontine tegmental area. Neuroscience.
1992;46(3):701-710. doi:10.1016/0306-4522(92)90156-V
Mounir S, Parent A. The expression of neurokinin-1 receptor at striatal and pallidal levels in normal
human brain. Neuroscience Research. 2002;44(1):71-81. doi:10.1016/S0168-0102(02)00087-1
Nambu A, Tokuno H, Takada M. Functional significance of the cortico-subthalamo-pallidal
“hyperdirect”
pathway.
Neuroscience
Research.
2002;43(2):111-117.
doi:10.1016/S0168-
0102(02)00027-5
Parent A, Hazrati LN. Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamocortical loop. Brain Res. Rev. 1995a;20:91–127. doi:10.1016/0165-0173(94)00007-C
Parent A, Hazrati LN. Functional anatomy of the basal ganglia. II. The place of subthalamic nucleus
and external pallidium in basal ganglia circuitry. Brain Research Reviews. 1995b;20(1):128-154.
doi:10.1016/0165-0173(94)00008-D
Poulin JF, Caronia G, Hofer C, et al. Mapping projections of molecularly defined dopamine neuron
subtypes using intersectional genetic approaches. Nature Neuroscience. 2018;21(9):1260-1271.
doi:10.1038/s41593-018-0203-4
Robledo P, Ferger J. Excitatory influence of rat subthalamic nucleus to substantia nigra pars reticulata
and the pallidal complex: electrophysiological data. Brain Res. 1990;518:47–54. doi: 10.1016/00068993(90)90952-8
Schultz W, Dayan P, Montague PR. A neural substrate of prediction and reward. Science.
83
1997;275(5306):1593-1599. doi:10.1126/science.275.5306.1593
Schultz W. Predictive reward signal of dopamine neurons. Journal of Neurophysiology.
1998;80(1):1-27. doi:10.1152/jn.1998.80.1.1
Schultz W. Multiple dopamine functions at different time courses. Annual Review of Neuroscience.
2007;30:259-288. doi:10.1146/annurev.neuro.28.061604.135722
Storace DA, Higgins NC, Read HL. Thalamic label patterns suggest primary and ventral auditory
fields are distinct core regions. Journal of Comparative Neurology. 2010;518(10):1630-1646.
doi:10.1002/cne.22345
Sunahara, R., Guan, HC., O'Dowd, B. et al. Cloning of the gene for a human dopamine D5 receptor
with higher affinity for dopamine than D1. Nature. 1991;350:614–619. doi:10.1038/350614a0
Suzuki M, Sakamoto T, Kashio A, Yamasoba T. Age-related morphological changes in the basement
membrane in the stria vascularis of C57BL/6 mice. Eur Arch Otorhinolaryngol. 2016;273(1):57-62.
doi: 10.1007/s00405-014-3478-4.
Tsukano H, Horie M, Hishida R, Takahashi K, Takebayashi H, Shibuki K. Quantitative map of
multiple auditory cortical regions with a stereotaxic fine-scale atlas of the mouse brain. Scientific
Reports. 2016;6(February):1-12. doi:10.1038/srep22315
Tsukano H, Horie M, Ohga S, et al. Reconsidering tonotopic maps in the auditory cortex and
lemniscal auditory thalamus in mice. Frontiers in Neural Circuits. 2017;11(February):1-8.
doi:10.3389/fncir.2017.00014
Tsukano H, Horie M, Takahashi K, Hishida R, Takebayashi H, Shibuki K. Independent tonotopy and
thalamocortical projection patterns in two adjacent parts of the classical primary auditory cortex in
84
mice. Neuroscience Letters. 2017;637:26-30. doi:10.1016/j.neulet.2016.11.062
Vallone D, Picetti R, Borrelli E. Structure and function of dopamine receptors. Neuroscience and
Biobehavioral Reviews. 2000;24(1):125-132. doi:10.1016/S0149-7634(99)00063-9
Wichmann T, Bergman H, DeLong MR. The primate subthalamic nucleus. III. Changes in motor
behavior and neuronal activity in the internal pallidum induced by subthalamic inactivation in the
MPTP
model
of
parkinsonism.
Journal
of
Neurophysiology.
1994;72(2):521-530.
doi:10.1152/jn.1994.72.2.521
Xiong Q, Znamenskiy P, Zador AM. Selective corticostriatal plasticity during acquisition of an
auditory discrimination task. Nature. 2015;521(7552):348-351. doi:10.1038/nature14225
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