The DOI matches its Crossref record; 63 of the 63 references it cites were found in a registry or an index.
Origin and Molecular Specification of Globus Pallidus Neurons
Open accessAbstract
The mechanisms controlling the assembly of brain nuclei are poorly understood. In the forebrain, it is typically assumed that the formation of nuclei follows a similar sequence of events that in the cortex. In this structure, projection neurons are generated sequentially from common progenitor cells and migrate radially to reach their final destination, whereas interneurons are generated remotely and arrive to the cortex through tangential migration. Using the globus pallidus as a model to study the formation of forebrain nuclei, we found that the development of this basal ganglia structure involves the generation of several distinct classes of projection neurons from relatively distant progenitor pools, which then assemble together through tangential migration. Our results thus suggest that tangential migration in the forebrain is not limited to interneurons, as previously thought, but also involves projection neurons and reveal that the assembly of forebrain nuclei is more complex than previously anticipated.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
In the citing paper
“the generation of cortical interneurons is largely limited to the dorsal and intermediate domains of the MGE, whereas the ventrocaudal domain specializes in the production of PV+ projection neurons for the globus pallidus”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Nóbrega-Pereira et al., 2010
In the citing paper
“Genetic ‘fate-mapping’ using Lhx8-Cre suggested that these neurons account for the majority, if not all of the cholinergic projection and interneuron populations within the nucleus basalis, medial septum, and striatum, respectively, as well as the majority of Pvalb-positive projection neurons in the globus pallidus5,6”
From Developmental diversification of cortical inhibitory interneurons (2018) · cites this paper as [5]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Specification of Cerebral Cortical Areas
Rakic, P. (1988) · Science · doi:10.1126/science.3291116 · Cited by 3,127 · cited 1×
“In the cortex, projection neurons arise to their final destination through radial migration, which serves to maintain relatively stable topological relationships between the ventricular zone and the underlying mantle (Rakic, 1988, 2007).”
Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus
Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121
Noctor, S. C., Martínez-Cerdeño, V., Ivic, L., & Kriegstein, A. R. (2004) · Nature Neuroscience · doi:10.1038/nn1172 · Cited by 2,229
Mode of cell migration to the superficial layers of fetal monkey neocortex
Rakic, P. (1972) · Journal of Comparative Neurology · doi:10.1002/cne.901450105 · Cited by 2,170
Neuronal subtype specification in the cerebral cortex
Molyneaux, B. J., Arlotta, P., Menezes, J. R. L., & Macklis, J. D. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2151 · Cited by 1,704
The neostriatal mosaic: multiple levels of compartmental organization
Gerfen, C. R. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90355-c · Cited by 1,471
A long, remarkable journey: Tangential migration in the telencephalon
Marín, Ó., & Rubenstein, J. L. R. (2001) · Nature reviews. Neuroscience · doi:10.1038/35097509 · Cited by 1,077
The origin and specification of cortical interneurons
Wonders, C. P., & Anderson, S. A. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1954 · Cited by 980 · cited 1×
“Neuronal diversity in the cerebral cortex also increases with the incorporation of interneurons born at remote locations and that reach the cortex through tangential migration (Corbin et al., 2001; Marín and Rubenstein, 2001; Wonders and Anderson, 2006).”
C ELL M IGRATION IN THE F OREBRAIN
Marín, Ó., & Rubenstein, J. L. R. (2003) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.041002.131058 · Cited by 957
Sussel, L., Marin, O., Kimura, S., & Rubenstein, J. L. R. (1999) · Development · doi:10.1242/dev.126.15.3359 · Cited by 873
Cited by
Sorted by citations
Development and Functional Diversification of Cortical Interneurons
Lim, L., Mi, D., Llorca, A., & Marín, O. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.009 · Cited by 714
“Interestingly, the generation of cortical interneurons is largely limited to the dorsal and intermediate domains of the MGE, whereas the ventrocaudal domain specializes in the production of PV+ projection neurons for the globus pallidus (Flandin et al., 2010; Nóbrega-Pereira et al., 2010).”
Nicholas, C. R., Chen, J., Tang, Y., Southwell, D. G., Chalmers, N., Vogt, D. L., Arnold, C. M., Chen, Y.-J. J., Stanley, E. G., Elefanty, A. G., et al. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.04.005 · Cited by 528
Developmental diversification of cortical inhibitory interneurons
Mayer, C., Hafemeister, C., Bandler, R. C., Machold, R., Batista Brito, R., Jaglin, X., Allaway, K., Butler, A., Fishell, G., & Satija, R. (2018) · Nature · doi:10.1038/nature25999 · Cited by 492
Non-epithelial stem cells and cortical interneuron production in the human ganglionic eminences
Hansen, D. V., Lui, J. H., Flandin, P., Yoshikawa, K., Rubenstein, J. L., Alvarez-Buylla, A., & Kriegstein, A. R. (2013) · Nature Neuroscience · doi:10.1038/nn.3541 · Cited by 328
Prototypic and arkypallidal neurons in the dopamine-intact external globus pallidus
Abdi, A., Mallet, N., Mohamed, F. Y., Sharott, A., Dodson, P. D., Nakamura, K. C., Suri, S., Avery, S. V., Larvin, J. T., Garas, F. N., et al. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4662-14.2015 · Cited by 247
Portmann, T., Yang, M., Mao, R., Panagiotakos, G., Ellegood, J., Dolen, G., Bader, P. L., Grueter, B. A., Goold, C., Fisher, E., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.03.036 · Cited by 245
Arkypallidal Cells Send a Stop Signal to Striatum
Mallet, N. P., Schmidt, R., Leventhal, D., Chen, F., Amer, N., Boraud, T., & Berke, J. D. (2016) · Neuron · doi:10.1016/j.neuron.2015.12.017 · Cited by 241
Amplification of progenitors in the mammalian telencephalon includes a new radial glial cell type
Pilz, G.-A., Shitamukai, A., Reillo, I., Pacary, E., Schwausch, J., Stahl, R., Ninkovic, J., Snippert, H. J. G., Clevers, H. C., Godinho, L., et al. (2013) · Nature Communications · doi:10.1038/ncomms3125 · Cited by 229
Mastro, K. J., Bouchard, R. S., Holt, H. A. K., & Gittis, A. H. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4646-13.2014 · Cited by 198
Mouse and human share conserved transcriptional programs for interneuron development
Shi, Y., Wang, M., Mi, D., Lu, T., Wang, B., Dong, H., Zhong, S., Chen, Y., Sun, L., Zhou, X., et al. (2021) · Science · doi:10.1126/science.abj6641 · Cited by 196
Dodson, P. D., Larvin, J. T., Duffell, J. M., Garas, F. N., Doig, N. M., Kessaris, N., Duguid, I., Bogacz, R., Butt, S. J. B., & Magill, P. J. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.007 · Cited by 167
Flandin, P., Zhao, Y., Vogt, D., Jeong, J., Long, J., Potter, G., Westphal, H., & Rubenstein, J. L. R. (2011) · Neuron · doi:10.1016/j.neuron.2011.04.020 · Cited by 155
McKinsey, G. L., Lindtner, S., Trzcinski, B., Visel, A., Pennacchio, L. A., Huylebroeck, D., Higashi, Y., & Rubenstein, J. L. R. (2013) · Neuron · doi:10.1016/j.neuron.2012.11.035 · Cited by 153
The external globus pallidus: progress and perspectives
Hegeman, D. J., Hong, E. S., Hernández, V. M., & Chan, C. S. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13196 · Cited by 157
Hernandez, V. M., Hegeman, D. J., Cui, Q., Kelver, D. A., Fiske, M. P., Glajch, K. E., Pitt, J. E., Huang, T. Y., Justice, N. J., & Chan, C. S. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4672-14.2015 · Cited by 148
New roles for the external globus pallidus in basal ganglia circuits and behavior
Gittis, A. H., Berke, J. D., Bevan, M. D., Chan, C. S., Mallet, N., Morrow, M. M., & Schmidt, R. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3252-14.2014 · Cited by 136
Miyoshi, G., Young, A., Petros, T., Karayannis, T., McKenzie Chang, M., Lavado, A., Iwano, T., Nakajima, M., Taniguchi, H., Huang, Z. J., et al. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.1164-15.2015 · Cited by 135
Npas1 + Pallidal Neurons Target Striatal Projection Neurons
Glajch, K. E., Kelver, D. A., Hegeman, D. J., Cui, Q., Xenias, H. S., Augustine, E. C., Hernández, V. M., Verma, N., Huang, T., Luo, M., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1720-15.2016 · Cited by 112
New Insights Into Cholinergic Neuron Diversity
Ahmed, N. Y., Knowles, R., & Dehorter, N. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00204 · Cited by 108
Pessoa, L., Medina, L., Hof, P. R., & Desfilis, E. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.09.021 · Cited by 105
Refocusing neuroscience: moving away from mental categories and towards complex behaviours
Pessoa, L., Medina, L. M., & Desfilis, E. (2021) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2020.0534 · Cited by 106
Npas1 + -Nkx2.1 + Neurons Are an Integral Part of the Cortico-pallido-cortical Loop
Abecassis, Z. A., Berceau, B. L., Win, P. H., García, D., Xenias, H. S., Cui, Q., Pamukcu, A., Cherian, S., Hernández, V. M., Chon, U., et al. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1199-19.2019 · Cited by 97
Dong, J., Hawes, S., Wu, J., Le, W., & Cai, H. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.645287 · Cited by 93
Cellular and Synaptic Dysfunctions in Parkinson’s Disease: Stepping Out of the Striatum
Mallet, N. P., Delgado-Zabalza, L., Chazalon, M., Miguélez, C., & Baufreton, J. (2019) · Cells · doi:10.3390/cells8091005 · Cited by 98
Apical versus basal neurogenesis directs cortical interneuron subclass fate
Petros, T. J., Bultje, R. S., Ross, M. E., Fishell, G., & Anderson, S. A. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.079 · Cited by 91
Bupesh, M., Legáz, I., Abellán, A., & Medina, L. M. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22581 · Cited by 89
Functionally Distinct Connectivity of Developmentally Targeted Striosome Neurons
McGregor, M. M., McKinsey, G. L., Girasole, A. E., Bair-Marshall, C. J., Rubenstein, J. L. R., & Nelson, A. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.076 · Cited by 80
Kuenzel, W. J., Medina, L. M., Csillag, A., Perkel, D. J., & Reiner, A. J. (2011) · Brain Research · doi:10.1016/j.brainres.2011.09.037 · Cited by 83
Parvalbumin + and Npas1 + Pallidal Neurons Have Distinct Circuit Topology and Function
Pamukcu, A., Cui, Q., Xenias, H. S., Berceau, B. L., Augustine, E. C., Fan, I., Chalasani, S., Hantman, A. W., Lerner, T. N., Boca, S. M., et al. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0361-20.2020 · Cited by 76
Critical Roles of the Direct GABAergic Pallido-cortical Pathway in Controlling Absence Seizures
Chen, M., Guo, D., Li, M., Ma, T., Wu, S., Ma, J., Cui, Y., Yang, X., Xu, P., & Yao, D. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004539 · Cited by 78
Identification of a direct GABA ergic pallidocortical pathway in rodents
Chen, M. C., Ferrari, L., Sacchet, M. D., Foland‐Ross, L. C., Qiu, M., Gotlib, I. H., Fuller, P. M., Arrigoni, E., & Lu, J. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12822 · Cited by 77
Bupesh, M., Abellán, A., & Medina, L. M. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22719 · Cited by 79
Review of bilirubin neurotoxicity I: molecular biology and neuropathology of disease
Riordan, S. M., & Shapiro, S. M. (2019) · Pediatric Research · doi:10.1038/s41390-019-0608-0 · Cited by 75
Human pallial MGE-type GABAergic interneuron cell therapy for chronic focal epilepsy
Bershteyn, M., Bröer, S., Parekh, M. B., Maury, Y., Havlicek, S., Kriks, S., Fuentealba, L. C., Lee, S., Zhou, R., Subramanyam, G., et al. (2023) · Cell stem cell · doi:10.1016/j.stem.2023.08.013 · Cited by 76
Molecular and functional definition of the developing human striatum
Onorati, M., Castiglioni, V., Biasci, D., Cesana, E., Menon, R., Vuono, R., Talpo, F., Goya, R. L., Lyons, P., Bulfamante, G., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3860 · Cited by 77
NPAS1 Represses the Generation of Specific Subtypes of Cortical Interneurons
Stanco, A., Pla, R., Vogt, D. L., Chen, Y., Mandal, S., Walker, J. M., Hunt, R. F., Lindtner, S., Erdman, C. A., Pieper, A. A., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.040 · Cited by 72
Self-citationRavikrishnan, A., Gandhi, P. J., Shelkar, G. P., Liu, J., Pavuluri, R., & Dravid, S. M. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.03.011 · Cited by 73
Developmental specification of forebrain cholinergic neurons
Allaway, K. C., & Machold, R. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2016.11.007 · Cited by 68
Dissociable Roles of Pallidal Neuron Subtypes in Regulating Motor Patterns
Cui, Q., Pamukcu, A., Cherian, S., Chang, I. Y. M., Berceau, B. L., Xenias, H. S., Higgs, M. H., Rajamanickam, S., Chen, Y., Du, X., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2210-20.2021 · Cited by 62
Chazalon, M., Paredes-Rodriguez, E., Morin, S., Martínez, A., Cristóvão‐Ferreira, S., Vaz, S. H., Sebastião, A. M., Panatier, A., Boué‐Grabot, É., Miguélez, C., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.04.014 · Cited by 70
Qian, S., Kumar, P., & Testai, F. D. (2022) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-022-01204-8 · Cited by 66
Radial glia in the ventral telencephalon
Turrero García, M., & Harwell, C. C. (2017) · FEBS Letters · doi:10.1002/1873-3468.12829 · Cited by 62
Cell and circuit complexity of the external globus pallidus
Courtney, C. D., Pamukcu, A., & Chan, C. S. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01368-7 · Cited by 59
Sonic hedgehogexpressing and responding cells generate neuronal diversity in the medial amygdala
Carney, R. S. E., Mangin, J., Hayes, L. N., Mansfield, K., Sousa, V. H., Fishell, G., Machold, R. P., Ahn, S., Gallo, V., & Corbin, J. G. (2010) · Neural Development · doi:10.1186/1749-8104-5-14 · Cited by 60
Wang, C., You, Y., Qi, D., Zhou, X., Wang, L., Wei, S., Zhang, Z., Huang, W., Liu, Z., Liu, F., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1758-14.2014 · Cited by 57
Sonic hedgehog signaling in the development of the mouse hypothalamus
Blaess, S., SzabÃ, N., Haddad-Tóvolli, R., Zhou, X., & Álvarez-Bolado, G. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00156 · Cited by 56
Interneuron development and dysfunction
Yang, J., Yang, X. W., & Tang, K. (2021) · FEBS Journal · doi:10.1111/febs.15872 · Cited by 54
Sp9 Regulates Medial Ganglionic Eminence-Derived Cortical Interneuron Development
Liu, Z., Zhang, Z., Lindtner, S., Li, Z., Xu, Z., Wei, S., Liang, Q., Wen, Y. F., Tao, G., You, Y., et al. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy133 · Cited by 53
Abrahao, K. P., & Lovinger, D. M. (2018) · The Journal of Physiology · doi:10.1113/jp276079 · Cited by 53
Ontogenetic expression of Sonic Hedgehog in the chicken subpallium
Bardet, S. M. (2010) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2010.00028 · Cited by 52
Developmental mechanisms for the generation of telencephalic interneurons
Corbin, J. G., & Butt, S. J. B. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20890 · Cited by 58
Active intermixing of indirect and direct neurons builds the striatal mosaic
Tinterri, A., Ménardy, F., Diana, M. A., Lokmane, L., Keita, M., Coulpier, F., Lemoine, S., Mailhes‐Hamon, C., Mathieu, B., Merchán, P., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07171-4 · Cited by 47
Mehler, M. F., Petronglo, J. R., Arteaga-Bracho, E. E., Gulinello, M. E., Winchester, M. L., Pichamoorthy, N., Young, S. K., Dejesus, C., Ishtiaq, H., Gökhan, Ş., et al. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2443-18.2018 · Cited by 49
Striatal circuit development and its alterations in Huntington's disease
Lebouc, M., Richard, Q., Garret, M., & Baufreton, J. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105076 · Cited by 45
Medina, L. M., & Abellán, A. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-369497-3.10007-x · Cited by 43
Evolutionary and Developmental Contributions for Understanding the Organization of the Basal Ganglia
Medina, L. M., Abellán, A., Vicario, A., & Desfilis, E. (2014) · Brain Behavior and Evolution · doi:10.1159/000357832 · Cited by 41
Synchrony in Parkinson's disease: importance of intrinsic properties of the external globus pallidus
Schwab, B. C., Heida, T., Zhao, Y., Marani, E., van Gils, S. A., & Wezel, R. J. A. V. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00060 · Cited by 37
Cellular birthdate predicts laminar and regional cholinergic projection topography in the forebrain
Allaway, K. C., Muñoz, W., Tremblay, R., Sherer, M., Herron, J., Rudy, B., Machold, R. P., & Fishell, G. (2020) · eLife · doi:10.7554/elife.63249 · Cited by 32
Joven, A., Morona, R., González, A., & Moreno, N. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23385 · Cited by 34
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
Distinct roles of cortical and pallidal β and γ frequencies in hemiparkinsonian and dyskinetic rats
Salvadè, A., D’Angelo, V., Giovanni, G. D., Tinkhauser, G., Sancesario, G., Städler, C., Möller, J. C., Stefani, A., Kaelin‐Lang, A., & Galati, S. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.11.005 · Cited by 35
Using a novel PV-Cre rat model to characterize pallidonigral cells and their terminations
Oh, Y.-M., Karube, F., TAKAHASHI, S. Y., Kobayashi, K., Takada, M., Uchigashima, M., Watanabe, M., Nishizawa, K., Kobayashi, K., & Fujiyama, F. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1346-2 · Cited by 30
Bupesh, M., Vicario, A., Abellán, A., Desfilis, E., & Medina, L. M. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0533-7 · Cited by 30
Neural Stem Cells Direct Axon Guidance via Their Radial Fiber Scaffold
Kaur, N., Han, W., Li, Z., Madrigal, M. P., Shim, S., Pochareddy, S., Gulden, F. O., Li, M., Xu, X., Xing, X., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.06.035 · Cited by 29
Frizzled3 Controls Axonal Polarity and Intermediate Target Entry during Striatal Pathway Development
Morello, F., Prasad, A. A., Rehberg, K., de Sá, R. V., Antón-Bolaños, N., Leyva‐Díaz, E., Adolfs, Y., Tissir, F., López‐Bendito, G., & Pasterkamp, R. J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1840-15.2015 · Cited by 28
Su-Feher, L., Rubin, A. N., Silberberg, S. N., Catta-Preta, R., Lim, K. J., Ypsilanti, A. R., Zdilar, I., McGinnis, C. S., McKinsey, G. L., Rubino, T. E., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2108760119 · Cited by 26
Wei, B. K., Huang, Z., He, S., Sun, C., You, Y., Liu, F., & Yang, Z. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.07.016 · Cited by 29
Transcriptomic and spatial organization of telencephalic GABAergic neurons
van Velthoven, C. T. J., Gao, Y., Kunst, M., Lee, C., McMillen, D., Chakka, A. B., Casper, T., Clark, M., Chakrabarty, R., Daniel, S. F., et al. (2025) · Nature · doi:10.1038/s41586-025-09296-1 · Cited by 32
Turkiewicz, J., Bhatt, R. R., Wang, H., Vora, P. P., Krause, B., Sauk, J. S., Jacobs, J. P., Bernstein, C. N., Kornelsen, J., Labus, J. S., et al. (2021) · NeuroImage Clinical · doi:10.1016/j.nicl.2021.102613 · Cited by 30
Organization of the Globus Pallidus
Kita, H., & Jaeger, D. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00013-1 · Cited by 25
Adult islet1 Expression Outlines Ventralized Derivatives Along Zebrafish Neuraxis
Baeuml, S. W., Biechl, D., & Wullimann, M. F. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00019 · Cited by 23
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
Garcı́a-Calero, E., & Scharff, C. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23174 · Cited by 24
St18 specifies globus pallidus projection neuron identity in MGE lineage
Nunnelly, L. F., Campbell, M., Lee, D. I., Dummer, P. D., Gu, G., Menon, V., & Au, E. (2022) · Nature Communications · doi:10.1038/s41467-022-35518-5 · Cited by 20
Four‐dimensional analysis of nucleogenesis of the pontine nucleus in the hindbrain
Shinohara, M., Zhu, Y., & Murakami, F. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23353 · Cited by 23
Zimmer‐Bensch, G. (2018) · Brain Research · doi:10.1016/j.brainres.2018.09.001 · Cited by 22
Qi, Z., Shen, K., Peng, J., Fan, X., Huang, H., Jiang, J., Lu, J., Wang, X., Fang, X., Chen, L., et al. (2022) · British Journal of Pharmacology · doi:10.1111/bph.16010 · Cited by 20
Substance P effects exclusively on prototypic neurons in mouse globus pallidus
Mizutani, K., TAKAHASHI, S. Y., Okamoto, S., Karube, F., & Fujiyama, F. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1453-8 · Cited by 20
Regional expression of Pax7 in the brain of Xenopus laevis during embryonic and larval development
Bandín, S., Morona, R., Moreno, N., & González, A. (2013) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00048 · Cited by 19
Malt, E. A., Juhasz, K., Malt, U. F., & Naumann, T. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00059 · Cited by 21
Neurogenesis in the Basal Ganglia
Rubenstein, J. L. R., & Campbell, K. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00097-6 · Cited by 14
Basal ganglia involvement in ARX patients: The reason for ARX patients very specific grasping?
Curie, A., Friocourt, G., Portes, V. D., Roy, A. C., Nazir, T. A., Amandine, B., Cheylus, A., Marcorelles, P., Retzepi, K., Maleki, N., et al. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.04.001 · Cited by 17
Fudge, J. L., Kelly, E. A., & Hackett, T. A. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1453-22.2022 · Cited by 14
Shen, C., Shen, B., Liu, D., Han, L., Zou, K., Gan, L., Ren, J., Wu, B., Tang, Y., Zhao, J., et al. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2024.101566 · Cited by 14
Arkypallidal neurons in basal ganglia circuits: Unveiling novel pallidostriatal loops?
Guilhemsang, L., & Mallet, N. P. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102814 · Cited by 12
Tangential migration of corridor guidepost neurons contributes to anxiety circuits
Tinterri, A., Deck, M., Keita, M., Mailhes‐Hamon, C., Rubin, A. N., Kessaris, N., Lokmane, L., Bielle, F., & Garel, S. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24330 · Cited by 12
Puelles, L., Stühmer, T., Rubenstein, J. L. R., & Dı́az, C. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25536 · Cited by 12
Bershteyn, M., Zhou, H., Fuentealba, L. C., Chen, C., Subramanyam, G., Cherkowsky, D., Sevilla, E. S., Hampel, P., Salvatierra, J., Sezan, M., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.06.010 · Cited by 14
PRISM: A Progenitor-Restricted Intersectional Fate Mapping Approach Redefines Forebrain Lineages
Poulin, J.-F., Luppi, M. P., Hofer, C., Caronia, G., Hsu, P.-K., Chan, C. S., & Awatramani, R. B. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.05.019 · Cited by 11
Fate of Neural Progenitor Cells Transplanted into Jaundiced and Nonjaundiced Rat Brains
Yang, F.-C., Riordan, S. M., Winter, M. K., Gan, L., Smith, P. G., Vivian, J. L., Shapiro, S. M., & Stanford, J. A. (2017) · Cell Transplantation · doi:10.3727/096368917x694840 · Cited by 10
Organization of the Globus Pallidus
Kita, H. (2010) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-374767-9.00013-5 · Cited by 11
Neurogenesis in the basal ganglia
Rubenstein, J. L. R., & Campbell, K. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00018-7 · Cited by 7
Tangential Migration in the Telencephalon
Marín, Ó. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-374245-2.00003-6 · Cited by 7
Troppoli, T. A., Yang, C. Z., Katsuki, F., Uygun, D. S., Lin, I., Aguilar, D. D., Spratt, T. J., Basheer, R., McNally, J. M., Chan, C. S., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2321410121 · Cited by 7
Yang, F.-C., Draper, J. M., Smith, P. G., Vivian, J. L., Shapiro, S. M., & Stanford, J. A. (2018) · Cell Transplantation · doi:10.1177/0963689718766327 · Cited by 6
Hindbrain Tangential Migration
Sotelo, C., & Chédotal, A. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00032-6 · Cited by 8
The transcriptomic and spatial organization of telencephalic GABAergic neuronal typesPreprint
van Velthoven, C. T. J., Gao, Y., Kunst, M., Lee, C., McMillen, D., Chakka, A. B., Casper, T., Clark, M., Chakrabarty, R., Daniel, S. F., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.18.599583 · Cited by 6
Transcriptomic insights into fate choice of pallial versus subpallial GABAergic neurons
Sun, L., Xiong, F., Huang, F., Dong, S., Zhu, P., Jiang, P., Zhang, B., Zhang, X., Sun, J., Peng, H., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60338-8 · Cited by 7
Siskos, N., Ververidis, C., Skavdis, G., & Grigoriou, M. E. (2021) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.785541 · Cited by 7
Transcriptional Regulation of Cortical Interneuron Development
Pai, E. L.-L., Vogt, D. L., Hu, J. S., & Rubenstein, J. L. R. (2024) · Oxford University Press eBooks · doi:10.1093/med/9780197549469.003.0047 · Cited by 6
Metadata
- Authors
- Nóbrega-Pereira, S., Gelman, D., Bartolini, G., Pla, R., Pierani, A., & Marín, O.
- Affiliations
- Consejo Superior de Investigaciones Científicas (ES)
- Centre National de la Recherche Scientifique (FR)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2010-02-24
- Volume
- 30
- Issue
- 8
- Pages
- 2824-2834
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6633933
- OpenAlex
- W2093983408
- Cited by
- 142
- References
- 63
- Citations by year
- 2026: 1 · 2025: 10 · 2024: 7 · 2023: 9 · 2022: 10 · 2021: 13 · 2020: 10 · 2019: 8 · 2018: 11 · 2017: 8 · 2016: 10 · 2015: 10 · 2014: 9 · 2013: 12 · 2012: 3
- FWCI
- 2.63
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion)
- Funders
- McKnight Foundation
- European Commission (005139)
- Centre National de la Recherche Scientifique
- Ministerio de Ciencia e Innovación (CSD2007-00023)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Keywords
- globus pallidus, neuronal specification, tangential migration, projection neurons, interneurons, basal ganglia development, neuronal migration
- MeSH terms
- Thyroid Nuclear Factor 1, Acetylcholine, Animals, Cell Differentiation, Cell Movement, Choline O-Acetyltransferase, DNA-Binding Proteins, gamma-Aminobutyric Acid, Globus Pallidus, Mice, Transgenic, Nerve Tissue Proteins, Neural Pathways, Neurons, Nuclear Proteins, Parvalbumins, Stem Cells, Transcription Factors, Biomarkers, Prosencephalon, Mice, Knockout, Gene Expression Regulation, Developmental, Mice, Basic Helix-Loop-Helix Proteins, Neurogenesis
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