The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.
Delineation of Multiple Subpallial Progenitor Domains by the Combinatorial Expression of Transcriptional Codes
Open accessAbstract
The mammalian telencephalon is considered the most complex of all biological structures. It comprises a large number of functionally and morphologically distinct types of neurons that coordinately control most aspects of cognition and behavior. The subpallium, for example, not only gives rise to multiple neuronal types that form the basal ganglia and parts of the amygdala and septum but also is the origin of an astonishing diversity of cortical interneurons. Despite our detailed knowledge on the molecular, morphological, and physiological properties of most of these neuronal populations, the mechanisms underlying their generation are still poorly understood. Here, we comprehensively analyzed the expression patterns of several transcription factors in the ventricular zone of the developing subpallium in the mouse to generate a detailed molecular map of the different progenitor domains present in this region. Our study demonstrates that the ventricular zone of the mouse subpallium contains at least 18 domains that are uniquely defined by the combinatorial expression of several transcription factors. Furthermore, the results of microtransplantation experiments in vivo corroborate that anatomically defined regions of the mouse subpallium, such as the medial ganglionic eminence, can be subdivided into functionally distinct domains.
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?
The cited source says what the claim attributes to it.
In the citing paper
“On the basis of the molecular signature and regional specificity of each subclass, the Subpallium-GABA neighbourhood (subclasses 39–90, total 1,051 clusters) was divided into 7 classes that are likely related to their distinct developmental origins29,30”
From A high-resolution transcriptomic and spatial atlas of cell types in the whole mouse brain (2023) · cites this paper as [29]
In the citing paper
“The subpallium of rodents and primates, including humans, can be subdivided into several progenitor domains each characterized by the expression of a specific combination of transcription factors”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Flames et al., 2007
In the citing paper
“Each progenitor domain in the MGE generates multiple types of cortical interneurons”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Flames et al., 2007
In the citing paper
“The ventricular zone (VZ) of the MGE, CGE and preoptic region can be subdivided into multiple domains of progenitor cells that are uniquely defined by the combinatorial expression of several transcription factors”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Flames et al., 2007
In the citing paper
“The POH, the most caudal progenitor domain in the preoptic region, lacks expression of Nkx2-1 and exhibit molecular similarities with the CGE”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Flames et al., 2007
In the citing paper
“the dorsal MGE has a strong bias toward the generation of SST+ interneurons, whereas the ventrocaudal domains produce a larger fraction of PV+ neurons”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Flames et al., 2007
In the citing paper
“Diversity is first apparent in the regional expression of a limited number of transcription factors within the ganglionic eminences (GEs)2,3.”
From Developmental diversification of cortical inhibitory interneurons (2018) · cites this paper as [2]
In the citing paper
“Two subdomains are found in the POA based on nonoverlapping expression profiles for Dbx1 and Nkx5.1”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [335]
In the citing paper
“most interneuron precursors emerging from the POA do not rely on downstream activation of Lhx6 to specify PV and SST interneurons”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [335]
In the citing paper
“which reinforces the view that this anatomical region contains a molecularly heterogeneous pool of progenitor cells (15).”
From Early emergence of cortical interneuron diversity in the mouse embryo (2018) · cites this paper as [15]
In the citing paper
“Although the molecular diversity of VZ cells was more limited than anticipated (15, 16), this analysis revealed diversity among SVZ progenitors (Fig. 2B and figs. S11 to S14).”
From Early emergence of cortical interneuron diversity in the mouse embryo (2018) · cites this paper as [15]
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
Echelard, Y., Epstein, D. J., St-Jacques, B., Shen, L., Mohler, J., McMahon, J. A., & McMahon, A. P. (1993) · Cell · doi:10.1016/0092-8674(93)90627-3 · Cited by 2,154
Neuronal specification in the spinal cord: inductive signals and transcriptional codes
Jessell, T. M. (2000) · Nature Reviews Genetics · doi:10.1038/35049541 · Cited by 2,089
Pax-6, a murine paired box gene, is expressed in the developing CNS
Walther, C., & Gruß, P. (1991) · Development · doi:10.1242/dev.113.4.1435 · Cited by 1,257
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 4×
“In addition, analysis of interneuron populations derived from the MGE and CGE suggests that these two regions may contain different progenitor pools (Xu et al., 2004; Butt et al., 2005; Wonders and Anderson, 2006).”
BackgroundInfluentialSussel, L., Marin, O., Kimura, S., & Rubenstein, J. L. R. (1999) · Development · doi:10.1242/dev.126.15.3359 · Cited by 873
Self-citationLavdas, A. A., Grigoriou, M., Pachnis, V., & Parnavelas, J. G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-18-07881.1999 · Cited by 765
Longitudinal organization of the anterior neural plate and neural tube
Shimamura, K., Hartigan-O’Connor, D. J., Martı́nez, S., Puelles, L., & Rubenstein, J. L. R. (1995) · Development · doi:10.1242/dev.121.12.3923 · Cited by 654
Self-citationOrigin and Molecular Specification of Striatal Interneurons
Marín, Ó., Anderson, S. A., & Rubenstein, J. L. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-16-06063.2000 · Cited by 643
Self-citationOrigins of Cortical Interneuron Subtypes
Xu, Q., Cobos, I., De La Cruz, E., Rubenstein, J. L., & Anderson, S. A. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.5667-03.2004 · Cited by 639
Self-citationSussel, L., Kalamaras, J., Hartigan-O’Connor, D. J., Meneses, J. J., Pedersen, R. A., Rubenstein, J. L. R., & German, M. S. (1998) · Development · doi:10.1242/dev.125.12.2213 · Cited by 626
Self-citation
Cited by
Sorted by citations
Items 101–200 of 553
Strano, A., Tuck, E. J., Stubbs, V. E. L., & Livesey, F. J. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107732 · Cited by 113
Petri, R., Malmevik, J., Fasching, L., Åkerblom, M., & Jakobsson, J. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.09.022 · Cited by 109
Abellán, A., & Medina, L. M. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22083 · Cited by 109
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
Contact Repulsion Controls the Dispersion and Final Distribution of Cajal-Retzius Cells
Villar‐Cerviño, V., Molano‐Mazón, M., Catchpole, T., Valdeolmillos, M., Henkemeyer, M. J., Martı́nez, L. M., Borrell, V., & Marín, Ó. (2013) · Neuron · doi:10.1016/j.neuron.2012.11.023 · Cited by 108
Tanaka, D. H., Yanagida, M., Zhu, Y., Mikami, S., Nagasawa, T., Miyazaki, J., Yanagawa, Y., Obata, K., & Murakami, F. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5446-08.2009 · Cited by 107
Genetic dissection of GABAergic neural circuits in mouse neocortex
Taniguchi, H. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00008 · Cited by 106
Sonic hedgehog functions through dynamic changes in temporal competence in the developing forebrain
Sousa, V. H., & Fishell, G. (2010) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2010.04.008 · Cited by 106
Kim, T., Yao, R., Monnell, T. E., Cho, J.-H., Vasudevan, A., Koh, A., Peeyush, K. T., Moon, M., Datta, D., Bolshakov, V. Y., et al. (2014) · Stem Cells · doi:10.1002/stem.1704 · Cited by 111
Decision making during interneuron migration in the developing cerebral cortex
Guo, J., & Anton, E. S. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2013.12.001 · Cited by 104
Medina, L. M., Bupesh, M., & Abellán, A. (2011) · Brain Behavior and Evolution · doi:10.1159/000330056 · Cited by 104
Primate-specific origins and migration of cortical GABAergic neurons
Petanjek, Z. (2009) · Frontiers in Neuroanatomy · doi:10.3389/neuro.05.026.2009 · Cited by 108
A neuronal migratory pathway crossing from diencephalon to telencephalon populates amygdala nuclei
García‐Moreno, F., Pedraza, M., Giovannantonio, L. G. D., Salvio, M. D., López‐Mascaraque, L., Simeone, A., & Carlos, J. (2010) · Nature Neuroscience · doi:10.1038/nn.2556 · Cited by 102
Interneuron origin and molecular diversity in the human fetal brain
Yu, Y., Zeng, Z., Xie, D., Chen, R., Sha, Y., Huang, S., Cai, W., Chen, W., Li, W., Ke, R., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00940-3 · Cited by 108
Characterization of Type I and Type II nNOS-Expressing Interneurons in the Barrel Cortex of Mouse
Perrenoud, Q., Geoffroy, H., Gauthier, B., Rancillac, A., Alfonsi, F., Kessaris, N., Rossier, J., Vitalis, T., & Gallopin, T. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00036 · Cited by 99
Code Biology – A New Science of Life
Barbieri, M. (2012) · Biosemiotics · doi:10.1007/s12304-012-9147-3 · Cited by 100
Morales-Delgado, N. (2011) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2011.00010 · Cited by 98
The topography of plaques in multiple sclerosis with special reference to cerebral plaques.
Fog, T. (1965) · PubMed · Cited by 97
Prenatal stress and inhibitory neuron systems: implications for neuropsychiatric disorders
Fine, R., Zhang, J., & Stevens, H. E. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.35 · Cited by 96
Abnormal wiring of CCK+ basket cells disrupts spatial information coding
del Pino, I., Brotons‐Mas, J. R., Marques–Smith, A., Marighetto, A., Frick, A., Marín, Ó., & Rico, B. (2017) · Nature Neuroscience · doi:10.1038/nn.4544 · Cited by 99
Soma, M., Aizawa, H., Ito, Y., Maekawa, M., Osumi, N., Nakahira, E., Okamoto, H., Tanaka, K., & Yuasa, S. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21945 · Cited by 94
Optimization of interneuron function by direct coupling of cell migration and axonal targeting
Lim, L., Pakan, J. M. P., Selten, M. M., Marques-Smith, A., Llorca, A., Bae, S. E., Rochefort, N. L., & Marín, O. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0162-9 · Cited by 93
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
Dlx1andDlx2Promote Interneuron GABA Synthesis, Synaptogenesis, and Dendritogenesis
Pla, R., Stanco, A., Howard, M. A., Rubin, A. N., Vogt, D. L., Mortimer, N., Cobos, I., Potter, G. B., Lindtner, S., Price, J. D., et al. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx241 · Cited by 103
Self-citationApical 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
Adult Neurogenesis in FishPreprint
Ganz, J., & Brand, M. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a019018 · Cited by 91
Molecules and Mechanisms Involved in the Generation and Migration of Cortical Interneurons
Hernandez-Miranda, L. R., Parnavelas, J. G., & Chiara, F. (2010) · ASN NEURO · doi:10.1042/an20090053 · Cited by 90
Bupesh, M., Legáz, I., Abellán, A., & Medina, L. M. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22581 · Cited by 89
Rubin, A. N., Alfonsi, F., Humphreys, M. P., Choi, C. K. P., Rocha, S. F., & Kessaris, N. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.6178-09.2010 · Cited by 87
GABAergic interneuron transplants to study development and treat disease
Tyson, J. A., & Anderson, S. A. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.01.003 · Cited by 90
Development and evolution of the subpallium
Moreno, N., González, A., & Rétaux, S. (2009) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2009.04.007 · Cited by 87
Loss of Gsx1 and Gsx2 function rescues distinct phenotypes in Dlx1/2 mutants
Wang, B., Long, J. E., Flandin, P., Pla, R., Waclaw, R. R., Campbell, K., & Rubenstein, J. L. R. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23242 · Cited by 85
Self-citationYang, Z., You, Y., & Levison, S. W. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21819 · Cited by 85
Prospective Isolation of Cortical Interneuron Precursors from Mouse Embryonic Stem Cells
Maroof, A. M., Brown, K. N., Shi, S., Studer, L., & Anderson, S. A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4255-09.2010 · Cited by 86
Production and organization of neocortical interneurons
Sultan, K. T., Brown, K. N., & Shi, S.-H. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00221 · Cited by 83
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
Vitalis, T., Ansorge, M. S., & Dayer, A. G. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00093 · Cited by 90
Human pluripotent stem cell–derived models and drug screening in CNS precision medicine
Silva, M. C., & Haggarty, S. J. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14012 · Cited by 88
Elshatory, Y. M., & Gan, L. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5730-07.2008 · Cited by 80
COUP-TFII controls amygdala patterning by regulating neuropilin expression
Tang, K., Rubenstein, J. L. R., Tsai, S. Y., & Tsai, M. (2012) · Development · doi:10.1242/dev.075564 · Cited by 80
Self-citationMa, T., Zhang, Q., Cai, Y., You, Y., Rubenstein, J. L. R., & Yang, Z. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr296 · Cited by 79
Self-citationSingle-cell RNA sequencing identifies distinct mouse medial ganglionic eminence cell types
Chen, Y.-J. J., Friedman, B. A., Ha, C., Durinck, S., Liu, J., Rubenstein, J. L. R., Seshagiri, S., & Modrusan, Z. D. (2017) · Scientific Reports · doi:10.1038/srep45656 · Cited by 80
Self-citationNeurons on the Move: Migration and Lamination of Cortical Interneurons
Faux, C. H., Rakić, S., Andrews, W. D., & Britto, J. M. (2012) · Neurosignals · doi:10.1159/000334489 · Cited by 88
ATR maintains select progenitors during nervous system development
Lee, Y., Shull, E. R. P., Frappart, P., Katyal, S., Enriquez-Rios, V. D., Zhao, J., Russell, H. R., Brown, E. J., & McKinnon, P. J. (2012) · The EMBO Journal · doi:10.1038/emboj.2011.493 · Cited by 78
Development of Cortical Interneurons
Chu, J., & Anderson, S. A. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.171 · Cited by 80
Puelles, L. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00020 · Cited by 76
Self-citationBupesh, M., Abellán, A., & Medina, L. M. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22719 · Cited by 79
Differential Regulation of Telencephalic Pallial–Subpallial Boundary Patterning by Pax6 and Gsh2
Carney, R. S. E., Cocas, L. A., Hirata, T., Mansfield, K., & Corbin, J. G. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn123 · Cited by 75
Neuregulin 3 Mediates Cortical Plate Invasion and Laminar Allocation of GABAergic Interneurons
Bartolini, G., Sánchez-Alcañiz, J. A., Osório, C., Valiente, M., García-Frigola, C., & Marín, O. (2017) · Cell Reports · doi:10.1016/j.celrep.2016.12.089 · Cited by 74
From sauropsids to mammals and back: New approaches to comparative cortical development
Montiel, J. F., Vasistha, N. A., García‐Moreno, F., & Molnár, Z. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23871 · Cited by 74
Neocortical neurogenesis and neuronal migration
Tan, X., & Shi, S. (2012) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.88 · Cited by 85
Spatio-temporal extension in site of origin for cortical calretinin neurons in primates
Hladnik, A., Džaja, D., Darmopil, S., Jovanov-MiloÅ¡ević, N., & Petanjek, Z. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00050 · Cited by 72
Serrano‐Saiz, E., Leyva‐Díaz, E., Cruz, E. D. L., & Hobert, O. (2018) · Current Biology · doi:10.1016/j.cub.2018.06.045 · Cited by 72
Islet1 as a marker of subdivisions and cell types in the developing forebrain of Xenopus
Moreno, N., Domínguez, L., Rétaux, S., & González, A. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.04.029 · Cited by 69
Cambray, S., Arber, C., Little, G. E., Dougalis, A., Paola, V. D., Ungless, M. A., Li, M. C., & Rodríguez, T. A. (2012) · Nature Communications · doi:10.1038/ncomms1817 · Cited by 71
Abellán, A., Vernier, B., Rétaux, S., & Medina, L. M. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22410 · Cited by 69
Xu, Z., Liang, Q., Song, X., Zhang, Z., Lindtner, S., Li, Z., Wen, Y. F., Liu, G., Guo, T., Qi, D., et al. (2018) · Development · doi:10.1242/dev.165456 · Cited by 69
Self-citationZimmer, G., Rudolph, J., Landmann, J., Gerstmann, K., Steinecke, A., Gampe, C., & Bolz, J. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4690-11.2011 · Cited by 68
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
NKX2-1 Is Required in the Embryonic Septum for Cholinergic System Development, Learning, and Memory
Magno, L., Barry, C., Schmidt‐Hieber, C., Theodotou, P., Häusser, M., & Kessaris, N. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.07.053 · Cited by 69
Moreno, N., Morona, R., López, J. M., & González, A. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22493 · Cited by 70
The plasticitome of cortical interneurons
McFarlan, A. R., Chou, C. Y. C., Watanabe, A., Cherepacha, N., Haddad, M. G., Owens, H., & Sjöström, P. J. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00663-9 · Cited by 74
Interneuron Transplantation as a Treatment for EpilepsyPreprint
Hunt, R. F., & Baraban, S. C. (2015) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a022376 · Cited by 68
Staal, J. A., Alexander, S. R., Liu, Y., Dickson, T. D., & Vickers, J. C. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022040 · Cited by 68
Canty, A. J., Dietze, J., Harvey, M., Enomoto, H., Milbrandt, J., & Ibáñez, C. F. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2658-09.2009 · Cited by 69
Characterization of the hypothalamus of Xenopus laevis during development. I. The alar regions
Domínguez, L., Morona, R., González, A., & Moreno, N. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23222 · Cited by 67
MTOR controls genesis and autophagy of GABAergic interneurons during brain development
Ka, M., Smith, A. L., & Kim, W.-Y. (2017) · Autophagy · doi:10.1080/15548627.2017.1327927 · Cited by 70
Lineage-dependent circuit assembly in the neocortex
Gao, P., Sultan, K. T., Zhang, X., & Shi, S. (2013) · Development · doi:10.1242/dev.087668 · Cited by 68
Pallio-Pallial Tangential Migrations and Growth Signaling: New Scenario for Cortical Evolution?
Puelles, L. (2011) · Brain Behavior and Evolution · doi:10.1159/000327905 · Cited by 69
Self-citationPlan of the Developing Vertebrate Nervous System
Puelles, L. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00118-0 · Cited by 64
Self-citationMolecular anatomy of the thalamic complex and the underlying transcription factors
Nagalski, A., Puelles, L., Dąbrowski, M., Węgierski, T., Kuźnicki, J., & Wisniewska, M. B. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1052-5 · Cited by 67
Self-citationCoup-TF1 and Coup-TF2 control subtype and laminar identity of MGE-derived neocortical interneurons
Hu, J. S., Vogt, D. L., Lindtner, S., Sandberg, M., Silberberg, S. N., & Rubenstein, J. L. R. (2017) · Development · doi:10.1242/dev.150664 · Cited by 65
Self-citationSilberberg, S. N., Taher, L., Lindtner, S., Sandberg, M., Nord, A. S., Vogt, D., Mckinsey, G. L., Hoch, R., Pattabiraman, K., Zhang, D., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.027 · Cited by 62
Self-citationRadial glia in the ventral telencephalon
Turrero García, M., & Harwell, C. C. (2017) · FEBS Letters · doi:10.1002/1873-3468.12829 · Cited by 62
The cell-type underpinnings of the human functional cortical connectome
Zhang, X.-H., Anderson, K. M., Dong, H.-M., Chopra, S., Dhamala, E., Emani, P. S., Gerstein, M., Margulies, D. S., & Holmes, A. J. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01812-2 · Cited by 67
Sánchez‐Arrones, L., Ferrán, J. L., Rodríguez‐Gallardo, L., & Puelles, L. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.08.012 · Cited by 62
Self-citationNeves, G., Shah, M. M., Liodis, P., Achimastou, A., Denaxa, M., Roalfe, G., Sesay, A. K., Walker, M. C., & Pachnis, V. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs159 · Cited by 62
Patterning of ventral telencephalon requires positive function of Gli transcription factors
Yu, W., Wang, Y., McDonnell, K., Stephen, D. N., & Bai, C. B. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.07.026 · Cited by 62
Bertacchi, M., Parisot, J., & Studer, M. (2018) · Brain Research · doi:10.1016/j.brainres.2018.04.024 · Cited by 64
Spatio-temporal expression of Pax6 in Xenopus forebrain
Moreno, N., Rétaux, S., & González, A. (2008) · Brain Research · doi:10.1016/j.brainres.2008.08.052 · Cited by 60
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
Differential effects of BMP signaling on parvalbumin and somatostatin interneuron differentiation
Mukhopadhyay, A., McGuire, T. L., Peng, C., & Kessler, J. A. (2009) · Development · doi:10.1242/dev.034439 · Cited by 60
Moreno, N., Domínguez, L., Morona, R., & González, A. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22762 · Cited by 59
Yilmazer‐Hanke, D. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374236-0.10022-7 · Cited by 61
Reptiles: A New Model for Brain Evo‐Devo Research
Nomura, T., Kawaguchi, M., Ono, K., & Murakami, Y. (2013) · Journal of Experimental Zoology Part B Molecular and Developmental Evolution · doi:10.1002/jez.b.22484 · Cited by 58
Development and Evolution of the Claustrum
Puelles, L. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-404566-8.00004-0 · Cited by 58
Self-citationConserved rules in embryonic development of cortical interneurons
Laclef, C., & Métin, C. (2018) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2017.09.017 · Cited by 57
Identification of the optic recess region as a morphogenetic entity in the zebrafish forebrain
Affaticati, P., Yamamoto, K., Rizzi, B., Bureau, C., Peyriéras, N., Pasqualini, C., Demarque, M., & Vernier, P. (2015) · Scientific Reports · doi:10.1038/srep08738 · Cited by 57
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
Mechanisms regulating GABAergic neuron development
Achim, K., Salminen, M., & Partanen, J. M. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1501-3 · Cited by 56
The Non-Evaginated Secondary Prosencephalon of Vertebrates
Moreno, N., & González, A. (2011) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2011.00012 · Cited by 56
Characterization of the bed nucleus of the stria terminalis in the forebrain of anuran amphibians
Moreno, N., Morona, R., López, J. M., Domínguez, L., Joven, A., Bandín, S., & González, A. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22694 · Cited by 59
Radial derivatives of the mouse ventral pallium traced with Dbx1-LacZ reporters
Puelles, L., Medina, L. M., Borello, U., Legáz, I., Teissier, A., Pierani, A., & Rubenstein, J. L. R. (2015) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2015.10.011 · Cited by 56
Self-citationGene Maps and Related Histogenetic Domains in the Forebrain and Midbrain
Puelles, L., Martı́nez, S., Martı́nez-de-la-Torre, M., & Rubenstein, J. L. R. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-374245-2.00001-2 · Cited by 56
Self-citationNeurogliaform cortical interneurons derive from cells in the preoptic area
Niquille, M., Limoni, G., Markopoulos, F., Cadilhac, C., Prados, J., Holtmaat, A., & Dayer, A. (2018) · eLife · doi:10.7554/elife.32017 · Cited by 55
Puelles, L., Morales-Delgado, N., Merchán, P., Castro‐Robles, B., Martinez-de-la-Torre, M., Dı́az, C., & Ferrán, J. L. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1086-8 · Cited by 55
Self-citationPaina, S., Garzotto, D., Marchis, S. D., Marino, M., Moiana, A., Conti, L., Cattaneo, E. F., Perera, M., Corte, G., Calautti, E., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3110-10.2011 · Cited by 55
Simpson, T. I., Pratt, T., Mason, J. O., & Price, D. J. (2009) · Neural Development · doi:10.1186/1749-8104-4-19 · Cited by 55
Shedding Light on Chandelier Cell Development, Connectivity, and Contribution to Neural Disorders
Gallo, N. B., Paul, A., & Aelst, L. V. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.05.003 · Cited by 55
Kaoru, T., Liu, F., Ishida, M., Oishi, T., Hayashi, M., Kitagawa, M., Shimoda, K., & Takahashi, H. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.12.004 · Cited by 56
Metadata
- Authors
- Flames, N., Pla, R., Gelman, D. M., Rubenstein, J. L. R., Puelles, L., & Marín, O.
- Affiliations
- Consejo Superior de Investigaciones Científicas (ES)
- University of California, San Francisco (US)
- Instituto de Salud Carlos III (ES)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2007-09-05
- Volume
- 27
- Issue
- 36
- Pages
- 9682-9695
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC4916652
- OpenAlex
- W2094703740
- Cited by
- 560
- References
- 61
- Citations by year
- 2026: 8 · 2025: 19 · 2024: 19 · 2023: 23 · 2022: 23 · 2021: 32 · 2020: 30 · 2019: 19 · 2018: 30 · 2017: 33 · 2016: 28 · 2015: 40 · 2014: 38 · 2013: 39 · 2012: 32
- FWCI
- 10.05
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion)
- Funders
- European Commission (005139)
- National Institute of Mental Health (R01MH49428, K05MH065670, R01MH049428)
- 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
- subpallium, transcription factors, combinatorial gene expression, ventricular zone, medial ganglionic eminence, basal ganglia, amygdala, septum, cortical interneurons, microtransplantation, mouse brain development, telencephalon
- MeSH terms
- Animals, Cerebral Ventricles, Mice, Transgenic, Stem Cells, Telencephalon, Transcription Factors, Brain Tissue Transplantation, Genes, Reporter, Gene Expression Regulation, Developmental, Embryonic Development, Green Fluorescent Proteins, Mice
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
