The caudal ganglionic eminence is a source of distinct cortical and subcortical cell populations

The rat nervous system

Paxinos, G. (1985) · Cited by 3,715

Autoradiographic Study of Cell Migration during Histogenesis of Cerebral Cortex in the Mouse

ANGEVINE, J. B., & SIDMAN, R. L. (1961) · Nature · doi:10.1038/192766b0 · Cited by 1,530

Interneuron Migration from Basal Forebrain to Neocortex: Dependence on Dlx Genes

Anderson, S. A., Eisenstat, D. D., Shi, L., & Rubenstein, J. L. R. (1997) · Science · doi:10.1126/science.278.5337.474 · Cited by 1,462

A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

Schaeren‐Wiemers, N., & Gerfin-Moser, A. (1993) · Histochemistry and Cell Biology · doi:10.1007/bf00267823 · Cited by 1,151

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

Loss of Nkx2.1 homeobox gene function results in a ventral to dorsal molecular respecification within the basal telencephalon: evidence for a transformation of the pallidum into the striatum

Sussel, L., Marin, O., Kimura, S., & Rubenstein, J. L. R. (1999) · Development · doi:10.1242/dev.126.15.3359 · Cited by 873

Tbr1 regulates differentiation of the preplate and layer 6

Hevner, R. F., Shi, L., Justice, N., Hsueh, Y.-P., Sheng, M., Smiga, S., Bulfone, A., Goffinet, A. M., Campagnoni, A. T., & Rubenstein, J. L. R. (2001) · Neuron · doi:10.1016/s0896-6273(01)00211-2 · Cited by 857

[22] Detection of messenger RNA by in Situ hybridization to tissue sections and whole mounts

Wilkinson, D. G., & Nieto, M. A. (1993) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(93)25025-w · Cited by 794

Cell Cycle Dependence of Laminar Determination in Developing Neocortex

McConnell, S. K., & Kaznowski, C. E. (1991) · Science · doi:10.1126/science.1925583 · Cited by 787

The medial ganglionic eminence gives rise to a population of early neurons in the developing cerebral cortex

Lavdas, 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

The origin of neocortical nitric oxide synthase-expressing inhibitory neurons

Jaglin, X. H., Hjerling‐Leffler, J., Fishell, G., & Batista‐Brito, R. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00044 · Cited by 35

Caudal Ganglionic Eminence Precursor Transplants Disperse and Integrate as Lineage-Specific Interneurons but Do Not Induce Cortical Plasticity

Larimer, P., Spatazza, J., Espinosa, J. S., Tang, Y., Kaneko, M., Hasenstaub, A. R., Stryker, M. P., & Álvarez-Buylla, A. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.06.071 · Cited by 34

Dynamic patterns of colocalization of calbindin, parvalbumin and GABA in subpopulations of mouse basolateral amygdalar cells during development

Dávila, J. C., Olmos, L., Legáz, I., Medina, L. M., Guirado, S., & Real, M. A. (2007) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2007.06.003 · Cited by 34

Dynamic expression of calretinin in embryonic and early fetal human cortex

González‐Gómez, M., & Meyer, G. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00041 · Cited by 34

Molecular and Electrophysiological Characterization of GABAergic Interneurons Expressing the Transcription Factor COUP-TFII in the Adult Human Temporal Cortex

Varga, C., Tamás, G., Barzó, P., Oláh, S., & Somogyi, P. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv045 · Cited by 34

Oxidative Damage and Defective DNA Repair is Linked to Apoptosis of Migrating Neurons and Progenitors During Cerebral Cortex Development in Ku70-Deficient Mice

Narasimhaiah, R., Tuchman, A., Lin, S. L., & Naegele, J. R. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh171 · Cited by 34

Perspectives on the Developmental Origins of Cortical Interneuron Diversity

Fishell, G. (2008) · Novartis Foundation symposium · doi:10.1002/9780470994030.ch3 · Cited by 34

An epigenome atlas of neural progenitors within the embryonic mouse forebrain

Rhodes, C. T., Thompson, J. J., Mitra, A., Asokumar, D., Lee, D. R., Lee, D. J., Zhang, Y., Jason, E., Dale, R., Rocha, P. P., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-31793-4 · Cited by 34

Psychedelic control of neuroimmune interactions governing fear

Chung, E. N., Lee, J., Polonio, C. M., Choi, J., Akl, C. F., Kilian, M., Weiß, W. M., Gunner, G., Ye, M., Heo, T. H., et al. (2025) · Nature · doi:10.1038/s41586-025-08880-9 · Cited by 39

JNK signaling is required for proper tangential migration and laminar allocation of cortical interneurons

Myers, A., Cunningham, J. G., Smith, S. E., Snow, J. P., Smoot, C. A., & Tucker, E. S. (2020) · Development · doi:10.1242/dev.180646 · Cited by 33

Modeling the Impact of Alcohol on Cortical Development in a Dish: Strategies from Mapping Neural Stem Cell Fate

Miranda, R. C., Santillano, D. R., Camarillo, C., & Dohrman, D. P. (2008) · Methods in molecular biology · doi:10.1007/978-1-59745-242-7_12 · Cited by 33

Systemic prenatal insults disrupt telencephalon development: Implications for potential interventions

Robinson, S. (2005) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2005.06.005 · Cited by 34

Medial Ganglionic Eminence Progenitors Transplanted into Hippocampus Integrate in a Functional and Subtype-Appropriate Manner

Hsieh, J.-Y., & Baraban, S. C. (2017) · eNeuro · doi:10.1523/eneuro.0359-16.2017 · Cited by 34

Regulation of the E/I-balance by the neural matrisome

Mueller-Buehl, C., Wegrzyn, D., Bauch, J., & Faissner, A. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1102334 · Cited by 35

Loss of Embryonic MET Signaling Alters Profiles of Hippocampal Interneurons

Martins, G. J., Plachez, C., & Powell, E. M. (2006) · Developmental Neuroscience · doi:10.1159/000096219 · Cited by 32

Cortical interneurons from human pluripotent stem cells: prospects for neurological and psychiatric disease

Arber, C., & Li, M. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00010 · Cited by 37

Tangential migration and proliferation of intermediate progenitors of GABAergic neurons in the mouse telencephalon

Wu, S., Esumi, S., Watanabe, K., Chen, J., Nakamura, K., Nakamura, K., Kometani, K., Minato, N., Yanagawa, Y., Akashi, K., et al. (2011) · Development · doi:10.1242/dev.063032 · Cited by 35

Cell-Autonomous Regulation of Dendritic Spine Density by PirB

Vidal, G. S., Djurisic, M. R., Brown, K., Sapp, R. W., & Shatz, C. J. (2016) · eNeuro · doi:10.1523/eneuro.0089-16.2016 · Cited by 31

COUP - TF Genes, Human Diseases, and the Development of the Central Nervous System in Murine Models

Yang, X. W., Feng, S., & Tang, K. (2017) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2016.12.002 · Cited by 30

Dynamic expression of tyrosine hydroxylase mRNA and protein in neurons of the striatum and amygdala of mice, and experimental evidence of their multiple embryonic origin

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

CBP regulates the differentiation of interneurons from ventral forebrain neural precursors during murine development

Tsui, D. C. C., Voronova, A., Gallagher, D., Kaplan, D. R., Miller, F. D., & Wang, J. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.11.005 · Cited by 32

Mechanisms of Cortical Differentiation

Adnani, L., Han, S., Li, S., Mattar, P. A., & Schuurmans, C. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2017.07.005 · Cited by 33

Distinct Functional Groups Emerge from the Intrinsic Properties of Molecularly Identified Entorhinal Interneurons and Principal Cells

Ferrante, M., Tahvildari, B., Duque, A., Hadzipasic, M., Salkoff, D. B., Zagha, E., Hasselmo, M. E., & McCormick, D. A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw143 · Cited by 30

NECAB1 and NECAB2 are Prevalent Calcium-Binding Proteins of CB1/CCK-Positive GABAergic Interneurons

Miczán, V., Kelemen, K., Glavinics, J. R., László, Z. I., Barti, B., Kenesei, K., Kisfali, M., & Katona, I. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa326 · Cited by 30

Generating neural diversity through spatial and temporal patterning

Sen, S. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.06.002 · Cited by 26

Heterotopic Transplantations Reveal Environmental Influences on Interneuron Diversity and Maturation

Quattrocolo, G., Fishell, G., & Petros, T. J. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.09.075 · Cited by 28

Elucidating the developmental trajectories of GABAergic cortical interneuron subtypes

Miyoshi, G. (2018) · Neuroscience Research · doi:10.1016/j.neures.2018.09.012 · Cited by 29

The Generation of Cortical Interneurons

Gelman, D. M., Marín, Ó., & Rubenstein, J. L. R. (2012) · Oxford University Press eBooks · doi:10.1093/med/9780199746545.003.0061 · Cited by 28

Development of Auditory Cortex Circuits

Chang, M., & Kanold, P. O. (2021) · Journal of the Association for Research in Otolaryngology · doi:10.1007/s10162-021-00794-3 · Cited by 29

Two specific populations of GABAergic neurons originating from the medial and the caudal ganglionic eminences aid in proper navigation of callosal axons

Niquille, M., Minocha, S., Hornung, J., Rufer, N., Valloton, D., Kessaris, N., Alfonsi, F., Vitalis, T., Yanagawa, Y., Devenoges, C., et al. (2013) · Developmental Neurobiology · doi:10.1002/dneu.22075 · Cited by 29

Sonic hedgehog expression in zebrafish forebrain identifies the teleostean pallidal signaling center and shows preglomerular complex and posterior tubercular dopamine cells to arise from shh cells

Wullimann, M. F., & Umeasalugo, K. E. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24825 · Cited by 27

Two epochs in the development of γ‐aminobutyric acidergic neurons in the ferret thalamus

Hayes, S. G., Murray, K. D., & Jones, E. G. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10749 · Cited by 27

Origin of the Cortical Layer I in Rodents

Jiménez, D., Rivera, R., López‐Mascaraque, L., & Carlos, J. (2003) · Developmental Neuroscience · doi:10.1159/000072260 · Cited by 27

Subpallial origin of part of the calbindin-positive neurons of the claustral complex and piriform cortex

Legáz, I., García‐López, M., & Medina, L. M. (2005) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2005.05.006 · Cited by 27

Cell Lineage Tracing and Cellular Diversity in Humans

Abyzov, A. S., & Vaccarino, F. M. (2020) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-083118-015241 · Cited by 28

Interplay of environmental signals and progenitor diversity on fate specification of cortical GABAergic neurons

Brandão, J. A., & Romcy-Pereira, R. N. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00149 · Cited by 29

Neurochemical characterization of tyrosine hydroxylase-immunoreactive interneurons in the developing rat cerebral cortex

Asmus, S. E., Anderson‐Baucum, E. K., Ball, M. W., Barnes, B. A., Bohnen, A. M., Brown, A. M., Hartley, L. J., Lally, M. C., Lundblad, T. M., Martin, J., et al. (2008) · Brain Research · doi:10.1016/j.brainres.2008.05.053 · Cited by 26

Decoding the transcriptional basis for GABAergic interneuron diversity in the mouse neocortex

Anastasiades, P. G., & Butt, S. J. B. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07904.x · Cited by 26

Toward a systems-oriented approach to the role of the extended amygdala in adaptive responding

Waraczynski, M. A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.05.015 · Cited by 28

Neuron–Oligodendrocyte Communication in Myelination of Cortical GABAergic Cells

Mazuir, E., Fricker, D., & Sol‐Foulon, N. (2021) · Life · doi:10.3390/life11030216 · Cited by 27

Milestones of Directed Differentiation of Mouse and Human Embryonic Stem Cells into Telencephalic Neurons Based on Neural Development In Vivo

Nat, R., & Dechant, G. (2010) · Stem Cells and Development · doi:10.1089/scd.2010.0417 · Cited by 25

Removal of Pax6 Partially Rescues the Loss of Ventral Structures in Shh Null Mice

Fuccillo, M. V., Rutlin, M. L., & Fishell, G. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhk023 · Cited by 25

The generation of cortical interneurons

Rubenstein, J. L. R. (2010) · Epilepsia · doi:10.1111/j.1528-1167.2010.02854.x · Cited by 24

Patterning ganglionic eminences in developing human brain organoids using a morphogen-gradient-inducing device

Pavon, N., Diep, K., Yang, F., Sebastian, R., Martinez-Martin, B., Ranjan, R., Sun, Y., & Pak, C. (2024) · Cell Reports Methods · doi:10.1016/j.crmeth.2023.100689 · Cited by 24

Localization of latexin-immunoreactive neurons in the adult cat cerebral cortex and claustrum/endopiriform formation

Arimatsu, Y., Nihonmatsu, I., & Hatanaka, Y. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.05.060 · Cited by 24

Astrocyte-Mediated Hepatocyte Growth Factor/Scatter Factor Supplementation Restores GABAergic Interneurons and Corrects Reversal Learning Deficits in Mice

Bissonette, G. B., Bae, M. H., Suresh, T., Jaffe, D. E., & Powell, E. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5268-09.2010 · Cited by 25

Impaired Organization of GABAergic Neurons Following Prenatal Hypoxia

Nisimov, H., Orenbuch, A., Pleasure, S. J., & Golan, H. M. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.05.021 · Cited by 24

Transplantation of GABAergic interneurons for cell-based therapy

Spatazza, J., Mancia, W., & Álvarez-Buylla, A. (2017) · Progress in brain research · doi:10.1016/bs.pbr.2016.11.005 · Cited by 25

Precise inhibitory microcircuit assembly of developmentally related neocortical interneurons in clusters

Zhang, X., Li, Z., Han, Z., Sultan, K. T., Huang, K., & Shi, S. (2017) · Nature Communications · doi:10.1038/ncomms16091 · Cited by 26

Development and function of the medial amygdala

Prakash, N., Irqeba, A. A., & Corbin, J. G. (2024) · Trends in Neurosciences · doi:10.1016/j.tins.2024.11.004 · Cited by 22

Cell Therapy Using GABAergic Neural Progenitors

Anderson, S. A., & Baraban, S. C. (2012) · Oxford University Press eBooks · doi:10.1093/med/9780199746545.003.0087 · Cited by 22

Colocalization of neuropeptides with calcium-binding proteins in the claustral interneurons during postnatal development of the rat

Kowiański, P., Dziewíatkowski, J., Moryś, J. M., Majak, K., Wojcik, S. P., Edelstein, L. R., Lietzau, G., & Moryś, J. (2009) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2009.06.020 · Cited by 22

Interneuron Progenitor Transplantation to Treat CNS Dysfunction

Chohan, M. O., & Moore, H. M. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00064 · Cited by 23

Impact of Ethanol on the Developing GABAergic System

Isayama, R. N., Leite, P. E. C., Lima, J. P. M., Uziel, D., & Yamasaki, E. N. (2009) · The Anatomical Record · doi:10.1002/ar.20966 · Cited by 22

miRNAs are Essential for the Survival and Maturation of Cortical Interneurons

Tuncdemir, S. N., Fishell, G., & Batista‐Brito, R. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht426 · Cited by 22

Identification and characterization of a novel transcript down‐regulated in Dlx1/Dlx2 and up‐regulated in Pax6 mutant telencephalon

Faedo, A., Quinn, J. C., Stoney, P. N., Long, J. E., Dye, C. A., Zollo, M., Rubenstein, J. L. R., Price, D. J., & Bulfone, A. (2004) · Developmental Dynamics · doi:10.1002/dvdy.20152 · Cited by 22

Evidence that the laminar fate of LGE/CGE-derived neocortical interneurons is dependent on their progenitor domains

Torigoe, M., Yamauchi, K., Kimura, T., Uemura, Y., & Murakami, F. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.3550-15.2016 · Cited by 21

ALK Amplification and Rearrangements Are Recurrent Targetable Events in Congenital and Adult Glioblastoma

Blandin, A.-F., Giglio, R. M., Graham, M. S., Garcia, G., Malinowski, S. W., Woods, J. K., Ramkissoon, S. H., Ramkissoon, L. A., Dubois, F. P. B., Schoolcraft, K., et al. (2023) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-21-3521 · Cited by 21

H3G34-Mutant Gliomas—A Review of Molecular Pathogenesis and Therapeutic Options

Nguyen, A. V. P., Soto, J. M., Gonzalez, S.-M. C., Murillo, J., Trumble, E. R., Shan, F. Y., & Huang, J. H. (2023) · Biomedicines · doi:10.3390/biomedicines11072002 · Cited by 22

Mapping arealisation of the visual cortex of non-primate species: lessons for development and evolution

Homman‐Ludiye, J. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00079 · Cited by 24

Cortical distribution of GABAergic interneurons is determined by migration time and brain size

Fazzari, P., Mortimer, N., Yabut, O., Vogt, D. L., & Pla, R. (2020) · Development · doi:10.1242/dev.185033 · Cited by 23

Lamination of the cerebral cortex is disturbed in Gli3 mutant mice

Friedrichs, M., Larralde, O., Skutella, T., & Theil, T. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.03.032 · Cited by 21

Charting the spatial transcriptome of the human cerebral cortex at single-cell resolution

Wei, S., Luo, M., Wang, P., Chen, R., Jin, X., Xu, C., Li, C., Lin, X., Xu, Z., Liu, H., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62793-9 · Cited by 20

Deciphering inhibitory neuron development: The paths to diversity

Bandler, R. C., & Mayer, C. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102691 · Cited by 22

Mechanisms of Development

ten Donkelaar, H. J., & Fritzsch, B. (2023) · Springer eBooks · doi:10.1007/978-3-031-26098-8_2 · Cited by 20

Postnatal development of tyrosine hydroxylase mRNA‐expressing neurons in mouse neostriatum

Masuda, M., Miura, M., Inoue, R., Imanishi, M., Saino‐Saito, S., Takada, M., Kobayashi, K., & Aosaki, T. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07873.x · Cited by 19

Serotonergic regulation of bipolar cell survival in the developing cerebral cortex

Wong, F. K., Selten, M. M., Rosés-Novella, C., Sreenivasan, V., Pallas‐Bazarra, N., Serafeimidou‐Pouliou, E., Hanusz-Godoy, A., Oozeer, F., Edwards, R. H., & Marín, Ó. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111037 · Cited by 20

Distribution of nitric oxide-producing neurons in the developing and adult mouse amygdalar basolateral complex

Olmos, J. L., Real, M. A., Medina, L. M., Guirado, S., & Dávila, J. C. (2005) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2005.04.002 · Cited by 19

Vesicular GABA Transporter Is Necessary for Transplant-Induced Critical Period Plasticity in Mouse Visual Cortex

Priya, R., Rakela, B., Kaneko, M., Spatazza, J., Larimer, P., Hoseini, M. S., Hasenstaub, A. R., Álvarez-Buylla, A., & Stryker, M. P. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1253-18.2019 · Cited by 19

PAFAH1B1 haploinsufficiency disrupts GABA neurons and synaptic E/I balance in the dentate gyrus

Dinday, M. T., Girskis, K. M., Lee, S., Baraban, S. C., & Hunt, R. F. (2017) · Scientific Reports · doi:10.1038/s41598-017-08809-x · Cited by 18

PDK1 regulates the survival of the developing cortical interneurons

Wei, Y., Han, X., & Zhao, C. (2020) · Molecular Brain · doi:10.1186/s13041-020-00604-6 · Cited by 18

FLRT2 and FLRT3 cooperate in maintaining the tangential migratory streams of cortical interneurons during development

Fleitas, C., Marfull-Oromí, P., Chauhan, D., del Toro, D., Peguera, B., Zammou, B., Rocandio, D., Klein, R., Espinet, C., & Egea, J. (2021) · The Journal of Neuroscience · doi:10.1523/jneurosci.0380-20.2021 · Cited by 18

Distinct Subdivisions in the Transition Between Telencephalon and Hypothalamus Produce Otp and Sim1 Cells for the Extended Amygdala in Sauropsids

Metwalli, A. H., Abellán, A., Freixes, J., Pross, A., Desfilis, E., & Medina, L. M. (2022) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2022.883537 · Cited by 18

NPY-, SOM- and VIP-containing interneurons in postnatal development of the rat claustrum

Kowiański, P., Moryś, J. M., Dziewíatkowski, J., Wojcik, S. P., Sidor-Kaczmarek, J., & Moryś, J. (2008) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2008.04.004 · Cited by 18

Sticking out of the crowd: the molecular identity and development of cholecystokinin‐containing basket cells

Keimpema, E., Straiker, A. J., Mackie, K., Harkany, T., & Hjerling‐Leffler, J. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2011.224386 · Cited by 18

Association of astrocytes with neurons and astrocytes derived from distinct progenitor domains in the subpallium

Torigoe, M., Yamauchi, K., Zhu, Y., Kobayashi, H., & Murakami, F. (2015) · Scientific Reports · doi:10.1038/srep12258 · Cited by 18

Cilia

Métin, C., & Pedraza, M. (2014) · The Neuroscientist · doi:10.1177/1073858414543151 · Cited by 20

Immediate effects of maternal separation on the development of interneurons derived from medial ganglionic eminence in the neonatal mouse hippocampus

Katahira, T., Miyazaki, N., & Motoyama, J. (2018) · Development Growth & Differentiation · doi:10.1111/dgd.12540 · Cited by 17

In vivo Optogenetic Approach to Study Neuron-Oligodendroglia Interactions in Mouse Pups

Ortolani, D., Manot-Saillet, B., Orduz, D., Ortíz, F. C., & Angulo, M. C. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00477 · Cited by 18

Differential Expression Hallmarks of Interneurons in Different Types of Focal Cortical Dysplasia

Liang, C., Zhang, C., Chen, X., Wang, L., Yue, J., An, N., Zhang, L., Liu, S., & Yang, H. (2020) · Journal of Molecular Neuroscience · doi:10.1007/s12031-020-01492-0 · Cited by 17

A role for sustained MAPK activity in the mouse ventral telencephalon

Talley, M. J., Nardini, D., Qin, S., Prada, C. E., Ehrman, L. A., & Waclaw, R. R. (2021) · Developmental Biology · doi:10.1016/j.ydbio.2021.03.019 · Cited by 17

Identification of Vulnerable Interneuron Subtypes in 15q13.3 Microdeletion Syndrome Using Single-Cell Transcriptomics

Malwade, S., Gasthaus, J., Bellardita, C., Andelic, M., Moric, B., Korshunova, I., Kiehn, O., Vasistha, N. A., & Khodosevich, K. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.09.012 · Cited by 18

Characterization of a subpopulation of developing cortical interneurons from human iPSCs within serum-free embryoid bodies

Nestor, M. W., Jacob, S., Sun, B. Q., Prè, D., Sproul, A. A., Hong, S. I., Woodard, C. M., Zimmer, M., Chinchalongporn, V., Arancio, O., et al. (2014) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00263.2014 · Cited by 17

Rostro-Caudal and Caudo-Rostral Migrations in the Telencephalon: Going Forward or Backward?

Ruiz-Reig, N., & Studer, M. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00692 · Cited by 21

Early regionalisation of the neocortex and the medial ganglionic eminence

Bellion, A., & Métin, C. (2005) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2005.07.010 · Cited by 17

Leucine‐rich glioma inactivated 1 (Lgi1), an epilepsy‐related secreted protein, has a nuclear localization signal and localizes to both the cytoplasm and the nucleus of the caudal ganglionic eminence neurons

Kusuzawa, S., Honda, T., Fukata, Y., Fukata, M., Kanatani, S., Tanaka, D. H., & Nakajima, K. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08129.x · Cited by 16

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