Dlx1 and Dlx2 Control Neuronal versus Oligodendroglial Cell Fate Acquisition in the Developing Forebrain

Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity

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

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

Competing waves of oligodendrocytes in the forebrain and postnatal elimination of an embryonic lineage

Kessaris, N., Fogarty, M., Iannarelli, P., Grist, M., Wegner, M., & Richardson, W. D. (2006) · Nature Neuroscience · doi:10.1038/nn1620 · Cited by 1,195

Common Developmental Requirement for Olig Function Indicates a Motor Neuron/Oligodendrocyte Connection

Lu, Q. R., Sun, T., Zhu, Z., Ma, N., Garcia, M., Stiles, C. D., & Rowitch, D. H. (2002) · Cell · doi:10.1016/s0092-8674(02)00678-5 · Cited by 1,087

The bHLH Transcription Factors OLIG2 and OLIG1 Couple Neuronal and Glial Subtype Specification

Zhou, Q., & Anderson, D. J. (2002) · Cell · doi:10.1016/s0092-8674(02)00677-3 · Cited by 1,059

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×

Origin of oligodendrocytes in the subventricular zone of the adult brain

Menn, B., Garcia-Verdugo, J. M., Yaschine, C., Gonzalez-Perez, O., Rowitch, D., & Alvarez-Buylla, A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1299-06.2006 · Cited by 972

Sonic hedgehog--regulated oligodendrocyte lineage genes encoding bHLH proteins in the mammalian central nervous system.

Lu, Q. R., Yuk, D.-I., Alberta, J., Zhu, Z.-M., Pawlitzky, I., Chan, J., McMahon, A., Stiles, C., & Rowitch, D. H. (2000) · Neuron · doi:10.1016/s0896-6273(00)80897-1 · Cited by 883

Homeobox gene Nkx2.2 and specification of neuronal identity by graded Sonic hedgehog signalling

Briscoe, J., Sussel, L., Serup, P., Hartigan-O'Connor, D., Jessell, T., Rubenstein, J., & Ericson, J. (1999) · Nature · doi:10.1038/19315 · Cited by 807

Sox10, a Novel Transcriptional Modulator in Glial Cells

Kuhlbrodt, K., Herbarth, B., Sock, E., Hermans-Borgmeyer, I., & Wegner, M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-01-00237.1998 · Cited by 781

Instructing neuronal identity during CNS development and astroglial-lineage reprogramming: Roles of NEUROG2 and ASCL1

Chouchane, M., & Costa, M. R. (2018) · Brain Research · doi:10.1016/j.brainres.2018.02.045 · Cited by 24

A gain-of-function senescence bypass screen identifies the homeobox transcription factor DLX2 as a regulator of ATM–p53 signalingPreprint

Wang, Y., Xu, Q., Sack, L. M., Kang, C., & Elledge, S. J. (2016) · Genes & Development · doi:10.1101/gad.271445.115 · Cited by 24

Gene Coexpression Networks in Human Brain Developmental Transcriptomes Implicate the Association of Long Noncoding RNAs with Intellectual Disability

Gudenas, B. L., & Wang, L. (2015) · Bioinformatics and Biology Insights · doi:10.4137/bbi.s29435 · Cited by 24

Polydendrocytes in development and myelin repair

Zuo, H., & Nishiyama, A. (2013) · Neuroscience Bulletin · doi:10.1007/s12264-013-1320-4 · Cited by 23

Mechanisms of Development

ten Donkelaar, H. J. (2006) · Springer eBooks · doi:10.1007/3-540-34659-7_2 · Cited by 22

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

Activity-dependent expression of neuronal PAS domain-containing protein 4 (npas4a) in the developing zebrafish brain

Klarić, T., Lardelli, M. T., Key, B., Koblar, S. A., & Lewis, M. D. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00148 · Cited by 25

Epigenetic Mechanisms Regulating Differentiation of Neural Stem/Precursor Cells

Adefuin, A. M. D., Kimura, A., Noguchi, H., Nakashima, K., & Namihira, M. (2014) · Epigenomics · doi:10.2217/epi.14.53 · Cited by 24

Making neurons from mature glia: A far-fetched dream?

Berninger, B. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.11.004 · Cited by 22

Gene-environment interactions in cortical interneuron development and dysfunction: A review of preclinical studies

Ansen-Wilson, L. J., & Lipinski, R. J. (2016) · NeuroToxicology · doi:10.1016/j.neuro.2016.12.002 · Cited by 25

Pleiotropic Functions for Transcription Factor Zscan10

Kraus, P., Vijayakumar, S., Yu, H., Xing, X., Lim, S. L., Adler, T., Aguilar‐Pimentel, J. A., Becker, L., Bohla, A., Garrett, L., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104568 · 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

Pharmacological Modulation of the Hedgehog Pathway Differentially Affects Dorsal/Ventral Patterning in Mouse and Human Embryonic Stem Cell Models of Telencephalic Development

Nat, R., Salti, A., Ceafalan, L. C., Ström, S., & Dechant, G. (2011) · Stem Cells and Development · doi:10.1089/scd.2011.0271 · Cited by 21

Sex-specific epigenetic development in the mouse hypothalamic arcuate nucleus pinpoints human genomic regions associated with body mass index

MacKay, H., Gunasekara, C., Yam, K., Srisai, D., Yalamanchili, H. K., Li, Y., Chen, R., Coarfa, C., & Waterland, R. A. (2022) · Science Advances · doi:10.1126/sciadv.abo3991 · Cited by 20

Pax6 limits the competence of developing cerebral cortical cells to respond to inductive intercellular signals

Manuel, M. N., Tan, K. B., Kozić, Z., Molinek, M., Marcos, T. S., Razak, F. M. A., Dobolyi, D., Dobie, R., Henderson, B. E. P., Henderson, N. C., et al. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001563 · Cited by 20

Mechanisms of Development

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

Multipotent precursors in the anterior and hippocampal subventricular zone display similar transcription factor signatures but their proliferation and maintenance are differentially regulated

García, C. C., Suh, Y., Obernier, K., Mandl, C., & Ciccolini, F. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.04.003 · Cited by 20

Presentation and integration of multiple signals that modulate oligodendrocyte lineage progression and myelination

Fekete, C. D., & Nishiyama, A. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1041853 · Cited by 21

Lineage tracing of dlx1a/2a and dlx5a/6a expressing cells in the developing zebrafish brain

Solek, C. M., Feng, S., Perin, S., Mendes, H. W., & Ekker, M. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.04.019 · Cited by 19

Progenies of NG2 glia: what do we learn from transgenic mouse models ?

Huang, W., Guo, Q., & Scheller, A. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.286950 · Cited by 20

Unbiased identification of novel transcription factors in striatal compartmentation and striosome maturation

Cirnaru, M., Song, S., Tshilenge, K., Corwin, C., Mleczko, J., Aguirre, C. G., Benlhabib, H., Bendl, J. M., Apontes, P., Fullard, J. F., et al. (2021) · eLife · doi:10.7554/elife.65979 · Cited by 18

Fate plasticity of adult hippocampal progenitors: biological relevance and therapeutic use

Jessberger, S., & Gage, F. H. (2009) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2008.11.003 · Cited by 19

Progressive divisions of multipotent neural progenitors generate late-born chandelier cells in the neocortex

Sultan, K. T., Liu, W. A., Li, Z.-L., Shen, Z., Li, Z., Zhang, X., Dean, O. R., Ma, J., & Shi, S. (2018) · Nature Communications · doi:10.1038/s41467-018-07055-7 · Cited by 20

Spatiotemporal transcriptome atlas of human embryos after gastrulation

Pan, J., Li, Y., Lin, Z., Lan, Q., Zhang, Y., Chen, H., Sui, S., Zhai, M., Zhang, G., Cheng, Y., et al. (2026) · Nature · doi:10.1038/s41586-026-10545-0 · Cited by 19

Decoding Neuronal Diversification by Multiplexed Single-cell RNA-Seq

Luginbühl, J., Kouno, T., Nakano, R., Chater, T. E., Sivaraman, D. M., Kishima, M., Roudnicky, F., Carninci, P., Plessy, C., & Shin, J. W. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.02.006 · Cited by 20

STAU2 binds a complex RNA cargo that changes temporally with production of diverse intermediate progenitor cells during mouse corticogenesis

Chowdhury, R., Wang, Y., Campbell, M., Goderie, S. K., Doyle, F., Tenenbaum, S. A., Kusek, G., Kiehl, T. R., Ansari, S. A., Boles, N. C., et al. (2021) · Development · doi:10.1242/dev.199376 · Cited by 17

NKCC1-Deficiency Results in Abnormal Proliferation of Neural Progenitor Cells of the Lateral Ganglionic Eminence

Magalhães, A. C., & Rivera, C. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00200 · Cited by 17

Myelin Restoration: Progress and Prospects for Human Cell Replacement Therapies

Potter, G. B., Rowitch, D. H., & Petryniak, M. A. (2011) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-011-0120-7 · Cited by 18

Proneural transcription factors Dlx2 and Pax6 are altered in adult SVZ neural precursor cells following striatal cell loss

Jones, K. S., & Connor, B. J. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.03.001 · Cited by 16

Annotating long intergenic non-coding RNAs under artificial selection during chicken domestication

Wang, Y.-M., Xu, H., Wang, M., Otecko, N. O., Ye, L., Wu, D., & Zhang, Y. (2017) · BMC Evolutionary Biology · doi:10.1186/s12862-017-1036-6 · Cited by 15

Refinement of the Region for Split Hand/Foot Malformation 5 on 2q31.1

Theisen, A. P., Rosenfeld, J. A., Shane-Carson, K., McBride, K. L., Atkin, J., Gaba, C., Hoo, J. J., Kurczynski, T. W., Schnur, R. E., Coffey, L. B., et al. (2010) · Molecular Syndromology · doi:10.1159/000328405 · Cited by 16

Cortical versus hippocampal network dysfunction in a human brain assembloid model of epilepsy and intellectual disability

McCrimmon, C. M., Toker, D., Pahos, M., Cao, Q., Lozano, K., Lin, J. J., Parent, J. M., Tidball, A. M., Zheng, J., Molnár, L., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116217 · Cited by 17

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

Olig2 defines a subset of neural stem cells that produce specific olfactory bulb interneuron subtypes in the subventricular zone of adult mice

del Águila, Á., Adam, M., Ullom, K., Shaw, N., Qin, S., Ehrman, J. M., Nardini, D., Salomone, J. R., Gebelein, B. A., Lü, Q., et al. (2022) · Development · doi:10.1242/dev.200028 · Cited by 15

Cross Talk between Cellular Redox Status, Metabolism, and p53 in Neural Stem Cell Biology

Forsberg, K., & Giovanni, S. D. (2014) · The Neuroscientist · doi:10.1177/1073858413514634 · Cited by 14

Deletion of FGF9 in GABAergic neurons causes epilepsy

Guo, M., Cui, C., Song, X., Jia, L., Li, D., Wang, X., Dong, H., Ma, Y., Liu, Y., Cui, Z., et al. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03478-1 · Cited by 16

Bioengineering the neurovascular niche to study the interaction of neural stem cells and endothelial cells

Winkelman, M. A., Koppes, A. N., Koppes, R. A., & Dai, G. (2021) · APL Bioengineering · doi:10.1063/5.0027211 · Cited by 14

Altered T-UCRs expression profile in the spinal cord of mice with neuropathic pain

Jiang, B., Tian, Y., Li-Na, H., & Gao, Y. (2016) · Translational Perioperative and Pain Medicine · doi:10.31480/2330-4871/038 · Cited by 14

Specification of GABAergic Neocortical Interneurons

Miyoshi, G., Machold, R. P., & Fishell, G. (2013) · Springer eBooks · doi:10.1007/978-4-431-54496-8_5 · Cited by 16

From neurodevelopment to neurodegeneration: utilizing human stem cell models to gain insight into Down syndrome

Watson, L. A., & Meharena, H. S. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1198129 · Cited by 13

Isolation of a novel rat neural progenitor clone that expresses dlx family transcription factors and gives rise to functional gabaergic neurons in culture

Li, H., Hader, A. T., Han, Y. R., Wong, J. A., Babiarz, J. P., Ricupero, C. L., Godfrey, S. B., Corradi, J., Fennell, M., Hart, R. P., et al. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20977 · Cited by 13

Ascl1 promotes tangential migration and confines migratory routes by induction of Ephb2 in the telencephalon

Liu, Y., Tsai, J., Chen, J.-L., Yang, W.-S., Chang, P., Cheng, P., Turner, D. L., Yanagawa, Y., Wang, T., & Yu, J. (2017) · Scientific Reports · doi:10.1038/srep42895 · Cited by 13

Identification and host response interaction study of SARS-CoV-2 encoded miRNA-like sequences: an in silico approach

Roy, S., Sharma, B., Mazid, M. I., Akhand, M. R. N., Das, M., Marufatuzzahan, M., Chowdhury, T. A., Azim, K. F., & Hasan, M. (2021) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2021.104451 · Cited by 14

Restriction of Neural Precursor Ability to Respond to Nurr1 by Early Regional Specification

Soldati, C., Cacci, E., Biagioni, S., Carucci, N., Lupo, G., Perrone‐Capano, C., Saggio, I., & Augusti-Tocco, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051798 · Cited by 13

GABA/Glutamate Neuron Differentiation Imbalance and Increased AKT/mTOR Signaling in CNTNAP2−/− Cerebral Organoids

Chalkiadaki, K., Statoulla, E., Zafeiri, M., Voudouri, G., Amvrosiadis, T., Typou, A., Theodoridou, N., Moschovas, D., Avgeropoulos, A., Samiotaki, M. K., et al. (2024) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2024.100413 · Cited by 13

Direct conversion of somatic cells towards oligodendroglial lineage cells: A novel strategy for enhancement of myelin repair

Yavarpour-Bali, H., Nakhaei-Nejad, M., Yazdi, A., & Ghasemi-Kasman, M. (2020) · Journal of Cellular Physiology · doi:10.1002/jcp.29195 · Cited by 10

Clonal origins of neocortical interneurons

Sultan, K. T., Shi, W., & Shi, S. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.01.010 · Cited by 13

Simultaneous profiling of spatial gene expression and chromatin accessibility for mouse brain developmentPreprint

Jiang, F., Zhou, X., Qian, Y., Zhu, M., Wang, L., Li, Z., Shen, Q., Qu, F., Cui, G., Chen, K., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.22.485333 · Cited by 12

Expression of dlx genes in the normal and regenerating brain of adult zebrafish

Mendes, H. W., Taktek, M., Duret, T., & Ekker, M. (2020) · PLoS ONE · doi:10.1371/journal.pone.0229549 · Cited by 11

HOXB13 controls cell state through super-enhancers

Aspuria, P.-J. P., Cheon, D., Gozo, M. C., Beach, J. A., Recouvreux, M. S., Walts, A. E., Karlan, B. Y., & Oršulić, S. (2020) · Experimental Cell Research · doi:10.1016/j.yexcr.2020.112039 · Cited by 11

Nucleoside diphosphate kinase Nm23-M1 involves in oligodendroglial versus neuronal cell fate decision in vitro

Owlanj, H., Yang, H. J., & Feng, Z. W. (2012) · Differentiation · doi:10.1016/j.diff.2012.08.007 · Cited by 11

Div-Seq: A single nucleus RNA-Seq method reveals dynamics of rare adult newborn neurons in the CNSPreprint

Habib, N., Li, Y., Heidenreich, M., Swiech, L. J., Trombetta, J. J., Zhang, F., & Regev, A. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/045989 · Cited by 11

Lineage Reprogramming: Genetic, Chemical, and Physical Cues for Cell Fate Conversion with a Focus on Neuronal Direct Reprogramming and Pluripotency Reprogramming

Umeyama, T., Matsuda, T., & Nakashima, K. (2024) · Cells · doi:10.3390/cells13080707 · Cited by 11

Switch-Like Roles for Polycomb Proteins from Neurodevelopment to Neurodegeneration

Hoffmann, A., Sportelli, V., Ziller, M. J., & Spengler, D. (2017) · Epigenomes · doi:10.3390/epigenomes1030021 · Cited by 10

Oligodendrogenesis and Myelin Formation in the Forebrain Require Platelet-derived Growth Factor Receptor-alpha

Hamashima, T., Ishii, Y., Nguyen, L. Q., Okuno, N., Sang, Y., Matsushima, T., Kurashige, Y., Takebayashi, H., Mori, H., Fujimori, T., et al. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.04.001 · Cited by 11

Transcriptional regulation of MGE progenitor proliferation by PRDM16 controls cortical GABAergic interneuron production

Garcίa, M. T., Baizabal, J., Tran, D. N., Peixoto, R. T., Wang, W., Xie, Y., Adam, M. A., English, L. A., Reid, C. M., Brito, S. I., et al. (2020) · Development · doi:10.1242/dev.187526 · Cited by 11

Multipotent radial glia sequentially deploy fate-restricted intermediate progenitors to diversify cortical interneuronsPreprint

Kelly, S. M., Raudales, R., Moissidis, M., & Huang, Z. J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/735019 · Cited by 9

Efficient Dlx2‐mediated astrocyte‐to‐neuron conversion and inhibition of neuroinflammation by NeuroD1

Liu, M., Xu, Y., Bai, X., Lin, J.-H., Xiang, Z., Wang, T., Xu, L., Li, W., & Chen, G. (2024) · Developmental Neurobiology · doi:10.1002/dneu.22951 · Cited by 9

The Many Lives of an Oligodendrocyte Precursor Cell

Buchanan, J., & Cheadle, L. (2025) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-112723-025806 · Cited by 11

The production and functions of caudal ganglionic eminence-derived inhibitory neurons

Horton, E. C., & Paredes, M. F. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2025.06.007 · Cited by 9

Olig1/2 Orchestrates Progenitor Cell Fates during Mammalian Cortical Gliogenesis and Gliomagenesis

Tian, Y., Wang, Z.-W., Yang, F., Zhang, W., Li, J., Yang, L., Fu, T.-Y., Zheng, W., Xu, Z.-J., Ma, T., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-64753-9 · Cited by 8

A Transposon-Mediated System for Flexible Control of Transgene Expression in Stem and Progenitor-Derived Lineages

Akhtar, A. A., Molina, J., Dutra‐Clarke, M., Kim, G. B., Levy, R., Schreiber-Stainthorp, W., Danielpour, M., & Breunig, J. J. (2015) · Stem Cell Reports · doi:10.1016/j.stemcr.2015.01.013 · Cited by 9

Directed differentiation of umbilical cord blood stem cells into cortical GABAergic neurons

Ali, H., Bayatti, N., Lindsay, S., Dashti, A. A., & Al‐Mulla, F. (2013) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2013-1934 · Cited by 9

Replicable Expansion and Differentiation of Neural Precursors from Adult Canine Skin

Duncan, T., Lowe, A., Sidhu, K., Sachdev, P. S., Lewis, T., Lin, R. C. Y., Sytnyk, V., & Valenzuela, M. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.07.008 · Cited by 9

Cell fate acquisition and reprogramming by the proneural transcription factor ASCL1

Lundie-Brown, J., Puletti, F., Philpott, A., & Azzarelli, R. (2025) · Open Biology · doi:10.1098/rsob.250018 · Cited by 10

Gestational stress induced differential expression of HDAC2 in male rat offspring hippocampus during development

Liao, L., Wang, X., Yao, X., Zhang, B., Zhou, L., & Huang, J. (2018) · Neuroscience Research · doi:10.1016/j.neures.2018.11.006 · Cited by 8

Lost highway(s): barriers to postnatal cortical neurogenesis and implications for brain repair

Akhtar, A. A., & Breunig, J. J. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00216 · Cited by 11

The Generation of Cortical Interneurons

Batista‐Brito, R., & Fishell, G. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00071-x · Cited by 9

Mechanisms of Development

ten Donkelaar, H. J. (2014) · Springer eBooks · doi:10.1007/978-3-642-54687-7_2 · Cited by 8

Intrinsic regulation of adult subventricular zone neural progenitor cells and the effect of brain injury.

Jones, K. S., & Connor, B. J. (2012) · Europe PMC (PubMed Central) · Cited by 8

Mouse cortical cellular diversification through lineage progression of radial gliaPreprint

Yang, L., Wang, Z., Gao, Y., Li, Z., Liu, G., Xu, Z., Zhang, Z., You, Y., Yang, Z., & Li, X. (2025) · Genes & Development · doi:10.1101/gad.352826.125 · Cited by 8

TempShift Reveals the Sequential Development of Human Neocortex and Skewed Developmental Timing of Down Syndrome Brains

Zhou, Y., Tao, L., & Zhu, Y. (2023) · Brain Sciences · doi:10.3390/brainsci13071070 · Cited by 7

Astrocytic Ephrin-B1 Regulates Oligodendrocyte Development and Myelination

Sutley-Koury, S. N., Anderson, A., Taitano-Johnson, C., Ajayi, M. T., Kulinich, A. O., Contreras, K., Regalado, J., Tiwari-Woodruff, S. K., & Ethell, I. M. (2024) · ASN NEURO · doi:10.1080/17590914.2024.2401753 · Cited by 8

Single-cell multimodal analysis in a case with reduced penetrance of Progranulin-Frontotemporal Dementia

Natarajan, K., Eisfeldt, J., Hammond, M., Patra, K., Laffita‐Mesa, J. M., Andrade‐Talavera, Y., Birtele, M., Öijerstedt, L., Fisahn, A., Parmar, M., et al. (2021) · Acta Neuropathologica Communications · doi:10.1186/s40478-021-01234-2 · Cited by 7

miR-17∼92 exerts stage-specific effects in adult V-SVZ neural stem cell lineages

Favaloro, F., DeLeo, A. M., Delgado, A. C., & Doetsch, F. K. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111773 · Cited by 7

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

Transposable elements resistant to epigenetic resetting in the human germline are epigenetic hotspots for development and diseasePreprint

Dietmann, S., Keogh, M. J., Tang, W. W. C., Magnúsdóttir, E., Kobayashi, T., Chinnery, P. F., & Surani, M. A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.19.998930 · Cited by 7

A developmental atlas of the mouse brain by single-cell mass cytometryPreprint

Deusen, A. L. V., Goggin, S. M., Williams, C. M., Keeler, A. B., Fread, K., Cheng, I., Deppmann, C. D., & Zunder, E. R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.27.501794 · Cited by 7

A comparative view of human and mouse telencephalon inhibitory neuron development

Chung, C., Girgiss, J., & Gleeson, J. G. (2025) · Development · doi:10.1242/dev.204306 · Cited by 6

Distinct requirements for Tcf3 and Tcf12 during oligodendrocyte development in the mouse telencephalon

Talley, M. J., Nardini, D., Ehrman, L. A., Lu, Q. R., & Waclaw, R. R. (2023) · Neural Development · doi:10.1186/s13064-023-00173-z · Cited by 5

Controlling the Expression Level of the Neuronal Reprogramming Factors for a Successful Reprogramming Outcome

Mseis-Jackson, N., Sharma, M., & Li, H. (2024) · Cells · doi:10.3390/cells13141223 · Cited by 6

Thyroid hormone regulation of adult hippocampal neurogenesis: Putative molecular and cellular mechanisms

Kapri, D., Fanibunda, S. E., & Vaidya, V. A. (2022) · Vitamins and hormones · doi:10.1016/bs.vh.2021.10.001 · Cited by 6

Long-Term Treatment with Bortezomib Induces Specific Methylation Changes in Differentiated Neuronal Cells

Łuczkowska, K., Taryma‐Leśniak, O., Bińkowski, J., Sokolowska, K. E., Strapagiel, D., Jarczak, J., Paczkowska, E., Machaliński, B., & Wojdacz, T. K. (2022) · Cancers · doi:10.3390/cancers14143402 · Cited by 6

Mechanisms of astrocyte development

Sardar, D., Cheng, Y.-T., Szewczyk, L., Deneen, B., & Molofsky, A. (2020) · Patterning and Cell Type Specification in the Developing CNS and PNS · doi:10.1016/b978-0-12-397265-1.00080-0 · Cited by 16

Endogenous neural stem cells characterization using omics approaches: Current knowledge in health and disease

Murtaj, V., Butti, E., Martino, G., & Panina‐Bordignon, P. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1125785 · Cited by 8

RNA-Seq time-course analysis of neural precursor cell transcriptome in response to herpes simplex Virus-1 infection

Wood, J. A., Chaparala, S., Bantang, C., Chattopadhyay, A., Wesesky, M. A., Kinchington, P. R., Nimgaonkar, V. L., Bloom, D. C., & D’Aiuto, L. (2024) · Journal of NeuroVirology · doi:10.1007/s13365-024-01198-8 · Cited by 4

Proneural Proteins and the Development of the Cerebral Cortex

Heng, J. I., & Guillemot, F. (2013) · Springer eBooks · doi:10.1007/978-4-431-54496-8_2 · Cited by 5

EphB1 controls long-range cortical axon guidance through a cell non-autonomous role in GABAergic cells

Assali, A., Chenaux, G., Cho, J. Y., Berto, S., Ehrlich, N. A., & Cowan, C. W. (2024) · Development · doi:10.1242/dev.201439 · Cited by 5

Transcriptional Dynamics at Brain Enhancers: from Functional Specialization to Neurodegeneration

Vermunt, M. W., & Creyghton, M. P. (2016) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-016-0689-7 · Cited by 5

The generation of cortical interneurons

Batista‐Brito, R., Ward, C., & Fishell, G. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00020-5 · Cited by 6

Transcription Factors of Direct Neuronal Reprogramming in Ontogenesis and Ex Vivo

Samoilova, E. M., Викторович, Б. В., & Baklaushev, V. P. (2021) · Molecular Biology · doi:10.1134/s0026893321040087 · Cited by 5

Telencephalic Neurogenesis Versus Telencephalic Differentiation of Pluripotent Stem Cells

Nat, R., Apostolova, G., & Dechant, G. (2013) · InTech eBooks · doi:10.5772/54251 · Cited by 7

Revealing the Impact of Mitochondrial Fitness During Early Neural Development Using Human Brain Organoids

Romero-Morales, A. I., & Gama, V. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.840265 · Cited by 5

The Role of PLAG1 in Mouse Brain Development and Neurogenesis

Gasperoni, J. G., Tran, S. C., Grommen, S. V. H., Groef, B. D., & Dworkin, S. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-03943-w · Cited by 4

Транскрипционные факторы прямого пронейронального репрограммирования в онтогенезе и ex vivo

Samoilova, E. M., Викторович, Б. В., & Baklaushev, V. P. (2021) · Molecular Biology · doi:10.31857/s0026898421050086 · Cited by 4

The gene encoding the mouse contactin‐1 axonal glycoprotein is regulated by the collier/Olf1/EBF family early B ‐Cell factor 2 transcription factor

Bizzoca, A., Picocci, S., Corsi, P., Arbia, S., Croci, L., Consalez, G. G., & Gennarini, G. (2015) · Developmental Neurobiology · doi:10.1002/dneu.22293 · Cited by 4

PAX6 LIMITS THE COMPETENCE OF DEVELOPING CEREBRAL CORTICAL CELLSPreprint

Manuel, M. N., Tan, K. B., Kozić, Z., Molinek, M., Marcos, T. S., Razak, F. M. A., Dobolyi, D., Dobie, R., Henderson, B. E. P., Henderson, N. C., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.03.478927 · Cited by 4

A comprehensive view of cell-type-specific temporal dynamics in human and mouse brainsPreprint

Lu, Z., Zhang, M., Lee, J., Sziraki, A., Anderson, S., Ge, S., Nelson, P. T., Zhou, W. Y., & Cao, J. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.01.509820 · Cited by 4

Comprehensive profiling of transcription factors for reprogramming human astrocytes to neuronal cells through endogenous CRISPR-based gene activationPreprint

Reisman, S. J., Halabi, D., Miller, S. E., Song, L., Geraghty, S., Sangvai, N., Rice, G., Safi, A., Crawford, G. E., & Gersbach, C. A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.11.681828 · Cited by 4

Notch and neural development

Breunig, J. J., & Nelson, B. R. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00013-8 · Cited by 2

Direct reprogramming of oligodendrocyte precursor cells into GABAergic inhibitory neurons by a single homeodomain transcription factor Dlx2

Boshans, L. L., Soh, H., Wood, W. M., Nolan, T. M., Măndoiu, I., Yanagawa, Y., Tzingounis, A. V., & Nishiyama, A. (2021) · Scientific Reports · doi:10.1038/s41598-021-82931-9 · Cited by 28

Regulation of cell fate decisions in the developing forebrain by DLX transcription factors

Nevin, M. (2020) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3-3cf4-wa60

The DLX/Notch axis is necessary for spatiotemporal regulation of neural cell fate

Leung, R. F., See, M., George, A. M., Barry, P. L., France, K., Charitakis, N., Ramialison, M., Faux, M. C., & Eisenstat, D. D. (2026) · Nature Communications · doi:10.1038/s41467-026-76838-0 · Cited by 1

Dlx and Olig transcription factors specify neuronal versus glial cell fate in the mammalian CNS.Preprint

Mamoor, S. (2025) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5281/zenodo.18012499

Dlx1/2 are Central and Essential Components in the Transcriptional Code for Generating Olfactory Bulb Interneurons

Guo, T., Liu, G., Du, H., Wen, Y. F., Wei, S., Li, Z., Tao, G., Shang, Z., Song, X., Zhang, Z., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz018 · Cited by 45