Local generation of glia is a major astrocyte source in postnatal cortex

A robust and high-throughput Cre reporting and characterization system for the whole mouse brain

Madisen, L., Zwingman, T. A., Sunkin, S. M., Oh, S. W., Zariwala, H. A., Gu, H., Ng, L. L., Palmiter, R. D., Hawrylycz, M. J., Jones, A. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2467 · Cited by 6,907

Subventricular zone astrocytes are neural stem cells in the adult mammalian brain

Doetsch, F., Caillé, I., Lim, D. A., García-Verdugo, J. M., & Alvarez-Buylla, A. (1999) · Cell · doi:10.1016/s0092-8674(00)80783-7 · Cited by 3,898

The Glial Nature of Embryonic and Adult Neural Stem Cells

Kriegstein, A., & Alvarez-Buylla, A. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135600 · Cited by 2,475

Equal numbers of neuronal and nonneuronal cells make the human brain an isometrically scaled-up primate brain

Azevedo, F. A. C., Carvalho, L. R. B., Grinberg, L. T., Farfel, J. M., Ferretti, R. E. L., Leite, R. E. P., Filho, W. J., Lent, R., & Herculano‐Houzel, S. (2009) · Journal of Comparative Neurology · doi:10.1002/cne.21974 · Cited by 2,337

Visualizing Spatiotemporal Dynamics of Multicellular Cell-Cycle Progression

Sakaue-Sawano, A., Kurokawa, H., Morimura, T., Hanyu, A., Hama, H., Osawa, H., Kashiwagi, S., Fukami, K., Miyata, T., Miyoshi, H., et al. (2008) · Cell · doi:10.1016/j.cell.2007.12.033 · Cited by 2,194

Cell death and control of cell survival in the oligodendrocyte lineage

Barres, B. A., Hart, I. K., Coles, H. S. R., Burne, J. F., Voyvodic, J. T., Richardson, W. D., & Raff, M. C. (1992) · Cell · doi:10.1016/0092-8674(92)90531-g · Cited by 1,345

Astrocyte-mediated control of cerebral blood flow

Takano, T., Tian, G.-F., Peng, W., Lou, N., Libionka, W., Han, X., & Nedergaard, M. (2005) · Nature Neuroscience · doi:10.1038/nn1623 · Cited by 1,137

Epidemiology and molecular pathology of glioma

Schwartzbaum, J., Fisher, J. L., Aldape, K., & Wrensch, M. (2006) · Nature Clinical Practice Neurology · doi:10.1038/ncpneuro0289 · Cited by 951

Astroglial Metabolic Networks Sustain Hippocampal Synaptic Transmission

Rouach, N., Koulakoff, A., Abudara, V., Willecke, K., & Giaume, C. (2008) · Science · doi:10.1126/science.1164022 · Cited by 912

In Vivo Fate Analysis Reveals the Multipotent and Self-Renewal Capacities of Sox2+ Neural Stem Cells in the Adult Hippocampus

Suh, H., Consiglio, A., Ray, J., Sawai, T., D’Amour, K. A., & Gage, F. H. (2007) · Cell stem cell · doi:10.1016/j.stem.2007.09.002 · Cited by 851

Expression of GFAP and Tau Following Blast Exposure in the Cerebral Cortex of Ferrets

Schwerin, S. C., Chatterjee, M., Hutchinson, E. B., Djankpa, F. T., Armstrong, R. C., McCabe, J. T., Perl, D. P., & Juliano, S. L. (2021) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlaa157 · Cited by 34

Caspr Controls the Temporal Specification of Neural Progenitor Cells through Notch Signaling in the Developing Mouse Cerebral Cortex

Wu, Z., Li, D., Huang, Y., Chen, X., Huang, W., Liu, C., Zhao, H., Xu, R., Cheng, M., Schachner, M., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv318 · Cited by 34

Macroglial diversity: white and grey areas and relevance to remyelination

Werkman, I. L., Lentferink, D. H., & Baron, W. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03586-9 · Cited by 33

Astrogenesis in the murine dentate gyrus is a life‐long and dynamic process

Schneider, J., Weigel, J., Wittmann, M., Švehla, P., Ehrt, S., Zheng, F., Elmzzahi, T., Karpf, J., Paniagua‐Herranz, L., Başak, O., et al. (2022) · The EMBO Journal · doi:10.15252/embj.2021110409 · Cited by 34

SOX2 is essential for astrocyte maturation and its deletion leads to hyperactive behavior in mice

Wang, Y., Zhang, S., Lan, Z., Doan, V., Kim, B., Liu, S., Zhu, M., Hull, V. L., Rihani, S., Zhang, C., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111842 · Cited by 32

The Pathological Activation of Microglia Is Modulated by Sexually Dimorphic Pathways

O'Connor, J. L., & Nissen, J. C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054739 · Cited by 33

Dual lineage origins contribute to neocortical astrocyte diversity

Zhou, J., Vitali, I., Roig‐Puiggros, S., Javed, A., Cantando, I., Puglisi, M., Bezzi, P., Jabaudon, D., Mayer, C., & Bocchi, R. (2025) · Nature Communications · doi:10.1038/s41467-025-61829-4 · Cited by 31

Natural and lesion‐induced decrease in cell proliferation in the medial nucleus of the trapezoid body during hearing development

Saliu, A., Adise, S., Xian, S., Kudelska, K., & Rodríguez‐Contreras, A. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23473 · Cited by 31

The Challenging Pathway of Treatment for Neurogenesis Impairment in Down Syndrome: Achievements and Perspectives

Stagni, F., & Bartesaghi, R. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.903729 · Cited by 33

Genetic Abnormalities, Clonal Evolution, and Cancer Stem Cells of Brain Tumors

Testa, U., Castelli, G., & Pelosi, E. (2018) · Medical Sciences · doi:10.3390/medsci6040085 · Cited by 33

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

You Do Not Mess with the Glia

Herculano‐Houzel, S., & Santos, S. D. (2018) · Neuroglia · doi:10.3390/neuroglia1010014 · Cited by 30

Many roles for oligodendrocyte precursor cells in physiology and pathology

Nishiyama, A., Serwanski, D. R., & Pfeiffer, F. (2021) · Neuropathology · doi:10.1111/neup.12732 · Cited by 31

Mechanics and self-organization in tissue development

Gómez‐Gálvez, P., Anbari, S., Escudero, L. M., & Buceta, J. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.07.003 · Cited by 29

Progress of Astrocyte-Neuron Crosstalk in Central Nervous System Diseases

Zhang, Y., Wang, Z., Xu, F., Liu, Z., Zhao, Y., Yang, L. Z., & Fang, W. (2024) · Neurochemical Research · doi:10.1007/s11064-024-04241-6 · Cited by 28

Chromatin-based epigenetics of adult subventricular zone neural stem cells

Gonzales-Roybal, G., & Lim, D. A. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2013.00194 · Cited by 30

A subpopulation of astrocyte progenitors defined by Sonic hedgehog signaling

Gingrich, E. C., Case, K., & Garcia, A. D. R. (2022) · Neural Development · doi:10.1186/s13064-021-00158-w · Cited by 28

BMP-Responsive Protease HtrA1 Is Differentially Expressed in Astrocytes and Regulates Astrocytic Development and Injury Response

Chen, J., Gulden, S. V., McGuire, T. L., Fleming, A. C., Oka, C., Kessler, J. A., & Peng, C. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2031-17.2018 · Cited by 28

Reprogramming astroglia into neurons with hallmarks of fast-spiking parvalbumin-positive interneurons by phospho-site–deficient Ascl1

Marichal, N., Péron, S., Beltrán-Arranz, A., Galante, C., Scarante, F. F., Wiffen, R., Schuurmans, C., Karow, M., Gascón, S., & Berninger, B. (2024) · Science Advances · doi:10.1126/sciadv.adl5935 · Cited by 28

Early Life Events and Maturation of the Dentate Gyrus: Implications for Neurons and Glial Cells

Aniol, V. A., Манолова, А. О., & Gulyaeva, N. V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23084261 · Cited by 28

Neuroinflammation: Molecular Mechanisms And Therapeutic Perspectives

Meccariello, R., Marino, M., Mele, E., Pastorino, G. M. G., Operto, F. F., Santoro, A., & Viggiano, A. (2022) · Central Nervous System Agents in Medicinal Chemistry · doi:10.2174/1871524922666220929153215 · Cited by 29

Very Low Efficiency of Direct Reprogramming of Astrocytes Into Neurons in the Brains of Young and Aged Mice After Cerebral Ischemia

Greșiță, A., Glăvan, D., Udriștoiu, I., Cătălin, B., Hermann, D. M., & Popa‐Wagner, A. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00334 · Cited by 27

Metabolic dynamics in astrocytes and microglia during post-natal development and their implications for autism spectrum disorders

Cantando, I., Centofanti, C., D’Alessandro, G., Limatola, C., & Bezzi, P. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1354259 · Cited by 27

Coordination of proliferation and neuronal differentiation by the retinoblastoma protein family

Ajioka, I. (2014) · Development Growth & Differentiation · doi:10.1111/dgd.12127 · Cited by 28

mGlu5-mediated signalling in developing astrocyte and the pathogenesis of autism spectrum disorders

Petrelli, F., & Bezzi, P. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.12.014 · Cited by 26

The glial perspective of autism spectrum disorder convergent evidence from postmortem brain and PET studies

Liao, X., Chen, M., & Li, Y. (2023) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2023.101064 · Cited by 25

Function and therapeutic value of astrocytes in diabetic cognitive impairment

Meng, F., Fu, J., Zhang, L., Guo, M., Zhuang, P., Yin, Q., & Zhang, Y. (2023) · Neurochemistry International · doi:10.1016/j.neuint.2023.105591 · Cited by 26

Origins and significance of astrogliosis in the multiple sclerosis model, MOG peptide EAE

Moreno, M. A., Guo, F., Ko, E. M., Bannerman, P. G. C., Soulika, A. M., & Pleasure, D. (2013) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2012.12.014 · Cited by 25

Developmental dynamics of neurogenesis and gliogenesis in the postnatal mammalian brain in health and disease: Historical and future perspectives

Nakafuku, M., & del Águila, Á. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.369 · Cited by 25

Retinoic Acid Is Required for Oligodendrocyte Precursor Cell Production and Differentiation in the Postnatal Mouse Corpus Callosum

Morrison, V. E., Smith, V. N., & Huang, J. K. (2019) · eNeuro · doi:10.1523/eneuro.0270-19.2019 · Cited by 27

Longitudinal scRNA-seq analysis in mouse and human informs optimization of rapid mouse astrocyte differentiation protocols

Frazel, P. W., Labib, D., Fisher, T., Brosh, R., Pirjanian, N., Marchildon, A. E., Boeke, J. D., Fossati, V., & Liddelow, S. A. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01424-2 · Cited by 24

Construction of the human forebrain

Jernigan, T. L., & Stiles, J. (2016) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1409 · Cited by 27

Reduction of neuronal activity mediated by blood-vessel regression in the adult brain

Gao, X., Chen, X.-J., Ye, M., Li, J.-L., Lu, N., Yao, D., Ci, B., Chen, F., Zheng, L., Yi, Y., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60308-0 · Cited by 24

Human Glioma–Initiating Cells Show a Distinct Immature Phenotype Resembling but Not Identical to NG2 Glia

Barrantes‐Freer, A., Kim, E. L., Bielańska, J., Giese, A., Mortensen, L. S., Schulz‐Schaeffer, W., Stadelmann, C., Brück, W., & Pardo, L. A. (2013) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31828afdbd · Cited by 24

Neuroglia: Definition, Classification, Evolution, Numbers, Development

(2013) · Wiley eBooks · doi:10.1002/9781118402061.ch3 · Cited by 27

On astrocyte-neuron interactions: broad insights from the striatum

Khakh, B. S. (2025) · Neuron · doi:10.1016/j.neuron.2025.08.009 · Cited by 23

Astroglial cells as neuroendocrine targets in forebrain development: Implications for sex differences in psychiatric disease

Rurak, G. M., Woodside, B. C., Aguilar‐Valles, A., & Salmaso, N. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100897 · Cited by 24

Prion Replication Elicits Cytopathic Changes in Differentiated Neurosphere Cultures

Iwamaru, Y., Takenouchi, T., Imamura, M., Shimizu, Y., Miyazawa, K., Mohri, S., Yokoyama, T., & Kitani, H. (2013) · Journal of Virology · doi:10.1128/jvi.00572-13 · Cited by 23

Developmental control of cortico-cerebral astrogenesis

Mallamaci, A. (2013) · The International Journal of Developmental Biology · doi:10.1387/ijdb.130148am · Cited by 26

Classic “broken cell” techniques and newer live cell methods for cell cycle assessment

Henderson, L. M., Bortone, D. S., Lim, C., & Zambon, A. C. (2013) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00006.2013 · Cited by 23

Clonal Mapping of Astrocytes in the Olfactory Bulb and Rostral Migratory Stream

García‐Marqués, J., & López‐Mascaraque, L. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw071 · Cited by 23

Neural stem cell heterogeneity in the mammalian forebrain

Adams, K. V., & Morshead, C. M. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.06.005 · Cited by 26

A functional perspective on astrocyte heterogeneity

Kwon, W., Williamson, M. R., & Deneen, B. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2025.06.009 · Cited by 22

Reprogramming cellular identity in vivo

Leaman, S., Marichal, N., & Berninger, B. (2022) · Development · doi:10.1242/dev.200433 · Cited by 22

Foxg1 Antagonizes Neocortical Stem Cell Progression to Astrogenesis

Falcone, C., Santo, M., Liuzzi, G., Cannizzaro, N., Grudina, C., Valencic, E., Peruzzotti‐Jametti, L., Pluchino, S., & Mallamaci, A. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz031 · Cited by 24

Astrocyte phenotypes: Emphasis on potential markers in neuroinflammation.

Bozic, I. D., Savić, D. Z., & Lavrnja, I. C. (2021) · PubMed · doi:10.14670/hh-18-284 · Cited by 22

Interactions between neural cells and blood vessels in central nervous system development

Morimoto, K., Tabata, H., Takahashi, R., & Nakajima, K. (2023) · BioEssays · doi:10.1002/bies.202300091 · Cited by 21

Intra-generational protein malnutrition impairs temporal astrogenesis in rat brain

Naik, A. A., Patro, N., Seth, P., & Patro, I. K. (2017) · Biology Open · doi:10.1242/bio.023432 · Cited by 21

An Overview of Extrinsic and Intrinsic Mechanisms Involved in Astrocyte Development in the Central Nervous System

Zarei‐Kheirabadi, M., Vaccaro, A. R., Rahimi‐Movaghar, V., Kiani, S., & Baharvand, H. (2019) · Stem Cells and Development · doi:10.1089/scd.2019.0189 · Cited by 21

Use of CRISPR/Cas9-mediated disruption of CNS cell type genes to profile transduction of AAV by neonatal intracerebroventricular delivery in mice

Torregrosa, T., Lehman, S., Hana, S., Marsh, G., Xu, S., Koszka, K., Mastrangelo, N., McCampbell, A., Henderson, C. E., & Lo, S. (2021) · Gene Therapy · doi:10.1038/s41434-021-00223-3 · Cited by 24

Radial stem astrocytes (aka neural stem cells): Identity, development, physio‐pathology, and therapeutic potential

Yeh, C., Wu, K., Huang, G., & Verkhratsky, A. (2023) · Acta Physiologica · doi:10.1111/apha.13967 · Cited by 20

Astrocytes in ischemic stroke: Crosstalk in central nervous system and therapeutic potential

Liu, J., Guo, Y., Zhang, Y., Zhao, X., Fu, R., Hua, S., & Xu, S. (2023) · Neuropathology · doi:10.1111/neup.12928 · Cited by 21

Single-Cell RNA-Sequencing in Astrocyte Development, Heterogeneity, and Disease

Gao, M.-Y., Wang, J., He, J. M., Gao, R., Zhang, Y., & Li, X. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01397-7 · Cited by 21

Spatiotemporal analyses of neural lineages after embryonic and postnatal progenitor targeting combining different reporters

Figueres‐Oñate, M., García‐Marqués, J., Pedraza, M., Carlos, J., & López‐Mascaraque, L. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00087 · Cited by 20

TheInk4a/ArfLocus Is a Barrier to Direct Neuronal Transdifferentiation

Price, J. D., Park, K.-Y., Chen, J., Salinas, R. D., Cho, M. J., Kriegstein, A. R., & Lim, D. A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3159-13.2014 · Cited by 24

NMDA receptor-dependent prostaglandin-endoperoxide synthase 2 induction in neurons promotes glial proliferation during brain development and injury

Zhou, J., Geng, Y., Su, T., Wang, Q., Ren, Y., Zhao, J., Fu, C., Weber, M., Lin, H., Kaminker, J. S., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110557 · Cited by 20

Origin, molecular specification, and stemness of astrocytes

Zheng, K., Huang, H., Yang, J., & Qiu, M. S. (2022) · Developmental Neurobiology · doi:10.1002/dneu.22863 · Cited by 19

Application of Small Molecules in the Central Nervous System Direct Neuronal Reprogramming

Wang, J., Chen, S., Pan, C., Li, G., & Tang, Z. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.799152 · Cited by 19

GFAP-Positive Progenitor Cell Production is Concentrated in Specific Encephalic Regions in Young Adult Mice

Guo, Z., Su, Y., & Lou, H. (2018) · Neuroscience Bulletin · doi:10.1007/s12264-018-0228-4 · Cited by 19

ZBTB20 is crucial for the specification of a subset of callosal projection neurons and astrocytes in the mammalian neocortex

de Araújo, J. A. M., Barão, S., Mateos-White, I., Espinosa, A., Costa, M. R., Gil, C., & Müller, U. (2021) · Development · doi:10.1242/dev.196642 · Cited by 20

Neogenin-YAP signaling in neocortical astrocytic differentiation

Huang, Z., & Xiong, W. (2016) · Neurogenesis · doi:10.1080/23262133.2016.1248735 · Cited by 19

Molecular divergence of mammalian astrocyte progenitor cells at early gliogenesis

Liu, J., Wu, X., & Lü, Q. (2022) · Development · doi:10.1242/dev.199985 · Cited by 19

Genesis of a functional astrocyte syncytium in the developing mouse hippocampus

Zhong, S., Kiyoshi, C. M., Du, Y., Wang, W., Luo, Y., Wu, X. Y., Taylor, A. T., Ma, B., Aten, S., Liu, X., et al. (2023) · Glia · doi:10.1002/glia.24327 · Cited by 19

Astrocytes in the adult dentate gyrus—balance between adult and developmental tasks

Chalmers, N., Masouti, E., & Beckervordersandforth, R. (2024) · Molecular Psychiatry · doi:10.1038/s41380-023-02386-4 · Cited by 19

Glial enriched gene expression profiling identifies novel factors regulating the proliferation of specific glial subtypes in the Drosophila brain

Avet‐Rochex, A., Maierbrugger, K. T., & Bateman, J. E. (2014) · Gene Expression Patterns · doi:10.1016/j.gep.2014.09.001 · Cited by 18

H2A.Z.1 crosstalk with H3K56-acetylation controls gliogenesis through the transcription of folate receptor

Su, L., Xia, W., Shen, T., Liang, Q., Wang, W., Li, H., & Jiao, J. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky585 · Cited by 20

Early Postnatal In Vivo Gliogenesis From Nestin-Lineage Progenitors Requires Cdk5

Petřík, D., Yun, S., Latchney, S. E., Kamrudin, S., LeBlanc, J. A., Bibb, J. A., & Eisch, A. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072819 · 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

Glial cells as therapeutic targets in progressive multiple sclerosis

Wilbanks, B., Maher, L., & Rodriguez, M. (2019) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2019.1614443 · Cited by 17

Vitamin C Recycling Regulates Neurite Growth in Neurospheres Differentiated In Vitro

Espinoza, F., Magdalena, R., Saldivia, N., Jara, N., Martínez, F., Ferrada, L., Salazar, K., Ávila, F., & Nualart, F. (2020) · Antioxidants · doi:10.3390/antiox9121276 · Cited by 17

In vivo Direct Conversion of Astrocytes to Neurons Maybe a Potential Alternative Strategy for Neurodegenerative Diseases

Wang, Y., Zhang, X., Chen, F., Song, N., & Xie, J. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.689276 · Cited by 18

Astrocytes Transplanted during Early Postnatal Development Integrate, Mature, and Survive Long Term in Mouse Cortex

Chierzi, S., Kacerovsky, J. B., Fok, A. H. K., Lahaie, S. C., Rosen, A. S., Farmer, W. T., & Murai, K. K. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0544-22.2023 · Cited by 17

SIMS: A deep-learning label transfer tool for single-cell RNA sequencing analysis

Gonzalez-Ferrer, J., Lehrer, J., O’Farrell, A., Paten, B., Teodorescu, M., Haussler, D. H., Jönsson, V. D., & Mostajo-Radji, M. A. (2024) · Cell Genomics · doi:10.1016/j.xgen.2024.100581 · Cited by 16

Asymmetric cell division: Implications for glioma development and treatment

Lewis, K., & Petritsch, C. K. (2013) · Translational Neuroscience · doi:10.2478/s13380-013-0148-8 · Cited by 16

Cortical Spreading Depolarization Stimulates Gliogenesis in the Rat Entorhinal Cortex

Urbach, A., Brueckner, J., & Witte, O. W. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2014.232 · Cited by 16

Derivation of an endogenous small RNA from double-stranded Sox4 sense and natural antisense transcripts in the mouse brain

Ling, K., Brautigan, P. J., Moore, S., Fraser, R., Cheah, P.-S., Raison, J. M., Babic, M., Lee, Y. K., Daish, T., Mattiske, D. M., et al. (2016) · Genomics · doi:10.1016/j.ygeno.2016.01.006 · Cited by 16

Astrocytes and Circadian Rhythms: An Emerging Astrocyte-Neuron Synergy in the Timekeeping System.

Mayo, O. B., Berdondini, L., & Tonelli, D. D. P. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9068-9_10 · Cited by 12

Differential Proliferation and Maturation of Subcortical Astrocytes During Postnatal Development

Shoneye, T., Orrego, A. T., Jarvis, R., Men, Y., Chiang, M. S. R., & Yang, Y. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00435 · Cited by 16

The anatomy of neuroepithelial tumours

Akeret, K., Weller, M., & Krayenbühl, N. (2023) · Brain · doi:10.1093/brain/awad138 · Cited by 16

Yin Yang 1 controls cerebellar astrocyte maturation

Mockenhaupt, K., Tyc, K. M., McQuiston, A. R., Gonsiewski, A. K., Zarei‐Kheirabadi, M., Hariprashad, A., Biswas, D. D., Gupta, A. S., Olex, A. L., Singh, S. K., et al. (2023) · Glia · doi:10.1002/glia.24434 · Cited by 15

Quantitative characterization of proliferative cells subpopulations in the hilus of the hippocampus of adult Wistar rats: an integrative study

García-Martínez, Y., Sánchez-Huerta, K., & Pacheco-Rosado, J. (2020) · Journal of Molecular Histology · doi:10.1007/s10735-020-09895-4 · Cited by 15

Astrocyte Dysfunction in Developmental Neurometabolic Diseases

Olivera‐Bravo, S., Isasi, E., Fernández, A. S., Casanova, G., Rosillo, J. C., & Barbeito, L. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-40764-7_11 · Cited by 15

Gestational zinc deficiency impairs brain astrogliogenesis in rats through multistep alterations of the JAK/STAT3 signaling pathway

Supasai, S., Adamo, A. M., Mathieu, P., Marino, R. C., Hellmers, A. C., Cremonini, E., & Oteiza, P. I. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102017 · Cited by 14

Evaluation of Glymphatic System Development in Neonatal Brain via Diffusion Analysis along the Perivascular Space Index

Lin, S., Guo, M., Liang, Q., Lin, X., Chen, S., Li, Y., Chen, P., & Qiu, Y. (2024) · Annals of Neurology · doi:10.1002/ana.27047 · Cited by 14

Astrocyte morphogenesis requires self-recognition

Lee, J. H., Sergeeva, A. P., Ahlsén, G., Mannepalli, S. M., Bahna, F. A., Goodman, K. M., Xu, R., Khakh, B. S., Weiner, J. A., Shapiro, L. S., et al. (2025) · Nature · doi:10.1038/s41586-025-09013-y · Cited by 14

Bulk and Mosaic Deletions of Egfr Reveal Regionally Defined Gliogenesis in the Developing Mouse Forebrain

Zhang, X., Xiao, G., Johnson, C. A., Cai, Y., Horowitz, Z. K., Mennicke, C. V., Coffey, R. J., Haider, M. A., Threadgill, D. W., Eliscu, R., et al. (2022) · iScience · doi:10.1016/j.isci.2023.106242 · Cited by 14

Neural Stem Cells in the Diabetic Brain

Bachor, T. P., & Suburo, Á. M. (2012) · Stem Cells International · doi:10.1155/2012/820790 · Cited by 14

Spatiotemporal control of mitochondrial network dynamics in astroglial cells

Göbel, J., Motori, E., & Bergami, M. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.06.191 · Cited by 15

Gaps and Doubts in Search to Recognize Glioblastoma Cellular Origin and Tumor Initiating Cells

Włodarczyk, A., Grot, D., Stoczyńska-Fidelus, E., & Rieske, P. (2020) · Journal of Oncology · doi:10.1155/2020/6783627 · Cited by 14

Role of Notch and its oncogenic signaling crosstalk in glioma and glioma stem cells

Sidhu, R. S., Guo, S., Wang, G., & Liu, M. (2025) · Gene · doi:10.1016/j.gene.2025.149761 · Cited by 13

NR3C1-mediated epigenetic regulation suppresses astrocytic immune responses in mice

Park, S., Park, H., Byun, Y. G., Wei, X., Eom, J., Joo, J., Lee, A., Diao, Y., Chung, W., & Jung, I. (2025) · Nature Communications · doi:10.1038/s41467-025-64088-5 · Cited by 13

Glial Cells of the Central Nervous System: A Potential Target in Chronic Prostatitis/Chronic Pelvic Pain Syndrome

Lao, Y., Li, Z., Bai, Y., Li, W., Wang, J., Wang, Y., Li, Q., & Dong, Z. (2023) · Pain Research and Management · doi:10.1155/2023/2061632 · Cited by 13

Preclinical studies of gene replacement therapy for CDKL5 deficiency disorder

Voronin, G. O., Narasimhan, J., Gittens, J., Sheedy, J., Lipari, P., Peters, M. M., DeMarco, S. J., Cao, L., Varganov, Y., Kim, M. J., et al. (2024) · Molecular Therapy · doi:10.1016/j.ymthe.2024.07.012 · Cited by 13

Premature Neural Progenitor Cell Differentiation Into Astrocytes in Retinoic Acid-Induced Spina Bifida Rat Model

Oria, M., Pathak, B., Li, Z., Bakri, K., Gouwens, K. R., Varela, M. F., Lampe, K., Murphy, K. P., Lin, C.-Y. J., & Peiro, J. L. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.888351 · Cited by 13

Crosstalk between Blood Vessels and Glia during the Central Nervous System Development

Tabata, H. (2022) · Life · doi:10.3390/life12111761 · Cited by 14

Uncovering cilia function in glial development

Bear, R. M., & Caspary, T. (2023) · Annals of Human Genetics · doi:10.1111/ahg.12519 · Cited by 13

Fucci-guided purification of hematopoietic stem cells with high repopulating activity

Yo, M., Sakaue-Sawano, A., Noda, S., Miyawaki, A., & Miyoshi, H. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.12.074 · Cited by 13

Enhanced proliferation of oligodendrocyte progenitor cells following retrovirus mediated Achaete-scute complex-like 1 overexpression in the postnatal cerebral cortex in vivo

Galante, C., Marichal, N., Scarante, F. F., Ghayad, L. M., Shi, Y., Schuurmans, C., Berninger, B., & Péron, S. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.919462 · Cited by 12

Temporal expression analysis of angiogenesis-related genes in brain development

Özkan, A., Biçer, A., Avşar, T., Şeker, A., Toktaş, Z. O., Bozkurt, S., Başak, A., & Kılıç, T. (2012) · Vascular Cell · doi:10.1186/2045-824x-4-16 · Cited by 12

Control of occlusion of middle cerebral artery in perinatal and neonatal mice with magnetic force

Jia, J., Peng, C., Wang, Y., Zheng, J., & Ge, W. (2018) · Molecular Brain · doi:10.1186/s13041-018-0389-0 · Cited by 12

Local production of astrocytes in the cerebral cortex

Ge, W.-P., & Jia, J.-M. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2015.08.057 · Cited by 58

Sourcing local produce

Welberg, L. (2012) · Nature reviews. Neuroscience · doi:10.1038/nrn3247

Astrogenesis versus astrogliosis

Koob, A. O. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.200798 · Cited by 4

The Germinative Zone Produces the Most Cortical Astrocytes after Neuronal Migration in the Developing Mammalian Brain

Gressèns, P., Richelme, C., Kadhim, H. J., Gadisseux, J., & Evrard, P. (2009) · Biology of the Neonate · doi:10.1159/000243526 · Cited by 141

Cortical astrocytes develop in a plastic manner at both clonal and cellular levels

Clavreul, S., Abdeladim, L., Hernández-Garzón, E., Niculescu, D., Durand, J., Ieng, S.-H., Barry‐Martinet, R., Bonvento, G., Beaurepaire, E., Livet, J., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12791-5 · Cited by 181