Slowly dividing neural progenitors are an embryonic origin of adult neural stem cells

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

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Adult Neurogenesis in the Mammalian Brain: Significant Answers and Significant Questions

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The Glial Nature of Embryonic and Adult Neural Stem Cells

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The cell biology of neurogenesis

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Defining the Epithelial Stem Cell Niche in Skin

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Hematopoietic Stem Cells Reversibly Switch from Dormancy to Self-Renewal during Homeostasis and Repair

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SOX2 Functions to Maintain Neural Progenitor Identity

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Molecular regulation of stem cell quiescence

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Roles of continuous neurogenesis in the structural and functional integrity of the adult forebrain

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Neural stem cells confer unique pinwheel architecture to the ventricular surface in neurogenic regions of the adult brain

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SETD4 cells contribute to brain development and maintain adult stem cell reservoir for neurogenesis

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Tracing the developmental origin of tissue stem cells

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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

The P-body protein 4E-T represses translation to regulate the balance between cell genesis and establishment of the postnatal NSC pool

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Metabolic Regulation and Related Molecular Mechanisms in Various Stem Cell Functions

Lee, H., & Hong, I. (2020) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x15666200512105347 · Cited by 7

Live Imaging Reveals Cerebellar Neural Stem Cell Dynamics and the Role of VNUT in Lineage Progression

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Embracing the heterogeneity of neural stem cells in the subventricular zone

Apostolou, S., & Donega, V. (2025) · Stem Cell Reports · doi:10.1016/j.stemcr.2025.102452 · Cited by 6

How Growth Cones Sense Extracellular Cues and Drive Neuronal Migration

Kanzawa, T., Nakajima, C., Sawada, M., & Sawamoto, K. (2025) · BioEssays · doi:10.1002/bies.70050 · Cited by 6

Growth/differentiation factor 15 controls ependymal and stem cell number in the V-SVZ

Baur, K., García, C. C., Şan, Ş., von Hahn, M., Strelau, J., Hölzl‐Wenig, G., Mandl, C., & Ciccolini, F. (2024) · Stem Cell Reports · doi:10.1016/j.stemcr.2024.01.008 · Cited by 6

Suppressor of Fused regulates the proliferation of postnatal neural stem and precursor cells via a Gli3-dependent mechanism

Gomez, H. G., Castillo, J. G., Noguchi, H., Aguilar, D., Pleasure, S. J., & Yabut, O. (2019) · Biology Open · doi:10.1242/bio.039248 · Cited by 6

Contributions of Single-Cell Approaches for Probing Heterogeneity and Dynamics of Neural Progenitors Throughout Life: Concise Review

Marcy, G., & Raineteau, O. (2019) · Stem Cells · doi:10.1002/stem.3071 · Cited by 7

Neurogenesis in zebrafish

Alunni, A., Coolen, M., Foucher, I., & Bally‐Cuif, L. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00026-6 · Cited by 6

Adult Neural Stem Cells: Constant Extension from Embryonic Ancestors

Cai, Y., & Yang, Z. (2019) · Neuroscience Bulletin · doi:10.1007/s12264-019-00396-3 · Cited by 6

Spatiotemporal transcriptome at single-cell resolution reveals key radial glial cell population in axolotl telencephalon development and regenerationPreprint

Wei, X., Fu, S., Li, H., Liu, Y., Wang, S., Feng, W., Yang, Y., Liu, X., Zeng, Y.-Y., Cheng, M., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.23.465550 · Cited by 6

Neural stem cells of the subventricular zone: A potential stem cell pool for brain repair in Parkinson’s disease

Verkerke, M., Werkman, M. H., & Donega, V. (2025) · Stem Cell Reports · doi:10.1016/j.stemcr.2025.102533 · Cited by 5

Generation of adult hippocampal neural stem cells occurs in the early postnatal dentate gyrus and depends on cyclin D2

Pastor-Alonso, O., Zahra, A. S., Kaske, B., García‐Moreno, F., Tetzlaff, F., Bockelmann, E., Grunwald, V., Martín‐Suárez, S., Riecken, K., Witte, O. W., et al. (2023) · The EMBO Journal · doi:10.1038/s44318-023-00011-2 · Cited by 9

Stem cells: slow and steady wins the race

Huttner, W. Β. (2015) · Nature Neuroscience · doi:10.1038/nn.4009 · Cited by 5

Regulation of the Brain Neural Niche by Soluble Molecule Akhirin

Kudo, M., & Ohta, K. (2021) · Journal of Developmental Biology · doi:10.3390/jdb9030029 · Cited by 5

Adult neurogenesis research in China

Luo, X., Xu, M., & Guo, W. (2023) · Development Growth & Differentiation · doi:10.1111/dgd.12900 · Cited by 5

Hindbrain rhombomere centers harbor a heterogenous population of dividing progenitors which rely on Notch signaling

Belmonte‐Mateos, C., Meister, L., & Pujades, C. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1268631 · Cited by 5

Advances in stem cells and regenerative medicine: single-cell dynamics, new models and translational perspectives

Twigger, A., & Scheel, C. (2017) · Development · doi:10.1242/dev.153569 · Cited by 4

Differential potentials of neural progenitors for the generation of neurons and non-neuronal cells in the developing amniote brain

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Neural stem cells among glia

Kriegstein, A. R., Subramanian, L., Obernier, K., & Álvarez-Buylla, A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00031-x · Cited by 5

Cyclin-dependent kinase inhibitor p18 regulates lineage transitions of excitatory neurons, astrocytes, and interneurons in the mouse cortex

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Ependymal and neural stem cells are close relatives

Lokka, G., Chantzara, A., Lygerou, Z., & Taraviras, S. L. (2025) · Stem Cell Reports · doi:10.1016/j.stemcr.2025.102574 · Cited by 4

Macrophage regulation of tumor cell dormancy and the dormant niche: an overview in solid tumors

Zhang, H., Ding, Y., Gu, L., Guo, A., Duan, W., Wang, X., & Zhang, B. (2025) · Cancer and Metastasis Reviews · doi:10.1007/s10555-025-10280-4 · Cited by 7

Prdm16 regulates the postnatal fate of embryonic radial glia via Vcam1-dependent mechanisms

Li, J., Godoy, M. I., Lu, Y., Zhang, A. J., Diamante, G., Rathbun, E. M., Tian, M., Ahn, I. S., Cebrián‐Silla, A., Álvarez-Buylla, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60895-y · Cited by 4

Adult human subventricular zone microglia promote a pro-neurogenic niche for neuronal progenitors in Parkinson’s disease

Pecoraro, S., Verkerke, M., Sluijs, J. A., Hof, B. V. H., van der Pol, S. M. A., van Strien, M. E., van der Kant, R., de Vries, C. J. M., de Vries, H. E., van de Berg, W. D. J., et al. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.06.017 · Cited by 4

Aging of the ventricular-subventricular zone neural stem cell niche

Merson, T. D. (2020) · Advances in stem cells and their niches · doi:10.1016/bs.asn.2020.07.001 · Cited by 4

Ascorbic acid and its transporter SVCT2 , affect radial glia cells differentiation in postnatal stages

Saldivia, N., Salazar, K., Cifuentes, M., Espinoza, F., Harrison, F. E., & Nualart, F. (2024) · Glia · doi:10.1002/glia.24498 · Cited by 4

Fluctuation of lysosomal protein degradation in neural stem cells of the postnatal mouse brain

Zhang, H., Ishii, K., Shibata, T., Ishii, S., Hirao, M., Lu, Z., Takamura, R., Kitano, S., Miyachi, H., Kageyama, R., et al. (2024) · Development · doi:10.1242/dev.202231 · Cited by 4

The laminar position, morphology, and gene expression profiles of cortical astrocytes are influenced by time of birth from ventricular/subventricular progenitors

Casasbuenas, D. L., Kortebi, I., Gora, C., Scott, E., Gomes, C., Oliveira, M. S., Sharma, T., Daniele, E., Olfat, A., Gibbs, R., et al. (2024) · Glia · doi:10.1002/glia.24578 · Cited by 5

Prdm16 and Vcam1 regulate the postnatal disappearance of embryonic radial glia and the ending of cortical neurogenesisPreprint

Li, J., Godoy, M. I., Zhang, A. J., Diamante, G., Ahn, I. S., Cebrián‐Silla, A., Álvarez-Buylla, A., Yang, X., Novitch, B. G., & Zhang, Y. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.14.528567 · Cited by 4

A specific olfactory bulb interneuron subtype Tpbg/5T4 generated at embryonic and neonatal stages

Tsuboi, A. (2024) · Frontiers in Neural Circuits · doi:10.3389/fncir.2024.1427378 · Cited by 3

Generating neurons in the embryonic and adult brain: compared principles and mechanisms

Chouly, M., & Bally‐Cuif, L. (2024) · Comptes Rendus Biologies · doi:10.5802/crbiol.167 · Cited by 4

Regulation of neural stem cells by innervating neurons

Dittmann, N. L., Chen, L., & Voronova, A. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.16287 · Cited by 3

Applications and Possible Mechanisms of ULK4 in Brain: Implications for Neuropsychiatric Disorders

Luo, W., Wang, J., & Chen, J. (2025) · Journal of Integrative Neuroscience · doi:10.31083/jin31350 · Cited by 3

Effects of thyroid disruption on neural cells stem fate in the mouse brain

Valcárcel-Hernández, V., Butruille, L., & Remaud, S. (2025) · La Presse Médicale · doi:10.1016/j.lpm.2025.104312 · Cited by 3

Heterogeneity of Neural Stem Cells in the Ventricular–Subventricular Zone

Rushing, G. V., Bollig, M. K., & Ihrie, R. A. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-24108-7_1 · Cited by 4

A Nucleolar Protein, Nepro, Is Essential for the Maintenance of Early Neural Stem Cells and Preimplantation Embryos

Saito, T. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-34436-8_6 · Cited by 3

“FlashMap” - A Semi-Automatic Tool for Rapid and Accurate Spatial Analysis of Marker Expression in the Subventricular Zone

Zweifel, S., Buquet, J., Caruso, L., Rousseau, D., & Raineteau, O. (2018) · Scientific Reports · doi:10.1038/s41598-018-33939-1 · Cited by 3

Life-Long Neural Stem Cells Are Fate-Specified at an Early Developmental Stage

Tanaka, A., Ishida, S., Fuchigami, T., Hayashi, Y., Kuroda, A., Ikenaka, K., Fukazawa, Y., & Hitoshi, S. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa200 · Cited by 3

Stem Cells and Asymmetric Cell Division

Sousa‐Nunes, R., & Hirth, F. (2016) · Springer eBooks · doi:10.1007/978-3-319-27583-3_3 · Cited by 3

Single cell analysis of the dorsal V-SVZ reveals differential quiescence of postnatal pallial and subpallial neural stem cells driven by TGFbeta/BMP-signallingPreprint

Marcy, G., Foucault, L., Babina, E., Texeraud, E., Zweifel, S., Heinrich, C., Hernández‐Vargas, H., Parras, C. M., Jabaudon, D., & Raineteau, O. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.20.492790 · Cited by 3

Gas1-high quiescent neural stem cells are multipotent and produce oligodendrocytes during aging and after demyelinating injury

Ding, C., Pan, Z., Yan, X., Zhou, R., Li, H., Chen, L., Wang, Y., & Zhang, Y. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003100 · Cited by 2

Multiomics reveal biomolecular shifts and ER stress in sleep-restricted women affecting NSC functions

Malik, V., Huang, X., Zhou, H., Bojar, R., Soni, R. K., Landry, D. W., Jelić, S., & Wang, J. (2025) · iScience · doi:10.1016/j.isci.2025.112510 · Cited by 2

Rnd3 deletion affects neuroblast behavior through the RhoA/ROCK pathway but not neural stem cells in postnatal mice subventricular zone

Solana-Orts, A., Belenguer, G., Ballester‐Lurbe, B., Gómez, O., Pérez‐Roger, I., Terrado, J., Poch, E., & Bizy, A. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1612177 · Cited by 2

Autocrine ECM molecules establish MSC quiescence during incisor development by disrupting WNT ligand trafficking process

Chen, Z., Cai, M., Wang, Y., Li, X., He, Y., Pu, H., Huang, J., Ye, L., Yang, R., Jing, J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-65705-z · Cited by 5

Update on the interaction of notch and Wnt/β-catenin signaling in neural stem cells and brain homeostasis during ischemic stroke

Hasanzadeh‐Moghadam, M., Mohammdnejad, D., Rahbarghazi‬, R., Mahmoudi, J., Hassanzadeh, A., Mafikandi, V., Nasrabadi, H. T., & Karimipour, M. (2026) · Tissue and Cell · doi:10.1016/j.tice.2026.103651 · Cited by 3

Protein homeostasis and degradation in quiescent neural stem cells

Kobayashi, T. (2024) · The Journal of Biochemistry · doi:10.1093/jb/mvae006 · Cited by 2

Arl2 GTPase associates with the centrosomal protein Cdk5rap2 to regulate cortical development via microtubule organization

Ma, D., Lin, K., Suresh, D., Lin, J., Gujar, M. R., Aung, H. Y., Tan, Y. S., Gao, Y., Vincent, A. S., Chen, T., et al. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002751 · Cited by 2

Arx revisited: involved in the development of GABAergic interneurons

Tsuboi, A., & Yoshihara, S.-I. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1563515 · Cited by 4

Experimental and Preclinical Tools to Explore the Main Neurological Impacts of Brain Irradiation: Current Insights and Perspectives

Mouton, L., Ribeiro, M., Mouthon, M., Boumezbeur, F., Bihan, D. L., Ricard, D., Boussin, F. D., & Verrelle, P. (2020) · Neuromethods · doi:10.1007/978-1-0716-0856-2_11 · Cited by 2

Non-canonical post-transcriptional RNA regulation of neural stem cell potential

Rolando, C., & Taylor, V. (2017) · Brain Plasticity · doi:10.3233/bpl-170046 · Cited by 2

Regeneration in the Olfactory Bulb

Malvaut, S., & Saghatelyan, A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.23883-2 · Cited by 2

Early fate bias in neuroepithelial progenitors of hippocampal neurogenesis

von Berlin, L., Westholm, J. O., Ratz, M., & Frisén, J. (2022) · Hippocampus · doi:10.1002/hipo.23482 · Cited by 2

Arachidonic acid level is related to early motor recovery following intracerebral hemorrhage with severe motor paralysis

Sato, T., Okumura, M., Takahashi, J., Kokubu, T., Tanabe, M., Onda, A., Komatsu, T., Sakuta, K., Sakai, K., Umehara, T., et al. (2023) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2023.102603 · Cited by 2

Dephosphorylation of 4EBP1/2 Induces Prenatal Neural Stem Cell QuiescencePreprint

Geben, L. C., Brockman, A. A., Chalkley, M. L., Sweet, S. R., Gallagher, J. E., Scheuing, A. L., Simerly, R. B., Ess, K. C., Irish, J. M., & Ihrie, R. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.14.528513 · Cited by 2

Proneural genes form a combinatorial code to diversify neocortical neural progenitor cellsPreprint

Moffat, A., Oproescu, A.-M., Okawa, S., Han, S., Vasan, L., Ghazale, H., Dennis, D. J., Zinyk, D. L., Guillemot, F., del Sol, A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.29.551096 · Cited by 2

Neurogenesis in the postnatal V-SVZ and the origin of interneuron diversity

Álvarez-Buylla, A., Merkle, F. T., Fuentealba, L. C., & Cebrián‐Silla, A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00022-9 · Cited by 1

Recent developments in 3D bioprinting for neural tissue engineering

Sharma, R., da Silva, V. A., Hangad, M. V., & Willerth, S. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95730-4.00012-3 · Cited by 1

Rb substantially compensates for the double loss of p130 and p107 in adult but not embryonic neural stem cell lineages

Swaidan, R., Daher, A., Bejjani, A. T., Atie, Y. E. E., Chehab, Y., Hamdan, R. B., Vandenbosch, R., Slack, R. S., Omais, S., & Ghanem, N. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-07815-6 · Cited by 3

Reduced Adult Neurogenesis in Humans Results From a Tradeoff Rather Than Direct Negative Selection

Morizet, D., & Bally‐Cuif, L. (2025) · BioEssays · doi:10.1002/bies.70041 · Cited by 3

P2X purinergic receptors are required for correct cortical development in human brain organoids

Benito-León, M., Serrano-López, J., Llorente-Sáez, C., Arribas-Blázquez, M., Olivos-Oré, L. A., Pravatà, V. M., Pérez‐Sen, R., Delicado, E. G., Drukker, M., Artalejo, A. R., et al. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110784 · Cited by 1

Beyond the canonical niche: how astrocytes carried neurogenic potential into the brain parenchyma

Fogli, M., Nato, G., Peretto, P. M., Buffo, A., & Luzzati, F. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1737065 · Cited by 2

Single-cell multiomic approaches define a gradual, spatially regulated epigenetic and transcriptional transition from embryonic to adult neural stem cells

Wang, B. S., Karamboulas, K., Tahmasian, N., Dennis, D. J., Kaplan, D. R., & Miller, F. D. (2026) · Stem Cell Reports · doi:10.1016/j.stemcr.2026.102967 · Cited by 1

A Butterfly Effect on Neural Stem Cells

Vanderhaeghen, P. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.015 · Cited by 1

The Future Vocation of Neural Stem Cells: Lineage Commitment in Brain Development and Evolution

Nomura, T., Gotoh, H., & Ono, K. (2017) · Neurochemical Research · doi:10.1007/s11064-017-2380-z · Cited by 1

Transcriptional control of neural stem cell activity

Kaise, T., & Kageyama, R. (2024) · Biochemical Society Transactions · doi:10.1042/bst20230439 · Cited by 1

Morphological classification of radial glia–like cells in the postnatal mouse subventricular zone

Yoshida, R., & Mori, T. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16503 · Cited by 1

An Unexpected Calm: Mfge8 Controls Stem Cell Quiescence and Maintenance

Okazaki, T., & Gotoh, Y. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.08.006 · Cited by 1

Cell biology of neuronal progenitor cells

Temple, S., Bai, Q., & Shen, Q. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00012-6 · Cited by 1

Imprinted genes Cdkn1c and Igf2 interact to promote terminal differentiation of adult NSCsPreprint

Lozano-Ureña, A., Jiménez-Villalba, E., Lázaro-Carot, L., Montalbán-Loro, R., Martínez-Gurrea, I., Nakayama, K. I., Kirstein, M., & Ferrón, S. R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.24.477488 · Cited by 1

Growth/differentiation factor 15 controls number of ependymal and neural stem cells in the ventricular-subventricular zonePreprint

Baur, K., Carrillo-García, C., Şan, Ş., von Hahn, M., Strelau, J., Hölzl-Wenig, G., Mandl, C., & Ciccolini, F. (2023) · bioRxiv · doi:10.1101/2022.12.02.518869 · Cited by 1

Self-balanced regulation by the long non-coding RNA Lockd on the cell cycle progression of cortical neural progenitor cells through counteracting cis and trans rolesPreprint

Qi, S.-J., Zheng, J., & Shen, Q. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.08.574564 · Cited by 1

YAP/TAZ create a physical niche for the maintenance of adult neural stem cell quiescencePreprint

Blasco-Chamarro, L., García-Bolufer, P., Duart-Abadía, P., Jordán‐Pla, A., Sirerol-Piquer, M. S., Carrillo-Barberà, P., Sgattoni, C., Mateos-White, I., Gil, C., Morante‐Redolat, J. M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.27.661955 · Cited by 1

Cell-cycle inhibition preserves robust development but rebalances lineages in mouse gastruloidsPreprint

Leonardi, M., Paychère, Y., & Naef, F. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.08.698406 · Cited by 1

Neurogenesis in Cancun: where science meets the sea

Hsieh, J., & Zhang, C. (2016) · Development · doi:10.1242/dev.138412

miRNA-Dependent and Independent Functions of the Microprocessor in the Regulation of Neural Stem Cell Biology

Erni, A., Rolando, C., & Taylor, V. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804402-5.00006-6

All Roads Lead to Rome: Hippocampal Stem Cells Hop(x) the Continuous Way

Bai, Q., & Shen, Q. (2019) · Cell stem cell · doi:10.1016/j.stem.2019.04.013

Role of the imprinted allele of the p57 Kip2 gene in mouse neocortical developmentPreprint

Imaizumi, Y., Furutachi, S., Watanabe, T., Miya, H., Kawaguchi, D., & Gotoh, Y. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/737692

Investigating the Effects of the Medulloblastoma Secretome on Neural Stem Cell Function

Simonetta, J. V. (2019) · TSpace (University of Toronto)

Loss of α7 nicotinic acetylcholine receptors in GABAergic interneurons causes sex-dependent impairments in postnatal neurogenesis and cognitive and social behaviorPreprint

Nacer, S. A., Otto, S., Letsinger, A. C., DeFilipp, J. S., Nikolova, V. D., Riddick, N. V., Stevanovic, K. D., Cushman, J. D., & Yakel, J. L. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.16.994111

Spatiotemporally Dependent Vascularization Regulates Neural Stem and Progenitor Cells

Mizutani, K. (2021) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.20-00198-1

Generation of Neurons and Their Integration in Pre-Existing Circuits in the Postnatal Brain: Signalling in Physiological and Regenerative Contexts

Mira, H., Díez del Corral, R., & Morales, A. V. (2020) · Frontiers research topics · doi:10.3389/978-2-88963-988-5

Faculty Opinions recommendation of Autocrine mfge8 signaling prevents developmental exhaustion of the adult neural stem cell pool.

Pardal, R. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733939109.793552964

Quiescencia y senescencia: enfoque traslacional al paciente oncológico y críticamente enfermo.

Moscoso, S. X. A., Montalvo-Villagómez, M., González, F. E. J., Páez, P. A. V., Montero, C. G. V., & Vélez-Páez, J. L. (2019) · Revista Ecuatoriana de Ciencia Tecnología e Innovación en Salud Pública · doi:10.31790/inspilip.v4i1.154

Autophagy is a cell-intrinsic driver of neural stem cell quiescence in hippocampal dentate gyrus developmentPreprint

Calatayud-Baselga, I., Casares-Crespo, L., Franch-Ibáñez, C., Guijarro-Nuez, J., Sanz, P., & Mira, H. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.03.539225

Exosomes Originating from Neural Stem Cells Undergoing Necroptosis Participate in Cellular Communication Following Spinal Cord InjuryPreprint

Li, S., Li, J., Chen, G., Zhang, P., Tong, K., Chen, N., & Liu, S. (2023) · Research Square · doi:10.21203/rs.3.rs-3673053/v1

Yukiko Gotoh: I am fascinated by the beauty of science

Emmenis, L. V. (2024) · The Journal of Experimental Medicine · doi:10.1084/jem.20240003

Arl2 Associates with Cdk5rap2 to Regulate Cortical Development via Microtubule OrganizationPreprint

Ma, D., Lin, K., Divya, S., Lin, J., Gujar, M. R., Aung, H. Y., Tan, Y. S., Gao, Y., Vincent, A. S., Chen, T., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.16.575964

Mitotic Activity and DNA Maintenance of Adult Neural Stem Cells is Regulated by Beclin1Preprint

Kalinina, A., Dhaliwal, J., Xue, Y., Vaculik, M., McCambley, M., Fong, B. C., Cook, D. P., Slack, R. S., & Lagace, D. C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.26.573092

Developmental emergence of quiescent-like neural progenitor cells in the zebrafish embryonic brainPreprint

Liu, Y., Lembke, C., & Paridaen, J. T. M. L. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.13.580083

From heparan glycobiology to stem cell therapy: a historical perspective

Nurcombe, V. (2024) · Academia Biology · doi:10.20935/acadbiol6196

Embryonic diversification of adult neural stem cells and ependymal cellsPreprint

Yamaguchi, S., Kuniya, T., Omiya, H., Suzuki, Y., Seki, M., Ukai, H., Fang, L., Harada, Y., Kawaguchi, D., & Gotoh, Y. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.12.593751

Both intrinsic and microenvironmental factors contribute to the regulation of stem cell quiescence

Zhou, P., Hu, M., Li, Q., & Yang, G. (2024) · Journal of Cellular Physiology · doi:10.1002/jcp.31325

The purinergic receptor P2Y 13 controls the activation and mode of division of adult ventricular–subventricular zone neural stem cells

Paniagua‐Herranz, L., Serrano-López, J., Llorente-Sáez, C., Pérez-Sanz, M. L., de Agustín-Durán, D., Duart-Abadía, P., Domingo-Muelas, A., Vincelle-Nieto, Á., Bragado, P., Manzano-Franco, D., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1101/2024.11.29.626065

Neural Stem Cells

Kempermann, G. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780197519233.003.0003

Characterization of quiescent subpopulations and proliferative compartments in glioblastomaPreprint

Mihalas, A. B., Mitchell, K., Arora, S., O’Connor, S. A., Patel, A. P., Plaisier, C. L., & Paddison, P. J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.03.680278

Cell-cycle-driven epigenetic resetting maintains meristematic cell fate for shoot branching

Guo, Y., Yang, Y., Shi, B., Wang, H., Cao, X., Peng, Z., He, Y., Xiao, J. Y., Tao, L., Wagner, D., et al. (2026) · Nature Plants · doi:10.1101/2025.10.22.683900 · Cited by 1

Stem cells: slow and steady wins the race

Huttner, W. Β. (2015) · Nature Neuroscience · doi:10.1038/nn.4009 · Cited by 5

Integrative analysis of the embryonic origin of adult neural stem cells in forebrain subventricular zones

Wu, H., Tang, K., Xu, R., Li, T., Liang, K., Wang, X., Huang, D., Yang, Y., Yin, Y., Xie, J., et al. (2026) · National Science Review · doi:10.1093/nsr/nwag516

Embryonic diversification of adult neural stem cells and ependymal cellsPreprint

Yamaguchi, S., Kuniya, T., Omiya, H., Suzuki, Y., Seki, M., Ukai, H., Fang, L., Harada, Y., Kawaguchi, D., & Gotoh, Y. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.12.593751

IL2 Neural stem cell regulation and brain development

Gotoh, Y. (2021) · Neuro-Oncology Advances · doi:10.1093/noajnl/vdab159.001

Developmental emergence of quiescent-like neural progenitor cells in the zebrafish embryonic brainPreprint

Liu, Y., Lembke, C., & Paridaen, J. T. M. L. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.13.580083