The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.
Selective Lengthening of the Cell Cycle in the Neurogenic Subpopulation of Neural Progenitor Cells during Mouse Brain Development
Open accessAbstract
During embryonic development of the mammalian brain, the average cell-cycle length of progenitor cells in the ventricular zone is known to increase. However, for any given region of the developing cortex and stage of neurogenesis, the length of the cell cycle is thought to be similar in the two coexisting subpopulations of progenitors [i.e., those undergoing (symmetric) proliferative divisions and those undergoing (either asymmetric or symmetric) neuron-generating divisions]. Using cumulative bromodeoxyuridine labeling of Tis21-green fluorescent protein knock-in mouse embryos, in which these two subpopulations of progenitors can be distinguished in vivo, we now show that at the onset as well as advanced stages of telencephalic neurogenesis, progenitors undergoing neuron-generating divisions are characterized by a significantly longer cell cycle than progenitors undergoing proliferative divisions. In addition, we find that the recently characterized neuronal progenitors dividing at the basal side of the ventricular zone and in the subventricular zone have a longer G 2 phase than those dividing at the ventricular surface. These findings are consistent with the hypothesis (Calegari and Huttner, 2003) that cell-cycle lengthening can causally contribute to neural progenitors switching from proliferative to neuron-generating divisions and may have important implications for the expansion of somatic stem cells in general.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Interestingly, G1/S transition rates might be associated with these cell decisions as symmetric divisions can have shorter G1/S transition times than asymmetric divisions [93, 101].”
From The ASD Living Biology: from cell proliferation to clinical phenotype (2019) · cites this paper as [101]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Noctor, S. C., Martínez-Cerdeño, V., Ivic, L., & Kriegstein, A. R. (2004) · Nature Neuroscience · doi:10.1038/nn1172 · Cited by 2,229
Rakic, P. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93934-p · Cited by 1,047
Haubensak, W. E., Attardo, A., Denk, W. T., & Huttner, W. Β. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308600100 · Cited by 1,004
Self-citationAsymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells
Miyata, T., Kawaguchi, A., Saito, K., Kawano, M., Muto, T., & Ogawa, M. (2004) · Development · doi:10.1242/dev.01173 · Cited by 791
Characterization of CNS Precursor Subtypes and Radial Glia
Hartfuss, E., Galli, R., Heins, N., & Götz, M. (2001) · Developmental Biology · doi:10.1006/dbio.2000.9962 · Cited by 755
Nowakowski, R. S., Lewin, S. B., & Miller, M. W. (1989) · Journal of Neurocytology · doi:10.1007/bf01190834 · Cited by 755
Signalling, cell cycle and pluripotency in embryonic stem cells
Burdon, T., Smith, A. T., & Savatier, P. (2002) · Trends in Cell Biology · doi:10.1016/s0962-8924(02)02352-8 · Cited by 727
The cell cycle of the pseudostratified ventricular epithelium of the embryonic murine cerebral wall
Takahashi, T., Nowakowski, R. S., & Caviness, V. S. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-09-06046.1995 · Cited by 673
Numbers, time and neocortical neuronogenesis: a general developmental and evolutionary model
Caviness, V. S., Takahashi, T., & Nowakowski, R. S. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93933-o · Cited by 566
Constructing the cerebral cortex: Neurogenesis and fate determination
McConnell, S. K. (1995) · Neuron · doi:10.1016/0896-6273(95)90168-x · Cited by 416
Cited by
Sorted by citations
Items 301–395 of 395
Drill, E. (2009) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 3
Simultaneous production of diverse neuronal subtypes during early corticogenesisPreprint
Magrinelli, E., Wagener, R. J., & Jabaudon, D. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/369678 · Cited by 3
A Human Accelerated Region participates in early human forebrain patterning and expansionPreprint
Acosta, S., Sidhaye, J., Fiore, L., Rollán, I., Iacono, G., Misharin, A. V., Takata, N., Sikora, M., Joshi, N., Xu, B., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/777235 · Cited by 3
A COMPARATIVE ANALYSIS OF CONVECTIVE HEAT TRANSFER IN A NUCLEAR ROCKET NOZZLE
Neumann, H., & Bettinger, P. J. (1963) · University of Michigan Library Repository · Cited by 3
MicroRNA-mediated neuronal detargeting alters astrocyte cell fate conversion trajectories in vivo
Ghazale, H., Pazos, M. R., Jung, S., Cao, K., Vasan, L., Hickmott, J. W., Zhang, L., Morshead, C. M., Wang, C., del Sol, A., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-09169-3 · Cited by 3
Laminin β2 Chain Regulates Cell Cycle Dynamics in the Developing Retina
Serjanov, D., Bachay, G., Hunter, D. D., & Brunken, W. J. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.802593 · Cited by 2
Dady, A., Davidson, L., Loyer, N., Rappich, S., Findlay, G. M., Sanders, T., Januschke, J., & Storey, K. G. (2025) · Development · doi:10.1242/dev.205082 · Cited by 2
Thomaidou, D., Politis, P., & Matsas, R. (2010) · Springer eBooks · doi:10.1007/978-1-60327-153-0_8 · Cited by 2
Regulation of Self-Renewing Divisions in Normal and Leukaemia Stem Cells
Viale, A., & Pelicci, P. G. (2010) · Springer eBooks · doi:10.1007/978-1-4419-1770-6_7 · Cited by 2
Etienne, O., Béry, A., Roque, T., Desmaze, C., & Boussin, F. D. (2014) · Journal of Visualized Experiments · doi:10.3791/51209 · Cited by 2
Expression of D-type cyclins in differentiating cells of the mouse spinal cord
Salles, P. D. A., Fortes, J. C., Guedes, M. I. F., & Weller, M. (2007) · Genetics and Molecular Biology · doi:10.1590/s1415-47572007000400032 · Cited by 2
Sanes, D. H., Reh, T. A., Harris, W. A., & Landgraf, M. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-803996-0.00003-4 · Cited by 2
Hatakeyama, J., & Shimamura, K. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy252 · Cited by 2
Wakeman, D. R., Hofmann, M. R., Teng, Y. D., & Snyder, E. Y. (2009) · Human cell culture · doi:10.1007/978-90-481-2269-1_1 · Cited by 2
Investigation of Sip1 gene interactions in the development of the mammalian telencephalon
Nityanandam, A. (2010) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3228 · Cited by 1
Spatiotemporal control of cell cycle acceleration during axolotl spinal cord regenerationPreprint
Costa, E. C., Otsuki, L., Albors, A. R., Tanaka, E. M., & Chara, O. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.10.941443 · Cited by 2
Human cortical organoids expose a differential function of GSK3 on direct and indirect neurogenesisPreprint
Tobon, A., Villa, C. E., Cheroni, C., Trattaro, S., Caporale, N., Conforti, P., Iennaco, R., Lachgar-Ruiz, M., Rigoli, M. T., de la Cruz, B. M., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/484741 · Cited by 2
CDK4/6 inhibitors display a class effect in inducing differentiation of neuroblastoma cells
Ferguson, K. M., Grealy, F. M. Y. A., & Philpott, A. (2025) · Wellcome Open Research · doi:10.12688/wellcomeopenres.23190.2 · Cited by 1
Ceccarelli, M., Micheli, L., D’Andrea, G., & Tirone, F. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2026.1775035 · Cited by 1
Cell Cycle Regulation in Brain Construction
Crespo, M., & Ross, M. E. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00094-0 · Cited by 1
Response to letter by Lenos and Tsaniklidou
Salomoni, P., & Calegari, F. (2010) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.07.003 · Cited by 1
Self-citationSanes, D. H., Reh, T. A., & Harris, W. A. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374539-2.00007-0 · Cited by 1
Ischemic Stroke Pathophysiology and Cell Therapy
Ren, C., Han, R., Shi, J., & Ji, X. (2016) · Springer eBooks · doi:10.1007/978-981-10-2929-5_1 · Cited by 1
Kempermann, G. (2010) · Oxford University Press eBooks · doi:10.1093/med/9780199729692.003.0009 · Cited by 1
Ocasio, J. K. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2752-5_3 · Cited by 1
Mestres, I., Atabay, A., Escolano, J.-C., Arndt, S., Schmidtke, K., Einsiedel, M., Patsonis, M., Castro, L. A. B., Yun, M. H., Bernhardt, N. R., et al. (2024) · Biology Open · doi:10.1242/bio.060359 · Cited by 1
Self-citationInhalation Anesthetics Play a Janus-Faced Role in Self-Renewal and Differentiation of Stem Cells
Hao, X., Li, Y., Gao, H., Wang, Z., & Fang, B. (2024) · Biomolecules · doi:10.3390/biom14091167 · Cited by 1
Caetano-Anollés, D. (2016) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign) · Cited by 1
Marín, A. B. S. (2012) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.41.2012.tde-08032013-105224 · Cited by 1
ON SIMULATING THE GENERATION OF MOSAICISM DURING MAMMALIAN CEREBRAL CORTICAL DEVELOPMENT
Case, M. A., & MacMillan, H. R. (2009) · Journal of Biological Systems · doi:10.1142/s0218339009002740 · Cited by 1
Regulation of m RNA Localization and Translation in Brain Development
Kikkawa, T., Naher, S., & Osumi, N. (2023) · Wiley eBooks · doi:10.1002/9781119860914.ch29 · Cited by 1
Area V1 Development, a Model System to Link Corticogenesis to Adult Cortex Structure and Function
Dehay, C., & Kennedy, H. (2023) · Wiley eBooks · doi:10.1002/9781119860914.ch4 · Cited by 3
Dady, A., Davidson, L., Loyer, N., Rappich, S., Findlay, G. M., Sanders, T., Januschke, J., & Storey, K. G. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.01.591467 · Cited by 1
Sierra, A., Pereira‐Iglesias, M., Martinson, W. D., Falcó, C., Maldonado-Teixidó, J., González-Domínguez, M., Senovilla-Ganzo, R., Benito, E., Beccari, S., Valero, J., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.03.685577 · Cited by 1
Neurogénesis y gliogénesis en el cerebro rostral del ratón adulto heterocigoto para Pax6 (+/SeyDey)
Curto, G. G. (2010) · Gredos (University of Salamanca) · doi:10.14201/gredos.76495 · Cited by 1
Coordinated neural progenitor adaptations drive primate neocortical downscalingPreprint
Tynianskaia, L., Betancourt, C. M. B., Grewe, E. M., Kniep, J. M., Liutikaite, N., Eşiyok, N., Heide, S., Rüger, N., Lindenwald, D. L., Drummer, C., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.19.706795 · Cited by 1
Chang, H., & Faust, P. L. (2020) · Columbia Undergraduate Science Journal · doi:10.7916/cusj.v2i0.5624
Arai, Y., Huttner, W. Β., & Calegari, F. (2010) · Springer eBooks · doi:10.1007/978-90-481-9075-1_13
Self-citationNeurogenesis in the Central Nervous System
Dubreuil, V., Farkas, L. M., Calegari, F., Kosodo, Y., & Huttner, W. Β. (2005) · Wiley eBooks · doi:10.1002/9783527619689.ch7
Self-citationFGF signaling in neurogenesis and patterning of the developing midbrain and anterior hindbrain
Lahti, L. (2012) · Työväentutkimus Vuosikirja
Neural stem cell characteristics affected by oncogenic pathways and in a human motoneuron disease
Kerosuo, L. (2009) · Työväentutkimus Vuosikirja
MicroRNAs' role in brain development and disease
Fineberg, S. K., Davidson, B. L., Anderson, M. G., Russo, A. F., Cornell, R. A., & Johnson, W. A. (2010) · doi:10.17077/etd.qahvaifc
Fibroblast Growth Factor Signalling in the Development of the Midbrain and Anterior Hindbrain
Saarimäki‐Vire, J. (2012) · Työväentutkimus Vuosikirja
Notch signaling in neuroepithelial development
Märki, S. D. (2009) · Zurich Open Repository and Archive (University of Zurich) · doi:10.3929/ethz-a-005900269
Length of cell cycle in neural development
Juan, G. U., & Xiao-Ping, C. H. E. N. (2011) · Hereditas (Beijing) · doi:10.3724/sp.j.1005.2011.01185
CHARACTERISATION OF Y-BOX PROTEIN 3 (MSY3) IN THE DEVELOPING MURINE CENTRAL NERVOUS SYSTEM
Grzyb, A. N. (2006) · Qucosa (Saxon State and University Library Dresden)
Amadei, G. (2016) · TSpace (University of Toronto)
The Role of Polarity Complex Proteins in Neural Progenitor Proliferation
Simmons, A. (2019) · TUScholarShare (Temple University)
Mann, B., Crawford, J. C., Reddy, K., Lott, J., Youn, Y. H., Gao, G., Guy, C. S., Chou, C., Darnell, D., Trivedi, S., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.19.464985
Heterogeneous Fates of Simultaneously-Born Neurons During Early CorticogenesisPreprint
Magrinelli, E., Klingler, E., Baumann, N., Wagener, R. J., Glangetas, C., Bellone, C., & Jabaudon, D. (2021) · Research Square · doi:10.21203/rs.3.rs-956593/v1
The Effect of Opiates on the Developing Cerebral Cortex
Sargeant, T. J. (2008) · doi:10.26686/wgtn.16934851.v1 · Cited by 1
Arai, Y., Huttner, W. Β., & Calegari, F. (2013) · Springer eBooks · doi:10.1007/978-94-007-5690-8_12
Self-citationFunction of MCPH1 in Neurogenesis
Gruber, R. (2011) · doi:10.53846/goediss-475
Kempermann, G. (2010) · Oxford University Press eBooks · doi:10.1093/med/9780199729692.003.0007
Ben‐Ari, Y. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733499087.793568939
Costa, E. C. (2022) · doi:10.35537/10915/139746
Glass, M. R., Stein, J. L., & Anton, E. S. (2023) · Wiley eBooks · doi:10.1002/9781119860914.ch25
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
Cho, S., Kim, J. H., & Kim, S. (2024) · Developmental Biology · doi:10.1016/j.ydbio.2024.09.003
CDK4/6 inhibitors display a class effect in inducing differentiation of neuroblastoma cells
Ferguson, K. M., Grealy, F. M. Y. A., & Philpott, A. (2024) · Wellcome Open Research · doi:10.12688/wellcomeopenres.23190.1 · Cited by 1
Somsen, H. B., Eigenhuis, K. N., Kuijpers-Korporaal, A. L., de Almeida, M. P., Ferrer, R. M., Kats, K. P., Dekker, M. R., Zuidweg, T., Azmani, Z., van den Hout, M. C. G. N., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.26.625369
McDermott, C. R., Gao, Z., Mirmajlesi, A. S., Ntim, C., Kimbark, K. D., Thomas, D., Mughal, Z., Zhang, X., Zhou, X., Popov, D., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.25.639888
Neural stem cell epigenomes and fate bias are temporally coordinated during corticogenesisPreprint
Shapira, Y., Noack, F., Vangelisti, S., Chong, F., Lifshitz, A., Tanay, A., & Bonev, B. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.03.647013
DTX4 regulates neural progenitor transitions during cortical developmentPreprint
Pedersen, E., Zhang, S., Dong, X., Vallone, V. B. F., Epifanova, E. A., Willecke, P. M., Lajkó, D., Schaub, T., Ambrozkiewicz, M. C., Textoris‐Taube, K., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.10.648213
Enright, J., Shiau, F., Zhang, X., Chen, S., Ruzycki, P. A., Blackshaw, S., & Clark, B. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.02.691925
Chen, X., Chen, Z.-Y., Qi, S., Huang, Q., Wei, L.-H., Chen, M., Li, H., Huang, N., Kang, Y.-X., Guo, Z., et al. (2026) · Cell Death Discovery · doi:10.1038/s41420-026-02974-7
Cheng, H.-Y., Liu, C., Nien, C.-W., Huang, H.-C., Zhao, H.-J., Nian, F., Chen, C., Custodio, H. M., Sisodiya, S. M., Lu, C. Y., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-69241-2
Yakoubi, W. E. (2012) · theses.fr (ABES) · doi:10.70675/c7f12aa8zb750z4a9ez8b33za3e1f7ab1093
Role of G1 phase regulators during corticogenesis
Pilaz, L. (2009) · theses.fr (ABES) · doi:10.70675/9f47e9acz5e06z4d39z83b5za3e00f543c58
Différenciation des cellules souches embryonnaires humaines vers l'hépatocyte
Funakoshi, N. (2011) · theses.fr (ABES) · doi:10.70675/124c2d82za8a6z4426zaff0z873bdb00a1fa
The brevity of G1 is an intrinsic determinant of naïve pluripotency
Coronado, D. (2011) · theses.fr (ABES) · doi:10.70675/dc890767z90e7z4923z977fz6127a0349fad
Reilly, M. L. (2018) · theses.fr (ABES) · doi:10.70675/dc69ccc1zaa2fz4147z8d1bzf306462e1009
The role of Notch signaling pathway during neural delamination in the vertebrate embryo
Baek, C. (2018) · theses.fr (ABES) · doi:10.70675/89032e52z6b8bz423bzb1d0zc7069afe33bd
Etude du rôle de la kinésine KIF21B au cours du développement cortical
Asselin, L. (2019) · theses.fr (ABES) · doi:10.70675/bd543948zdb0fz4298zae3fzf4fc50923d78
Hurtado, D. V. (2019) · theses.fr (ABES) · doi:10.70675/11c3ab93z927ez47ffz8c02z50f6aca0d59d
Carpentieri, J. A. (2020) · theses.fr (ABES) · doi:10.70675/1e00c88fzf627z42c5za72ez7da656ac6044
Molins, E. A. G. (2020) · theses.fr (ABES) · doi:10.70675/252d1be2z22e8z4378zb146zfd4ec7fa46a7
Development and specification of cortical areas in the non human primate
Pace, C. (2020) · theses.fr (ABES) · doi:10.70675/b7094400z9034z4ec5zb776zde051009bafa
Penisson, M. (2020) · theses.fr (ABES) · doi:10.70675/ad2c850ezf9cfz4390za05azc0cd02a0c5f0
Shapira, Y., Noack, F., Vangelisti, S., Chong, F., Lifshitz, A., Tanay, A., & Bonev, B. (2026) · Genes & Development · doi:10.1101/gad.353090.125
Steller: a high-resolution platform for spatial clonal tracing of mammalian brain developmentPreprint
Li, Z., Wang, C., Guo, C., Liao, Y., Chen, C., Xing, Q., Pei, W., & Peng, G. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.16.732634
Mechanical constraints regulate embryonic stem cell mitosis in the developing brain
Marthiens, V., Jawish, L., Malosse, M., Basto, C., Krndija, D., Macé, A., Laigna, E., Terrizzano, A., Peyret, C., Pan, T., et al. (2026) · The EMBO Journal · doi:10.1038/s44318-026-00848-3 · Cited by 1
Cell-cycle control of chromatin creates a therapeutic window for epigenetic therapy in tumorsPreprint
Hayatigolkhatmi, K., Valzelli, R., Ceccacci, E., Hosseini, A., Menna, O. E., Romanenghi, M., Pallavicini, I., Soda, E., Ejlli, O., Villa, E., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.03.748889
Hostetler, J. E., Shiau, F., Zhang, X., Chen, S., Ruzycki, P. A., Blackshaw, S., & Clark, B. S. (2026) · Developmental Biology · doi:10.1016/j.ydbio.2026.09.002
Coordinated neural progenitor adaptations contribute to primate neocortical downscaling
Tynianskaia, L., Betancourt, C. M. B., Grewe, E. M., Kniep, J., Liutikaite, N., Eşiyok, N., Göloğlu, İ. B., Heide, S., Rüger, N., Lindenwald, D. L., et al. (2026) · Science Advances · doi:10.1126/sciadv.aeg5563 · Cited by 1
Metadata
- Authors
- Calegari, F., Haubensak, W., Haffner, C., & Huttner, W. B.
- Affiliations
- Max Planck Institute of Molecular Cell Biology and Genetics (DE)
- California Institute of Technology (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2005-07-13
- Volume
- 25
- Issue
- 28
- Pages
- 6533-6538
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6725437
- OpenAlex
- W1999970417
- Cited by
- 396
- References
- 23
- Citations by year
- 2026: 10 · 2025: 16 · 2024: 11 · 2023: 11 · 2022: 16 · 2021: 19 · 2020: 25 · 2019: 19 · 2018: 22 · 2017: 18 · 2016: 17 · 2015: 23 · 2014: 23 · 2013: 15 · 2012: 24
- FWCI
- 4.92
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Max Planck Institute for Plasma Physics (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- Deutsche Forschungsgemeinschaft (SPP1109)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Keywords
- neural progenitor cells, neurogenesis, telencephalic development, ventricular zone, subventricular zone, G2 phase, TIS21, BrdU labeling, mouse embryo, adult stem cells
- MeSH terms
- Animals, Brain, Cell Cycle, Cell Differentiation, Cell Division, Gestational Age, Mice, Inbred C57BL, Neuroglia, Neurons, Recombinant Fusion Proteins, Stem Cells, Telencephalon, Time Factors, Genes, Tumor Suppressor, Immediate-Early Proteins, Genes, Reporter, Gene Expression Regulation, Developmental, Tumor Suppressor Proteins, Green Fluorescent Proteins, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
