Alternative functions of core cell cycle regulators in neuronal migration, neuronal maturation, and synaptic plasticity
Open accessAbstract
Recent studies have demonstrated that boundaries separating a cycling cell from a postmitotic neuron are not as concrete as expected. Novel and unique physiological functions in neurons have been ascribed for proteins fundamentally required for cell cycle progression and control. These "core" cell cycle regulators serve diverse postmitotic functions that span various developmental stages of a neuron, including neuronal migration, axonal elongation, axon pruning, dendrite morphogenesis, and synaptic maturation and plasticity. In this review, we detail the nonproliferative postmitotic roles that these cell cycle proteins have recently been reported to play, the significance of their expression in neurons, mechanistic insight when available, and future prospects.
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DYRK1A can phosphorylate and possibly regulate Cyclin D1 (G1-to-S phase transition and cell proliferation) and p27 (neuronal differentiation and cell cycle exit).
“This mechanism of action could be attributed to the ability of DYRK1A to phosphorylate and possibly regulate Cyclin D1 (G1-to-S phase transition and cell proliferation) and p27 (neuronal differentiation and cell cycle exit) (Frank and Tsai, 2009; Hindley and Philpott, 2012; Najas et al., 2015; Tejedor and Hammerle, 2011).”
From Sex-specific developmental alterations in DYRK1A expression in the brain of a Down syndrome mouse model (2024) · cites this paper as Frank and Tsai, 2009
The Cell cycle section describes cyclin D complexes promoting G1 progression, and the Neuronal differentiation and migration section links p27Kip1 to neuronal differentiation and inhibition of G1 CDKs (page numbers unavailable). But no passage found for DYRK1A phosphorylating or regulating either protein; the paper instead describes CDK5 phosphorylating p27Kip1. (LLM, conf=0.82)
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Cites
DNA Replication in Eukaryotic Cells
Bell, S. P., & Dutta, A. (2002) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.71.110601.135425 · Cited by 2,065 · see citing works
Genetic Control of the Cell Division Cycle in Yeast
Hartwell, L. H., Culotti, J. G., Pringle, J. R., & Reid, B. J. (1974) · Science · doi:10.1126/science.183.4120.46 · Cited by 1,567 · see citing works
The self-tuning neuron: synaptic scaling of excitatory synapses
Turrigiano, G. G. (2008) · Cell · doi:10.1016/j.cell.2008.10.008 · Cited by 1,533 · see citing works
Fero, M. L., Rivkin, M. J., Tasch, M., Porter, P. L., Carow, C. E., Firpo, E. J., Polyák, K., Tsai, L., Broudy, V. C., Perlmutter, R. M., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)81239-8 · Cited by 1,459 · see citing works
Self-citationChen, M. S., Huber, A. B., van der Haar, M. E., Frank, M., Schnell, L., Spillmann, A. A., Christ, F., & Schwab, M. E. (2000) · Nature · doi:10.1038/35000219 · Cited by 1,445 · see citing works
Ubiquitin ligases: cell-cycle control and cancer
Nakayama, K. I., & Nakayama, K. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1881 · Cited by 1,441 · see citing works
The anaphase promoting complex/cyclosome: a machine designed to destroy
Peters, J.-M. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1988 · Cited by 1,315 · see citing works
Retinoblastoma protein recruits histone deacetylase to repress transcription
Brehm, A., Miska, E. A., McCance, D. J., Reid, J. L., Bannister, A. J., & Kouzarides, T. (1998) · Nature · doi:10.1038/35404 · Cited by 1,231 · see citing works
Giacinti, C., & Giordano, A. (2006) · Oncogene · doi:10.1038/sj.onc.1209615 · Cited by 1,218 · see citing works
Cohesin mediates transcriptional insulation by CCCTC-binding factor
Wendt, K. S., Yoshida, K., Itoh, T., Bando, M., Koch, B., Schirghuber, E., Tsutsumi, S., Nagae, G., Ishihara, K., Mishiro, T., et al. (2008) · Nature · doi:10.1038/nature06634 · Cited by 1,193 · see citing works
CDK inhibitors: Cell cycle regulators and beyond
Besson, A., Dowdy, S. F., & Roberts, J. M. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.01.013 · Cited by 1,152 · see citing works
Identification of the Nogo inhibitor of axon regeneration as a Reticulon protein
GrandPré, T., Nakamura, F., Vartanian, T. K., & Strittmatter, S. M. (2000) · Nature · doi:10.1038/35000226 · Cited by 1,139 · see citing works
Polo-like kinases and the orchestration of cell division
Barr, F. A., Silljé, H. H. W., & Nigg, E. A. (2004) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1401 · Cited by 1,092 · see citing works
Dhavan, R., & Tsai, L. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35096019 · Cited by 1,052 · see citing works
Self-citationGeminin, an inhibitor of DNA replication, is degraded during mitosis.
Mcgarry, T., & Kirschner, M. (1998) · Cell · doi:10.1016/s0092-8674(00)81209-x · Cited by 988 · see citing works
Rb Interacts with Histone Deacetylase to Repress Transcription
Luo, R. X., Postigo, A. A., & Dean, D. C. (1998) · Cell · doi:10.1016/s0092-8674(00)80940-x · Cited by 957 · see citing works
Nevins, J. R. (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.7.699 · Cited by 920 · see citing works
Sudakin, V., Chan, G. K. T., & Yen, T. J. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.200102093 · Cited by 907 · see citing works
Crystal structure of the p27Kip1 cyclin-dependent-kinase inibitor bound to the cyclin A–Cdk2 complex
Russo, A. A., Jeffrey, P. D., Patten, A. K., Massagué, J., & Pavletich, N. P. (1996) · Nature · doi:10.1038/382325a0 · Cited by 907 · see citing works
Retinoblastoma protein represses transcription by recruiting a histone deacetylase
Magnaghi-Jaulin, L., Groisman, R., Naguibneva, I., Robin, P., Lorain, S., Levillain, J. P., Troalen, F., Trouche, D., & Harel‐Bellan, A. (1998) · Nature · doi:10.1038/35410 · Cited by 906 · see citing works
Cohesins Functionally Associate with CTCF on Mammalian Chromosome Arms
Parelho, V., Hadjur, S., Spivakov, M., Leleu, M., Sauer, S., Gregson, H. C., Jarmuz, A., Canzonetta, C., Webster, Z., Nesterova, T., et al. (2008) · Cell · doi:10.1016/j.cell.2008.01.011 · Cited by 900 · see citing works
Mutations in aurora prevent centrosome separation leading to the formation of monopolar spindles
Glover, D. M., Leibowitz, M. H., McLean, D., & Parry, H. D. (1995) · Cell · doi:10.1016/0092-8674(95)90374-7 · Cited by 838 · see citing works
The murine gene p27Kip1 is haplo-insufficient for tumour suppression
Fero, M. L., Randel, E., Gurley, K. E., Roberts, J. M., & Kemp, C. J. (1998) · Nature · doi:10.1038/24179 · Cited by 784 · see citing works
Coordination of Growth and Cell Division in the Drosophila Wing
Neufeld, T. P., de la Cruz, A. F. A., Johnston, L. A., & Edgar, B. A. (1998) · Cell · doi:10.1016/s0092-8674(00)81462-2 · Cited by 769 · see citing works
GENETIC CONTROL OF THE CELL DIVISION CYCLE IN YEAST: V. GENETIC ANALYSIS OF cdc MUTANTS
Hartwell, L. H., Mortimer, R., Culotti, J. G., & Culotti, M. (1973) · Genetics · doi:10.1093/genetics/74.2.267 · Cited by 740 · see citing works
The KEN box: an APC recognition signal distinct from the D box targeted by Cdh1Preprint
Pfleger, C. M., & Kirschner, M. W. (2000) · Genes & Development · doi:10.1101/gad.14.6.655 · Cited by 733 · see citing works
The Phosphatase Cdc14 Triggers Mitotic Exit by Reversal of Cdk-Dependent Phosphorylation
Visintin, R., Craig, K. L., Hwang, E. S., Prinz, S., Tyers, M., & Amon, A. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80286-5 · Cited by 725 · see citing works
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 · see citing works
Trekking across the Brain: The Journey of Neuronal Migration
Ayala, R., Shu, T., & Tsai, L.-H. (2007) · Cell · doi:10.1016/j.cell.2006.12.021 · Cited by 620 · see citing works
Self-citationThe E2F1–3 transcription factors are essential for cellular proliferation
Wu, L., Timmers, C. D., Maiti, B., Saavedra, H. I., Sang, L., Chong, G. T., Nuckolls, F., Giangrande, P. H., Wright, F. A., Field, S. J., et al. (2001) · Nature · doi:10.1038/35106593 · Cited by 620 · see citing works
THE STRUCTURE AND FUNCTION OF SMC AND KLEISIN COMPLEXES
Nasmyth, K., & Haering, C. H. (2005) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.74.082803.133219 · Cited by 612 · see citing works
Chromosomal Cohesin Forms a Ring
Gruber, S., Haering, C. H., & Nasmyth, K. (2003) · Cell · doi:10.1016/s0092-8674(03)00162-4 · Cited by 603 · see citing works
Fang, G., Yu, H., & Kirschner, M. W. (1998) · Genes & Development · doi:10.1101/gad.12.12.1871 · Cited by 597 · see citing works
A Self-Enabling TGFβ Response Coupled to Stress Signaling
Kang, Y., Chen, C.-R., & Massagué, J. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00109-6 · Cited by 548 · see citing works
CTCF physically links cohesin to chromatin
Rubio, E. D., Reiss, D. J., Welcsh, P. L., Disteche, C. M., Filippova, G. N., Baliga, N. S., Aebersold, R., Ranish, J. A., & Krumm, A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801273105 · Cited by 511 · see citing works
Control of Cyclin Ubiquitination by CDK-Regulated Binding of Hct1 to the Anaphase Promoting Complex
Zachariae, W., Schwab, M., Nasmyth, K., & Seufert, W. (1998) · Science · doi:10.1126/science.282.5394.1721 · Cited by 511 · see citing works
Cell cycle regulation in the postmitotic neuron: oxymoron or new biology?
Herrup, K., & Yang, Y. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2124 · Cited by 507 · see citing works
Control of the SCFSkp2–Cks1 ubiquitin ligase by the APC/CCdh1 ubiquitin ligase
Bashir, T., Dorrello, N. V., Amador, V., Guardavaccaro, D., & Pagano, M. (2004) · Nature · doi:10.1038/nature02330 · Cited by 504 · see citing works
Degradation of the SCF component Skp2 in cell-cycle phase G1 by the anaphase-promoting complex
Wei, W., Ayad, N. G., Wan, Y., Zhang, G.-J., Kirschner, M. W., & Kaelin, W. G. (2004) · Nature · doi:10.1038/nature02381 · Cited by 495 · see citing works
Wu, L., Wells, D., Tay, J., Mendis, D., Abbott, M.-A., Barnitt, A., Quinlan, E., Heynen, A., Fallon, J. R., & Richter, J. D. (1998) · Neuron · doi:10.1016/s0896-6273(00)80630-3 · Cited by 488 · cited 2× · see citing works
“Building on work that originally implicated CPEB-1 in synaptic activity-induced polyadenylation and translation of CaMKII mRNA (Wu et al., 1998), Huang et al.”
p27 Kip1 modulates cell migration through the regulation of RhoA activationPreprint
Besson, A., Gurian-West, M., Schmidt, A., Hall, A., & Roberts, J. M. (2004) · Genes & Development · doi:10.1101/gad.1185504 · Cited by 487 · see citing works
Polo on the Rise—from Mitotic Entry to Cytokinesis with Plk1
Petronczki, M. P., Lénárt, P., & Peters, J. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.04.014 · Cited by 485 · see citing works
M-phase kinases induce phospho-dependent ubiquitination of somatic Wee1 by SCF <sup>β-TrCP</sup>
Watanabe, N., Arai, H., Nishihara, Y., Taniguchi, M., Watanabe, N., Hunter, T., & Osada, H. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307700101 · Cited by 472 · see citing works
X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations
Musio, A., Selicorni, A., Focarelli, M. L., Gervasini, C., Milani, D., Russo, S., Vezzoni, P., & Larizza, L. (2006) · Nature Genetics · doi:10.1038/ng1779 · Cited by 468 · see citing works
Geley, S., Kramer, E., Gieffers, C., Gannon, J., Peters, J., & Hunt, T. (2001) · Journal of Cell Biology · doi:10.1083/jcb.153.1.137 · Cited by 462 · see citing works
Mitotic Regulation of the APC Activator Proteins CDC20 and CDH1
Kramer, E. R., Scheuringer, N., Podtelejnikov, A. V., Mann, M., & Peters, J. (2000) · Molecular Biology of the Cell · doi:10.1091/mbc.11.5.1555 · Cited by 455 · see citing works
Hauf, S., Roitinger, E., Koch, B., Dittrich, C. M., Mechtler, K., & Peters, J. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030069 · Cited by 438 · see citing works
Si, K., Giustetto, M., Etkin, A., Hsu, R., Janisiewicz, A. M., Miniaci, M. C., Kim, J., Zhu, H., & Kandel, E. R. (2003) · Cell · doi:10.1016/s0092-8674(03)01021-3 · Cited by 432 · see citing works
Mitotic regulation of the human anaphase‐promoting complex by phosphorylation
Kraft, C., Herzog, F., Gieffers, C., Mechtler, K., Hagting, A., Pines, J., & Peters, J. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg627 · Cited by 421 · see citing works
The Aurora kinase family in cell division and cancer
Vader, G., & Lens, S. M. A. (2008) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2008.07.003 · Cited by 421 · see citing works
Association of the Origin Recognition Complex with Heterochromatin and HP1 in Higher Eukaryotes
Pak, D. T. S., Pflumm, M. F., Chesnokov, I. N., Huang, D. W., Kellum, R., Marr, J., Romanowski, P., & Botchan, M. R. (1997) · Cell · doi:10.1016/s0092-8674(00)80415-8 · Cited by 408 · see citing works
Axon Pruning during Drosophila Metamorphosis
Watts, R. J., Hoopfer, E. D., & Luo, L. (2003) · Neuron · doi:10.1016/s0896-6273(03)00295-2 · Cited by 376 · see citing works
Calegari, F., & Huttner, W. Β. (2003) · Journal of Cell Science · doi:10.1242/jcs.00825 · Cited by 367 · see citing works
p27 kip1 independently promotes neuronal differentiation and migration in the cerebral cortexPreprint
Nguyen, L., Besson, A., Heng, J. I., Schuurmans, C. J., Teboul, L., Parras, C. M., Philpott, A., Roberts, J. M., & Guillemot, F. (2006) · Genes & Development · doi:10.1101/gad.377106 · Cited by 367 · see citing works
Stedman, W., Kang, H., Lin, S., Kissil, J. L., Bartolomei, M. S., & Lieberman, P. M. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.1 · Cited by 366 · see citing works
Cdh1-APC Controls Axonal Growth and Patterning in the Mammalian Brain
Konishi, Y., Stegmüller, J., Matsuda, T., Bonni, S., & Bonni, A. (2004) · Science · doi:10.1126/science.1093712 · Cited by 363 · see citing works
Ordered proteolysis in anaphase inactivates Plk1 to contribute to proper mitotic exit in human cells
Lindon, C., & Pines, J. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200309035 · Cited by 358 · see citing works
Margottin-Goguet, F., Hsu, J. Y., Loktev, A. V., Hsieh, H.-M., Reimann, J. D. R., & Jackson, P. K. (2003) · Developmental Cell · doi:10.1016/s1534-5807(03)00153-9 · Cited by 337 · see citing works
Losada, A., Hirano, M., & Hirano, T. (2002) · Genes & Development · doi:10.1101/gad.249202 · Cited by 335 · see citing works
Méndez, J., Zou-Yang, X. H., Kim, S. Y., Hidaka, M., Tansey, W. P., & Stillman, B. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00467-7 · Cited by 320 · see citing works
Bagri, A., Cheng, H.-J., Yaron, A., Pleasure, S. J., & Tessier‐Lavigne, M. (2003) · Cell · doi:10.1016/s0092-8674(03)00267-8 · Cited by 319 · see citing works
APC/C and SCF: Controlling Each Other and the Cell Cycle
Vodermaier, H. C. (2004) · Current Biology · doi:10.1016/j.cub.2004.09.020 · Cited by 318 · see citing works
Identification and Characterization of Sa/Scc3p Subunits in the Xenopus and Human Cohesin Complexes
Losada, A., Yokochi, T., Kobayashi, R., & Hirano, T. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.150.3.405 · Cited by 315 · see citing works
INK4 proteins, a family of mammalian CDK inhibitors with novel biological functions
Cánepa, E. T., Scassa, M. É., Ceruti, J. M., Marazita, M. C., Carcagno, A. L., Sirkin, P. F., & Ogara, M. F. (2007) · IUBMB Life · doi:10.1080/15216540701488358 · Cited by 314 · see citing works
Littlepage, L. E., & RUDERMAN, J. V. (2002) · Genes & Development · doi:10.1101/gad.1007302 · Cited by 308 · see citing works
Polo-Like Kinases: A Team in Control of the Division
van de Weerdt, B. C. M., & Medema, R. H. (2006) · Cell Cycle · doi:10.4161/cc.5.8.2692 · Cited by 301 · see citing works
Kotani, S., Tugendreich, S., Fujii, M., Jorgensen, P.-M., Watanabe, N., Höög, C., Hieter, P., & Todokoro, K. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80037-4 · Cited by 301 · see citing works
Targeted Protein Degradation and Synapse Remodeling by an Inducible Protein Kinase
Pak, D. T. S., & Sheng, M. (2003) · Science · doi:10.1126/science.1082475 · Cited by 299 · see citing works
Degradation of Id2 by the anaphase-promoting complex couples cell cycle exit and axonal growth
Lasorella, A., Stegmüller, J., Guardavaccaro, D., Liu, G., Carro, M. S., Rothschild, G., de la Torre-Ubieta, L., Pagano, M., Bonni, A., & Iavarone, A. (2006) · Nature · doi:10.1038/nature04895 · Cited by 298 · see citing works
Huang, Y.-S., Jung, M.-Y., Sarkissian, M., & Richter, J. (2002) · EMBO Journal · doi:10.1093/emboj/21.9.2139 · Cited by 290 · see citing works
Peschiaroli, A., Dorrello, N. V., Guardavaccaro, D., Venere, M., Halazonetis, T., Sherman, N. E., & Pagano, M. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.06.013 · Cited by 289 · see citing works
Evidence that Loading of Cohesin Onto Chromosomes Involves Opening of Its SMC Hinge
Gruber, S., Arumugam, P., Katou, Y., Kuglitsch, D., Helmhart, W., Shirahige, K., & Nasmyth, K. (2006) · Cell · doi:10.1016/j.cell.2006.08.048 · Cited by 287 · see citing works
Phosphorylation of CDC25B by Aurora-A at the centrosome contributes to the G2–M transition
Dutertre, S., Cazalès, M., Quaranta, M., Froment, C., Trabut, V., Dozier, C., Mirey, G., Bouché, J., Theis‐Febvre, N., Schmitt, E., et al. (2004) · Journal of Cell Science · doi:10.1242/jcs.01108 · Cited by 284 · see citing works
Cell-Type-Specific TEV Protease Cleavage Reveals Cohesin Functions in Drosophila Neurons
Pauli, A., Althoff, F., Oliveira, R. A., Heidmann, S. K., Schuldiner, O., Lehner, C. F., Dickson, B. J., & Nasmyth, K. (2008) · Developmental Cell · doi:10.1016/j.devcel.2007.12.009 · Cited by 276 · see citing works
Kawauchi, T., Chihama, K., Nabeshima, Y., & Hoshino, M. (2005) · Nature Cell Biology · doi:10.1038/ncb1338 · Cited by 273 · see citing works
Aurora kinases, aneuploidy and cancer, a coincidence or a real link?
Giet, R., Petretti, C., & Prigent, C. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.03.004 · Cited by 263 · see citing works
Mitosis: a matter of getting rid of the right protein at the right time
Pines, J. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.11.006 · Cited by 262 · see citing works
Human Orc2 localizes to centrosomes, centromeres and heterochromatin during chromosome inheritance
Prasanth, S. G., Prasanth, K. V., Siddiqui, K., Spector, D. L., & Stillman, B. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600255 · Cited by 260 · see citing works
Ferreira, R., Magnaghi-Jaulin, L., Robin, P., Harel‐Bellan, A., & Trouche, D. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.18.10493 · Cited by 251 · see citing works
Schuldiner, O., Berdnik, D., Levy, J. M., Wu, J., Luginbuhl, D. J., Gontang, A. C., & Luo, L. (2008) · Developmental Cell · doi:10.1016/j.devcel.2007.11.001 · Cited by 246 · see citing works
Revisiting the Role of the Mother Centriole in Centriole Biogenesis
Rodrigues-Martins, A., Riparbelli, M. G., Callaini, G., Glover, D. M., & Bettencourt‐Dias, M. (2007) · Science · doi:10.1126/science.1142950 · Cited by 245 · see citing works
Orc6 Involved in DNA Replication, Chromosome Segregation, and Cytokinesis
Prasanth, S. G., Prasanth, K. V., & Stillman, B. (2002) · Science · doi:10.1126/science.1072802 · Cited by 236 · see citing works
Substrate recognition by the Cdc20 and Cdh1 components of the anaphase-promoting complexPreprint
Pfleger, C. M., Lee, E. N., & Kirschner, M. W. (2001) · Genes & Development · doi:10.1101/gad.918201 · Cited by 236 · see citing works
Cyclin-Dependent Kinases and S Phase Control in Mammalian Cells
Woo, R. A., & Poon, R. Y. C. (2003) · Cell Cycle · doi:10.4161/cc.2.4.468 · Cited by 234 · see citing works
Zheng, X., Wang, J., Haerry, T. E., Wu, A. Y.-H., Martin, J. L., O’Connor, M. B., Lee, C.-H. J., & Lee, T. (2003) · Cell · doi:10.1016/s0092-8674(03)00072-2 · Cited by 233 · see citing works
Seeburg, D. P., Feliú-Mójer, M. I., Gaiottino, J., Pak, D. T. S., & Sheng, M. (2008) · Neuron · doi:10.1016/j.neuron.2008.03.021 · Cited by 230 · see citing works
Cyclin-dependent kinase (CDK) phosphorylation destabilizes somatic Wee1 via multiple pathways
Watanabe, N., Arai, H., Iwasaki, J.-I., Shiina, M., Ogata, K., Hunter, T. R., & Osada, H. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500410102 · Cited by 229 · see citing works
Polo-like Kinase-1 Controls Proteasome-Dependent Degradation of Claspin during Checkpoint Recovery
Mamely, I., van Vugt, M. A., Smits, V. A., Semple, J. I., Lemmens, B., Perrakis, A., Medema, R. H., & Freire, R. (2006) · Current Biology · doi:10.1016/j.cub.2006.08.026 · Cited by 227 · see citing works
Independent Regulation of Synaptic Size and Activity by the Anaphase-Promoting Complex
van Roessel, P., Elliott, D. A., Robinson, I. M., Prokop, A., & Brand, A. H. (2004) · Cell · doi:10.1016/j.cell.2004.11.028 · Cited by 220 · see citing works
Moshe, Y., Boulaire, J., Pagano, M., & Hershko, A. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402442101 · Cited by 213 · see citing works
McAllister, S. S., Becker‐Hapak, M., Pintucci, G., Pagano, M., & Dowdy, S. F. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.23.1.216-228.2003 · Cited by 212 · see citing works
Cohesin Complex Promotes Transcriptional Termination between Convergent Genes in S. pombe
Gullerová, M., & Proudfoot, N. J. (2008) · Cell · doi:10.1016/j.cell.2008.02.040 · Cited by 208 · see citing works
Misulovin, Z., Schwartz, Y. B., Li, X., Kahn, T. G., Gause, M., MacArthur, S., Fay, J. C., Eisen, M. B., Pirrotta, V., Biggin, M. D., et al. (2007) · Chromosoma · doi:10.1007/s00412-007-0129-1 · Cited by 208 · see citing works
Plk4 haploinsufficiency causes mitotic infidelity and carcinogenesis
Ko, M. A., Rosario, C. O., Hudson, J. W., Kulkarni, S., Pollett, A. F., Dennis, J. W., & Swallow, C. J. (2005) · Nature Genetics · doi:10.1038/ng1605 · Cited by 205 · see citing works
Kauselmann, G., Weiler, M., Wulff, P., Jessberger, S., Konietzko, U., Scafidi, J., Staubli, U., Bereiter‐Hahn, J., Strebhardt, K., & Kuhl, D. (1999) · The EMBO Journal · doi:10.1093/emboj/18.20.5528 · Cited by 205 · see citing works
Cip/Kip proteins: more than just CDKs inhibitors: Figure 1.Preprint
Denicourt, C., & Dowdy, S. F. (2004) · Genes & Development · doi:10.1101/gad.1205304 · Cited by 203 · see citing works
Functional contribution of Pds5 to cohesin-mediated cohesion in human cells and Xenopus egg extracts
Losada, A., Yokochi, T., & Hirano, T. (2005) · Journal of Cell Science · doi:10.1242/jcs.02355 · Cited by 195 · see citing works
Identification of an Early-Growth-Response Gene Encoding a Novel Putative Protein Kinase
Simmons, D. L., Neel, B. G., Stevens, R. E., Evett, G. E., & Erikson, R. L. (1992) · Molecular and Cellular Biology · doi:10.1128/mcb.12.9.4164-4169.1992 · Cited by 195 · see citing works
Theis, M., Si, K., & Kandel, E. R. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1133424100 · Cited by 194 · see citing works
Donohue, P. J., Alberts, G. F., Guo, Y. H., & Winkles, J. A. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.17.10351 · Cited by 192 · see citing works
A Centrosomal Cdc20-APC Pathway Controls Dendrite Morphogenesis in Postmitotic Neurons
Kim, A. H., Puram, S. V., Bilimoria, P. M., Ikeuchi, Y., Keough, S., Wong, M., Rowitch, D. H., & Bonni, A. (2009) · Cell · doi:10.1016/j.cell.2008.11.050 · Cited by 189 · see citing works
Leone, G. W., Nuckolls, F., Ishida, S., Adams, M., Sears, R. C., Jakoi, L., Miron, A., & Nevins, J. R. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.10.3626-3632.2000 · Cited by 187 · see citing works
Expression of the CDH1-associated form of the anaphase-promoting complex in postmitotic neurons
Gieffers, C., Peters, B. H., Kramer, E. R., Dotti, C. G., & Peters, J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.20.11317 · Cited by 185 · see citing works
Golan, A., Yudkovsky, Y., & Hershko, A. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m111476200 · Cited by 173 · see citing works
Differential Functions of the Aurora-B and Aurora-C Kinases in Mammalian Spermatogenesis
Kimmins, S., Crosio, C., Kotaja, N., Hirayama, J., Monaco, L., Höög, C., van Duin, M., Gossen, J. A., & Sassone‐Corsi, P. (2006) · Molecular Endocrinology · doi:10.1210/me.2006-0332 · Cited by 168 · see citing works
Juo, P., & Kaplan, J. M. (2004) · Current Biology · doi:10.1016/j.cub.2004.11.010 · Cited by 164 · see citing works
Cytoplasmic p21Cip1 Is Involved in Ras-induced Inhibition of the ROCK/LIMK/Cofilin Pathway
Lee, S., & Helfman, D. M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m306968200 · Cited by 163 · see citing works
Gallo, G. (2006) · Journal of Cell Science · doi:10.1242/jcs.03084 · Cited by 163 · see citing works
Cell-Intrinsic Regulation of Axonal Morphogenesis by the Cdh1-APC Target SnoN
Stegmüller, J., Konishi, Y., Huynh, M. A., Yuan, Z., DiBacco, S., & Bonni, A. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.034 · Cited by 163 · see citing works
Alarcón, J. M., Hodgman, R., Theis, M., Huang, Y., Kandel, E. R., & Richter, J. D. (2004) · Learning & Memory · doi:10.1101/lm.72704 · Cited by 160 · see citing works
Cytoplasmic p21Cip1/WAF1 regulates neurite remodeling by inhibiting Rho-kinase activity
Tanaka, H., Yamashita, T., Asada, M., Mizutani, S., Yoshikawa, H., & Tohyama, M. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200202071 · Cited by 157 · see citing works
Li, M., Shin, Y.-H., Hou, L., Huang, X., Wei, Z., Klann, E., & Zhang, P. (2008) · Nature Cell Biology · doi:10.1038/ncb1768 · Cited by 156 · see citing works
Ferguson, K. L., Vanderluit, J. L., Hébert, J. M., McIntosh, W. C., Tibbo, E., MacLaurin, J. G., Park, D. S., Wallace, V. A., Vooijs, M., McConnell, S. K., et al. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf338 · Cited by 156 · see citing works
Dynamic localization and functional implications of Aurora-C kinase during male mouse meiosis
Tang, C.-J. C., Lin, C., & Tang, T. K. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2005.11.036 · Cited by 152 · see citing works
Sun, A., Bagella, L., Tutton, S., Romano, G., & Giordano, A. (2007) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21609 · Cited by 152 · see citing works
Late mitotic failure in mice lacking Sak, a polo-like kinase
Hudson, J. W., Kozarova, A., Cheung, P., Macmillan, J. C., Swallow, C. J., Cross, J. C., & Dennis, J. W. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00117-8 · Cited by 152 · see citing works
Polo-like Kinase-2 Is Required for Centriole Duplication in Mammalian Cells
Warnke, S., Kemmler, S., Hames, R. S., Tsai, H.-L., Hoffmann‐Rohrer, U., Fry, A. M., & Hoffmann, I. (2004) · Current Biology · doi:10.1016/j.cub.2004.06.059 · Cited by 150 · see citing works
Winkles, J. A., & Alberts, G. F. (2005) · Oncogene · doi:10.1038/sj.onc.1208219 · Cited by 148 · see citing works
Complex Transcriptional Regulatory Mechanisms Control Expression of the E2F3 Locus
Adams, M. R., Sears, R. C., Nuckolls, F., Leone, G. W., & Nevins, J. R. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.10.3633-3639.2000 · Cited by 146 · see citing works
Dorsett, D. (2006) · Chromosoma · doi:10.1007/s00412-006-0072-6 · Cited by 145 · see citing works
Essential role of Id2 in negative regulation of IgE class switching
Sugai, M., Gonda, H., Kusunoki, T., Katakai, T., Yokota, Y., & Shimizu, A. (2002) · Nature Immunology · doi:10.1038/ni874 · Cited by 140 · see citing works
Plk1- and β-TrCP–dependent degradation of Bora controls mitotic progression
Seki, A., Coppinger, J. A., Du, H., Jang, C., Yates, J. R., & Fang, G. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200712027 · Cited by 134 · see citing works
Boynton, S., & Tully, T. (1992) · Genetics · doi:10.1093/genetics/131.3.655 · Cited by 133 · see citing works
Reduction of Cytosolic p27Kip1 Inhibits Cancer Cell Motility, Survival, and Tumorigenicity
Wu, F. Y., Wang, S. E., Sanders, M. E., Shin, I., Rojo, F., Baselga, J. M., & Arteaga, C. L. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-3304 · Cited by 130 · see citing works
Sarkissian, M., Méndez, R., & Richter, J. D. (2004) · Genes & Development · doi:10.1101/gad.1136004 · Cited by 130 · see citing works
Sørensen, C. S., Lukas, C., Kramer, E. R., Peters, J., Bártek, J., & Lukas, J. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.11.3692-3703.2001 · Cited by 128 · see citing works
Liu, J., & Krantz, I. D. (2008) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.9.081307.164211 · Cited by 126 · see citing works
The brain-specific activator p35 allows Cdk5 to escape inhibition by p27Kip1 in neurons.
Lee, M., Nikolić, M., Baptista, C. A., Lai, E., Tsai, L., & Massagué, J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.8.3259 · Cited by 124 · see citing works
Self-citationCell Cycle Dependent Regulation of the Origin Recognition Complex
Depamphilis, M. (2004) · Cell Cycle · doi:10.4161/cc.4.1.1333 · Cited by 123 · see citing works
RB, the conductor that orchestrates life, death and differentiation
Khidr, L., & Chen, P.-L. (2006) · Oncogene · doi:10.1038/sj.onc.1209612 · Cited by 123 · see citing works
Aurora A, mitotic entry, and spindle bipolarity
Liu, Q., & RUDERMAN, J. V. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601425103 · Cited by 120 · see citing works
Bi-directional signaling by Semaphorin 1a during central synapse formation in Drosophila
Godenschwege, T. A., Hu, H., Shan-Crofts, X., Goodman, C. S., & Murphey, R. K. (2002) · Nature Neuroscience · doi:10.1038/nn976 · Cited by 118 · see citing works
p57Kip2 Regulates Actin Dynamics by Binding and Translocating LIM-kinase 1 to the Nucleus
Yokoo, T., Toyoshima, H., Miura, M., Wang, Y., Iida, K., Suzuki, H., Sone, H., Shimano, H., Gotoda, T., Nishimori, S., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m309334200 · Cited by 115 · see citing works
Expression of INK4 inhibitors of cyclin D-dependent kinases during mouse brain development.
Zindy, F., Soares, H. D., Herzog, K., Morgan, J., Sherr, C. J., & Roussel, M. F. (1997) · PubMed · Cited by 114 · see citing works
Degradation of human Aurora‐A protein kinase is mediated by hCdh1
Taguchi, S.-I., Honda, K., Sugiura, K., Yamaguchi, A., Furukawa, K., & Urano, T. (2002) · FEBS Letters · doi:10.1016/s0014-5793(02)02711-4 · Cited by 113 · see citing works
Spatial Regulation of an E3 Ubiquitin Ligase Directs Selective Synapse Elimination
Ding, M., Chao, D. L., Wang, G., & Shen, K. (2007) · Science · doi:10.1126/science.1145727 · Cited by 110 · see citing works
Chesnokov, I. N., Chesnokova, O. N., & Botchan, M. R. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1633580100 · Cited by 108 · see citing works
Cell cycle molecules and vertebrate neuron death: E2F at the hub
Greene, L. A., Biswas, S. C., & Liu, D. X. (2003) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401341 · Cited by 108 · see citing works
Specificity of E2F1, E2F2, and E2F3 in mediating phenotypes induced by loss of Rb.
Saavedra, H. I., Wu, L., de Bruin, A., Timmers, C. D., Rosol, T. J., Weinstein, M. B., Robinson, M. L., & Leone, G. W. (2002) · PubMed · Cited by 108 · see citing works
The Origin Recognition Complex Functions in Sister-Chromatid Cohesion in Saccharomyces cerevisiae
Shimada, K., & Gasser, S. M. (2007) · Cell · doi:10.1016/j.cell.2006.11.045 · Cited by 106 · see citing works
Pinto, S., Quintana, D. G., Smith, P., Mihalek, R., Hou, Z.-H., Boynton, S., Jones, C. J., Hendricks, M., Velinzon, K., Wohlschlegel, J. A., et al. (1999) · Neuron · doi:10.1016/s0896-6273(00)80752-7 · Cited by 105 · see citing works
Zhang, B., Jain, S. R., Song, H., Fu, M., Heuckeroth, R. O., Erlich, J. M., Jay, P. Y., & Milbrandt, J. (2007) · Development · doi:10.1242/dev.005884 · Cited by 104 · see citing works
The APC/C and CBP/p300 cooperate to regulate transcription and cell-cycle progression
Turnell, A. S., Stewart, G. S., Grand, R. J. A., Rookes, S. M., Martin, A., Yamano, H., Elledge, S. J., & Gallimore, P. H. (2005) · Nature · doi:10.1038/nature04151 · Cited by 100 · see citing works
Why do Neurons Enter the Cell Cycle?
Kruman, I. I. (2004) · Cell Cycle · doi:10.4161/cc.3.6.901 · Cited by 99 · see citing works
The mechanism of sister chromatid cohesion
Uhlmann, F. (2004) · Experimental Cell Research · doi:10.1016/j.yexcr.2004.03.005 · Cited by 98 · see citing works
The many faces of the origin recognition complex
Sasaki, T., & Gilbert, D. M. (2007) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2007.04.007 · Cited by 98 · see citing works
Siegel, P. M., Shu, W., & Massagué, J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m301413200 · Cited by 95 · see citing works
Toyoda, Y., & Yanagida, M. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-11-1089 · Cited by 95 · see citing works
Zearfoss, N. R., Alarcón, J. M., Trifilieff, P., Kandel, E. R., & Richter, J. D. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1756-08.2008 · Cited by 93 · see citing works
Li, C., Vassilev, A. P., & Depamphilis, M. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.13.5875-5886.2004 · Cited by 93 · see citing works
The cell cycle as a therapeutic target for Alzheimer's disease
Neve, R. L., & McPhie, D. L. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2005.09.005 · Cited by 92 · see citing works
Liu, X.-B., Low, L. K., Jones, E. G., & Cheng, H.-J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2648-05.2005 · Cited by 91 · see citing works
Rb-Mediated Neuronal Differentiation through Cell-Cycle–Independent Regulation of E2f3a
Chen, D., Opavsky, R., Pacal, M., Tanimoto, N., Wenzel, P., Seeliger, M. W., Leone, G., & Bremner, R. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050179 · Cited by 91 · see citing works
Unique Requirement for Rb/E2F3 in Neuronal Migration: Evidence for Cell Cycle-Independent Functions
McClellan, K. A., Ruzhynsky, V. A., Douda, D. N., Vanderluit, J. L., Ferguson, K. L., Chen, D., Bremner, R., Park, D. S., Leone, G., & Slack, R. S. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.02100-06 · Cited by 88 · see citing works
Goukassian, D. A., Díez‐Juan, A., Asahara, T., Schratzberger, P., Silver, M., Murayama, T., Isner, J. M., & Andrés, V. (2001) · The FASEB Journal · doi:10.1096/fj.01-0065com · Cited by 88 · see citing works
Itoh, Y., Masuyama, N., Nakayama, K., Nakayama, K., & Gotoh, Y. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m609944200 · Cited by 87 · see citing works
TGFβ-Smad2 Signaling Regulates the Cdh1-APC/SnoN Pathway of Axonal Morphogenesis
Stegmüller, J., Huynh, M. A., Yuan, Z., Konishi, Y., & Bonni, A. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.3061-07.2008 · Cited by 86 · see citing works
latheo, a Drosophila Gene Involved in Learning, Regulates Functional Synaptic Plasticity
Rohrbough, J. C., Pinto, S., Mihalek, R., Tully, T., & Broadie, K. S. (1999) · Neuron · doi:10.1016/s0896-6273(00)80753-9 · Cited by 84 · see citing works
Conn, C. W., Hennigan, R. F., Dai, W. H., Sánchez, Y., & Stambrook, P. J. (2000) · PubMed · Cited by 81 · see citing works
Strachan, T. (2005) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2005.04.005 · Cited by 73 · see citing works
Why do neurons enter the cell cycle?
Kruman (2004) · PubMed · Cited by 67 · see citing works
A cell‐autonomous requirement for the cell cycle regulatory protein, Rb, in neuronal migration
Ferguson, K. L., McClellan, K. A., Vanderluit, J. L., McIntosh, W. C., Schuurmans, C., Polleux, F., & Slack, R. S. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600887 · Cited by 65 · see citing works
Requirements for dE2F function in proliferating cells and in post‐mitotic differentiating cells.
Brook, A., Xie, J. E., Du, W., & Dyson, N. J. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00737.x · Cited by 65 · see citing works
The origin recognition core complex regulates dendrite and spine development in postmitotic neurons
Huang, Z. D., Zang, K., & Reichardt, L. F. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200505075 · Cited by 63 · see citing works
Cambronne, X. A., Seeburg, D. P., Sheng, M., & Harper, J. W. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m802475200 · Cited by 61 · see citing works
Alzheimer's disease and the cell cycle
Raina, A. K., Zhu, X., & Smith, M. A. (2004) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2004-1496 · Cited by 43 · see citing works
Cuvier, O., Lutzmann, M., & Méchali, M. (2006) · Current Biology · doi:10.1016/j.cub.2006.01.059 · Cited by 24 · see citing works
The chromosome glue gets a little stickier
McNairn, A. J., & Gerton, J. L. (2008) · Trends in Genetics · doi:10.1016/j.tig.2008.06.002 · Cited by 19 · see citing works
p27Kip1 Promotes Migration of Metastatic Hepatocellular Carcinoma Cells
Wang, X. Q., Lui, E. L. H., Cai, Q., Ching, W. Y. P., Liu, K. S. Y., Poon, R. T. P., & Fan, S. T. (2008) · Tumor Biology · doi:10.1159/000152939 · Cited by 14 · see citing works
Conway, A.-M., James, A. B., Zang, J., & MORRIS, B. J. (2007) · Synapse · doi:10.1002/syn.20387 · Cited by 9 · see citing works
Flagged first, then by citations
3 of the 173 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- Russo AA Jeffrey PD Patten AK Massague J Pavletich NP Crystal structure of the p27Kip1 cyclin-dependent-kinase inhibitor bound to the cyclin ACdk2 complex Nature 1996 382 325 331 8684460
- Tanaka H Yamashita T Asada M Mizutani S Yoshikawa H Tohyama M Cytoplasmic p21(Cip1/WAF1) regulates neurite remodeling by inhibiting Rhokinase activity J Cell Biol 2002 158 321 329 12119358 PMC2173114
Cited by
Sorted by citations
Gumy, L. F., Yeo, G. S. H., Tung, Y. L., Zivraj, K. H., Willis, D. E., Coppola, G., Lam, B., Twiss, J. L., Holt, C. E., & Fawcett, J. W. (2010) · RNA · doi:10.1261/rna.2386111 · Cited by 367 · see citing works
Subcellular Profiling Reveals Distinct and Developmentally Regulated Repertoire of Growth Cone mRNAs
Zivraj, K. H., Tung, Y. C. L., Piper, M., Gumy, L., Fawcett, J. W., Yeo, G. S. H., & Holt, C. E. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.1800-10.2010 · Cited by 315 · see citing works
microRNA as Repressors of Stress-Induced Anxiety: The Case of Amygdalar miR-34
Haramati, S., Navon, I., Issler, O., Ezra-Nevo, G., Gil, S., Zwang, R., Hornstein, E., & Chen, A. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.1673-11.2011 · Cited by 252 · see citing works
Neuronal cell cycle: the neuron itself and its circumstances
Frade, J. M., & Ovejero-Benito, M. C. (2015) · Cell Cycle · doi:10.1080/15384101.2015.1004937 · Cited by 245 · see citing works
Physiological Relevance of Cell Cycle Kinases
Malumbres, M. (2011) · Physiological Reviews · doi:10.1152/physrev.00025.2010 · Cited by 215 · see citing works
Soppa, U., Schumacher, J., Florencio Ortiz, V., Pasqualon, T., Tejedor, F., & Becker, W. (2014) · Cell Cycle · doi:10.4161/cc.29104 · Cited by 189 · see citing works
CB2 Cannabinoid Receptors Promote Neural Progenitor Cell Proliferation via mTORC1 Signaling
Palazuelos, J., Ortega, Z., Díaz-Alonso, J., Guzmán, M., & Galve‐Roperh, I. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.291294 · Cited by 173 · see citing works
Is senescence-associated β-galactosidase a marker of neuronal senescence?
Piechota, M. J., Sunderland, P., Wysocka, A., Nalberczak‐Skóra, M., Śliwińska, M. A., Radwańska, K., & Sikora, E. (2016) · Oncotarget · doi:10.18632/oncotarget.12752 · Cited by 156 · see citing works
Neocortical neurogenesis and the etiology of autism spectrum disorder
Packer, A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.03.002 · Cited by 138 · see citing works
Should I stay or should I go? Becoming a granule cell
Chédotal, A. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.01.004 · Cited by 143 · see citing works
Cell Cycle Activation and Aneuploid Neurons in Alzheimer's Disease
Arendt, T. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8262-0 · Cited by 133 · see citing works
REST and CoREST Modulate Neuronal Subtype Specification, Maturation and Maintenance
Abrajano, J. J., Qureshi, I., Gökhan, Ş., Zheng, D., Bergman, A., & Mehler, M. F. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007936 · Cited by 134 · see citing works
Cell cycle regulates cell type in theArabidopsissepal
Roeder, A., Cunha, A., Ohno, C. K., & Meyerowitz, E. M. (2012) · Development · doi:10.1242/dev.082925 · Cited by 124 · see citing works
Whole transcriptome profiling reveals the RNA content of motor axons
Briese, M., Saal-Bauernschubert, L., Appenzeller, S., Moradi, M., Baluapuri, A., & Sendtner, M. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv1027 · Cited by 113 · see citing works
Goriely, A., McGrath, J. J., Hultman, C. M., Wilkie, A. O. M., & Malaspina, D. (2013) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2013.12101352 · Cited by 96 · see citing works
Li, H., Zhu, Y., Morozov, Y. M., Chen, X., Page, S. C., Rannals, M. D., Maher, B. J., & RAKIC, P. T. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0353-0 · Cited by 94 · see citing works
Frank, C. L., Ge, X., Xie, Z., Zhou, Y., & Tsai, L. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.140699 · Cited by 93 · see citing works
Self-citationGLS2 is transcriptionally regulated by p73 and contributes to neuronal differentiation
Velletri, T., Romeo, F., Tucci, P., Peschiaroli, A., Annicchiarico‐Petruzzelli, M., Niklison-Chirou, M. V., Amelio, I., Knight, R. A., Mak, T. W., Melino, G., et al. (2013) · Cell Cycle · doi:10.4161/cc.26771 · Cited by 87 · see citing works
Gu, X., Fu, C., Lin, L., Liu, S., Su, X., Li, A., Wu, Q., Jia, C., Zhang, P., Chen, L., et al. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.25927 · Cited by 71 · see citing works
Barrio-Alonso, E., Hernández‐Vivanco, A., Walton, C. C., Perea, G., & Frade, J. M. (2018) · Scientific Reports · doi:10.1038/s41598-018-32708-4 · Cited by 65 · see citing works
van Leeuwen, L. A. G., & Hoozemans, J. J. M. (2015) · Acta Neuropathologica · doi:10.1007/s00401-015-1382-7 · Cited by 60 · see citing works
The functional variant rs34330 of CDKN1B is associated with risk of neuroblastoma
Capasso, M., McDaniel, L., Cimmino, F., Cirino, A., Formicola, D., Russell, M. R., Raman, P., Cole, K. A., & Diskin, S. J. (2017) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.13226 · Cited by 57 · see citing works
ID2: A negative transcription factor regulating oligodendroglia differentiation
Chen, X., Zhang, Y., Cai, Q., & Yao, Z. (2012) · Journal of Neuroscience Research · doi:10.1002/jnr.22826 · Cited by 54 · see citing works
The Rb/E2F Pathway Modulates Neurogenesis through Direct Regulation of the Dlx1/Dlx2 Bigene Cluster
Ghanem, N., Andrusiak, M. G., Svoboda, D. S., Lafi, S. M. A., Julian, L. M., McClellan, K. A., Repentigny, Y. D., Kothary, R., Ekker, M., Blais, A., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1344-12.2012 · Cited by 48 · see citing works
Kawauchi, T., Shikanai, M., & Kosodo, Y. (2013) · Genes to Cells · doi:10.1111/gtc.12029 · Cited by 47 · see citing works
Proliferative reactive gliosis is compatible with glial metabolic support and neuronal function
Vázquez-Chona, F., Swan, A. G., Ferrell, W. D., Jiang, L., Baehr, W., Chien, W., Fero, M. L., Marc, R. E., & Levine, E. M. (2011) · BMC Neuroscience · doi:10.1186/1471-2202-12-98 · Cited by 45 · see citing works
Region and Cell Type Distribution of TCF4 in the Postnatal Mouse Brain
Kim, H., Berens, N., Ochandarena, N. E., & Philpot, B. D. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.00042 · Cited by 46 · see citing works
Khazaei, M. R., & Püschel, A. W. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.055897 · Cited by 43 · see citing works
Hong, J., Zhang, H., Kawase‐Koga, Y., & Sun, T. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00151 · Cited by 44 · see citing works
Patrício, P., Mateus‐Pinheiro, A., Sousa, N., & Pinto, L. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8422-x · Cited by 38 · see citing works
Cortical neurons gradually attain a post-mitotic state
de Anda, F. C., Madabhushi, R., Rei, D., Meng, J., Gräff, J., Durak, O., Meletis, K., Richter, M., Schwanke, B., Mungenast, A. E., et al. (2016) · Cell Research · doi:10.1038/cr.2016.76 · Cited by 35 · see citing works
Self-citationHernández‐Ortega, K., Quiroz‐Baez, R., & Arias, C. (2011) · Neuroscience Bulletin · doi:10.1007/s12264-011-1002-z · Cited by 36 · see citing works
Chirivella, L., Kirstein, M., Ferrón, S., Domingo-Muelas, A., Durupt, F. C., Acosta-Umanzor, C., Cano-Jaimez, M., Pérez-Sánchez, F., Barbacid, M., Ortega, S., et al. (2017) · Stem Cells · doi:10.1002/stem.2694 · Cited by 33 · see citing works
Primary neurons can enter M-phase
Walton, C. C., Zhang, W., Patiño-Parrado, I., Barrio-Alonso, E., Garrido, J. J., & Frade, J. M. (2019) · Scientific Reports · doi:10.1038/s41598-019-40462-4 · Cited by 35 · see citing works
Yamada, M., Hirotsune, S., & Wynshaw-Boris, A. J. (2010) · Cell Adhesion & Migration · doi:10.4161/cam.4.2.10715 · Cited by 35 · see citing works
Molecular control of brain size: Regulators of neural stem cell life, death and beyond
Joseph, B., & Hermanson, O. (2010) · Experimental Cell Research · doi:10.1016/j.yexcr.2010.03.012 · Cited by 34 · see citing works
Müller, M., Lutter, D., & Püschel, A. W. (2009) · Journal of Cell Science · doi:10.1242/jcs.058230 · Cited by 33 · see citing works
Tsunekawa, Y., Kikkawa, T., & Osumi, N. (2014) · Development Growth & Differentiation · doi:10.1111/dgd.12135 · Cited by 30 · see citing works
Paolo, A. D., Eastman, G., Mesquita-Ribeiro, R., Farías, J., Macklin, A. M., Kislinger, T., Colburn, N. H., Munroe, D. J., Sosa, J. R. S., Dajas‐Bailador, F., et al. (2020) · RNA · doi:10.1261/rna.075424.120 · Cited by 28 · see citing works
Wesley, U. V., Hatcher, J. F., & Dempsey, R. J. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8829-z · Cited by 28 · see citing works
Catts, V. S., Catts, S. V., Jablensky, A. V., Chandler, D., Weickert, C. S., & Lavin, M. F. (2011) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2011.565073 · Cited by 28 · see citing works
Moon, H., Jeon, S. G., Kim, J.-I., Kim, H. S., Lee, S. H., Kim, D., Park, S., Moon, M., & Chung, H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms21010004 · Cited by 28 · see citing works
Chao, A., Chen, C.-H., Wu, M.-H., Hou, B.-Y., & Yang, D. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2019.118628 · Cited by 27 · see citing works
Liu, D., Ander, B. P., & Sharp, F. R. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.11.013 · Cited by 27 · see citing works
Pacal, M., & Bremner, R. (2012) · Developmental Dynamics · doi:10.1002/dvdy.23840 · Cited by 27 · see citing works
Bilitou, A., & Ohnuma, S. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22223 · Cited by 26 · see citing works
Coordination of proliferation and neuronal differentiation by the retinoblastoma protein family
Ajioka, I. (2014) · Development Growth & Differentiation · doi:10.1111/dgd.12127 · Cited by 26 · see citing works
Application of the Neurosphere Assay for DNT Hazard Assessment: Challenges and Limitations
Baumann, J., Dach, K., Barenys, M., Giersiefer, S., Goniwiecha, J., Lein, P. J., & Fritsche, E. (2015) · Methods in pharmacology and toxicology · doi:10.1007/7653_2015_49 · Cited by 24 · see citing works
Trk activation in the secretory pathway promotes Golgi fragmentation
Schecterson, L. C., Hudson, M. P., Ko, H. M., Philippidou, P., Akmentin, W., Wiley, J. C., Rosenblum, E., Chao, M. V., Halegoua, S., & Bothwell, M. A. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.01.007 · Cited by 23 · see citing works
The transcription factor MEF2C restrains microglial overactivation by inhibiting kinase CDK2
Hu, X., Wu, J., Shi, L., Wang, F., He, K., Tan, P., Hu, Y., Yang, Y., Wang, D., Ma, T., et al. (2025) · Immunity · doi:10.1016/j.immuni.2025.02.026 · Cited by 23 · see citing works
Mesquita-Ribeiro, R., Fort, R. S., Rathbone, A., Farías, J., Lucci, C., James, V. H., Sotelo-Silveira, J. R., Duhagon, M. A., & Dajas‐Bailador, F. (2021) · RNA Biology · doi:10.1080/15476286.2021.2000792 · Cited by 21 · see citing works
Phf21b imprints the spatiotemporal epigenetic switch essential for neural stem cell differentiationPreprint
Basu, A., Mestres, I., Sahu, S. K., Tiwari, N., Khongwir, B., Baumgart, J., Singh, A. P., Calegari, F., & Tiwari, V. K. (2020) · Genes & Development · doi:10.1101/gad.333906.119 · Cited by 22 · see citing works
Common pathways for growth and for plasticity
Knafo, S., & Esteban, J. A. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.02.008 · Cited by 21 · see citing works
Core cell cycle machinery is crucially involved in both life and death of post-mitotic neurons
Marlier, Q., D’aes, T., Verteneuil, S., Vandenbosch, R., & Malgrange, B. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03548-1 · Cited by 20 · see citing works
Jiang, P., Scarpa, J. R., Gao, V. D., Vitaterna, M. H., Kasarskis, A., & Turek, F. W. (2019) · Scientific Reports · doi:10.1038/s41598-019-41248-4 · Cited by 20 · see citing works
He, Z., & Yu, Q. (2018) · BMC Genomics · doi:10.1186/s12864-018-4649-2 · Cited by 20 · see citing works
Yoon, G., Lim, Y.-H., Jo, D., Ryu, J., Song, J., & Kim, Y. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01303-x · Cited by 19 · see citing works
Mitogen Synergy: An Emerging Route to Boosting Human Beta Cell Proliferation
Shcheglova, E. G., Błaszczyk, K., & Borowiak, M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.734597 · Cited by 16 · see citing works
Web Service Composition Optimization Based on Improved Artificial Bee Colony Algorithm
He, J., Chen, L., Wang, X., & Li, Y. (2013) · Journal of Networks · doi:10.4304/jnw.8.9.2143-2149 · Cited by 17 · see citing works
Chen, X., Feng, L., Cai, B., Chen, G., & Chen, G. (2017) · PubMed Central · Cited by 17 · see citing works
Pin1 inhibition activates cyclin D and produces neurodegenerative pathology
Atabay, K. D., & Karabay, A. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07259.x · Cited by 17 · see citing works
Chen, M. J., Ng, J. M. J., Peng, Z. F., Manikandan, J., Yap, Y. W., Llanos, R. M., Beart, P. M., & Cheung, N. S. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2012.12.015 · Cited by 17 · see citing works
Poncelet, L., Garigliany, M., Ando, K., Franssen, M., Desmecht, D. J.-M., & Brion, J. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1249546 · Cited by 17 · see citing works
Advani, D., & Kumar, P. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04130-7 · Cited by 16 · see citing works
Incontro, S., Ciruela, F., Ziff, E. B., Hofmann, F. B., Sánchez‐Prieto, J., & Torres, M. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.03.021 · Cited by 16 · see citing works
Shukla, M., & Vincent, B. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230314142505 · Cited by 15 · see citing works
Ioannidis, V., Pandey, R., Bauer, H. F., Schön, M., Bockmann, J., Boeckers, T. M., & Lutz, A.-K. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02362-y · Cited by 15 · see citing works
Alternative Functions of Cell Cycle-Related and DNA Repair Proteins in Post-mitotic Neurons
Akagawa, R., Nabeshima, Y., & Kawauchi, T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.753175 · Cited by 13 · see citing works
Branch, M. R., & Hepler, J. R. (2017) · PLoS ONE · doi:10.1371/journal.pone.0184497 · Cited by 15 · see citing works
Fu, X., Lui, K. N.-C., Tang, C. S.-M., Ng, R. K., Lai, F. P.-L., Lau, S.-T., Li, Z., García-Barceló, M.-M., Sham, P. C., Tam, P. K. H., et al. (2020) · Genome Research · doi:10.1101/gr.264473.120 · Cited by 14 · see citing works
Wang, Y., He, G., He, L., & McGrath, J. J. (2011) · Schizophrenia Research · doi:10.1016/j.schres.2011.05.009 · Cited by 13 · see citing works
Neğiş, Y., Yıldız, A., Korulu, Ş., & Karabay, A. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.03.100 · Cited by 12 · see citing works
Mokhtari, M., Narayanan, B., Hamm, J. P., Soh, P., Calhoun, V. D., Ruaño, G., Kocherla, M., Windemuth, A., Clementz, B. A., Tamminga, C. A., et al. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv147 · Cited by 11 · see citing works
Identification of a transcriptional signature found in multiple models of ASD and related disordersPreprint
Thudium, S., Palozola, K. C., L'Her, É., & Korb, E. (2022) · Genome Research · doi:10.1101/gr.276591.122 · Cited by 10 · see citing works
Hawley, L. E., Stringer, M., Deal, A. J., Folz, A., Goodlett, C. R., & Roper, R. J. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106359 · Cited by 10 · see citing works
“…be attributed to the ability of DYRK1A to phosphorylate and possibly regulate Cyclin D1 (G 1 -to-S phase transition and cell proliferation) and p27 (neuronal differentiation and cell cycle exit) (Frank and Tsai, 2009; Hindley and Philpott, 2012; Najas et al., 2015; Tejedor and Hammerle, 2011).”
Schizophrenia and cancer: Is angiogenesis a missed link?
Lopes, R., Soares, R. A., Figueiredo‐Braga, M., & Coelho, R. C. (2014) · Life Sciences · doi:10.1016/j.lfs.2013.12.023 · Cited by 10 · see citing works
γ-Taxilin temporally regulates centrosome disjunction in a Nek2A-dependent manner
Makiyama, T., Higashi, S., Sakane, H., Nogami, S., & Shirataki, H. (2017) · Experimental Cell Research · doi:10.1016/j.yexcr.2017.12.004 · Cited by 10 · see citing works
Cell death in HeLa mediated by thermoplastic polyurethane with co-immobilized IFN-γ plus TNF-α
Guan, Y., Zheng, Z., Li, Z., & Liu, J. (2011) · Acta Biomaterialia · doi:10.1016/j.actbio.2011.11.023 · Cited by 10 · see citing works
Cell cycle checkpoints and pathogenesis of HIV-1 infection: a brief overview
Kurapati, K. R. V., Samikkannu, T., Atluri, V. S. R., & Nair, M. (2014) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp-2014-0018 · Cited by 9 · see citing works
Fajardo, J., MILTHORPE, B. K., & Santos, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144867 · Cited by 9 · see citing works
Transcriptional insights on the regenerative mechanics of axotomized neurons in vitro
Ng, J. M. J., Chen, M. J., Leung, J. Y. K., Peng, Z. F., Manikandan, J., Qi, R. Z., Chuah, M. I., West, A. K., Vickers, J. C., Lu, J., et al. (2011) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2011.01361.x · Cited by 9 · see citing works
Cyclin beyond the Cell Cycle: New Partners at the Synapse
Ghose, A., & Shashidhara, L. S. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.09.015 · Cited by 9 · see citing works
Thackray, A. M., Lam, B., Razak, A. S. A., Yeo, G. S. H., & Bujdoso, R. (2020) · Biochemical Journal · doi:10.1042/bcj20190872 · Cited by 9 · see citing works
Prion-induced neurotoxicity: Possible role for cell cycle activity and DNA damage response
Bujdoso, R. (2015) · World Journal of Virology · doi:10.5501/wjv.v4.i3.188 · Cited by 7 · see citing works
Protein arginine methyltransferases as regulators of cellular stress
Zaccarelli‐Magalhães, J., Citadin, C. T., Langman, J., Smith, D. J., Matuguma, L. H., Lin, H. W., & Udo, M. S. B. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.115060 · Cited by 6 · see citing works
Expression of Cyclin-D1 in Astrocytes Varies During Aging
Ciapa, B., & Granon, S. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00104 · Cited by 8 · see citing works
Aurora A moonlights in neurite extension
Lefkowitz, G. K., & Gleeson, J. G. (2009) · Nature Cell Biology · doi:10.1038/ncb0909-1053 · Cited by 7 · see citing works
Prostate Cancer Related JAZF1 Gene is Associated with Schizophrenia.
Wang, K., Zuo, L., Owusu, D., Pan, Y., & Luο, X. (2014) · PubMed · Cited by 7 · see citing works
Prion disease modelled in Drosophila
Bujdoso, R., Smith, A. D. P., Fleck, O., Spiropoulos, J., Andréoletti, O., & Thackray, A. M. (2022) · Cell and Tissue Research · doi:10.1007/s00441-022-03586-0 · Cited by 6 · see citing works
Kawauchi, T., & Nabeshima, Y. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00064 · Cited by 6 · see citing works
Novel structure in the nuclei of honey bee brain neurons revealed by immunostaining
Hurd, P. J., Grübel, K., Wojciechowski, M., Maleszka, R., & Rößler, W. (2021) · Scientific Reports · doi:10.1038/s41598-021-86078-5 · Cited by 6 · see citing works
Behavior of intracellular lipid droplets during cell division in HuH7 hepatoma cells.
Makiyama, T., Obama, T., Watanabe, Y., Chatani, M., Azetsu, Y., Kawaguchi, K., Imanaka, T., & Itabe, H. (2023) · Experimental Cell Research · doi:10.1016/j.yexcr.2023.113855 · Cited by 4 · see citing works
Towers, E. B., Shapiro, D. A., Abel, J. M., Bakhti‐Suroosh, A., Kupkova, K., Auble, D., Grant, P. A., & Lynch, W. J. (2023) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2023.01.007 · Cited by 5 · see citing works
Cellular prion protein activates Caspase 3 for apoptotic defense mechanism in astrocytes
Marques, C. M. S., Pedron, T., Batista, B. L., & Cerchiaro, G. (2021) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-021-04078-5 · Cited by 5 · see citing works
Two Faces of Evil: Cancer and Neurodegeneration
Curran, T., & Christen, Y. (2010) · Research and perspectives in Alzheimer's disease · doi:10.1007/978-3-642-16602-0 · Cited by 5 · see citing works
Cell Cycle Phase Transitions: Signposts for Aberrant Cell Cycle Reentry in Dying Mature Neurons
Liu, D. (2011) · Journal of Cytology & Histology · doi:10.4172/2157-7099.1000e101 · Cited by 4 · see citing works
Kajitani, K., Wafa, K., Pasumarthi, K. B. S., & Robertson, G. S. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.04.042 · Cited by 3 · see citing works
Editorial: Non-cell Cycle Functions of Cell Cycle Regulators
Liu, S., Chan, G. K. T., & Li, W. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00122 · Cited by 3 · see citing works
Pancreatic β-Cell Senescence: Mechanisms and Association with Diabetes
Ahmed, S. M., Elshenawy, S. E., Sedky, S., Elmehrath, A. O., & El‐Badri, N. (2021) · European Medical Journal · doi:10.33590/emj/20-00128 · Cited by 4 · see citing works
Did axons evolve by activating cytokinesis during interphase? A hypothesis on the origin of neurons
Miller, K. E., Oprea, F., Alam, S., Grodsky, A., & Craig, E. M. (2025) · Molecular Biology of the Cell · doi:10.1091/mbc.e24-12-0585 · Cited by 1 · see citing works
- Authors
- Frank, C. L., & Tsai, L.-H.
- Affiliations
- Howard Hughes Medical Institute (US)
- Broad Institute (US)
- Corresponding author
- Tsai, Li-Huei
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2009-05
- Volume
- 62
- Issue
- 3
- Pages
- 312-326
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC2757047
- OpenAlex
- W2009951375
- Cited by
- 118
- References
- 173
- Citations by year
- 2026: 5 · 2025: 2 · 2024: 4 · 2023: 5 · 2022: 4 · 2021: 6 · 2020: 9 · 2019: 7 · 2018: 3 · 2017: 6 · 2016: 4 · 2015: 7 · 2014: 8 · 2013: 10 · 2012: 7
- FWCI
- 1.14
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc-sa)
- Funders
- Howard Hughes Medical Institute
- National Institute on Aging (P01AG27916, P01AG027916)
- National Institute of Neurological Disorders and Stroke (R01 NS51876, R01NS051874)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- postmitotic neurons, neuronal migration, neuronal maturation, synaptic plasticity, axon elongation, axon pruning, dendrite morphogenesis, synapse maturation, cell cycle proteins
- MeSH terms
- Animals, Cell Movement, Gene Expression Regulation, Humans, Synaptic Transmission, Neuronal Plasticity, Neurons, Cell Cycle Proteins, Cell Proliferation, Neurogenesis
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