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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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“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
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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
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
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
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
Self-citationUbiquitin ligases: cell-cycle control and cancer
Nakayama, K. I., & Nakayama, K. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1881 · Cited by 1,450
Chen, 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
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
Giacinti, C., & Giordano, A. (2006) · Oncogene · doi:10.1038/sj.onc.1209615 · Cited by 1,263
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
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
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Soppa, U., Schumacher, J., Florencio Ortiz, V., Pasqualon, T., Tejedor, F., & Becker, W. (2014) · Cell Cycle · doi:10.4161/cc.29104 · Cited by 189
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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
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 163
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Packer, A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.03.002 · Cited by 138
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Chédotal, A. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.01.004 · Cited by 145
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Arendt, T. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8262-0 · Cited by 138
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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
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Roeder, A., Cunha, A., Ohno, C. K., & Meyerowitz, E. M. (2012) · Development · doi:10.1242/dev.082925 · Cited by 128
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 123
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 110
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 97
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
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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
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
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 67
van Leeuwen, L. A. G., & Hoozemans, J. J. M. (2015) · Acta Neuropathologica · doi:10.1007/s00401-015-1382-7 · Cited by 64
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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
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Chen, X., Zhang, Y., Cai, Q., & Yao, Z. (2012) · Journal of Neuroscience Research · doi:10.1002/jnr.22826 · Cited by 54
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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
Kawauchi, T., Shikanai, M., & Kosodo, Y. (2013) · Genes to Cells · doi:10.1111/gtc.12029 · Cited by 46
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 46
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 48
Hong, J., Zhang, H., Kawase‐Koga, Y., & Sun, T. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00151 · Cited by 44
Khazaei, M. R., & Püschel, A. W. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.055897 · Cited by 43
Patrício, P., Mateus‐Pinheiro, A., Sousa, N., & Pinto, L. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8422-x · Cited by 39
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 36
Self-citationHernández‐Ortega, K., Quiroz‐Baez, R., & Arias, C. (2011) · Neuroscience Bulletin · doi:10.1007/s12264-011-1002-z · Cited by 36
Chirivella, L., Kirstein, M., Ferrón, S. R., Domingo-Muelas, A., Durupt, F. C., Umanzor, C. A., Cano‐Jaimez, M., Pérez‐Sánchez, F., Barbacid, M., Ortega, S., et al. (2017) · Stem Cells · doi:10.1002/stem.2694 · Cited by 35
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
Yamada, M., Hirotsune, S., & Wynshaw-Boris, A. J. (2010) · Cell Adhesion & Migration · doi:10.4161/cam.4.2.10715 · Cited by 37
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
Müller, M., Lutter, D., & Püschel, A. W. (2009) · Journal of Cell Science · doi:10.1242/jcs.058230 · Cited by 35
Tsunekawa, Y., Kikkawa, T., & Osumi, N. (2014) · Development Growth & Differentiation · doi:10.1111/dgd.12135 · Cited by 30
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 29
Wesley, U. V., Hatcher, J. F., & Dempsey, R. J. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8829-z · Cited by 28
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
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 29
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
Liu, D., Ander, B. P., & Sharp, F. R. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.11.013 · Cited by 27
Pacal, M., & Bremner, R. (2012) · Developmental Dynamics · doi:10.1002/dvdy.23840 · Cited by 26
Bilitou, A., & Ohnuma, S. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22223 · Cited by 26
Coordination of proliferation and neuronal differentiation by the retinoblastoma protein family
Ajioka, I. (2014) · Development Growth & Differentiation · doi:10.1111/dgd.12127 · Cited by 28
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
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
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
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 26
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 24
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 24
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 23
Jiang, P., Scarpa, J. R., Gao, V., Vitaterna, M. H., Kasarskis, A., & Turek, F. W. (2019) · Scientific Reports · doi:10.1038/s41598-019-41248-4 · Cited by 20
He, Z., & Yu, Q. (2018) · BMC Genomics · doi:10.1186/s12864-018-4649-2 · Cited by 19
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 20
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 18
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 18
Chen, X., Feng, L., Cai, B., Chen, G., & Chen, G. (2017) · PubMed Central · Cited by 17
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
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
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
Advani, D., & Kumar, P. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04130-7 · Cited by 16
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
Shukla, M., & Vincent, B. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230314142505 · Cited by 17
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 18
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
Branch, M. R., & Hepler, J. R. (2017) · PLoS ONE · doi:10.1371/journal.pone.0184497 · Cited by 15
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
Wang, Y., He, G., He, L., & McGrath, J. J. (2011) · Schizophrenia Research · doi:10.1016/j.schres.2011.05.009 · Cited by 13
Neğiş, Y., Yıldız, A., Korulu, Ş., & Karabay, A. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.03.100 · Cited by 12
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
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
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
“…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
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
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
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
Fajardo, J., MILTHORPE, B. K., & Santos, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144867 · Cited by 9
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
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
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
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
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
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 9
Aurora A moonlights in neurite extension
Lefkowitz, G. K., & Gleeson, J. G. (2009) · Nature Cell Biology · doi:10.1038/ncb0909-1053 · Cited by 7
Prostate Cancer Related JAZF1 Gene is Associated with Schizophrenia.
Wang, K., Zuo, L., Owusu, D., Pan, Y., & Luο, X. (2014) · PubMed · Cited by 7
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
Kawauchi, T., & Nabeshima, Y. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00064 · Cited by 6
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
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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
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Metadata
- 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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