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Motor skill learning requires active central myelination
Open accessAbstract
Myelin-forming oligodendrocytes (OLs) are formed continuously in the healthy adult brain. In this work, we study the function of these late-forming cells and the myelin they produce. Learning a new motor skill (such as juggling) alters the structure of the brain’s white matter, which contains many OLs, suggesting that late-born OLs might contribute to motor learning. Consistent with this idea, we show that production of newly formed OLs is briefly accelerated in mice that learn a new skill (running on a “complex wheel” with irregularly spaced rungs). By genetically manipulating the transcription factor myelin regulatory factor in OL precursors, we blocked production of new OLs during adulthood without affecting preexisting OLs or myelin. This prevented the mice from mastering the complex wheel. Thus, generation of new OLs and myelin is important for learning motor skills.
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“In the mouse, motor learning or motor behavioral improvements require proliferation and differentiation of oligodendrocyte precursor cells (OPCs) in the white matter and motor cortex (Gibson et al., 2014 ; McKenzie et al., 2014 ; Xiao et al., 2016 ).”
From Motor learning requires myelination to reduce asynchrony and spontaneity in neural activity (2020) · cites this paper as McKenzie et al., 2014
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“We focused on the primary motor cortex (M1), as the proliferation and differentiation of M1 OPCs is accelerated, and the activity of M1 cortical neurons dynamically changes during motor learning (Huber et al., 2012 ; Masamizu et al., 2014 ; McKenzie et al., 2014 ; Peters, Chen, & Komiyama, 2014 ; Xiao et al., 2016 ).”
From Motor learning requires myelination to reduce asynchrony and spontaneity in neural activity (2020) · cites this paper as McKenzie et al., 2014
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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“In such a case, the synchronous input of myelinated long‐range axons connecting distant areas, and information processes with a high signal‐to‐noise ratio, may be important (Gibson et al., 2014 ; McKenzie et al., 2014 ; Xiao et al., 2016 ).”
From Motor learning requires myelination to reduce asynchrony and spontaneity in neural activity (2020) · cites this paper as McKenzie et al., 2014
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In the citing paper
“These assessed motor learning ability using a running wheel with irregularly spaced rungs, in which the mice had to coordinate many parts of the body to avoid missing their step, even in the first session.”
From Motor learning requires myelination to reduce asynchrony and spontaneity in neural activity (2020) · cites this paper as McKenzie et al., 2014
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“running on the wheel leads to an increase in the number of proliferating OPCs after 4 days, followed by an increase in oligodendrocytes after 8 days (20).”
From Oligodendrocyte heterogeneity in the mouse juvenile and adult central nervous system (2016) · cites this paper as [20]
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“increased motor skills were already apparent after 2 days in wild type mice, but not in mutant mice that were unable to synthesize new myelin (20)”
From Oligodendrocyte heterogeneity in the mouse juvenile and adult central nervous system (2016) · cites this paper as [20]
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“the density of BCAS1+ oligodendrocytes in the cortex remains high throughout life—in stark contrast to the white matter—supporting a physiological role in neuronal function, e.g. as effectors of adaptive cortical myelination and circuit modulation.49,50”
From BCAS1-positive oligodendrocytes enable efficient cortical remyelination in multiple sclerosis (2025) · cites this paper as [50]
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“It is now known that task learning can alter dMRI attributes (Hofstetter et al., 2013; McKenzie et al., 2014; Sampaio-Baptista et al., 2013; Xiao et al., 2016)”
From The cingulum bundle: Anatomy, function, and dysfunction (2018) · cites this paper as McKenzie et al., 2014
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“Recent evidence in animal models indicates that ongoing myelin remodeling throughout life may be important for learning, behavior, and cognition throughout adulthood (Liu et al., 2012; McKenzie et al., 2014).”
From Down Syndrome Developmental Brain Transcriptome Reveals Defective Oligodendrocyte Differentiation and Myelination (2016) · cites this paper as McKenzie et al., 2014
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“Genetic deletion of myelin regulatory factor causes deficient maturation of OPCs in mature mice, resulting in impaired motor learning (McKenzie et al., 2014 ; Xiao et al., 2016 ).”
From Motor learning requires myelination to reduce asynchrony and spontaneity in neural activity (2020) · cites this paper as McKenzie et al., 2014
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In the citing paper
“In contrast to our results, the effect of impaired myelin regulation was detected from the beginning of motor training in other studies (McKenzie et al., 2014 ; Xiao et al., 2016 ).”
From Motor learning requires myelination to reduce asynchrony and spontaneity in neural activity (2020) · cites this paper as McKenzie et al., 2014
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“a process that requires active myelination (20).”
From Oligodendrocyte heterogeneity in the mouse juvenile and adult central nervous system (2016) · cites this paper as [20]
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“suggesting that oligodendrocyte lineage cells contribute to learning already within the first 2 days.”
From Oligodendrocyte heterogeneity in the mouse juvenile and adult central nervous system (2016) · cites this paper as [20]
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“Indeed, the growing realisation that experience can alter white matter microstructure (Metzler-Baddeley et al., 2017; (McKenzie et al., 2014) Zatorre et al., 2012) highlights the problems of separating cause from effect.”
From The cingulum bundle: Anatomy, function, and dysfunction (2018) · cites this paper as McKenzie et al., 2014
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Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121
Training induces changes in white-matter architecture
Scholz, J., Klein, M. C., Behrens, T. E. J., & Johansen-Berg, H. (2009) · Nature Neuroscience · doi:10.1038/nn.2412 · Cited by 1,508
Neuronal activity promotes oligodendrogenesis and adaptive myelination in the mammalian brain
Gibson, E. M., Purger, D., Mount, C. W., Goldstein, A. K., Lin, G. L., Wood, L. S., Inema, I., Miller, S. E., Bieri, G., Zuchero, J. B., et al. (2014) · Science · doi:10.1126/science.1252304 · Cited by 1,472
Cognitive Neuroscience and the Study of Memory
Milner, B. A., Squire, L. R., & Kandel, E. R. (1998) · Neuron · doi:10.1016/s0896-6273(00)80987-3 · Cited by 1,335
Extensive piano practicing has regionally specific effects on white matter development
Bengtsson, S. L., Nagy, Z., Skare, S., Forsman, L., Forssberg, H., & Ullén, F. (2005) · Nature Neuroscience · doi:10.1038/nn1516 · Cited by 1,193
A Developmental Switch in the Response of DRG Neurons to ETS Transcription Factor Signaling
Hippenmeyer, S., Pecho‐Vrieseling, E., Sigrist, M., Portmann, T., Laengle, C., Ladle, D. R., & Arber, S. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030159 · Cited by 1,111
PDGFRA/NG2 glia generate myelinating oligodendrocytes and piriform projection neurons in adult mice
Rivers, L. E., Young, K. M., Rizzi, M., Jamen, F., Psachoulia, K., Wade, A., Kessaris, N., & Richardson, W. D. (2008) · Nature Neuroscience · doi:10.1038/nn.2220 · Cited by 961
Self-citationA critical period for social experience-dependent oligodendrocyte maturation and myelination
Makinodan, M., Rosen, K. M., Ito, S., & Corfas, G. (2012) · Science · doi:10.1126/science.1220845 · Cited by 922
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Grillner, S. E. (2006) · Neuron · doi:10.1016/j.neuron.2006.11.008 · Cited by 920
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Young, K. M., Psachoulia, K., Tripathi, R. B., Dunn, S.-J., Cossell, L., Attwell, D., Tohyama, K., & Richardson, W. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.006 · Cited by 919
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Rastoldo, G., Mahmoudi, N. E., Marouane, E., Péricat, D., Watabe, I., Toneto, A., López‐Juárez, A., Chabbert, C., & Tighilet, B. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101899 · Cited by 34
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Chen, L., Ren, S.-Y., Li, R., Liu, K., Chen, J., Yang, Y., Deng, Y.-B., Wang, H.-Z., Xiao, L., Mei, F., et al. (2021) · Neuroscience Bulletin · doi:10.1007/s12264-021-00745-1 · Cited by 34
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Capilla‐González, V., Bonsu, J. M., Redmond, K. J., García‐Verdugo, J. M., & Quiñones‐Hinojosa, A. (2016) · Stem Cell Research · doi:10.1016/j.scr.2016.02.031 · Cited by 35
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Hill, R., Nishiyama, A., & Hughes, E. G. (2023) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041425 · Cited by 36
Simoes, R. V., Muñoz‐Moreno, E., Cruz-Lemini, M., Eixarch, E., Bargalló, N., Cortés, M. S., & Gratacós, E. (2016) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2016.09.089 · Cited by 33
Boulanger, J. J., & Messier, C. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.08.018 · Cited by 35
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Hasan, M., Murugappan, S., Jun, W., Ramkrishnan, A. S., Iqbal, Z., Lee, Y., & Li, Y. (2019) · The FASEB Journal · doi:10.1096/fj.201900910r · Cited by 35
Samudyata, S., Castelo‐Branco, G., & Liu, J. (2020) · Glia · doi:10.1002/glia.23820 · Cited by 34
Chen, X., Wang, F., Gan, J., Zhang, Z., Liang, X., Li, T., Huang, N., Zhao, X., Mei, F., & Xiao, L. (2020) · Neuroscience Bulletin · doi:10.1007/s12264-019-00449-7 · Cited by 33
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Ghosh, T., Almeida, R., Zhao, C., Mannioui, A., Martin, E., Fleet, A., Chen, C. Z.-Y., Assinck, P., Ellams, S., González, G. A., et al. (2024) · Cell · doi:10.1016/j.cell.2024.01.011 · Cited by 39
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Du, X., Zhang, Z., Zhou, H., & Zhou, J. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00843-0 · Cited by 32
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Madrid, L., Initiative, A. D. N., Moreno–Grau, S., Ahmad, S., González-Pérez, A., de Rojas, I., Xia, R., Adami, P. V. M., García‐González, P., Kleineidam, L., et al. (2021) · Aging · doi:10.18632/aging.202950 · Cited by 33
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Huang, H.-T., Ho, C.-H., Sung, H.-Y., Lee, L., Chen, W.-P., Chen, Y.-W., Chen, C., Yang, C., & Tzeng, S. (2021) · Scientific Reports · doi:10.1038/s41598-021-85972-2 · Cited by 31
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Martins‐Macedo, J., Lepore, A. C., Domingues, H. S., Salgado, A. J., Gomes, E. D., & Pinto, L. (2020) · Glia · doi:10.1002/glia.23922 · Cited by 31
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Palhol, J. S. C., Balia, M., Terán, F. S.-R., Labarchède, M., Gontier, É., & Battefeld, A. (2023) · Fluids and Barriers of the CNS · doi:10.1186/s12987-023-00425-4 · Cited by 30
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Sullivan, G. M., Knutsen, A. K., Peruzzotti‐Jametti, L., Korotcov, A. V., Bosomtwi, A., Dardzinski, B. J., Bernstock, J. D., Rizzi, S., Edenhofer, F., Pluchino, S., et al. (2020) · Acta Neuropathologica Communications · doi:10.1186/s40478-020-00960-3 · Cited by 29
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Hou, J., Bi, H., Ye, Z., Huang, W., Zou, G., Zou, X., Shi, Y. S., Shen, Y., Ma, Q., Kirchhoff, F., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2455-19.2021 · Cited by 29
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Faw, T. D., Lakhani, B., Schmalbrock, P., Knopp, M. V., Lohse, K. R., Kramer, J. L. K., Liu, H., Nguyen, H. T., Phillips, E. G., Bratasz, A., et al. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113853 · Cited by 29
Tang, J., Liang, X., Dou, X., Qi, Y., Yang, C., Luo, Y., Chao, F., Zhang, L., Xiao, Q., Jiang, L. H., et al. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01747-3 · Cited by 33
Zhang, Y., Cheng, L., Liu, Y., Zhang, R., Wu, Z., Cheng, K., & Zhang, X. (2022) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.1c07594 · Cited by 29
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Zhao, Q. C., Zhu, Y., Ren, Y., Yin, S., Yu, L., Huang, R., Song, S., Hu, X., Zhu, R., Cheng, L., et al. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1049562 · Cited by 27
Chen, X., Zhang, W., Li, T., Guo, Y., Tian, Y., Wang, F., Liu, S., Shen, H., Feng, Y., & Xiao, L. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00467 · Cited by 30
Keiner, S., Niv, F., Neumann, S., Steinbach, T., Schmeer, C. W., Hornung, K., Schlenker, Y., Förster, M., Witte, O. W., & Redecker, C. (2017) · BMC Neuroscience · doi:10.1186/s12868-017-0347-2 · Cited by 32
Dong, W., Bai, J., Yuan, Q., Zhang, Y., Zhang, Y., Zhang, Z., Yang, M., Li, H., Zhao, Z., & Jiang, H. (2025) · EBioMedicine · doi:10.1016/j.ebiom.2025.105791 · Cited by 29
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Nicholson, M., Wood, R. J., Gonsalvez, D. G., Hannan, A. J., Fletcher, J. L., Xiao, J., & Murray, S. S. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15840 · Cited by 27
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Sampaio‐Baptista, C., Neyedli, H. F., Sanders, Z., Diosi, K., Havard, D., Huang, Y., Andersson, J., Lührs, M., Goebel, R., & Johansen‐Berg, H. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109890 · Cited by 26
Vancamp, P., Blay, K. L., Butruille, L., Sébillot, A., Boelen, A., DEMENEIX, B. A., & Remaud, S. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.01.002 · Cited by 28
The nociceptin receptor inhibits axonal regeneration and recovery from spinal cord injury
Sekine, Y., Siegel, C. S., Sekine-Konno, T., Cafferty, W. B. J., & Strittmatter, S. M. (2018) · Science Signaling · doi:10.1126/scisignal.aao4180 · Cited by 26
Autophagic degradation of CNS myelin maintains axon integrity
Ktena, N., Kaplanis, S. I., Kolotuev, I., Georgilis, A., Stavroulaki, V., Kallergi, E., Nikoletopoulou, V., Karagogeos, D., & Savvaki, M. (2022) · Cell Stress · doi:10.15698/cst2022.12.274 · Cited by 28
Milbocker, K. A., Smith, I. F., & Klintsova, A. Y. (2023) · Brain Plasticity · doi:10.3233/bpl-230151 · Cited by 29
The differing roles of NREM and REM sleep in the slow enhancement of skills and schemas
Pereira, S. I. R., & Lewis, P. A. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.12.005 · Cited by 29
Shimizu, T., Ishida, A., Hagiwara, M., Ueda, Y., Hattori, A., Tajiri, N., & Hida, H. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.07.002 · Cited by 27
Autoantibodies against NMDA receptor 1 modify rather than cause encephalitis
Wilke, J. B. H., Hindermann, M., Berghoff, S. A., Zihsler, S., Arinrad, S., Ronnenberg, A., Barnkothe, N., Steixner-Kumar, A. A., Röglin, S., STÖCKER, W., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01238-3 · Cited by 26
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Wang, S., Wang, Y., & Zou, S. (2022) · Current Issues in Molecular Biology · doi:10.3390/cimb44050149 · Cited by 24
Tissue-Engineered Models of the Human Brain: State-of-the-Art Analysis and Challenges
Tarricone, G., Carmagnola, I., & Chiono, V. (2022) · Journal of Functional Biomaterials · doi:10.3390/jfb13030146 · Cited by 30
The Shh receptor Boc is important for myelin formation and repair
Zakaria, M., Ferent, J., Hristovska, I., Laouarem, Y., Zahaf, A., Kassoussi, A., Mayeur, M.-E., Pascual, O., Charron, F., & Traiffort, É. (2019) · Development · doi:10.1242/dev.172502 · Cited by 28
Kasuga, Y., Fudge, A. D., Zhang, Y., & Li, H. (2019) · Glia · doi:10.1002/glia.23684 · Cited by 23
Self-citationRegulation of lipid synthesis in myelin modulates neural activity and is required for motor learning
Kato, D., Aoyama, Y., Nishida, K., Takahashi, Y., Sakamoto, T., Takeda, I., Tatematsu, T., Go, S., Saito, Y., Kunishima, S., et al. (2023) · Glia · doi:10.1002/glia.24441 · Cited by 25
Cai, Y., Pinheiro‐de‐Sousa, I., Slobodyanyuk, M., Chen, F., Huynh, T., Kanyo, J. E., Tang, P., Fuentes, L. A., Braker, A., Welch, R., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-01973-8 · Cited by 34
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O’Rourke, M., Cullen, C. L., Auderset, L., Pitman, K. A., Achatz, D. E., Gasperini, R., & Young, K. M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0162858 · Cited by 30
Gallardo, N. D. L. V., Peñalva, R. G., Dittmer, M., Naughton, M., Falconer, J., Moffat, J., de la Fuente, A. G., Hombrebueno, J. R., Lin, Z., Perbal, B., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1922089117 · Cited by 25
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Sengottuvel, V., Hota, M., Oh, J., Galam, D. L. A., Wong, B. H., Wenk, M. R., Ghosh, S., Torta, F. T., & Silver, D. L. (2023) · Journal of Clinical Investigation · doi:10.1172/jci164118 · Cited by 25
Zhou, B., Feng, C., Sun, S., Chen, X., Zhuansun, D., Wang, D., Yu, X., Meng, X., Xiao, J., Wu, L., et al. (2024) · Developmental Cell · doi:10.1016/j.devcel.2024.03.034 · Cited by 29
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Teo, R. T. Y., Bardile, C. F., Tay, Y. L., Yusof, N. A. B. M., Kreidy, C., Tan, L. J., & Pouladi, M. A. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1579-1 · Cited by 25
White matter alterations in Williams syndrome related to behavioral and motor impairments
Nir, A., & Barak, B. (2020) · Glia · doi:10.1002/glia.23868 · Cited by 26
Mercier, O., Quilichini, P., Magalon, K., Gil, F., Ghestem, A., Richard, F., Boudier, T., Cayre, M., & Durbec, P. (2024) · Glia · doi:10.1002/glia.24513 · Cited by 25
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Zollinger, D. R., Baalman, K. L., & Rasband, M. N. (2015) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100913-013107 · Cited by 24
Tanaka, T., Ohno, N., Osanai, Y., Saitoh, S., Thai, T. Q., Nishimura, K., Shinjo, T., Takemura, S., Tatsumi, K., & Wanaka, A. (2021) · Glia · doi:10.1002/glia.24055 · Cited by 25
Disrupted myelination network in the cingulate cortex of Parkinson's disease
Xie, S., Yang, J., Huang, S., Fan, Y., Xu, T., He, J., Guo, J., Ji, X., Wang, Z., Li, P., et al. (2022) · IET Systems Biology · doi:10.1049/syb2.12043 · Cited by 26
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Wang, J., Yang, L., Jiang, M., Zhao, C., Liu, X., Berry, K., Waisman, A., Langseth, A. J., Novitch, B. G., Bergles, D. E., et al. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0237-22.2022 · Cited by 23
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Tseng, C., Chien, Y., Lee, N., Hsu, Y., Peng, S., Tseng, W. I., & Hwu, W. (2019) · Annals of Neurology · doi:10.1002/ana.25467 · Cited by 24
Development of the Nervous System
Yuskaitis, C. J., & Pomeroy, S. L. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-35214-7.00131-1 · Cited by 24
Rapid cycle deliberate practice approach on resuscitation training: A systematic review
Abelairas‐Gómez, C., Cortegiani, A., Sawyer, T., Greif, R. T., Donoghue, A. J., Anderson, N., Bhanji, F., Breckwoldt, J., Cheng, A., Eastwood, K., et al. (2024) · Resuscitation Plus · doi:10.1016/j.resplu.2024.100648 · Cited by 23
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Ghorbani, S., Li, C., Lozinski, B. M., Moezzi, D., D’Mello, C., Dong, Y., Visser, F., Li, H., Silva, C., Khakpour, M., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci176910 · Cited by 23
Self-citationIntegrin-Linked Kinase (ILK) Deletion Disrupts Oligodendrocyte Development by Altering Cell Cycle
Hussain, R., & Macklin, W. B. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2113-16.2016 · Cited by 22
The effects of developmental and current niches on oligodendrocyte precursor dynamics and fate
Boshans, L. L., Sherafat, A., & Nishiyama, A. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.134593 · Cited by 24
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Hide, T., & Komohara, Y. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-37184-5_8 · Cited by 23
Guzman, K., Brink, L. E., Bey, G. R., Bodnar, R. J., Kuang, L., Xing, B., Sullivan, M. L. G., Park, H. J., Koppes, E., Zhu, H., et al. (2020) · Glia · doi:10.1002/glia.23825 · Cited by 23
Mediavilla, T., Özalay, Ö., Estévez-Silva, H. M., Frias, B., Orädd, G., Sultan, F. R., Brozzoli, C., Garzón, B., Lövdén, M., & Marcellino, D. J. (2022) · eLife · doi:10.7554/elife.77432 · Cited by 26
Metadata
- Authors
- McKenzie, I. A., Ohayon, D., Li, H., Paes de Faria, J., Emery, B., Tohyama, K., & Richardson, W. D.
- Affiliations
- University College London (GB)
- The Wolfson Institute for Biomedical Research, University College London, Gower Street, London WC1E 6BT, UK.
- The University of Melbourne (AU)
- Iwate Medical University (JP)
- Corresponding author
- McKenzie, Ian A.
- Ohayon, David
- Richardson, William D.
- Venue
- Science
- Published
- 2014-10-17
- Volume
- 346
- Issue
- 6207
- Pages
- 318-322
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC6324726
- OpenAlex
- W2085529478
- Cited by
- 1,177
- References
- 36
- Citations by year
- 2026: 68 · 2025: 90 · 2024: 103 · 2023: 107 · 2022: 101 · 2021: 146 · 2020: 108 · 2019: 122 · 2018: 83 · 2017: 101 · 2016: 88 · 2015: 53 · 2014: 3
- FWCI
- 28.41
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Wellcome Trust (100269, 100269/Z/12/Z, 066745)
- Biotechnology and Biological Sciences Research Council (BB/L003236/1)
- Japan Society for the Promotion of Science (24650181)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Keywords
- motor skill learning, oligodendrocyte myelination, adult neurogenesis, white matter plasticity, oligodendrocyte precursor cells, juggling
- MeSH terms
- Animals, Brain, Humans, Learning, Male, Mice, Transgenic, Motor Skills, Myelin Sheath, Synaptic Transmission, Oligodendroglia, Mental Recall, Transcription Factors, Gene Deletion, Cell Proliferation, Mice
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