The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.
Regulation of Oligodendrocyte Differentiation and Myelination
Abstract
Despite the importance of myelin for the rapid conduction of action potentials, the molecular bases of oligodendrocyte differentiation and central nervous system (CNS) myelination are still incompletely understood. Recent results have greatly advanced this understanding, identifying new transcriptional regulators of myelin gene expression, elucidating vital roles for microRNAs in controlling myelination, and clarifying the extracellular signaling mechanisms that orchestrate the development of myelin. Studies have also demonstrated an unexpected level of plasticity of myelin in the adult CNS. These recent advances provide new insight into how remyelination may be stimulated in demyelinating disorders such as multiple sclerosis.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Myelin formation by oligodendrocytes surrounding axons in the central nervous system regulates conduction velocity (CV), which is a key component of fast and efficient information processing in the brain (Emery, 2010 ; Fields, 2008 ; Nave, 2010 ).”
From Motor learning requires myelination to reduce asynchrony and spontaneity in neural activity (2020) · cites this paper as Emery, 2010
In the citing paper
“Myelin formation by oligodendrocytes surrounding axons in the central nervous system regulates conduction velocity (CV), which is a key component of fast and efficient information processing in the brain (Emery, 2010 ; Fields, 2008 ; Nave, 2010 ).”
From Motor learning requires myelination to reduce asynchrony and spontaneity in neural activity (2020) · cites this paper as Emery, 2010
In the citing paper
“To that end, we have selected a 2.2 kb region upstream of the transcription start site in the human MAG gene and two truncated variants, that harbor an abundance of binding motifs for transcription factors known to regulate gene activity and myelination in oligodendrocytes or Schwann cells (Emery, 2010).”
From Recombinant Human Myelin-Associated Glycoprotein Promoter Drives Selective AAV-Mediated Transgene Expression in Oligodendrocytes (2016) · cites this paper as Emery, 2010
In the citing paper
“This discrepancy could be due to OPCs differentiating into pre-myelinating oligodendrocytes [14] (also see below), which are not myelinating the axons due to continuous cuprizone lesion.”
From Strain differences in cuprizone induced demyelination (2017) · cites this paper as [14]
In the citing paper
“MicroRNAs (miRs) regulate diverse molecular and cellular processes including oligodendrocyte (OL) precursor cell (OPC) proliferation and differentiation in rodents.”
From Regulation of miRNA 219 and miRNA Clusters 338 and 17-92 in Oligodendrocytes (2012) · cites this paper as Emery, 2010
Citations
Cites
Cahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129
Self-citationTraining 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
Structural maturation of neural pathways in children and adolescents: in vivo study
Paus, T., Zijdenbos, A., Worsley, K., Collins, D. L., Blumenthal, J., Giedd, J. N., Rapoport, J. L., & Evans, A. C. (1999) · Science · doi:10.1126/science.283.5409.1908 · Cited by 1,322
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 translational profiling approach for the molecular characterization of CNS cell types
Heiman, M., Schaefer, A., Gong, S., Peterson, J. D., Day, M., Ramsey, K. E., Suárez-Fariñas, M., Schwarz, C., Stephan, D. A., Surmeier, D. J., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.028 · Cited by 1,134
Lu, Q. R., Sun, T., Zhu, Z., Ma, N., Garcia, M., Stiles, C. D., & Rowitch, D. H. (2002) · Cell · doi:10.1016/s0092-8674(02)00678-5 · Cited by 1,087
Glutamatergic synapses on oligodendrocyte precursor cells in the hippocampus
Bergles, D. E., Roberts, J. D. B., Somogyi, P., & Jahr, C. E. (2000) · Nature · doi:10.1038/35012083 · Cited by 1,062
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
Oligodendrocyte dysfunction in schizophrenia and bipolar disorder.
Tkachev, D., Mimmack, M., Ryan, M. M., Wayland, M., Freeman, T., Jones, P., Starkey, M., Webster, M., Yolken, R., & Bahn, S. (2003) · The Lancet · doi:10.1016/s0140-6736(03)14289-4 · Cited by 940
Benes, F. M. (1994) · Archives of General Psychiatry · doi:10.1001/archpsyc.1994.03950060041004 · Cited by 744
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 654
Promotion of Remyelination by Sulfasalazine in a Transgenic Zebrafish Model of Demyelination
Kim, S., Lee, Y.-I., Chang, K.-Y., Lee, D.-W., Cho, S. C., Ha, Y. W., Na, J. E., Rhyu, I. J., Park, S. C., & Park, H. (2015) · Molecules and Cells · doi:10.14348/molcells.2015.0246 · Cited by 26
Pinocembrin Promotes OPC Differentiation and Remyelination via the mTOR Signaling Pathway
Shao, Q., Zhao, M., Pei, W., Pu, Y., Liu, M., Liu, W., Yu, Z., Chen, K., Liu, H., Deng, B., et al. (2021) · Neuroscience Bulletin · doi:10.1007/s12264-021-00696-7 · Cited by 25
Extracellular Vesicles, Stem Cells and the Role of miRNAs in Neurodegeneration
MARATOVICH, B. A., Al-Yozbaki, M., George, A., Niyazova, R. Y., Sharipov, K. O., Byrne, L. J., & Wilson, C. M. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210817150141 · Cited by 27
Cristobal, C. D., Wang, C.-Y., Zuo, Z., Smith, J. A., Lindeke-Myers, A., Bellen, H. J., & Lee, H. K. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1517-21.2022 · Cited by 28
Park, S., Ahn, E. S., & Kim, Y. (2014) · Cell Biology International · doi:10.1002/cbin.10401 · Cited by 25
Impaired Remyelination in a Mouse Model of Huntington Disease
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
Stimulating myelin restoration with BDNF: a promising therapeutic approach for Alzheimer's disease
Zota, I., Chanoumidou, K., Gravanis, A., & Charalampopoulos, I. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1422130 · Cited by 25
Vasistha, N. A., Johnstone, M., Barton, S. K., Mayerl, S. E., Selvaraj, B. T., Thomson, P. A., Dando, O., Grünewald, E., Alloza, C., Bastin, M. E., et al. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0505-2 · Cited by 21
Oligodendrocyte differentiation alters tRNA modifications and codon optimality-mediated mRNA decay
Martin, S., Allan, K. C., Pinkard, O. W., Sweet, T. J., Tesar, P. J., & Coller, J. (2022) · Nature Communications · doi:10.1038/s41467-022-32766-3 · Cited by 25
Olig2Ablation in Immature Oligodendrocytes Does Not Enhance CNS Myelination and Remyelination
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
Oligodendrocyte lineage cells: Advances in development, disease, and heterogeneity
Wang, J., Gao, M.-Y., Gao, R., Zhao, K., Zhang, Y., & Li, X. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15728 · Cited by 24
A Critical Cell-Intrinsic Role for Serum Response Factor in Glial Specification in the CNS
Lu, P., & Ramanan, N. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5633-11.2012 · Cited by 27
Schmidt, F., van den Eijnden, M., Gobert, R. P., Saborı́o, G. P., Carboni, S., Alliod, C., Pouly, S., Staugaitis, S. M., Dutta, R., Trapp, B. D., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040457 · Cited by 24
Remyelinating strategies in multiple sclerosis
Luessi, F., Kuhlmann, T., & Zipp, F. (2014) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.2014.969241 · Cited by 24
Morrison, V. E., Smith, V. N., & Huang, J. K. (2019) · eNeuro · doi:10.1523/eneuro.0270-19.2019 · Cited by 27
Moyon, S., Liang, J., & Casaccia, P. (2015) · Brain Research · doi:10.1016/j.brainres.2015.06.009 · 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
Integrin-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
Stage‐specific regulation of oligodendrocyte development by Hedgehog signaling in the spinal cord
Xu, X., Yu, Q., Fang, M., Yi, M., Yang, A., Xie, B., Yang, J., Zhang, Z., Dai, Z., & Qiu, M. S. (2019) · Glia · doi:10.1002/glia.23729 · Cited by 23
WWOX-Related Neurodevelopmental Disorders: Models and Future Perspectives
Steinberg, D. J., & Aqeilan, R. I. (2021) · Cells · doi:10.3390/cells10113082 · Cited by 22
Huang, Z., Zhang, Y., Ma, X., Feng, Y., Zong, X., Jordan, J. D., & Zhang, Q. (2023) · Theranostics · doi:10.7150/thno.78777 · Cited by 24
Social Experience-Dependent Myelination: An Implication for Psychiatric Disorders
Toritsuka, M., Makinodan, M., & Kishimoto, T. (2015) · Neural Plasticity · doi:10.1155/2015/465345 · Cited by 24
A method for deriving homogenous population of oligodendrocytes from mouse embryonic stem cells
Neman, J., & de Vellis, J. (2012) · Developmental Neurobiology · doi:10.1002/dneu.22008 · Cited by 23
Li, Z., Yao, F., Li, C., Cheng, W., Qi, L., Yu, S., Zhang, L., Zha, X., & Jing, J. (2018) · Journal of Orthopaedic Research® · doi:10.1002/jor.24172 · Cited by 23
Uncovering the biology of myelin with optical imaging of the live brain
Hill, R., & Grutzendler, J. (2019) · Glia · doi:10.1002/glia.23635 · Cited by 23
Agenesis and Hypomyelination of Corpus Callosum in Mice Lacking Nsun5, an RNA Methyltransferase
Yuan, Z., Chen, P., Zhang, T., Shen, B., & Chen, L. (2019) · Cells · doi:10.3390/cells8060552 · Cited by 23
Wang, C., Deneen, B., & Tzeng, S. (2019) · Glia · doi:10.1002/glia.23660 · Cited by 23
White matter disturbances in phenylketonuria: Possible underlying mechanisms
Ferreira, B. K., Rodrigues, M. T., STRECK, E. L., Ferreira, G. C., & Schuck, P. F. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24598 · Cited by 25
Development of type I/II oligodendrocytes regulated by teneurin-4 in the murine spinal cord
Hayashi, C., Suzuki, N., Takahashi, R., & Akazawa, C. (2020) · Scientific Reports · doi:10.1038/s41598-020-65485-0 · Cited by 24
Thymosin beta4 promotes oligodendrogenesis in the demyelinating central nervous system
Zhang, J., Zhang, Z. G., Li, Y., Lü, M., Zhang, Y., Elias, S. B., & Chopp, M. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.01.010 · Cited by 24
OPALIN is an LGI1 receptor promoting oligodendrocyte differentiation
Teng, X., Hu, P., Zhang, C.-M., Zhang, Q.-X., Yang, G., Zang, Y., Liu, Z., Chen, G., & Shi, Y. S. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2403652121 · Cited by 22
The shifting landscape of the preterm brain
Kratimenos, P., Sanidas, G., Simonti, G., Byrd, C. E., & Gallo, V. (2025) · Neuron · doi:10.1016/j.neuron.2025.03.024 · Cited by 28
Pazhouhandeh, M., Sahraian, M. A., Siadat, S. D., Fateh, A., Vaziri, F., Tabrizi, F. H. A., Ajorloo, F., Arshadi, A. K., Fatemi, E., Piri‐Gavgani, S., et al. (2017) · Clinical & Experimental Immunology · doi:10.1111/cei.13087 · Cited by 22
Rapid and Specific Immunomagnetic Isolation of Mouse Primary Oligodendrocytes
Flores‐Obando, R. E., Freidin, M. M., & Abrams, C. K. (2018) · Journal of Visualized Experiments · doi:10.3791/57543 · Cited by 23
Histone Deacetylase SIRT1 Mediates C5b-9-Induced Cell Cycle in Oligodendrocytes
Tatomir, A., Rao, G. G., Boodhoo, D., Vlaicu, S. I., Beltrand, A., Anselmo, F., Rus, V., & Rus, H. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00619 · Cited by 22
Chronic Exposure to Alcohol Inhibits New Myelin Generation in Adult Mouse Brain
Guo, F., Zhang, Y., Liu, K., Huang, X., Li, R., Wang, S., Wang, F., Xiao, L., Mei, F., & Li, T. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.732602 · Cited by 22
Wei, W., Yin, Y., Zhang, Y., Li, X., Li, M., Guo, W., Wang, Q., Deng, W., Ma, X., Zhao, L., et al. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab337 · Cited by 21
Wang, X., Zang, J., Yang, Y., Lu, S., Guan, Q., Ye, D., Wang, Z., Zhou, H., Li, K., Wang, Q., et al. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.749244 · Cited by 22
Epigenetic Mechanisms Regulating Differentiation of Neural Stem/Precursor Cells
Adefuin, A. M. D., Kimura, A., Noguchi, H., Nakashima, K., & Namihira, M. (2014) · Epigenomics · doi:10.2217/epi.14.53 · Cited by 24
Inhibitory milieu at the multiple sclerosis lesion site and the challenges for remyelination
Galloway, D. A., Gowing, E., Setayeshgar, S., & Kothary, R. (2019) · Glia · doi:10.1002/glia.23711 · Cited by 23
Dong, F., Liu, D., Jiang, F., Liu, Y., Wu, X., Qu, X., Liu, J., Chen, Y., Fan, H., & Yao, R. (2020) · Neuroscience Bulletin · doi:10.1007/s12264-020-00583-7 · Cited by 22
Lee, J. B., Affeldt, B. M., Gamboa, Y., Hamer, M., Dunn, J. F., Pardo, A. C., & Obenaus, A. (2018) · Developmental Neuroscience · doi:10.1159/000494134 · Cited by 21
Nie, B.-X., Zhao, G., Yuan, X.-F., Yu, L.-X., Zhang, J., Yuan, Y., Liu, Y. Z., Hu, J., Song, E., Zhou, Y., et al. (2021) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2021.102053 · Cited by 21
Emerging mitochondrial‐mediated mechanisms involved in oligodendrocyte development
Gil, M., & Gama, V. (2022) · Journal of Neuroscience Research · doi:10.1002/jnr.25151 · Cited by 24
Myelination dictates axonal viscoelasticity
Chuang, Y., Alcantara, A., Fabris, G., Abderezaei, J., Lu, T., Melendez‐Vasquez, C. V., & Kurt, M. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.15954 · Cited by 20
Zhou, L., Shao, C., Xu, S., Ma, J., Xie, Y., Zhou, L., Teng, P., Wang, Y., Qiu, M. S., & Shen, Y. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8678-9 · Cited by 21
Unwrapping Neurotrophic Cytokines and Histone Modification
Roe, C. (2016) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-016-0330-y · Cited by 21
Liang, S., Yin, N., & Faiola, F. (2019) · Stem Cells and Development · doi:10.1089/scd.2019.0007 · Cited by 21
Schwann cells: Rescuers of central demyelination
García-Díaz, B., & Evercooren, A. B. (2020) · Glia · doi:10.1002/glia.23788 · Cited by 21
Scott, K., O’Rourke, R., Gillen, A. E., & Appel, B. (2020) · Development · doi:10.1242/dev.191023 · Cited by 21
Epigenetic Mechanisms Underlying Adult Post Stroke Neurogenesis
Liu, X., Fan, B., Chopp, M., & Zhang, Z. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21176179 · Cited by 23
Intra- and intercellular trafficking in sphingolipid metabolism in myelination
Wattenberg, B. W. (2018) · Advances in Biological Regulation · doi:10.1016/j.jbior.2018.11.002 · Cited by 21
POLR3-Related Leukodystrophy: Exploring Potential Therapeutic Approaches
Perrier, S., Michell‐Robinson, M. A., & Bernard, G. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.631802 · Cited by 23
Tauheed, A. M., Ayo, J. O., & Kawu, M. U. (2016) · Pathophysiology · doi:10.1016/j.pathophys.2016.05.007 · Cited by 23
Investigation of Oligodendrocyte Precursor Cell Differentiation by Quantitative Proteomics
Schoor, C., Brocke‐Ahmadinejad, N., Gieselmann, V., & Winter, D. (2019) · PROTEOMICS · doi:10.1002/pmic.201900057 · Cited by 20
Joly, O., Rousié, D., Jissendi, P., Rousié, M., & Frankó, E. (2014) · European Spine Journal · doi:10.1007/s00586-014-3435-3 · Cited by 21
Myelin and traumatic brain injury: The copper deficiency hypothesis
Klevay, L. M. (2013) · Medical Hypotheses · doi:10.1016/j.mehy.2013.09.011 · Cited by 20
Kupferman, A., & Leibowitz, H. M. (1975) · PubMed · Cited by 20
Fekete, C. D., & Nishiyama, A. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1041853 · Cited by 21
Whole Transcriptome Screening Reveals Myelination Deficits in Dysplastic Human Temporal Neocortex
Donkels, C., Pfeifer, D., Janz, P., Huber, S., Nakagawa, J. M., Prinz, M., Schulze‐Bonhage, A., Weyerbrock, A., Zentner, J., & Haas, C. A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv346 · Cited by 18
The extracellular domain of teneurin-4 promotes cell adhesion for oligodendrocyte differentiation
Hayashi, C., Suzuki, N., Mabuchi, Y., Kikura, N., Hosoda, Y., de Vega, S., & Akazawa, C. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.12.002 · Cited by 19
Jamet, M., Dupuis, L., & de Aguilar, J. G. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1375330 · Cited by 18
MicroRNAs: A Light into the “Black Box” of Neuropediatric Diseases?
Omran, A. G., Elimam, D., Shalaby, S., Peng, J., & Yin, F. (2012) · NeuroMolecular Medicine · doi:10.1007/s12017-012-8193-y · Cited by 18
Sirt2 epigenetically down-regulates PDGFRα expression and promotes CG4 cell differentiation
Fang, N., Cheng, J., Zhang, C., Chen, K., Zhang, C., Hu, Z., Bi, R., Furber, K. L., Thangaraj, M. P., Nazarali, A. J., et al. (2019) · Cell Cycle · doi:10.1080/15384101.2019.1609818 · Cited by 18
Xue, Y., Zhu, X., Yan, W., Zhang, Z., Cui, E., Wu, Y., Li, C., Pan, J., Yan, Q., Chai, X., et al. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.860280 · Cited by 19
Deng, X., Hu, Z., Zhou, S., Wu, Y., Fu, M., Zhou, C., Sun, J., Gao, X., & Huang, Y. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14510 · Cited by 19
Wang, W., Wang, Y., Su, L., Zhang, M., Zhang, T., Zhao, J., Ma, H., Zhang, D., Ji, F., Jiao, R. D., et al. (2024) · Advanced Science · doi:10.1002/advs.202308508 · Cited by 18
Novel roles of oligodendrocyte precursor cells in the developing and damaged brain
Maki, T. (2017) · Clinical and Experimental Neuroimmunology · doi:10.1111/cen3.12358 · Cited by 18
Lukoshe, A., van den Bosch, G. E., van der Lugt, A., Kushner, S. A., Hokken‐Koelega, A. C. S., & White, T. J. H. (2017) · Schizophrenia Bulletin · doi:10.1093/schbul/sbx052 · Cited by 18
Are Sigma Receptor Modulators a Weapon Against Multiple Sclerosis Disease?
Collina, S., Rui, M., Stotani, S., Bignardi, E., Rossi, D., Curti, D., Giordanetto, F., Malacrida, A., Scuteri, A., & Cavaletti, G. (2017) · Future Medicinal Chemistry · doi:10.4155/fmc-2017-0122 · Cited by 17
Arcuri, C., Mecca, C., Giambanco, I., & Donato, R. (2019) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2019.04.005 · Cited by 19
Li, S., Zheng, J., Chai, L., Lin, M., Zeng, R., Lu, J., & Bian, J. T. (2019) · Developmental Neuroscience · doi:10.1159/000499364 · Cited by 18
Meco, E., Zheng, W., Sharma, A. H., & Lampe, K. J. (2020) · Biomacromolecules · doi:10.1021/acs.biomac.0c00828 · Cited by 18
Oligodendrocytes Development and Wnt Signaling Pathway
Soomro, S. H., Jie, J., & Fu, H. Q. (2018) · International Journal of Human Anatomy · doi:10.14302/issn.2577-2279.ijha-18-2407 · Cited by 19
Aspirin Promotes Oligodendroglial Differentiation Through Inhibition of Wnt Signaling Pathway
Huang, N., Dong, C., Wu, X., Chen, X., Zhang, X., Niu, J., Shen, H., & Xiao, L. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9241-z · Cited by 17
Oligodendrocytes and myelination: pioneering new frontiers in cognitive neuroscience
Zhang, N., Yi, R., Zhong, F., Lu, Y., Chen, W., Ke, Z., Zhang, Y., Zhou, L., Wang, P., & Wei, L. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1618468 · Cited by 22
Regulation of Glial Function by Noncoding RNA in Central Nervous System Disease
Bai, Y., Ren, H., Bian, L., Zhou, Y., Wang, X., Xiong, Z., Liu, Z., Han, B., & Yao, H. (2022) · Neuroscience Bulletin · doi:10.1007/s12264-022-00950-6 · Cited by 16
Environmental tobacco smoke in the early postnatal period induces impairment in brain myelination
Torres, L. H., Annoni, R., Balestrin, N. T., Coleto, P. L., Duro, S. D. O., Garcia, R. C. T., Pacheco-Neto, M., Mauad, T., Camarini, R., Britto, L. R., et al. (2014) · Archives of Toxicology · doi:10.1007/s00204-014-1343-2 · Cited by 16
Cdon, a cell surface protein, mediates oligodendrocyte differentiation and myelination
Wang, L., & Almazán, G. (2016) · Glia · doi:10.1002/glia.22980 · Cited by 17
Li, F., Zhou, M., Liu, N., Yang, Y.-Y., Xing, H.-Y., Lu, Y., & Liu, X.-X. (2019) · Neural Plasticity · doi:10.1155/2019/9610687 · Cited by 17
Glial cells as therapeutic targets in progressive multiple sclerosis
Wilbanks, B., Maher, L., & Rodriguez, M. (2019) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2019.1614443 · Cited by 17
Livin’ On The Edge: glia shape nervous system transition zones
Fontenas, L., & Kucenas, S. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.09.008 · Cited by 17
Go and stop signals for glial regeneration
Hidalgo, A., & Logan, A. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.10.011 · Cited by 16
Chen, X., Liu, H., Gan, J., Wang, X., Yu, G., Li, T., Liang, X., Yu, B., & Xiao, L. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00984 · Cited by 17
Buttigieg, J. A., Eftekharpour, E., Karimi‐Abdolrezaee, S., & Fehlings, M. G. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07789.x · Cited by 17
Cation Channel TMEM63A Autonomously Facilitates Oligodendrocyte Differentiation at an Early Stage
Wang, Y., Wu, D., Zhan, Y., Li, F., Zang, Y., Teng, X., Zhang, L., Duan, G., Wang, H., Xu, R., et al. (2025) · Neuroscience Bulletin · doi:10.1007/s12264-024-01338-4 · Cited by 16
Fu, W., Che, X., Tan, J., Cui, S., Ma, Y., Xu, D., Long, H., Yang, X., Wen, T., & He, Z. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14452 · Cited by 16
Deep brain stimulation induces white matter remodeling and functional changes to brain-wide networks
Fujimoto, S. H., Fujimoto, A., Elorette, C., Seltzer, A., Andraka, E., Herbert, K., Verma, G., Janssen, W. G. M., Fleysher, L., Folloni, D., et al. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02301-4 · Cited by 17
CLC-2 is a positive modulator of oligodendrocyte precursor cell differentiation and myelination
Hou, X., Zhang, R., Wang, J., Li, Y., Li, F., Zhang, Y., Zheng, X., Shen, Y., Wang, Y., & Zhou, L. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.8439 · Cited by 16
Repurposing of omeprazole for oligodendrocyte differentiation and remyelination
Zhu, K., Sun, J., Zheng, K., Zou, Z., Wu, X., Wang, Y.-Q., Wu, G.-C., Harris, R. A., & Wang, J. (2018) · Brain Research · doi:10.1016/j.brainres.2018.12.037 · Cited by 16
Dynamic Lamin B1-Gene Association During Oligodendrocyte Progenitor Differentiation
Yattah, C., Hernandez, M., Huang, D., Park, H., Liao, W., & Casaccia, P. (2020) · Neurochemical Research · doi:10.1007/s11064-019-02941-y · Cited by 16
TRO19622 promotes myelin repair in a rat model of demyelination
Li, Y., Zhang, Y., Han, W., Hu, F., Qian, Y., & Chen, Q. (2013) · International Journal of Neuroscience · doi:10.3109/00207454.2013.804523 · Cited by 16
Gonsior, C., Binamé, F., Frühbeis, C., Bauer, N., Hoch-Kraft, P., Luhmann, H. J., Trotter, J., & White, R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0089423 · Cited by 16
Morris, J. K., Chomyk, A. M., Song, P., Parker, N., Deckard, S. A., Trapp, B. D., Pimplikar, S. W., & Dutta, R. (2015) · Invertebrate Neuroscience · doi:10.1007/s10158-015-0180-1 · Cited by 17
Manipulating oligodendrocyte intrinsic regeneration mechanism to promote remyelination
Binamé, F., Pham-Van, L. D., & Bagnard, D. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03852-4 · Cited by 16
Thirty years of BDNF study in central myelination: From biology to therapy
Xiao, J. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15968 · Cited by 16
Brain-peripheral cell crosstalk in white matter damage and repair
Hayakawa, K., & Lo, E. H. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2015.08.006 · Cited by 15
Kelly, S., Morris, D. W., Mothersill, O., Rose, E. J., Fahey, C., O'Brien, C. L., O’Hanlon, E., Gill, M., Corvin, A. P., & Donohoe, G. J. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.05.002 · Cited by 15
C21orf91 Regulates Oligodendroglial Precursor Cell Fate—A Switch in the Glial Lineage?
Reiche, L., Göttle, P., Lane, L., Duek, P. D., Park, M., Azim, K., Schütte, J., Manousi, A., Schira‐Heinen, J., & Küry, P. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.653075 · Cited by 17
Suo, N., He, B., Cui, S.-H., Yang, Y., Wang, M., Yuan, Q., & Xie, X. (2022) · Glia · doi:10.1002/glia.24233 · Cited by 15
Metadata
- Authors
- Emery, B.
- Affiliations
- The University of Melbourne (AU)
- Corresponding author
- Emery, Ben
- ORCID
- Emery, Ben
- Venue
- Science
- Published
- 2010-11-05
- Volume
- 330
- Issue
- 6005
- Pages
- 779-782
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2001810970
- Cited by
- 653
- References
- 54
- Citations by year
- 2026: 28 · 2025: 23 · 2024: 37 · 2023: 32 · 2022: 50 · 2021: 46 · 2020: 45 · 2019: 50 · 2018: 32 · 2017: 35 · 2016: 40 · 2015: 54 · 2014: 51 · 2013: 50 · 2012: 39
- FWCI
- 3.25
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- oligodendrocyte differentiation, myelination, myelin gene expression, transcription factors, microRNA, extracellular signaling, myelin plasticity, remyelination, demyelinating disease, multiple sclerosis, central nervous system
- MeSH terms
- Animals, Axons, Cell Differentiation, Central Nervous System, Demyelinating Diseases, Gene Expression Regulation, Humans, Myelin Sheath, Oligodendroglia, Transcription, Genetic, Signal Transduction, MicroRNAs, Chromatin Assembly and Disassembly
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review