The DOI matches its Crossref record; 38 of the 39 references it cites were found in a registry or an index.
Dynamics of oligodendrocyte generation in multiple sclerosis
Open accessAbstract
Oligodendrocytes wrap nerve fibres in the central nervous system with layers of specialized cell membrane to form myelin sheaths 1. Myelin is destroyed by the immune system in multiple sclerosis, but myelin is thought to regenerate and neurological function can be recovered. In animal models of demyelinating disease, myelin is regenerated by newly generated oligodendrocytes, and remaining mature oligodendrocytes do not seem to contribute to this process 2-4. Given the major differences in the dynamics of oligodendrocyte generation and adaptive myelination between rodents and humans 5-9, it is not clear how well experimental animal models reflect the situation in multiple sclerosis. Here, by measuring the integration of 14 C derived from nuclear testing in genomic DNA 10, we assess the dynamics of oligodendrocyte generation in patients with multiple sclerosis. The generation of new oligodendrocytes was increased several-fold in normal-appearing white matter in a subset of individuals with very aggressive multiple sclerosis, but not in most subjects with the disease, demonstrating an inherent potential to substantially increase oligodendrocyte generation that fails in most patients. Oligodendrocytes in shadow plaques-thinly myelinated lesions that are thought to represent remyelinated areas-were old in patients with multiple sclerosis. The absence of new oligodendrocytes in shadow plaques suggests that remyelination of lesions occurs transiently or not at all, or that myelin is regenerated by pre-existing, and not new, oligodendrocytes in multiple sclerosis. We report unexpected oligodendrocyte generation dynamics in multiple sclerosis, and this should guide the use of current, and the development of new, therapies.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Additionally, findings from some studies suggest that adult oligodendrocytes, which withstand the demyelinating event, may also contribute to myelin repair [101,102].”
From How to Use the Cuprizone Model to Study De- and Remyelination (2024) · cites this paper as [102]
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“oligodendrocyte precursor cells in cortex and white matter were shown to differ in their propensity for terminal differentiation, and cortical oligodendrocytes reach their final number much later in life than in the white matter, as inferred from 14C incorporation.48”
From BCAS1-positive oligodendrocytes enable efficient cortical remyelination in multiple sclerosis (2025) · cites this paper as [48]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Axonal transection in the lesions of multiple sclerosis
Trapp, B. D., Peterson, J., Ransohoff, R. M., Rudick, R., Mörk, S., & Bö, L. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801293380502 · Cited by 4,029
Evidence for Cardiomyocyte Renewal in Humans
Bergmann, O., Bhardwaj, R. D., Bernard, S., Zdunek, S., Barnabé-Heider, F., Walsh, S., Zupicich, J., Alkass, K., Buchholz, B. A., Druid, H., et al. (2009) · Science · doi:10.1126/science.1164680 · Cited by 3,130
Self-citationDynamics of hippocampal neurogenesis in adult humans
Spalding, K. L., Bergmann, O., Alkass, K., Bernard, S., Salehpour, M., Huttner, H. B., Boström, E., Westerlund, I., Vial, C., Buchholz, B. A., et al. (2013) · Cell · doi:10.1016/j.cell.2013.05.002 · Cited by 1,841
Self-citationNeuronal 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
Motor skill learning requires active central myelination
McKenzie, I. A., Ohayon, D., Li, H., Paes de Faria, J., Emery, B., Tohyama, K., & Richardson, W. D. (2014) · Science · doi:10.1126/science.1254960 · Cited by 1,177
Premyelinating Oligodendrocytes in Chronic Lesions of Multiple Sclerosis
Chang, A., Tourtellotte, W. W., Rudick, R., & Trapp, B. D. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa010994 · Cited by 991
Myelination of the Nervous System: Mechanisms and Functions
Nave, K.-A., & Werner, H. B. (2014) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100913-013101 · Cited by 983
Neurogenesis in the striatum of the adult human brain
Ernst, A., Alkass, K., Bernard, S., Salehpour, M., Perl, S., Tisdale, J., Possnert, G., Druid, H., & Frisén, J. (2014) · Cell · doi:10.1016/j.cell.2014.01.044 · Cited by 937
Self-citationKuhlmann, T., Miron, V., Cuo, Q., Wegner, C., Antel, J., & Bruck, W. (2008) · Brain · doi:10.1093/brain/awn096 · Cited by 864
Altered human oligodendrocyte heterogeneity in multiple sclerosis
Jäkel, S., Agirre, E., Mendanha Falcão, A., van Bruggen, D., Lee, K. W., Knuesel, I., Malhotra, D., ffrench-Constant, C., Williams, A., & Castelo-Branco, G. (2019) · Nature · doi:10.1038/s41586-019-0903-2 · Cited by 854
Cited by
Sorted by citations
Items 301–381 of 381
Oligodendrocytes interactions with glial cells and neurons in demyelinating disease
He, J., Sun, Q., Li, X., Du, R., Xue, H., Zhang, Y., & Li, X. (2025) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2025105 · Cited by 1
Sobel, R. A., Hinojoza, J., & Zoabi, M. (2026) · Journal of Neuropathology and Experimental Neurology · doi:10.1093/jnen/nlag018
Glial cells in chronic inflammation: diversity, dysfunction and therapeutic targeting
Lee, H., Rone, J. M., Lee, J.-H., & Quintana, F. J. (2026) · Nature reviews. Immunology · doi:10.1038/s41577-026-01313-2 · Cited by 3
The GPR17 agonist galinex restores oligodendrocyte maturation under inflammatory conditions
Silva, J. H. C. E., Marangon, D., Boccazzi, M., Raffaele, S., Cignitti, N., Bavetta, M., Arisi, I., Fumagalli, M., Abbracchio, M. P., & Lecca, D. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1838997 · Cited by 1
Pereira, C. D., Martins, F., Marques, F., Sousa, J. C., & Rebelo, S. (2020) · Springer eBooks · doi:10.1007/978-3-030-44436-5_1 · Cited by 2
BDNF-TrkB Signaling in Lifelong Central Nervous System Myelination and Myelin Repair
Nicholson, M., Yoo, S., Craig, G. A., Murray, S. S., & Fletcher, J. L. (2021) · Springer eBooks · doi:10.1007/978-3-030-71519-9_219-1 · Cited by 2
Casanova, G., Rosillo, J. C., Jiménez, M., Fernández, A. S., Rodao, M., Martínez, G. F., Isasi, E., Gau, N. P., Otero, G., Cabrera, M., et al. (2023) · International Journal of Developmental Neuroscience · doi:10.1002/jdn.10256 · Cited by 1
Neuroglial components of brain lesions may provide new therapeutic strategies for multiple sclerosis
Khanghahi, A. M., Rayatpour, A., Baharvand, H., & Javan, M. (2023) · Neurological Sciences · doi:10.1007/s10072-023-06915-5 · Cited by 1
Wobbly hedgehog syndrome- a progressive neurodegenerative disease
Doss, G. A., Radecki, D. Z., Kethireddy, A., Reilly, M. J., Pohly, A. E., August, B. K., Duncan, I. D., & Samanta, J. (2023) · Experimental Neurology · doi:10.1016/j.expneurol.2023.114520 · Cited by 1
Bardy-Lagarde, M., Asbelaoui, N., & Ghoumari, A. M. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00439 · Cited by 1
Role of Oligodendrocyte Lineage Cells in White Matter Injury
Pieczonka, K., Zhang, O., Kouhzaei, S., Velumian, A. A., & Fehlings, M. G. (2025) · Advances in neurobiology · doi:10.1007/978-3-031-87919-7_11 · Cited by 1
Detection and Analysis of Critical Dynamic Properties of Oligodendrocyte Differentiation
Nikolov, S. G., Wolkenhauer, O., Nenov, M., & Vera, J. (2022) · Mathematics · doi:10.3390/math10162928 · Cited by 1
BDNF-TrkB Signaling in Lifelong Central Nervous System Myelination and Myelin Repair
Nicholson, M., Yoo, S., Craig, G. A., Murray, S. S., & Fletcher, J. L. (2022) · Springer eBooks · doi:10.1007/978-3-031-15080-7_219 · Cited by 1
Chamling, X., Kallman, A., Berlinicke, C., Devkota, P., Mertz, J. L., Chang, C. K. W., Kaushik, A. M., Chen, L., Calabresi, P. A., Mao, H., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.07.328971 · Cited by 1
Cunniffe, N. (2021) · Apollo (University of Cambridge) · doi:10.17863/cam.77136 · Cited by 1
GABA B R agonist baclofen promotes central nervous system remyelinationPreprint
Serrano‐Regal, M. P., Bayón‐Cordero, L., Chara, J. C., Tepavčević, V., Ochoa-Bueno, B. I., Matute, C., & Sánchez‐Gómez, M. V. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.28.478233 · Cited by 1
Zhao, Q. X., Fan, P., Gu, Q., Mo, X., Tan, X., Zhou, X., Yang, F., Zhou, X., & Li, Q. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.17.618899 · Cited by 1
Oligodendrocyte studies reveal limits on remyelination
Fyfe, I. (2019) · Nature Reviews Neurology · doi:10.1038/s41582-019-0149-5
A SY-Stematic approach towards understanding stem cell biology
Pilz, G.-A., & Knobloch, M. (2019) · Development · doi:10.1242/dev.177220
Demyelinating conditions regulated by ROS pathways outside and inside the brain
Carlström, K. E. (2020) · Figshare
LRP1 is a negative regulator of oligodendrogenesis in the adult mouse central nervous system
Auderset, L. (2020) · UTAS Research Repository · doi:10.25959/100.00034806
Age and axon-specific forms of cortical remyelination by divergent populations of NG2-gliaPreprint
Chapman, T. W., Olveda, G. E., Pereira, E., & Hill, R. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.12.09.414755
The Role of MERTK in Central Inflammatory Demyelination
Dwyer, C. (2020) · Minerva Access (University of Melbourne)
Cholesterol metabolism in mouse models of Multiple Sclerosis
Berghoff, S. A. (2020) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8239
Investigation of myelin maintenance and turnover by inducible MBP knock-out in adult mice
Meschkat, M. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7679
Julian, K. A., & Imitola, J. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85765-9.00001-1
(2021) · Elsevier eBooks · doi:10.1016/b978-3-437-22085-2.00028-8
Nejad, R. K. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8737
Beckmann, N., Neuhaus, A., Zurbruegg, S., Joller, S., Feuerbach, D., Doelemeyer, A., Schweizer, T., Rudin, S., Neumann, U., Berth, R., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1431273/v1
Lyons, D. A., & Almeida, R. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.738031512.793575106
Neuroinflammation in Multiple Sclerosis
Prasad, P., Roth, L., Ionescu, R.-B., Willis, C. M., Nicaise, A. M., Krzak, G., Peruzzotti‐Jametti, L., & Pluchino, S. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00267-4
Wang, S., Xiong, B., Tian, Y., Hu, Q., Jiang, X., Zhang, J., Chen, L., Wang, R., Li, M., Zhou, X. J., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2639575/v1
Sajjad, M., Zahoor, I., Rashid, F., Rattan, R., & Giri, S. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.19.533192
Patent Highlights August–September 2022
Mucke, H. A. (2023) · Pharmaceutical Patent Analyst · doi:10.4155/ppa-2022-0049
Mouse model of multiple sclerosis induced by disrupting vesicular transport in oligodendrocytesPreprint
Chow, C. H., Huang, M., Rai, J., Harada, H., Eide, S., Sun, H., Feng, Z., Monnier, P. P., Okamoto, K., Zhang, L., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.24.554669
Vitamin D mechanisms of protection in multiple sclerosis
Hayes, C. E., Astier, A., & Lincoln, M. R. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-91338-6.00051-3
Tunley, S. (2024) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.25201913
A Human iPSC-derived Organoid System to Model Myelin Destruction and RepairPreprint
Ramesan, S., Mason, J., Swanson, M. E. V., Mills, S. A., Turner, B. J., Rutar, M., Gonsalvez, D. G., & Barton, S. K. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.19.594912
Oligodendrocytes in multiple sclerosis
Pernin, F., Kuhlmann, T., Kennedy, T. E., & Antel, J. P. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-823848-6.00009-9
Anand, M. A. V., Manjula, K. S., & Wang, C. (2024) · Journal of physiological investigation. · doi:10.4103/ejpi.ejpi-d-24-00043 · Cited by 1
Impacts of hnRNP A1 Splicing Inhibition on the Brain Remyelination Proteome
Brandão‐Teles, C., Carregari, V. C., Reis‐de‐Oliveira, G., Smith, B. J., Chaves, Y. C., Santos, A. V. S., Pinheiro, E. M. D. C., Oliveira, C. C., Vieira, A. S., Crunfli, F., et al. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.16304
Cellular Senescence in Multiple Sclerosis (MS)
Dahiya, R., Dahiya, S., Siddique, R., Thapa, R., Bhat, A. A., Hussain, M. S., Singh, T. G., Singh, S. K., Gupta, S., Deb, P. K., et al. (2025) · Springer eBooks · doi:10.1007/978-981-96-8873-9_11
Gao, M., Xu, R., Ping, L., Lingtong, L., Xiao, H., Wang, Q., Jiangli, Z., & Cheng, Y. (2025) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2025.111712
Villani, A., Wittmann, J., Wyss, T., Mallona, I., Ortiz, I. S., Tichy, N., Biermeier, C. M., Pena, M., Pal, A. A., Gilmour, D. T., et al. (2026) · Communications Biology · doi:10.1038/s42003-026-09948-6 · Cited by 1
Yang, C., Ma, Y., Lu, Q., Qu, Y., Li, Y., Cheng, S., Xiao, C., Chen, J., Wang, C., Wang, F., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26388863
Seeker, L. A., Bestard-Cuche, N., Jäkel, S., Kazakou, N.-L., Bøstrand, S. M. K., Wagstaff, L. J., Cholewa-Waclaw, J., Kilpatrick, A. M., van Bruggen, D., Kabbe, M., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26591057
Seeker, L. A., Bestard-Cuche, N., Jäkel, S., Kazakou, N.-L., Bøstrand, S. M. K., Wagstaff, L. J., Cholewa-Waclaw, J., Kilpatrick, A. M., van Bruggen, D., Kabbe, M., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26591051
Seeker, L. A., Bestard-Cuche, N., Jäkel, S., Kazakou, N.-L., Bøstrand, S. M. K., Wagstaff, L. J., Cholewa-Waclaw, J., Kilpatrick, A. M., van Bruggen, D., Kabbe, M., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26591048
Seeker, L. A., Bestard-Cuche, N., Jäkel, S., Kazakou, N.-L., Bøstrand, S. M. K., Wagstaff, L. J., Cholewa-Waclaw, J., Kilpatrick, A. M., van Bruggen, D., Kabbe, M., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26591063
Beckmann, N., Neuhaus, A., Zurbruegg, S., Volkmer, P., Patiño, C., Joller, S., Feuerbach, D., Doelemeyer, A., Schweizer, T., Rudin, S., et al. (2023) · Figshare · doi:10.6084/m9.figshare.22598837
Lohrberg, M., Winkler, A., Franz, J., van der Meer, F., Ruhwedel, T., Sirmpilatze, N., Dadarwal, R., Löber-Handwerker, R., Esser, D. S., Wiegand, K., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13488672
Seeker, L. A., Bestard-Cuche, N., Jäkel, S., Kazakou, N.-L., Bøstrand, S. M. K., Wagstaff, L. J., Cholewa-Waclaw, J., Kilpatrick, A. M., van Bruggen, D., Kabbe, M., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26591060
Seeker, L. A., Bestard-Cuche, N., Jäkel, S., Kazakou, N.-L., Bøstrand, S. M. K., Wagstaff, L. J., Cholewa-Waclaw, J., Kilpatrick, A. M., van Bruggen, D., Kabbe, M., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26591054
A dive into the untapped potential of marine compounds in counteracting neurodegeneration
Costa, I., Barbosa, D. J., Remião, F., Sousa, M. E., & Silva, R. (2026) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2026.108982
Healing through movement: narrative review on exercise and neurological disorders
Essa, S. M., Kakar, A., Khosa, N. A., Ibrahim, I. A., Jovanovic, M., Mclaughlin, M. L., Ibrahim, M. M., & Riddle, K. (2025) · Asia-Pacific Journal of Surgical & Experimental Pathology · doi:10.32948/ajsep.2025.10.28
Liu, L., Ji, J., Zhang, J., Zhang, Y., Xie, G., Yao, Y., Chen, H., Liao, F., Fu, C., Liu, Y., et al. (2026) · Cell Biomaterials · doi:10.1016/j.celbio.2026.100426
Macrophage activation profiles of multiple sclerosis patients
Fransson, J. (2019) · theses.fr (ABES) · doi:10.70675/361929ebz66c2z48dbz83a1z8955d8b54716
Along-tract and across-plexus propagation of tissue damage in multiple sclerosis
Ricigliano, V. A. G. (2021) · theses.fr (ABES) · doi:10.70675/d9e05903zbf45z4f3cz9290z50f80f3e4ead
Investigation of regulatory plasma cells in health and disease
Bui, T. C. (2022) · theses.fr (ABES) · doi:10.70675/65ea40a7zbe2dz4f33z969bz1fa9a07e0174
Lazzarotto, A. (2023) · theses.fr (ABES) · doi:10.70675/245e2c82zb2bdz4b9dzbd16zc18dbdc9732b
Preclinical gene therapy using recombinant AAV vectors in mouse models of two human diseases
Günes, Y. Ö. (2022) · theses.fr (ABES) · doi:10.70675/52c9a808z1652z42c4zae82zc812b95f1723
Pharmacogenomic identification of small molecules promoting oligodendrogenesis and myelin repair
Huré, J.-B. (2022) · theses.fr (ABES) · doi:10.70675/17691e80z7bacz455fzba89z49fef7be0512
Masson, M. L. P. (2024) · theses.fr (ABES) · doi:10.70675/7f680c8dz2453z40c7z9047z982a66a8bfd5
Briggs, F. B. S., Montini, F., Spurlock, C. F., Ryan, C., Bailey, J. N. C., Trapl, E., Shaginurova, G. I., Wylezinski, L. S., Sesler, C. L., Fereidan-Esfahani, M., et al. (2026) · Environmental Research · doi:10.1016/j.envres.2026.124763
Chow, C. H., Huang, M., Regmi, A., Rai, J., Harada, H., Eide, S., Sun, H., Feng, Z., Monnier, P. P., Okamoto, K., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-73381-w
Microenvironmental Regulation of Central Nervous System Myelination and Remyelination
Wang, Y., Tan, L., Lao, L., Huang, X., Zhang, S., & Sun, H. (2026) · Journal of Integrative Neuroscience · doi:10.31083/jin43257
Martinez, C. S., Lopez, S., Hernandez, D. P., Figueroa, A., Lorenzo, K. D. L., Rodriguez, J., Radhakrishnan, V., Rodriguez, M. R., Winkler, A. M., Cisneros-Mejorado, A., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.01.729333
18:2 Cholesterol Ester is a Novel Prognostic Biomarker of Disease Progression in Multiple Sclerosis
Torres, P., Gil-Sánchez, A., Saldaña, A. S., Quibus, L., Murillo, E. S. P., Ruiz‐Fernández, E., Peralta, S., Solana, M. J., Brieva, L., & González‐Mingot, C. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-05915-8
Myelin Repair as a Neuroprotective Strategy for Multiple Sclerosis: From Bench to Bedside
Battah, T., Mastorodemos, V., Struecker, E., Mitsikostas, D. D., & Papadopoulos, D. (2026) · Medicina · doi:10.3390/medicina62061183
Ploughman, M., Cattaneo, D., Marazzini, F., Bray, N. W., & Fritz, N. E. (2026) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-026-01501-6
A novel small molecule remyelination therapy for multiple sclerosis
Yang, Y., Bai, B., Knutsen, L. J. S., Hamlyn, R. J., Cui, Q., Antel, J. P., Macklin, W. B., Medicetty, S., & Trapp, B. D. (2026) · npj Drug Discovery. · doi:10.1038/s44386-026-00060-7
Oligodendrocytes in central nervous system health and disease
Ryan, L. J., & Miron, V. E. (2026) · Cell · doi:10.1016/j.cell.2026.08.003
A human-induced pluripotent stem cell-derived spheroid model to investigate myelin injury and repair
Ramesan, S., Mason, J., Kumar, S. S., Swanson, M. E. V., Korneev, D., Mills, S. A., Mathangasinghe, Y., Andres, A., Loh, L. J., Fraser, T. D., et al. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02457-z
Mechanisms and therapeutic strategies for central and peripheral remyelination
Zhan, J., Jo, J., Cristobal, C. D., Jeong, D. J., Park, H. T., & Lee, H. K. (2026) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2026.102964
Metadata
- Authors
- Yeung, M. S. Y., Djelloul, M., Steiner, E., Bernard, S., Salehpour, M., Possnert, G., Brundin, L., & Frisén, J.
- Affiliations
- Karolinska Institutet (SE)
- Lyon 1 Université (FR)
- Uppsala University (SE)
- Karolinska University Hospital (SE)
- Corresponding author
- Frisén, Jonas
- ORCID
- Venue
- Nature
- Published
- 2019-01-23
- Volume
- 566
- Issue
- 7745
- Pages
- 538-542
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC6420067
- OpenAlex
- W2913848851
- Cited by
- 376
- References
- 39
- Citations by year
- 2026: 23 · 2025: 50 · 2024: 50 · 2023: 51 · 2022: 58 · 2021: 53 · 2020: 58 · 2019: 32
- FWCI
- 36.99
- Type
- journal article
- Language
- en
- Update notices
- correction (2019-02-05)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion, other-oa)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Cleveland Clinic
- Torsten Söderbergs Stiftelse
- Swedish Cancer Foundation
- Multiple Sclerosis Society (207495)
- Knut och Alice Wallenbergs Stiftelse
- Vetenskapsrådet
- Lerner Research Institute, Cleveland Clinic
- Topics
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Keywords
- multiple sclerosis, oligodendrocyte generation, remyelination, normal-appearing white matter, demyelinating disease, disease aggressiveness
- MeSH terms
- Remyelination, Adult, Aging, Cell Differentiation, Cell Separation, Female, Humans, Male, Multiple Sclerosis, Myelin Sheath, Oligodendroglia, Case-Control Studies, Age of Onset, Cell Proliferation, White Matter
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