The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
Myelin Impairs CNS Remyelination by Inhibiting Oligodendrocyte Precursor Cell Differentiation
Open accessAbstract
Demyelination in the adult CNS can be followed by extensive repair. However, in multiple sclerosis, the differentiation of oligodendrocyte lineage cells present in demyelinated lesions is often inhibited by unknown factors. In this study, we test whether myelin debris, a feature of demyelinated lesions and an in vitro inhibitor of oligodendrocyte precursor differentiation, affects remyelination efficiency. Focal demyelinating lesions were created in the adult rat brainstem, and the naturally generated myelin debris was augmented by the addition of purified myelin. After quantification of myelin basic protein mRNA expression from lesion material obtained by laser capture microdissection and supported by histological data, we found a significant impairment of remyelination, attributable to an arrest of the differentiation and not the recruitment of oligodendrocyte precursor cells. These data identify myelin as an inhibitor of remyelination as well as its well documented inhibition of axon regeneration.
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
“they also exhibit regenerative properties through the phagocytosis of myelin debris3, 4 and secretion of growth/neurotrophic factors5.”
From M2 microglia and macrophages drive oligodendrocyte differentiation during CNS remyelination (2013) · cites this paper as [3]
In the citing paper
“Efficient myelin debris removal and clearance by phagocytic cells are critical to eliminate inhibitory signals interfering with OPC activation, recruitment to the site of demyelination and/or differentiation into myelinating mature OLs [14, 26, 27].”
From TREM2 activation on microglia promotes myelin debris clearance and remyelination in a model of multiple sclerosis (2020) · cites this paper as [26]
In the citing paper
“One critical role for microglia during demyelination is the clearance of myelin debris, which acts as an inhibitor of remyelination [192–194].”
From Oligodendrocyte death and myelin loss in the cuprizone model: an updated overview of the intrinsic and extrinsic causes of cuprizone demyelination (2022) · cites this paper as [194]
In the citing paper
“Long-term demyelination occurs post-SCI, with lipid-containing myelin debris being absorbed and processed by inflammatory cells, including microglia—a process crucial for paving the way for regenerative reactions and inflammation resolution [9–11].”
From miR-223 accelerates lipid droplets clearance in microglia following spinal cord injury by upregulating ABCA1 (2024) · cites this paper as [9]
Citations
Cites
MYELINATION IN RAT BRAIN: METHOD OF MYELIN ISOLATION1
Norton, W. T., & Poduslo, S. E. (1973) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1973.tb07519.x · Cited by 1,413
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
Caroni, P., & Schwab, M. E. (1988) · Neuron · doi:10.1016/0896-6273(88)90212-7 · Cited by 886
Myelin-associated inhibitors of axonal regeneration in the adult mammalian CNS
Filbin, M. T. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1195 · Cited by 873
Why does remyelination fail in multiple sclerosis?
Franklin, R. J. M. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn917 · Cited by 862
Self-citationLINGO-1 is a component of the Nogo-66 receptor/p75 signaling complex
Mi, S., Lee, X., Shao, Z., Thill, G., Ji, B., Relton, J. K., Levesque, M., Allaire, N., Perrin, S., Sands, B., et al. (2004) · Nature Neuroscience · doi:10.1038/nn1188 · Cited by 827
p75 interacts with the Nogo receptor as a co-receptor for Nogo, MAG and OMgp
Wang, K., Kim, J. A., Sivasankaran, R., Segal, R. A., & He, Z. (2002) · Nature · doi:10.1038/nature01176 · Cited by 824
Proliferation and Differentiation of Progenitor Cells Throughout the Intact Adult Rat Spinal Cord
Horner, P. J., Power, A. E., Kempermann, G., Kuhn, H. G., Palmer, T. D., Winkler, J., Thal, L. J., & Gage, F. H. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-06-02218.2000 · Cited by 777
NG2-Positive Oligodendrocyte Progenitor Cells in Adult Human Brain and Multiple Sclerosis Lesions
Chang, A., Nishiyama, A., Peterson, J. W., Prineas, J. W., & Trapp, B. D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-17-06404.2000 · Cited by 711
LINGO-1 negatively regulates myelination by oligodendrocytes
Mi, S., Miller, R. H., Lee, X., Scott, M. L., Shulag-Morskaya, S., Shao, Z., Chang, J., Thill, G., Levesque, M., Zhang, M., et al. (2005) · Nature Neuroscience · doi:10.1038/nn1460 · Cited by 628
Flagged first, then by citations
Cited by
Sorted by citations
Items 601–700 of 774
Shultz, R. B., Hai, N., & Zhong, Y. (2024) · Journal of Neural Engineering · doi:10.1088/1741-2552/ad29d5 · Cited by 3
Signaling pathways that regulate glial development and early migration—oligodendrocytes
Fancy, S. P. J., & Miller, R. H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00035-7 · Cited by 2
White Matter Repair in Subcortical Stroke
Sözmen, E. G., & Carmichael, S. T. (2013) · Springer eBooks · doi:10.1007/978-1-4614-9123-1_12 · Cited by 3
Microglia: roles and rules in brain traumatic injury
Alvis-Miranda, H. R., Alcalá‐Cerra, G., & Moscote‐Salazar, L. R. (2013) · Romanian Neurosurgery · doi:10.2478/v10282-012-0019-9 · Cited by 3
Mausner-Fainberg, K., Kolb, H., Penn, M., Regev, K., Vaknin‐Dembinsky, A., Gadoth, A., Kestenbaum, M., & Karni, A. (2016) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2016.01.019 · Cited by 3
Kira, J., & Isobe, N. (2019) · Contemporary clinical neuroscience · doi:10.1007/978-3-030-19515-1_15 · Cited by 4
Fransson, J., Bachelin, C., Deknuydt, F., Ichou, F., Guillot‐Noël, L., Ponnaiah, M., Gloaguen, A., Maillart, É., Stankoff, B., Tenenhaus, A., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.13.426327 · Cited by 3
Oligomeric amyloid beta prevents myelination in a clusterin-dependent mannerPreprint
Beiter, R. M., Raghavan, T. P., Suchocki, O., Ennerfelt, H. E., Rivet-Noor, C. R., Merchak, A. R., Phillips, J. L., Bathe, T., Lukens, J. R., Prokop, S., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-4415143/v1 · Cited by 3
Dissecting the evolving cellular landscape of a remyelinating microenvironment
Melchor, G. S., Baydyuk, M., Manavi, Z., Hu, J., & Huang, J. K. (2024) · doi:10.1101/2024.12.25.630253 · Cited by 3
Depletion of Microglia Increases Cortical Oligodendrocyte Density During Remyelination
Loo, H. K., Gallegos, J., Mialki, C., Perrin, G. E., Malloy, T., & Orthmann‐Murphy, J. L. (2026) · Glia · doi:10.1002/glia.70120 · Cited by 2
“In the setting of demyelinating injury, microglia remove myelin debris by phagocytosis (Yamasaki et al. 2014), thereby eliminating at least one barrier to OPC differentiation (Kotter 2006; Plemel et al. 2013).”
Wang, Q., Zeng, F., Fang, C., Sun, Y., Zhao, X., Rong, X., Zhang, H., & Xu, Y. (2024) · Brain Research · doi:10.1016/j.brainres.2024.149106 · Cited by 3
Niacin produces an inconsistent treatment response in the EAE model of multiple sclerosis
Wuerch, E. C., Mirzaei, R., & Yong, V. W. (2024) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2024.578421 · Cited by 2
Serrano‐Regal, M. P., Camacho-Toledano, C., Alonso-García, I., Ortega, M. C., Machín-Díaz, I., Lebrón‐Galán, R., García-Arocha, J., Calahorra, L., Nieto‐Díaz, M., & Clemente, D. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.106919 · Cited by 2
Oligodendroglia in Ageing and Age-Dependent Neurodegenerative Diseases
Niu, J., Verkhratsky, A., Butt, A. M., & Yi, C. (2025) · Advances in neurobiology · doi:10.1007/978-3-031-87919-7_13 · Cited by 4
Hu, Y., Tang, K., Hu, H., 米红波, Li, X., Wang, H., Liu, J., Xia, Y., Huang, W., Kirchhoff, F., et al. (2026) · Journal of Neuroinflammation · doi:10.1186/s12974-026-03782-7 · Cited by 4
Neuroglia in traumatic brain injury: Pathophysiology and therapeutic targeting
Suk, K. (2026) · Brain Network Disorders · doi:10.1016/j.bnd.2026.03.002 · Cited by 2
Mechanisms of Plasticity Remodeling and Recovery
Zheng, Z., Chen, J., & Chopp, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-69424-7.00011-9 · Cited by 2
Mata, P., Sagartzazu‐Aizpurua, M., Berehova, N., Miranda, J. I., Montilla, A., Bosch-Juan, M., Sánchez‐Gómez, M. V., Matute, C., Pérez‐Samartín, A., Aizpurua, J. M., et al. (2025) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2025.117862 · Cited by 2
Alcohol and Its Impact on Myelin
Guerri, C., & Pascual, M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800213-1.00039-0 · Cited by 2
Model Systems to Define Remyelination Therapies
Miller, R. H., Karl, M. T., Tognatta, R., Pajoohesh‐Ganji, A., & Abu-Rub, M. (2018) · InTech eBooks · doi:10.5772/intechopen.76318 · Cited by 2
Brunois, C., & Ris, L. (2019) · Contemporary clinical neuroscience · doi:10.1007/978-3-030-19515-1_9 · Cited by 2
Neuroinflammation in Neurological Disorders
Kira, J. (2013) · Advances in neurobiology · doi:10.1007/978-1-4614-8313-7_2 · Cited by 2
Vitamin D and Multiple Sclerosis: An Open-Ended Story
Scazzone, C., Agnello, L., Sasso, B. L., Ciaccio, A. M., Giglio, R. V., Bivona, G., & Ciaccio, M. (2019) · The Open Biochemistry Journal · doi:10.2174/1874091x01913010088 · Cited by 2
Kesselring, J., Comı, G., & Thompson, A. J. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511781698.002 · Cited by 2
IRF5 regulates microglial myelin clearance and cholesterol metabolism after demyelinationPreprint
Montilla, A., Zabala, A., Calvo, I., Mata, P., Tomé, I., Koster, M., Sierra, A., Kooistra, S. M., Soria, F. N., Eggen, B. J. L., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.14.553274 · Cited by 2
Tsai, H., Piya, S., Wang, J., Zhu, J. K., Hu, W., Gehrke, A. R., Cao, S., Guise, A. J., Chan, S. J., Sheehan, M. J., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.07.637125 · Cited by 2
The best basic science paper in MS in 2013: Antimuscarinic therapies in remyelination
Green, A. (2014) · Multiple Sclerosis Journal · doi:10.1177/1352458514558679 · Cited by 1
Pietro, A. A. D., & Pasquini, L. A. (2024) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2024.103937 · Cited by 1
Circulating platelets modulate oligodendrocyte progenitor cell differentiation during remyelination
Philp, A. R., Reyes, C. R., Mansilla, J. B., Sharma, A., Zhao, C., Valenzuela‐Krugmann, C., Rawji, K. S., Martinez, G. A. G., Dimas, P., Hinrichsen, B., et al. (2024) · eLife · doi:10.7554/elife.91757.3 · Cited by 1
Self-citationMado, H., Stasiniewicz, A., Nafalska, N., Stopyra, M., Furgoł, T., Jezierzański, M. M., Kisielewska, W., Kubicka, K., Niedziela, N., Sowa, P., et al. (2026) · Molecular Immunology · doi:10.1016/j.molimm.2026.02.005 · Cited by 1
Zhao, Y., Hu, H., Wang, J., Hu, Y., Yang, L., Wu, Z., Zhao, S., Wang, X., Mu, Y., Zheng, M., et al. (2026) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2026.111823 · Cited by 1
Song, C., Lee, Y., & Kim, M. S. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1813048 · Cited by 1
Deng, Y., He, Q., Yao, B., Chen, X., Cheng, G., Xu, M., Hu, J., Graça, L., Zhu, X., Zhang, X., et al. (2026) · Science Signaling · doi:10.1126/scisignal.aea4402 · Cited by 1
Microglial Function in MS Pathology
Kilpatrick, T. J., & Jokubaitis, V. (2012) · Springer eBooks · doi:10.1007/978-1-4614-2218-1_3 · Cited by 1
Antigen-Presenting Cells in the Central Nervous System
Koning, N., Ilarregui, J. M., García-Vallejo, J. J., & van Kooyk, Y. (2013) · Springer eBooks · doi:10.1007/978-1-4614-7953-6_4 · Cited by 1
Mikroglia im Kontext der Multiplen Sklerose
Hoepner, R., Gold, R., & Faissner, S. (2014) · Nervenheilkunde · doi:10.1055/s-0038-1627744 · Cited by 1
Macrophages and Microglia in Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis
Mishra, M. K., & Yong, V. W. (2013) · Springer eBooks · doi:10.1007/978-1-4614-7953-6_9 · Cited by 1
Pourabdolhossein, F., Javan, M., Mirnajafi-Zadeh, S. J., Dehghan, S., Sherafat, M. A., Mozafari, S., & Ahmadiani, A. (2011) · KAUMS Journal · Cited by 1
The effect of interleukin 17 on oligodendrocyte proliferation and differentiation
Tetteh, S. (2012) · doi:10.7282/t3s18192 · Cited by 1
Neural Stem Cells and Demyelinating Disease
Crawford, A. H., & Franklin, R. J. M. (2014) · Stem cell biology and regenerative medicine · doi:10.1007/978-1-4939-1908-6_8 · Cited by 1
Self-citationBéchet, S., & Dev, K. K. (2024) · Biomedicines · doi:10.3390/biomedicines12030594 · Cited by 1
Garcia, J. C., Bueno, R. J., Salla, M., Serra, I. M., Seeger, B., Akbari, N., Sperber, P. S., Stachelscheid, H., Infante‐Duarte, C., Paul, F., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-57066-2 · Cited by 1
Origin, Diversity, and Roles of Microglia
Ris, L. (2024) · Springer eBooks · doi:10.1007/978-3-031-24297-7_9-1 · Cited by 1
Kira, J., & Isobe, N. (2024) · Springer eBooks · doi:10.1007/978-3-031-60006-7_15 · Cited by 2
Napoli, M. D., Smith, C. J., Hopkins, S. J., Popa‐Wagner, A., Bugă, A. M., & SLEVIN, M. A. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1071-7_11 · Cited by 1
Multiple Sclerosis: Etiology and Mechanism, with Special Reference to Asians
Kira, J. (2016) · Springer eBooks · doi:10.1007/978-4-431-55594-0_5 · Cited by 1
Evercooren, A. B., Lachapelle, F., Nait‐Oumesmar, B., & Pham-Dinh, D. (2007) · Revue Neurologique · doi:10.1016/s0035-3787(07)90459-2 · Cited by 1
Microglial LRP1 modulates neuroinflammation via control of the NF-κB pathway in autoimmunity
Chuang, T. Y. (2016) · doi:10.18130/v3h31c · 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
Montilla, A., Zabala, A., Er-Lukowiak, M., Rissiek, B., Magnus, T. U., Rodríguez-Iglesias, N., Sierra, A., Matute, C., & Domercq, M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.10.495612 · Cited by 1
Impairment of autophagy-lysosomal activity near the chronically implanted microelectrodesPreprint
Chen, K., Padilla, C. G., Kiselyov, K. I., & Kozai, T. D. Y. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.31.543108 · Cited by 1
Funaki, M., Nio‐Kobayashi, J., Suzuki, R., & Bandô, Y. (2023) · Preprints.org · doi:10.20944/preprints202311.0095.v1 · Cited by 1
The concentration of myelin debris-like particles in the normal rat optic nervePreprint
Kawano, J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.19.643597 · Cited by 1
Peng, M., Zeng, M., Tian, H., He, C., Zhang, L., Zhao, Z., Luo, Y., Li, X., Xia, F., Liu, S., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.19.689382 · Cited by 1
Späte, E., Higgins, K. P., Kim, Y., Mangana, C., Komarek, L., Teymouri, M., Gerwig, U. C., Melzer, S., Sadowski, B., Ruhwedel, T., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.05.692364 · Cited by 1
The cuprizone model and multiple sclerosis : disparities and similarities
Kipp, M., & Baumgärtner, W. (2011) · RWTH Publications (RWTH Aachen)
The Role of Transcription Factors in Regulating Adult Neurogenesis after Excitotoxic Brain Injury
Jones, K. (2012) · ResearchSpace (University of Auckland)
Conditional regulation of Hoxa2 gene expression in CG4 cells
Wang, J. (2007) · University Library - University of Saskatchewan (University of Saskatchewan)
Innate Immunity in the CNS – A Focus on the Myeloid Cell
Moore, C. S., Durafourt, B. A., & Antel, J. P. (2014) · Wiley eBooks · doi:10.1002/9781118406557.ch2
The contribution of brain reorganisation to recovery inpatients with optic neuritis
Jenkins, T. M. (2010) · UCL Discovery (University College London)
Modelling Multiple Sclerosis In Vitro and the Influence of Activated Macrophages
Vereyken, E. J. F., Dijkstra, C. D., & Teunisse, C. E. (2011) · InTech eBooks · doi:10.5772/30525
Regulation of Oligodendrocyte Differentiation: Relevance for Remyelination
Maier, O. (2012) · InTech eBooks · doi:10.5772/37892
Effects of Macrophages and Monocytes in Remyelination of the CNS
Natrajan, M. S., Bielekova, B., & Franklin, R. J. M. (2015) · Wiley eBooks · doi:10.1002/9781118732748.ch13
Self-citationKuypers, N. J. (2014) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/786
Antel, J. P., & Miron, V. E. (2012) · Springer eBooks · doi:10.1007/978-1-4614-2218-1_9
Stiles, T. L. (2013) · eScholarship (California Digital Library)
Mechanisms of Plasticity, Remodeling and Recovery
Zhang, Z. G., & Chopp, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-323-29544-4.00011-6
Neuroendocrine Checkpoints of Innate Immune Responses in Multiple Sclerosis
Deckx, N., Berneman, Z. N., & Cools, N. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801914-6.00012-x
Remyelination in the Central Nervous System
(1989) · KARGER eBooks · doi:10.1159/isbn.978-3-8055-8766-2
The adult human oligodendrocyte precursor cell: a key player in myelin repair
Rist, J. M., & Franklin, R. J. M. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511781698.007
Self-citationThe oligodendrocyte "processosome": novel regulators of differentiation and myelination
da Silva, A. F. B. (2015) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.34626/1zbe-vq61
Water Homeostasis Dysfunctions and Edema in Neuroinflammatory Disease
Petry, K. G., & Bikfalvi, A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803196-4.00018-7
On the role of macrophages, microglia and the extracellular matrix in remyelination
Wang, P. (2018) · University of Groningen research database (University of Groningen / Centre for Information Technology)
Remyelination in Multiple Sclerosis
Bir, S. C., Chernyshev, O. Y., & Minagar, A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811709-5.00008-9
The Role of Galectin-3 in Stroke and Diseases of the Cerebrovascular System
Venkatraman, A., Khawaja, A. M., & Kumar, N. (2018) · Med One · doi:10.20900/mo.20180009
Signalisation par les récepteurs toll-like dans un contexte d'excitotoxicité
Larochelle, A. (2014) · Corpus Université Laval (Université Laval)
McMurran, C. E., de la Fuente, A. G., Peñalva, R. G., Menachem-Zidon, O. B., Dombrowski, Y., González, G. A., Zhao, C., Krause, F. N., Young, A. M. H., Griffin, J. L., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/575829
Self-citationSiddiqui, T. A. (2016) · TSpace (University of Toronto)
Aging exacerbates myelin disruption and axon injury following demyelination
Michaels, N. J. (2019) · doi:10.11575/prism/36466
Glial Cell Plasticity During Development and Myelinopathies
Morris, A. (2017) · doi:10.18130/v3v07q
Emerging Drugs and Targets for Remyelination in Multiple Sclerosis
Wagstaff, L. J., & Williams, A. (2019) · Royal Society of Chemistry eBooks · doi:10.1039/9781788016070-00197
Role of the NLR gene family members in neuroinflammation and demyelination in the CNS
Jha, S. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/e2yp-8441
Characterising the role of AMIGO3 in oligodendrocytes and demyelinating diseases
Foale, S. (2019) · University of Birmingham Institutional Research Archive (University of Birmingham)
Ozsvár, A. (2020) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.10270
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
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
XuYang, C.-J., & Liao, W. (2011)
Ding, Z., Han, Q.-X., Song, L., Wang, Q., Han, G., Chu, G.-G., Li, Y., Chai, Z., Yu, J., Xiao, B., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-531893/v1 · Cited by 1
Mendiola, A. S., Church, K. A., Cardona, S. M., Vanegas, D., Garcia, S. A., Macklin, W. B., Lira, S. A., Ransohoff, R. M., Kokovay, E., Lin, C. A., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.06.06.447262
Luo, J. X. X. (2021) · eScholarship@McGill (McGill) · doi:10.82308/21669
C-64 進行非小細胞癌に対するCDDP+VDS+MMC療法とCDDP+VDS+IFX療法の検討
西, 耕., 中積, 泰., 水島, 豊., 中村, 裕., 山之内, 菊., 斉藤, 元., 藤村, 政., 岡藤, 和., 飴嶋, 慎., & 金森, 一. (1992) · 肺癌
Nejad, R. K. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8737
The role of astrocytic RFX4_v3 in demyelination
Paap, F. (2015) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5062
Microglia activation and regulation of remyelination in the central nervous system
Su, M. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7399
Neuroaxonale Schädigung in experimentellen Modellen der multiplen Sklerose
Escher, A. (2008) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-1328
Preclinical model of multiple sclerosis: Focal, chemical or viral demyelination
Tsirka, S. E., & Nissen, J. C. (2022) · Methods in cell biology · doi:10.1016/bs.mcb.2021.12.010
Metadata
- Authors
- Kotter, M. R., Li, W.-W., Zhao, C., & Franklin, R. J. M.
- Affiliations
- University of Cambridge (GB)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2006-01-04
- Volume
- 26
- Issue
- 1
- Pages
- 328-332
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6674302
- OpenAlex
- W2094044389
- Cited by
- 768
- References
- 30
- Citations by year
- 2026: 24 · 2025: 39 · 2024: 63 · 2023: 56 · 2022: 48 · 2021: 56 · 2020: 46 · 2019: 58 · 2018: 34 · 2017: 41 · 2016: 39 · 2015: 40 · 2014: 34 · 2013: 43 · 2012: 25
- FWCI
- 15.22
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, public-domain)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Raymond and Beverly Sackler Foundation
- Multiple Sclerosis Society
- Austrian Science Fund
- Topics
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- remyelination, myelin debris, oligodendrocyte precursor cells, oligodendrocyte differentiation, demyelination, multiple sclerosis, myelin basic protein, demyelinating lesions, axon regeneration, central nervous system repair
- MeSH terms
- Animals, Cell Differentiation, Central Nervous System, Female, Growth Inhibitors, Myelin Sheath, Nerve Fibers, Myelinated, Neural Inhibition, Oligodendroglia, Stem Cells, Rats, Sprague-Dawley, Rats
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