The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Episodic demyelination and subsequent remyelination within the murine central nervous system: changes in axonal calibre
Abstract
Exposure of young adult C57BL/6 mice to cuprizone in the diet initiated profound and synchronous demyelination of the corpus callosum, which was virtually complete by 4 weeks of exposure. Interestingly, even in the face of a continued exposure to cuprizone, there was spontaneous remyelination 2 weeks later. This remyelination preferentially involved smaller calibre axons. There was a suggestion of yet another cycle of demyelination (at 10 weeks) and remyelination (at 12 weeks), but by 16 weeks of exposure, the regenerative capacity was exhausted and the animals were near death. The relapsing–remitting pattern suggests this may be a useful model for certain human demyelinating disorders. In contrast to the above chronic model, the corpus callosum from mice exposed to cuprizone for only 6 weeks continued to remyelinate, with 67% of the axons being myelinated or remyelinated at 10 weeks. Interestingly, a significant reduction in the mean value for axonal diameter was observed during acute demyelination. Upon remyelination, however, the axonal calibre distribution returned to near‐normal. In contrast, when mice were maintained on a cuprizone diet for 16 weeks, the mean value for axonal diameter was reduced to 60% of normal. These results provide further evidence that the interactions between oligodendrocytes and axons alter axonal calibre.
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
“In contrast, the continuous exposure of C57BL/6 mice to cuprizone results in a pattern of two cycles of demyelination and remyelination, followed by chronic demyelination from which animals do not recover 36, 39.”
From SJL Mice Exposed to Cuprizone Intoxication Reveal Strain and Gender Pattern Differences in Demyelination (2009) · cites this paper as [36]
In the citing paper
“Thus, unlike male C57BL/6 mice, which show three cycles of demyelination while on continuous exposure to cuprizone over 13 weeks (36), SJL mice appear to demyelinate gradually once during these time points; however, the demyelination is incomplete.”
From SJL Mice Exposed to Cuprizone Intoxication Reveal Strain and Gender Pattern Differences in Demyelination (2009) · cites this paper as [36]
In the citing paper
“Previous studies have shown that LFB–PAS scores are reflective to the trends in demyelination when compared with percent myelinated fibers that are counted in electron micrographs 29, 36.”
From SJL Mice Exposed to Cuprizone Intoxication Reveal Strain and Gender Pattern Differences in Demyelination (2009) · cites this paper as [36]
In the citing paper
“In addition, C57BL/6 mice experience a spontaneous partial remyelination after 6 weeks and then continue to demyelinate further when exposed continuously to cuprizone 36, 39.”
From SJL Mice Exposed to Cuprizone Intoxication Reveal Strain and Gender Pattern Differences in Demyelination (2009) · cites this paper as [36]
In the citing paper
“Indeed, long-term feeding of cuprizone induces an episodic sequence of demyelinating and remyelinating events, which becomes ineffective over time, progressing to a chronic state of demyelination [26].”
From How to Use the Cuprizone Model to Study De- and Remyelination (2024) · cites this paper as [26]
In the citing paper
“Mason and colleagues rarely observed necrotic axons but showed a mean decrease in axonal caliber, indicating some kind of axonal injury or dysfunction that might impair remyelination [26].”
From How to Use the Cuprizone Model to Study De- and Remyelination (2024) · cites this paper as [26]
Citations
Cites
WEINSHENKER, B. G., BASS, B., RICE, G. P. A., NOSEWORTHY, J., CARRIERE, W., BASKERVILLE, J., & EBERS, G. C. (1989) · Brain · doi:10.1093/brain/112.1.133 · Cited by 1,452
The natural history of multiple sclerosis:a geographically based study
Cottrell, D. A., Kremenchutzky, M., Rice, G. P., Koopman, W. J., Hader, W. J., Baskerville, J., & Ebers, G. C. (1999) · Brain · doi:10.1093/brain/122.4.625 · Cited by 1,169
de Waegh, S. M., Lee, V. M. ‐., & Brady, S. T. (1992) · Cell · doi:10.1016/0092-8674(92)90183-d · Cited by 743
Coetzee, T., Fujita, N., Dupree, J. L., Shi, R., Blight, A. R., Suzuki, K., Suzuki, K., & Popko, B. (1996) · Cell · doi:10.1016/s0092-8674(00)80093-8 · Cited by 624
Self-citationWolswijk, G. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-02-00601.1998 · Cited by 562
Endogenous progenitors remyelinate demyelinated axons in the adult CNS
Gensert, J. M., & Goldman, J. E. (1997) · Neuron · doi:10.1016/s0896-6273(00)80359-1 · Cited by 544
ATLAS OF THE MOUSE BRAIN AND SPINAL CORD
Strich, S. J. (1972) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.35.3.422-b · Cited by 538
Microglial/macrophage accumulation during cuprizone-induced demyelination in C57BL/6 mice
Hiremath, M. M., Saito, Y., Knapp, G. W., Ting, J. P.-Y., Suzuki, K., & Matsushima, G. K. (1998) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(98)00168-4 · Cited by 412
Self-citation(1978) · PubMed · Cited by 297
Nixon, R. A., Paskevich, P. A., Sihag, R. K., & Thayer, C. Y. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.126.4.1031 · Cited by 277
Research works printed but not linked: 2
- Ludwin SK., 1978, Central nervous system demyelination and remyelination in the mouse, Lab Invest, 39, 597
- Ludwin SK., 1980, Chronic demyelination inhibits remyelination in the central nervous system, Lab Invest, 43, 382
Cited by
Sorted by citations
Items 101–172 of 172
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
Tavares, E. R., Silva-Gotay, A., Riad, W. V., Bengston, L., & Richardson, H. N. (2019) · Brain Sciences · doi:10.3390/brainsci9070167 · Cited by 30
Khoja, S., Liu, X.-B., Truong, B., Nitzahn, M., Lambert, J., Eliav, A., Nasser, E., Randolph, E., Burke, K. E., White, R. A., et al. (2022) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2022.04.012 · Cited by 26
Krämer, J., Brück, W., Zipp, F., Cerina, M., Groppa, S., & Meuth, S. G. (2019) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2019.101663 · Cited by 27
Experimental studies of g-ratio MRI in ex vivo mouse brain
West, K. L., Kelm, N. D., Carson, R. P., Alexander, D. C., Gochberg, D. F., & Does, M. D. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.11.064 · Cited by 23
Hepatic arginase deficiency fosters dysmyelination during postnatal CNS development
Liu, X.-B., Haney, J. R., Cantero, G., Lambert, J., Otero‐García, M., Truong, B., Gropman, A. L., Cobos, I., Cederbaum, S. D., & Lipshutz, G. S. (2019) · JCI Insight · doi:10.1172/jci.insight.130260 · Cited by 25
Edgar, J. M., & Griffiths, I. R. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374709-9.00005-5 · Cited by 25
Thapaliya, K., Vegh, V., Bollmann, S., & Barth, M. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.11.029 · Cited by 23
Exercise modulates the levels of growth inhibitor genes before and after multiple sclerosis
Shahidi, S. H., Kordi, M. R., Rajabi, H., Malm, C., Shah, F. K., & Quchan, A. H. S. K. (2020) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2020.577172 · Cited by 22
Saitta, K. S., Lercher, L. D., Sainato, D. M., Patel, A., Huang, Y., McAuliffe, G., & Dreyfus, C. F. (2021) · Glia · doi:10.1002/glia.24003 · Cited by 23
Franco‐Pons, N., Tomàs-Roig, J., Roig, B., Auladell, C., Martorell, L., & Vilella, E. (2008) · Journal of Molecular Neuroscience · doi:10.1007/s12031-008-9151-x · Cited by 24
Colmenares, A. M., Prytherch, B., Thomas, M. L., & Burzynska, A. Z. (2023) · Imaging Neuroscience · doi:10.1162/imag_a_00045 · Cited by 24
Heterogeneity in oligodendroglia: Is it relevant to mouse models and human disease?
Ornelas, I. M., McLane, L. E., Saliu, A., Evangelou, A. V., Khandker, L., & Wood, T. L. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23900 · Cited by 22
Huang, Y., Song, Y. J., Isaac, M., Miretzky, S., Patel, A., McAuliffe, W. G., & Dreyfus, C. F. (2020) · ASN NEURO · doi:10.1177/1759091420957464 · Cited by 19
Structural adaption of axons during de‐ and remyelination in the Cuprizone mouse model
Pfeiffer, F., Frommer‐Kaestle, G., & Fallier‐Becker, P. (2019) · Brain Pathology · doi:10.1111/bpa.12748 · Cited by 22
Hoyos, H. C., Marder, M., Ulrich, R., Gudi, V., Stangel, M., Rabinovich, G. A., Pasquini, L. A., & Pasquini, J. M. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-40764-7_15 · Cited by 21
Laquinimod Supports Remyelination in Non-Supportive Environments
Nyamoya, S., Steinle, J., Chrzanowski, U., Kaye, J., Schmitz, C., Beyer, C., & Kipp, M. (2019) · Cells · doi:10.3390/cells8111363 · Cited by 19
Multiple Sclerosis: Basic and Clinical
Buzzard, K. A., Chan, W. H., Kilpatrick, T. J., & Murray, S. S. (2017) · Advances in neurobiology · doi:10.1007/978-3-319-57193-5_8 · Cited by 26
Chew, L., Ming, X., Mcellin, B. M., Dupree, J. L., Hong, E., Catron, M. A., Fauveau, M., Nait‐Oumesmar, B., & Gallo, V. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.10.121 · Cited by 19
Rühling, S., Kramer, F., Schmutz, S., Amor, S., Jiangshan, Z., Schmitz, C., Kipp, M., & Hochstrasser, T. (2019) · Molecular Neurobiology · doi:10.1007/s12035-018-1353-9 · Cited by 18
Fatemi, A. S., Wilson, M. A., Phillips, A. W., McMahon, M. T., Zhang, J., Smith, S. A., Arauz, E. J., Falahati, S., Gummadavelli, A., Bodagala, H., et al. (2011) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2011.68 · Cited by 17
Hertanu, A., Soustelle, L., Buron, J., Priellec, J. L., Cayre, M., Troter, A. L., Prévost, V., Ranjeva, J., Varma, G., Alsop, D. C., et al. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119785 · Cited by 16
Compromised Myelin and Axonal Molecular Organization Following Adult-Onset Sulfatide Depletion
Dustin, E., Suárez‐Pozos, E., Stotesberry, C., Qiu, S., Palavicini, J. P., Han, X., & Dupree, J. L. (2023) · Biomedicines · doi:10.3390/biomedicines11051431 · Cited by 15
Kalakh, S., & Mouihate, A. (2015) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12237 · Cited by 16
Remyelination by Endogenous Glia
Franklin, R. J. M., & Goldman, J. E. (2004) · Elsevier eBooks · doi:10.1016/b978-012439510-7/50060-7 · Cited by 15
Feng, Y., Feng, F., Zheng, C., Zhou, Z., Jiang, M., Liu, Z., Xie, F., Sun, X., & Wu, Z. (2019) · International Journal of Biological Sciences · doi:10.7150/ijbs.35266 · Cited by 14
The Rabbit Brachial Plexus as a Model for Nerve Repair Surgery—Histomorphometric Analysis
Reichert, P., Kiełbowicz, Z., Dzięgiel, P., Puła, B., Kuryszko, J. J., Gosk, J., & Bocheńska, A. (2014) · The Anatomical Record · doi:10.1002/ar.23058 · Cited by 13
Long lasting behavioural effects on cuprizone fed mice after neurotoxicant withdrawal
Tomàs-Roig, J., Torrente, M., Cabré, M., Vilella, E., & Colomina, M. T. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.01.036 · Cited by 15
Adult‐onset depletion of sulfatide leads to axonal degeneration with relative myelin sparing
Dustin, E., McQuiston, A. R., Honke, K., Palavicini, J. P., Han, X., & Dupree, J. L. (2023) · Glia · doi:10.1002/glia.24423 · Cited by 11
Cuprizone markedly decreases kynurenic acid levels in the rodent brain tissue and plasma
Polyák, H., Cseh, E. K., Bohár, Z., Rajda, C., Zádori, D., Klivènyi, P., Toldi, J., & Vécsei, L. (2021) · Heliyon · doi:10.1016/j.heliyon.2021.e06124 · Cited by 14
Richards, K., Jancovski, N., Hanssen, E. G., Connelly, A., & Petrou, S. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147157 · Cited by 9
Edgar, J. M., & Griffiths, I. R. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-396460-1.00007-x · Cited by 13
Tian, K., Zhang, F., Jiang, H., Wang, B., & Han, S. (2016) · Journal of Anatomy · doi:10.1111/joa.12541 · Cited by 10
Siponimod supports remyelination in the non-supportive environment
Krüger, J., Behrangi, N., Schliep, D., Heinig, L., Vankriekelsvenne, E., Wigger, N., & Kipp, M. (2025) · Scientific Reports · doi:10.1038/s41598-025-87825-8 · Cited by 9
Role and Mechanism of Microglia in White Matter Injury Recovery in Ischemic Stroke
Guo, Y., Shang, Y., Yao, J., & Bi, X. (2025) · Immunity Inflammation and Disease · doi:10.1002/iid3.70226 · Cited by 12
Rossi, E. G., Marenna, S., Castoldi, V., Comı, G., & Leocani, L. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.114972 · Cited by 9
Remyelination as Neuroprotection
Howe, C. L., & Rodriguez, M. (2005) · Elsevier eBooks · doi:10.1016/b978-012738761-1/50028-6 · Cited by 8
Lanthionine Ketimine Ethyl Ester Accelerates Remyelination in a Mouse Model of Multiple Sclerosis
Dupree, J. L., Paez, P. M., Tiwari-Woodruff, S. K., Denton, T. T., Hensley, K., Angeliu, C. G., Boullerne, A. I., Kalinin, S., Egge, S., Cheli, V. T., et al. (2022) · ASN NEURO · doi:10.1177/17590914221112352 · Cited by 7
Symmetric data-driven fusion of diffusion tensor MRI: Age differences in white matter
Colmenares, A. M., Hefner, M. B., Calhoun, V. D., Salerno, E. A., Fanning, J. T., Gothe, N. P., McAuley, E., Kramer, A. F., & Burzynska, A. Z. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1094313 · Cited by 6
The development of myelin repair agents for treatment of multiple sclerosis
Murphy, R., Murphy, K. J., & Pickering, M. (2013) · Bioengineered · doi:10.4161/bioe.22835 · Cited by 6
Zarini, D., Pasbakhsh, P., Mojaverrostami, S., Amirizadeh, S., Hashemi, M., Shabani, M., Noshadian, M., & Kashani, I. R. (2024) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2023.101630 · Cited by 5
Neves, K. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804042-3.00047-6 · Cited by 4
Jurczak, W. J., Rule, S. A., Townsend, W. M., Tucker, D. L., Sarholz, B., Scheele, J., Gribben, J. G., & Zinzani, P. L. (2018) · Annals of Oncology · doi:10.1093/annonc/mdy286.010 · Cited by 3
Influence of 7T GRE-MRI Signal Compartment Model Choice on Tissue Parameters
Thapaliya, K., Vegh, V., Bollmann, S., & Barth, M. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00271 · Cited by 3
3D inversion recovery ultrashort echo time MRI can detect demyelination in cuprizone-treated mice
Searleman, A. C., Ma, Y., Sampath, S. C., Sampath, S. C., Bussell, R., Chang, E. Y., Deaton, L. M., Schumacher, A. M., & Du, J. (2024) · Frontiers in Neuroimaging · doi:10.3389/fnimg.2024.1356713 · Cited by 2
Utrera, J., Romero, R., Verdaguer, E., Junyent, F., & Auladell, C. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07928.x · Cited by 2
Remyelination in Multiple Sclerosis
Stangel, M., Pul, R., Skripuletz, T., Trebst, C., Voß, E. V., & Gudi, V. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-384913-7.00009-5 · Cited by 3
Thomason, E. J., Suárez‐Pozos, E., Afshari, F. S., Rosenberg, P. A., Dupree, J. L., & Fuss, B. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.905299 · Cited by 2
Effects of recombinant human erythropoietin in the cuprizone mouse model of de- and remyelination
Hagemeyer, N. (2012) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-1472 · Cited by 2
Ebrahimbabaei, A., Osanloo, M., Ghanbariasad, A., & Shojaeifard, M. B. (2026) · Molecular Neurobiology · doi:10.1007/s12035-025-05632-8 · Cited by 1
Bardile, C. F., Priego, M., Sidik, H., Tano, V., Langley, S. R., Pouladi, M. A., & Morfini, G. A. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70356 · Cited by 1
Oxidative Stress and Neurodegeneration
Pasquini, J. M., Pasquini, L. A., & Quintá, H. R. (2016) · Springer eBooks · doi:10.1007/978-3-319-45865-6_20 · Cited by 1
TRP channels as potential target molecules for pharmacotherapy of neurological diseases
Kormos, V., Kriszta, G., Al-Omari, A., Rozmer, K., Konkoly, J., Pozsgai, G., & Pintér, E. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-18653-0.00011-3 · Cited by 1
Immune mediators of central nervous system demyelination and remyelination
Chen, V. S. (2008) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/v4b9-9109 · Cited by 1
Die Rolle der Beta-Sekretase bei der Myelinisierung im Zentralen Nervensystem
Treiber, H. (2014) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-4444
Kuypers, N. J. (2014) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/786
Axon Initial Segment Stability in Multiple Sclerosis
Thummala, S. K. (2015) · VCU Scholars Compass (Virginia Commonwealth University) · doi:10.25772/gptb-a885
De - und Remyelinisierung in Dopaminrezeptor-defizienten Mäusen
Schultz, K. (2012) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-1535
The Regenerative Response of Endogenous Neural Stem/Progenitor Cells to Traumatic Brain Injury
Sullivan, G. M. (2014) · Defense Technical Information Center (DTIC) · doi:10.21236/ad1012867
Sex differences and the protective influence of estrogen in a mouse model of demyelinating disease
Taylor, L. C. (2008) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/5t0s-5k20
Lipid organisation and dynamics in the myelin membrane sheets
Steshenko, O. (2014) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-4620
Schüle, S. (2013) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3851
Schultz, V. (2015) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-4890
The role of astrocytic RFX4_v3 in demyelination
Paap, F. (2015) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5062
Effects of dimethyl fumarate in two animal models of MS
Traffehn, S. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6275
Svendsen, O. B., Hasegawa, R., Yang, R. R., Uzuncayir, M. A., Conoan, N. H., Hasselholt, S., Midtgaard, J., Xu, N.-L., Lee, F. S. Y., & Nyengaard, J. R. (2024) · Brain Mechanisms · doi:10.1016/j.bramec.2024.202483
Postmortem Validation of Quantitative MRI for White Matter Hyperintensities in Alzheimer’s DiseasePreprint
Mojtabai, M., Kumar, R., Honnorat, N., Li, K., Wang, D. H., Li, J., Lee, R. F., Richardson, T. E., Cavazos, J. E., Bouhrara, M., et al. (2025) · medRxiv · doi:10.1101/2025.08.05.25332820
Dai, X., Zhang, J., Li, X., Chen, Y., Qiao, Y., Zhang, S., Chen, K. W., Ai, L., Peng, D., & Zhang, Z. (2026) · Frontiers in Neurology · doi:10.3389/fneur.2025.1658712
Myelin imaging in MRI using ultra-short echo time sequences
Soustelle, L. (2018) · theses.fr (ABES) · doi:10.70675/7606cd78z6ce3z466fzbba0z59ebf521f1d9
Metadata
- Authors
- Mason, J. L., Langaman, C., Morell, P., Suzuki, K., & Matsushima, G. K.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Corresponding author
- Matsushima, G. K.
- ORCID
- Suzuki, K.
- Venue
- Neuropathology and Applied Neurobiology
- Publisher
- Wiley
- Published
- 2001-02
- Volume
- 27
- Issue
- 1
- Pages
- 50-58
- ISSN
- 0305-1846 (ISSN-L)
- 1365-2990
- OpenAlex
- W2156549416
- Cited by
- 172
- References
- 27
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 6 · 2023: 5 · 2022: 4 · 2021: 3 · 2020: 6 · 2019: 13 · 2018: 6 · 2017: 8 · 2016: 13 · 2015: 12 · 2014: 9 · 2013: 6 · 2012: 4
- FWCI
- 3.32
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuropathology and Applied Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Multiple Sclerosis Society
- National Institutes of Health (RG2754A1, 5r01ns011615-29, 5r01ns037815-05, 5r29ns035372-05)
- National Institute of Neurological Disorders and Stroke (NS 24453, NS37815, R01NS024453, NS-11615, NS-35372)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Keywords
- cuprizone, demyelination, remyelination, axon diameter, corpus callosum, demyelinating disease, C57BL/6 mice
- MeSH terms
- Amidines, Animals, Axons, Central Nervous System, Chronic Disease, Corpus Callosum, Cuprizone, Demyelinating Diseases, Disease Models, Animal, Fluorescent Dyes, Mice, Inbred C57BL, Microscopy, Electron, Nerve Fibers, Myelinated, Recurrence, Remission, Spontaneous, Cell Size, Mice
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