The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Identification of myelin-associated glycoprotein as a major myelin-derived inhibitor of neurite growth
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.
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
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
Absence of Wallerian Degeneration does not Hinder Regeneration in Peripheral Nerve
Lunn, E. R., Perry, V. H., Brown, M. C., Rosen, H., & Gordon, S. (1989) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1989.tb00771.x · Cited by 646
Two contrary functions of tenascin: Dissection of the active sites by recombinant tenascin fragments
Spring, J., Beck, K., & Chiquet-Ehrismann, R. (1989) · Cell · doi:10.1016/0092-8674(89)90294-8 · Cited by 413
Cited by
Biology of Oligodendrocyte and Myelin in the Mammalian Central Nervous System
Baumann, N., & Pham-Dinh, D. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.2.871 · Cited by 1,828
White matter in learning, cognition, and psychiatric disorders
Fields, R. D. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.04.001 · Cited by 1,337
Schnaar, R. L., Gerardy-Schahn, R., & Hildebrandt, H. (2014) · Physiological Reviews · doi:10.1152/physrev.00033.2013 · Cited by 745
The bright side of the glial scar in CNS repair
Rolls, A., Shechter, R., & Schwartz, M. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2591 · Cited by 674
Experience-driven plasticity of visual cortex limited by myelin and nogo receptor
McGee, A. W., Yang, Y., Fischer, Q. S., Daw, N. W., & Strittmatter, S. M. (2005) · Science · doi:10.1126/science.1114362 · Cited by 643
Davies, S. J. A., Goucher, D. R., Doller, C., & Silver, J. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-14-05810.1999 · Cited by 606
Why is Wallerian degeneration in the CNS so slow?
Vargas, M. E., & Barres, B. A. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094354 · Cited by 510
Linking oligodendrocyte and myelin dysfunction to neurocircuitry abnormalities in schizophrenia
Takahashi, N., Sakurai, T., Davis, K. L., & Buxbaum, J. D. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.09.004 · Cited by 337
Macrophages in spinal cord injury: Phenotypic and functional change from exposure to myelin debris
Wang, X., Cao, K., Sun, X., Chen, Y., Duan, Z., Sun, L., Guo, L., Bai, P., Sun, D., Fan, J., et al. (2015) · Glia · doi:10.1002/glia.22774 · Cited by 288
Vyas, A. A., Patel, H. V., Fromholt, S. E., Heffer-Lauc, M., Vyas, K. A., Dang, J., Schachner, M., & Schnaar, R. L. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.072211699 · Cited by 272
Neural Stem Cell Transplantation for Neurodegenerative Diseases
De Gioia, R., Biella, F., Citterio, G., Rizzo, F., Abati, E., Nizzardo, M., Bresolin, N., Comi, G. P., & Corti, S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21093103 · Cited by 247
The digital revolution and adolescent brain evolution
Giedd, J. N. (2012) · Journal of Adolescent Health · doi:10.1016/j.jadohealth.2012.06.002 · Cited by 185
Macrophage phagocytosis after spinal cord injury: when friends become foes
Van Broeckhoven, J., Sommer, D., Dooley, D., Hendrix, S., & Franssen, A. J. P. M. (2021) · Brain · doi:10.1093/brain/awab250 · Cited by 172
Receptor protein tyrosine phosphatase sigma inhibits axon regrowth in the adult injured CNS
Sapieha, P. S., Duplan, L., Uetani, N., Joly, S., Tremblay, M. L., Kennedy, T. E., & Di Polo, A. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.10.011 · Cited by 106
Jackson Snipes, G., & Suter, U. (1997) · Subcellular Biochemistry · doi:10.1007/978-1-4615-5901-6_7 · Cited by 77
Collins, B. E., Ito, H., Sawada, N., Ishida, H., Kiso, M., & Schnaar, R. L. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.53.37637 · Cited by 73
Macrophages and microglia in central nervous system injury: are they helpful or harmful?
Schwartz, M. (2003) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200304000-00001 · Cited by 207
Gopalakrishnan, S. M., Teusch, N., Imhof, C., Bakker, M. H. M., Schurdak, M., Burns, D. J., & Warrior, U. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21671 · Cited by 62
Sun, J. (2004) · Glycobiology · doi:10.1093/glycob/cwh107 · Cited by 56
Chevalier, A. C., & Rosenberger, T. A. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14032 · Cited by 50
Pourabdolhossein, F., Mozafari, S., Morvan-Dubois, G., Mirnajafi-Zadeh, J., Lopez-Juarez, A., Pierre-Simons, J., Demeneix, B. A., & Javan, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0106378 · Cited by 47
Biomaterial Approaches to Modulate Reactive Astroglial Response
Zuidema, J. M., Gilbert, R. J., & Gottipati, M. K. (2018) · Cells Tissues Organs · doi:10.1159/000494667 · Cited by 46
Mehta, N. R., Nguyen, T., Bullen, J. W., Griffin, J. W., & Schnaar, R. L. (2010) · ACS Chemical Neuroscience · doi:10.1021/cn900029p · Cited by 38
Gene expression-based modeling of human cortical synaptic density
Goyal, M. S., & Raichle, M. E. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1303453110 · Cited by 37
Overexpression of myelin-associated glycoprotein after axotomy of the perforant pathway
Mingorance, A., Fontana, X., Soriano, E., & del Río, J. A. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.03.016 · Cited by 24
Axons regulate the distribution of Schwann cell microtubules
Kidd, G., Andrews, S., & Trapp, B. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-03-00946.1996 · Cited by 23
SIGLEC-4 (MAG) antagonists: From the natural carbohydrate epitope to glycomimetics
Schwardt, O., Kelm, S., & Ernst, B. (2013) · Topics in current chemistry · doi:10.1007/128_2013_498 · Cited by 14
Metadata
- Authors
- McKerracher, L., David, S., Jackson, D. L., Kottis, V., Dunn, R. J., & Braun, P. E.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 1994-10
- Volume
- 13
- Issue
- 4
- Pages
- 805-811
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2025778924
- Cited by
- 1,126
- References
- 3
- FWCI
- 13.47
- Type
- journal article
- Language
- en
- Open access
- closed
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
