The DOI matches its Crossref record; 40 of the 41 references it cites were found in a registry or an index.
Differentiation and Death of Premyelinating Oligodendrocytes in Developing Rodent Brain
Open accessAbstract
Previous studies have indicated that newly formed oligodendrocytes are dynamic cells whose production, survival, and differentiation depend upon axonal influences. This study has characterized the appearance and fate of newly formed oligodendrocytes in developing rat brain. Oligodendrocytes appear in predictable locations and radially extend DM-20-positive processes that cover 80-microm domains in the cortex and 40-microm domains in the corpus callosum. These premyelinating oligodendrocytes have one of two fates: they myelinate axons or degenerate. Between 7 and 21 d after birth, approximately 20% of premyelinating oligodendrocytes identified in the cerebral cortex were degenerating. Oligodendrocytes that ensheathed axons expressed and selectively targeted proteolipid protein to compact myelin and did not degenerate. These observations support the hypothesis that axonal influences affect oligodendrocyte survival, differentiation, and expression of proteolipid protein gene products.
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 source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In the developing neocortex, ∼20% of premyelinating OLs die between P7 and P11 (Trapp et al., 1997).”
From Oligodendrocyte Dynamics in the Healthy Adult CNS: Evidence for Myelin Remodeling (2013) · cites this paper as Trapp et al., 1997
Experimental — accuracy not yet measuredIn the citing paper
“The timing of their appearance coincides with the onset of myelination, during which large numbers of newly formed oligodendrocytes die (Barres et al., 1992; Trapp et al., 1997).”
From Developmental Heterogeneity of Microglia and Brain Myeloid Cells Revealed by Deep Single-Cell RNA Sequencing (2019) · cites this paper as Trapp et al., 1997
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
RAFF, M. C., Miller, R. H., & Noble, M. (1983) · Nature · doi:10.1038/303390a0 · Cited by 2,030
Programmed Cell Death and the Control of Cell Survival: Lessons from the Nervous System
RAFF, M. C., Barres, B. A., Burne, J. F., Coles, H., Ishizaki, Y., & Jacobson, M. D. (1993) · Science · doi:10.1126/science.8235590 · Cited by 1,450
Cell death and control of cell survival in the oligodendrocyte lineage
Barres, B. A., Hart, I. K., Coles, H. S. R., Burne, J. F., Voyvodic, J. T., Richardson, W. D., & Raff, M. C. (1992) · Cell · doi:10.1016/0092-8674(92)90531-g · Cited by 1,345
A role for platelet-derived growth factor in normal gliogenesis in the central nervous system
Richardson, W. D., Pringle, N. P., Mosley, M. J., Westermark, B., & Dubois-Dalcg, M. (1988) · Cell · doi:10.1016/0092-8674(88)90392-3 · Cited by 774
The oligodendrocyte and its many cellular processes
PFEIFFER, S., WARRINGTON, A., & BANSAL, R. (1993) · Trends in Cell Biology · doi:10.1016/0962-8924(93)90213-k · Cited by 737
Levison, S. W., & Goldman, J. E. (1993) · Neuron · doi:10.1016/0896-6273(93)90311-e · Cited by 725
Proliferation of oligodendrocyte precursor cells depends on electrical activity in axons
Barres, B. A., & Raff, M. C. (1993) · Nature · doi:10.1038/361258a0 · Cited by 673
Pringle, N. P., & Richardson, W. D. (1993) · Development · doi:10.1242/dev.117.2.525 · Cited by 510
Pringle, N. P., Mudhar, H. S., Collarini, E. J., & Richardson, W. D. (1992) · Development · doi:10.1242/dev.115.2.535 · Cited by 443
Polarity of Epithelial and Neuronal Cells
Rodriguez-Boulan, E. J., & Powell, S. K. (1992) · Annual Review of Cell Biology · doi:10.1146/annurev.cb.08.110192.002143 · Cited by 430
Flagged first, then by citations
1 of the 41 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Nishiyama, 1996, Interaction between NG2 proteoglycan and PDGF α receptor on 02A progenitor cells is required for optimal response to PDGF, J Neurosci Res, 43, 315, 10.1002/(SICI)1097-4547(19960201)43:3<315::AID-JNR6>3.0.CO;2-M · DOI
Cited by
Sorted by citations
Items 301–393 of 393
Arinrad, S., Depp, C., Siems, S. B., Sasmita, A. O., Eichel‐Vogel, M. A., Ronnenberg, A., Hammerschmidt, K., Lüders, K. A., Werner, H. B., Ehrenreich, H., et al. (2023) · eLife · doi:10.7554/elife.70792 · Cited by 9
Cleavage of VAMP2/3 Affects Oligodendrocyte Lineage Development in the Developing Mouse Spinal Cord
Fekete, C. D., Horning, R. Z., Doron, M. S., & Nishiyama, A. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.2206-21.2023 · Cited by 9
Self-citationThomson, C. E., Vouyiouklis, D. A., Barrie, J. A., Wease, K. N., & Montague, P. (2005) · Developmental Neuroscience · doi:10.1159/000084530 · Cited by 8
Is cell migration or proliferation dominant in the formation of linear arrays of oligodendrocytes?
Walsh, D. M., Röth, P. T., Holmes, W. R., Landman, K. A., Merson, T. D., & Hughes, B. D. (2016) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2016.06.028 · Cited by 8
NG2/HMP Proteoglycan as a Cancer Therapeutic Target
Chekenya, M., & Immervoll, H. (2006) · Humana Press eBooks · doi:10.1385/1-59745-208-4:93 · Cited by 8
Approaches to the Study of Diseases Involving Oligodendroglial Death
Back, S. A., & Volpe, J. J. (1999) · Humana Press eBooks · doi:10.1007/978-1-4612-1602-5_19 · Cited by 8
Vana, N., van Loo, K. M. J., Waardenberg, A. J., Tießen, M., Cases‐Cunillera, S., Sun, W., Quatraccioni, A., Schoch, S., & Dietrich, D. (2023) · Glia · doi:10.1002/glia.24388 · Cited by 7
Butt, A. M., Niu, J., Yi, C., & Verkhratsky, A. (2026) · Physiological Reviews · doi:10.1152/physrev.00023.2025 · Cited by 7
Attack of the Clones: Microglia in Health and Disease
Manjally, A. V., & Tay, T. L. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.831747 · Cited by 7
mRNA Localization to the Endoplasmic Reticulum in Plant Endosperm Cells
Zhang, L., Si, Q., Yang, K., Zhang, W., Okita, T. W., & Tian, L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113511 · Cited by 8
Bouchard, E. L., Meireles, A. M., & Talbot, W. S. (2023) · Glia · doi:10.1002/glia.24473 · Cited by 7
ffrench‐Constant, C. (2004) · Elsevier eBooks · doi:10.1016/b978-012439510-7/50078-4 · Cited by 9
Increased apoptosis and hypomyelination in cerebral white matter of macular mutant mouse brain
Takikita, S., Takano, T., Narita, T., & Maruo, Y. (2015) · Molecular Genetics and Metabolism Reports · doi:10.1016/j.ymgmr.2015.05.005 · Cited by 7
Dysmyelination In Mice and the Proteolipid Protein Gene Family
Dimou, L., Klugmann, M., Werner, H. B., Jung, M., Nave, K., & Griffiths, I. R. (1999) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4685-6_21 · Cited by 7
KAJIGAYA, H., Tanaka, K. F., Hayashi, A., Suzuki, A., Ishibashi, T., Ikenaka, K., & Baba, H. (2011) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.87.415 · Cited by 7
Transient Upregulation of Procaspase-3 during Oligodendrocyte Fate Decisions
Kamen, Y., Chapman, T. W., Piedra, E. T., Ciolkowski, M. E., & Hill, R. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.2066-24.2025 · Cited by 6
Olude, M. A., Bello, S. T., Mustapha, O., Olopade, F. E., Plendl, J., Ihunwo, A. O., & Olopade, J. O. (2018) · Anatomia Histologia Embryologia · doi:10.1111/ahe.12348 · Cited by 6
Plasticity in oligodendrocyte lineage progression: An OPC puzzle on our nerves
Craig, G. A., Yoo, S., D'Araujo, T. Y., & Xiao, J. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14845 · Cited by 6
Orian, J. M., Ahern, A. J., Ayers, M. M., Levine, J. M., Tapp, L. D., & Reynolds, R. (2001) · Journal of Neuroscience Research · doi:10.1002/jnr.1196 · Cited by 6
Bhambri, A., Thai, P., Wei, S., Bae, H., Reynolds, P., Barbosa, D., Sharma, T., Yu, Z., Xing, C., Kim, J. H., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-02110-1 · Cited by 7
Pantazou, V., Roux, T., Moreira, V. O., Lubetzki, C., & Desmazières, A. (2021) · Life · doi:10.3390/life11030231 · Cited by 6
Visualization of myelin‐forming oligodendrocytes in the adult mouse brain
Yokoyama, K., Hiraoka, Y., Abe, Y., & Tanaka, K. F. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16218 · Cited by 5
Parrilla, M., León-Lobera, F., Lillo, C., Arévalo, R., Aijón, J., Lara, J. M., & Velasco, A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0154703 · Cited by 5
Models of Pelizeaus-Merzbacher-Disease
Nave, K., & Griffiths, I. R. (2004) · Elsevier eBooks · doi:10.1016/b978-012439510-7/50100-5 · Cited by 5
Sypecka, J. (2003) · PubMed · Cited by 4
Joshi, S., Frondelli, M. J., Zanin, J. P., Levison, S. W., & Friedman, W. (2023) · Glia · doi:10.1002/glia.24430 · Cited by 3
Neuron–glial interactions and neurotransmitter signaling to cells of the oligodendrocyte lineage
Call, C. L., Biase, L. M. D., & Bergles, D. E. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00036-9 · Cited by 3
Biase, L. M. D., & Bergles, D. E. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00133-7 · Cited by 3
Defective myelination in an RNA polymerase III mutant leukodystrophic mousePreprint
Merheb, E., Cui, M.-H., DuBois, J. C., Branch, C. A., Gulinello, M., Shafit‐Zagardo, B., Moir, R. D., & Willis, I. M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.12.09.418657 · Cited by 3
A COMPARATIVE ANALYSIS OF CONVECTIVE HEAT TRANSFER IN A NUCLEAR ROCKET NOZZLE
Neumann, H., & Bettinger, P. J. (1963) · University of Michigan Library Repository · Cited by 3
Regulation of oligodendrocyte lineage development by VAMP2/3 in the developing mouse spinal cordPreprint
Fekete, C. D., Horning, R. Z., Doron, M. S., & Nishiyama, A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.10.507429 · Cited by 3
Self-citationRies, C., Štark, T., Boulat, B., Ruhwedel, T., Delling, J. P., Infante, A. M., von Poblotzki, J., Ulivi, A. F., von Mücke-Heim, I.-A., Chang, S., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116474 · Cited by 3
Effect of postlactation iron deficiency on the composition of fatty acids of whole brain myelin
Romero, M. D. S. C., Pliego-Rivero, F. B., Moreno-Altamirano, B., & Otero, G. (2010) · Nutritional Neuroscience · doi:10.1179/147683010x12611460764606 · Cited by 2
Clayton, B. L. L., Allan, K. C., Nevin, Z. S., Elitt, M. S., & Tesar, P. J. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814409-1.00013-6 · Cited by 2
Zacher, A., Grabinski, M., Console‐Meyer, L., Felmy, F., & Pätz, C. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1561312 · Cited by 1
Developmental Profiling of Structural and Functional Maturation in Mouse Corpus Callosum
Johnson, H., Beall, M., Latifi, S., Peng, J., & Sun, W. (2026) · Glia · doi:10.1002/glia.70152 · 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. (2021) · Springer eBooks · doi:10.1007/978-3-030-71519-9_219-1 · Cited by 2
Манолова, А. О., & Gulyaeva, N. V. (2023) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093023050125 · Cited by 1
Effect of Cytoskeletal Linker Protein GAS2L1 on Oligodendrocyte and Myelin Development
Zou, Y., Jin, Y., Yang, Y., Zhang, L., Feng, Y., Yu, L., Xu, Z., He, Y., Zheng, W., Wang, S., et al. (2025) · Glia · doi:10.1002/glia.24658 · Cited by 1
Neuroprotection in Demyelinating Diseases: The Therapeutic Potential of the Neurotrophins
Xiao, J., Hughes, R. A., & Murray, S. S. (2014) · Springer eBooks · doi:10.1007/978-1-4614-5836-4_36 · Cited by 1
A Small Molecule Induces Oligodendrogenesis Leading to Myelin Sheath Repair
Nye, S. H., & Yarger, J. G. (2017) · 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
Lyons, D. A., & Almeida, R. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732872241.793545529 · Cited by 1
Autophagy collaborates with apoptosis pathways to control myelination specificity and functionPreprint
Zhang, T., Bae, H., Bhambri, A., Zhang, Y., Barbosa, D., Xue, J., Wazir, S., Mulinyawe, S. B., Kim, J. H., & Sun, L. O. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.31.522394 · Cited by 1
Bhambri, A., Thai, P., Wei, S., Bae, H., Barbosa, D., Sharma, T., Yu, Z., Xing, C., Kim, J. H., Yu, G., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.27.630559 · Cited by 1
Nave, K. (1999) · Springer eBooks · doi:10.1007/978-3-662-07096-3_12 · Cited by 1
Hienola, A. (2007) · Työväentutkimus Vuosikirja
Buser, A. (2008) · edoc (University of Basel) · doi:10.5451/unibas-004587317
Histologie de la glie et oligodendrogenèse
Varlet, P. (2005) · Neurochirurgie · doi:10.1016/s0028-3770(05)83483-6
Charakterisierung der subzellulären Lokalisation von Myelinproteinen in der Shiverer-Maus.
Winter, C. (2010) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-814
Dhaunchak, A. S. (2006) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3205
Trapp, B. D., & Herrup, K. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-5316-3.00007-1
Self-citationStem Cell Biology in the Central Nervous System
Horner, P. J., & Nutt, S. E. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-5316-3.00006-x
Characterization, differentiation and therapeutic application of NG2+ progenitor cells
Ju, P. J. (2013) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/53654
Identification of a unique oligodendrocyte subpopulation in mouse brain
Khojasteh-Fard, M. (2018) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7076 · Cited by 1
Demyelinating conditions regulated by ROS pathways outside and inside the brain
Carlström, K. E. (2020) · Figshare
Neural Injury at the Molecular Level
Kim, D. H., Vaccaro, A. R., Henderson, F. C., & Benzel, E. C. (2005) · Elsevier eBooks · doi:10.1016/b978-0-443-06616-0.50011-0
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
Luo, J. X. X. (2021) · eScholarship@McGill (McGill) · doi:10.82308/21669
White matter integrity of the frontal brain and its relevance for catatonia and executive function
Arinrad, S. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8974
Pinch2 is a novel regulator of myelination in the Central Nervous SystemPreprint
de Faria, J. P., Vale-Silva, R. S., Fässler, R., Werner, H. B., & Relvas, J. B. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.04.483000
Neural Injury at the Molecular Level
Mullin, J. P., Wathen, C. A., Walsh, K. M., Kim, D. H., Vaccaro, A. R., Henderson, F. C., & Benzel, E. C. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-40030-5.00019-8
Lu, Q. R., & Berry, K. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734515510.793570329
Lyons, D. A., & Almeida, R. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.738031512.793575106
Lyons, D. A., & Almeida, R. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734515510.793553839
Focal adhesion kinase, a major regulator of oligodendrocyte morphological maturation and myelination
Lafrenaye, A. D. (2010) · VCU Scholars Compass (Virginia Commonwealth University) · doi:10.25772/9rxs-er88
Sasmita, A. O. (2024) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10403
Манолова, А. О., & Gulyaeva, N. V. (2023) · Российский физиологический журнал им И М Сеченова · doi:10.31857/s0869813923090078 · Cited by 1
Wang, Y., Egert, A., Schenke, M., Smirnova, L., & Kincaid, B. (2025) · Elsevier eBooks · doi:10.1016/b978-0-323-95488-4.00187-x
Are Oligodendrocytes the Culprits or Victims in Alzheimer's Disease
Rapaka, D., Saniotis, A., Henneberg, M., & Bitra, V. R. (2025) · Physiological Research · doi:10.33549/physiolres.935451
Prado-Rivera, M. A., Jagersma, J. D., & Olivier, J. D. A. (2025) · Current topics in behavioral neurosciences · doi:10.1007/7854_2025_602
Tanaka, M., Morita, C., Izawa, T., Yamate, J., Franklin, R. J. M., Kuramoto, T., Serikawa, T., & Kuwamura, M. (2025) · Veterinary Pathology · doi:10.1177/03009858251379486
Schenck, J. K., Karl, M. T., Paredes, C. C., Bastin, A., Pushkarsky, T., Břicháček, B., Miller, R. H., & Bukrinsky, M. (2024) · Figshare · doi:10.6084/m9.figshare.26719980
Macklin, W. B., & Allen, T. E. (2026) · Science · doi:10.1126/science.aee4609
Self-citationZi, H., Goldbrunner, A., Askari, S., Eichenseer, K., Misgeld, T., & Snaidero, N. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.15.705957
Premyelinating Oligodendrocyte Survival Governs CNS RemyelinationPreprint
Stockton, M. E., Wentling, M., Corchado, Y. I. M., Kucera, A. J., Karas, S., Seabrook, T. A., Mutschler, C., Osso, L. A., Schuster, K. H., Nunes, G. D. F., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.23.707571 · Cited by 1
Rôles des androgènes et de leur récepteur AR dans le dimorphisme et la réparation de la myéline
Abi‐Ghanem, C. (2016) · theses.fr (ABES) · doi:10.70675/c7a8d4f5z2330z4437z89a4z7ddf73a92b07
The role of Chd7 & Chd8 chromatin remodelers in oligodendrogenesis and (re)myelination
Marie, C. (2017) · theses.fr (ABES) · doi:10.70675/01ff9606zc0a7z47a8za3f4ze4f886e3bb00
Gliogenèse hypothalamique et contrôle de la fonction de reproduction
Martin, M. J. (2021) · theses.fr (ABES) · doi:10.70675/0650653dz87dez4961z9536z23565f173f47
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
Self-citationMolecular mechanisms involved in oligodendrocyte development
Coelho, R. P. (2008) · VCU Scholars Compass (Virginia Commonwealth University) · doi:10.25772/fx70-ha31
Electrical responses of oligodendrocytes to pathological stimuli
Kołodziejczyk, K. (2011) · UCL Discovery (University College London)
Dey, H. T. (2012) · Digital Archive @ GSU · doi:10.57709/3489823
Expression of the PLP Gene and a PLP-LacZ Transgene in Oligodendrocytes
Duchala, C. S., & Macklin, W. B. (1997) · Springer eBooks · doi:10.1007/978-1-4615-5949-8_16
Self-citationMutations of Myelination-Associated Genes That Affect Axonal Integrity
Nave, K., & Werner, H. B. (2005) · Elsevier eBooks · doi:10.1016/b978-012738761-1/50022-5
- Self-citation
Metadata
- Authors
- Trapp, B. D., Nishiyama, A., Cheng, D., & Macklin, W.
- Affiliations
- Cleveland Clinic (US)
- Venue
- The Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 1997-04-21
- Volume
- 137
- Issue
- 2
- Pages
- 459-468
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC2139778
- OpenAlex
- W2097849969
- Cited by
- 395
- References
- 41
- Citations by year
- 2026: 7 · 2025: 10 · 2024: 9 · 2023: 16 · 2022: 14 · 2021: 23 · 2020: 26 · 2019: 16 · 2018: 13 · 2017: 15 · 2016: 12 · 2015: 13 · 2014: 13 · 2013: 10 · 2012: 7
- FWCI
- 4.80
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Journal of Cell Biology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Funders
- National Multiple Sclerosis Society
- Multiple Sclerosis Society
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (NS25304, R01NS029818, R01NS025304, NS 29818)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Neonatal and fetal brain pathology
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Keywords
- oligodendrocyte differentiation, oligodendrocyte death, myelination, proteolipid protein, DM20, oligodendrocyte survival, cerebral cortex, corpus callosum, postnatal brain development
- MeSH terms
- Animals, Axons, Brain, Cell Differentiation, Cerebral Cortex, Chromatin, Corpus Callosum, Nerve Tissue Proteins, Oligodendroglia, Cell Death, Rats, Sprague-Dawley, Myelin Proteolipid Protein, 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