The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Microtubule Stabilization Reduces Scarring and Causes Axon Regeneration After Spinal Cord Injury
Open accessAbstract
Taxol stimulates the capacity of axons to grow after spinal cord injury.
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Cites
Chondroitinase ABC promotes functional recovery after spinal cord injury
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Microtubule stabilization specifies initial neuronal polarization
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Differential trafficking of Kif5c on tyrosinated and detyrosinated microtubules in live cells
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Sustained axon regeneration induced by co-deletion of PTEN and SOCS3
Sun, F., Park, K. K., Belin, S., Wang, D., Lu, T., Chen, G., Zhang, K., Yeung, C., Feng, G., Yankner, B. A., et al. (2011) · Nature · doi:10.1038/nature10594 · Cited by 754
Microglia are an essential component of the neuroprotective scar that forms after spinal cord injury
Bellver-Landete, V., Bretheau, F., Mailhot, B., Vallières, N., Lessard, M., Janelle, M.-E., Vernoux, N., Tremblay, M.-È., Fuehrmann, T., Shoichet, M. S., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08446-0 · Cited by 594
Cai, R., Pan, C., Ghasemigharagoz, A., Todorov, M. I., Förstera, B., Zhao, S., Bhatia, H. S., Parra-Damas, A., Mrowka, L., Theodorou, D., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0301-3 · Cited by 470
Axonal transport: Driving synaptic function
Guedes-Dias, P., & Holzbaur, E. L. F. (2019) · Science · doi:10.1126/science.aaw9997 · Cited by 355
Regulation of axonal regeneration after mammalian spinal cord injury
Zheng, B., & Tuszynski, M. H. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00562-y · Cited by 328
CNS fibroblasts form a fibrotic scar in response to immune cell infiltration.
Dorrier, C. E., Aran, D., Haenelt, E. A., Sheehy, R. N., Hoi, K. K., Pintarić, L., Chen, Y., Lizama, C. O., Cautivo, K. M., Weiner, G. A., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-020-00770-9 · Cited by 199
Cytoskeleton dynamics in axon regeneration
Blanquie, O., & Bradke, F. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.02.024 · Cited by 189
Self-citationLatremoliere, A., Cheng, L., DeLisle, M., Wu, C., Chew, S., Hutchinson, E. B., Sheridan, A., Alexandre, C., Latremoliere, F., Sheu, S.-H., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.07.029 · Cited by 183
Geoffroy, C. G., Hilton, B. J., Tetzlaff, W., & Zheng, B. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.03.028 · Cited by 159
Kim, G.-W., Li, L., Gorbani, M., You, L., & Yang, X.-J. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.464792 · Cited by 141
Developing therapeutic approaches to tau, selected kinases, and related neuronal protein targets
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Dock GEFs and their therapeutic potential: Neuroprotection and axon regeneration
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Cellular cartography: Towards an atlas of the neuronal microtubule cytoskeleton
Iwanski, M. K., & Kapitein, L. C. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1052245 · Cited by 38
Self-citationNoh, M. R., Woo, C.-H., Park, M.-J., In Kim, J., & Park, K. M. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.02.001 · Cited by 33
Rehabilitation enhances epothilone-induced locomotor recovery after spinal cord injury
Griffin, J. M., Hingorani Jai Prakash, S., Bockemühl, T., Benner, J. M., Schaffran, B., Moreno-Manzano, V., Büschges, A., & Bradke, F. (2022) · Brain Communications · doi:10.1093/braincomms/fcad005 · Cited by 19
Self-citationBiotolerability of Intracortical Microelectrodes
Fernández, E., & Botella, P. (2018) · Advanced Biosystems · doi:10.1002/adbi.201700115 · Cited by 11
In situ structural mechanism of epothilone-B-induced CNS axon regeneration
Bodakuntla, S., Taira, K., Yamada, Y., Alvarez-Brecht, P., Cada, A. K., Basnet, N., Zhang, R., Martinez-Sanchez, A., Biertümpfel, C., & Mizuno, N. (2025) · Nature · doi:10.1038/s41586-025-09654-z · Cited by 9
Microtubules in the axon are GDP bound but adopt a stable GTP-like expanded state
Zehr, E. A., Sun, S., Sarbanes, S. L., & Roll-Mecak, A. (2026) · Nature Structural & Molecular Biology · doi:10.1038/s41594-026-01787-7 · Cited by 8
Meiring, J. C. M., Mahapatra, V., Liu, R., Gravett, M. S. C., Morren, D., Saunders, H. A. J., Choi, S. R., Pelster José, A., Karhanova, A., Metallidou, I., et al. (2026) · Nature Cell Biology · doi:10.1038/s41556-026-02079-4
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Metadata
- Authors
- Hellal, F., Hurtado, A., Ruschel, J., Flynn, K. C., Laskowski, C. J., Umlauf, M., Kapitein, L. C., Strikis, D., Lemmon, V., Bixby, J., Hoogenraad, C. C., & Bradke, F.
- Venue
- Science
- Published
- 2011-02-18
- Volume
- 331
- Issue
- 6019
- Pages
- 928-931
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2058116209
- Cited by
- 588
- References
- 4
- FWCI
- 16.91
- Type
- journal article
- Language
- en
- Open access
- green
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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.
