The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
The Kinetochore
Open accessAbstract
A critical requirement for mitosis is the distribution of genetic material to the two daughter cells. The central player in this process is the macromolecular kinetochore structure, which binds to both chromosomal DNA and spindle microtubule polymers to direct chromosome alignment and segregation. This review will discuss the key kinetochore activities required for mitotic chromosome segregation, including the recognition of a specific site on each chromosome, kinetochore assembly and the formation of kinetochore-microtubule connections, the generation of force to drive chromosome segregation, and the regulation of kinetochore function to ensure that chromosome segregation occurs with high fidelity.
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Citations
Cites
The spindle-assembly checkpoint in space and time
Musacchio, A., & Salmon, E. D. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2163 · Cited by 2,227
Boveri revisited: chromosomal instability, aneuploidy and tumorigenesis
Holland, A. J., & Cleveland, D. W. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2718 · Cited by 859
Sensing centromere tension: Aurora B and the regulation of kinetochore function
Lampson, M. A., & Cheeseman, I. M. (2011) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.10.007 · Cited by 375
Self-citationFoley, E. A., Maldonado, M., & Kapoor, T. M. (2011) · Nature Cell Biology · doi:10.1038/ncb2327 · Cited by 267
Cited by
The molecular biology of spindle assembly checkpoint signaling dynamics.
Musacchio, A. (2015) · Current Biology · doi:10.1016/j.cub.2015.08.051 · Cited by 778
The phenotypic landscape of essential human genes
Funk, L., Su, K.-C., Ly, J., Feldman, D., Singh, A., Moodie, B., Blainey, P. C., & Cheeseman, I. M. (2022) · Cell · doi:10.1016/j.cell.2022.10.017 · Cited by 160
Self-citationBUB-1-bound PLK-1 directs CDC-20 kinetochore recruitment to ensure timely embryonic mitoses
Houston, J., Ohta, M., Gómez-Cavazos, J. S., Deep, A., Corbett, K. D., Oegema, K., Lara-Gonzalez, P., Kim, T., & Desai, A. (2023) · Current Biology · doi:10.1016/j.cub.2023.04.021 · Cited by 13
Ludzia, P., Ishii, M., Deák, G., Spanos, C., Wilson, M. D., Redfield, C., & Akiyoshi, B. (2025) · Structure · doi:10.1016/j.str.2024.10.031 · Cited by 6
Tarasovetc, E. V., Sissoko, G. B., Maiorov, A., Mukhina, A. S., Ataullakhanov, F. I., Cheeseman, I. M., & Grishchuk, E. L. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2401344121 · Cited by 4
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Metadata
- Authors
- Cheeseman, I. M.
- Venue
- Cold Spring Harbor Perspectives in Biology
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2014-07-01
- Volume
- 6
- Issue
- 7
- Pages
- a015826-a015826
- ISSN
- 1943-0264 (ISSN-L)
- OpenAlex
- W4229736484
- Cited by
- 298
- References
- 4
- Type
- posted content
- Language
- en
- Open access
- bronze
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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.
