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Human Zw10 and ROD are mitotic checkpoint proteins that bind to kinetochores
Abstract
Here we show that human Zeste White 10 (Zw10) and Rough deal (Rod) are new components of the mitotic checkpoint, as cells lacking these proteins at kinetochores fail to arrest in mitosis when exposed to microtubule inhibitors. Checkpoint failure and premature mitotic exit may explain why cells defective for hZw10 and hRod divide with lagging chromosomes. As Zw10 and Rod are not conserved in yeast, our data, combined with an accompanying study of Drosophila Zw10 and Rod, indicate that metazoans may require an elaborate spindle checkpoint to monitor complex kinetochore functions.
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“the kinetochore-associated protein (KNTC1), a regulator of the mitotic checkpoint70,71, which demonstrated moderate to strong lethal effects when knocked out in almost every cell line except for those with a KRAS G12V allele”
From The origins and genetic interactions of KRAS mutations are allele- and tissue-specific (2021) · cites this paper as [70]
Citations
Cites
Mutations of mitotic checkpoint genes in human cancers
Cahill, D. P., Lengauer, C., Yu, J., Riggins, G. J., Willson, J. K. V., Markowitz, S. D., Kinzler, K. W., & Vogelstein, B. (1998) · Nature · doi:10.1038/32688 · Cited by 1,490
Feedback control of mitosis in budding yeast
Li, R., & Murray, A. W. (1991) · Cell · doi:10.1016/0092-8674(81)90015-5 · Cited by 1,174
S. cerevisiae genes required for cell cycle arrest in response to loss of microtubule function
Hoyt, M. A., Totis, L., & Roberts, B. T. (1991) · Cell · doi:10.1016/0092-8674(81)90014-3 · Cited by 1,138
Association of Spindle Assembly Checkpoint Component XMAD2 with Unattached Kinetochores
Chen, R., Waters, J. C., Salmon, E. D., & Murray, A. W. (1996) · Science · doi:10.1126/science.274.5285.242 · Cited by 783
How Cells Get the Right Chromosomes
Nicklas, R. B. (1997) · Science · doi:10.1126/science.275.5300.632 · Cited by 619
Identification of a Human Mitotic Checkpoint Gene: hsMAD2
Li, Y., & Benezra, R. (1996) · Science · doi:10.1126/science.274.5285.246 · Cited by 597
Taylor, S. S., & McKeon, F. (1997) · Cell · doi:10.1016/s0092-8674(00)80255-x · Cited by 540
Human T Cell Leukemia Virus Type 1 Oncoprotein Tax Targets the Human Mitotic Checkpoint Protein MAD1
Jin, D., Spencer, F. A., & Jeang, K.-T. (1998) · Cell · doi:10.1016/s0092-8674(00)81148-4 · Cited by 525
Rieder, C. L., Schultz, A., Cole, R. W., & Sluder, G. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.127.5.1301 · Cited by 506
Rieder, C. L., & Alexander, S. P. H. (1990) · The Journal of Cell Biology · doi:10.1083/jcb.110.1.81 · Cited by 488
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The mitotic checkpoint complex (MCC): looking back and forth after 15 years
Liu, S., & Zhang, H. (2016) · AIMS molecular science · doi:10.3934/molsci.2016.4.597 · Cited by 47
PinX1 Is a Novel Microtubule-binding Protein Essential for Accurate Chromosome Segregation
Yuan, K., Li, N., Jiang, K., Zhu, T., Huo, Y., Wang, C., Lü, J., Shaw, A., Thomas, K., Zhang, J., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.001990 · Cited by 44
Vallee, R. B., Varma, D., & Dujardin, D. (2006) · Cell Cycle · doi:10.4161/cc.5.21.3395 · Cited by 43
Moonlighting functions of the NRZ (mammalian Dsl1) complex
Tagaya, M., Arasaki, K., Inoue, H., & Kimura, H. (2014) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2014.00025 · Cited by 42
Recent Progress on the Localization of the Spindle Assembly Checkpoint Machinery to Kinetochores
Dou, Z., Prifti, D. K., Gui, P., Liu, X., Elowe, S., & Yao, X. (2019) · Cells · doi:10.3390/cells8030278 · Cited by 40
Famulski, J. K., Vos, L. J., Rattner, J. B., & Chan, G. K. T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016494 · Cited by 41
Self-citationInducing precocious anaphase in cultured mammalian cells
Canman, J. C., Salmon, E. D., & Fang, G. (2002) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.10032 · Cited by 40
Mitotic checkpoint defects in human cancers and their implications to chemotherapy
Wang, X. (2007) · Frontiers in bioscience · doi:10.2741/2827 · Cited by 39
The kinetochore and spindle checkpoint in mammals
Kops, G. J. P. L. (2008) · Frontiers in bioscience · doi:10.2741/2953 · Cited by 38
G2 histone methylation is required for the proper segregation of chromosomes
Heit, R., Rattner, J. B., Chan, G. K. T., & Hendzel, M. J. (2009) · Journal of Cell Science · doi:10.1242/jcs.045351 · Cited by 39
Self-citationYeh, P.-C., Yeh, C.-C., Chen, Y.-C., & Juang, Y. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.299131 · Cited by 34
Kuijt, T. E. F., Omerzu, M., Saurin, A. T., & Kops, G. J. P. L. (2014) · Chromosoma · doi:10.1007/s00412-014-0458-9 · Cited by 37
Qiu, H., Huang, J., Xiang, C., Li, R., Zuo, E., Zhang, Y., Li, S., & Cheng, X. (2020) · Technology in Cancer Research & Treatment · doi:10.1177/1533033820980112 · Cited by 34
Spatial Rule-Based Modeling: A Method and Its Application to the Human Mitotic Kinetochore
Ibrahim, B., Henze, R., Gruenert, G., Egbert, M. D., Huwald, J., & Dittrich, P. (2013) · Cells · doi:10.3390/cells2030506 · Cited by 34
Brunet, S., & Vernos, I. (2001) · EMBO Reports · doi:10.1093/emb0-reports/kve158 · Cited by 33
The ESCRT protein Chmp4c regulates mitotic spindle checkpoint signaling
Petsalaki, E., Dandoulaki, M., & Zachos, G. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201709005 · Cited by 32
Cep57 is a Mis12-interacting kinetochore protein involved in kinetochore targeting of Mad1–Mad2
Zhou, H., Wang, T., Zheng, T., Teng, J., & Chen, J. (2016) · Nature Communications · doi:10.1038/ncomms10151 · Cited by 30
Ayoub, A. T., El-Magd, R. M. A., Xiao, J., Lewis, C. W., Tilli, T. M., Arakawa, K., Nindita, Y., Chan, G. K. T., Sun, L., Glover, M., et al. (2016) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6b01264 · Cited by 30
Self-citationChromosome motors on the move. From motion to spindle checkpoint activity.
Brunet, S., & Vernos, I. (2001) · Europe PMC (PubMed Central) · doi:10.1093/embo-reports/kve158 · Cited by 30
Liška, F., Mancini, M., Krupková, M., Chylíková, B., Krenová, D., Šeda, O., Šilhavý, J., Mlejnek, P., Landa, V., Zídek, V., et al. (2013) · American Journal of Hypertension · doi:10.1093/ajh/hpt156 · Cited by 28
MAD1: Kinetochore Receptors and Catalytic Mechanisms
Luo, Y., Ahmad, E., & Liu, S. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00051 · Cited by 29
Liu, C., Min, L., Wang, Y., Li, P., Wu, Y., & Zhang, S. (2019) · International Journal of Oncology · doi:10.3892/ijo.2019.4672 · Cited by 29
A network medicine approach to build a comprehensive atlas for the prognosis of human cancer
Zhang, F., Ren, C., Lau, K. K., Zheng, Z., Lu, G., Yi, Z., Zhao, Y., Su, F., Zhang, S., Zhang, B., et al. (2016) · Briefings in Bioinformatics · doi:10.1093/bib/bbw076 · Cited by 26
Kadura, S., & Sazer, S. (2005) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.20072 · Cited by 26
Masson, I. L., Saveanu, C., Chevalier, A., Namane, A., Gobin, R., Fromont‐Racine, M., Jacquier, A., & Mann, C. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.02844.x · Cited by 25
Loss of RanGAP1 drives chromosome instability and rapid tumorigenesis of osteosarcoma
Gong, Y., Zou, S., Deng, D., Wang, L., Hu, H., Qiu, Z., Wei, T., Yang, P., Zhou, J., Zhang, Y., et al. (2023) · Developmental Cell · doi:10.1016/j.devcel.2022.12.012 · Cited by 24
Key players in chromosome segregation in Caenorhabditis elegans
Kitagawa, R. (2009) · Frontiers in bioscience · doi:10.2741/3323 · Cited by 24
Nordihydroguaiaretic Acid Affects Multiple Dynein-Dynactin Functions in Interphase and Mitotic Cells
Arasaki, K., Tani, K., Yoshimori, T., Stephens, D. J., & Tagaya, M. (2006) · Molecular Pharmacology · doi:10.1124/mol.106.029611 · Cited by 24
Analysis of Bub3 spindle checkpoint function inXenopusegg extracts
Campbell, L., & Hardwick, K. (2003) · Journal of Cell Science · doi:10.1242/jcs.00255 · Cited by 23
shRNA‑mediated knockdown of KNTC1 inhibits non-small-cell lung cancer through regulating PSMB8
Liu, R., Liu, R., Guo, Z., Ren, J., Huang, J., Luo, Q., & Tan, Q. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05140-w · Cited by 22
Mitotic catenation is monitored and resolved by a PKCε-regulated pathway
Brownlow, N., Soliman, T. N., Zicha, D., Collinson, L., & Parker, P. J. (2014) · Nature Communications · doi:10.1038/ncomms6685 · Cited by 22
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Musio, A., Mariani, T., Montagna, C., Zambroni, D., Ascoli, C., Ried, T., & Vezzoni, P. (2004) · Gene · doi:10.1016/j.gene.2004.01.028 · Cited by 21
Tong, H., 谢俊杰, Liu, X., Peng, C., Shen, B., & Zhu, Z. (2022) · Cellular Signalling · doi:10.1016/j.cellsig.2022.110498 · Cited by 20
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Liu, Y. (2006) · Frontiers in bioscience · doi:10.2741/2272 · Cited by 19
Vos, L. J., Famulski, J. K., & Chan, G. K. T. (2011) · Biochemical Journal · doi:10.1042/bj20110137 · Cited by 19
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Modulations of cell cycle checkpoints during HCV associated disease
Sarfraz, S., Hamid, S. S., Ali, A., Jafri, W., & Siddiqui, A. A. (2009) · BMC Infectious Diseases · doi:10.1186/1471-2334-9-125 · Cited by 17
Zombies Never Die: The Double Life Bub1 Lives in Mitosis
Zhang, Y., Song, C., Wang, L., Jiang, H., Zhai, Y., Wang, Y., Fang, J., & Zhang, G. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.870745 · Cited by 14
Cao, S., Xiao, S., Zhang, J., & Li, S. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1147366 · Cited by 13
Chen, Y., Fang, S.-T., Yeh, P.-C., Yang, H., Chen, S.-Y., Chang, C.-J., Zhai, W., Chen, Y. C., & Juang, Y. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.12.007 · Cited by 13
Mu, K., Li, L., Yang, Q., Zhang, T., Gao, P., Meng, B., Liu, Z., Wang, Y., & Zhou, G. (2011) · Histopathology · doi:10.1111/j.1365-2559.2011.03780.x · Cited by 13
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Inoue, M., Arasaki, K., Ueda, A., Aoki, T., & Tagaya, M. (2008) · Genes to Cells · doi:10.1111/j.1365-2443.2008.01215.x · Cited by 13
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Kim, H., Cho, Y. S., Kim, H., Jho, S., Son, B., Choi, J. Y., Kim, S., Lee, B. C., Bhak, J., & Jang, G. (2013) · Scientific Reports · doi:10.1038/srep02998 · Cited by 13
Castro, A., Vigneron, S., Lorca, T., & Labbé, J. (2003) · médecine/sciences · doi:10.1051/medsci/2003193309 · Cited by 13
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Deng, Y., Huang, H., Shi, J., & Jin, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911892 · Cited by 12
Heit, R., Underhill, D. A., Chan, G. K. T., & Hendzel, M. J. (2006) · Biochemistry and Cell Biology · doi:10.1139/o06-080 · Cited by 12
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Liu, S., Majeed, W., Grigaitis, P., Betts, M. J., Climer, L. K., Starkuviene, V., & Storrie, B. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00126 · Cited by 8
Ishikawa, A., Fujii, H., Fukui, T., Kido, A., Katsuya, N., Sentani, K., Kuraoka, K., Tazuma, S., Sudo, T., Serikawa, M., et al. (2022) · Pathology - Research and Practice · doi:10.1016/j.prp.2022.154277 · Cited by 10
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Lu, Y., Wang, Z., Ge, L., Chen, N., & Liu, H. (2009) · Cell Structure and Function · doi:10.1247/csf.08040 · Cited by 9
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Zhou, M. L., Duan, L., Chen, J., Li, Y., Yin, Z., Song, S., Cao, Y., Luo, P., Hu, F., Yang, G., et al. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01513-0 · Cited by 8
Tarailo‐Graovac, M., Wang, J., Chu, J. S., Tu, D. K., Baillie, D. L., & Chen, N. (2010) · BMC Cell Biology · doi:10.1186/1471-2121-11-71 · Cited by 8
Anaphase‐promoting complex/cyclosome‐Cdc‐20 promotes Zwint‐1 degradation
He, Y., Li, R., Gu, L., Deng, H., Zhao, Y., Guo, Y., Yu, S., & Wang, G. (2020) · Cell Biochemistry and Function · doi:10.1002/cbf.3499 · Cited by 8
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Self-citationSpindly attachments: Figure 1.Preprint
Çivril, F., & Musacchio, A. (2008) · Genes & Development · doi:10.1101/gad.1719208 · Cited by 8
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Campos-León, K., Wijendra, K., Siddiqa, A., Pentland, I., Feeney, K. M., Knapman, A., Davies, R. C., Androphy, E. J., & Parish, J. L. (2016) · Journal of Virology · doi:10.1128/jvi.02305-16 · Cited by 6
Ouni, E., Peaucelle, A., Ghasemi, R., Facchinetti, F., Opitz, M., Bigot, L., Sauvat, A., Kepp, O., Jaulin, F., Loriot, Y., et al. (2025) · Cell Biomaterials · doi:10.1016/j.celbio.2025.100149 · Cited by 5
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Bellah, S. F., Yang, F., Xiong, F., Dou, Z., Yao, X., & Liu, X. (2024) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjae026 · Cited by 5
Altenfeld, A., Wohlgemuth, S., Wehenkel, A. M., Vetter, I. R., & Musacchio, A. (2015) · Acta Crystallographica Section F Structural Biology Communications · doi:10.1107/s2053230x15004343 · Cited by 5
Progress in studies of ZW10, a proper chromosome segregation protein
Lu, Y., Yao, N., Liu, X., Chen, N., & Liu, H. (2008) · Biochemistry (Moscow) Supplement Series A Membrane and Cell Biology · doi:10.1134/s1990747808020025 · Cited by 5
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Stukenberg, P. T., & Burke, D. J. (2004) · Humana Press eBooks · doi:10.1385/1-59259-788-2:083 · Cited by 5
Javed, M., Bukhari, R. S., Rasool, R., Alhomrani, M., Alghamdi, S. A., Habeeballah, H. H., Ramzan, F., Baothman, B. K., Kashif, M., Almaghrabi, S. A., et al. (2023) · PubMed Central · Cited by 4
Yan, D., Wei, T., Dong, X., Luo, C. W., Tie, H., Lǚ, Z., Wang, Z., Jiang, H., Chen, J., Gan, L., et al. (2024) · Aquaculture · doi:10.1016/j.aquaculture.2024.741446 · Cited by 3
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Hoffmann, I. (2006) · Springer eBooks · doi:10.1007/b138827 · Cited by 3
The RZZ Complex Facilitates Mad1 Binding to Bub1 Ensuring Efficient Checkpoint SignalingPreprint
Zhang, G., Kruse, T., & Nilsson, J. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3193407 · Cited by 3
Famulski, J. K., Vos, L. J., Rattner, J. B., & Chan, G. K. T. (2011) · PLoS ONE · doi:10.1371/annotation/272736a3-6a7a-44ba-bbae-fd5d7e97d651 · Cited by 3
Self-citationThe Role of the Kinetochore in Spindle Checkpoint Signaling
Stukenberg, P. T., & Burke, D. J. (2008) · Springer eBooks · doi:10.1007/978-0-387-69076-6_11 · Cited by 2
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Huang, H., & Yen, T. J. (2010) · Springer eBooks · doi:10.1007/978-1-4419-1770-6_4 · Cited by 2
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Self-citationWang, J., Ding, Z., Shu, W., & Zhuge, Y. (2023) · Cellular Signalling · doi:10.1016/j.cellsig.2023.110728 · Cited by 2
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Zhong, L., Dong, Y., & Liu, S. (2024) · Molecular Carcinogenesis · doi:10.1002/mc.23748 · Cited by 1
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Liu, Z., Liu, H., Sun, Y., Lang, H., Xing, J., Qian, Y., Xie, Q., Yang, X., Yan, J., Ye, D., et al. (2025) · Industrial Crops and Products · doi:10.1016/j.indcrop.2025.120558 · Cited by 1
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Chen, K., Su, H., Pei, F., Chen, X., Xu, M., Chai, F., & Luo, Y. (2026) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-026-03651-4 · Cited by 1
Bellah, S. F., & Billah, S. (2026) · Oriental Pharmacy and Experimental Medicine · doi:10.1007/s13596-026-00905-6 · Cited by 1
Rs2459976 inZW10gene associated with congenital heart diseases in Chinese Han population
Sun, C., Sun, C. C., Cheng, R., Shi, S., Han, Y., Li, X., Zhi, J., Li, F.-F., & Liu, S. (2017) · Oncotarget · doi:10.18632/oncotarget.23240 · Cited by 1
Steimle, J. D., Laforest, B., Nadadur, R. D., Broman, M., & Moskowitz, I. P. G. (2020) · Springer eBooks · doi:10.1007/978-981-15-1185-1_51 · Cited by 1
Ibrahim, B. (2008) · Common Library Network (Der Gemeinsame Bibliotheksverbund) · Cited by 1
Identification of key genes and their microRNAs in glioma: Evidence from bioinformatic analysisPreprint
Wen, X., Fu, M., Wu, W., Zeng, Z., & Zheng, K. (2020) · doi:10.21203/rs.3.rs-27708/v1 · Cited by 1
Mitotic Chromosome Segregation Control
Xue, Y., Fu, C., Miao, Y., Yao, J., Dou, Z., Zhang, J., Brako, L., & Yao, X. (2007) · Springer eBooks · doi:10.1007/978-4-431-30130-1_3
Characterisation of the spindle assembly checkpoint in mammalian oocytes
Vogt, E.-J. (2009) · PUB – Publications at Bielefeld University (Bielefeld University)
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Cahill, D. P. (2003) · Humana Press eBooks · doi:10.1007/978-1-59259-313-2_2
hMad1 in the spindle assembly checkpoint : characterization of interacting partners
Lluesma, S. M. (2002) · Archive ouverte UNIGE (University of Geneva) · doi:10.13097/archive-ouverte/unige:145
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Kwak, S. (2008) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/mn1v-vr34
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Kuznetsova, A. A. (2013) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.16812
Terret, M., & Verlhac, M. (2004) · OpenGrey (Institut de l'Information Scientifique et Technique)
Identification of regulatory phosphorylation sites on the human kinetochore
Zettl, S. (2009) · University of Vienna · doi:10.25365/thesis.6708
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Camps, J. (2005) · Dipòsit Digital de Documents de la UAB (Universitat Autònoma de Barcelona)
Hüber, D. (2009) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-1350
Metadata
- Authors
- Chan, G. K. T., Jablonski, S. A., Starr, D. A., Goldberg, M. L., & Yen, T. J.
- Affiliations
- Fox Chase Cancer Center (US)
- University of Colorado Boulder (US)
- Cornell University (US)
- Corresponding author
- Yen, T. J.
- Venue
- Nature Cell Biology
- Published
- 2000-11-14
- Volume
- 2
- Issue
- 12
- Pages
- 944-947
- ISSN
- 1465-7392 (ISSN-L)
- 1476-4679
- OpenAlex
- W1540858422
- Cited by
- 217
- References
- 31
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 6 · 2023: 7 · 2022: 6 · 2021: 2 · 2020: 10 · 2019: 5 · 2018: 8 · 2017: 5 · 2016: 6 · 2015: 3 · 2014: 5 · 2013: 8 · 2012: 2
- FWCI
- 5.28
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (P30CA006927, CA06927)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- ZW10, rods, spindle assembly checkpoint, kinetochore, microtubule inhibitors, mitotic arrest, lagging chromosomes, chromosome segregation, Drosophila, animal evolution
- MeSH terms
- Binding Sites, Chromosomal Proteins, Non-Histone, HeLa Cells, Humans, Microscopy, Fluorescence, Microtubules, Mitosis, Spindle Apparatus, Protein Binding, Nocodazole, Kinetochores, Cell Cycle Proteins
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 ›
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