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作 者:Xia Ding Feng Yan Phil Yao Zhihong Yang Weihong Wan Xiwei Wang Jing Liu Xinjiao Gao Ariane Abrieu Tongge Zhu Jiancun Zhang Zhen Dou Xuebiao Yao
机构地区:[1]Anhui Key Laboratory for Cellular Dynamics and Chemical Biology, Hefei 230027, China [2]Georgia Cancer Coalition, Atlanta, GA 30310, USA [3]Beijing University of Chinese Medicine, Beijing 100026, China [4]Proteomics Research Laboratory, Beijing 100086, China [5]Universites Montpellier, 34293 Montpellier, France
出 处:《Cell Research》2010年第12期1386-1389,共4页细胞研究(英文版)
基 金:Acknowledgments We thank members of our groups for insightful discussion during the course of this study. This work was initiated by the chemical biology grant PGX-t from the Proteomics Research Laboratory, and supported in part by Chinese Academy of Sciences Grants (KSCX2-YW-H-10 and KSCX2-YW-R195), 973 projects (2002CB713700; 2010CB912103), National Natural Science Foundation of China (90913016), and Georgia Cancer Coalition Eminent Scholar Award.
摘 要:Dear Editor, Chromosome movements during mitosis are orches- trated primarily by the interaction of spindle microtu- bules with the kinetochore [1], the site for attachment of spindle microtubules to the centromere. The kinetochore has an active function in chromosomal segregation through microtubule-based motors located at or near it [1-2]. CENP-E is a microtubule-based kinesin motor [3],
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