Human Cdc14B Promotes Progression through Mitosis by Dephosphorylating Cdc25 and Regulating Cdk1/Cyclin B Activity
出版年份 2011 全文链接
标题
Human Cdc14B Promotes Progression through Mitosis by Dephosphorylating Cdc25 and Regulating Cdk1/Cyclin B Activity
作者
关键词
-
出版物
PLoS One
Volume 6, Issue 2, Pages e14711
出版商
Public Library of Science (PLoS)
发表日期
2011-02-18
DOI
10.1371/journal.pone.0014711
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- The nucleolar phosphataseCdc14Bis dispensable for chromosome segregation and mitotic exit in human cells
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- Cdc25 Phosphatases Are Required for Timely Assembly of CDK1-Cyclin B at the G2/M Transition
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- Vertebrate cells genetically deficient for Cdc14A or Cdc14B retain DNA damage checkpoint proficiency but are impaired in DNA repair
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- Live-cell imaging RNAi screen identifies PP2A–B55α and importin-β1 as key mitotic exit regulators in human cells
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- Phosphorylation of Skp2 regulated by CDK2 and Cdc14B protects it from degradation by APCCdh1 in G1 phase
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- Cdc14B depletion leads to centriole amplification, and its overexpression prevents unscheduled centriole duplication
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- Birth and Rapid Subcellular Adaptation of a Hominoid-Specific CDC14 Protein
- (2008) Lia Rosso et al. PLOS BIOLOGY
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