生物
非整倍体
染色体不稳定性
染色体
基因组不稳定性
有丝分裂
遗传学
染色体分离
疾病
变色
DNA损伤
基因
DNA
病理
医学
作者
Robin M. Ricke,Jan M. van Deursen
标识
DOI:10.1083/jcb.201301061
摘要
Aneuploidy, an aberrant number of chromosomes, has been recognized as a feature of human malignancies for over a century, but compelling evidence for causality was largely lacking until mouse models for chromosome number instability were used. These in vivo studies have not only uncovered important new insights into the extremely complex aneuploidy–cancer relationship but also into the molecular mechanisms underlying proper and aberrant chromosome segregation. A series of diverse mouse models for the mitotic checkpoint protein BubR1 has provided evidence for a provocative novel link between aneuploidization and the development of age-related pathologies.
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