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An unbiased, quantitative and versatile method for determining misaligned and lagging chromosome during mitosis

机译：一种无偏，定量和多功能的方法，用于在有丝分裂期间测定未对血液和滞后染色体的方法

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Luciano Gama Braga; Diogjena Katerina Prifti; Chantal Garand; Pawan Kumar Saini; Sabine Elowe;
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1. Nucleoporin Translocated Promoter Region (Tpr) Associates with Dynein Complex, Preventing Chromosome Lagging Formation during Mitosis [J] . Hiroshi Nakano, Tatsuyoshi Funasaka, Chieko Hashizume, The Journal of biological chemistry . 2010,第14期

机译：核常素易位启动子区（TPR）与Dynein复合物相关联，在有丝分裂期间防止染色体滞后形成
2. Quantitative microscopy uncovers ploidy changes during mitosis in live Drosophila embryos and their effect on nuclear size Quantitative microscopy uncovers ploidy changes during mitosis in live Drosophila embryos and their effect on nuclear size Quantitative microscopy uncovers ploidy changes during mitosis in live Drosophila embryos and their effect on nuclear size [J] . Martin Wasser, Wee Choo Puah, Rambabu Chinta Biology Open . 2017,第3期

机译：定量显微镜发现果蝇活体胚胎有丝分裂期间的倍性变化及其对核大小的影响定量显微镜发现果蝇活体胚胎有丝分裂期间的倍性变化及其对核大小的影响定量显微镜揭示果蝇活体胚胎的有丝分裂期间的倍性变化及其对核的影响尺寸
3. Multisite phosphorylation determines the formation of Ska–Ndc80 macro-complexes that are essential for chromosome segregation during mitosis [J] . Qian Zhang, Liqiao Hu, Yujue Chen, Molecular biology of the cell . 2020,第17期

机译：多立体磷酸化决定了在有丝分裂期间对染色体隔离至关重要的SKA-NDC80宏观复合物的形成
4. Chromosome mechanics in vivo: quantitative analysis of nonrigid 3D chromosome motion in Drosophila embryos [C] . Wallace F. Marshall, Univ. of California/San Francisco, San Francisco, Optical Diagnostics of Living Cells and Biofluids . 1996

机译：体内的染色体力学：果蝇胚胎中非刚性3D染色体运动的定量分析
5. Mathematical models of chromosome motility during mitosis. [D] . Shtylla, Blerta. 2011

机译：有丝分裂期间染色体运动的数学模型。
6. Nucleoporin Translocated Promoter Region (Tpr) Associates with Dynein Complex Preventing Chromosome Lagging Formation during Mitosis [O] . Hiroshi Nakano, Tatsuyoshi Funasaka, Chieko Hashizume, 2010

机译：核蛋白转运位点启动子区域（Tpr）与Dynein复合物缔合防止有丝分裂期间染色体的滞后形成
7. A quantitative and semiautomated method for determining misaligned and lagging chromosomes during mitosis [O] . Luciano Gama Braga, Diogjena Katerina Prifti, Chantal Garand, 2021

机译：用于测定有丝分裂中未对血液和滞后染色体的定量和半报道方法
8. Defects in Histone H3.3 Phosphorylation and ATRX Recruitment to Misaligned Chromosomes during Mitosis Contribute to the Development of Pediatric Glioblastomas. [R] . Hinchcliffe, E. H. 2015

机译：组蛋白缺陷H3.3磷酸化和aTRX招募到有丝分裂期间错位的染色体有助于小儿胶质母细胞瘤的发展。

An unbiased, quantitative and versatile method for determining misaligned and lagging chromosome during mitosis

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