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1 yed in akir-1 mutants and are accompanied by lagging chromosomes.
2 ls overexpressing Mad2 display high rates of lagging chromosomes.
3 rora B through Chk1, preventing formation of lagging chromosomes.
4 micronuclei form when mitotic errors produce lagging chromosomes.
5 defects such as centrosome amplification and lagging chromosomes.
6 metaphase plate and an increase in anaphase lagging chromosomes.
7 indles and asymmetric, bipolar spindles with lagging chromosomes.
8 utations cause chromosome missegregation and lagging chromosomes.
9 ore defects within the regions of misaligned/lagging chromosomes.
10 n early mitosis, but few anaphase cells show lagging chromosomes.
11 events merotelic kinetochores from producing lagging chromosomes.
15 luding premature chromatid separation (PCS), lagging chromosomes, anaphase bridges, micronuclei, cent
17 it from MII, there is a dramatic increase in lagging chromosomes and an inhibition of cytokinesis.
19 ore anaphase onset, but ZW10 mutants exhibit lagging chromosomes and irregular chromosome segregation
23 errors in chromosome segregation (including lagging chromosomes), and abnormalities in spindle morph
28 indle morphology, increased the frequency of lagging chromosomes, and inhibited the proliferation of
29 wn of the Twins B subunit led to bridged and lagging chromosomes, and knockdown of the B' Widerborst
31 tion and aberrant mitosis with misaligned or lagging chromosomes are significantly increased in Ptpn1
32 festing disorganized spindle, misaligned and lagging chromosomes as well as micronucleated cells.
33 ypes associated with zw10 and rod mutations: lagging chromosomes at anaphase and precocious sister ch
35 ing division, these cells frequently exhibit lagging chromosomes at both metaphase and anaphase, sugg
36 1.16% of untreated anaphase cells exhibiting lagging chromosomes at the spindle equator, and this per
37 uploidy phenotype involved the occurrence of lagging chromosomes but not chromosome bridges, indicati
38 High levels of mBub3 remain associated with lagging chromosomes but not with correctly aligned chrom
41 rebral cortical neuroblasts in situ detected lagging chromosomes during mitosis, suggesting the norma
48 d during mitosis, we show that a majority of lagging chromosomes in anaphase segregate to the correct
50 tly show alignment defects during metaphase, lagging chromosomes in anaphase, and chromatin bridges d
51 efects in chromosome alignment in metaphase, lagging chromosomes in anaphase, failure of cytokinesis
52 damage and consequent chromatin bridges and lagging chromosomes in anaphase, frequently leading to c
53 ith merotelic kinetochores often manifest as lagging chromosomes in anaphase, suggesting that lagging
56 Kif2a-depleted animal caps have anaphase lagging chromosomes in stage 9 and 10 embryos and subseq
57 s allows the correction and reintegration of lagging chromosomes in the main nuclei before completion
58 bit mitotic defects including misaligned and lagging chromosomes, multipolar spindles, and increased
59 nd thereby, delays abscission in response to lagging chromosomes, nuclear pore defects, and tension f
61 show chromosome segregation defects such as lagging chromosomes on the spindle during anaphase and h
62 t mitoses, including misaligned chromosomes, lagging chromosomes, polylobed nuclei, and delayed passa
63 ly inactive Smurf2 results in misaligned and lagging chromosomes, premature anaphase onset, and defec
64 increase in anaphase-lagging cells, with the lagging chromosomes showing reduced centromere protein C
67 Extended anaphases, chromosome bridges, and lagging chromosomes were frequent during these polyploid
70 rized by chromosomal bridges in anaphase and lagging chromosomes, without affecting spindle checkpoin
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