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1 nded DNA breaks, and improper segregation of sister chromosomes.
2 mosome supercoiling and remove links between sister chromosomes.
3 during cell division to physically separate sister chromosomes.
4 oteolysis and delayed mitotic disjunction of sister chromosomes.
5 ndergo anaphase B and successfully segregate sister chromosomes.
6 ed direct evidence for active segregation of sister chromosomes.
7 egrates, by utilizing transposon ends on two sister chromosomes.
8 annealing of DNA ends generated in different sister chromosomes after transposase nicks DNA near part
9 n studied extensively in the case of dimeric sister chromosomes and when chromosome organization is i
10 g Bacillus subtilis sporulation, segregating sister chromosomes are anchored to cell poles and the ch
12 ominant DNA markers, as would be expected if sister chromosomes are rejoined, rather than the 3:1 rat
14 to invaginate, the termini of the completed sister chromosomes are transiently held apart at the cel
17 ration after replication and movement of the sister chromosomes away from the division septum prior t
18 ought to depend on the physical proximity of sister chromosomes, because it is inhibited when chromos
19 nd other effects is that thus far replicated sister chromosomes become spatially separated (individua
20 ell and acts to align and stretch duplicated sister chromosomes before their ultimate segregation int
21 poisomerase-mediated entanglements until all sister chromosomes bi-orient along the spindle apparatus
22 n response to the tension that is exerted on sister chromosomes by the forces of the spindle that wil
23 translocase that facilitates decatenation of sister chromosomes by TopIV and resolution of chromosome
25 the nuclear pore, Ig gene hypermutation, and sister chromosome cohesion have all been demonstrated or
27 e findings show that, in addition to loss of sister chromosome cohesion, successful anaphase requires
29 e cyclin B (CYC-B(S)) in Drosophila embryos, sister chromosomes disjoined normally but their anaphase
30 nome condensation and orderly convergence of sister chromosomes, diverse stress conditions prime bact
31 , formed by homologous recombination between sister chromosomes during DNA replication, are resolved
32 dinates cohesin removal with decatenation of sister chromosomes during mitosis in mammalian cells.
34 Dimer replicon products have experienced a sister-chromosome exchange event in addition to deletion
35 pansion events are accompanied by reciprocal sister-chromosome exchange, producing dimeric plasmids c
36 rearrangements: simple replication slippage, sister-chromosome exchange-associated slippage, and sing
38 pleted human cells accumulate fragile sites, sister chromosome exchanges, and double strand breaks at
40 f the genome during mitosis by ensuring that sister chromosomes form bipolar attachments with microtu
42 s imply that segregation of Escherichia coli sister chromosomes is not a smooth continuous process bu
44 , formed by homologous recombination between sister chromosomes, normally require cell division to be
45 al steps in the resolution and separation of sister chromosomes occur at the replication terminus, wh
48 some cancer cells or in natural endocycles, sister chromosomes remain paired and produce four-strand
50 y, we demonstrate that these barriers affect sister chromosome segregation by visualizing specific ch
51 hat consequently, the arm regions of mitotic sister chromosomes separate precociously while cohesion
53 vealing a requirement for Cdc20 in efficient sister chromosome separation and chromosome-microtubule
55 nction of the protease separase in promoting sister chromosome separation, the role of separase durin
57 omosome cohesion model, replication produces sister chromosomes that are paired along much of their l
58 omologues reveal that bivalents form between sister chromosomes, the genetically identical products o
59 d Mps1, may prevent premature disjunction of sister chromosomes, the other, consisting of Bfa1 and Bu
60 oint tension magnitude for properly attached sister chromosomes to facilitate robust mechanochemical
62 ssion until microtubules attach each pair of sister chromosomes to opposite poles of the mitotic spin
64 tion of DNA are the driving forces that move sister chromosomes toward their respective origins, whic
65 e removal of cohesion and catenation between sister chromosomes, two physical linkages established du
67 that FtsK segregates the terminus region of sister chromosomes whether they are monomeric or dimeric
68 ough a nonrandom, zipper-like convergence of sister chromosomes, which is proposed to rely on the rec
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