ライフサイエンスコーパス: spindle apparatus

1 sions depend on the precise placement of the spindle apparatus.

2 y contributing to the formation of a bipolar spindle apparatus.

3 the formation of a microtubule-based bipolar spindle apparatus.

4 icrotubules emanating from both poles of the spindle apparatus.

5 l all sister chromosomes bi-orient along the spindle apparatus.

6 ormation of a microtubule (MT)-based bipolar spindle apparatus.

7 ndensation, nuclear kinesis, and assembly of spindle apparatus.

8 g mitosis, when clathrin concentrates at the spindle apparatus.

9 replicated sister chromatids to the mitotic spindle apparatus.

10 whereas a pool of Nup96 colocalized with the spindle apparatus.

11 factors required for assembly of the mitotic spindle apparatus.

12 TACC4 proteins could no longer target to the spindle apparatus.

13 nce showed that PP5 localizes to the mitotic spindle apparatus.

14 attern but no direct colocalization with the spindle apparatus.

15 hromosome segregation depends on the mitotic spindle apparatus, a bipolar array of microtubules nucle

16 The localization of Esp1 to the spindle apparatus, analyzed by live cell imaging, is reg

17 Integrity of the microtubule spindle apparatus and intact cell division checkpoints a

18 the attachment of chromosomes to the mitotic spindle apparatus and is required for faithful chromosom

19 critical component of the centrosome/mitotic spindle apparatus and its absence triggers p53-mediated

20 his context appears to depend on the mitotic spindle apparatus and midzone microtubules.

21 s (MSCs), which monitor the integrity of the spindle apparatus and prevent cells from progressing int

22 he separation of duplicate chromatids by the spindle apparatus and the delivery of one set of chromos

23 (4%) had anticytoplasmic (mitochondrial and spindle apparatus) antibodies with a titer of 80 and two

24 osphorylation is closely associated with the spindle apparatus at centrosomes and kinetochores.

25 dominant role in assembly of the microtubule spindle apparatus at mitosis.

26 The microtubule spindle apparatus dictates the plane of cell cleavage in

27 family and is associated with the centrosome-spindle apparatus during cell cycling.

28 Eukaryotic chromosomes are anchored to a spindle apparatus during mitosis, but no such structure

29 el fraction of Cdc6 that associates with the spindle apparatus during mitosis.

30 also appeared to associated with the mitotic spindle apparatus during mitosis.

31 riatal cells, HAP-1 localized to the mitotic spindle apparatus, especially at spindle poles and on ve

32 , are the only structural constituent of the spindle apparatus essential for cleavage furrow inductio

33 Structural constituents of the spindle apparatus essential for cleavage induction remai

34 ine/threonine phosphorylation as the mitotic spindle apparatus forms, and this phosphorylation persis

35 This protein localizes to the spindle apparatus in a cell cycle- and microtubule-depen

36 chromosomes and with the absence of mitotic spindle apparatus in cytoplasm.

37 s in functional localization of TACC4 to the spindle apparatus in mitotic cells.

38 uitous even though it is associated with the spindle apparatus in mitotic cells.

39 chromosomes did not align correctly onto the spindle apparatus in the majority of Mlh1(-/-) spermatoc

40 ation that was most prominent in the mitotic spindle apparatus in variant HT1080 human fibrosarcoma c

41 d improves the integrity of the microtubular spindle apparatus in young and old oocytes.

42 and abrogates EG5 recruitment to the mitotic spindle apparatus, leading to spindle disorganization.

43 Kinetochore fibres (K-fibres) of the spindle apparatus move chromosomes during mitosis.

44 PRL-1 relocalizes to the centrosomes and the spindle apparatus, proximal to the centrosomes, in a far

45 be involved in regulating the stability of a spindle apparatus regulator(s).

46 show that LIN-5 is a novel component of the spindle apparatus required for chromosome and spindle mo

47 s spindle matrix that embeds the microtubule spindle apparatus, stretching from pole to pole.

48 of communication between chromosomes and the spindle apparatus that may be widely conserved among euk

49 become correctly attached to the microtubule spindle apparatus via their kinetochores.

50 Normal microtubule architecture or spindle apparatus was absent in these cells; instead, pu

51 teraction of an apparently symmetric mitotic spindle apparatus with a clearly polarized cell cortex.

52 Models of the spindle apparatus with linear chromatin springs that mat

53 oint proteins monitor the interaction of the spindle apparatus with the kinetochores, halting anaphas

54 location of TACC4 from the centrosome to the spindle apparatus with the majority of TACC4 at the spin