ライフサイエンスコーパス: spindle apparatus

1 yotes requires the regulated assembly of the spindle apparatus.

2 attern but no direct colocalization with the spindle apparatus.

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

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

5 icrotubules emanating from both poles of 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 sions depend on the precise placement of the spindle apparatus.

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

15 ires amphitelic chromosome attachment to the spindle apparatus.

16 l MTOC, before joining it to the rest of the spindle apparatus.

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

18 microtubules needed to assemble the mitotic spindle apparatus(1).

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

20 Proteins associated with the spindle apparatus, a cytoskeletal structure that ensures

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

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

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

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

25 deSUMOylation of key target proteins in the spindle apparatus and kinetochore may be involved with s

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

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

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

29 ter, determines the eventual location of the spindle apparatus and ultimately the cytokinetic furrow.

30 (4%) had anticytoplasmic (mitochondrial and spindle apparatus) antibodies with a titer of 80 and two

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

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

33 um (ER) concentrates around the poles of the spindle apparatus by associating with astral microtubule

34 n the posttranslational modifications of the spindle apparatus by SUMO and its SENP proteases.

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

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

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

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

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

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

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

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

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

44 The acentrosomal spindle apparatus has kinetochore fibers organized and c

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

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

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

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

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

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

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

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

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

54 ted and new cellular structures, such as the spindle apparatus, must be assembled.

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

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

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

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

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

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

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

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

63 re fibers are assembled and unified into the spindle apparatus with convergent poles.

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

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

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