ライフサイエンスコーパス: interpolar

1 eminal nucleus and the interface between the interpolar and caudal subnuclei were labeled ipsilateral

2 plate resulted in spindle movement along the interpolar axis at a velocity slightly slower than micro

3 ned area that is radially displaced from the interpolar central spindle.

4 rage velocity of 0.89 microns/min, until the interpolar distance was reduced by 22-62%.

5 98/+ mutants revealed improper regulation of interpolar (iMT) and kinetochore (kMT) microtubules in a

6 depends on a persistent kinesin-5-generated interpolar (ip) microtubule (MT) sliding filament mechan

7 to test the hypothesis that it slides apart interpolar (ip) microtubules (MT), thereby controlling p

8 LP3A inhibition disrupts the organization of interpolar (ip) MTs and produces short spindles.

9 pindle poles, which allows outwardly sliding interpolar (ip) MTs to drive pole-pole separation.

10 Interpolar methane gradient (IPG) data from ice cores su

11 that the suppression of poleward flux within interpolar microtubule (ipMT) bundles of Drosophila embr

12 s process is driven by a kinesin-5-generated interpolar microtubule (MT; ipMT) sliding filament mecha

13 mplex suddenly concentrates to the center of interpolar microtubule bundles during anaphase is unclea

14 est of spindle elongation, and initiation of interpolar microtubule depolymerization.

15 e pairing represents an intermediate step in interpolar microtubule formation.

16 hat Ipl1p regulates both the kinetochore and interpolar microtubule plus ends to regulate its various

17 motors persistently slide apart antiparallel interpolar microtubules (ipMTs).

18 ometaphase, puncta of both motors aligned on interpolar microtubules (MTs [ipMTs]), and motor perturb

19 localize and segregate along the peripheral interpolar microtubules and are abnormally positioned in

20 inetochore proteins have been observed along interpolar microtubules and at the midzone during anapha

21 phorylation (S360A) results in spindles with interpolar microtubules and high-angle, antiparallel mic

22 duced Klp3a function results in disorganized interpolar microtubules and shortened spindles.

23 the BimC family that cross-link antiparallel interpolar microtubules and slide them past each other.

24 Events in the specification of the interpolar microtubules are poorly understood.

25 at Ndc10p is transported to the plus-ends of interpolar microtubules at the midzone during anaphase,

26 lided with an unyielding cell cortex and the interpolar microtubules buckled outward as they continue

27 on each chromosome, while approximately four interpolar microtubules emanate from each pole and inter

28 Our findings suggest that the number of interpolar microtubules formed during spindle assembly i

29 manate from each pole and interdigitate with interpolar microtubules from the opposite spindle to pro

30 studies demonstrate an unsuspected role for interpolar microtubules in driving acentric segregation.

31 appearing to be excluded from the overlap of interpolar microtubules in the central spindle.

32 esin-6 protein that is required for bundling interpolar microtubules located within the central spind

33 cient to separate the spindle poles, whereas interpolar microtubules maintain the velocity of pole di

34 , these findings suggest that Stu1p binds to interpolar microtubules of the mitotic spindle and plays

35 e cdc20 spindles contained a large number of interpolar microtubules organized in a "core bundle." A

36 In anaphase, the plus ends of the interpolar microtubules show strong KRIT1 staining and,

37 erization pressure from growing plus ends of interpolar microtubules whose minus ends are anchored in

38 posite structure composed of kinetochore and interpolar microtubules, the kinetochore, and organized

39 es in the search and capture of antiparallel interpolar microtubules, where it aids in generating for

40 chores or pair to form antiparallel pairs or interpolar microtubules, which span the two spindle pole

41 periphery of the spindle in association with interpolar microtubules.

42 rrelated with the number and organization of interpolar microtubules.

43 is radially displaced from condensin and the interpolar microtubules.

44 a normal number of microtubules but lacking interpolar microtubules.

45 r microtubules: kinetochore microtubules and interpolar microtubules.

46 between spindle elongation and the growth of interpolar microtubules.

47 organization and function of kinetochore and interpolar microtubules.

48 ys but with poorly organized kinetochore and interpolar microtubules.

49 These interpolar MT bundles are parallel near the poles and an

50 ox (BCB), localize along the length of these interpolar MT bundles, being concentrated in the midzone

51 KLP61F-GFP localizes to interpolar MT bundles, half spindles, and asters, and is

52 F motors form cross-links between MTs within interpolar MT bundles.

53 ractions with the MT lattice expected during interpolar MT cross-linking.

54 ases, the activity of TOGL2 is essential for interpolar MT stability, whereas TOGL1 is not involved.

55 dle but concentrate in the overlap region of interpolar MTs (ipMTs) at anaphase B onset.

56 hore microtubules (kMTs) and approximately 8 interpolar MTs (ipMTs).

57 se A, fluorescent punctae on kinetochore and interpolar MTs flux toward the poles at 0.03 microm/s, t

58 Ts in anastral spindles, and perhaps also to interpolar MTs in astral spindles.

59 nd during anaphase B, fluorescent punctae on interpolar MTs move away from the spindle equator at the

60 In cells, She1 stabilizes interpolar MTs, preventing spindle deformations during m

61 dle stability by cross-linking anti-parallel interpolar MTs.

62 during cycle 13, by Ncd, which localizes to interpolar MTs.

63 CB2 immunostaining was detected in the interpolar part of spinal 5th nucleus of wild type but n

64 in function but only occurred if the initial interpolar separation was less than twice the microtubul

65 r kinetochores during early mitosis, and the interpolar spindle as it elongates in anaphase B.

66 P) is a plus-end-directed motor localized to interpolar spindle microtubules and to the spindle poles

67 oper force balance between kinesin motors on interpolar spindle microtubules is critical for correcti