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1 periphery of the spindle in association with interpolar microtubules.
2 a normal number of microtubules but lacking interpolar microtubules.
3 r microtubules: kinetochore microtubules and interpolar microtubules.
4 between spindle elongation and the growth of interpolar microtubules.
5 organization and function of kinetochore and interpolar microtubules.
6 ys but with poorly organized kinetochore and interpolar microtubules.
7 rs Cin8 (kinesin-5) and Kar3 (kinesin-14) to interpolar microtubules.
8 rrelated with the number and organization of interpolar microtubules.
9 is radially displaced from condensin and the interpolar microtubules.
10 localize and segregate along the peripheral interpolar microtubules and are abnormally positioned in
11 inetochore proteins have been observed along interpolar microtubules and at the midzone during anapha
12 phorylation (S360A) results in spindles with interpolar microtubules and high-angle, antiparallel mic
14 the BimC family that cross-link antiparallel interpolar microtubules and slide them past each other.
16 at Ndc10p is transported to the plus-ends of interpolar microtubules at the midzone during anaphase,
17 lided with an unyielding cell cortex and the interpolar microtubules buckled outward as they continue
18 mplex suddenly concentrates to the center of interpolar microtubule bundles during anaphase is unclea
20 on each chromosome, while approximately four interpolar microtubules emanate from each pole and inter
23 manate from each pole and interdigitate with interpolar microtubules from the opposite spindle to pro
24 studies demonstrate an unsuspected role for interpolar microtubules in driving acentric segregation.
26 that the suppression of poleward flux within interpolar microtubule (ipMT) bundles of Drosophila embr
28 esin-6 protein that is required for bundling interpolar microtubules located within the central spind
29 cient to separate the spindle poles, whereas interpolar microtubules maintain the velocity of pole di
30 s process is driven by a kinesin-5-generated interpolar microtubule (MT; ipMT) sliding filament mecha
31 ometaphase, puncta of both motors aligned on interpolar microtubules (MTs [ipMTs]), and motor perturb
32 , these findings suggest that Stu1p binds to interpolar microtubules of the mitotic spindle and plays
33 e cdc20 spindles contained a large number of interpolar microtubules organized in a "core bundle." A
34 hat Ipl1p regulates both the kinetochore and interpolar microtubule plus ends to regulate its various
36 transmit forces to chromosomes, antiparallel interpolar microtubules support spindle structure, and a
37 posite structure composed of kinetochore and interpolar microtubules, the kinetochore, and organized
38 During anaphase B, molecular motors slide interpolar microtubules to elongate the mitotic spindle,
39 inesin-14D1-dependent mechanism that employs interpolar microtubules to regulate the organization of
40 te spindle poles but neither kinetochore nor interpolar microtubules, unlike in mitotic mouse fibrobl
41 es in the search and capture of antiparallel interpolar microtubules, where it aids in generating for
42 chores or pair to form antiparallel pairs or interpolar microtubules, which span the two spindle pole
43 erization pressure from growing plus ends of interpolar microtubules whose minus ends are anchored in