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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 rrelated with the number and organization of interpolar microtubules.
8 is radially displaced from condensin and the interpolar microtubules.
9  localize and segregate along the peripheral interpolar microtubules and are abnormally positioned in
10 inetochore proteins have been observed along interpolar microtubules and at the midzone during anapha
11 phorylation (S360A) results in spindles with interpolar microtubules and high-angle, antiparallel mic
12 duced Klp3a function results in disorganized interpolar microtubules and shortened spindles.
13 the BimC family that cross-link antiparallel interpolar microtubules and slide them past each other.
14           Events in the specification of the interpolar microtubules are poorly understood.
15 at Ndc10p is transported to the plus-ends of interpolar microtubules at the midzone during anaphase,
16 lided with an unyielding cell cortex and the interpolar microtubules buckled outward as they continue
17 mplex suddenly concentrates to the center of interpolar microtubule bundles during anaphase is unclea
18 est of spindle elongation, and initiation of interpolar microtubule depolymerization.
19 on each chromosome, while approximately four interpolar microtubules emanate from each pole and inter
20 e pairing represents an intermediate step in interpolar microtubule formation.
21      Our findings suggest that the number of interpolar microtubules formed during spindle assembly i
22 manate from each pole and interdigitate with interpolar microtubules from the opposite spindle to pro
23  studies demonstrate an unsuspected role for interpolar microtubules in driving acentric segregation.
24 appearing to be excluded from the overlap of interpolar microtubules in the central spindle.
25 that the suppression of poleward flux within interpolar microtubule (ipMT) bundles of Drosophila embr
26 motors persistently slide apart antiparallel interpolar microtubules (ipMTs).
27 esin-6 protein that is required for bundling interpolar microtubules located within the central spind
28 cient to separate the spindle poles, whereas interpolar microtubules maintain the velocity of pole di
29 s process is driven by a kinesin-5-generated interpolar microtubule (MT; ipMT) sliding filament mecha
30 ometaphase, puncta of both motors aligned on interpolar microtubules (MTs [ipMTs]), and motor perturb
31 , these findings suggest that Stu1p binds to interpolar microtubules of the mitotic spindle and plays
32 e cdc20 spindles contained a large number of interpolar microtubules organized in a "core bundle." A
33 hat Ipl1p regulates both the kinetochore and interpolar microtubule plus ends to regulate its various
34            In anaphase, the plus ends of the interpolar microtubules show strong KRIT1 staining and,
35 posite structure composed of kinetochore and interpolar microtubules, the kinetochore, and organized
36 es in the search and capture of antiparallel interpolar microtubules, where it aids in generating for
37 chores or pair to form antiparallel pairs or interpolar microtubules, which span the two spindle pole
38 erization pressure from growing plus ends of interpolar microtubules whose minus ends are anchored in

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