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1 eminal nucleus and the interface between the interpolar and caudal subnuclei were labeled ipsilateral
2 lly divided into three classes: kinetochore, interpolar, and astral microtubules (kMTs, iMTs, and aMT
3 plate resulted in spindle movement along the interpolar axis at a velocity slightly slower than micro
4 lied either by interdigitating MTs that form interpolar bundles or by astral MTs connected to the cel
5 ned area that is radially displaced from the interpolar central spindle.
6                          We suggest that the interpolar climate synchronization within these inferred
7 rage velocity of 0.89 microns/min, until the interpolar distance was reduced by 22-62%.
8 98/+ mutants revealed improper regulation of interpolar (iMT) and kinetochore (kMT) microtubules in a
9  depends on a persistent kinesin-5-generated interpolar (ip) microtubule (MT) sliding filament mechan
10  to test the hypothesis that it slides apart interpolar (ip) microtubules (MT), thereby controlling p
11 LP3A inhibition disrupts the organization of interpolar (ip) MTs and produces short spindles.
12 pindle poles, which allows outwardly sliding interpolar (ip) MTs to drive pole-pole separation.
13                                              Interpolar methane gradient (IPG) data from ice cores su
14 that the suppression of poleward flux within interpolar microtubule (ipMT) bundles of Drosophila embr
15 s process is driven by a kinesin-5-generated interpolar microtubule (MT; ipMT) sliding filament mecha
16 mplex suddenly concentrates to the center of interpolar microtubule bundles during anaphase is unclea
17 est of spindle elongation, and initiation of interpolar microtubule depolymerization.
18 e pairing represents an intermediate step in interpolar microtubule formation.
19 hat Ipl1p regulates both the kinetochore and interpolar microtubule plus ends to regulate its various
20 motors persistently slide apart antiparallel interpolar microtubules (ipMTs).
21 ometaphase, puncta of both motors aligned on interpolar microtubules (MTs [ipMTs]), and motor perturb
22  localize and segregate along the peripheral interpolar microtubules and are abnormally positioned in
23 inetochore proteins have been observed along interpolar microtubules and at the midzone during anapha
24 phorylation (S360A) results in spindles with interpolar microtubules and high-angle, antiparallel mic
25 duced Klp3a function results in disorganized interpolar microtubules and shortened spindles.
26 the BimC family that cross-link antiparallel interpolar microtubules and slide them past each other.
27           Events in the specification of the interpolar microtubules are poorly understood.
28 at Ndc10p is transported to the plus-ends of interpolar microtubules at the midzone during anaphase,
29 lided with an unyielding cell cortex and the interpolar microtubules buckled outward as they continue
30 on each chromosome, while approximately four interpolar microtubules emanate from each pole and inter
31      Our findings suggest that the number of interpolar microtubules formed during spindle assembly i
32 manate from each pole and interdigitate with interpolar microtubules from the opposite spindle to pro
33  studies demonstrate an unsuspected role for interpolar microtubules in driving acentric segregation.
34 appearing to be excluded from the overlap of interpolar microtubules in the central spindle.
35 esin-6 protein that is required for bundling interpolar microtubules located within the central spind
36 cient to separate the spindle poles, whereas interpolar microtubules maintain the velocity of pole di
37 , these findings suggest that Stu1p binds to interpolar microtubules of the mitotic spindle and plays
38 e cdc20 spindles contained a large number of interpolar microtubules organized in a "core bundle." A
39            In anaphase, the plus ends of the interpolar microtubules show strong KRIT1 staining and,
40 transmit forces to chromosomes, antiparallel interpolar microtubules support spindle structure, and a
41    During anaphase B, molecular motors slide interpolar microtubules to elongate the mitotic spindle,
42 inesin-14D1-dependent mechanism that employs interpolar microtubules to regulate the organization of
43 erization pressure from growing plus ends of interpolar microtubules whose minus ends are anchored in
44 posite structure composed of kinetochore and interpolar microtubules, the kinetochore, and organized
45 te spindle poles but neither kinetochore nor interpolar microtubules, unlike in mitotic mouse fibrobl
46 es in the search and capture of antiparallel interpolar microtubules, where it aids in generating for
47 chores or pair to form antiparallel pairs or interpolar microtubules, which span the two spindle pole
48 rrelated with the number and organization of interpolar microtubules.
49 is radially displaced from condensin and the interpolar microtubules.
50  a normal number of microtubules but lacking interpolar microtubules.
51 periphery of the spindle in association with interpolar microtubules.
52 r microtubules: kinetochore microtubules and interpolar microtubules.
53 between spindle elongation and the growth of interpolar microtubules.
54 organization and function of kinetochore and interpolar microtubules.
55 ys but with poorly organized kinetochore and interpolar microtubules.
56 rs Cin8 (kinesin-5) and Kar3 (kinesin-14) to interpolar microtubules.
57                                        These interpolar MT bundles are parallel near the poles and an
58 ox (BCB), localize along the length of these interpolar MT bundles, being concentrated in the midzone
59                      KLP61F-GFP localizes to interpolar MT bundles, half spindles, and asters, and is
60 F motors form cross-links between MTs within interpolar MT bundles.
61 ractions with the MT lattice expected during interpolar MT cross-linking.
62 ases, the activity of TOGL2 is essential for interpolar MT stability, whereas TOGL1 is not involved.
63 dle but concentrate in the overlap region of interpolar MTs (ipMTs) at anaphase B onset.
64 hore microtubules (kMTs) and approximately 8 interpolar MTs (ipMTs).
65 se A, fluorescent punctae on kinetochore and interpolar MTs flux toward the poles at 0.03 microm/s, t
66 Ts in anastral spindles, and perhaps also to interpolar MTs in astral spindles.
67 nd during anaphase B, fluorescent punctae on interpolar MTs move away from the spindle equator at the
68                    In cells, She1 stabilizes interpolar MTs, preventing spindle deformations during m
69 dle stability by cross-linking anti-parallel interpolar MTs.
70  during cycle 13, by Ncd, which localizes to interpolar MTs.
71       CB2 immunostaining was detected in the interpolar part of spinal 5th nucleus of wild type but n
72 in function but only occurred if the initial interpolar separation was less than twice the microtubul
73 r kinetochores during early mitosis, and the interpolar spindle as it elongates in anaphase B.
74 P) is a plus-end-directed motor localized to interpolar spindle microtubules and to the spindle poles
75 oper force balance between kinesin motors on interpolar spindle microtubules is critical for correcti
76 d in decreased spindle polyglutamylation and interpolar spindle, as well as congression failure, mito