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1 ring oogenesis and female meiosis is usually acentrosomal.
2 phase and followed the fate of the resultant acentrosomal and centrosomal daughter cells.
3 most cell types, oocytes of many species are acentrosomal and must organize spindles in their absence
4                           Here, we show that acentrosomal Arabidopsis cells that are mutant for the k
5 plant cortical microtubule array is a unique acentrosomal array that is essential for plant morphogen
6                                        These acentrosomal arrays support essential cell functions suc
7 organized by imaging microtubule dynamics in acentrosomal basal cytoplasts derived from these cells.
8 meiosis I in mouse oocytes, formation of the acentrosomal bipolar spindle takes 3-4 h, and stabilizat
9                                     Although acentrosomal cells become polyploid, polyploidy is not s
10                                         Many acentrosomal cells exhibit prolonged spindle assembly, c
11 id not alter already-formed Golgi complexes, acentrosomal cells fail to reassemble an integral comple
12 By contrast, during this period, none of the acentrosomal cells had entered S phase.
13      Here, we find that the mitotic delay in acentrosomal cells is enforced by the SAC in a MPS1-depe
14                                 Apoptosis of acentrosomal cells is mediated by JNK signaling, which a
15 experiments reveal that microtubules form in acentrosomal cells randomly within the cytoplasm.
16                                 Karyoplasts (acentrosomal cells) entered and completed mitosis.
17 ell-free extracts and experimentally derived acentrosomal cells, randomly oriented microtubules (MTs)
18  microtubule (MT)-dependent MT nucleation in acentrosomal cells.
19 quired for bipolar cell division to occur in acentrosomal cells.
20  TRIM37 is required for cell cycle arrest in acentrosomal cells.
21                                          The acentrosomal cortical microtubules (MTs) of higher plant
22 go a normal anaphase and usually produce two acentrosomal daughter cells.
23            An excess of Shot induces ectopic acentrosomal luminal branching points in the embryonic a
24                                Plants employ acentrosomal mechanisms to organize cortical microtubule
25 PLK-1 as a key player that promotes faithful acentrosomal meiosis in oocytes and demonstrates that it
26                                              Acentrosomal meiosis in oocytes represents a gametogenic
27 the length and maintaining bipolarity of the acentrosomal meiotic spindle and in promoting the contac
28  required for the proper organization of the acentrosomal meiotic spindle in Drosophila melanogaster
29                                          The acentrosomal meiotic spindle poles do not have centriole
30 etochore for constraining chromosomes in the acentrosomal meiotic spindle.
31 gmin in stabilizing the bipolar shape of the acentrosomal meiotic spindle.
32 ) in mammalian oocytes is carried out by the acentrosomal MI spindles.
33  yeast, nuclear-independent, self-organized, acentrosomal microtubule arrays are structurally and fun
34 s vital for the formation and maintenance of acentrosomal microtubule arrays.
35 rosome function and reveal a multi-component acentrosomal microtubule assembly pathway to establish i
36 , although Nek2B is not required to organize acentrosomal microtubule asters, we show that addition o
37 sin network interacts with the minus ends of acentrosomal microtubule bundles through the cytolinker
38             Developing arbors have extensive acentrosomal microtubule dynamics, and here, we report a
39 is an essential regulator of centrosomal and acentrosomal microtubule formation, yet its structure is
40  organization regulates the role of Golgi in acentrosomal microtubule growth in dendrites and in dend
41 l parameters for the self-organization of an acentrosomal microtubule network.
42 rs are sufficient to generate a steady-state acentrosomal microtubule network.
43 well understood, but less is known about how acentrosomal microtubule networks are formed.
44  al. demonstrate that Golgi outposts mediate acentrosomal microtubule nucleation and reveal it is cru
45                           Here, we show that acentrosomal microtubule nucleation in plant cells invol
46 hese results identify a direct mechanism for acentrosomal microtubule nucleation within neurons and r
47 h is known about the structures that promote acentrosomal microtubule nucleation, less is known about
48 nd therefore provide a model system to study acentrosomal microtubule nucleation.
49                                  We identify acentrosomal microtubule organizing centers localized in
50 caused aberrant PLK1 aggregation that led to acentrosomal microtubule-organizing center (aMTOC) forma
51  satellite organelle that can function as an acentrosomal microtubule-organizing center (MTOC), nucle
52 tposts, an organelle that can function as an acentrosomal microtubule-organizing center (MTOC).
53                           We also show that (acentrosomal) microtubule asters fail to assemble in vit
54 nized independently of a centrosome, but how acentrosomal microtubules arrays form and whether they a
55                         How neurons generate acentrosomal microtubules remains unclear.
56    We find that inactivating TRIM37 improves acentrosomal mitosis because TRIM37 prevents PLK4 from s
57 rgery, vertebrate somatic cells form bipolar acentrosomal mitotic spindles, but the fate of these cel
58 dividual microtubules form stable, polarized acentrosomal MT arrays spanning the axon and dendrite to
59 -GCP6 (the non-core GCPs) may be involved in acentrosomal MT nucleation in plant cells.
60                                         This acentrosomal nucleation requires gamma-tubulin and CP309
61 al centrosome system, which is distinct from acentrosomal oocyte meiosis, but its specific regulatory
62 ng that none were entirely selective for the acentrosomal pathway.
63 horing complex is used to recruit katanin in acentrosomal plant cells.
64                                          The acentrosomal pole lacks pericentrin, gamma-tubulin, and
65 lls eventually formed bipolar spindles by an acentrosomal pole-focusing mechanism.
66  formed that contain one centrosomal and one acentrosomal pole.
67 on pathways from chromatin, spindle MTs, and acentrosomal poles all contribute to robust bipolar spin
68  numerous microtubule plus ends growing from acentrosomal poles toward the metaphase plate.
69 or Nek6 function did not induce formation of acentrosomal poles, meaning that multipolar spindles wer
70 ugmin-independent MT nucleation process from acentrosomal poles, which becomes increasingly active ov
71 ein is required to maintain the integrity of acentrosomal poles; removal of dynein from bipolar spind
72 that produces a bipolar structure during the acentrosomal process of oocyte meiotic spindle assembly.
73  that EDE1, but not AUG8, is associated with acentrosomal spindle and phragmoplast MT arrays in patte
74                                          The acentrosomal spindle apparatus has kinetochore fibers or
75                 Low TRIM37 levels accelerate acentrosomal spindle assembly and improve proliferation
76                            Here we show that acentrosomal spindle assembly following PLK4 inhibition
77 ontrast, elevated TRIM37 expression inhibits acentrosomal spindle assembly through a distinct mechani
78  centrosome-less cells that exhibit delayed, acentrosomal spindle assembly(4).
79 This screen identified 197 genes involved in acentrosomal spindle assembly, eight of which had no pre
80 hibition, whereas high TRIM37 levels inhibit acentrosomal spindle assembly, leading to mitotic failur
81  M phase, required for the initial stages of acentrosomal spindle assembly.
82  oocyte-specific function of kinetochores in acentrosomal spindle bipolarization in mice, and provide
83 is showed robust microtubule assembly of the acentrosomal spindle but frequent chromosome misalignmen
84                                      Bipolar acentrosomal spindle formation during meiosis in oocytes
85 own to nucleate microtubules, mechanisms for acentrosomal spindle formation remain unclear.
86 e the organization of kinetochore fibers for acentrosomal spindle morphogenesis.
87 so required for establishing and maintaining acentrosomal spindle organization and for preventing exc
88 GSK3 beta) were found to be enriched at both acentrosomal spindle poles and the kinetochore region.
89 equired for the formation and maintenance of acentrosomal spindle poles in extracts prepared from Xen
90                           Mouse eggs contain acentrosomal spindle poles when arrested at meiotic meta
91 nt to understand the mechanisms that promote acentrosomal spindle stability.
92 gregation occurs in Drosophila oocytes on an acentrosomal spindle, which raises interesting questions
93  the rapid capture of all chromosomes by the acentrosomal spindle.
94 cks centrosomes, but the mechanisms by which acentrosomal spindles are organized and function are lar
95 y results from mitotic exit occurring before acentrosomal spindles can become bipolar.
96 s undergo mitotic arrest with barrel-shaped, acentrosomal spindles during the rapid cycles of syncyti
97 s undergo mitotic arrest with barrel-shaped, acentrosomal spindles during the rapid S-M cycles of syn
98 ess in Caenorhabditis elegans, detailing how acentrosomal spindles form and revealing mechanisms requ
99 e not required for chromosome segregation on acentrosomal spindles in Caenorhabditis elegans oocytes,
100 a timely manner to promote elongation of the acentrosomal spindles that segregate homologous chromoso
101  (a microtubule-plus-end binding protein) in acentrosomal spindles, we also demonstrate that the spin
102 aphase central spindle functions to organize acentrosomal spindles.
103 crotubule minus ends in both centrosomal and acentrosomal spindles.
104 refore chromosome segregation is mediated by acentrosomal spindles.

 
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