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1 les spore morphogenesis to the completion of chromosome segregation.
2 ortant for sister centromere orientation and chromosome segregation.
3 somes entail poorly understood mechanisms of chromosome segregation.
4 ir, DNA replication, chromatid cohesion, and chromosome segregation.
5 ed from APC activity, leading to error-prone chromosome segregation.
6 tochore assembly during mitosis and accurate chromosome segregation.
7 growth, cell division, DNA replication, and chromosome segregation.
8 loss of genetic information through unequal chromosome segregation.
9 c spindle assembly, spindle positioning, and chromosome segregation.
10 n of cohesion among sister chromatids during chromosome segregation.
11 bilizes k-MT attachments to promote faithful chromosome segregation.
12 at the centromere helps to facilitate proper chromosome segregation.
13 chromosome organization to support faithful chromosome segregation.
14 link chromosomes to dynamic microtubules for chromosome segregation.
15 dence of a specific role for tubulin CTTs in chromosome segregation.
16 tubule structures, is essential for accurate chromosome segregation.
17 in gene silencing, chromosome packaging, and chromosome segregation.
18 some alignment, but there were no defects in chromosome segregation.
19 romeric protein, plays critical functions in chromosome segregation.
20 ssociation, which is essential for effective chromosome segregation.
21 removal of centromeric cohesins and faithful chromosome segregation.
22 heterochromatin decompaction and defects in chromosome segregation.
23 ting that Cdc55 might have a role in meiotic chromosome segregation.
24 ining chromosome-microtubule coupling during chromosome segregation.
25 s essential to separate DNA replication from chromosome segregation.
26 isassembly of SC proteins to ensure accurate chromosome segregation.
27 x (MCC), which inhibits the APC/C and delays chromosome segregation.
28 versus high tension is critical for accurate chromosome segregation.
29 ch are involved in cell cycle regulation and chromosome segregation.
30 tiple parallel mechanisms to ensure accurate chromosome segregation.
31 c insight into the basis for accuracy during chromosome segregation.
32 unresolved replication intermediates impair chromosome segregation.
33 en replicated chromatids that interfere with chromosome segregation.
34 l complex (SC) is crucial for proper meiotic chromosome segregation.
35 NA repair, chromatin regulation, and mitotic chromosome segregation.
36 in mitosis and thus ensures the fidelity of chromosome segregation.
37 cohesin and opens the cohesin ring to allow chromosome segregation.
38 T repeats per Spc105 are needed for accurate chromosome segregation.
39 sister chromatid cohesion to ensure faithful chromosome segregation.
40 ly important for proper spindle assembly and chromosome segregation.
41 promotes checkpoint inactivation and timely chromosome segregation.
42 hat is essential for DNA damage response and chromosome segregation.
43 ing proper anaphase B spindle elongation and chromosome segregation.
44 eckpoint signaling, resulting in error-prone chromosome segregation.
45 ndent on timely DNA replication and accurate chromosome segregation.
46 ic cell cycle, microtubule organization, and chromosome segregation.
47 netochore and is required to ensure faithful chromosome segregation.
48 of Hec1 S165 by Nek2 is required for proper chromosome segregation.
49 icrotubules (MTs) are important for accurate chromosome segregation.
50 nk homologous chromosomes and drive faithful chromosome segregation.
51 Centromeres are essential for proper chromosome segregation.
52 wn spindle assembly checkpoint that monitors chromosome segregation.
53 correction function is essential for proper chromosome segregation.
54 eading to impaired anaphase B and incomplete chromosome segregation.
55 in chromatin and are essential for accurate chromosome segregation.
56 lluminates a process critical for successful chromosome segregation.
57 ading to varied effects on transcription and chromosome segregation.
58 hromosome to regulate processes critical for chromosome segregation.
59 te recombination intermediate resolution and chromosome segregation.
60 e contribution of specific classes of MTs in chromosome segregation.
61 requirement for ligand binding in regulating chromosome segregation.
62 om Psh1-mediated ubiquitination for faithful chromosome segregation.
63 s are removed before they can prevent normal chromosome segregation.
64 diversity in the progeny, as well as proper chromosome segregation.
65 ase is followed by two consecutive rounds of chromosome segregation.
66 esolve mitotic interlinks, thus facilitating chromosome segregation.
67 r DNA-repair synthesis that ensures faithful chromosome segregation.
68 r designation, and ensuring accurate meiotic chromosome segregation.
69 uding homologous pairing, recombination, and chromosome segregation.
70 ric chromatin and the mitotic spindle during chromosome segregation.
71 ect improper attachments and ensure faithful chromosome segregation.
72 es and spindle microtubules is essential for chromosome segregation.
73 osed by Ipl1 kinase is critical for faithful chromosome segregation.
74 nt re-entanglements, and complete failure in chromosome segregation.
75 otes checkpoint signaling to ensure accurate chromosome segregation.
76 protein implicated in spindle stability and chromosome segregation.
77 ed parABS partitioning system in plasmid and chromosome segregation.
78 ere integrity independently of their role in chromosome segregation.
79 in mitosis and thus ensures the fidelity of chromosome segregation.
80 ponents in sister centromere orientation and chromosome segregation.
81 y dispensable, and in fact act as brakes for chromosome segregation.
82 protein (IAP) family, regulates mitosis and chromosome segregation.
83 regulation roles for H2A phosphorylation in chromosome segregation.
84 lope breakdown (NEBD) is required for proper chromosome segregation.
85 e features are well suited to support robust chromosome segregation.
86 lving and have roles in genome stability and chromosome segregation.
87 and their resolution is essential for proper chromosome segregation.
88 bule attachments is essential for successful chromosome segregation.
89 n nucleating kinetochores at centromeres for chromosome segregation.
90 microtubule polymers and facilitate optimal chromosome segregation.
91 longer in mitosis, indicative of problems in chromosome segregation.
92 ysical links that are essential for accurate chromosome segregation.
93 le processes coordinate spindle assembly and chromosome segregation.
94 maintaining centromere function and faithful chromosomes segregation.
101 nvolved in other cellular processes, such as chromosome segregation and cell cycle regulation, emphas
105 strictly required for spindle organization, chromosome segregation and cytokinesis in meiotic cells.
107 important at distinct stages of the meiotic chromosome segregation and differentiation program were
108 and rigid form they need to undergo faithful chromosome segregation and division in a crowded tissue
109 merase II (topo II), an enzyme essential for chromosome segregation and DNA supercoiling homeostasis.
113 y key nuclear roles in modulating chromatin, chromosome segregation and germline gene expression via
114 activates expression of genes that regulate chromosome segregation and is critical for maintaining g
117 ly specialized chromatin domains that enable chromosome segregation and orchestrate faithful cell div
118 phabeta-tubulin that have essential roles in chromosome segregation and organization of the cytoplasm
120 des a unique mechanism by which cells ensure chromosome segregation and preserve genome integrity.
121 bipolar spindles exhibit reduced fidelity of chromosome segregation and promote genetic instability.
122 that is necessary and sufficient for proper chromosome segregation and provide evidence that this fu
125 er/dif recombination is tuned to both act in chromosome segregation and stably maintain mobile elemen
127 orphology and a maternal-effect on embryonic chromosome segregation and survival, which was completel
128 f centrosome number is critical for accurate chromosome segregation and the maintenance of genomic in
129 ighlight the biological function of TOP2A in chromosome segregation and the mechanisms that regulate
130 spindle is efficiently assembled to achieve chromosome segregation and then rapidly disassembled as
131 lly adopt a rounded shape to ensure faithful chromosome segregation and to promote morphogenesis.
132 a phenomenon with wide-ranging importance in chromosome segregation and, in multicellular organisms,
133 are unique chromosomal domains that control chromosome segregation, and are epigenetically specified
135 Aurora B, one of the main kinases regulating chromosome segregation, and controls its subcellular loc
136 condensed mitotic structures that facilitate chromosome segregation, and decondensed interphase struc
137 ubiquitin ligase that mediates high-fidelity chromosome segregation, and describe the mechanisms that
138 timate relationship between DNA replication, chromosome segregation, and division site selection in t
139 esses, including transcriptional regulation, chromosome segregation, and heterochromatin formation, i
140 tinct cell cycle roles, in cell division and chromosome segregation, and highlights that cell probabl
142 ding phenomics, transcriptomics, proteomics, chromosome segregation, and replication analysis-to prov
143 hore-dependent mechanisms that drive mitotic chromosome segregation are well understood, in oocytes o
144 e H3 variant CENP-A is required for accurate chromosome segregation as a foundation for kinetochore a
145 kinesis and identify cell wall synthesis and chromosome segregation as limiting processes of cytokine
146 crossovers during meiosis I ensures accurate chromosome segregation at the first meiotic division.
147 us chromosomes and is essential for accurate chromosome segregation at the first meiotic division.
148 on plane positioning is crucial for faithful chromosome segregation but also influences cell size, po
149 res control genetic inheritance by directing chromosome segregation but are not genetically encoded t
150 tive for plus-end tracking facilitate proper chromosome segregation but display spindle positioning d
151 peculate that NUSAP1 contributes to accurate chromosome segregation by acting as a co-factor for RanB
152 tem, the mitotic checkpoint ensures faithful chromosome segregation by delaying anaphase onset even w
153 lex regulates transcription, DNA repair, and chromosome segregation by dynamically entrapping chromos
154 emonstrate that these barriers affect sister chromosome segregation by visualizing specific chromosom
155 and Psc3 promotes UPD by uniquely affecting chromosome segregation, causing a reductional segregatio
156 cytotoxic analog (SM15) was shown to produce chromosome segregation defects in cancer cells by inhibi
157 the two forms of PP2A by quantifying meiotic chromosome segregation defects in double or triple mutan
167 ggest that Cdc55 is required for reductional chromosome segregation during achiasmate meiosis and thi
176 e, and it is caused by a failure of accurate chromosome segregation during gametogenesis or early emb
178 ect of cytoplasmic volume on the fidelity of chromosome segregation during meiosis in mouse oocytes.
181 ka) protein complex is required for accurate chromosome segregation during mitosis [1-6] and consists
185 a role in nuclear-to-cytoplasm transport and chromosome segregation during mitosis, cellular prolifer
191 in formation at centromeres, allowing proper chromosome segregation during mitotic growth and G0 entr
192 to direct kinetochore disassembly-dependent chromosome segregation during oocyte meiosis I and nucle
193 owever, we also found that random homologous chromosome segregation during ploidy reduction can expos
197 olume may be the reason the SAC is weak, and chromosome segregation error-prone, in mammalian oocytes
199 gesting that its untimely activation induces chromosome segregation errors and paradoxically undermin
200 ative stress during meiotic prophase induces chromosome segregation errors and support the model that
201 at was specifically marked by a lacO repeat, chromosome segregation errors and the appearance of aneu
202 abnormality contributing to infertility, and chromosome segregation errors are common during female m
205 ly attributed to the exponential increase in chromosome segregation errors in the oocyte with age.
206 ch the kinetochore prevents the incidence of chromosome segregation errors that generate aneuploid ga
207 deficient cells fail to biorient and display chromosome segregation errors underlying suppressed KT-M
208 humans oocyte meiotic divisions are prone to chromosome segregation errors, a leading cause of freque
209 inappropriate PLK1 activity contributing to chromosome segregation errors, formation of micronuclei,
211 est was not a result of a prolonged mitosis, chromosome segregation errors, or cytokinesis failure.
212 nderstand how the mitotic kinase PLK1 drives chromosome segregation errors, with a specific focus on
216 e resolution defects are a frequent cause of chromosome segregation failure and consequent aneuploidi
219 ukaryotic gene repression and contributes to chromosome segregation fidelity and genome stability.
220 The spindle plays a vital role in accurate chromosome segregation fidelity and is a therapeutic tar
221 t is unknown whether CPC dysfunction affects chromosome segregation fidelity in cancers and, if so, h
222 xpression of most mitotic regulators impairs chromosome segregation fidelity, certain manipulations o
224 me-wide maps (meiomaps) of recombination and chromosome segregation for the three products of human f
225 to govern basic cellular processes, such as chromosome segregation, gene expression, cell division,
227 shed and maintained before the initiation of chromosome segregation has not been experimentally estab
230 nding the mechano-molecular underpinnings of chromosome segregation; however, existing kinetochore fo
231 s of the mitotic spindle, which orchestrates chromosome segregation in all Eukaryotes and positions t
233 It persists throughout mitosis, biasing chromosome segregation in anaphase by causing daughter c
240 t that, despite the dispensability of proper chromosome segregation in megakaryocytes, an endomitotic
244 f specific cell-cycle proteins to coordinate chromosome segregation in mitosis and entry into the G1
251 ressor mutations in cdc55 affect reductional chromosome segregation in the absence of recombination,
252 rveillance mechanism that prevents premature chromosome segregation in the presence of unattached or
253 eltapkl1Delta spindle is fully competent for chromosome segregation independently of motor activity,
260 beit via distinct molecular mechanisms, host chromosome segregation machineries for self-preservation
264 transcription sites in 3'-end processing and chromosome segregation mutants, and 3) transcripts being
266 ific factors to drive the unique reductional chromosome segregation of meiosis I, which also results
271 ch is required for the efficient splicing of chromosome segregation related genes, probably by stabil
273 ub, which links DNA replication, repair, and chromosome segregation, represents a novel target for th
278 hway acts at centromeres to promote faithful chromosome segregation, revealing functions of R loops a
279 cr1Delta), which mapped to genes involved in chromosome segregation, RNA polymerase-associated factor
280 tate have been shown to influence or trigger chromosome segregation, sporulation, aerotaxis, and soci
281 somerase II is similarly required for linear chromosome segregation, suggesting that linear chromosom
282 les assemble close to the cell's center, but chromosome segregation takes place at the cell periphery
283 two especially potent challenges to meiotic chromosome segregation that probably necessitate adaptiv
286 her DNA transactions, such as expression and chromosome segregation, that is summarized, with referen
288 a B as a catalytic subunit, ensures faithful chromosome segregation through destabilizing incorrect m
289 a cells induces mitotic delay and defects in chromosome segregation through mitogen-activated protein
293 ologically entraps chromosomes and regulates chromosome segregation, transcription, and DNA repair.
294 ) T cells show persistent catenations during chromosome segregation, triggering DNA damage in diploid
295 tween meiotic replication fork stability and chromosome segregation, two processes with major implica
296 role of the nucleoporin MEL-28 in mediating chromosome segregation via its interaction with PP1 at t
297 he broadly conserved role of microtubules in chromosome segregation, we have a limited understanding
299 ocalize and function with the CPC to support chromosome segregation yet retains catalytic activity in
300 Centromeres mediate the conserved process of chromosome segregation, yet centromeric DNA and the cent
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