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1 s, the mitotic checkpoint (also known as the spindle assembly checkpoint).
2 d load-bearing capacity and silencing of the spindle assembly checkpoint.
3 llels with the mode of action of Mad2 in the spindle assembly checkpoint.
4 ubule polymerization and satisfaction of the spindle assembly checkpoint.
5 tive microtubule nucleation pathways and the spindle assembly checkpoint.
6 7(C70R) mutation does not affect the mitotic spindle assembly checkpoint.
7 ts contribution seems to be relevant for the spindle assembly checkpoint.
8 be induced in the mouse by inactivating the spindle assembly checkpoint.
9 d in G2 phase and mitosis, suggesting a weak spindle assembly checkpoint.
10 D2L1) in a screen for genes required for the spindle assembly checkpoint.
11 damage response, whereas Mps1 regulates the spindle assembly checkpoint.
12 re-microtubule associations and regulate the spindle assembly checkpoint.
13 Moreover, a lack of CK2 activates the spindle assembly checkpoint.
14 ule lattice and, thus, the activation of the spindle assembly checkpoint.
15 ids, the tel1 mec1 diploids had a functional spindle assembly checkpoint.
16 Mps1 is an essential component of the spindle assembly checkpoint.
17 t interact with spindle microtubules and the spindle assembly checkpoint.
18 to mitotic stress by abrogating the mitotic spindle assembly checkpoint.
19 actor transmitting the tension status to the spindle assembly checkpoint.
20 has also been implicated in inactivating the spindle assembly checkpoint.
21 hromatin staining, indicative of an extended spindle assembly checkpoint.
22 ssion of Mad2, an essential component of the spindle assembly checkpoint.
23 otein 1 (MAD1) is a component of the mitotic spindle assembly checkpoint.
24 se to microtubule stress, independent of the spindle assembly checkpoint.
25 pole and missegregate in the absence of the spindle assembly checkpoint.
26 ) and control cell-cycle progression via the spindle assembly checkpoint.
27 ining, indicating that DRT/DMC activates the spindle assembly checkpoint.
28 s, causing mitotic arrest and activating the spindle assembly checkpoint.
29 ase and is one of the main components of the spindle assembly checkpoint.
30 hts the contribution of p53 in regulation of spindle assembly checkpoint.
31 hase of the cell cycle, independently of the spindle assembly checkpoint.
32 ndle disruptions cause the engagement of the spindle assembly checkpoint.
33 , thereby resulting in the activation of the spindle assembly checkpoint.
34 ential roles in chromosome alignment and the spindle assembly checkpoint.
35 ependent regulation of MT attachment and the spindle-assembly checkpoint.
36 checkpoints and a recently reported mitotic spindle-assembly checkpoint.
37 ansient activation of the S phase, G2/M, and spindle assembly checkpoints.
38 detailed knowledge of the components of the spindle assembly checkpoint, a molecular explanation of
40 kinetochore-microtubule attachment, mitotic/spindle-assembly checkpoint, accurate chromosome segrega
41 y regulator of meiotic recombination and the spindle assembly checkpoint, acting on signaling protein
42 vels of KT proteins, including CENP-C(Cnp3), spindle assembly checkpoint activation, and chromosome s
43 itotic progression is halted attributable to spindle assembly checkpoint activation, and chromosomes
48 in p31(comet) is implicated in silencing the spindle assembly checkpoint after all kinetochores are a
50 fects in mitotic spindle formation, cellular spindle assembly checkpoint and centrosome amplification
52 and interphase microtubule organization, the spindle assembly checkpoint and cytokinesis through its
53 omosomal passenger protein that mediates the spindle assembly checkpoint and cytokinesis, and also fu
54 ur analysis expands our understanding of the spindle assembly checkpoint and identifies new candidate
55 found that FA signaling is essential for the spindle assembly checkpoint and is therefore required fo
56 anaphase is delayed due to activation of the spindle assembly checkpoint and lagging sister chromatid
58 cells undergo normal mitoses with an intact spindle assembly checkpoint and that they are able to co
59 llmark of cancer, due to attenuations in the spindle assembly checkpoint and the post-mitotic checkpo
60 APC(Cdc20), antimitotic agents activate the spindle-assembly checkpoint and induce apoptosis after p
61 arily conserved protein kinase, required for spindle-assembly checkpoint and, in some organisms, for
63 on, arrested cells in mitosis, activated the spindle assembly checkpoint, and triggered mitotic catas
64 ched include genes that regulate the mitotic spindle assembly checkpoint, apoptosis, and the cytosoli
66 at DNA damage-induced wild-type p53 leads to spindle assembly checkpoint arrest by repressing UBE2C,
69 metaphase plate, possibly due to a defective spindle-assembly checkpoint, as well as of frayed and un
70 appear to rely on several components of the spindle assembly checkpoint but does require the kinetoc
71 etochore-associated kinase Mps1 controls the spindle assembly checkpoint, but the regulation of its k
72 reviously undescribed regulatory role in the spindle assembly checkpoint by recruiting Plk1 to kineto
73 ), promotes the inactivation of the mitotic (spindle assembly) checkpoint by disassembling the mitoti
74 ng anaphase progression by activation of the spindle assembly checkpoint caused a loss of condensatio
75 INPP5E in human and murine cells impairs the spindle assembly checkpoint, centrosome and spindle func
77 me instability (W-CIN) we down-regulated the spindle assembly checkpoint component BUB1 and the mitot
79 the Mos-MEK1-MAPK-p90(Rsk) cascade utilizes spindle-assembly-checkpoint components to effect metapha
80 adipogenesis, DNA replication, mitosis, and spindle assembly checkpoint control were all highly repr
82 dle poles, we identified novel roles for the spindle assembly checkpoint, cortical actin cytoskeleton
83 TRIP13 action in vitro, and in cells causes spindle assembly checkpoint defects consistent with loss
85 The mitotic checkpoint, also known as the spindle assembly checkpoint, delays anaphase onset until
88 stmitotic checkpoint after adaptation to the spindle assembly checkpoint, E7-expressing cells replica
91 rmation of a bipolar mitotic spindle and the spindle assembly checkpoint, ensuring proper spindle fun
93 , but maintains kinetochore localization and spindle assembly checkpoint function, indicating that TP
94 By depolymerizing microtubules and mutating spindle assembly checkpoint function, we demonstrate tha
95 troduced into the monopolar spindle 1 (Mps1) spindle-assembly checkpoint gene so that Cre-mediated re
96 sufficiency or heterozygous mutations in the spindle assembly checkpoint genes BUB1 and BUB3 in 2.9%
97 examined the genetic interactions with four spindle assembly checkpoint genes to identify nonessenti
98 ion, to identify the individual roles of the spindle assembly checkpoint genes within the checkpoint,
99 s in the APC co-activator fzy-1 and in three spindle assembly checkpoint genes, mdf-1, mdf-2, and mdf
104 ne H3 plays a crucial role in activating the spindle assembly checkpoint in response to a defect in m
111 findings establish that in mammalian MI, the spindle assembly checkpoint is unable to sustain meiotic
112 ipts also indicated that the strength of the spindle assembly checkpoint is weakened and that higher
114 c arrest deficient 2 (Mad2), a member of the spindle assembly checkpoint, is present on DRT/DMC chrom
117 ne-121 site on histone H2A, a target of Bub1 spindle assembly checkpoint kinase, sensitizes gammaH2A-
118 with NHEJ deficiency upon disruption are two spindle assembly checkpoint kinases, Bub1 and Bub2.
119 rmal chromosome alignment and activating the spindle assembly checkpoint, leading to arrest in a prom
121 dies provide evidence that components of the spindle assembly checkpoint may regulate the metaphase-t
124 synthetic genetic array (SGA) analysis using spindle assembly checkpoint mutants mad1, mad2, mad3, an
125 und 228 synthetic interactions with the four spindle assembly checkpoint mutants with substantial ove
126 e found shared interactions between pairs of spindle assembly checkpoint mutants, suggesting addition
127 ed to the spindle, kinetochores activate the spindle assembly checkpoint network, which in turn block
128 eukaryotic signaling pathways including the spindle assembly checkpoint, numerous DNA recombination/
131 The mitotic checkpoint (also known as the spindle assembly checkpoint) prevents premature anaphase
132 show that mutant mice with low levels of the spindle assembly checkpoint protein BubR1 develop progre
134 xhibit normal kinetochore recruitment of the spindle assembly checkpoint protein BubR1 without restor
135 conserved HORMA domain family, including the spindle assembly checkpoint protein MAD2 and the meiotic
139 ng than by differences in mitotic spindle or spindle assembly checkpoint proteins and that antimitoti
141 ers of the mitotic spindle and by recruiting spindle assembly checkpoint proteins Mad1 and Mad2.
142 accharomyces pombe MCC (a complex of mitotic spindle assembly checkpoint proteins Mad2, Mad3 and APC/
143 rence reflects a more permissive role of the spindle assembly checkpoint, rather than solely reflecti
145 Correspondingly, cyclin B accumulation and spindle assembly checkpoint (SAC) activation were observ
146 r62 depleted cells show spindle instability, spindle assembly checkpoint (SAC) activation, mitotic ar
147 mproperly attached kinetochores activate the spindle assembly checkpoint (SAC) and by an unknown mech
148 resting in meiosis I through activity of the Spindle Assembly Checkpoint (SAC) and DNA Damage Respons
150 eso1 (eso1-H17) is due to activation of the spindle assembly checkpoint (SAC) and is associated with
151 eveloped surveillance mechanisms such as the spindle assembly checkpoint (SAC) and the DNA damage res
154 the triple-Glu mutant failed to satisfy the spindle assembly checkpoint (SAC) at metaphase because p
157 east, both the DNA damage checkpoint and the spindle assembly checkpoint (SAC) block cells prior to a
158 pore complex (NPC) protein implicated in the spindle assembly checkpoint (SAC) by an unknown mechanis
163 ences of aneuploidy has relied on perturbing spindle assembly checkpoint (SAC) components, but interp
168 unattached/weakly attached kinetochores, the spindle assembly checkpoint (SAC) delays exit from mitos
172 chore-microtubule (KT-MT) attachment and the spindle assembly checkpoint (SAC) during cell division a
185 morigenesis model derived from knocking down spindle assembly checkpoint (SAC) genes and preventing a
188 DNA damage activates a pathway involving the spindle assembly checkpoint (SAC) in response to chemica
189 hether APC-deficient cells have a functional spindle assembly checkpoint (SAC) in vivo by examining t
194 correction, chromosome biorientation and the spindle assembly checkpoint (SAC) is complicated by thei
203 ginally described as a core component of the spindle assembly checkpoint (SAC) mechanism in yeast.
208 amage-induced apoptotic response and mitotic spindle assembly checkpoint (SAC) override in human tumo
210 ensure accurate chromosome segregation, the spindle assembly checkpoint (SAC) prevents anaphase unti
213 , a cell surveillance mechanism known as the spindle assembly checkpoint (SAC) produces an inhibitory
214 ole localization of gamma-tubulin and showed spindle assembly checkpoint (SAC) protein Bub3 at the ki
217 ~1 h, and this is due to an earlier onset of spindle assembly checkpoint (SAC) satisfaction and APC(C
218 premature mitotic exit is due to defects in spindle assembly checkpoint (SAC) signaling, such that c
220 ched to the spindle; this is achieved by the Spindle Assembly Checkpoint (SAC) that inhibits the Anap
221 rapeutic agents such as taxanes activate the spindle assembly checkpoint (SAC) to arrest anaphase ons
222 hanosensitive signaling cascade known as the spindle assembly checkpoint (SAC) to detect and signal t
223 have evolved a signaling pathway called the spindle assembly checkpoint (SAC) to increase the fideli
224 mproper kinetochore attachments activate the spindle assembly checkpoint (SAC) to prevent anaphase on
225 APC/C coactivator, Cdc20, is targeted by the spindle assembly checkpoint (SAC) to restrict APC/C acti
226 titioning during cell division relies on the Spindle Assembly Checkpoint (SAC), a conserved signaling
227 K protein kinase) is a core component of the spindle assembly checkpoint (SAC), a genome-surveillance
228 (Mps1) is a central component of the mitotic spindle assembly checkpoint (SAC), a sensing mechanism t
229 itors or Plk1-null cells is triggered by the spindle assembly checkpoint (SAC), and can be rescued in
230 e I causes acceleration of MI, bypass of the spindle assembly checkpoint (SAC), and loss of interchro
231 Two key components are centrosomes and the spindle assembly checkpoint (SAC), and mutations affecti
232 urea, leading to secondary activation of the spindle assembly checkpoint (SAC), aneuploidy, and letha
233 PCM, form multipolar spindles, activate the spindle assembly checkpoint (SAC), arrest in mitosis, an
234 MPS1 kinase is an essential component of the spindle assembly checkpoint (SAC), but its functioning m
235 ce phenotype that requires components of the spindle assembly checkpoint (SAC), including Bub3 and Ma
236 RIP13 and have substantial impairment of the spindle assembly checkpoint (SAC), leading to a high rat
237 th Aurora inhibitors still have a functional spindle assembly checkpoint (SAC), since the checkpoint
238 is to cell cycle arrest independently of the spindle assembly checkpoint (SAC), suggesting that while
239 descriptions of the G1-S checkpoint and the spindle assembly checkpoint (SAC), the EGF signalling pa
240 error correction mechanism [1, 2] and by the spindle assembly checkpoint (SAC), which delays cell-cyc
242 ulin ring complex (gamma-TuRC) activates the spindle assembly checkpoint (SAC), which led them to sug
243 opolar spindle 1 (Mps1) is essential for the spindle assembly checkpoint (SAC), which prevents anapha
245 es identical mitotic defects that initiate a spindle assembly checkpoint (SAC)-dependent mitotic dela
270 This transition is essential to satisfy the spindle-assembly checkpoint (SAC) and couple MT-generate
271 in kinase MPS1 is a crucial component of the spindle assembly checkpoint signal and is aberrantly ove
273 ere impaired, resulting in the activation of spindle assembly checkpoint signaling and, ultimately, e
274 port that the nuclear pore complex scaffolds spindle assembly checkpoint signaling in interphase, pro
277 compromised bipolar attachment and premature spindle assembly checkpoint silencing in the mutant cell
282 spindle 1 kinase (Mps-1) is a kinase of the spindle assembly checkpoint that controls cell division
283 s mechanism of aneuploidy bypasses the known spindle assembly checkpoint that monitors chromosome seg
285 ding cells use a surveillance mechanism, the spindle assembly checkpoint, that monitors the attachmen
286 and p31(comet) collaborate to inactivate the spindle assembly checkpoint through MAD2 conformational
287 s possible that a lowered sensitivity of the spindle assembly checkpoint to certain types of chromoso
288 s to the spindle microtubules and signal the spindle assembly checkpoint to delay mitotic exit until
289 tension at the kinetochore that silences the spindle assembly checkpoint to ensure faithful chromosom
291 on due to erroneous attachment activates the spindle assembly checkpoint, which corrects the mistakes
292 d the kinetochore microtubules activates the spindle assembly checkpoint, which delays anaphase by bl
293 ssociated with defects in DNA repair and the spindle assembly checkpoint, which in turn can lead to p
295 The arrest is dependent on activation of the spindle assembly checkpoint, which results in anaphase-p
296 regulation of genes involved in the mitotic spindle assembly checkpoint, which results in inhibition
297 cell cycle as in Opisthokonts; however, the spindle assembly checkpoint, which targets the APC in Op
298 a a Cdk1/MAPK-dependent stabilization of the spindle assembly checkpoint, which when inhibited leads
300 on leads to a constitutive activation of the spindle-assembly checkpoint, which therefore causes a la
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