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1 genetic alterations that deregulate the G1/S cell cycle checkpoint.
2 on, rather than an indirect consequence of a cell cycle checkpoint.
3 tial mediator of the DNA damage response and cell cycle checkpoint.
4 step in the initiation and amplification of cell cycle checkpoint.
5 at PGCs prior to sex determination lack a G1 cell cycle checkpoint.
6 specific mitotic arrest mediated by the Mad2 cell cycle checkpoint.
7 Rad3 related) and CHK1 kinases to induce the cell cycle checkpoint.
8 escribed as important regulators of the G2-M cell cycle checkpoint.
9 grade signals to specifically enforce a G1-S cell cycle checkpoint.
10 Gln checkpoint and before the mTOR-mediated cell cycle checkpoint.
11 bition of ATR or CHK1, but also defects G2-M cell cycle checkpoint.
12 system ensures mitotic entry independent of cell cycle checkpoint.
13 n of cellular DNA damage and activation of a cell cycle checkpoint.
14 caspase-8 to override the p53-dependent G2/M cell-cycle checkpoint.
15 in sensing general DNA damage and mediating cell-cycle checkpoint.
16 cer cells to override the p53-dependent G2/M cell-cycle checkpoint.
17 f cyclin-dependent kinases 2 and 4/6 at G1/S cell-cycle checkpoint.
18 s normally triggers a precise precytokinesis cell-cycle checkpoint.
19 oprotein from HPV degrades p53 and abrogates cell cycle checkpoints.
20 enome integrity by regulating DNA repair and cell cycle checkpoints.
21 Human cells contain G1 and G2 cell cycle checkpoints.
22 cute homology-directed DNA damage repair and cell cycle checkpoints.
23 rades the tumor suppressor p53 and abrogates cell cycle checkpoints.
24 ontrol of DNA damage repair and signaling to cell cycle checkpoints.
25 g in ATM/Chk2 inactivation and abrogation of cell cycle checkpoints.
26 t timer to trigger the MBT and activation of cell cycle checkpoints.
27 DDR) activates downstream pathways including cell cycle checkpoints.
28 ns, including DNA breaks, and can compromise cell cycle checkpoints.
29 M/Chk2 and ATR/Chk1 pathways and appropriate cell cycle checkpoints.
30 ive proteins and reverses DNA damage-induced cell cycle checkpoints.
31 critical residues of EBNA3C in bypassing the cell cycle checkpoints.
32 n the initiation of both DNA replication and cell cycle checkpoints.
33 cluding the initiation of DNA damage-induced cell cycle checkpoints.
34 tered cell cycle dynamics and the failure of cell cycle checkpoints.
35 ng is known about how T. brucei controls its cell cycle checkpoints.
36 351 activates CHK1 as well as the S and G2/M cell cycle checkpoints.
37 Biologically, these conditions correspond to cell cycle checkpoints.
38 n actionable dependence on ATR/CHK1-mediated cell cycle checkpoints.
39 pigenetic silencing of CDKN1A and release of cell cycle checkpoints.
40 ously described, but also regulates multiple cell cycle checkpoints.
41 ontrols progression of mitosis by activating cell cycle checkpoints.
42 mosome instability in cancer cells that lack cell cycle checkpoints.
43 nous cell divisions without growth phases or cell cycle checkpoints.
44 lar oncogenes need to circumvent DDR-induced cell-cycle checkpoints.
45 protein involved in DNA repair pathways and cell-cycle checkpoints.
46 response to DNA damage and is essential for cell-cycle checkpoints.
47 nment, as well as an amplification of G(1)/S cell-cycle checkpoints.
48 tors that normally coordinate DNA repair and cell-cycle checkpoints.
49 ponse and, in particular, intra-S and G(2)/M cell-cycle checkpoints.
50 s illegitimate joining of DSBs and activates cell-cycle checkpoints.
51 pt and irreversible nature of three specific cell-cycle checkpoints.
52 y M. oryzae requires two independent S-phase cell-cycle checkpoints.
53 ncluding the onset of bulk transcription and cell-cycle checkpoints.
54 nonical regulatory mechanisms that establish cell-cycle checkpoints.
57 tify strong synergistic interactions between cell-cycle checkpoint-abrogating Chk1- and MK2 inhibitor
60 horylation, induced PARP cleavage, abrogated cell cycle checkpoint activation and attenuated the form
63 ults demonstrate that targeted inhibition of cell cycle checkpoint activation following ionizing radi
64 l an important role for RECQ1 in controlling cell cycle checkpoint activation in response to gemcitab
66 rivaled by marked activation of DNA damage, cell cycle checkpoint activation, and mitotic catastroph
67 tranded DNA and may determine telomere size, cell cycle checkpoint activation, and, ultimately, tempe
72 trol ultimately causes extensive DNA damage, cell-cycle checkpoint activation and cell death whereas
74 WAC-dependent transcription is important for cell-cycle checkpoint activation in response to genotoxi
75 of signaling cascades, chromatin remodeling, cell-cycle checkpoint activation, and repair of the DSB.
76 ular functions, including DNA damage repair, cell-cycle checkpoint activation, gene transcriptional r
78 reduces IR-induced apoptosis by influencing cell-cycle checkpoint activity, potentially allowing for
81 , supernumerary centrosomes, and compromised cell-cycle checkpoints, allowing accumulation of chromos
82 ted tissue, and through deactivation of G2/M cell-cycle checkpoint allows the cell-cycle progression
85 ologous recombination DNA repair and Chk1 in cell cycle checkpoint and DNA repair, creating opportuni
90 of the conventional DNA damage-induced G2/M cell cycle checkpoint and the spindle assembly checkpoin
91 d enrichment of DNA replication, cell cycle, cell cycle checkpoint and TNF pathways in selinexor trea
92 BRCA1 E3 ligase activity regulates the G2/M cell cycle checkpoint and, thus, contributes to maintena
93 BRCA1 E3 ligase activity regulates the G2/M cell cycle checkpoint and, thus, contributes to maintena
94 The mammalian MMR proteins also activate cell cycle checkpoints and apoptosis in response to pers
95 d in the regulation of the G(1)-S and G(2)-M cell cycle checkpoints and death receptor/apoptosis sign
97 karyotic genomic integrity is safeguarded by cell cycle checkpoints and DNA repair pathways, collecti
98 hat sense stalled replication forks activate cell cycle checkpoints and DNA repair processes, which m
102 pathway that regulates cell cycle arrest at cell cycle checkpoints and facilitates the repair of dsD
103 1 (Chk1) is an essential kinase required for cell cycle checkpoints and for coordination of DNA synth
104 polyomaviruses in primary cells with intact cell cycle checkpoints and how the activation might be l
106 1 kinase inhibitor AZD1775 (WEE1i) overrides cell cycle checkpoints and is being studied in HNSCC reg
107 le regulators, bypasses the need for S-phase cell cycle checkpoints and predisposes to genomic instab
108 intenance of genomic integrity by activating cell cycle checkpoints and promoting repair of DNA doubl
109 ibition of CHK1 abrogates DNA damage-induced cell cycle checkpoints and sensitizes p53 deficient canc
110 hibitor Pif1 resulted in the inactivation of cell cycle checkpoints and the subsequent rescue of temp
112 ioresistance and that combined inhibition of cell-cycle checkpoint and DNA repair targets provides th
117 ine protein kinase, is centrally involved in cell-cycle checkpoints and cellular response to DNA dama
118 multiple pathways, including DDR signaling, cell-cycle checkpoints and damage repair, ESC differenti
125 at orchestrate chromatin structural changes, cell-cycle checkpoints and multiple enzymatic activities
127 age, propagate injury DNA messages, regulate cell cycle checkpoints, and alter the microenvironment.
129 relevant pathways including stress response, cell cycle checkpoints, and cell migration/adhesion.
131 d cellular gene expression, activates G(2)-M cell cycle checkpoints, and is essential for viral sprea
132 s, cellular signaling, nuclear architecture, cell cycle checkpoints, and other cellular activities co
134 excision repair (NER) and the ATR-dependent cell cycle checkpoint are the major pathways responsible
136 , is crisis, the state that cells reach when cell cycle checkpoints are impaired and cells can no lon
140 ismatch repair (MMR) triggers prolonged G(2) cell cycle checkpoint arrest after alkylation damage fro
141 nal DNA mismatch repair (MMR) stimulate G(2) cell cycle checkpoint arrest and apoptosis in response t
142 omplexes of protein interactions that govern cell cycle checkpoint arrest and repair of the DNA lesio
144 they are highly reliant on the Chk1-mediated cell cycle checkpoint arrest, indicating that HR repair
146 cle progression, focusing on the G1 and G2/M cell cycle checkpoints, as well as on related essential
147 igger a characteristic 'VSG synthesis block' cell-cycle checkpoint, as some cells reinitiated S phase
148 es typically lead to progression through the cell-cycle checkpoints, as well as increased cell migrat
149 ion mutants, the latter of which affects the cell cycle checkpoint ATAXIA TELANGIECTASIA-MUTATED AND
150 her than erasing their signalling history at cell-cycle checkpoints before mitosis, mother cells tran
152 ability of ATR inhibition to abrogate the G2 cell cycle checkpoint both contributed to the synergisti
154 s, replication inhibitors did not activate a cell cycle checkpoint, but they did activate a process t
155 s predominantly engaged in the regulation of cell cycle checkpoints by p21Cip1 and does not trigger a
158 ic expression of miR-421 resulted in S-phase cell cycle checkpoint changes and an increased sensitivi
161 f transcription, cell cycle lengthening, and cell cycle checkpoints comprise the midblastula transiti
162 ified over two decades ago and linked to the cell cycle checkpoint concept proposed by Weinert and Ha
163 r to MRL mice, providing a firm link between cell cycle checkpoint control and tissue regeneration.
164 f MK2 in inflammation, Hsp27 regulation, and cell cycle checkpoint control with a focus on brain path
167 he DNA damage response comprises DNA repair, cell-cycle checkpoint control, and DNA damage-induced ap
172 copy BRCA1 loss in centrosome amplification, cell-cycle checkpoint defects, DNA damage and genomic in
173 but not all, of the proteins contributing to cell cycle checkpoint deficiencies in RA T cells, via a
174 nation of multiple cellular events including cell cycle checkpoint, DNA repair, transcription, and ap
175 ys that maintain genomic stability including cell cycle checkpoints, DNA repair, protein ubiquitinati
179 YC2 in controlling a G1-to-S light-dependent cell cycle checkpoint, dsCYC2 silencing decreases the ra
181 hibits alterations in DNA repair enzymes and cell-cycle checkpoints, elucidation of factors enabling
184 ant, als3-1, resulted in identification of a cell cycle checkpoint factor, ALUMINUM TOLERANT2 (ALT2),
186 was integral to signaling that regulated the cell cycle checkpoint, focal adhesion, and actin remodel
187 rexpress oncogenes that specifically perturb cell-cycle checkpoints (for example, E7 from human papil
189 Thus, we hypothesize that ATM performs a cell cycle checkpoint function to protect post-mitotic n
192 molecular level, NONO bound to the p16-Ink4A cell cycle checkpoint gene and potentiated its circadian
193 s from this mouse pointed to the role of the cell cycle checkpoint gene CDKN1a, or p21(cip1/waf1).
195 ilar to the loss-of-function mutants for the cell cycle checkpoint genes ATAXIA TELANGIECTASIA AND RA
197 provides additional insight into the role of cell-cycle checkpoint genes in neurodevelopmental disord
198 free survival and resistance to knockdown of cell-cycle checkpoint genes in triple-negative/basal-lik
199 ive signals, based in part on derangement of cell cycle checkpoints governed by cilia and centrosomes
200 gene and protein expression that reestablish cell cycle checkpoints, halt protein translation, and pr
201 e 1 (CHK1)-mediated S-phase and G(2)-M-phase cell-cycle checkpoints has been a promising therapeutic
203 the apical protein kinase that initiates the cell cycle checkpoint in response to DNA damage and repl
204 ortholog of human ATM kinase and initiates a cell cycle checkpoint in response to dsDNA breaks (DSBs)
205 e part of a signaling cascade that induces a cell cycle checkpoint in response to ROS-induced DNA dam
206 echanism for co-targeting DNA damage-induced cell cycle checkpoints in combination with repair of cis
207 d Skp2 expression may overcome p53-dependent cell cycle checkpoints in melanoma cells and highlight S
210 on of G arrest by p18 bypasses a homeostatic cell-cycle checkpoint in iPCs for PC differentiation.
211 s, mechanisms that attenuate DDR and disrupt cell-cycle checkpoints in sporadic cancers are not well
212 ion of HPV1 E4 in cells is known to activate cell cycle checkpoints, inhibiting G(2)-to-M transition
213 rrest, which is cytotoxic when combined with cell-cycle checkpoint inhibition and constitutes a novel
214 increased micronuclei formation utilizing a cell cycle checkpoint inhibitor to drive cell cycle prog
216 our findings show a rationale for combining cell-cycle checkpoint inhibitors with the novel non-CPT
217 ive regulator of p53 stability when the G(1) cell cycle checkpoint is activated and provides an expla
221 Understanding the regulatory principles of cell cycle checkpoints is important because loss of chec
222 cytotoxicity when depleted, with loss of the cell cycle checkpoint kinase 1 (CHK1/CHEK1) being the mo
223 ough ataxia-telangiectasia mutated (ATM) and cell cycle checkpoint kinase 2 (CHK2), a DNA damage resp
225 Particularly CHEK1, which encodes for the cell cycle checkpoint kinase CHK1, is significantly over
226 trate that phosphorylation at Thr-288 by the cell cycle checkpoint kinase CHK2 is involved in this pr
229 hetic lethal relationship exists between the cell cycle checkpoint kinase MK2 and the tumor suppresso
231 small-molecule inhibitors targeting the G2/M cell cycle checkpoint kinase, CHK1, in a variety of non-
232 ed DNA, and the ATR targets RPA2 and Chk1, a cell cycle checkpoint kinase, were not phosphorylated.
233 eting ataxia-telangiectasia and Rad3-related/cell-cycle checkpoint kinase 1 (CHK1)-mediated S-phase a
238 matin alterations recruit the DNA repair and cell cycle checkpoint machinery to restore genome integr
239 of PKCdelta in the DNA damage-induced G(2)/M cell cycle checkpoint may be a critical component of its
240 These results suggest that a p53-dependent cell cycle checkpoint monitors changes of cellular NS le
241 atory cytokine mRNA decay, AUF1 destabilizes cell-cycle checkpoint mRNAs, preventing cellular senesce
242 ordinate cell-signaling pathways involved in cell-cycle checkpoints, nuclear localization, gene trans
245 ed response including several DNA repair and cell cycle checkpoint pathways is activated to ensure fa
246 damage response, including highly conserved cell cycle checkpoint pathways that prevent cells with D
247 tenance mechanisms, involving DNA repair and cell-cycle checkpoint pathways, initiate genetic instabi
250 is heterogeneity may reflect a relaxation of cell cycle checkpoints, possibly increasing the ability
251 implicate a novel mechanism by which loss of cell cycle checkpoints promotes BRCA1-associated tumorig
252 In addition, deletion of Ku80 along with the cell cycle checkpoint protein, p53, dramatically increas
253 stabilizes quadruplex mRNA that encodes the cell-cycle checkpoint protein kinase Aurora A to a great
255 vealed that pathways involved in cell cycle, cell cycle checkpoints, protein-ubiquitination, and apop
256 nd BRCT domain of the tandem BRCT repeats of cell cycle checkpoint proteins MDC1 (mediator of DNA dam
259 ermore, SpHst4 interacts with SpMyh1 and the cell cycle checkpoint Rad9-Rad1-Hus1 (9-1-1) complex.
260 esults in relaxed chromatin structure, rapid cell-cycle checkpoint recovery and enhanced survival aft
265 Moreover, RAs control the expression of cell-cycle checkpoint regulators such as p27(Kip1), p57(
267 acts with CHK1, a key effector kinase in the cell cycle checkpoint response, and regulates its phosph
268 ting of CycG2 attenuates doxorubicin-induced cell cycle checkpoint responses in multiple cell lines.
271 n human cells but also adversely affects the cell cycle checkpoint, resulting in profound chromosomal
272 ed through into mitosis because of defective cell cycle checkpoints, resulting in cell death by mitot
273 ation (IR)-induced DNA damage, activation of cell cycle checkpoints results in cell cycle arrest, all
276 generate regions of ssDNA that then trigger cell cycle checkpoint signaling and DSB repair by homolo
277 pon which to build additional aspects of the cell cycle checkpoint signaling network, including those
278 RCT) domains, present in many DNA repair and cell cycle checkpoint signaling proteins, are phosphopro
279 e essential for telomere length maintenance, cell cycle checkpoint signaling, meiotic recombination,
280 Thus targeting DNA replication and G2-M cell cycle checkpoint simultaneously by cisplatin and WE
281 aled that rtel1 mutant plants show activated cell cycle checkpoints, specific sensitivity to DNA cros
282 egulates cellulose production independent of cell cycle checkpoint systems that are controlled by div
284 f miR-221 and miR-222 is tightly linked to a cell cycle checkpoint that ensures cell survival by coor
285 her increase in E2F7, which induces a second cell cycle checkpoint that prevents unconstrained cell d
287 plays a well-characterized role in the major cell-cycle checkpoint that regulates chromosome segregat
288 oliferation and may also compromise multiple cell-cycle checkpoints that maintain genomic integrity,
289 ich mediates relaxation of the intra-S phase cell-cycle checkpoint; this facilitates viral oncogene-d
290 inase (MK2) and simultaneously controls both cell cycle checkpoints through distinct target mRNAs, bu
291 to simultaneously control the G1/S and G2/M cell cycle checkpoints through transcriptional induction
292 ty of Cre-LoxP conditional disruption of the cell cycle checkpoint tumor-suppressor genes Trp53 and R
293 threshold of YneA required to establish the cell cycle checkpoint, uncovering a new regulatory step
294 We showed here that E7 abrogated the G1 cell cycle checkpoint under hypoxia and analyzed key cel
296 ure of MYH activity is its coordination with cell cycle checkpoint via interaction with the Rad9-Rad1
297 s, where it functions in repair and triggers cell-cycle checkpoints via activation of the ataxia-tela
298 53 (via inhibition of MDM2) or impairment of cell cycle checkpoints (via inhibition of CHK1/2 or WEE1
299 lung cancer cells displayed a defective G1/S cell cycle checkpoint, were unable to resolve DNA damage
300 Cyclin-dependent kinases (CDKs) coordinate cell cycle checkpoints with DNA repair mechanisms that t