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1 rapidly signal fork stalling to activate the S phase checkpoint.
2 g that death was not preventable post the G1-S phase checkpoint.
3 OP blocking most, if not all, aspects of the S phase checkpoint.
4 syndrome 1 (NBS1), and is required for intra-S phase checkpoint.
5  is not induced by IR but also affects intra-S phase checkpoint.
6 A damage checkpoint independent of the intra-S phase checkpoint.
7 to ionizing radiation (IR) to activate intra-S phase checkpoint.
8  DNA replication forks and a mediator of the S phase checkpoint.
9 nding domain for recruitment to IRIF and the S phase checkpoint.
10 orks, but which is compromised for the intra-S phase checkpoint.
11  repair, telomere maintenance, and the intra-S phase checkpoint.
12 were associated with activation of the intra-S phase checkpoint.
13 by STAT3, leading to relaxation of the intra-S phase checkpoint.
14  transcription of ASE1, which depends on the S phase checkpoint.
15    This Top1-dependent process activates the S phase checkpoint.
16 e stability distinct from its role in the G1-S phase checkpoint.
17 a readout for activation of the ATR-mediated S phase checkpoint.
18 LL on damage to DNA, and thus compromise the S-phase checkpoint.
19 rigin activity and is modulated by the intra-S-phase checkpoint.
20 nto how cells recover from activation of the S-phase checkpoint.
21 d stalled replication forks during the intra-S-phase checkpoint.
22 iency in the forks required to establish the S-phase checkpoint.
23 complex (MRN) plays an essential role in the S-phase checkpoint.
24 ivate the signaling cascades involved in the S-phase checkpoint.
25 at Ser-343, which results in a defect in the S-phase checkpoint.
26 d cell cycle progression via an ATR-mediated S-phase checkpoint.
27 ependent cell survival required a functional S-phase checkpoint.
28 stranded breaks (DSBs) and activation of the S-phase checkpoint.
29  the ionizing radiation (IR)-inducible intra-S-phase checkpoint.
30 ion forks is a key step in activation of the S-phase checkpoint.
31 ingly, this accumulation is not dependent on S-phase checkpoint.
32 nates stalled forks, thereby attenuating the S-phase checkpoint.
33  be an important target of the Chk1-mediated S-phase checkpoint.
34  DNA damage, replication is inhibited by the S-phase checkpoint.
35 diol epoxide (BPDE) induces a Chk1-dependent S-phase checkpoint.
36 and functions upstream of rad-5/clk-2 in the S-phase checkpoint.
37 ed for normal recovery from the BPDE-induced S-phase checkpoint.
38 c25A is a major mechanism for damage-induced S-phase checkpoint.
39 ugh maintenance of an ATR and Chk1-dependent S-phase checkpoint.
40 ases polkappa and poleta in the BPDE-induced S-phase checkpoint.
41 hat loss of CDK2 activity activates an intra-S-phase checkpoint.
42 icularly enriched for genes that support the S-phase checkpoint.
43 at leads to this slowing is called the intra-S-phase checkpoint.
44 n radiosensitivity and a defect in the intra-S-phase checkpoint.
45 al for the efficient activation of the intra-S-phase checkpoint.
46 stream effector of ATM activity in the intra-S-phase checkpoint.
47 therapy, at least in part, by regulating the S-phase checkpoint.
48 ATRIP)-ATR complex, and this compromised the S-phase checkpoint.
49 (stalled fork) and is protected by the inter-S-phase checkpoint.
50 n and a potential role for PP2A in the intra-S-phase checkpoint.
51  to introduce a G2 in embryos that lacked an S-phase checkpoint.
52 tion licensing through the activation of the S-phase checkpoint.
53 ation forks and activates the Cds1-dependent S-phase checkpoint.
54 hase lengthens, which delays mitosis via the S-phase checkpoint.
55 nates DNA damage-induced G2/M, G1, and intra S phase checkpoints.
56 ce show defective recovery from BPDE-induced S-phase checkpoints.
57  that Cks overexpression abrogates the intra-S-phase checkpoint, a major barrier to oncogene-mediated
58 rikingly, phosphorylation of Mrc1 during the S phase checkpoint abolishes Pol2N binding, but not Pol2
59                                          The S-phase checkpoint activated at replication forks coordi
60 we report that Chk1p has a role in the intra-S-phase checkpoint activated when yeast cells replicate
61     Arrest was accompanied by DNA damage and S phase checkpoint activation and required ATR or ATM ki
62         Therefore, Trp53 is required for the S phase checkpoint activation observed in Fancd2 mutant
63 R-induced foci (IRIF) formation of R/M/N and S phase checkpoint activation, but only the BRCT domain
64 nd intermediate levels of UV sensitivity and S phase checkpoint activation, but similar levels of Mre
65 d breaks repair and DNA damage-induced intra-S phase checkpoint activation.
66    Intriguingly, an ATM inhibitor suppressed S-phase checkpoint activation after exposure to replicat
67  involved in replication fork stabilization, S-phase checkpoint activation and establishment of siste
68 E-822, to prevent chemotherapy-induced intra-S-phase checkpoint activation and evaluated the antitumo
69 processing is not necessary for ATR-mediated S-phase checkpoint activation and that the lesion recogn
70 oduces replication-dependent DNA lesions and S-phase checkpoint activation following DPC formation.
71 BS cells are radiosensitive and defective in S-phase checkpoint activation following irradiation.
72 DR), promotes cellular survival and prevents S-phase checkpoint activation in budding yeast undergoin
73          Each of these agents also triggered S-phase checkpoint activation in parental ES cells, as i
74         Following ionizing radiation-induced S-phase checkpoint activation, Tax-expressing cells prog
75 cell cycle re-entry after DNA damage-induced S-phase checkpoint activation.
76 duced p21(Waf1/Cip1) and MDM2, demonstrating S-phase checkpoint activation.
77 k1 phosphorylation, and abolished UV-induced S-phase checkpoint activation.
78 sphorylation of Chk2 and Smc1, necessary for S-phase checkpoint activation.
79                                   This intra-S-phase checkpoint actively regulates DNA synthesis by i
80 ia RPA and directly control the amplitude of S phase checkpoint activity and the subsequent deactivat
81  Ino80, function to attenuate and deactivate S phase checkpoint activity.
82                                         Both S-phase checkpoint activity and H3K4me are crucial for f
83 langiectasia and Rad3 related (ATR)-mediated S phase checkpoint acts as a surveillance mechanism to p
84 akage syndrome protein, known to mediate the S phase checkpoint after DNA damage.
85 cells from interphase arrest and loss of the S-phase checkpoint after DNA damage, accompanied by high
86                             Furthermore, the S-phase checkpoint after UV irradiation was defective in
87 rosine phosphorylation mediated by the intra-S-phase checkpoint, allowing cells to continue replicati
88 UV exposure, a defective UV responsive intra-S phase checkpoint and a specific pattern of genomic ins
89  and SMC3 acetylation are required for intra-S phase checkpoint and cellular survival after IR.
90 nase is necessary for both activation of the S phase checkpoint and for efficient DNA damage repair r
91 Tipin complex plays an important role in the S phase checkpoint and replication fork stability in met
92                                         Both S phase checkpoint and SCC defects are phenocopied by H3
93 prevent mitotic catastrophe, function in the S-phase checkpoint and also cooperate with atm-1 in the
94 re equally important for triggering of intra-S-phase checkpoint and ATM signaling promoted recovery o
95 n important role for the p21-dependent intra-S-phase checkpoint and extensive rereplication, whereas
96 log of the human ATR/ATM genes, controls the S-phase checkpoint and prevents replication fork collaps
97 sion of MDC1 expression results in defective S-phase checkpoint and reduced apoptosis in response to
98 /Tim1 complex plays an important role in the S-phase checkpoint and replication fork stability.
99 st cancer cells is preceded by activation of S-phase checkpoint and selective induction of E2F1, a re
100 e to degrade cyclin D1 compromises the intra-S-phase checkpoint and suggest that cyclin D1 degradatio
101 requires the coordinated action of the intra-S-phase checkpoint and the Fanconi anaemia pathway, whic
102 ication fork arrest, activation of the intra-S phase checkpoint, and global defects in chromatin stru
103 eplication stress and activation of an intra-S phase checkpoint, and suppressed the growth of VHL-/-
104 ologous recombination, telomere maintenance, S-phase checkpoint, and genome stability during replicat
105         Neither the DNA damage nor the intra-S phase checkpoints are activated in the first cell cycl
106 ment, as well as DNA damage-induced G2/M and S phase checkpoint arrest and radiation survival are dep
107 lution triggers anaphase, is dispensable for S phase checkpoint arrest.
108 esulfonate, inducers of DNA damage and intra-S-phase checkpoint arrest in all examined eukaryotes.
109                                              S-phase checkpoint arrest was incomplete, however, allow
110 f Chk1 was associated with inefficient inter-S phase checkpoint, as Hsp72 depleted cells failed to ha
111 be explained by co-dependence on a single G1/S-phase checkpoint, as S phase and zygotic polarization
112 on--with zygotes having to pass through a G1/S-phase checkpoint before the polarization axis can be f
113 We propose that S phase arrest activates the S phase checkpoint blocking mitosis onset and inhibiting
114 d independently of the replication-dependent S phase checkpoint but by similar conditions involving t
115          Esc4p is not required for the intra-S-phase checkpoint but is essential for resumption of ch
116  the ataxia telangiectasia mutated-dependent S-phase checkpoint, but rather closely resembled a previ
117 of NBN is required for the activation of the S-phase checkpoint, but the mechanism whereby these phos
118 ally induce and activate p53 and activate an S phase checkpoint by modifying the Nijmegen breakage sy
119 tive phosphorylation by CK2 may affect intra-S phase checkpoint by modulating SMC3 phosphorylation by
120                          Bypass of the intra-S-phase checkpoint by caffeine activates many new origin
121                       Induction of the intra-S-phase checkpoint by hydroxyurea (HU) inhibits Rad52 fo
122 phase and that activating the Rad3 dependent S-phase checkpoint by inhibiting DNA replication had lit
123 g a high threshold for the ATR-Chk1-mediated S-phase checkpoint by promptly repairing DNA breaks that
124 eveal a novel pathway, defended by the intra-S-phase checkpoint, by which MDM2 induces unscheduled or
125 in response to cytarabine (ara-C) induced an S-phase checkpoint characterized by the inhibition of Cd
126 lizing or restarting replication forks under S phase checkpoint conditions.
127 n the absence and presence of DNA damage and S-phase checkpoint conditions.
128                                    The intra-S-phase checkpoint contributed to the high-level of fork
129 as a missing link between p53 activation and S phase checkpoint control designed to eliminate replica
130 lication machinery plays additional roles in S phase checkpoint control, although the identities of t
131            We propose that Ddk modulates the S-phase checkpoint control by attenuating checkpoint sig
132 ion of Nbs1-S343A mutant disrupted the intra-S-phase checkpoint, decreased homologous recombinational
133  proteins after IR, they exhibit a defective S-phase checkpoint, decreased survival, and increased ch
134 phosphorylation of Ser-1067 as well as intra-S phase checkpoint defect.
135 int competent, but set1Delta displays a mild S phase checkpoint defect.
136               53BP1(-/-) cells show a slight S-phase checkpoint defect and prolonged G(2)/M arrest af
137 horylation of ATM on Ser 1981, and caused an S-phase checkpoint defect in DNA-damaged cells.
138 e ATM kinase inhibitor KU 55933 results in a S-phase checkpoint defect similar to that observed in WR
139 pts checkpoint signaling and causes an intra-S-phase checkpoint defect.
140 eletion mutants (dot1Delta) are G1 and intra-S phase checkpoint defective after ionizing radiation bu
141      Nbs1(DeltaC/DeltaC) cells exhibit intra-S-phase checkpoint defects, but are otherwise indistingu
142 not S516A or DeltaSET mutant MLL rescues the S-phase checkpoint defects.
143 ent causes a persistent Mec1-dependent intra-S-phase checkpoint delay characterized by slow DNA repai
144 -R696W, we discovered that pol3-R696W causes S-phase checkpoint-dependent elevation of dNTP pools.
145 xia causes replication arrest independent of S-phase checkpoint, DNA damage response, or transformati
146                   Multiple pathways, such as S-phase checkpoints, DNA replication, recombination, chr
147 at BID plays an unexpected role in the intra-S phase checkpoint downstream of DNA damage distinct fro
148 id-type genomic abnormalities, indicative of S-phase checkpoint dysfunction.
149  (MRN) complex is required for mediating the S-phase checkpoint following UV treatment, but the under
150 n of RPA2, a critical event in mediating the S-phase checkpoint following UV treatment.
151                             We find that the S-phase checkpoint function of Sgs1p is dispensable for
152  of mismatch repair function restored normal S-phase checkpoint function.
153 gradation, thereby preventing attenuation of S-phase checkpoint functions and a compromised capacity
154           These data indicate that the intra-S-phase checkpoint functions to block late origin firing
155 F1 has also been implicated in regulating an S phase checkpoint, however its role in this checkpoint
156 w MRN affects DNA replication to control the S-phase checkpoint, however, remains unclear.
157 at Snm1B-deficient cells exhibit a defective S phase checkpoint in response to MMC, but not to IR, an
158 wo mechanisms are involved in regulating the S-phase checkpoint in an MRN-dependent manner following
159  involved in ATM pathway activation and in a S-phase checkpoint in cells exposed to DNA interstrand c
160 netic studies indicate the role of an intact S-phase checkpoint in maintaining genome integrity.
161 owed that DDK is an important target for the S-phase checkpoint in mammalian cells to suppress replic
162  an important mechanism underlying the intra-S-phase checkpoint in mammalian cells.
163 ubstrate of ATM and ATR to mediate the intra-S-phase checkpoint in mammalian cells.
164          Although the basic framework of the S-phase checkpoint in multicellular organisms has been o
165  as to how MDC1 regulates NBS1 and the intra-S-phase checkpoint in response to DNA damage.
166 ation, G2-M checkpoint arrest, and the intra-S-phase checkpoint in response to ionizing radiation.
167 air system is required for activation of the S-phase checkpoint in response to ionizing radiation.
168 r, DDK-null cells fail to activate the intra-S-phase checkpoint in the presence of hydroxyurea-induce
169  overexpress Cks1 or Cks2 override the intra-S-phase checkpoint in the presence of replication stress
170 ilon (Pol epsilon) was shown to activate the S-phase checkpoint in yeast in response to replicative s
171  failed to recover from the UV light-induced S-phase checkpoint), in sharp contrast to Polk(-/-) MEFs
172                            Recovery from the S-phase checkpoint includes inactivation of checkpoint s
173 s(checkpoint kinase 1) (Grp(Chk1))-dependent S-phase checkpoint, increased levels of CycB drives cyto
174 se pathway and show that deregulation of the S-phase checkpoint incurred by MLL translocations probab
175 ever, dun1Delta cells are proficient for the S-phase-checkpoint-induced anaphase block.
176 e Dun1p, yeast Chk1p is not required for the S-phase-checkpoint-induced anaphase block.
177               During replication stress, the S-phase checkpoint inhibits the DDK- and CDK-dependent a
178  bromodeoxyuridine incorporation to evaluate S phase checkpoint integrity, monoubiquitination of Fanc
179                       Furthermore, the intra-S-phase checkpoint is activated in Orc2-S188A-expressing
180 uce early mitotic entry, but reversal of the S-phase checkpoint is compromised by pairwise cyclin kno
181                     Interestingly, the intra-S-phase checkpoint is crucial for the cellular response
182 ether, our study demonstrates that the intra-S-phase checkpoint is exerted by Chk1 not only upon repl
183 ssion yeast, the signal activating the intra-S-phase checkpoint is generated only when replication fo
184 ec1, a key regulatory ATR-like kinase in the S-phase checkpoint, is required for both normal chromati
185 t treated with hydroxyurea (HU) activate the S phase checkpoint kinase Rad53, which prevents DNA repl
186 mitant phosphorylation and activation of the S phase checkpoint kinase, Rad53.
187                                          The S-phase checkpoint kinase and telomere maintenance facto
188                                    The intra-S-phase checkpoint kinase Chk1 phosphorylates Cdc25A to
189 phorylation of S331 is mediated by CHK1, the S-phase checkpoint kinase implicated in the Fanconi anem
190 ilon depend on damage uninducible (Dun)1, an S-phase checkpoint kinase that maintains dNTP levels dur
191 evidenced by autophosphorylation of ATR, the S-phase checkpoint kinase, and by recruitment of ATR and
192                                          The S-phase checkpoint kinases Mec1 and Rad53 in the budding
193 signals from active replication forks to the S-phase checkpoint machinery in human cells.
194 to be an essential target inactivated by the S-phase checkpoint machinery that inhibits DNA replicati
195 o present evidence suggesting that the intra-S-phase checkpoint makes a relatively minor contribution
196 ons argue that Drf1 is regulated by an intra-S-phase checkpoint mechanism that down-regulates the loa
197 se progression to G2 by modulating the intra-S phase checkpoint mediated by Chk1.
198  the loading onto chromatin of various intra-S-phase checkpoint mediators and found that NONO favours
199 mined the expression and activation of known S-phase checkpoint mediators in FdUrd-treated SW620 and
200                       The DNA replication or S-phase checkpoint monitors the integrity of DNA synthes
201                                              S-phase checkpoint mutants fail to stabilize Dia2 in res
202                            In contrast, most S-phase checkpoint mutants were synthetically lethal in
203 to better understand replication dynamics in S-phase checkpoint mutants, we developed a replication o
204 ign MLL as a novel effector in the mammalian S-phase checkpoint network and identify checkpoint dysfu
205  treatment with SN-38 and UCN-01 resulted in S-phase checkpoint override, an amplified DNA damage res
206  cdk2 have only been implicated in the intra-S phase checkpoint pathway after DNA damage.
207                                          The S phase checkpoint pathway preserves genome stability by
208 lecular mechanisms by which the ATR-mediated S phase checkpoint pathway prevents DNA rereplication an
209 urthermore, cells lacking H2A.Z required the S-phase checkpoint pathway for survival.
210 iated proteolysis and that activation of the S-phase checkpoint pathway inhibits Dia2 protein degrada
211                  During DNA replication, the S-phase checkpoint pathway responds to replication stres
212 h many chemotherapy drugs activate the intra-S-phase checkpoint pathway to block S-phase progression,
213  signaling through the conserved Mec1/Rad53, S-phase checkpoint pathway to induce the expression and
214 rity of the Pol binding module and block the S-phase checkpoint pathway, downstream of the Mec1 kinas
215 quire NBS1, a component of the IR-responsive S-phase checkpoint pathway.
216 ons as an effector in the ATM/NBS1-dependent S-phase checkpoint pathway.
217 the absence of Rtt/genome caretakers trigger S-phase checkpoint pathways to stimulate Ty1 reverse tra
218     Here, we show that either or both of two S-phase checkpoint pathways, the replication stress path
219                                          The S-phase checkpoint phenotype was independent of Nbs1 sta
220 ombination), mec1Delta tel1Delta (DNA damage/S-phase checkpoints), pif1Delta (maintenance of mitochon
221 hases of replication and triggers the "intra-S phase checkpoint." Previous work with budding yeast ha
222 iency in HCT116 is associated with defective S-phase checkpoint, prolonged G2 arrest, and hypersensit
223                       Such compromised intra-S phase checkpoints promoted gene amplification independ
224                                          The S phase checkpoint protects the genome from spontaneous
225                                    The intra-S phase checkpoint protein complex Tof1/Csm3 of Saccharo
226 evel of global control mediated by the intra-S-phase checkpoint protein complex of Tof1p and Csm3p th
227 e function of DNA polymerase epsilon and the S-phase checkpoint protein Mec1.
228 droxyurea (HU) treatment activates the intra-S phase checkpoint proteins Cds1 and Mrc1 to prevent rep
229                Third, deletions of the intra-S phase checkpoint proteins Tof1 and Csm3 abolished fork
230  F-box protein Dia2 as a novel player in the S-phase checkpoint recovery pathway.
231 ring DNA replication reinitiation during the S-phase checkpoint recovery.
232  Dia2 contributes to Mrc1 degradation during S-phase checkpoint recovery.
233 ased recruitment of Mre11 to IRIF, abrogated S phase checkpoint, reduced activation of ATM, Chk1, and
234  much is known about how and where the intra-S-phase checkpoint regulates origins of replication in h
235  1 (whose products regulate G(2) and G(1) or S phase checkpoints, respectively) after the cells have
236                            The budding yeast S phase checkpoint responds to hydroxyurea-induced nucle
237 ndent pathway plays an important role in the S phase checkpoint response following ionizing irradiati
238                                          The S phase checkpoint response slows down replication in th
239  may be an additional step in regulating the S phase checkpoint response to DNA damage on the leading
240 n stabilizing stalled replication forks, the S phase checkpoint response, and suppressing genetic cro
241 tes, disruption of DNA replication causes an S phase checkpoint response, which regulates multiple pr
242 s essential for the DNA damage-induced intra-S phase checkpoint response.
243 ATR-dependent phosphorylation of Chk2 or the S-phase checkpoint response after ionising radiation.
244 DM2 transgenic mice enter S phase and induce S-phase checkpoint response earlier than lung cells from
245  not inhibited during the DNA-damage-induced S-phase checkpoint response in Xenopus egg extracts and
246       Wild-type Tetrahymena elicits an intra-S-phase checkpoint response that is induced by hydroxyur
247 V fibroblasts lacking poleta showed a normal S-phase checkpoint response to BPDE (but failed to recov
248 nduces replication stress eliciting an early S-phase checkpoint response to inhibit further firing of
249 s is required for establishment of the intra-S-phase checkpoint response.
250 on, PP5 is required to elicit an appropriate S-phase checkpoint response.
251 uring S phase activate the S-phase and intra-S-phase checkpoint responses, respectively, regulated by
252 ion (IR), Hus1-deficient cells showed intact S-phase checkpoint responses.
253 he nucleus and not the cytoplasm to modulate S-phase checkpoint responses: alpha-syn up-regulates his
254                                Thus, the MRN S-phase checkpoint role is separate from its Ctp1- and r
255 ctedly, induction of the p21-dependent intra-S-phase checkpoint seemed to be independent of both Cdt1
256 replication, whereas the ATR-dependent intra-S-phase checkpoint seemed to play a less dominant role.
257       The Chk1 kinase is a major effector of S phase checkpoint signaling during the cellular respons
258 cks on the same RPA70N surface that recruits S phase checkpoint signaling proteins to chromatin.
259          Inhibition of RPA/ATR/Chk1-mediated S-phase checkpoint signaling partially inhibited BPDE-in
260 rk at a replication fork pause site restores S-phase checkpoint signaling to chk1Delta dun1Delta cell
261 unctions as an upstream regulator to monitor S-phase checkpoint signaling.
262  that Ddk plays an active role in regulating S-phase checkpoint signaling.
263               In the absence of a functional S-phase checkpoint, stalled replication forks collapse a
264                                    The intra-S-phase checkpoint suppresses origin firing after the lo
265 x6-dependent Chk1 degradation contributes to S phase checkpoint termination and that a defect in this
266 angiectasia and Rad3-related (ATR)-dependent S phase checkpoint that inhibits replication fork progre
267 e during DNA-replication arrest requires the S phase checkpoint that inhibits the S phase CDK.
268 DNA replication elongation trigger the intra-S phase checkpoint that leads to the activation of the C
269  yeast, DNA replication stress activates the S phase checkpoint that stabilizes replication forks and
270 essoria on the rice leaf surface requires an S-phase checkpoint that acts through the DNA damage resp
271 r cell types, leads to override of the intra-S-phase checkpoint that blocks DNA replication in respon
272 intaining the integrity of the genome is the S-phase checkpoint that functions to prevent DNA replica
273 n and suppresses the ATM/ATR-dependent intra-S-phase checkpoint that inhibits origin firing.
274 ent with MMC is part of a caffeine-sensitive S-phase checkpoint that is controlled by xATR.
275 s that are stalled by DNA damage activate an S-phase checkpoint that prevents irreversible fork arres
276 ely resistant to FdUrd, have an intact early S-phase checkpoint that protects against FdUrd-induced D
277 e for aberrant Gli1 in the regulation of the S-phase checkpoint that suppresses replication stress an
278 completion of both double-stranded break and S-phase checkpoints that should arrest all replication w
279 cy, consequently causes abnormalities in the S-phase checkpoint, the G(2)/M checkpoint, the spindle c
280     Based on synthetic phenotypes, the intra-S-phase checkpoint, the SRS2 inhibitor of recombination,
281 es by their sensitivity to activation by the S-phase checkpoint, thereby, providing an effective mech
282 uced DNA damage signaling and controls intra-S-phase checkpoint through CHK2 activation.
283 horylation of Dbf4 is critical for the intra-S-phase checkpoint to inhibit DNA replication.
284 wever, most dying neurons do not pass the G1/S-phase checkpoint to resume DNA synthesis.
285 Rad17 are required for the activation of the S-phase checkpoint to suppress DNA synthesis in response
286 larization involves a novel, DDR-independent S-phase checkpoint, triggered by appressorium turgor gen
287 ent of replication forks in coordinating the S-phase checkpoint using dun1Delta cells that have a def
288 ting for DNA synthesis when the BPDE-induced S-phase checkpoint was active.
289                               4) The G(1) to S-phase checkpoint was intact in primary and spontaneous
290 y, the ability of cytarabine to activate the S-phase checkpoint was severely compromised in Rad9(-/-)
291 ation initiation and elongation to the intra-S-phase checkpoint, we examined cells treated with the s
292 o investigate other potential targets of the S-phase checkpoint, we tested the effects of BPDE on the
293 stream and downstream of ATR to regulate the S-phase checkpoint when replication forks are stalled.
294 in Pol1 renders yeast cells dependent on the S phase checkpoint, whereas truncation of Pol1 at amino
295                    HU treatment triggers the S-phase checkpoint, which arrests cells at S-phase, inhi
296 damage and may also play a role in the intra-S-phase checkpoint, which delays the replication of dama
297 V-induced DNA damage by activating the intra-S-phase checkpoint, which prevents replication fork coll
298 otes activate a signaling pathway called the S-phase checkpoint, which produces a multifaceted respon
299 re not caused by defects in the ATM-mediated S-phase checkpoint, which was intact in primary Fancd2 m
300 atively involving the activation of an intra-S-phase checkpoint, would also inhibit tumor proliferati

 
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