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1 e.g., sterol biosynthesis) or not (e.g., DNA replication initiation).
2  genes cause disruption of the origin of DNA replication initiation.
3 -phase and define potential locations of DNA replication initiation.
4  cells imparts a rapid and complete block to replication initiation.
5  helicases that are central to bidirectional replication initiation.
6  changes, which are likely incompatible with replication initiation.
7 reaction that exhibits hallmarks of cellular replication initiation.
8 orylation, each previously shown to regulate replication initiation.
9  parapsilosis also employs recombination for replication initiation.
10 ediate chromosome segregation independent of replication initiation.
11 our understanding of mechanisms that control replication initiation.
12 bly of the GINS complex but is essential for replication initiation.
13  repair in addition to its essential role in replication initiation.
14 hereupon a dihexamer forms, resulting in DNA replication initiation.
15 to E2F1, which results in the termination of replication initiation.
16 ng partners on chromatin and facilitates DNA replication initiation.
17 ents lead to reverse transcription and viral replication initiation.
18 lay in establishing the genomic landscape of replication initiation.
19 es adjacent to one side of the major site of replication initiation.
20 45 and GINS helicase-activating proteins and replication initiation.
21 pBP1-treslin interaction is critical for DNA replication initiation.
22 ity may be a common mechanism for regulating replication initiation.
23 o the molecular mechanisms of eukaryotic DNA replication initiation.
24 by cyclin-dependent kinases is essential for replication initiation.
25 ucidated concerning their functional role in replication initiation.
26 omplexes of these proteins are necessary for replication initiation.
27 lows origin licensing and prevents premature replication initiation.
28 e dnaA promoter to control the timing of DNA replication initiation.
29 ggesting that LPS phosphorylation stimulates replication initiation.
30 tin structure plays an important role in DNA replication initiation.
31  protein that may act as an activator of DNA replication initiation.
32 ng the viability of mutants defective in DNA replication initiation.
33 effects of a primary activity regulating DNA replication initiation.
34  is the focus of several pathways to control replication initiation.
35 allows Cdc45 loading and derepression of DNA replication initiation.
36  of ParA halts segregation without affecting replication initiation.
37 for origin licensing, a prerequisite for DNA replication initiation.
38 BNA1 at sites of active transcription or DNA replication initiation.
39 e oriC to locally melt the DNA duplex during replication initiation.
40 tional importance of OGRE/G4 elements in DNA replication initiation.
41 ., constant growth increments) that start at replication initiation.
42 case is the committed step in eukaryotic DNA replication initiation.
43  recruitment during reactivation to preclude replication initiation.
44 g cell physiology, separate from its role in replication initiation.
45 ycle exit by functioning at a step after DNA replication initiation.
46 Mcm10 are factors that are also required for replication initiation.
47 possibly be independent from its role in DNA replication initiation.
48 s and epigenetic modifications in regulating replication initiation.
49 CD2 reduces the number of potential sites of replication initiation.
50 e a common G-rich motif and exhibit elevated replication initiation.
51 ive an analytical expression for the rate of replication initiation.
52 ouble hexamer that facilitates bidirectional replication initiation.
53 ts of the pre-replication complex during DNA replication initiation.
54 howed that AZ-27 inhibited transcription and replication initiation.
55 synthesis and shortens S phase by increasing replication initiation.
56 scuss here the molecular choreography of DNA replication initiation across the three domains of life,
57 c2 or Cdt1 suffice to recruit all downstream replication initiation activities to a prospective origi
58 se cyclin-dependent kinases (CDKs) stimulate replication initiation and accelerate progression throug
59 etabolic complex is enriched at sites of DNA replication initiation and associated with proliferating
60             DDK plays essential roles in DNA replication initiation and checkpoint activation.
61  We used RNAi against Cdc7 kinase to inhibit replication initiation and dissect this checkpoint in fi
62 e helicase 4 (RECQL4) plays crucial roles in replication initiation and DNA repair; however, the cont
63                 This enzyme is implicated in replication initiation and DNA topology restoration and
64 se, consistent with the observation that DNA replication initiation and elongation are impaired in so
65 chanism by which a checkpoint kinase targets replication initiation and elongation complexes, which m
66       To investigate the contribution of DNA replication initiation and elongation to the intra-S-pha
67  we establish that RbN directly inhibits DNA replication initiation and elongation using a bipartite
68 ates WEE1-MCM2 signaling, which inhibits DNA replication initiation and enables BRCA1-deficient cells
69 dimer is required both for activation of DNA replication initiation and for interaction with Spo0J.
70  multiple processes, including inhibition of replication initiation and fork stabilization.
71 ct relationship between sites of reduced DNA replication initiation and genetic damage.
72 phed mechanisms, often through the action of replication initiation and helicase-loader proteins.
73 lication stress is caused by deregulation of replication initiation and increased interference betwee
74 s in plasmid origins and participate both in replication initiation and its control.
75 Here, we review our current understanding of replication initiation and its regulation, describe mech
76 rates by primase may influence regulation of replication initiation and Okazaki fragments processing.
77 lays a key role in determining the timing of replication initiation and origin usage.
78 aA, DnaD, and DnaB to help properly regulate replication initiation and perhaps are analogous to the
79 mage, BRCA1 deficiency markedly enhances DNA replication initiation and preferably impairs DNA replic
80 he importance of protein acetylation for DNA replication initiation and progression, and suggests tha
81 of the response regulator CtrA represses DNA replication initiation and regulates the transcription o
82 se relationship between the durations of DNA replication initiation and replication.
83 h chloramphenicol relieves inhibition of DNA replication initiation and RNA synthesis in HipA-arreste
84       A genome-scale correlation between DNA replication initiation and RNA transcription, which is e
85  data help explain how CDK activity controls replication initiation and suggest that replication prog
86                      These data suggest that replication initiation and termination are coupled to tr
87 ntified and quantitatively compared sites of replication initiation and termination in untransformed
88  investigated the role of YabA in regulating replication initiation and the activity of DnaA as a tra
89 ole of protein kinase CK2 in controlling DNA replication initiation and the expression levels of repl
90    We demonstrate that SLD-2 is required for replication initiation and the nuclear retention of a cr
91  activate CtrA-dependent genes following DNA replication initiation and the reaccumulation of CtrA.
92 se checkpoint in mammalian cells to suppress replication initiation and to protect replication forks.
93 dent pathway mediating the inhibition of DNA replication initiation, and a SpoT-independent pathway(s
94 r fundamental understanding of bacterial DNA replication initiation, and because of the conserved str
95 that confers stable episome maintenance, DNA replication initiation, and chromatin organization funct
96 ssion can support organized, yet stochastic, replication initiation, and its absence could explain in
97 f pre-replication complex (pre-RC) assembly, replication initiation, and micrococcal nuclease (MNase)
98 K is an S-phase-specific kinase required for replication initiation, and the DNA primase-polymerase i
99            We also found that DnaN activates replication initiation apparently through effects on Yab
100 r, these results show that cell division and replication initiation are independently controlled at t
101                          Perturbation of DNA replication initiation arrests human cells in G1, pointi
102                                 By picturing replication initiation as a two-state system and conside
103 tion of SirA enforces diploidy by inhibiting replication initiation as B. subtilis cells develop into
104 r mechanism(s) of action at a distance, i.e. replication initiation at a considerable distance from t
105 h a model, suggesting that RepID facilitates replication initiation at a distinct group of human repl
106 , RecQ4, Treslin, and Drf1--are limiting for replication initiation at increasing N/C ratios in vitro
107     Previous work in Leishmania detected DNA replication initiation at just a single region in each c
108 nt gram positive bacteria and is involved in replication initiation at oriC and re-start of collapsed
109 onsistent with models in which YabA inhibits replication initiation at oriC, and perhaps DnaA functio
110 ound that YabA function is mainly limited to replication initiation at oriC.
111 nations of chromosomal orc genes showed that replication initiation at oriC1 requires orc7 but not or
112 bility by providing a checkpoint that delays replication initiation at OriP.
113 icase loading, and is a pivotal event during replication initiation at replication origins.
114 iates diagnostic of canonical bi-directional replication initiation at the centrally located bi-direc
115 r by viral protein-driven multiple rounds of replication initiation at viral origins.
116 itutions of the 3 residues are functional in replication initiation but are immune to inhibition by S
117 ria regulate the frequency and timing of DNA replication initiation by controlling the activity of th
118  Soj is a dynamic protein that regulates DNA replication initiation by either inhibiting or activatin
119               Bacteria control the timing of replication initiation by regulating the activity of Dna
120            This suggests that defects in DNA replication initiation can lead to activation of the DNA
121                  By clearly defining the DNA replication initiation checkpoint in hypoxic cells, we n
122 n is dependent on polar remodeling and a DNA replication initiation checkpoint that is tightly integr
123 gin domain plays a role in the regulation of replication initiation, chromosome organization, and DNA
124 een E1 and E2, preventing pre-initiation and replication initiation complex formation.
125 promotes DNA unwinding and the assembly of a replication initiation complex.
126  loss of OBP function or OBP itself from the replication initiation complex.
127 prereplication complexes but were present in replication initiation complexes on ori-Lyt.
128 were observed for 11 and 15 on corresponding replication initiation complexes.
129  of transcription and the enhancement of DNA replication initiation, contains two GAGGC sequences arr
130 l oligomer in vivo and that the frequency of replication initiation correlates with the extent of Dna
131 ependent phenotype as the rid phenotype (for replication initiation defective).
132                           Here we identify a replication-initiation determinant (RepID) protein that
133 Displaced Mcm2-7 double hexamers support DNA replication initiation distal to the loading site in vit
134 al states in response to both nucleotide and replication initiation/elongation factors.
135 clease activity, DNA synthesis is slowed and replication initiation events are more frequent.
136 ifferent cell types and host ~80% of all DNA replication initiation events in any cell population.
137 veal that the role of limiting the number of replication initiation events is to prevent DNA topologi
138 its associated E3s are rescued by increasing replication initiation events through mutating two maste
139 hosphorylation modulates the distribution of replication initiation events to insure genomic stabilit
140  of replication initiation sites showed that replication initiation events were absent from transcrip
141 s with high rates of transcription, very few replication initiation events were detected.
142                           Moreover, very few replication initiation events were observed when two ect
143 me-wide massively parallel sequencing to map replication initiation events, thereby creating a databa
144  sequences strongly affected the location of replication initiation events, whereas histone modificat
145  progression while reducing the frequency of replication initiation events.
146 ine the spatial and temporal organization of replication initiation events.
147 ally required throughout the S-phase for all replication initiation events.
148 ather acts as a tunable rheostat to regulate replication initiation events.
149 nes the timing of both the next division and replication initiation events.
150 pends on the spatial and temporal pattern of replication initiation events.
151 ormal replication fork progression and fewer replication-initiation events.
152 expressed proteins identified, Cdc6 is a DNA replication initiation factor and exhibits oncogenic act
153 uggest that WDHD1 may also function as a DNA replication initiation factor as well as a G1 checkpoint
154 osis in fission yeast has identified the DNA replication initiation factor cdc18 (known as CDC6 in ot
155 phogenetic protein (BMP) pathway and the DNA replication initiation factor Cdc6.
156 es the DNA damage-induced degradation of the replication initiation factor Cdt1 via the CRL4(Cdt2) E3
157                       Interestingly, the DNA replication initiation factor Cdt1, whose uncontrolled e
158              Geminin is known to inhibit the replication initiation factor Cdt1.
159 ecognition complex (ORC) is an essential DNA replication initiation factor conserved in all eukaryote
160 eplication by targeting the highly conserved replication initiation factor DnaA.
161 ta-TRCP)-dependent degradation of a limiting replication initiation factor Drf1.
162                           The eukaryotic DNA replication initiation factor Mcm10 is essential for bot
163              We identified a mutation of the replication initiation factor Sld3, Sld3-m16, that is sp
164                And-1/Ctf4 is therefore a new replication initiation factor that brings together the M
165 ation of cell division cycle 6 (Cdc6), a DNA replication initiation factor, by polo-like kinase 1 (Pl
166 ted by a region homologous to the yeast Sld2 replication initiation factor, followed by a cysteine-ri
167 es, replication protein A encoding gene, DNA replication initiation factor, securin gene, nucleosome
168 inus of RECQ4 shares homology with yeast DNA replication initiation factor, Sld2, and is vital for em
169 ingly, pX increases expression of endogenous replication initiation factors Cdc6 and Cdtl while suppr
170 n fires is related to its ability to recruit replication initiation factors that are limiting within
171 on is a member of an expanding subset of DNA replication initiation factors that are not strictly req
172 teases regulate DNA replication by degrading replication initiation factors, suggesting a model in wh
173                                By inhibiting replication initiation factors, we show that Cyclin E-in
174 of genetic material depends on essential DNA replication initiation factors.
175 The ability of Cdks to differentially effect replication initiation, factory activation, and progress
176      Bacillus subtilis DnaD is needed during replication initiation for assembly of the replicative h
177 LE may play a role in recombination-mediated replication initiation found in the mitochondria of mamm
178                       Despite an increase in replication initiation frequency, cells lacking Mus81 us
179 e levels were generally associated with high replication initiation frequency.
180  and its kinase activity is required for DNA replication initiation from each origin.
181         Under such conditions, uncoupling of replication initiation from mitotic progression led to a
182 is essential for deoxyribonucleic acid (DNA) replication initiation from yeast to humans.
183 but rapidly adapted through mutations in the replication initiation gene trfA1.
184                                A role in DNA replication initiation has been demonstrated and mapped
185 ly been shown to regulate DnaA-dependent DNA replication initiation; however, the mechanism underlyin
186 ctionally address their requirements for DNA replication initiation in a series of independent approa
187         yabA encodes a negative regulator of replication initiation in Bacillus subtilis and homologu
188                YabA, a negative regulator of replication initiation in Bacillus subtilis, interacts w
189                Our results shed light on why replication initiation in bacteria is limited to a singl
190  regulatory mechanism for the control of DNA replication initiation in bacteria.
191 nding of the molecular details that underpin replication initiation in bacteria.
192            SeqA protein negatively regulates replication initiation in Escherichia coli and is also p
193 ew insight into the mechanisms that regulate replication initiation in Escherichia coli.
194 rved uncertainty on the position and time of replication initiation in eukaryote cell populations.
195 se and show that MCM2 deficiency reduces DNA replication initiation in gene-rich regions of the genom
196  that the optimal cell cycle progression and replication initiation in M. tuberculosis requires that
197                  The genetic aspects of oriC replication initiation in Mycobacterium tuberculosis are
198  MRN at origin-proximal sites to control DNA replication initiation in response to DNA damage, thereb
199  and regulation are diverged features of DNA replication initiation in T. brucei, providing new insig
200 , indicating that ATR kinase activity limits replication initiation in the absence of damage.
201 TDs to bind multiple partners to orchestrate replication initiation in the bacterial cell.
202  basis for further mechanistic dissection of replication initiation in vertebrates.
203 hromatin-binding studies show that E4 blocks replication initiation in vitro by preventing loading of
204 the set of yeast core factors sufficient for replication initiation in vitro is conserved in metazoa.
205 portant for downregulating CtrA prior to DNA replication initiation in vivo but that other phosphatas
206                                       During replication initiation in vivo, it is not known if these
207                           Failure to inhibit replication initiation indeed causes increased DNA caten
208                                              Replication initiation is a key event in the cell cycle
209  an understanding of the complexities of how replication initiation is controlled and coordinated wit
210  and an origin-proximal promoter involved in replication initiation is delayed.
211                               Control of DNA replication initiation is essential for bacterial cells
212                               Control of DNA replication initiation is essential for cell growth.
213                               Control of DNA replication initiation is essential for normal cell grow
214 ear how this association is terminated after replication initiation is finished.
215 ols the MBT and shows that the regulation of replication initiation is fundamental for normal embryog
216 g metazoan development and proposes that DNA replication initiation is governed differently in mitoti
217                                   Eukaryotic replication initiation is highly regulated and dynamic.
218     In summary, these findings indicate that replication initiation is influenced by transcription in
219                   During replication stress, replication initiation is stimulated downstream of genes
220 th variability, invalidating the notion that replication initiation is the principal trigger for cell
221 me being circular, reinforcing the idea that replication initiation is triggered repeatedly by fork c
222           How Mcm10 is localized to sites of replication initiation is unclear, as current models ind
223                                     Zones of replication initiation (IZs) were detected throughout S
224  kinase and CDK targets at origins regulates replication initiation kinetics during S-phase and estab
225              Our data suggest that increased replication initiation leads to slow replication fork pr
226                We purified components of the replication initiation machinery and studied their inter
227                     Here, we report that the replication initiation machinery of D. melanogaster unex
228  modelling have yielded detailed genome-wide replication initiation maps.
229                                              Replication initiation must be a carefully regulated pro
230 ate that elevated levels of helicase perturb replication initiation not only at origins of replicatio
231  of Hda is tightly controlled to ensure that replication initiation occurs only once per cell cycle.
232 lays a key role during the transcription and replication initiation of vRNA genome.
233  but these were not directly associated with replication initiation or ongoing chromosome replication
234 ular processes of transcription, DNA repair, replication initiation, or polymerase elongation and the
235 m DNA molecules, as well as in bidirectional replication initiation outside of the main replication o
236                                              Replication initiation peaks were AT rich, and >50% of t
237 riments, and we discovered that cell size at replication initiation per origin, namely the initiation
238 initiation sites at oriC1 were determined by replication initiation point analysis and found to map d
239 plication programme employs subtelomeric DNA replication initiation, possibly extending beyond S phas
240 gin involves interactions of the RK2 plasmid replication initiation protein (TrfA) with both the poly
241  the ubiquitously conserved bacterial master replication initiation protein DnaA at the oriC but stru
242 a a transcriptional response mediated by the replication initiation protein DnaA.
243                        Here we show that the replication initiation protein Sld3 is phosphorylated by
244 the ability of Cdk2 to phosphorylate the key replication initiation protein treslin in vitro Furtherm
245 Overall, this study reveals that TbMCM-BP, a replication initiation protein, also guides the initiati
246 biting expression or function of the plasmid replication initiation protein, RepE.
247 hough they do not resemble any characterized replication initiation protein.
248                    Nicking is performed by a replication-initiation protein (Rep) that directly binds
249 lication caused by overexpression of various replication initiation proteins such as Dpb11 and Sld2.
250 ies of hypomorphic alleles of genes encoding replication initiation proteins suggest the question of
251                                              Replication initiation proteins, known as prereplicative
252 t-range IncP-1 plasmids generally encode two replication initiation proteins, TrfA1 and TrfA2.
253              DnaD and DnaB are essential DNA-replication-initiation proteins in low-G+C content Gram-
254                             Lowering the DNA replication initiation rate by introducing the dnaA(Sx)
255 tion and the beta-globin Replicator, the DNA replication-Initiation Region from the beta-globin locus
256 which corresponds with previously mapped DNA replication initiation regions and is demarcated by loca
257                               Eukaryotic DNA replication initiation relies on the origin recognition
258 six essential ATPases whose contributions to replication initiation remain unclear.
259                              Plasmid encoded replication initiation (Rep) proteins recruit host helic
260 into three measurable variables representing replication initiation, replication-division cycle, and
261 ication elongation, mutants defective in DNA replication initiation require the Chk1 kinase.
262                Template unwinding during DNA replication initiation requires the loading of the MCM h
263 or PPP2R2A deficiency-induced alterations of replication initiation/RS and sensitivity to ATR/CHK1 in
264 mplexes in a manner that exposes a potential replication initiation site.
265 ries of restriction fragments that contained replication initiation sites (bubbles) in vivo.
266 nct DNA-protein interactions at subgroups of replication initiation sites (replication origins) modul
267 ntiate TNR instability; therefore, we mapped replication initiation sites and prereplication complex
268 s short primers revealed the presence of two replication initiation sites at the template strand and
269 findings indicate that Mcm10 is localized to replication initiation sites by directly binding MCM thr
270 by HU suggests that there are many potential replication initiation sites in permissive parts of the
271                                   Mapping of replication initiation sites in the HAC revealed that re
272                   High-resolution mapping of replication initiation sites showed that replication ini
273                 Data presented here identify replication initiation sites throughout the genome, prov
274 n events, thereby creating a database of all replication initiation sites within nonrepetitive DNA in
275         Orc2 and Mcm4 bound near each of the replication initiation sites, but a dramatic change in (
276 s, resulting in a corresponding shift in DNA replication initiation sites.
277  define a new mechanism for targeting ORC to replication initiation sites.
278 inant (RepID) protein that binds a subset of replication-initiation sites.
279 These data suggest a conserved mechanism for replication initiation: Sld3/Treslin coordinates Cdc45 r
280 rapid cell lethality, disrupts the timing of replication initiation, slows replication elongation, an
281 e of the 3'-CCUGU motif completely abolished replication initiation, suggesting a crucial role of thi
282 ry - the factors that demarcate sites of the replication initiation, termed origins - are diverged fr
283  essential for replisome assembly during DNA replication initiation that is vulnerable to inhibition
284                This is due to the absence of replication initiation that would typically occur upstre
285                                       During replication initiation, the core component of the helica
286                                Shortly after replication initiation, the duplicated origins move as a
287 cation resumed from oriC after inhibition of replication initiation, these high levels of binding dec
288 sents a repressive compartment that inhibits replication initiation, thus maintaining the boundaries
289 nctionally distinct Rpd3 complexes to affect replication initiation timing supports the idea that his
290 e-cell growth rates, cell division sizes and replication initiation volumes.
291 n gene expression, separate from its role in replication initiation, we analyzed changes in mRNA leve
292  vitro assay for eukaryotic origin-dependent replication initiation, we investigated the control of t
293 t explain how monomers outcompete dimers for replication initiation when plasmid copy number and pi s
294 ity could also provide the physical basis of replication initiation where a double-hexamer idly encir
295 propose a model for Sld3-mediated control of replication initiation, wherein Sld3 manages the proper
296 kinase-independent function for AURKA in DNA replication initiation whose inhibition through a class
297 ribe the reconstitution of budding yeast DNA replication initiation with 16 purified replication fact
298 ee extracts we established a system to study replication initiation within linear telomeric DNA subst
299 upport predominantly chromosome-internal DNA replication initiation within S phase.
300          In S-phase, the checkpoint inhibits replication initiation, yet the function of this global

 
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