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1 enes encoding the Pol3 and Cdc27 subunits of DNA polymerase delta.
2 to mutations affecting ORC, Mcm proteins, or DNA polymerase delta.
3 lap endonuclease 1 (FEN1), DNA ligase I, and DNA polymerase delta.
4 topoisomerase III, replication protein A and DNA polymerase delta.
5 reconstitute fully active recombinant human DNA polymerase delta.
6 6, and p12 have been assigned as subunits of DNA polymerase delta.
7 isiae, POL3 encodes the catalytic subunit of DNA polymerase delta.
8 rier for the strand displacement activity of DNA polymerase delta.
9 utation in the 3'-->5' exonuclease domain of DNA polymerase delta.
10 , a temperature-sensitive mutation affecting DNA polymerase delta.
11 replication protein A (RPA), RFC, PCNA, and DNA polymerase delta.
12 (PCNA), a requisite processivity factor for DNA polymerase delta.
13 at supported PCNA-dependent DNA synthesis by DNA polymerase delta.
14 p50 interacts with the catalytic subunit of DNA polymerase delta.
15 art on the 3'-to-5' proofreading activity of DNA polymerase delta.
16 in other genes, including the gene encoding DNA polymerase delta.
17 (13D5) inhibited the activity of calf thymus DNA polymerase delta.
18 similarity to the small subunit of mammalian DNA polymerase delta.
19 NA polymerase III, the analogue of mammalian DNA polymerase delta.
20 ar antigen (PCNA), a processivity factor for DNA polymerase delta.
21 l peptides of the catalytic subunit of human DNA polymerase delta.
22 merase epsilon as compared to lagging-strand DNA polymerase delta.
23 0 (RPA70), replication factor C1 (RFC1), and DNA polymerase delta.
24 ssDNA template and inhibits DNA synthesis by DNA polymerase delta.
25 e first evidence for the targeting of PP1 to DNA polymerase delta.
26 coimmunoprecipitate with Hys2, a subunit of DNA polymerase delta.
27 ncer-cell DNA replication and interacts with DNA polymerase delta.
28 flap by the strand displacement activity of DNA polymerase delta.
29 for cells with defects in the lagging-strand DNA polymerase delta.
30 , Rad27p, or the proofreading exonuclease of DNA polymerase delta.
31 d27p, or the DNA proofreading exonuclease of DNA polymerase delta.
32 late translesion synthesis by Pol zeta or by DNA polymerase delta.
33 tigen (PCNA), replication factor C (RFC) and DNA polymerase delta.
37 of CRL4(Cdt2), i.e. the direct regulation of DNA polymerase delta, adding to its known functions in t
38 such as DNA polymerase beta and subunits of DNA polymerase delta along with the EBV-encoded DNase BG
39 cts were competent for DNA replication using DNA polymerases delta, alpha, and possibly epsilon, with
41 tion depends on the proofreading activity of DNA polymerase-delta, although the repair proteins Msh2,
42 The repair reaction displays specificity for DNA polymerase delta, an effect that presumably reflects
47 ding motif, includes a sequence conserved in DNA polymerase delta and implicated in its PCNA binding.
48 teins which bound to PCNA-Sepharose included DNA polymerase delta and straightepsilon, PCNA, the 37 a
49 udding yeast) that impede the interaction of DNA polymerase delta and the 5'-flap endonuclease Rad27/
50 etween cdc19+ and genes encoding subunits of DNA polymerase delta and the replication initiator cdc18
52 ences within FRA16D by the replicative human DNA polymerases delta and alpha, and with human cell-fre
53 of defects in the exonuclease activities of DNA polymerases delta and epsilon (conferred by the pol3
54 yotes, processive DNA synthesis catalyzed by DNA polymerases delta and epsilon (pol delta and epsilon
55 east, we confirm the strand specificities of DNA polymerases delta and epsilon and show that the PCNA
58 The resulting excision gap is filled in by DNA polymerases delta and epsilon as revealed by the 'ph
59 3'-->5' exonuclease activity of replicative DNA polymerases delta and epsilon but did not enhance th
61 proofreading) by the exonuclease activity of DNA polymerases delta and epsilon, and post-replication
62 ar antigen (PCNA), a processivity factor for DNA polymerases delta and epsilon, is essential for both
63 ar antigen (PCNA), a processivity factor for DNA polymerases delta and epsilon, is involved in DNA re
70 s with somatic mutations in two of the major DNA polymerases, delta and epsilon, that replicate the g
72 This sequence was found to be present on DNA polymerase delta, and a peptide conforming to this s
73 r antigen clamp loader replication factor C, DNA polymerase delta, and DNA ligase I in the absence of
76 involved in DNA synthesis, such as PCNA and DNA polymerase delta, are concentrated in perinucleolar
77 argue that DNA polymerase zeta, rather than DNA polymerase delta as previously suggested, is respons
79 red for PCNA-dependent BER (AP endonuclease, DNA polymerases delta, beta and DNA ligase, and FEN1 end
80 s arrest is not due to 5-FU lesions blocking DNA polymerase delta but instead depends, in part, on th
81 ed capacity in enhancing the processivity of DNA polymerase delta but showed no deficiency in stimula
82 merase, and the most pure fraction contained DNA polymerase delta but was free of detectable DNA poly
84 re isolated with highly purified calf thymus DNA polymerase delta by conventional chromatography.
87 or the replicative RFC in the PCNA-dependent DNA polymerase delta-catalyzed DNA replication reaction.
88 unwound large (CTG)(n) hairpins and promoted DNA polymerase delta-catalyzed DNA synthesis using a (CT
89 to its native counterpart in (i) supporting DNA polymerase delta-catalyzed PCNA-dependent DNA chain
91 Likewise, expression of the intracellular DNA polymerase delta cofactor/proliferating-cell nuclear
96 cteristic for authentic RF-C: stimulation of DNA polymerase delta DNA synthesis on singly primed sing
98 BER factors flap endonuclease 1 (FEN-1) and DNA polymerase delta/epsilon was also observed, suggesti
99 ovement through undamaged DNA slows down and DNA polymerase delta fails to associate with replicating
101 o of the several sites involved in tethering DNA polymerase delta for processive DNA synthesis during
102 inity purification of recombinant p50 and of DNA polymerase delta from calf thymus or HeLa extracts.
103 er, rigorous purification of human or bovine DNA polymerase delta from natural sources has usually yi
104 ing of Okazaki fragments) and POL3 (encoding DNA polymerase delta) genes on the stability of a minisa
106 tated with human p50, as well as calf thymus DNA polymerase delta heterodimer, but not with p125 alon
107 ome maintenance complex component (MCM7) and DNA polymerase delta hindering replication fork progress
108 d to enhance the processivity of calf thymus DNA polymerase delta holoenzyme similar to calf thymus P
112 serve as the lagging strand replicase, like DNA polymerase delta in eukaryotes, but instead function
113 th pol3+, which encodes the large subunit of DNA polymerase delta in fission yeast, and the Cdc1 prot
115 hese observations, we infer a requirement of DNA polymerase delta in post-replicative bypass of UV-da
116 antly alter the ability of PCNA to stimulate DNA polymerase delta in the absence of RFC but substanti
117 we have evaluated possible participation of DNA polymerase delta in the excision step of repair.
118 he coding region of the catalytic subunit of DNA polymerase delta in XP variant cell lines revealed t
119 antigen (PCNA), the processivity factor for DNA polymerase delta, in mature cells of Nicotiana benth
120 ed levels of Pol3p, the catalytic subunit of DNA polymerase delta, induce instability at these same s
122 se results suggest that the small subunit of DNA polymerase delta is essential for functional interac
123 roliferating cell nuclear antigen (PCNA) and DNA polymerase delta is essential for processive DNA syn
124 POLD1 gene encoding the catalytic subunit of DNA polymerase delta is G/C-rich and does not contain a
125 de that both the quantity and the quality of DNA polymerase delta is important in ensuring genome sta
127 establish that the interaction of PCNA with DNA polymerase delta is mediated through the small subun
129 h repair to the depleted extract, indicating DNA polymerase delta is required for mismatch repair in
134 at degradation of p12, the fourth subunit of DNA polymerase delta, is critical for inhibiting fork pr
135 rast to the native heterodimeric calf thymus DNA polymerase delta, is not responsive to stimulation b
136 pared with those of the native heterodimeric DNA polymerase delta isolated from fetal calf thymus, an
137 root of the clade containing all eukaryotic DNA polymerase delta members but that this clade does no
138 in the "proofreading" exonuclease domain of DNA polymerase delta) mutations were synthetically letha
139 action cannot be promoted by the replicative DNA polymerase delta or by other TLS polymerases such as
140 n in this process have suggested that either DNA polymerase delta or DNA polymerase epsilon may be in
141 can facilitate DNA replication by tethering DNA polymerase delta or DNA polymerase epsilon to the DN
142 nuclear antigen onto DNA, where it recruits DNA polymerase delta or epsilon to the primer terminus a
143 achieved by including highly purified human DNA polymerase delta or epsilon, PCNA, RFC, and DNA liga
146 (PCNA) is a processivity factor required for DNA polymerase delta (or epsilon)-catalyzed DNA synthesi
148 nstrated that the catalytic subunit of human DNA polymerase delta (p125) expressed in baculovirus-inf
149 gh small but detectable levels were seen for DNA polymerases delta (+PCNA) and straightepsilon (- PCN
151 model whereby the high-fidelity replicative DNA polymerase delta performs recombination-associated D
155 ed for processive DNA synthesis catalyzed by DNA polymerase delta (pol delta) and polymerase epsilon.
156 ectrophoresis, is formed between calf thymus DNA polymerase delta (pol delta) and synthetic oligonucl
157 aturation requires the coordinated action of DNA polymerase delta (Pol delta) and the FLAP endonuclea
158 itiated by an RNA/DNA primer and extended by DNA polymerase delta (pol delta) and the replication cla
160 ability to promote DNA synthesis by purified DNA polymerase delta (pol delta) both on unmodified temp
163 DNA helicase that partially co-purifies with DNA polymerase delta (pol delta) from fetal bovine thymu
165 the p12 subunit in the function of the human DNA polymerase delta (Pol delta) holoenzyme by comparing
166 we constructed a series of recombinant human DNA polymerase delta (Pol delta) in which one or two of
170 replication and in several types of repair, DNA polymerase delta (pol delta) is assisted by replicat
178 (PCNA) promotes DNA synthesis by calf thymus DNA polymerase delta (pol delta) past several chemically
182 ouble mutant allele, which causes defects in DNA polymerase delta (Pol delta) proofreading (pol3-01)
183 of proliferating cell nuclear antigen, yeast DNA polymerase delta (Pol delta) replicated DNA at a rat
184 telomere damage to establish predominance of DNA polymerase delta (Pol delta) through its POLD3 subun
185 dihydroguanine (8-oxoG) by fetal calf thymus DNA polymerase delta (pol delta) was examined by steady-
186 at interacts with the small subunit (p50) of DNA polymerase delta (pol delta) was identified in a two
187 analysis of the 3'-->5' exonuclease of yeast DNA polymerase delta (Pol delta) we have discerned addit
188 dination of strand displacement synthesis by DNA polymerase delta (Pol delta) with 5.-flap cutting by
189 ow here that WRN functionally interacts with DNA polymerase delta (pol delta), a eukaryotic polymeras
191 ough tight coordination of the activities of DNA polymerase delta (Pol delta), flap endonuclease 1 (F
192 ed to study complexes formed among mammalian DNA polymerase delta (pol delta), proliferating cell nuc
193 lizing antibodies suggested a role for yeast DNA polymerase delta (Pol delta), RFC and PCNA in LLR re
195 an will be more internal errors generated by DNA polymerase delta (Pol delta), which takes over for P
196 iscontinuous strand that takes place in both DNA polymerase delta (Pol delta)- and DNA polymerase (Po
202 positions of components of the DNA-dependent DNA polymerase delta (pol delta).proliferating cell nucl
205 The mutator effects of mutations in the DNA polymerase delta (POL3) gene and the recombinational
206 on with three essential replication enzymes: DNA polymerase delta (POLD1), DNA primase (PRIM1), and m
214 tation (D400A) in the proofreading domain of DNA polymerase delta (poldelta, encoded by the Pold1 gen
215 tigen (PCNA) for functional interaction with DNA polymerases delta (Poldelta) and epsilon (Pol epsilo
217 tations in the POLD1 and POLE genes encoding DNA polymerases delta (Poldelta) and varepsilon (Polvare
221 the Bloom syndrome helicase (BLM) stimulates DNA polymerase delta progression across telomeric G-rich
222 synthesis and progression by the replicative DNA polymerase delta/proliferating cell nuclear antigen/
223 ombination-associated DNA synthesis and that DNA polymerase delta promotes recombination-associated D
224 Finally, a diploid strain with a defect in DNA polymerase delta proofreading exhibits a higher muta
227 ns of 4 to 14 bases to examine the impact of DNA polymerase delta proofreading on mutation avoidance.
228 ion at L604 in the polymerase active site of DNA polymerase delta reduces life span, increases genomi
229 a reaction requiring S. pombe Uve1p, Rad2p, DNA polymerase delta, replication factor C, proliferatin
230 of the catalytic and small subunits of human DNA polymerase delta results in formation of a stable, f
231 the processivity or proofreading activity of DNA polymerase delta shortened hetDNA length or reduced
232 ffects of recombinant p50 on the activity of DNA polymerase delta showed that p50 is able to slightly
233 of DNA ligase III, while those catalyzed by DNA polymerase delta/straightepsilon appeared to be more
235 , DNA polymerase zeta, Rev1 protein, and the DNA polymerase delta subunit, Pol32, in the bypass of an
236 air; however, the identity of the subunit of DNA polymerase delta that directly interacts with PCNA h
237 m of yeast Rad51, Rad54, RPA, PCNA, RFC, and DNA polymerase delta that loading of PCNA by RFC targets
238 by heterozygosity for a missense mutation in DNA polymerase delta that reduces its proofreading activ
239 fect in the catalytic subunit of replicative DNA polymerase delta that results in increased rates of
240 nuclear antigen, replication protein A, and DNA polymerase delta that supports Exo1-independent repa
241 determine which of the two subunits of core DNA polymerase delta, the 125-kDa catalytic subunit or t
242 aturation by the PCNA-coordinated actions of DNA polymerase delta, the flap endonuclease FEN1, and DN
244 epsilon incorporated the analogs showed that DNA polymerase delta, the most sensitive of the DNA poly
245 strand displacement synthesis carried out by DNA polymerase delta, the PCNA clamp, its loader RFC, an
247 In results presented here, Pif1 promoted DNA polymerase delta to displace strands that achieve a
248 the ability of the p125 catalytic subunit of DNA polymerase delta to engage in protein-protein intera
249 se delta that loading of PCNA by RFC targets DNA polymerase delta to the D loop formed by Rad51 prote
250 ta1N, proliferating cell nuclear antigen and DNA polymerase delta was found to repair substrates cont
251 The fidelity of Schizosaccharomyces pombe DNA polymerase delta was measured in the presence or abs
255 ability of ATM to stimulate DNA synthesis by DNA polymerase delta, which is implicated in both DNA re
258 t is essential for functional interaction of DNA polymerase delta with PCNA and for highly processive
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