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1 sors is strictly dependent on topB (encoding topoisomerase III).
2 uld explain its functional coordination with topoisomerase III.
3 e IIIalpha and Schizosaccharomyces pombe DNA topoisomerase III.
4  possess topoisomerase IB appear to lack DNA topoisomerase III.
5       We cloned cDNA encoding Drosophila DNA topoisomerase III.
6 ifth was sufficient for interaction with DNA topoisomerase III.
7  the protein it encodes has been denoted DNA topoisomerase III.
8                                     However, topoisomerase III alpha and Bloom helicase can dissolve
9 ses: reverse gyrase and a protein complex of topoisomerase III alpha and Bloom helicase.
10  larger protein complex ('BLMcx') containing topoisomerase III alpha, RMI1, RMI2 and replication prot
11 ad low amino acid sequence similarity to DNA topoisomerase III, an enzyme that relaxes DNA supercoils
12 s human BLM and yeast Sgs1 interact with DNA topoisomerase III and are thought to act on stalled repl
13 ginally identified in S.cerevisiae ) between topoisomerase III and DNA helicases of the RecQ family,
14                    Rqh1 forms a complex with topoisomerase III and is proposed to process or disrupt
15   YjhX inhibits only topoisomerase I but not topoisomerase III and IV in vitro.
16 nlinking, we demonstrated directly that both topoisomerase III and topoisomerase IV were efficient at
17 PG0104, which is highly similar (57%) to DNA topoisomerase III, and PG0121, which has high similarity
18 ge site sequence analysis suggest that it is topoisomerase III, and therefore we named it "NeqTop3."
19                           RecQ helicases and topoisomerase III are both required for genome stability
20             Helicases of the RecQ family and topoisomerase III are evolutionarily conserved proteins
21                            Overexpression of topoisomerase III at the nonpermissive temperature was s
22                         Escherichia coli DNA topoisomerase III belongs to the type IA family of DNA t
23 gh-throughput screen for compounds that trap topoisomerase III beta (TOP3B poisons) by developing a C
24 tween the appearance of chromosome-bound DNA topoisomerase III beta and Rad51, a protein known to be
25 es of wild-type mice also indicates that DNA topoisomerase III beta becomes prominently associated wi
26 hromosomal defects in germ cells lacking DNA topoisomerase III beta, and this interpretation is suppo
27 ion of the mouse TOP3 beta gene encoding DNA topoisomerase III beta, one of the two mammalian type IA
28              Additionally, the expression of topoisomerase III beta, which exhibited a clear pattern
29                                              Topoisomerase III-beta (Top3b) reduces nucleic acid tors
30                                              Topoisomerase III-beta (TOP3B), the only RNA topoisomera
31 lved crystal structures of wild-type E. coli topoisomerase III bound to an eight-base ssDNA molecule
32 d 33% sequence identity to Bacillus subtilis topoisomerase III (bsTopo III) and Escherichia coli topo
33 g the putative DNA binding cavity of E. coli topoisomerase III, creating a molecule that can be coval
34 merase III (bsTopo III) and Escherichia coli topoisomerase III (ecTopo III) respectively.
35                    In budding yeast, loss of topoisomerase III, encoded by the TOP3 gene, leads to a
36  out physiological functions associated with topoisomerase III enzyme in other bacteria.
37 ficant sequence similarity to genes encoding topoisomerase III enzymes in other eukaryotic species.
38    RecQ-like DNA helicases pair with cognate topoisomerase III enzymes to function in the maintenance
39 protein is a member of the beta-subfamily of topoisomerase III enzymes.
40 hly conserved CXXC motifs not found in other topoisomerase III enzymes.
41                                          DNA topoisomerase III from Escherichia coli belongs to the t
42                                          The topoisomerase III gene ( top3 (+)) from Schizosaccharomy
43 ination of gene structure for a second human topoisomerase III gene.
44                               The removal of topoisomerase III has no effect on the accumulation of c
45                           A human homolog of topoisomerase III has previously been identified.
46             In sgs1 top3 cells devoid of DNA topoisomerase III, however, expression of full-length Sg
47 lution, of an inactive mutant of E. coli DNA topoisomerase III in a non-covalent complex with an 8-ba
48    These data are consistent with a role for topoisomerase III in disentangling recombination interme
49 omerase III/IV mutant, indicating a role for topoisomerase III in recombination.
50 nce points to the role of RecQ helicases and topoisomerase III in regulating homologous recombination
51 nd a bias against deleting the gene encoding topoisomerase III in ruvC53 or DeltaruvABC backgrounds c
52             We show here that the removal of topoisomerase III in temperature sensitive topoisomerase
53 dies on the interaction between Sgs1 and DNA topoisomerase III in vitro and in vivo.
54 ies can be catalyzed by Escherichia coli DNA topoisomerase III, indicating that this enzyme can act a
55 mbination, including the helicase domain and topoisomerase III interaction domain, are essential.
56                                              Topoisomerase III interacts with DNA helicase SGS1 and t
57                                      Whereas topoisomerase III is a more efficient decatenase than to
58 which the association of a RecQ helicase and topoisomerase III is important for facilitating decatena
59          The presence of more than one human topoisomerase III is reminiscent of mammalian topoisomer
60                    The physiological role of topoisomerase III is unclear for any organism.
61                              Because the DNA topoisomerase III isozymes are likely to interact with h
62 rome genes are likely to act in concert with topoisomerase III isozymes in human cells.
63  mice points to the possibility that the DNA topoisomerase III isozymes might be involved in the path
64 ion of ruvABC allows the construction of the topoisomerase III/IV double mutant.
65 escued the synthetic lethality of the double topoisomerase III/IV mutant, indicating a role for topoi
66                            We postulate that topoisomerase III may be deregulated in A-T cells and th
67  type IA topoisomerases, including mammalian topoisomerase III, may also help link the enzyme activit
68 lly rescue the slow growth defect of a yeast topoisomerase III mutant.
69 resolution reaction is specific for the RecQ-topoisomerase III pair and is mediated by interaction of
70 e III; therefore, these results suggest that topoisomerase III participates in orderly and efficient
71  and in vivo data indicate that Sgs1 and DNA topoisomerase III physically interact and that this inte
72 Thus, mechanisms by which RecQ helicases and topoisomerase III proteins cooperate to maintain genomic
73                           RecQ helicases and topoisomerase III proteins interact physically and funct
74    The cellular function of Escherichia coli topoisomerase III remains elusive.
75 eukaryotes are well established, the role of topoisomerase III remains poorly defined.
76 hromosome maintenance, including p53, BRCA1, topoisomerase III, replication protein A and DNA polymer
77                           Shorter pauses for topoisomerase III result in a higher decatenation rate.
78  cerevisiae, loss of the TOP3 gene, encoding topoisomerase III, results in a phenotype of slow growth
79                                          The topoisomerase III RuvC double mutants that can be constr
80                                 In addition, topoisomerase III shows a strong dependence on the cross
81  IV and is unlikely to define a new role for topoisomerase III; therefore, these results suggest that
82 ll-length ORF for hTOP3, the first mammalian topoisomerase III to be identified.
83 residues 1-283, inhibited the binding of DNA topoisomerase III to single-stranded DNA.
84 uman BLM and yeast Sgs1, form a complex with topoisomerase III (Top3) and are thought to act during D
85 B activity prevents the proper regulation of topoisomerase III (Top3) function, disrupting a recombin
86 mportant and has been implicated in Sgs1-DNA topoisomerase III (Top3) interaction.
87                                          The topoisomerase III (Top3)-Rmi1 heterodimer, which catalyz
88 ng tricks, with a particular emphasis on DNA topoisomerase III (TOP3).
89 DNA helicases are known to interact with DNA topoisomerase III (Top3).
90                  Together, RecQ helicase and topoisomerase III (Topo III) of Escherichia coli compris
91  has been identified in Escherichia coli DNA topoisomerase III (Topo III) that is essential for Topo
92 his activity specifically stimulates E. coli topoisomerase III (Topo III) to fully catenate dsDNA mol
93 ogy simplification activity, and for E. coli topoisomerase III (topo III), a type IA topoisomerase th
94 Escherichia coli topB, the gene encoding DNA topoisomerase III (Topo III).
95        The largest gene product of the novel topoisomerase III was expressed and shown to interact wi
96                               Eukaryotic DNA topoisomerase III was first identified by studying the h
97                               topB, encoding topoisomerase III, was identified as a high copy suppres
98              Using Escherichia coli RecQ and topoisomerase III, we demonstrate a second activity for
99  DNA-bound, catalytically inactive mutant of topoisomerase III where DNA binding realigns catalytic r