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1 operty that distinguishes it from Thermotoga endonuclease V.
2 g reveals a novel 3'-exonuclease activity in endonuclease V.
3 , or xanthine in a similar manner to E. coli endonuclease V.
4  a homologue of the bacteriophage T4-encoded endonuclease V.
5 lobutane pyrimidine dimer-specific enzyme T4 endonuclease V.
6 r reveals a novel 3'-exonuclease activity in endonuclease V.
7 cis-syn dimer-specific cleavage with T4 denV endonuclease V.
8  DNA required for specific recognition by T4 endonuclease V.
9 onucleosomes and substantial reduction of T4 endonuclease V accessibility to cyclobutane pyrimidine d
10   Binding analysis indicates that Salmonella endonuclease V achieves tight binding to deoxyuridine-co
11  human alkyltransferase, suggesting that the endonuclease V activity may also repair a promutagenic l
12 her the deficiency nor the overproduction of endonuclease V affected the growth of the single-strande
13 ll-known inosine-dependent endonuclease, Tma endonuclease V also exhibits inosine-dependent 3'-exonuc
14 ysis using 3'-labeled DNA indicates that Tma endonuclease V also possesses non-specific 5'-exonucleas
15                                              Endonuclease V, an enzyme known for its enzymatic activi
16 omology between the PIWI domain of Ago-2 and endonuclease V and identified potential active-site amin
17 ically inhibits cleavage at the cs CTD by T4 endonuclease V and photoreversal by UV photolyase.
18  found in many DNA repair enzymes such as T4 endonuclease V and uracil DNA glycosylase.
19 indicates that the active site of Salmonella endonuclease V can accommodate pyrimidine-containing mis
20 , E89, D110, and H214 in Thermotoga maritima endonuclease V catalysis.
21  generated by deoxyuridine incorporation and endonuclease V cleavage.
22          The bacterial DNA repair enzyme, T4 endonuclease V, delivered intracellularly, increases the
23 cally compromised mutants (E23Q and E23D) of endonuclease V demonstrate altered affinities for the py
24                                              Endonuclease V (deoxyinosine 3' endonuclease), the produ
25            Previous work with the classic T4 endonuclease V digestion of DNA from irradiated Drosophi
26 ylguanine-DNA alkyltransferase (AGT) with an endonuclease V domain.
27 se challenges, we show that Escherichia coli Endonuclease V (eEndoV), an inosine-cleaving enzyme, can
28                                              Endonuclease V, encoded by the nfi gene, initiates remov
29                                              Endonuclease V (endo V) recognizes a broad range of aber
30                                              Endonuclease V (endo V) recognizes and cleaves deoxyinos
31                                              Endonuclease V (EndoV) cleaves the second phosphodiester
32                                           T4 Endonuclease V (EndoV) is a base excision repair enzyme
33                                              Endonuclease V (EndoV) is a ubiquitous protein present i
34                                              Endonuclease V (EndoV) is an enzyme with specificity for
35 ation scanning method that sequentially used endonuclease V (EndoV) to nick at mismatches and DNA lig
36                             Here, we utilize Endonuclease V (EndoV), which binds specifically to inos
37                                   Salmonella endonuclease V exhibits limited turnover on cleavage of
38                                   Within the endonuclease V family, the substrate specificities are d
39 ndonuclease to 3'-exonuclease mode switch by endonuclease V for removal of deaminated base lesions du
40           Under optimal cleavage conditions, endonuclease V forms two stable complexes with DNA conta
41                                              Endonuclease V from bacteriophage T4, is a cis-syn pyrim
42                                              Endonuclease V from Escherichia coli has a wide substrat
43 totypical enzyme studied for this pathway is endonuclease V from the bacteriophage T4 (T4 bacteriopha
44                               A thermostable endonuclease V from the hyperthermophilic bacterium Ther
45 ed deamination lesion cleavage activities of endonuclease V from the macrophage-residing pathogen, Sa
46                                       Unlike endonuclease V from Thermotoga maritima, Salmonella endo
47 the endonuclease and exonuclease activity in endonuclease V from Thermotoga maritima.
48                            Disruption of the endonuclease V gene, nfi, rescues the HAP sensitivity di
49 A lethality is suppressed by inactivation of endonuclease V (gpnfi) specific for DNA-hypoxanthines/xa
50 oxyuridine-specific endonuclease activity of endonuclease V has a divalent metal requirement similar
51                   These results suggest that endonuclease V has a significant role in the repair of d
52                                              Endonuclease V has been combined with a high-fidelity DN
53  replication, the T[c,s]T was detected by T4 endonuclease V in about one-half (46 +/- 9%) of the clos
54                                           T4 endonuclease V-incised DNA was processed in the same way
55                     Our results suggest that endonuclease V incision of DNA containing HAP leads to i
56 rations greater than those determined for T4 endonuclease V, indicating a possibly stronger electrost
57  by the pyrimidine dimer-specific enzyme, T4 endonuclease V, indicating that complete replication of
58                                              Endonuclease V initiates repair of deaminated base damag
59                                   The enzyme endonuclease V initiates repair of deaminated DNA bases
60 his capability to demonstrate EndoVIPER-seq (Endonuclease V inosine precipitation enrichment sequenci
61                                              Endonuclease V is a deoxyinosine 3'-endonuclease which i
62                                           T4 endonuclease V is a glycosylase/apurinic (AP) lyase that
63                                              Endonuclease V is a pyrimidine dimer-specific DNA glycos
64                                              Endonuclease V is an enzyme that initiates a conserved D
65                                              Endonuclease V is an enzyme that initiates a conserved D
66  recognition and strand nicking mechanism of endonuclease V is presented.
67                                              Endonuclease V is specific for single-stranded DNA or fo
68 th other enzymes known to use base flipping, endonuclease V is unique in that it moves the base oppos
69 guing possibility that there may be other T4 endonuclease V-like enzymes with specificity toward othe
70 e notion that two metal ions are involved in endonuclease V-mediated catalysis.
71 or removal of deaminated base lesions during endonuclease V-mediated repair.
72                                      An nfi (endonuclease V) mutant and a recA mutant were selectivel
73                                      An nfi (endonuclease V) mutant was grown anaerobically with nitr
74 s generated when replication forks encounter endonuclease V-nicked DNA.
75                                              Endonuclease V nicks damaged DNA at the second phosphodi
76 tructure, provide a detailed architecture of endonuclease V-nontarget DNA interactions.
77                                              Endonuclease V obtained from Thermotoga maritima prefere
78 ining the activity of endonuclease IV and T4 endonuclease V on highly purified and UVA-irradiated pUC
79 y purified native and synthetic DNA using T4 endonuclease V, photolyase, and anti-CPD antibodies stro
80  binding site for the dimer-specific T4 denV endonuclease V repair enzyme by chemical and enzymatic f
81 air, initiated by uracil-DNA glycosylase and endonuclease V, respectively.
82 e find that only approximately 60% of the T4 endonuclease V-sensitive sites, which are commonly count
83                                 Wild type T4 endonuclease V shows an 8-fold decreased affinity for a
84 imers, are also revealed using the enzyme T4 endonuclease V (T4 endo V).
85 se (Fpg), endonuclease III (endo III) and T4-endonuclease V (T4-endo V) to characterize DNA lesions.
86                      Liposomes containing T4 endonuclease V (T4N5) were applied to the site of UV exp
87 ogs and catalytically inactive mutants of T4 endonuclease V, this study investigates the discrete ste
88          A metal ion enhances the binding of endonuclease V to double-stranded and single-stranded ox
89 e conserved positions of Thermotoga maritima endonuclease V to identify amino acid residues involved
90                           EndoV-seq utilizes Endonuclease V to nick the inosine-containing DNA strand
91 tifs of the thermostable Thermotoga maritima endonuclease V to probe for residues that affect DNA-pro
92                               The binding of endonuclease V to this duplex was analyzed by gel mobili
93 ophoresis separation of UV-irradiated and T4 Endonuclease V treated plasmids.
94 ion of the supercoiled plasmid assay with T4 Endonuclease V treatment of irradiated plasmids and AFM
95 inosine- and mismatch-specific activities of endonuclease V was found to have different divalent meta
96   Recently, the first sequence homolog of T4 endonuclease V was identified from chlorella virus Param
97 eas liposomes containing heat-inactivated T4 endonuclease V were ineffective.
98 ine keratinocytes in vitro with liposomal T4 endonuclease V, which accelerates the repair of cyclobut
99 stic nature in the active site of Salmonella endonuclease V, which allows the enzyme to enfold both p
100 ystal structure of a catalytically deficient endonuclease V with pyrimidine dimer-containing DNA, fou
101 ed pyrimidine dimer-specific glycosylase, T4 endonuclease V, with its substrate DNA.

 
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