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1 o one encoding ribosomal protein P0/apurinic/apyrimidinic endonuclease.
2 I, poly(ADP-ribose) polymerase, and apurinic/apyrimidinic endonuclease.
3 uclease-1, DNA polymerase beta, and apurinic/apyrimidinic endonuclease.
4 L1 retrotransposon and also to the apurinic/apyrimidinic endonucleases.
5 ediates by the specific activity of apurinic/apyrimidinic endonucleases.
6 opting a G-quadruplex fold in which apurinic/apyrimidinic endonuclease 1 (APE1) binds, but inefficien
14 we determined the ability of human apurinic/apyrimidinic endonuclease 1 (APE1) to cleave at apurinic
17 P-BER), including DNA glycosylases, apurinic/apyrimidinic endonuclease 1 (APE1), DNA polymerase beta
18 ntial base excision repair protein, apurinic/apyrimidinic endonuclease 1 (APE1), plays an important r
19 d by DNA polymerase beta (Polbeta), apurinic/apyrimidinic endonuclease 1 (APE1), poly(ADP-ribose) pol
20 hosphate dehydrogenase (GAPDH) with apurinic/apyrimidinic endonuclease 1 (Ape1), the major oxidized D
22 sential base-excision repair enzyme apurinic/apyrimidinic endonuclease 1 (APE1)/redox effector factor
23 lases and the downstream processing apurinic/apyrimidinic endonuclease 1 (APE1)] can be tested simult
24 ession of critical DNA repair genes apurinic/apyrimidinic endonuclease 1 (Apex1) and DNA polymerase b
26 ins, we demonstrate here a role for apurinic/apyrimidinic endonuclease 1 in pri-miRNA processing and
28 r mechanisms underlying the role of apurinic/apyrimidinic endonuclease 1 in these processes are still
30 show that endonuclease activity of apurinic/apyrimidinic endonuclease 1 is required for the processi
32 rmediate, the DNA is channeled from apurinic/apyrimidinic endonuclease 1 to DNA polymerase beta and t
33 acterization of the interactomes of apurinic/apyrimidinic endonuclease 1 with RNA and other proteins,
35 e reactive geometry observed in the apurinic/apyrimidinic endonuclease 1, explaining the dephosphoryl
38 tiate radiotherapy, we investigated apurinic/apyrimidinic endonuclease 1/redox factor-1 (APE1/Ref-1)
42 und that recombinant purified human apurinic/apyrimidinic endonuclease-1 (APE1) and APE1 from human c
47 tly reported that the expression of apurinic/apyrimidinic endonuclease-1/redox factor-1 (APE-1/Ref-1)
48 or the base excision repair enzyme, apurinic/apyrimidinic endonuclease 2 (APE2) protein develop relat
50 nuclease activities of Rrp1 include apurinic/apyrimidinic endonuclease, 3'-phosphodiesterase, 3'-phos
51 ly of DNA repair enzymes, including apurinic/apyrimidinic endonuclease activity and repair activities
52 d with an increase in mitochondrial apurinic/apyrimidinic endonuclease activity in both H2O2- and O2-
54 p53 did not influence mitochondrial apurinic/apyrimidinic endonuclease activity measured by incision
58 e transcription regulator FoxD3 and apurinic/apyrimidinic endonuclease and the presence of chromosome
59 cil DNA glycosylase (UL2), cellular apurinic/apyrimidinic endonuclease, and DNA ligase IIIalpha-XRCC1
61 3-methyladenine DNA glycosylase and apurinic/apyrimidinic endonuclease, and, paradoxically, with incr
64 e endonucleolytic activity of human apurinic/apyrimidinic endonuclease (AP endo) is a major factor in
69 ied 12 property-based motifs in the apurinic/apyrimidinic endonuclease (APE) family of DNA-repair enz
70 o assess the possible role of human apurinic/apyrimidinic endonuclease (Ape) in double-strand break r
75 ll lines accumulated high levels of apurinic/apyrimidinic endonuclease (APE-1/Ref-1, redox effector-1
78 NA damage is initiated by the major apurinic/apyrimidinic endonuclease Ape1, which specifically recog
79 singly, this enzyme was found to be apurinic/apyrimidinic endonuclease (APE1) (), a well characterize
84 hMYH is associated in vivo with apurinic/apyrimidinic endonuclease (APE1), proliferating cell nuc
87 a ribosomal protein that is also an apurinic/apyrimidinic endonuclease, binds to YA in ovary and embr
88 tudies in vitro indicate that after apurinic-apyrimidinic endonuclease cleaves immediately upstream o
89 asic site; this site was incised by apurinic/apyrimidinic endonuclease creating a nick with 3'-hydrox
90 an proteins uracil-DNA glycosylase, apurinic/apyrimidinic endonuclease, DNA polymerase beta and DNA l
91 e excision repair proteins, such as apurinic/apyrimidinic endonuclease, DNA polymerase beta, and liga
92 an enzymes: uracil-DNA glycosylase, apurinic/apyrimidinic endonuclease, DNA polymerase beta, flap end
93 DNA glycosylase, strand scission by apurinic/apyrimidinic endonuclease, DNA resynthesis and ligation.
94 abasic sites, which are excised by apurinic/apyrimidinic endonucleases, eventually generating double
95 59 amino acids with homology to the apurinic/apyrimidinic endonuclease family of DNA repair enzymes.
96 r ung and mutY glycosylase and xthA apurinic/apyrimidinic endonuclease genes in H. pylori, mutants of
97 The structure of the major human apurinic/ apyrimidinic endonuclease (HAP1) has been solved at 2.2
98 shock protein 70 (HSP70) with human apurinic/apyrimidinic endonuclease (HAP1) was demonstrated by coi
100 tions of uracil-DNA glycosylase and apurinic/apyrimidinic endonuclease, human pol gamma was able to f
101 age and the additional depletion of apurinic/apyrimidinic endonuclease I (APE1) confers hypersensitiv
102 dehydrogenase and DNA repair enzyme apurinic/apyrimidinic endonuclease I protect smooth muscle cells
103 ition to its primary activity as an apurinic/apyrimidinic endonuclease in BER, Ape1 also possesses 3'
104 ssed at high levels relative to the apurinic/apyrimidinic endonuclease, increases spontaneous mutatio
107 extraribosomal functions, including apurnic-apyrimidinic endonuclease-like activity suggested to be
112 I, FAPY DNA glycosylase, both known apurinic/apyrimidinic endonucleases, or DNA deoxyribophosphodiest
116 air enzyme, Redox effector factor-1/apurinic/apyrimidinic endonuclease (Ref-1/Ape), facilitates DNA b
117 nd U/G mispairs in double-stranded DNA; (ii) apyrimidinic endonuclease that cleaves double-stranded D
118 that is related in sequence to the apurinic-apyrimidinic endonucleases that participate in DNA repai
119 wo endonuclease III homologs and an apurinic/apyrimidinic endonuclease) that might account for this a
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