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1 on between the ligand's alkyl chloride and a guanine residue.
2  complementary bond to O6 of the alternative guanine residue.
3  at all mismatches except those containing a guanine residue.
4 stem loop recognition motif by exchange of a guanine residue.
5 bases 3' of a syn-DMBADE-modified adenine or guanine residue.
6 ovalently intercalated on the 5' face of the guanine residue.
7  whereas all 76 other complex isolates had a guanine residue.
8 s consisting of a planar arrangement of four guanine residues.
9 ch are stabilized by the hydrogen bonding of guanine residues.
10 derivatives as well as oxidized cytosine and guanine residues.
11 yl aminofluorene adducted- and cisplatinated-guanine residues.
12 ed by MMR by increasing mutations at runs of guanine residues.
13 encodes a pathway capable of modification of guanine residues.
14 ficity aptamers and is composed of complexed guanine residues.
15                    Mutations of the critical guanine residues (-135/-136) decreased the formation of
16 as located by primer extension analysis to a guanine residue 8 bp 5' of the malA start codon.
17 eaks and in base excision repair of oxidized guanine residues (8-oxoguanine) by aiding the localizati
18 that include steroid-dependent protection of guanine residues -889 and -885 and hypersensitivity of a
19 ppery sequence of six adenine residues and a guanine residue (A6G) and a 3' secondary structure.
20 ded chlorambucil was shown to label a target guanine residue adjacent to its binding site in 80% effi
21 these, 63 and 36%, respectively, occurred at guanine residues along the cII gene.
22 aining a dynamic equilibrium of extrahelical guanine residues also suggested that the nickel complex
23 B and Sp1 were modified site-specifically at guanine residues and electrophoretic mobility shift assa
24 ide core sequence has eight highly conserved guanine residues and forms a G-quadruplex structure.
25 ates reactive oxygen species that can damage guanine residues and lead to the production of 8-oxoguan
26                The inability of SP to cut at guanine residues and the favoring of A-T-rich regions di
27 ng a simulated annealing protocol showed the guanine residues and the tether lay approximately in a p
28 ched when PdC is paired with a complementary guanine residue, and thus is greatly enhanced upon forma
29        No sequences containing just a single guanine residue are acceptable.
30 ite and established the importance of the 5'-guanine residue as critical for high affinity binding.
31  +1 and +7 and a pseudotemplated 5' terminal guanine residue as key for activation.
32  highly conserved sequence consisting of six guanine residues at the 3' end of the PPT (hereafter ref
33 n and interference showed that CcpA contacts guanine residues at the outer bounds of amyO with higher
34 short as 8 bases, and (iii) substitutions of guanine residues caused at an increased frequency by the
35 show that MG preferentially makes adducts on guanine residues, causing DNA damage.
36  cytosine residues are fully paired with the guanine residues, each using two Hoogsteen hydrogen bond
37 idine enhancement that occurs selectively at guanine residues either in RNA or in DNA at low Mg2+ con
38 iting site where the insertion of one or two guanine residues encodes, respectively, additional V and
39 y)Cl]+ bind DNA covalently at the N7 site of guanine residues forming mono-dentate adducts.
40 cca americana), removes specific adenine and guanine residues from the highly conserved, alpha-sarcin
41 le-stranded regions and, to a lesser extent, guanine residues from wobble base-pairs in hairpin stems
42 ddition, we observe a single hypermethylated guanine residue (G128), located within the Rev high-affi
43 oss-link bridges the 2-amino position of two guanine residues, G4 and G22.
44 tion-mediated PCR delineated the position of guanine residues important to vimentin expression.
45 ue with the N(2)-amino group of the opposing guanine residue in 5'-CAp sequences to generate hemiamin
46 terminus of the downstream (D+) segment to a guanine residue in a purine-rich tract in pol (AAAAGAAGA
47                     Spontaneous oxidation of guanine residues in DNA generates 8-oxoguanine (oxoG).
48 redominantly to the exocyclic amino group of guanine residues in DNA in vivo and in vitro.
49                To achieve platination of the guanine residues in duplex II the central linker remains
50 e major sites of oxidation being the central guanine residues in each telomeric repeat.
51 d covalent probe designed to target unpaired guanine residues in structured RNAs is reported.
52 ple-stranded complex and usually occurred at guanine residues in the flanking double-stranded DNA.
53                                              Guanine residues in the genome are vulnerable to attack
54                                          The guanine residues in the loop stabilize the duplex as a r
55 udies suggest that the major groove edges of guanine residues in Watson-Crick G.C base-pairs could po
56 h a concomitant displacement of the modified guanine residue into the minor groove in the methylated
57  signal amplification: (1) a large amount of guanine residues introduced on the electrode surface thr
58                             The two opposing guanine residues involved in the cross-link were identif
59  of the electrophile toward the nucleophilic guanine residue is important for efficient covalent bond
60                                  A conserved guanine residue is positioned to act as the general base
61 SJG-136 (NSC 694501) selectively cross-links guanine residues located on opposite strands of DNA, and
62 propenals can transfer oxopropenyl groups to guanine residues of DNA to yield pyrimodopurinone (M(1)G
63 ns of both the loop thymine residues and the guanine residues of the adjacent quartet.
64 as significantly reduced compared with other guanine residues of the flanking regions in both in vitr
65 ween the polyaromatic core of the ligand and guanine residues of the outer G-quartets.
66  of the cytosine residue flanking the target guanine residue on the 5'-side.
67 rom the reaction of a DNA abasic site with a guanine residue on the opposing strand of the double hel
68 n interstrand cross-link via reaction with a guanine residue on the opposing strand.
69  conjugates that would react with a specific guanine residue on the template strand of the HER-2/neu
70 , with protein-DNA contact points located on guanine residues on both DNA strands within and just adj
71 e results suggest that the 2-amino groups of guanine residues on both strands of the nucleic acid pla
72 , determined that the modifications occur at guanine residues on either strand separated by 3 bp.
73 ypass did occur, pol gamma misincorporated a guanine residue opposite the 3'-thymine of the dimer onl
74 er as well as two stimulus-specific enhanced guanine residues possibly due to alterations in chromati
75  interact with DNA (AZB016) or cleave DNA at guanine residues, presumably through alkylation of the N
76   Likewise, point mutations of the protected guanine residues profoundly attenuated the response to t
77 10-tetrahydrobenzo[a]pyrene (anti-BPDE) with guanine residues prompted us to study the efficiencies o
78 ethylation patterns surrounding the targeted guanine residues strongly affect their probability to be
79 n addition, nickel-dependent modification of guanine residues surrounding the three-helix junction of
80 sion site to produce a bulge and tipping the guanine residues; the two guanines and the tether attain
81 ion of the efficiency of oxidative damage at guanine residues through long-range charge transport was
82 ichael addition of the N(2)-amino group of a guanine residue to the electrophilic sugar remnant gener
83                  Acrolein reacts with DNA at guanine residues to form the exocyclic adduct, 8-hydroxy
84  in the consensus binding sequence (CB) with guanine residues was evaluated both in vitro and in vivo
85  sites were primarily at or one base 3' to a guanine residue, which correlated well with the distribu
86 te bound the duplex and alkylated the target guanine residues with high efficiency.
87 ion with DNA results in DNA damage mainly at guanine residues, with products from thymine oxidation a
88 tic cross-linking (clamping) of two selected guanine residues within an RNA.
89   8-Oxoguanine is formed by the oxidation of guanine residues within DNA by reactive oxygen species,
90 o confirm that FA preferentially mutagenizes guanine residues within single-stranded DNA (ssDNA).
91  vivo revealed methylation protection of all guanine residues within the d(GA)(n).d(TC)(n).
92 oint mutations were introduced into specific guanine residues within the G-quadruplex-forming region
93 al level by frameshift mutations in a run of guanine residues within the hpuA sequence encoding the m
94  observed that the overall reactivity of the guanine residues within this tract toward DMS was signif
95 tituting a guanine analogue, 6MI, for single guanine residues within UV1C extends the DNAzyme's activ