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1 Nase II activity is also sensitive to the 3'-neighboring base.
2 h base flipping depends on the stacking with neighboring bases.
3 pping rather than from direct recognition of neighboring bases.
4 ctions that perturb the electron orbitals of neighboring bases.
5 t electron transfer (hole migration) between neighboring bases.
6 pared with the free nucleoside, depending on neighboring bases.
7 these 2-APs are no longer stacked onto their neighboring bases.
8 and base-unstacking and to the nature of the neighboring bases.
9 tween each anomer of the abasic site and the neighboring bases.
10 ained partial stacking interactions with its neighboring bases.
11 pear to be dependent upon the composition of neighboring bases.
12 s the expression of the interdependencies of neighboring bases.
13 equences by including the interdependence of neighboring bases.
14 orotation angle of the sugar ring for the 5'-neighboring base A6, as determined from scalar coupling
15 en base pairs, stacking interactions between neighboring bases and long-range intra- and inter-backbo
16 intrastrand (vertical) interactions between neighboring bases; and (ii) formation of double helices
20 res were examined; the influence of specific neighboring bases, as opposed to the general A + T conte
21 terms, of the relative positions of pairs of neighboring bases (both intra- and interstrand) in Carte
22 uanine maintained stacking interactions with neighboring bases but was not Watson-Crick hydrogen bond
23 oxygen; (iv) there is no involvement of the neighboring bases by way of inter- or intrastrand cross-
24 a given base mutates "to." We find that both neighboring bases have a significant effect on the mutat
25 rds, we sought to determine what effects the neighboring bases have on what a given base mutates "to.
29 onsistent with a model where altered risk at neighboring bases is linked to lesion formation at the f
31 otency by only 2-3-fold, suggesting that two neighboring bases may be sufficient for significant inte
32 ackbone and decreased base interactions with neighboring bases might be the origin of the decreased s
34 ven when (CP)G and (CP)C are incorporated as neighboring bases on the same strand, their efficiency o
35 rises from base stacking and collisions with neighboring bases only but is insensitive to base-pairin
37 structural analysis of the effect of the 5'-neighboring base pair on recognition of an intrahelical
42 the extent of carcinogenic interaction with neighboring base pairs and the thermodynamic properties
43 d pi-pi stacking interaction energy with the neighboring base pairs compared to the natural S-CPT.
44 show that this wobble base pair destabilizes neighboring base pairs on only one side of the wobble.
46 N is the unpaired base and X.X' and Z.Z' the neighboring base pairs, could be well-represented (+/-0.
47 ions between the intercalated ligand and the neighboring base pairs, provide <50% of the thermodynami
48 ring at the misincorporation site and at the neighboring base pairs, the observed inhibition of relig
49 e lesion is dominated by the identity of the neighboring base pairs, with the cross strand partner ba
57 hin reads by comparing position-specific and neighboring base quality scores with the distribution of
58 c stacking and collisional interactions with neighboring bases, respectively (see the preceding paper
59 n the trimers bring it into proximity of the neighboring bases, resulting in efficient charge transfe
60 otides were used to explore the influence of neighboring base sequence context on the mutagenic poten
61 are apparently mediated by interactions with neighboring bases, spectral changes that occur as probe-
63 imarily to collisional interactions with the neighboring bases, the absence of dynamic quenching in t
64 f thymine is due to methyl interactions with neighboring bases, thus adding to our understanding of t
68 increasing the solvent accessibility of the neighboring bases while maintaining the overall hairpin
69 the base stacking between the f(5)C and the neighboring bases while not causing significant global a