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1 GT/-3', producing four base 3'-OH overhangs (sticky ends).
2 DNA template adjacent to the gene, leaving a sticky end.
3 ze on a nucleosome, generating two vacant CD sticky ends.
4 ell-structured branched DNA motifs tailed by sticky ends.
5 ity, was also constructed by the addition of sticky ends.
6 the intermolecular contacts are directed by 'sticky' ends.
7 sembly of cohesive single-stranded segments (sticky ends).5, 6 Methods that exploit the sequence addr
8 and of DNA composed entirely of concatenated sticky ends and that binds to four local neighbours duri
9 re is also a logical equivalence between DNA sticky ends and Wang tile edges.
10 tent state in which two unbound chromodomain sticky ends appear exposed.
11 ends are flanked by a pair of dyes; when the sticky ends are disrupted, the dyes separate, and the fl
12                                        Those sticky ends are flanked by a pair of dyes; when the stic
13 -assembly processes, with complementary DNA "sticky ends" as one of the most notable examples.
14 ate configurations, for example, homodimers, sticky-ended assemblies, and antiparallel arrangements.
15 aspartate to stabilize the triple helix in a sticky-ended assembly.
16                                Complementary sticky ends associate with each other preferentially and
17 ation of the three different tiles and three sticky end association strategies.
18 bility and cooperativity of a network of DNA sticky-end associations could lead to greater control ov
19 son-Crick base-pairs and a two-nucleotide 5'-sticky end at each end of the duplex.
20 nucleosomal distance, suggesting that the CD sticky ends bridge nearby methylated nucleosomes.
21 on an edge adjacent to the binding site; the sticky ends can be disrupted if the protein binds with s
22                                          The sticky ends cohere with one another, so the molecules fo
23 ination of synthetic stable branched DNA and sticky-ended cohesion has led to the development of stru
24 hnology combines branched DNA junctions with sticky-ended cohesion to create self-assembling macromol
25 uous arrays facilitated by sequence-specific sticky-ended cohesion.
26  produce well-ordered 2D periodic arrays via sticky-ended cohesion.
27 embled into objects and networks directed by sticky-ended cohesion.
28 e combination of branched DNA molecules and 'sticky' ends creates a powerful molecular assembly kit f
29 work, we demonstrate for the first time that sticky ended dimers are not a prerequisite for alpha-hel
30 f such nanofibers has been the formation of "sticky ended" dimers through careful selection of electr
31 s and is analogous to the "reprogramming" of sticky-ends displayed on the DNA tiles.
32                                              Sticky-ended DNA duplexes can associate spontaneously in
33 at the modified base, and the other across a sticky-ended DNA junction.
34 irections of propagation associated with the sticky ends do not share the same plane, but extend to f
35 in charged pairs, and is inspired by similar sticky-ended fibrillation designs applied in DNA and coi
36                               Complementary 'sticky ends' form specific inter-particle links and repr
37 ion electron microscopy indicate that these "sticky-ended" fragments self-assemble via intermolecular
38 the interior of the frame through prescribed sticky end interactions.
39 cifically designed arm lengths and intertile sticky-end interactions can be used to form sophisticate
40 ation with complementary single-stranded DNA sticky ends is increasingly used for guiding the self-as
41                          The strength of the sticky ends is readily varied, so that the ability of th
42 e multiple cloning site via either blunt- or sticky-end ligation not only serves as a highly efficien
43 on-Crick complementary single-stranded DNA ("sticky end") linking strategies.
44 inside aquafoldamers can be created via the "sticky" end-mediated formation of 1D chiral helical stac
45                             Free energies of sticky-end mismatches are also calculated for determinin
46 ive adsorption properties of the two 12-base sticky ends of the DNA molecules to partially immobilize
47 rmation of the 12 base-pair single-stranded "sticky" ends of mature lambda DNA.
48 f the duplex, thus forming the 12-base-pair "sticky" ends of the mature genome.
49      The two DX molecules are also joined by sticky ends on an edge adjacent to the binding site; the
50 ary the number of linkers, the length of the sticky ends on the linker, and linker architecture and m
51 shared-stem design for the LNA-MB to prevent sticky-end pairing.
52 Functionalized with DNA with single-stranded sticky ends, patches on different particles can form hig
53 nd the generation of unique, non-palindromic sticky ends permits the formation of seamless junctions
54  the number and the relative position of DNA sticky-ends play a significant role in the stability of
55 r backbone, self-complementary "palindromic" sticky ends readily form intraparticle hairpins and loop
56 DNA target hybridizes this signal probe, the sticky end remains free to hybridize another target lead
57                            Efficient NHEJ of sticky ends requires the Ku70 and Ku80 proteins and the
58 ally modified with DNA bearing complementary sticky end sequences.
59 modifications (1) confirms the importance of sticky-end stacking, (2) confirms the identity of the in
60 the solution an oligonucleotide duplex with 'sticky ends' that are complementary to the two grafted s
61 tural units are programmed by the design of 'sticky ends' that associate according to Watson-Crick co
62                             For our 11 base "sticky ends," the limit is 73 distinct sequences with no
63                                              Sticky ends thus created are uniform across the assembly
64 chieved using reactants with non-palindromic sticky ends to maximize specificity.
65 ranched DNA molecules are linked together by sticky ends to produce objects, periodic arrays, and nan
66 , we find that the backbone that tethers the sticky ends to the surface can have a significant impact
67                                   These had "sticky-ends" to promote the formation of long fibers.
68 methylene blue (a redox moiety) label and a "sticky end." When a DNA target hybridizes this signal pr
69 l are the free energies of ligation for each sticky end, which can be estimated by the calculator fro

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