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1 pairs that connect neighboring layers of DNA double helices.
2 nsible for the pronounced destabilization of double helices.
3 by dimer formation, promoting supramolecular double helices.
4  assembly into left-handed gold nanoparticle double helices.
5  be replicated in the same way as simple DNA double helices.
6 dyad axis that relates two flanking parallel double helices.
7 ins nearly identical to those of DNA and RNA double helices.
8  stack with each other and with the flanking double helices.
9           Bulge loops introduce bends in RNA double helices.
10 A triple helix, analogous to A-RNA and B-DNA double helices.
11 single-stranded polymers or short oligomeric double helices.
12                      How do helicases unwind double helices?
13  extended minor-groove interactions with RNA double helices, a quintuple-base motif that transitions
14 -correlation-mediated attraction between RNA double helices, a recently proposed model for early coll
15 e of hybridization events that yields nicked double helices analogous to alternating copolymers.
16 extraordinary sphere configurations, such as double helices and rhombohedra.
17 rmediate between canonical A-type and B-type double helices, and has mixed structural characteristics
18 inner core is made of multiple connected DNA double helices, and the outer shell is composed of regul
19 ting the shape of tetrahedral containers, of double helices, and, supreme wonder, of the Borromean ri
20 DNA hybrids argued that the grooves of these double helices are also dehydrated relative to bulk solu
21                        The gold nanoparticle double helices are highly regular, spatially complex, an
22                                          The double helices are interpenetrated by the unreacted diol
23                        The expanded-diameter double helices are more thermodynamically stable than th
24         In the crystal, these oligomers form double helices around twofold symmetry axes.
25 custom-shaped bundle of tightly cross-linked double helices, arrayed in parallel to their helical axe
26  that accounts for the elastic energy of DNA double helices as well as for the chiral nature of the d
27 een neighboring bases; and (ii) formation of double helices by association (docking) of single helica
28 ducing 3D shapes formed as pleated layers of double helices constrained to a honeycomb lattice.
29  bonds are more transient throughout the DNA double helices containing an abasic site.
30           The complex binds two distinct DNA double helices corresponding to the arms of a plectonemi
31  and Cu(I) fall into two classes; bimetallic double helices ([Cu(2)L(2)](2+)) and monometallic ([CuL]
32 nzene-1,3,5-tricarboxamides (BTAs) that form double helices, fibers that were long thought to be chai
33 at associate by base pairing to produce four double helices flanking a junction point.
34 association into long-lived partially paired double helices, followed by reversible association of th
35 ucture is that the two adjacent parallel DNA double helices form crossovers at every point possible.
36 short staple strands into parallel arrays of double helices, has proven a powerful method for custom
37 plexes can associate spontaneously into long double helices; however, such self-assembly is much less
38 nucleoside triphosphate hydrolysis to unwind double helices in essentially every metabolic pathway in
39  this crystal is similar to the alignment of double helices in parallel Holliday junctions.
40 ces minimize electrostatic repulsion between double helices in several ways.
41 nce of end-to-end length for a series of DNA double helices in solution, using small-angle x-ray scat
42 s transition correlated with the assembly of double helices in the ribozyme core.
43         We present the first anion-templated double helices induced by halogen bonds (XBs) and stabil
44 ms a dodecahedral structure in which the RNA double helices, interacting closely with the inner capsi
45 ick interactions that help arrange canonical double helices into tertiary structures.
46 t arise from the stacking of short, separate double helices, not all of which are A-form, and in many
47                        Fifty-nine years ago, double helices of poly(rA) were first proposed to form a
48 s lack built-in support even for base pairs, double helices, or hairpin loops.
49 ity structures in which rigid bundles of DNA double helices resist compressive forces exerted by segm
50 t, 3DNA can handle antiparallel and parallel double helices, single-stranded structures, triplexes, q
51 ular poly(dG).poly(dC) and poly(dA).poly(dT) double helices, stretched from compressed states of 2.0
52 is of electrostatic interactions between DNA double helices suggests that in some situations these pr
53 a crossover and which are modeled to contain double helices that are exactly parallel or antiparallel
54 c assembly motif comprises adjacent parallel double helices that crossover at every possible point ov
55 s in all registers at pH 3.5 to form stacked double helices that span the crystal.
56 taposition of backbones between parallel DNA double helices, the molecules form a paranemic structure
57                  We show IHF bridges two DNA double helices through non-specific recognition that giv
58 the topoisomerases in passing DNA strands or double helices through one another and their importance
59 which slowly converts into single-handed HCP double helices through partial fragmentation and self-so
60 er, so the molecules form continuous 10-fold double helices throughout the crystal, with each strand
61          A helical structure transition from double helices to single helices is observed as the pept
62 mers to change fiber morphology from racemic double helices to single helices with a preferred handed
63  repair through its ability to bring two DNA double helices together.
64      The sequence-dependent structure of DNA double helices was studied extensively during the past 1
65                Left-handed gold nanoparticle double helices were prepared using a new method that all
66 es, creating intertwined nanomagnetic cobalt double helices, where curvature, torsion, chirality and
67 sting as a mixture of right- and left-handed double helices, which eventually undergo an inversion of
68 d pattern of crossovers between adjacent DNA double helices, whose conformation often deviates from t
69 ulate the global folding and interactions of double helices with hundreds of basepairs.
70 ain complementary 'meta-base pairs' can form double helices with programmed handedness and helical pi
71 -dimensional vectorial magnetic state of the double helices with soft-X-ray magnetic laminography(12,
72 ons suggests strongly that only nucleic acid double helices with the A structure support efficient te