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1  of both of the proteins from nsDNA (plasmid unpairing).
2       Divalent metal ions were essential for unpairing.
3 capturing the -11A subsequent to spontaneous unpairing.
4 t -11 of the template strand in overall base unpairing.
5 veral other positions did not affect thymine unpairing.
6 ons confer a high propensity for stable base unpairing.
7 r of the stem loop structure that allows DNA unpairing.
8 hin MARs that is highly potentiated for base unpairing.
9 strates and products that were indicative of unpairing.
10  promoter that has been partly pre-opened by unpairing a short segment of the transcription bubble.
11                                          The unpairing allows a nanoscale cavity to form at the junct
12 acids are not required for double nucleotide unpairing and appear to act cooperatively, whereas the h
13 e its fluorescence is sensitive to both base-unpairing and base-unstacking and to the nature of the n
14 ally, PAM-distal mismatches result in duplex unpairing and induce a conformational change in the Cas9
15          Our results support a model whereby unpairing and unstacking of the terminal base pairs is a
16  distortion activity is consistent with both unpairing and unstacking of the three terminal base pair
17  formation, but this can be bypassed by base unpairing, and even a completely single-stranded signal
18                          We suggest that DNA unpairing around the signal-coding border is essential f
19 fixed distance, the kinetic rates for strand unpairing at fixed applied force, and the rupture force
20 he protospacer at PAM + 1 and increases with unpairing at PAM + 2 and + 3.
21 f unpaired thymine residues, we studied base unpairing at the -10 region during isomerization upon RN
22 er upon RNA polymerase binding involves base unpairing at the -10 region.
23                Additionally, we detected the unpairing-dependent loss of a transcript during meiotic
24                      We also investigate the unpairing dynamics in the strong coupling regime and fin
25  bending, the ssDNA gateway, and double-base unpairing flanking the scissile phosphate control precis
26         Previous studies have indicated that unpairing, "fraying," of the viral DNA ends by IN contri
27  cellular stress induces fast and reversible unpairing in a Z4/CAP-H2 dependent manner.
28 alysis and chemical probing indicate greater unpairing in A+T-rich sequences in other regions of the
29 d atomic force microscopy detected local DNA unpairing in supercoiled plasmids.
30 erhelical energy required to initiate duplex unpairing is essentially length-independent from eight t
31                 Cohesin-mediated pairing and unpairing likely provides a counting mechanism for evenl
32      From these results we propose that such unpairing may enhance both the processing and the joinin
33 es utilize variations of a basic pairing and unpairing mechanism for faithful segregation during mito
34 vivo analysis suggests neither profound base unpairing nor protein binding within the MT-I R/Y sequen
35 r at the -11 position of P1 and P3 prevented unpairing not only at that position but also at the othe
36 as never been clear, however, whether duplex unpairing occurs during mitotic replication or during st
37 In plasmids containing five repeats, minimal unpairing of (ATTCT)(5).(AGAAT)(5) occurred while 2D gel
38 g-a) motif is utilized in the "unzipping" or unpairing of bases that occurs when RT binds a malleable
39        Pathways featured: (i) unstacking and unpairing of L2 and S2 nucleobases without preQ1-exposin
40 (WT) and Vglut3 (+/-), noise exposure caused unpairing of presynaptic ribbons and presynaptic Ca(V)1.
41 th our previous observations indicating that unpairing of target DNA promotes the joining reaction.
42         Sequence alterations that facilitate unpairing of the bases at the signal/coding border activ
43 of electrons to antibonding orbitals) and by unpairing of the bonding electrons, such as in the tripl
44  are conducive to topological stress-induced unpairing of the double helix and have critical roles in
45 e that binding of CCE1 results in a complete unpairing of the four central base-pairs of the junction
46 dependent Cas12a off-target binding requires unpairing of the protospacer at PAM + 1 and increases wi
47                                              Unpairing of the two base pairs downstream of the primer
48 te-limiting physical step, such as substrate unpairing or helical arch ordering, that occurs after su
49 f well mixed As, Ts, and Cs confer high base unpairing propensity under negative superhelical strain.
50 izing a special DNA context with strong base-unpairing propensity.
51  with an ATC sequence context with high base-unpairing propensity.
52  displacement synthesis and suggest that the unpairing reaction is mediated by an intimate associatio
53 65-kDa major fragment containing both a base-unpairing region (BUR)-binding domain and a homeodomain.
54 e the core unwinding element within the base-unpairing region.
55                                    Such base unpairing regions (BURs) are typically found in scaffold
56                                    Such base-unpairing regions (BURs) are typically identified within
57                                         Base-unpairing regions (BURs) contain a specialized DNA conte
58 ibute is the presence of stress-induced base-unpairing regions (BURs).
59 nces Satb1 binding and Satb1 stabilizes base unpairing regions against melting by molecular machines.
60 e show that these defects can be repaired by unpairing short (3 or 5 bp) DNA segments spanning the tr
61 is specificity arises from double nucleotide unpairing that places the scissile phosphate diester on
62                The other half is utilized in unpairing the +1 to +2/+3 GG/G sequence for initiation.
63     This specificity is proposed to arise by unpairing the 5'-end of duplex to permit the scissile ph
64 everse transcriptase plays an active role in unpairing the DNA ahead of the translocating polymerase.
65 and hairpin products, as well as likely base unpairing to produce single-stranded (ss) DNA near the c
66 ere we monitored DNA bending by FRET and DNA unpairing using 2-aminopurine exciton pair CD to determi
67 ow that the kinetics of DNA base pairing and unpairing, which are fundamental to both the biological