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1 ion of the MMLV dimerization initiation site kissing loop.
2 that were fluorescently labelled in and near kissing loops.
5 By monitoring the folding of the aptamer, kissing loop, and riboswitch expression platform, we est
6 n that the Tar-Tar(*) complex, an archetypal kissing loop, can form without Mg(2+), so long as high c
7 In contrast sequences involved in forming a kissing loop complex are not absolutely required, but ar
8 ormation of an extended duplex rather than a kissing loop complex because the short stems are not sta
9 The degree of cation accumulation around the kissing loop complex was also inversely proportional to
10 two other RNAs, an adenine riboswitch and a kissing loop complex, become more stable by 2-3 kcal/mol
12 it requires as much force to break the MMLV kissing-loop complex as is required to unfold an 11-bp R
13 op interface is critical in the formation of kissing loop complexes and that in the absence of Mg(2+)
16 rived from the ColE1 plasmid to associate as kissing loop complexes in the presence and absence of di
17 in the unusual stability of other retroviral kissing-loop complexes such as the HIV dimerization site
28 Escherichia coli btuB riboswitch contains a kissing loop interaction that is in close proximity to t
29 Using this system, we determine that the kissing-loop interaction between 5BSL3.2 and 3' SL2 is r
30 bilizes an unusual long-range intramolecular kissing-loop interaction that controls mRNA expression.
31 o engages in a stable, long-distance RNA-RNA kissing-loop interaction with a 12-bp 5'-coding-region h
32 contains an apical loop capable of forming a kissing-loop interaction with a 5' proximal hairpin and
33 Most 3'CITEs participate in a long-distance kissing-loop interaction with a 5' proximal hairpin to d
34 the PEMV PTE that engages in a long-distance kissing-loop interaction with a coding sequence hairpin
35 or eIF4F complex and to engage in an RNA-RNA kissing-loop interaction with a hairpin loop located at
37 iform is not an absolute requirement for the kissing-loop interaction, suggesting a model in which tr
38 iation has been proposed to occur through a "kissing-loop" interaction involving a specific RNA stem-
42 involves the fast formation of an unstable "kissing" loop intermediate, followed by a slower convers
43 the fast formation of an unstable extended "kissing" loop intermediate, followed by a slower strand
46 ubstrate stem loop I (SLI)-stem loop V (SLV) kissing loop junction of the Varkud Satellite ribozyme h
49 nucleocapsid (NC) to the hinge region of the kissing-loop (KL) dimer formed by stemloop 1 (SL1) can h
51 sociated with the disruption of a long-range kissing-loop (KL) interaction is substantially decreased
54 ranscriptional expression possibly through a kissing loop model bridging TRX 3'- and 5'-UTRs through
61 ribozyme core via three tertiary contacts: a kissing loop (P14), a metal core-receptor interaction, a
62 and therefore differs significantly from the kissing loop palindromes utilized to initiate dimerizati
63 Finally, we show that both the poly(U) and kissing-loop RNA elements can function outside of their
65 ection pathway resembles that of an isolated kissing loop similar to P14, and the rate along the indu
67 ed metastable configuration consisting of a "kissing loop" stabilized by flanking helical domains; th
68 slated region (3'UTR), the ribosome-binding, kissing-loop T-shaped structure (kl-TSS) and eukaryotic
69 EMV) 3' translational enhancer, known as the kissing-loop T-shaped structure (kl-TSS), binds to 40S s
70 tifunctional element is designated a kl-TSS (kissing-loop T-shaped structure) to distinguish it from
71 B coding region, 5BSL3.2, forms a functional kissing-loop tertiary structure with part of the 3' NTR,
72 These oligomers self-associate to form a kissing loop that thermally rearranges into a more stabl
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