ライフサイエンスコーパス: complementary RNA

1 ther singly or in combination with wild-type complementary RNA.

2 when a TP-modified ODN is hybridized to its complementary RNA.

3 escent reporter signal upon hybridization to complementary RNA.

4 orthern-biased MOE nucleotides hybridized to complementary RNA.

5 heteroduplexes composed of modified DNA and complementary RNA.

6 rocessively along a DNA template, creating a complementary RNA.

7 rresponding mRNA but also virion RNA and its complementary RNA.

8 ifications and measured their affinities for complementary RNA.

9 guided by endogenous or viral sRNAs, targets complementary RNAs.

10 e types of 2'-O-modified ribonucleotides and complementary RNAs.

11 increase in hybridization affinity toward a complementary RNA (1.5 degrees C per modification) and a

12 -base loop region, forms a 1:1 duplex with a complementary RNA 18-mer, mini-TAR RNA.

13 ce 5'-G-G-C-G-C-C-C-G-A-A-3' was annealed to complementary RNA (5'-u-u-c-g-g-g-c-g-c-c-3') and crysta

14 resistant to nucleases, formed duplexes with complementary RNA (A-form), and, as chimeric oligomers c

15 itiation codon region of the HER-2 mRNA, and complementary RNA and DNA ODNs, were used in this study.

16 LNA) bases have remarkably high affinity for complementary RNA and DNA sequences.

17 on the affinity of the oligonucleotides for complementary RNA and on nuclease stability was evaluate

18 fluorescence signal in the presence of fully complementary RNAs and selectivity against single nucleo

19 ing affinity of the oligonucleotides for the complementary RNA (and not for DNA).

20 t both types formed A-form duplexes with the complementary RNA, and the melting temperatures were in

21 corresponding plus-strand panhandles of the complementary RNA are recognized with lower affinity.

22 During replication, two complementary RNAs are also detected: an exact complemen

23 units are able to form heteromers when their complementary RNAs are injected into oocytes, whether fu

24 y to the provided RNA replicon and using the complementary RNA as template to synthesize new TBSV rep

25 DNA) clone and determine the distribution of complementary RNA at the tissue and cellular levels.

26 of the finger 5-finger 6 interface to form a complementary RNA binding surface.

27 -3'-deoxyribonucleotides bind selectively to complementary RNA but not to DNA.

28 nwinding induces an efficient annealing of a complementary RNA by making the unwound strand more acce

29 oligomers does not decrease the affinity for complementary RNA compared to 2'-O-alkyl substituents of

30 By expressing two self-complementary RNA constructions designed to initiate RNA

31 itiates on the vRNA 3' terminus, producing a complementary RNA (cRNA) intermediate, which serves as a

32 Radioactive complementary RNA (cRNA) probes were prepared from cDNAs

33 er allowing competitive binding with CRP and complementary RNA (cRNA) strands in pure form and co-mix

34 transcribed by T7 RNA polymerase to generate complementary RNA (cRNA), which then was used to hybridi

35 3-1) or by injection of in vitro transcribed complementary RNAs (cRNAs) into Xenopus oocytes.

36 bone and showed no discrimination in Tm with complementary RNA, demonstrating that 6'-F substitution

37 tes the suppression of CIITA pIV possibly by complementary RNA-DNA binding to an inhibitory domain on

38 stable complex depends on the presence of a complementary RNA-DNA hybrid that is at least 9 bp in le

39 The crystal structure of a self-complementary RNA duplex r(GGGCGCUCC)2with non-adjacent

40 The equilibrium folding of a series of self-complementary RNA duplexes and the unmodified yeast tRNA

41 are reported for duplex formation of 48 self-complementary RNA duplexes containing Watson-Crick termi

42 are reported for duplex formation of 40 self-complementary RNA duplexes containing wobble terminal ba

43 of LQT, we injected oocytes with mutant HERG complementary RNAs, either singly or in combination with

44 Oocytes injected with low levels of NBCn1-B complementary RNA exhibit a Na+ conductance that 4,4-dii

45 lexes of single or double-linked probes with complementary RNA exhibited sensitivity to RNase H diges

46 Xenopus laevis oocytes injected with the complementary RNA for oapt1 demonstrated higher uptake o

47 lementary DNA, then generates biotin-labeled complementary RNA from the cDNA.

48 lular components capable of synthesizing new complementary RNAs from existing RNA templates.

49 tranded RNA (dsRNA) produced by annealing of complementary RNAs generated during viral infection.

50 One is a complementary RNA identical in size to the input RNA tem

51 e that the Cmr complex cleaves an endogenous complementary RNA in Pyrococcus furiosus, providing dire

52 sis (Arabidopsis thaliana) plants and CYBDOM complementary RNA-injected Xenopus laevis oocytes.

53 rs through de novo initiation and involves a complementary RNA intermediate.

54 nesis, was found to catalyze assimilation of complementary RNA into a homologous region of a DNA dupl

55 Complementary RNA is also shown to displace the bound an

56 ression via a RNase H mechanism in which the complementary RNA is degraded by RNase H.

57 hosphocholine-mediated Ca2+ release when its complementary RNA is injected into Xenopus oocytes.

58 odification systems, it is not known whether complementary RNA is involved in chloroplast editing sit

59 ause the binding affinity of 2'-O-meRNAs for complementary RNA is low relative to analogous PNAs.

60 e or interference caused by annealing of the complementary RNAs, leading to degradation.

61 tion that several nucleotide residues of non-complementary RNA located upstream of the RNA-DNA hybrid

62 ial reversal of RNA-mediated phenotypes with complementary RNA molecules.

63 n region of c-myc mRNA and the corresponding complementary RNA oligomer were used for this study.

64 ment of sR8 guide region accessibility using complementary RNA oligonucleotide probes revealed signif

65 not StpA-NterL, promotes strand annealing of complementary RNA oligonucleotides and in vitro trans-sp

66 The use of complementary RNA or DNA sequences to selectively interf

67 ted from any double-stranded RNA and degrade complementary RNAs; others are encoded by genes and repr

68 r with complementary DNA (PNA:DNA) than with complementary RNA (PNA:RNA).

69 Complementary RNA prepared from RNA of the HCjE cells wa

70 thout passing through a promoter by adding a complementary RNA primer and core Escherichia coli RNA p

71 Northern analysis using a VMAT2 complementary RNA probe revealed a single 4 kb mRNA spec

72 n this study, we have used an antibody and a complementary RNA probe to explore the distribution of n

73 dization histochemistry using a 35S-labelled complementary RNA probe.

74 akly sensitive with highly sensitive subunit complementary RNAs produces functional heteromeric chann

75 ma(E)-dependent sRNA, MicL (mRNA-interfering complementary RNA regulator of Lpp), transcribed from a

76 enables quick localization of potential near-complementary RNA-RNA interactions between given query a

77 pendence is similar to that for Watson-Crick complementary RNA/RNA duplexes, which suggests that the

78 oximately 22-nucleotide miRNAs, which target complementary RNA sequences.

79 into small RNAs that promote degradation of complementary RNA sequences.

80 Spectroscopic melting experiments against complementary RNA showed increases of 3-4 degreesC per m

81 ments of modified oligodeoxynucleotides with complementary RNA showed slightly sequence-dependent dup

82 he affinity of antisense oligonucleotides to complementary RNA similar to 2'-O-MOE-modified ASOs as c

83 A to double-stranded RNA by synthesis of the complementary RNA strand.

84 NA chimera was constructed and annealed to a complementary RNA strand.

85 phosphoramidates form stable duplexes with a complementary RNA strand.

86 lex purification uses on-column annealing of complementary RNA strands, followed by separation of the

87 replication silencer, that can down-regulate complementary RNA synthesis of a positive-strand RNA vir

88 ation, the hammerhead ribozyme must cleave a complementary RNA target without deleterious effects fro

89 nts that promote site-specific cleavage on a complementary RNA target.

90 nd small RNAs and use them as guides to find complementary RNA targets and induce gene silencing.

91 FFPE-RNA, are used as primers for the RT of complementary RNA templates contained in a sense-RNA lib

92 While complementary RNA that guides nucleotides for alteration

93 In Xenopus oocytes injected with aquaporin 1 complementary RNA, the application of forskolin or cycli

94 es that hybridize to a surface modified with complementary RNA; the motion is achieved through the ad

95 r duplex with an alpha-tocopherol-conjugated complementary RNA (Toc-HDO) is significantly more potent

96 e binding of several large sets of probes to complementary RNA transcripts.

97 w FRET and fluorescence anisotropy show that complementary RNAs transiently form a ternary complex wi

98 protein complexes to regulate expression of complementary RNAs via base pairing.

99 SOs can be designed to induce degradation of complementary RNAs via the RNase H pathway and much is u

100 Release of Hfq upon addition of complementary RNA was faster than duplex formation, sugg

101 change from stem-loop to duplex RNA-DNA when complementary RNA was present.

102 Complementary RNAs were expressed in Xenopus oocytes for

103 ed by the zwitterionic oligonucleotides with complementary RNAs were not substrates for RNase H.

104 Pairing of the complementary RNAs would be predicted to occlude the rot