ライフサイエンスコーパス: antisense strand

1 while the intron-encoded protein cleaves the antisense strand.

2 originating from two different places in the antisense strand.

3 ereas the intron-encoded protein cleaves the antisense strand.

4 for a substrate that contained a 2'-methoxy antisense strand.

5 base 10 and 11 relative to the 5' end of the antisense strand.

6 A precursors, rasiRNAs arise mainly from the antisense strand.

7 ethylation of the Ets site (5'CCGGAG) on the antisense strand.

8 oop and a U1-4 3' overhang at the end of the antisense strand.

9 lement C3 gene locus which is encoded on the antisense strand.

10 yme (class I aaRS homolog) via its sense and antisense strands.

11 at are different for the converted sense and antisense strands.

12 A sequence with high identity to the 736 antisense strand (17 of 19 bases) is present within the

13 anscriptional products of both the sense and antisense strands across the IIa-IIx-IIb MHC gene locus.

14 iRAPs encoded in the antisense strand also promote gene expression by reducin

15 ghest potential to form strong duplexes with antisense strands also have the greatest tendency to be

16 ApoE AS1 is transcribed from the antisense strand and is complementary to exon 4 of ApoE

17 r occurred in untranslated leader sequences, antisense strands, and intergenic regions.

18 found only at the expected frequency on the antisense strands, and they are underrepresented within

19 The antisense strands are isolated and hybridised with a sen

20 ly generated from the sense strand at Map2b, antisense strand at Nefl, and both strands at Vim were i

21 been directed to the genomic features of the antisense strand at the HD locus, though the presence of

22 It is probably generated in the antisense strand between the consensus bases 3'-AA and T

23 ch silencer function of 5'SHS is mediated by antisense strand binding proteins, possibly by stabilizi

24 predominantly dissociated into the sense and antisense strands by collisional activation.

25 Antisense-strand cleavage requires additional interactio

26 Antisense-strand cleavage requires additional interactio

27 hich cDNAs are incorporated at a nick at the antisense-strand cleavage site.

28 artial or complete reverse splicing, and the antisense strand cleaved by the intron-encoded protein.

29 at relatively low temperatures, whereas the antisense strand, d(AGAAT)9, does not form a structure e

30 s can act directly to mediate RNAi, with the antisense strand determining mRNA target specificity.

31 s C virus replicon RNA dissociates, and only antisense strand distributes in the cytoplasm of the cel

32 We demonstrate that the sense and antisense strand DNA mutagenesis at the immunoglobulin h

33 The distribution of sense and antisense strand DNA mutations on transcribed duplex DNA

34 racteristically interacted with the unwound, antisense strand E7 siRNA.

35 The antisense strand encodes miR-214, which is transcribed b

36 lecule selected to target ICAM-1 through its antisense strand exhibited broad anti-TNF activities.

37 The HTLV genome antisense-strand genes hbz and aph-2 are often the only

38 ne might produce functional species from its antisense strand has not been examined.

39 encing complex (RISC) assembly the guide (or antisense) strand has to separate from its complementary

40 subject to non-coding transcription of their antisense strand; however the genome-wide role for antis

41 pelling hairpin structures on both sense and antisense strands; however, the possibility that a miRNA

42 tion depends on the presence of a functional antisense strand in the siRNA duplex, suggesting that vi

43 d 4,000 predicted ORFs was observed from the antisense strand, indicating that most of the genome is

44 are well tolerated on the sense, but not the antisense, strand, indicating that the two trigger stran

45 tebrates are endogenously processed on their antisense strands into mature miRNAs with distinct seeds

46 ctive than native siRNA if the center of the antisense strand is not modified.

47 5' hydroxyl termini of antisense strands isolated from human cells were phospho

48 y associated with ANA modification of the 5'-antisense strand may be due to reduced phosphorylation a

49 The addition of a G at 5' end of the antisense strand may enhance the efficacy of gene silenc

50 Introducing an additional mismatch in the antisense strand may improve the selectivity.

51 Southwestern blot analysis revealed that the antisense strand of 5'SHS binds to nuclear proteins of m

52 study identified 45 321 tags that match the antisense strand of 9804 known mRNA sequences, 6606 of w

53 tron (e.g. mirtrons in animals), or from the antisense strand of a protein coding gene (natural antis

54 e (COIN module) that lies inertly within the antisense strand of a resident gene.

55 he status of the 5' hydroxyl terminus of the antisense strand of a siRNA determines RNAi activity, wh

56 Finally, we show that on the antisense strand of Alus, a non-CpG site just downstream

57 chromosome-wide effects of ASAR6 map to the antisense strand of an L1 retrotransposon within ASAR6 R

58 ng RNA (lncRNA) that is transcribed from the antisense strand of homeobox C gene locus in chromosome

59 A basic leucine zipper region located in the antisense strand of HTLV-1, believed to play a role in v

60 eveal a new open reading frame, ORF0, on the antisense strand of human LINE-1 encoding a small regula

61 HTLV-1 encodes a protein from the antisense strand of its proviral genome, the HTLV-1 basi

62 the antisense SAGE tags originated from the antisense strand of known mRNA sequences included in the

63 ), a recombinant protein translated from the antisense strand of PR3 cDNA.

64 ous screens missed small RNAs encoded on the antisense strand of protein-coding genes and small RNAs

65 The study of the antisense strand of siRNAs demonstrated that activity de

66 the mismatches were centrally placed in the antisense strand of small interfering RNAs.

67 non-coding RNA (lncRNA) that arises from the antisense strand of SMN, SMN-AS1, which is enriched in n

68 The antisense strand of such a mismatched RNA requires a 5'-

69 using a cryptic polyadenylation site in the antisense strand of the adjacent MPP1 gene, normally loc

70 erated transgenic Arabidopsis expressing the antisense strand of the AtRanBP1c gene to understand the

71 were detected by their hybridization to the antisense strand of the complementary promoter-directed

72 n 50 makes contacts with two guanines on the antisense strand of the DNA, adjacent to the TAAT core D

73 The antisense strand of the dsRNA determined target specific

74 A novel 2986-base transcript encoded by the antisense strand of the HRES-1 human endogenous retrovir

75 The antisense strand of the HTLV-1 genome encodes HBZ, a nov

76 The antisense strand of the HTLV-1 genome encodes HTLV-1 bas

77 PH-2), whose messenger RNA is encoded by the antisense strand of the HTLV-2 genome.

78 The antisense strand of the HTLV-2 proviral genome also enco

79 Targeting the antisense strand of the L1 within ectopically expressed

80 of a validated novel miRNA derived from the antisense strand of the miR-203 locus, which plays a rol

81 We also found transcripts from the antisense strand of the mudrA gene in all cell types in

82 This putative protein is encoded on the antisense strand of the provirus genome and entirely ove

83 rough RNAPII promoters are recognized by the antisense strand of the siRNA and function as a recognit

84 er seed region (positions 2-7 or 2-8) of the antisense strand of the siRNA.

85 It is not clear whether the antisense strand of the siRNAs bind directly to DNA or t

86 class that is processed from both sense and antisense strands of approximately 130 endogenous transc

87 Both sense and antisense strands of CRM and CentC, but not small interf

88 sequenced unambiguously using the sense and antisense strands of DNA.

89 ipelines that allow the mapping of sense and antisense strands of mitochondrial and RefSeq genes, the

90 sfection into mammalian cells, the sense and antisense strands of the duplex are transcribed by these

91 leotide tiling arrays representing sense and antisense strands of the entire nonrepetitive sequence o

92 sequence is obtained from both the sense and antisense strands of the insert region.

93 1 from class II, as complementary sense and antisense strands of the same ancestral gene.

94 RNAs (siRNAs) derive from both the sense and antisense strands of their double-stranded RNA precursor

95 The activity did not bind to the antisense strand or to an RNA with three mutations in th

96 tation studies reveal that the 5' end of the antisense strand, or "seed" sequence, is critical for ac

97 nds, while modification at the 5' end of the antisense strand resulted in complete loss of activity.

98 The 2'-O-MOE modification in the antisense strand resulted in less active siRNA construct

99 ediated transcription and translation of the antisense strand resulted in production of a 18.5-kDa pr

100 the dissociation of the individual sense and antisense strand siRNA anions was studied using ion trap

101 y exert their activities exclusively via the antisense strand that binds and silences designated targ

102 This is followed by removal of antisense strands to generate an ssDNA pool for subseque

103 s approach is complicated by the presence of antisense strand transcription of expanded GGCCCC repeat

104 In addition, we detected previously unknown antisense strand transcription that produced natural ant

105 ral C4'alpha-epimer monomers in the sense or antisense strands triggered RNAi-mediated gene silencing

106 rotein gene (VSV-GFP) and one expressing the antisense strand (VSV-PFG).

107 odified ribonucleotides at the 5'-end of the antisense strand were less active relative to the 3'-mod

108 Both the sense and antisense strands were analyzed independently, and sever

109 -F sugar was generally well-tolerated on the antisense strand, whereas the 2'-O-Me showed significant

110 ations at or near the 3' end of the sense or antisense strands, while modification at the 5' end of t

111 gene, ZNF127AS, that is transcribed from the antisense strand with a different transcript size and pa

112 ences derive from a template on the sense or antisense strand with similar frequency.