ライフサイエンスコーパス: polyadenylated RNA

1 y can be harnessed to identify alternatively polyadenylated RNA.

2 s that contain pre-mRNA splicing factors and polyadenylated RNA.

3 O2 into enlarged nuclear speckles containing polyadenylated RNA.

4 ripts accounted for approximately 20% of the polyadenylated RNA.

5 opy that the complex can circularize capped, polyadenylated RNA.

6 nscripts (BARTs) are the most abundant viral polyadenylated RNA.

7 BRPCs without detection of KDR despite using polyadenylated RNA.

8 d protein uptake and nuclear accumulation of polyadenylated RNA.

9 on of ORF59 RNA and RBM15's association with polyadenylated RNAs.

10 e is proposed to explain the accumulation of polyadenylated RNAs.

11 solution of oligo(dT) hybridized to a large polyadenylated RNA (1.0 x 10(-7) cm2/s).

12 Following RNA extraction and isolation of polyadenylated RNA, a 5'-RNA adapter that includes an Mm

13 We now demonstrate that Slr1 binds to polyadenylated RNA and that its intracellular localizati

14 en the steady-state levels of CAR1-specific, polyadenylated RNA and the degree of arginase induction

15 rent biochemistries, with one examining only polyadenylated RNA and the other total RNA.

16 t hydroxymethylcytosine preferentially marks polyadenylated RNAs and is deposited by Tet in Drosophil

17 el approach to prepare 3' end fragments from polyadenylated RNA, and mapped the position of the poly(

18 onine serine repeat protein (Gts1p), nuclear polyadenylated RNA-binding protein 3, and minichromosome

19 everse transcriptase is used to quantify the polyadenylated RNA by extension of a biotinylated oligo-

20 wn without the inducer contained very little polyadenylated RNA capable of hybridizing to the isolate

21 ogy from Pacific Biosciences to sequence the polyadenylated RNA complement of a pooled set of 20 huma

22 he continually transcribed XIST gene and its polyadenylated RNA consistently localize to a nuclear re

23 cing coincides with nuclear retention of non-polyadenylated RNA derived from MuDR and recently descri

24 e cloned gene was used as a probe to analyze polyadenylated RNA derived from wild-type and mutant cel

25 We sequenced polyadenylated RNA-derived complementary DNAs from 92 ps

26 he viral genome is a single 7,400-nucleotide polyadenylated RNA encoding 11 proteins in a single open

27 ntified in a screen for strains defective in polyadenylated RNA export.

28 utated alleles of GLE2 displayed blockage of polyadenylated RNA export; however, nuclear protein impo

29 Electrophoretic analysis of polyadenylated RNA, followed by transfer to nitrocellulo

30 tation of the NES in Gle1 prevents export of polyadenylated RNA from the nucleus.

31 generation sequencing to analyze and compare polyadenylated RNAs from abortive MOCV infections of sev

32 Picornaviruses have 3' polyadenylated RNA genomes, but the mechanisms by which

33 that SRp20 and 9G8 can be UV cross-linked to polyadenylated RNA in both the nucleus and cytoplasm of

34 tes, was coincident with the accumulation of polyadenylated RNA in the nucleus.

35 BP significantly reduces both its binding to polyadenylated RNA in vivo and its ability to prevent de

36 Taken together with the low abundance of polyadenylated RNAs in maize mitochondria, our results a

37 tochondria, where they are directly bound to polyadenylated RNAs in vivo.

38 nantly in the nucleus and is associated with polyadenylated RNAs in vivo.

39 DNA molecules that had been synthesized from polyadenylated RNA isolated from 3-week-old plants.

40 The cDNA library was constructed from polyadenylated RNA isolated from the suppressed UACC-903

41 cterized an abundant late 1.7-kb cytoplasmic polyadenylated RNA (L1.7 RNA) transcribed from the bovin

42 associations of human nuclear and cytosolic polyadenylated RNAs longer than 200 nucleotides (nt) and

43 e been constructed with the use of cytosolic polyadenylated RNA obtained from 11 human cell lines.

44 entary DNA samples, reverse-transcribed from polyadenylated RNA obtained from human liver tissue.

45 short (14 base) expressed sequence tags from polyadenylated RNA obtained from vastus lateralis muscle

46 Finally, we demonstrate that degradation of polyadenylated RNAs occurs in the 3' to 5' direction thr

47 Furthermore, a polyadenylated RNA of 1.4 kb was identified downstream o

48 A polyadenylated RNA of 3.0 kb (T3.0) is transcribed from

49 with complementary DNAs transcribed from the polyadenylated RNAs of a variety of normal and neoplasti

50 n of 32P-labelled cDNAs synthesized from the polyadenylated RNAs of the white blood cells from patien

51 ination of nonpolyadenylated as well as some polyadenylated RNA polymerase II transcripts.

52 sequencing, to determine the 5' ends of the polyadenylated RNAs produced during HDV genome replicati

53 can be polyadenylated in vitro, and similar polyadenylated RNA products are detectable in vivo.

54 two transcripts, 1.3 and 1.1 kb in size, in polyadenylated RNA purified from leaf tissues of mature,

55 Formation of the 3' end of these non-polyadenylated RNAs requires a specialized 3' box elemen

56 This transcription is observed in polyadenylated RNA samples and appears to be derived fro

57 degrades polyadenylated as compared with non-polyadenylated RNA substrates corresponding to the 3' UT

58 cell cytoplasmic S100 extracts and exogenous polyadenylated RNA substrates that reproduces regulated

59 toplasm after its nuclear export, to degrade polyadenylated RNAs, such as mRNAs, pre-mRNAs, or those

60 rved regions of the genome and include small polyadenylated RNAs (T0.7 and T1.1) as well as most of t

61 ughput method for reliable identification of polyadenylated RNA termini, and we apply this method, ca

62 referred to as the antigenome, and an 800-nt polyadenylated RNA that could act as the mRNA for the de

63 rine Upregulated Gene 1 (TUG1) is a spliced, polyadenylated RNA that does not encode any open reading

64 is-1 gene is expressed as a 3-kb spliced and polyadenylated RNA that is believed to function in the a

65 trated that XTUT7 repressed translation of a polyadenylated RNA, to which it added a distinct number

66 quantification of the full range of cellular polyadenylated RNA transcripts using a Helicos Genetic A

67 Because RBDmap relies on the isolation of polyadenylated RNA via oligo(dT), it will not provide RN

68 The nuclear/cytoplasmic (n/c) ratio of polyadenylated RNAs was 3.8, while the n/c ratio for rib

69 Non-coding non-polyadenylated RNAs were among the key Hox targets, with

70 Men epsilon is a 3.2-kb polyadenylated RNA, whereas Men beta is an approximately

71 The mouse His-1 gene encodes a spliced and polyadenylated RNA with no long open reading frame (ORF)

72 number that gave rise to heterogeneous Trf4p-polyadenylated RNAs with lengths of approximately 250-50

73 In addition, sar1 sar3 plants accumulate polyadenylated RNA within the nucleus, indicating that S