ライフサイエンスコーパス: RNA precursor

1 from a stem-loop structured single-stranded RNA precursor.

2 factor enhances the binding of Hrp1p to the RNA precursor.

3 erase that transcribes the 45S ribosomal (r) RNA precursor.

4 ucleotide miRNAs from longer double-stranded RNA precursors.

5 t productively with a diversity of noncoding RNA precursors.

6 script turnover and maturation of structured RNA precursors.

7 A species may not arise from double-stranded RNA precursors.

8 uced from endogenous single-stranded hairpin RNA precursors.

9 ively process, rather than destroy, specific RNA precursors.

10 ar to be processed from long double-stranded RNA precursors.

11 terfering RNAs (siRNAs) from double-stranded RNA precursors.

12 urns over RNA but also processes certain key RNA precursors.

13 n the substrate and catalytic domains of the RNA precursors.

14 ) genome was studied by using nonreplicative RNA precursors.

15 ed for the accumulation of certain noncoding RNA precursors and for the role of the Saccharomyces cer

16 and enhancer-associated RNAs (eRNAs), micro-RNA precursors and repeat-derived RNAs.

17 During RNAi, long double-stranded RNA precursors are processed by Dicer proteins into appr

18 t work has also suggested that some transfer RNA precursors are processed in the nucleolus.

19 olated mitochondria incorporate radiolabeled RNA precursors, as well as DNA precursors, into replicat

20 ed transcription and processing of ribosomal RNA precursors, as well as the translation of specific r

21 microRNAs are generated from double-stranded RNA precursors by the Dicer endonucleases, and function

22 ntrons are removed from eukaryotic messenger RNA precursors by the spliceosome in two transesterifica

23 ering RNA against the loop region of a micro-RNA precursor can be used to deplete the micro-RNA.

24 ition of nuclear export of shRNA or premicro-RNA precursors, competition for the Exportin 5 nuclear e

25 mor cell invasion, and H19, a long noncoding RNA precursor for an RB-targeting microRNA.

26 s RNase E cleavage of a representative small-RNA precursor for interaction with a mRNA target.

27 The enzyme Dicer cleaves double-stranded RNA precursors, generating short interfering RNAs and mi

28 RNA precursors give rise to mRNA after splicing of intro

29 NA turnover and quality control of ribosomal RNA precursors in many bacterial species.

30 rotein levels of MRPP1 and an increase in mt-RNA precursors indicative of impaired mt-RNA processing

31 hat processes microRNA and small interfering RNA precursors into their short mature forms, enabling t

32 ervening sequences from eukaryotic messenger RNA precursors is carried out by the spliceosome, a comp

33 is well known that the splicing of messenger RNA precursors is generally repressed on heat shock, but

34 The splicing of transfer RNA precursors is similar in Eucarya and Archaea.

35 se E for processing 9S RNA (the ribosomal 5S RNA precursor) is repressed in the presence of the ribos

36 port the synthesis of highly enantioenriched RNA precursor molecules from racemic starting materials,

37 Nearly all eukaryotic messenger RNA precursors must undergo cleavage and polyadenylation

38 ngs also illustrate that dicing of the viral RNA precursors of primary and secondary siRNA is insuffi

39 biting siRNA processing from double-stranded RNA precursors or by destabilizing siRNAs.

40 s-splicing reactions with a target messenger RNA precursor (pre-mRNA).

41 es have shown that copy numbers of ribosomal-RNA precursor (pre-rRNA) of specific pathogen species re

42 oding sequences of most eukaryotic messenger RNA precursors (pre-mRNAs) are interrupted by non-coding

43 Eukaryotic messenger RNA precursors (pre-mRNAs) synthesized by RNA polymerase

44 Most eukaryotic messenger RNA precursors (pre-mRNAs) undergo extensive maturationa

45 and polyadenylation of eukaryotic messenger RNA precursors (pre-mRNAs); it also participates in tran

46 Eukaryotic transfer RNA precursors (pre-tRNAs) contain a 5' leader preceding

47 d antisense strands of their double-stranded RNA precursors, rasiRNAs arise mainly from the antisense

48 Polyadenylation of messenger RNA precursors requires a complex protein machinery that

49 d in a stepwise process from double-stranded RNA precursors that are embedded in long RNA polymerase

50 We propose that defective stable RNA precursors that are poorly converted to their mature

51 rom much longer sequences of double-stranded RNA precursors through cleavage by Dicer or a Dicer-like

52 m of protein-coding regions in polycistronic RNA precursors through trans splicing.

53 Introns are removed from nuclear messenger RNA precursors through two sequential phospho-transester

54 entify the contribution of a predicted micro-RNA precursor to the pool of mature micro-RNA in a given

55 allows the locations of the double-stranded RNA precursors to be inferred.

56 No aberrant processing of RNA precursors was observed.

57 s that accumulate for essentially all stable RNA precursors when RNA maturation is slowed because of

58 CL1) in plants, to catalyze processing of an RNA precursor with a fold-back structure.