ライフサイエンスコーパス: mRNA precursor

1 for specific polyadenylation of the cleaved mRNA precursor.

2 plicing pathway of the sulfonylurea-receptor mRNA precursor.

3 ntisense endo-siRNAs match histone mRNAs and mRNA precursors.

4 in that plays important roles in splicing of mRNA precursors.

5 he nucleolytic processing of gRNA, rRNA, and mRNA precursors.

6 ein complex essential for polyadenylation of mRNA precursors.

7 rtant function for SUMO in the processing of mRNA precursors.

8 s in capping, splicing, and 3' processing of mRNA precursors.

9 ription and co-transcriptional processing of mRNA precursors.

10 derived from a small RNA, the SL RNA, to all mRNA precursors.

11 east, which are required for the splicing of mRNA precursors.

12 anscription and processing of messenger RNA (mRNA) precursors.

13 ssenger RNA (mRNA) transcripts from a single mRNA precursor and contributes to the complexity of our

14 lays critical roles both in transcription of mRNA precursors and in the processing reactions needed t

15 ce that PARylation can control processing of mRNA precursors, and also identify PARP1 as a regulator

16 n transcription and subsequent processing of mRNA precursors, and interactions between the transcript

17 lays an essential role in polyadenylation of mRNA precursors, and it has long been thought that mamma

18 acterium Escherichia coli processes rRNA and mRNA precursors, and its catalytic action can regulate g

19 ce that transcription and polyadenylation of mRNA precursors are both affected in vivo by UV treatmen

20 Transcription and processing of mRNA precursors are coordinated events that require nume

21 ecessary for 3' processing of polyadenylated mRNA precursors are well known.

22 include alterations in the structure of the mRNA precursors as well as the addition and perhaps even

23 a critical role not only in transcription of mRNA precursors but also in their subsequent processing.

24 We propose that recognition of mRNA precursors by the SCANR complex is in kinetic compe

25 scriptional level and involves maturation of mRNA precursors by trans splicing of a 39-nucleotide min

26 gnal sequences surrounding a poly(A) site on mRNA precursor, cleaves at that site, and adds a poly(A)

27 Alternative splicing of mRNA precursors enables cells to generate different prot

28 Relatively more C1 INH mRNA precursor (heterogeneous nuclear RNA [hnRNA]) was d

29 ctor required for cleavage of the 3' ends of mRNA precursor in Saccharomyces cerevisiae, has been sho

30 of Swd2, cleavage and polyadenylation of the mRNA precursor in vitro are completely normal.

31 RNAP II) is responsible for transcription of mRNA precursors in eukaryotic cells.

32 specific binding of the polymerase to capped mRNA precursors in the nucleus of infected cells.

33 ecifically inhibits ongoing transcription of mRNA precursors in vivo and both transcription and RNAP

34 , the poly(A) tail added at the 3' end of an mRNA precursor is essential for the regulation of mRNA s

35 Alternative splicing of mRNA precursors is a nearly ubiquitous and extremely fle

36 Polyadenylation of mRNA precursors is a two-step reaction requiring multipl

37 The splicing of nascent mRNA precursors is an essential step for the expression

38 Polyadenylation of mRNA precursors is frequently coupled to transcription b

39 Polyadenylation of mRNA precursors is mediated by a large multisubunit prot

40 umans, it has been observed that splicing of mRNA precursors is repressed upon heat shock.

41 We show that the 3' end cleavage of HIV-1 mRNA precursors is specifically reduced in N91-eIF3f exp

42 Maturation of mRNA precursors often occurs simultaneously with their s

43 estigations demonstrate that the stalling of mRNA precursors on spliceosomes is required for siRNA ac

44 Processing of mRNA precursors (pre-mRNAs) by polyadenylation is an ess

45 Splicing of mRNA precursors (pre-mRNAs) comprises a series of ATP-de

46 Polyadenylation of mammalian mRNA precursors requires at least two signal sequences i

47 The splicing of mammalian mRNA precursors requires both protein phosphorylation an

48 Alternative promoter usage and mRNA precursor splicing produce three amino-terminal iso

49 We show that intron-containing mRNA precursors template siRNA synthesis.

50 are the alternatively spliced variants of an mRNA precursor that is transcribed from a single human M

51 ts, but the machinery for removing them from mRNA precursors was entirely unknown.

52 s by alternative splicing of its transcribed mRNA precursor with differential distribution of these i