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1  SG-PB docking, and impaired preservation of polyadenylated mRNA.
2 ion factors, mRNA binding proteins, and most polyadenylated mRNA.
3 form lacking it, eIF4G-1a(DM), but only with polyadenylated mRNA.
4 lly activate the translation of a capped and polyadenylated mRNA.
5 Or gene array, producing a mature capped and polyadenylated mRNA.
6 lls with nonpolyadenylated mRNA but not with polyadenylated mRNA.
7  3'-end processing and nuclear export of non-polyadenylated mRNAs.
8 istone genes that encode histone variants as polyadenylated mRNAs.
9 amyxoviruses produce capped, methylated, and polyadenylated mRNAs.
10 all capped RNAs, and selection of capped and polyadenylated mRNAs.
11 , similar to the mechanism of translation of polyadenylated mRNAs.
12 ns two sets of histone genes that encode non-polyadenylated mRNAs.
13 etween 3' end formation of histone mRNAs and polyadenylated mRNAs.
14 turbing the overall cellular distribution of polyadenylated mRNAs.
15 stone H1 genes encodes detectable amounts of polyadenylated mRNAs.
16 ion-dependent histone mRNAs and encodes only polyadenylated mRNAs.
17 minators in this system, producing truncated polyadenylated mRNAs.
18 ime of the day modulates the accumulation of polyadenylated mRNAs.
19  eIF4F subunit interactions with full-length polyadenylated mRNAs.
20 t PRMT5 inhibition in mammalian cells causes polyadenylated mRNA and Smith antigen (Sm) protein accum
21 association even in yeast cells deficient in polyadenylated mRNA and/or Rpl46.
22  in parallel the native 5' ends of uncapped, polyadenylated mRNAs and 3' ends of capped mRNAs from th
23                            Both genes encode polyadenylated mRNAs and are highly expressed in vegetat
24                                              Polyadenylated mRNAs and replication-dependent histone m
25 mplexes-one specifically crafted to generate polyadenylated mRNAs and the other to generate nonpolyad
26                     Since PABP1 binds to all polyadenylated mRNAs, and is involved in translation ini
27  requires shortened/no poly(A)-tail targets; polyadenylated mRNAs are partially activated upon PAIP2
28                      During heat shock, most polyadenylated mRNAs are retained in the nucleus, wherea
29 e clock and/or the time of the day regulates polyadenylated mRNAs bound by ribosomes in response to h
30 nuclear export and also 3'-end processing of polyadenylated mRNAs, but whether such regulation also e
31         Together, these results suggest that polyadenylated mRNAs can enter P-bodies, and an mRNP com
32 ate of labeling of rp mRNA relative to total polyadenylated mRNA changed very little after stimulatio
33 f the maize cell line P3377.5' capped and 3' polyadenylated mRNA constructs containing the firefly ge
34                                          All polyadenylated mRNAs contain sequence of variable length
35 the prototype VZV genome isomer, expresses a polyadenylated mRNA containing a splice within the 3' un
36            PABPC1 antagonizes uridylation of polyadenylated mRNAs, contributing to the specificity fo
37                               Genes encoding polyadenylated mRNAs depend on their poly(A) signals for
38  synthesized during replication is a 0.8-kb, polyadenylated mRNA encoding the hepatitis delta antigen
39 addition, RNase R stalls in the body of many polyadenylated mRNAs, especially at G-rich sequences tha
40  the antigenome, and (iii) the less abundant polyadenylated mRNA for the small delta protein.
41 of target mRNAs produce diagnostic uncapped, polyadenylated mRNA fragments.
42 d of the genome followed by 5'-capped and 3'-polyadenylated mRNAs from internal genes by a stop-start
43 xon 2 resulting in the production of a small polyadenylated mRNA (HTTexon1) that encodes the highly p
44  stem-loop, the H1c gene expresses a longer, polyadenylated mRNA in differentiated cells, although in
45  We demonstrate that hos1 mutants accumulate polyadenylated mRNA in the nucleus and that the circadia
46 crete set of pathways for the degradation of polyadenylated mRNAs in eukaryotic cells have been descr
47                        They are expressed as polyadenylated mRNAs in fibroblasts differentiated in vi
48  of this system, including the prevalence of polyadenylated mRNAs in the bacterium, are still poorly
49 t the M3 protein is encoded by an unspliced, polyadenylated mRNA initiating at bp 7294 and terminatin
50       Our results reveal how FMRP sequesters polyadenylated mRNAs into stabilized and translationally
51                     We established that this polyadenylated mRNA is 0.8 kb in length and its 5' end b
52 adaptors that flag alternatively spliced and polyadenylated mRNA isoforms as cargo ready for the cyto
53 roteins (sFlt1s) produced from alternatively polyadenylated mRNA isoforms.
54 ssed in terminally differentiated tissues as polyadenylated mRNAs, likely serving as replacement hist
55 eta-lactamase family generate the 3' ends of polyadenylated mRNAs, nonpolyadenylated histone mRNAs, a
56                                          Non-polyadenylated mRNAs of replication-dependent histones (
57 n-independent histones, which are encoded by polyadenylated mRNAs, persists outside of S phase.
58 otein factors necessary for 3' processing of polyadenylated mRNA precursors are well known.
59 Transcription termination for genes encoding polyadenylated mRNAs requires a functional poly(A) signa
60 s, Nipah and Ebola, produce 5'-capped and 3'-polyadenylated mRNAs resembling higher eukaryotic mRNAs.
61  are needed for the translation of capped or polyadenylated mRNA, respectively.
62     Analysis of the cellular distribution of polyadenylated mRNAs revealed more pronounced nuclear mR
63 ause mtDNA is transcribed and processed into polyadenylated mRNAs reverse transcription coupled to PC
64 f genomic RNA replication and positive-sense polyadenylated mRNA(s) were synthesized.
65 t did not stimulate translation of uncapped, polyadenylated mRNA suggested additional Pab1p-dependent
66 er half of human genes produce alternatively polyadenylated mRNAs, suggesting that regulated polyaden
67 he oligo(dT)-primed reverse transcription of polyadenylated mRNA templates used to generate EST cDNA
68 its exact complement (the antigenome), and a polyadenylated mRNA that acts as a template for the smal
69  principally to a genomic region producing a polyadenylated mRNA that encodes a protein.
70 elongs to the picornavirus superfamily, is a polyadenylated mRNA that is naturally uncapped and yet i
71 nt splicing of exon 1 HTT results in a short polyadenylated mRNA that is translated into an exon 1 HT
72 erminal portion of DUX4 and (iii) capped and polyadenylated mRNAs that contain the double-homeobox do
73 alone caused an increase in the synthesis of polyadenylated mRNA, the majority of which was due to a
74  inserted gene into the predicted subgenomic polyadenylated mRNA was demonstrated by Northern (RNA) b
75 bed exclusively in testis, where the spliced polyadenylated mRNA was detected.
76                           About 70% of total polyadenylated mRNA was in the polysome fraction in all
77          The ratio of cytoplasmic to nuclear polyadenylated mRNA was increased in the presence of SM,
78 ated in vitro and also when m(7)G-capped and polyadenylated mRNA was transiently transfected into 293
79                                              Polyadenylated mRNAs were captured by oligo-dT primers a
80 s the genomic RNA to produce five capped and polyadenylated mRNAs with the 5'-terminal structure 7mGp
81 e show that sequencing of oligo(dT)-selected polyadenylated mRNAs, without considering the orientatio