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1 erase that transcribes the 45S ribosomal (r) RNA precursor.
2  from a stem-loop structured single-stranded RNA precursor.
3  factor enhances the binding of Hrp1p to the RNA precursor.
4 rden by autocatalytically splicing out of an RNA precursor.
5 n homochiral ribose-aminooxazoline (RAO), an RNA precursor.
6 ucleotide miRNAs from longer double-stranded RNA precursors.
7 t productively with a diversity of noncoding RNA precursors.
8 nt RNAend-seq to measure processing rates of RNA precursors.
9 script turnover and maturation of structured RNA precursors.
10 A species may not arise from double-stranded RNA precursors.
11 uced from endogenous single-stranded hairpin RNA precursors.
12 ively process, rather than destroy, specific RNA precursors.
13 ar to be processed from long double-stranded RNA precursors.
14 terfering RNAs (siRNAs) from double-stranded RNA precursors.
15 urns over RNA but also processes certain key RNA precursors.
16 n the substrate and catalytic domains of the RNA precursors.
17 ) genome was studied by using nonreplicative RNA precursors.
18 noRNA that directly interacts with ribosomal RNA precursors.
19 ed for the accumulation of certain noncoding RNA precursors and for the role of the Saccharomyces cer
20 s, which are produced as long non-coding (nc)RNA precursors and promote recognition of DSBs.
21  and enhancer-associated RNAs (eRNAs), micro-RNA precursors and repeat-derived RNAs.
22            During RNAi, long double-stranded RNA precursors are processed by Dicer proteins into appr
23 t work has also suggested that some transfer RNA precursors are processed in the nucleolus.
24 olated mitochondria incorporate radiolabeled RNA precursors, as well as DNA precursors, into replicat
25 ed transcription and processing of ribosomal RNA precursors, as well as the translation of specific r
26 microRNAs are generated from double-stranded RNA precursors by the Dicer endonucleases, and function
27 ntrons are removed from eukaryotic messenger RNA precursors by the spliceosome in two transesterifica
28 ering RNA against the loop region of a micro-RNA precursor can be used to deplete the micro-RNA.
29 ition of nuclear export of shRNA or premicro-RNA precursors, competition for the Exportin 5 nuclear e
30 c genes by RNA polymerase II (Pol II) yields RNA precursors containing introns that must be spliced o
31 were most often derived from double-stranded RNA precursors copied from spliced mRNAs.
32 mor cell invasion, and H19, a long noncoding RNA precursor for an RB-targeting microRNA.
33 s RNase E cleavage of a representative small-RNA precursor for interaction with a mRNA target.
34  from which RDR2 synthesizes double-stranded RNA precursors for small interfering RNAs (siRNAs) that
35     The enzyme Dicer cleaves double-stranded RNA precursors, generating short interfering RNAs and mi
36                                              RNA precursors give rise to mRNA after splicing of intro
37 NA turnover and quality control of ribosomal RNA precursors in many bacterial species.
38 rotein levels of MRPP1 and an increase in mt-RNA precursors indicative of impaired mt-RNA processing
39 hat processes microRNA and small interfering RNA precursors into their short mature forms, enabling t
40 ervening sequences from eukaryotic messenger RNA precursors is carried out by the spliceosome, a comp
41 is well known that the splicing of messenger RNA precursors is generally repressed on heat shock, but
42                     The splicing of transfer RNA precursors is similar in Eucarya and Archaea.
43 se E for processing 9S RNA (the ribosomal 5S RNA precursor) is repressed in the presence of the ribos
44 port the synthesis of highly enantioenriched RNA precursor molecules from racemic starting materials,
45 predominant binding of the 45S pre-ribosomal RNA precursor molecules.
46                                              RNA precursors, monomers, active ribozymes, oligonucleot
47              Nearly all eukaryotic messenger RNA precursors must undergo cleavage and polyadenylation
48 ngs also illustrate that dicing of the viral RNA precursors of primary and secondary siRNA is insuffi
49 ion of racemic ribo-aminooxazoline (RAO), an RNA precursor, on magnetite (Fe(3)O(4)) surfaces, achiev
50 biting siRNA processing from double-stranded RNA precursors or by destabilizing siRNAs.
51 rocycle adducts are subunits of the proposed RNA precursor, peptide nucleic acids (PNAs).
52 s-splicing reactions with a target messenger RNA precursor (pre-mRNA).
53 es have shown that copy numbers of ribosomal-RNA precursor (pre-rRNA) of specific pathogen species re
54 A polymerase I (Pol I) synthesizes ribosomal RNA precursor (pre-rRNA), which comprises most of RNA in
55 e spliceosome removes introns from messenger RNA precursors (pre-mRNA).
56 oding sequences of most eukaryotic messenger RNA precursors (pre-mRNAs) are interrupted by non-coding
57                         Eukaryotic messenger RNA precursors (pre-mRNAs) synthesized by RNA polymerase
58                    Most eukaryotic messenger RNA precursors (pre-mRNAs) undergo extensive maturationa
59  and polyadenylation of eukaryotic messenger RNA precursors (pre-mRNAs); it also participates in tran
60                    Introns of human transfer RNA precursors (pre-tRNAs) are excised by the tRNA splic
61                          Eukaryotic transfer RNA precursors (pre-tRNAs) contain a 5' leader preceding
62 d antisense strands of their double-stranded RNA precursors, rasiRNAs arise mainly from the antisense
63                 Polyadenylation of messenger RNA precursors requires a complex protein machinery that
64            During synthesis of the ribosomal RNA precursor, RNA polymerase I (Pol I) monitors DNA int
65  3'-untranslated region (3'-UTR) of a larger RNA precursor that possesses characteristics of mRNA inc
66 d in a stepwise process from double-stranded RNA precursors that are embedded in long RNA polymerase
67             We propose that defective stable RNA precursors that are poorly converted to their mature
68 rom much longer sequences of double-stranded RNA precursors through cleavage by Dicer or a Dicer-like
69 m of protein-coding regions in polycistronic RNA precursors through trans splicing.
70   Introns are removed from nuclear messenger RNA precursors through two sequential phospho-transester
71 entify the contribution of a predicted micro-RNA precursor to the pool of mature micro-RNA in a given
72  allows the locations of the double-stranded RNA precursors to be inferred.
73 quentially assembles on eukaryotic messenger RNA precursors to remove introns (pre-mRNA splicing), a
74                    No aberrant processing of RNA precursors was observed.
75 s that accumulate for essentially all stable RNA precursors when RNA maturation is slowed because of
76 ter release from polycistronic mitochondrial RNA precursors, which is essential for mitochondrial rib
77 nce systems depend on the synthesis of small RNA precursors whose sequences define the target spectru
78 CL1) in plants, to catalyze processing of an RNA precursor with a fold-back structure.