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1 ing the excision of either the coding or non-coding strand.
2 iption, resulting in G-to-A mutations in the coding strand.
3 cription-coupled repair on coding versus non-coding strand.
4 uency was threefold greater than that of the coding strand.
5  owing to the fragility of the displaced DNA coding strand.
6 anscribed strand is repaired faster than the coding strand.
7 equence from -141 to -170 (C1) is on the non-coding strand.
8  regions of the genome is faster than in the coding strand.
9  excess of C-->T changes was observed on the coding strand.
10 n the noncoding strand and -74 to -53 on the coding strand.
11 ded by a pyrimidine-rich sequence in the DNA coding strand.
12 no difference was observed for noncoding and coding strands.
13  strands identified a deletion of a T in the coding strand and a corresponding loss of an A in the no
14 ion, which is located from -66 to -17 on the coding strand and contains four TT(A/T/C)ACA-like repeat
15 ase II are repaired faster than those in the coding strand and nontranscribed regions of the genome.
16  intronic sequences are transcribed from the coding strand and that a given intron can be processed i
17 ne sequence from -171 to -200 (C2) is on the coding strand and the adjacent polypurine sequence from
18 late (bottom) strand lags behind that of the coding strand, and complete methylation of both strands
19 agenized, integrated into VR as a single non-coding strand, and then partially converted to the paren
20  strand, on differences between template and coding strand associated with transcription-coupled repa
21 f these observations it is proposed that the coding strand bias is generated by selection to code hig
22 n deaminates C in single-stranded DNA or the coding-strand DNA that is being transcribed but not in d
23 ding sequence (GAGGAA) is located on the non-coding strand from position -40 to -45 relative to the t
24  higher rates of cytosine deamination on the coding strand has been observed in enterobacteria.
25 emplate strand in exon 2, I-TwoI cleaves the coding strand in exon 1.
26 lose proximity to upstream genes on the same coding strand in most genomes are significantly higher i
27  asymmetry, an excess of G+T over A+C on the coding strand, in most genes.
28                     Methylation at +7 on the coding strand increases RFX1 complex formation in gel sh
29 adruplex-forming sequences (PQS) in promoter-coding strands, initiating base excision repair (BER) by
30 roblasts contains minimal methylation on the coding strand (<4%) with variable methylation on the tem
31 rays to determine the genomic boundaries and coding strand of 153 RNS-induced transcripts.
32 rallel and anti-parallel readings of the non-coding strand of DNA have displayed biological activity,
33  are defined as those generated from the non-coding strand of DNA, and represent a peptide analog to
34 ignificant repression of quadruplexes in the coding strand of exonic regions, which suggests that qua
35  adducts located in the template but not the coding strand of genes block elongation by RNA polymeras
36 ithin intergenic regions and on the opposite coding strand of known ORFs.
37 the first time, oriented antiparallel to the coding strand of L1 open reading frame-1.
38                      When CAG is in the ADE2 coding strand of strains harboring the ARS, the repeat t
39                      When CTG is in the ADE2 coding strand of strains harboring the ARS, the repeat t
40 ated DNA strand breaks induced by CPT in the coding strand of the 18S rRNA gene of human colon carcin
41 clear proteins that bind specifically to the coding strand of the 47-base pair enhancer and suppress
42 sion positioned at codon 60 or 61 of the non-coding strand of the human c-Ha- ras1 gene were inserted
43                 Here we show that the A-rich coding strand of the human LINE-1 contains multiple func
44                                          The coding strand of the survivin gene was extensively compl
45  that specifically interacts with the upper (coding) strand of the regulatory element was isolated by
46 ast, any new mutation in the nontranscribed (coding) strand remains unexpressed until the cells enter
47                       crRNAs that target the coding strand repress expression only down to 88%, where
48 r reverse orientations packaged noncoding or coding strands, respectively.
49 n beta-globin gene contains an 18-nucleotide coding strand sequence centered at codon 6 and capable o
50            The DNA strand corresponds to the coding strand sequence while the RNA strand represents t
51                              Pyrimidine-rich coding strand sequences were found immediately upstream
52 but an approximately 10-fold higher level of coding strand-specific RNA polymerase II (Pol II)-mediat
53 uced as a DNA form by transformation or as a coding strand transcript by electroporation.
54 rgeting was nine times more effective with a coding strand vector.
55                                Moreover, the coding strand viral RNA levels increased by 33-, 32-, an
56 d the probability of having an undamaged CAT coding strand was calculated by the Poisson distribution
57 ng synthesis of cDNA suggested that only the coding strand was transcribed in vivo.

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