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1 , we also noted editing within a specific 13 nucleotide motif.
2 nmt1) is governed by the presence of a three-nucleotide motif.
3 promoter is unaffected by deletion of the 5-nucleotide motif.
4 ment is flanked by duplications of an AAGGCT nucleotide motif.
5 refore is insufficient to fully characterize nucleotide motifs.
6 to a sum of energies assigned to individual nucleotide motifs.
7 ty and extensive repetition of in-frame CDR3 nucleotide motifs.
8 ethylation, mainly at symmetrical CG and CHG nucleotide motifs.
9 within these substrates revealed a conserved nucleotide motif 5' of the tagging site, which is requir
10 e P RNA and group I and II introns, this six-nucleotide motif adopts a distinctive local structure th
12 These effects should constrain heavily the nucleotide motif composition of the most abundant mRNAs
16 f a region with several repeats of 18- or 20-nucleotide motifs in the 5' untranslated region (5' UTR)
19 ave a high proportion of their CpG and CpNpG nucleotide motifs modified with 5-methylcytosine (5mC).
20 nd use this to identify the integration site nucleotide motifs of five retroviruses of different gene
21 caused by either selection against specific nucleotide motifs or context-dependent mutation biases.
23 s, we identified an evolutionarily conserved nucleotide motif present in slr-2 stress-responsive gene
24 uggest the ability for a divergent synthetic nucleotide motif recognition pattern of the receptor inv
27 eophylline-binding RNA aptamer contains a 15 nucleotide motif that is required for high-affinity liga
28 quence of the existence of a non-palindromic nucleotide motif that occurs in approximately equal prop
29 al excess of mutations within a novel hybrid nucleotide motif: the signature of somatic hypermutation
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