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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
11            We found that Atoh1 binds to a 10 nucleotide motif (AtEAM) to directly regulate genes invo
12   These effects should constrain heavily the nucleotide motif composition of the most abundant mRNAs
13 y cases, the presence of conserved genes and nucleotide motifs confirms the predictions.
14             In a test set of thirty-two 6-20-nucleotide motifs, FARFAR recapitulated 50% of the exper
15         To build this model, we first search nucleotide motifs in a target gene set.
16 f a region with several repeats of 18- or 20-nucleotide motifs in the 5' untranslated region (5' UTR)
17 66 (C6666) 5' of an essential cis -acting 11 nucleotide motif known as the mooring sequence.
18                                       A nine-nucleotide motif located in the 5' untranslated region (
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.
22                         This may explain why nucleotide motif preferences are very similar in transcr
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
25 r flanking sequences, suggesting a divergent nucleotide motif recognition pattern of TLR9.
26                     Here, we identified a 51-nucleotide motif that is present 11.49 times more often
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
30 ion consisting of 38 tandem repeats of a 143-nucleotide motif was detected in M. barkeri.
31                   The sites share the TGAGRG nucleotide motif (where R is A or G).
32                  These findings identify a 5-nucleotide motif within the ica promoter region that has

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