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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  to a sum of energies assigned to individual nucleotide motifs.
6 refore is insufficient to fully characterize nucleotide motifs.
7 ty and extensive repetition of in-frame CDR3 nucleotide motifs.
8 s) are consecutive repetitions of one to six nucleotide motifs.
9 ethylation, mainly at symmetrical CG and CHG nucleotide motifs.
10 within these substrates revealed a conserved nucleotide motif 5' of the tagging site, which is requir
11 e P RNA and group I and II introns, this six-nucleotide motif adopts a distinctive local structure th
12            We found that Atoh1 binds to a 10 nucleotide motif (AtEAM) to directly regulate genes invo
13 am of the target site, named Target Adjacent nucleotide Motif, can promote miRNA cleavage but not miR
14   These effects should constrain heavily the nucleotide motif composition of the most abundant mRNAs
15 y cases, the presence of conserved genes and nucleotide motifs confirms the predictions.
16             In a test set of thirty-two 6-20-nucleotide motifs, FARFAR recapitulated 50% of the exper
17         To build this model, we first search nucleotide motifs in a target gene set.
18 f a region with several repeats of 18- or 20-nucleotide motifs in the 5' untranslated region (5' UTR)
19 66 (C6666) 5' of an essential cis -acting 11 nucleotide motif known as the mooring sequence.
20                                       A nine-nucleotide motif located in the 5' untranslated region (
21 ave a high proportion of their CpG and CpNpG nucleotide motifs modified with 5-methylcytosine (5mC).
22 IC) and Ataxin-1 like (ATXN1L) binds to an 8-nucleotide motif near IFN and ISG promoters and prevents
23 ich merges mutated gene information with tri-nucleotide motif of mutated sites, for colorectal cancer
24 nd use this to identify the integration site nucleotide motifs of five retroviruses of different gene
25  caused by either selection against specific nucleotide motifs or context-dependent mutation biases.
26                         This may explain why nucleotide motif preferences are very similar in transcr
27 s, we identified an evolutionarily conserved nucleotide motif present in slr-2 stress-responsive gene
28                                         A 14 nucleotide motif, present in four copies in P(METE), was
29 uggest the ability for a divergent synthetic nucleotide motif recognition pattern of the receptor inv
30 r flanking sequences, suggesting a divergent nucleotide motif recognition pattern of TLR9.
31            Unique dipeptide-coding uORFs and nucleotide motifs, such as '5'-UGA(C/G)GG-3', are found
32                     Here, we identified a 51-nucleotide motif that is present 11.49 times more often
33 eophylline-binding RNA aptamer contains a 15 nucleotide motif that is required for high-affinity liga
34 quence of the existence of a non-palindromic nucleotide motif that occurs in approximately equal prop
35 al excess of mutations within a novel hybrid nucleotide motif: the signature of somatic hypermutation
36 ion consisting of 38 tandem repeats of a 143-nucleotide motif was detected in M. barkeri.
37                   The sites share the TGAGRG nucleotide motif (where R is A or G).
38                  These findings identify a 5-nucleotide motif within the ica promoter region that has