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1 ng region to a 2474-nucleotide region of the intergenic sequence.
2 oughly proportional to the ratio of genic to intergenic sequence.
3 replace, or enhance transcription from, the intergenic sequence.
4 meric signaling motif, originally called the intergenic sequence.
5 t sites, one of which was located within the intergenic sequence.
6 ic fusion sites, none possessing a canonical intergenic sequence.
7 to that of randomly selected, untranscribed intergenic sequences.
8 cleosomes at the interface between genic and intergenic sequences.
9 nes, pseudogenes, repeats, and nonrepetitive intergenic sequences.
10 nant analysis model to distinguish PETs from intergenic sequences.
11 ut the genome, including both the coding and intergenic sequences.
12 Cs are then extended to account for flanking intergenic sequences.
13 ession for 41% of the probes in intronic and intergenic sequences.
14 e-wide codon bias may also be predicted from intergenic sequences.
15 h of these parameters may be calculated from intergenic sequences.
16 introns contain significantly less SNPs than intergenic sequences.
17 lar protein and to reflect the extent of the intergenic sequences.
18 the tricross logic is inherently specific to intergenic sequences.
19 and tools, much remains to be discovered in 'intergenic' sequences.
21 bind in vitro to the negative strand of the intergenic sequence, a cis-acting element found in the l
22 ice MULEs capture guanine-cytosine (GC)-rich intergenic sequences, albeit at a much lower frequency.
23 cetyltransferase (CAT) gene placed behind an intergenic sequence and a 3'-end sequence with various d
24 lication of an HPIV3 minireplicon, while the intergenic sequence and N gene start signal (IS/Ngs, bas
26 tified clusters of conserved region-specific intergenic sequences and have verified our assembly by g
27 th 1.2 kb of 5' flanking sequence, 1.1 kb of intergenic sequence, and the whole TNF-alpha gene with 3
29 We used a fine mapping approach to show that intergenic sequences approximately 58-69 kb 5' to the tb
31 show that substitutions in long introns and intergenic sequences are clustered, such that there is a
32 which occurs in no more than six chloroplast intergenic sequences, are significantly shared by promot
33 downstream mRNA synthesis, thus defining the intergenic sequence as an essential sequence element of
36 ransformed Arabidopsis plants harboring this intergenic sequence between head-to-head oriented green
39 of the ribosomal DNA (rDNA) repeats and the intergenic sequence between the locus encoding the secon
40 y four residues (U4 tract) and a 22-base M-F intergenic sequence between the M gene end and F gene st
41 A region of high acetylation located in the intergenic sequences between HLA-DRB1 and HLA-DQA1 was d
42 cale comparative analysis of slowly evolving intergenic sequences can provide valuable insights into
43 ns: Our results show that most NETs resemble intergenic sequences, casting doubts on the quality of s
45 uirements for the search, tricross found 101 intergenic sequences conserved among the three organisms
48 the researcher to query gene data as well as intergenic sequence data based on a number of criteria.
49 I apply the method to recently collected intergenic sequence data from humans and the great apes.
52 tions in cancer have identified mutations in intergenic sequences encoding regulatory elements-and in
53 ta suggest that the polymerase "samples" the intergenic sequences following polyadenylation and termi
55 ulation occurred preferentially at conserved intergenic sequences, frequently near genes regulating p
56 ctive interfering (DI) RNA that contained an intergenic sequence from which subgenomic DI RNA is synt
58 14), which contained a different foreign M-F intergenic sequence, grew to similar or slightly higher
62 ence time in the coding sequences (CDSs) and intergenic sequences (IGSs) is the same between human an
65 is study we further assessed the role of the intergenic sequence in the transcriptional regulation of
66 ficial sequences that are modeled after real intergenic sequences in terms of composition, complexity
67 frequencies of NETs are similar to those of intergenic sequences in the genome, and they differ from
68 hly diverse, complex assemblies of conserved intergenic sequences (including genes hicA and hicB) wit
69 re also distinctly nonrandom with respect to intergenic sequences, including a strong bias toward mic
70 ived from the 5' prophage whereas most of an intergenic sequence, intergenic region 1, is always deri
72 duction near genes compared with the rest of intergenic sequences is greater in a species with larger
73 distribution of insertions between ORFs and intergenic sequences is roughly proportional to the rati
74 n gene organization, and the presence of the intergenic sequences is verified by reverse transcriptio
75 t is positively correlated with intronic and intergenic sequence length and is generally remarkably s
77 directs human meiotic crossover hot spots to intergenic sequence motifs, whereas budding yeast hot sp
78 y developed to facilitate the examination of intergenic sequences, none of the tricross logic is inhe
79 ded that there are unlikely motifs shared by intergenic sequences of most of chloroplast genes, indic
81 roteins tend to be partially duplicated, and intergenic sequences or neighboring genes are included i
82 dinucleotide combinations, single nucleotide intergenic sequences, or no intergenic sequence at all.
84 utative mammary-specific enhancer within the intergenic sequences separating the two Stat5 genes.
85 d gene starts, gene stops, and trinucleotide intergenic sequences similar to those in paramyxoviruses
86 to unicellular eukaryotes due to the larger intergenic sequence space and the increased complexity i
88 gapless coverage over gene space as well as intergenic sequences such as centromeres, telomeres, tra
89 ng patterns and regions of protection on the intergenic sequence, suggesting that MsvR may play a rol
91 uit fly Drosophila melanogaster relies on an intergenic sequence termed the IRER (irradiation-respons
92 s susceptible to intrinsic termination at an intergenic sequence that conforms to a bacterial intrins
93 ato golden mosaic virus (TGMV) contains a 5' intergenic sequence that includes the overlapping AL61 p
95 (76%) of the insertions were distributed in intergenic sequences that contained 31% of the promoters
96 TTTT (T(8)) and was reduced >70% by archaeal intergenic sequences that contained oligo(T) sequences.
97 t retrotransposons, MuDR DNA transposons and intergenic sequences that contribute to the 47.8-kb size
99 f genomic loci (encompassing both intra- and intergenic sequences) that are required or beneficial fo
100 des with gamma1 and gamma2 loci separated by intergenic sequences (the fifth clade being the cebid ma
101 cognized by Rap1 is found in both coding and intergenic sequences, the binding of Rap1 to the genome
102 s within the plasmid-encoded ureRp and ureDp intergenic sequences to regions of 68 bp and 86 bp, resp
104 d tRNA(Leu) transcripts with a 59-nucleotide intergenic sequence were identified by reverse transcrip
107 fragmented, lacking skewed GC and repetitive intergenic sequences, which are gaining importance due t
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