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1 ignals and a suboptimal context for the Tnp2 translation initiation codon.
2 a 36-nucleotide insertion near the core gene translation initiation codon.
3  is not translated due to the lack of an AUG translation initiation codon.
4 exhibit a homozygous substitution in the AMN translation initiation codon.
5 which is located 1498 bp upstream of the eas translation initiation codon.
6 me reading frame as the unique physiological translation initiation codon.
7 bp upstream from the first nucleotide of the translation initiation codon.
8 bp upstream from the first nucleotide of the translation initiation codon.
9  region and utilizes an ATG in exon 3 as its translation initiation codon.
10 phobic leader sequence closely following the translation initiation codon.
11 tains an in-frame stop-codon and an in-frame translation initiation codon.
12 at this molecule is generated by an internal translation initiation codon.
13 ein was dependent upon an artificially added translation initiation codon.
14 o a position 178 nucleotides upstream of the translation initiation codon.
15  localized 314 bases upstream from the first translation initiation codon.
16 NA signal(s), a process that also requires a translation initiation codon.
17 all have long leader RNAs preceding the Ag43 translation initiation codon.
18 is located 192 nucleotides upstream from the translation initiation codon.
19 is located 182 nucleotides upstream from the translation initiation codon.
20 nd, all four basonuclin mRNA shared the same translation initiation codon.
21 apped to an adenine residue 601 nt 5' of the translation initiation codon.
22 the gene, approximately 2 kb upstream of the translation initiation codon.
23 ertion of the microsatellite upstream of the translation initiation codon.
24 eotides, respectively, upstream from the ATG translation initiation codon.
25 site is an A residue 80 base pairs 5' of the translation initiation codon.
26  5' untranslated region just upstream of the translation initiation codon.
27 start site was tified 146 bp upstream of the translation initiation codon.
28  extended 82 nucleotides downstream from the translation initiation codon.
29 1 bp upstream of the first nucleotide of the translation initiation codon.
30 moter to a region 162-168 bp upstream of the translation initiation codon.
31 as identified 21 nucleotides upstream of the translation initiation codon.
32 tide positions -330 and -93, relative to the translation initiation codon.
33  that precedes the third exon containing the translation initiation codon.
34 f the rpsL mRNA to be 199 bp upstream of the translation initiation codon.
35 ting protein sequence by providing alternate translation initiation codons.
36 e first nucleotide of each of the respective translation initiation codons.
37 nique mRNA by alternative utilization of two translation initiation codons.
38 inding site pattern to refine predictions of translation initiation codons.
39 rnative mRNA splicing and utilization of two translation initiation codons.
40 by functional synonymous variations near the translation initiation codon affect the translation effi
41 42 (human) or 440 (mouse) bp upstream of the translation initiation codon, agreeing with the transcri
42                      Elimination of the uORF translation initiation codon also eliminated Arg-specifi
43                   The first exon encodes the translation initiation codon and a 5' untranslated regio
44 cripts are also produced that lack the first translation initiation codon and rely on a second in-fra
45 is elements for initiation at the downstream translation initiation codon and their inhibitory effect
46  mutations are both in exon 2 and affect the translation initiation codon and/or the secretion of ame
47 HC bound peptides, we identified the non-AUG translation initiation codons and established that their
48 are not found in M. senile mtDNA: unorthodox translation initiation codons and partial translation te
49 ligonucleotides complementary to the 5' NCR, translation initiation codon, and core protein coding se
50 that lacks an ATG triplet to function as the translation initiation codon, and the actual amino termi
51 hich is followed by five nucleotides, an ATG translation initiation codon, and the second open readin
52 he importance of sequences downstream of the translation initiation codon are dependent on the indivi
53 etermine if mRNA sequences downstream of the translation initiation codon are important for translati
54                       The sequence 5' to the translation initiation codon, as a part of the 5' stem-l
55 ation site is located 462 bp upstream of the translation initiation codon ATG as determined by 5'-RAC
56                       Point mutations in the translation initiation codon (ATG-->ATA) and in codon 31
57                                 Two such non-translation initiation codon (AUG)-initiated upstream op
58 ppears to originate solely from the upstream translation initiation codon (AUG-1) residing in exon 2'
59  Human angiotensinogen mRNA has two in-phase translation initiation codons (AUG) starting upstream 39
60 quence and suggests that the bovine tuftelin translation initiation codon be re-assigned to a more 5'
61 d be identified within 800bp upstream of the translation initiation codon, but the 5'-flanking region
62 dent on conversion of an ACG codon to an AUG translation initiation codon by mRNA editing, a safety f
63  to a 57-bp region localized upstream of the translation initiation codon by transfection of reporter
64  for enhancement was not because of upstream translation initiation codons contained in unspliced tra
65                                 Changing the translation initiation codon context substantially incre
66 and is spliced to exon 6, which contains the translation initiation codon corresponding to Met-200 of
67                                          The translation initiation codon for BCL-XL is located in BC
68 tal and a proximal promoter, upstream of the translation initiation codon for GIP.
69  of an ACG codon to an AUG codon creates the translation initiation codon for the psbL and ndhD trans
70    In the K-12 leader sequence, two in-frame translation initiation codons have been identified, one
71 e mouse PRSS17 gene sequence upstream of the translation initiation codon identified two potential tr
72                                     Multiple translation initiation codons in different reading frame
73                          The presence of two translation initiation codons in SPAST allows synthesis
74                           In eukaryotes, the translation initiation codon is generally identified by
75                                      The ATG translation initiation codon is located in exon 2, and t
76                           Recognition of the translation initiation codon is thought to require disso
77 n, which is 17 nucleotides upstream from the translation initiation codon, is conserved, as observed
78                             Re-assigning the translation initiation codon lengthens the tuftelin prot
79 ed that a previously unidentified downstream translation initiation codon located in exon 8 can regul
80 t to link up the gfp* coding region with the translation initiation codon of aadA.
81 we demonstrate that a c.2T>C mutation in the translation initiation codon of KDM5C results in transla
82 le aromatic amino acids were found 5' of the translation initiation codon of TBF1 and shown to affect
83 rom -282 to -264 nucleotides upstream of the translation initiation codon of the CD155 gene, which we
84 dG-dT) oligonucleotide immediately after the translation initiation codon of the enhanced GFP (EGFP)
85  inserted a "lox-stop-lox" (LoxTB) 5' of the translation initiation codon of the mouse Mc3r gene and
86  elements a similar distance upstream of the translation initiation codon of the rpsL gene, but these
87                        In contrast, when the translation initiation codon of the TCV CP was altered t
88 eukaryotic 40S ribosomal subunit locates the translation initiation codon on an mRNA via the so-calle
89 s (RLM-RACE) between -61 and -32 bp from the translation initiation codon.Reverse transcription-PCR a
90                         A mutation in the 1a translation initiation codon significantly decreased RNA
91 capability than the complex that scans for a translation initiation codon since a hairpin structure s
92 out single nucleotide deletions close to the translation initiation codons, that pDEST17 is intrinsic
93 r a small region immediately upstream of the translation initiation codon, there is no obvious sequen
94                                          The translation initiation codon was identified within the s
95 f DNA sequence immediately upstream from the translation initiation codon was not essential for promo
96 able to express vpu due to a mutation in its translation initiation codon, was able to replicate in p
97               The int gene has two alternate translation initiation codons within the extensively ove

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