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1 on of fluorescence signal from MBs targeting nontranslated 28S rRNA remained the same in normal and t
2 g short hairpin RNA (shRNA) targeting the 5' nontranslated conserved region of the HCV genome for inh
3 by the presence of an Alu sequence in the 3' nontranslated end of the longer species.
4 element (+20 to +40) is located in the first nontranslated exon of the human apoB gene, and apoB regu
5                  The 17 coding exons and two nontranslated exons of TSRC1 span 10 kb of genomic DNA.
6 lysome-bound (translated) and polysome-free (nontranslated) fractions by sucrose density centrifugati
7 anscripts containing wild-type or mutated 5' nontranslated GBV-B RNA (5'NTR) segments, placed between
8 ied from a genome-internal site, into the 5'-nontranslated genomic region (mono-crePV).
9                                              Nontranslated intergenic regions (IGRs) compose 10-15% o
10 retrotransposon and sequences similar to the nontranslated leader sequence of AT-P5C1, a gene for pyr
11                                  In oocytes, nontranslated maternal mRNAs are packaged by protein int
12  biological studies reporting high levels of nontranslated mRNA during early embryonic development.
13 ted with the production of a group of small, nontranslated, polyadenylylated RNAs (POLADS) produced d
14 aged or whether genomic packaging requires a nontranslated population of RNAs.
15 green fluorescent protein expressed from the nontranslated portions of BMV RNA1 and RNA2, suggesting
16                                       The 3' nontranslated region (3'NTR) of the SIN genome carries m
17 mechanism of RNA-RNA recombination at the 3' nontranslated region (3'NTR) of the Sindbis virus (SIN)
18 hat we have identified as a binder of HCV 3' nontranslated region (3'NTR).
19 ardiovirulence phenotype localizes to the 5' nontranslated region (5' NTR).
20            The regions sequenced were the 5'-nontranslated region (5'-NTR) (350 nucleotides [nt]), ca
21 g all but the first eight residues of the 5' nontranslated region (5'NTR) of HCV, resulted in a letha
22 nce replaced an analogous sequence in the 5' nontranslated region (5'NTR) of the GBV-B genome.
23 ssay targets the conserved regions in the 5' nontranslated region (5'NTR) of the parechovirus genome
24 he viral genome contains a highly structured nontranslated region (5'NTR) which folds to form an inte
25  sequence differences observed within the 5' nontranslated region (NTR) and 3' NTR were predicted to
26                           The enterovirus 5' nontranslated region (NTR) contains an internal ribosome
27                                       The 3' nontranslated region (NTR) contains several of these ele
28 nternal ribosome entry site (IRES) in the 5' nontranslated region (NTR) has been implicated as a cis-
29                                       The 5'-nontranslated region (NTR) of hepatitis C virus (HCV) co
30  Chimeric poliovirus RNAs, possessing the 5' nontranslated region (NTR) of hepatitis C virus in place
31                          Furthermore, the 3' nontranslated region (NTR) of RNA 3 constituted a hot sp
32 y analyses with the coat protein (CP) and 5' nontranslated region (NTR) of RNA 3 suggested subdivisio
33 n all regions of the genome except in the 5'-nontranslated region (NTR), where they are known to clus
34 s RNA genome is flanked at either end with a nontranslated region (NTR).
35 psid protein (CP)-coding sequence and the 3' nontranslated region (NTR).
36 onserved regions of the GBV-C genome (the 5' nontranslated region and the nonstructural protein-codin
37 ent locations in the genome including the 5' nontranslated region and within the open reading frame.
38             Our results show that the HCV 3' nontranslated region consists of four elements (positive
39                      Mutations within the 5' nontranslated region demonstrated that the CPm origin of
40 which the NS3 ORF is preceded only by the 5' nontranslated region did not replicate to detectable lev
41 ncluding those derived from the structured 3'nontranslated region highly potent for RIG-I activation,
42                           The role of the 5' nontranslated region in the replication of hepatitis A v
43                              The observed 5' nontranslated region mutation rate in this patient ( app
44                                         A 3' nontranslated region mutation which inhibited negative-s
45               Sequences from the putative 5' nontranslated region of GB virus A were isolated from my
46 al ribosomal entry site (IRES) within the 5' nontranslated region of its genome.
47                                       The 5' nontranslated region of poliovirus RNA contains two high
48 al ribosomal entry site (IRES) within the 5' nontranslated region of PV with its counterpart from hum
49      All adapting mutations mapped to the 5'-nontranslated region of PV1(RIPO).
50 es of genomic regions 2b, CP, MP, and the 3' nontranslated region of RNA3.
51  multiple instability elements within the 3'-nontranslated region of the GA mRNA and mediate its pH-r
52 ong poly(C) tracts (61 to 146 C's) at the 5' nontranslated region of the genome, and variants of thes
53                                       The 3' nontranslated region of the genomes of Sindbis virus (SI
54 epeat of an 8-base AU sequence within the 3'-nontranslated region of the glutaminase mRNA binds a uni
55                   Various segments of the 3'-nontranslated region of the renal glutaminase (GA) mRNA
56 ogenicity depends on sequences within the 5' nontranslated region of the virus.
57 ) 29 or a deletion up to nt 40 in the HCV 5' nontranslated region relieved the replication block, yie
58 ghtly more sensitive than our in-house EV 5' nontranslated region RT-snPCR assay, detecting as few as
59 e was constructed in which the poliovirus 5' nontranslated region was fused to the gene encoding luci
60                                       The 5' nontranslated region was the target for all of the PCR a
61 icons spanning 496 nucleotides within the 5' nontranslated region were generated directly from the ce
62 ve (or incomplete) mRNA processing in the 5'-nontranslated region, a phenomenon found in analysis of
63 e to elements in the intron, the flanking 3'-nontranslated region, or to elements existing even farth
64 es downstream of the parental or chimeric 5' nontranslated region, viral capsid antigens were synthes
65 nternal ribosome entry site (IRES) in the 5'-nontranslated region, were found to be involved in the o
66  both the 6K and E1 genes, as well as the 3' nontranslated region, were replaced with the correspondi
67 etween RHA and the S fragment in the FMDV 5' nontranslated region.
68 e 5' terminus, 2C helicase, ORF2, and the 3' nontranslated region.
69 at eight codons and one nucleotide in the 5' nontranslated region.
70 al ribosomal entry site (IRES) within its 5' nontranslated region.
71                                       The 3' nontranslated regions (3'NTRs) of reovirus mRNAs contain
72 e-sense RNA viruses, the 3'- and 5'-terminal nontranslated regions (NTRs) of the BUNV S, M, and L seg
73 is-replicating RNA elements in the 5' and 3' nontranslated regions (NTRs) of the hepatitis C virus (H
74    The three BUNV segments possess 3' and 5' nontranslated regions (NTRs) that signal two RNA synthes
75 from clones containing mutations in their 5' nontranslated regions (NTRs) were assayed for RNA produc
76 eading frame is flanked by the existing PIV3 nontranslated regions and transcription signals.
77                               Exchange of 5'-nontranslated regions between the two CVB3 strains demon
78 NA sequences and structures in the 5' and 3' nontranslated regions of poliovirus RNA interact with ho
79                          Alignment of the 5' nontranslated regions of RNA 3 for 26 strains of CMV sug
80 in (E) gene and/or replacement of 5'- and 3'-nontranslated regions on dengue virus replication in hum
81 dification) in cloned, terminally deleted 5'-nontranslated regions were confined to the cloverleaf do
82 em-loop structures located in the 5'- and 3'-nontranslated regions, genome replication of picornaviru
83 hough both viruses appear to contain long 5' nontranslated regions, the sites of polyprotein initiati
84 rises elements within both the 3' and the 5' nontranslated regions.
85 rved among related Flavivirus and Pestivirus nontranslated regions.
86 s with common protein coding but distinct 5' nontranslated regions.
87  We describe a mutational analysis of the 3' nontranslated RNA (3'NTR) signals required for replicati
88                                       The 5' nontranslated RNA (5'NTR) of a genotype 1b hepatitis C v
89                          Mutations in the 5' nontranslated RNA (5'NTR) of an attenuated, cell culture
90 titutions at three sites within the viral 5' nontranslated RNA (5'NTR): G(107)-->A, C(204)-->A, and G
91 In Escherichia coli, the gcvB gene encodes a nontranslated RNA (referred to as GcvB) that regulates O
92 e presence of at least 523 nucleotides of 5' nontranslated RNA containing multiple AUG codons, sugges
93 acts with two additional sites in the HAV 5'-nontranslated RNA, one located between nucleotides 1-148
94  GTL2 (gene trap locus 2) gene encodes for a nontranslated RNA.
95 ribosomal entry segment (IRES) within the 5'-nontranslated RNA.
96 erase III transcription of genes that encode nontranslated RNAs, potentially to control cell growth.
97 ns, defective interfering RNAs and DNAs, and nontranslated RNAs.
98 ranslation of bicistronic RNAs containing 5' nontranslated sequences within the intercistronic space
99 and EBV nuclear antigens (EBNAs), as well as nontranslated viral RNAs, such as the EBV-encoded small

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