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1  enhance transcription directed by the viral internal promoter.
2 dividing cells, with the proper choice of an internal promoter.
3 activation domain and is synthesized from an internal promoter.
4 transcription factor IIIA (TFIIIA) to the 5S internal promoter.
5 ay also be transcribed independently from an internal promoter.
6 f human L1 (L1Hs) houses a poorly understood internal promoter.
7 lternative transcription initiation using an internal promoter.
8 the native 5'-flanking region in addition to internal promoter.
9 not produced because of the activation of an internal promoter.
10 iption of this gene is controlled by a novel internal promoter.
11 d from the simian foamy virus type 1 (SFV-1) internal promoter.
12 rs to result from the use of an alternative, internal promoter.
13 nnrT and nnrU genes can be expressed from an internal promoter.
14  domain-lacking product, EVI1, because of an internal promoter.
15 ophin-gene products are also transcribed via internal promoters.
16 chia coli have been reported to also contain internal promoters.
17  genes may be independently transcribed from internal promoters.
18 operon can be independently transcribed from internal promoters.
19 ne, RIM2beta and 2gamma are transcribed from internal promoters.
20 II transcription from both gene external and internal promoters.
21  levels of gene expression than vectors with internal promoters.
22 provide an alternative to HIV-1 vectors with internal promoters.
23 ap8 operon was much stronger than any of the internal promoters.
24 ges in premature elongation terminations and internal promoters' activity.
25 Interestingly, a wild-type vector without an internal promoter also successfully transduced neurons i
26 ucible form of the gene is expressed from an internal promoter and encodes a novel intracellular form
27                      RIZ2 is generated by an internal promoter and lacks an NH2-terminal motif of RIZ
28         Here we identify the location of the internal promoter and provide information on how this pr
29 ed regions in transcripts initiated from the internal promoter and the long terminal repeat is sugges
30 minal repeat (non-LTR) retrotransposons lack internal promoters and are co-transcribed with their hos
31        This transcription unit features both internal promoters and internal polyadenylation signals,
32 ession patterns that suggest the presence of internal promoters and regulatory sequences in the opero
33 n male-specific PKD and core IL2 neurons via internal promoters and remote enhancer elements located
34 ed to the prototype SFV-3 sequence, the LTR, internal promoter, and FV transactivator (ORF-1) showed
35 ed as a large operon with at least five weak internal promoters, and the long polycistronic transcrip
36                Instead, we found a conserved internal promoter at the precise position where divergen
37 the Bel-1 target site located within the HFV internal promoter binds Bel-1 with a significantly highe
38   Furthermore, the unique arrangement of the internal promoter boxes (one A and two B boxes) is conse
39                   The presence of additional internal promoters cannot be excluded.
40                Retroviral vectors containing internal promoters, chromatin insulators, and self-inact
41               A short form, expressed via an internal promoter, consists solely of the Atrophin domai
42 onse in vivo when substituted into the SFV-1 internal promoter context.
43 whereas transcription that originates at the internal promoter creates transcripts that receive SL1.
44 s: (1) alternative splicing, (2) whether the internal promoter Cronos isoform was disrupted, and (3)
45              In addition, we showed that the internal promoters, despite their weak activities, were
46 rily in body-wall and pharyngeal muscle, one internal promoter directing expression of UNC-89-C prima
47 -89-C primarily in body-wall muscle, and one internal promoter directing expression of UNC-89-D prima
48               The possible roles of the CRII internal promoter element in paramyxovirus RNA replicati
49 pment: this zinc finger protein binds to the internal promoter element of the 5 S ribosomal RNA genes
50 nscription factor IIIA (TFIIIA) binds to the internal promoter element of the 5 S rRNA gene through n
51 binding site for Bel-1, derived from the HFV internal promoter element, and show that this short DNA
52 mmalian systems, which depend principally on internal promoter elements for tRNA gene transcription,
53  is required for transcription of genes with internal promoter elements, and contains TBP, a TFIIIB"
54 DNA binding sites located in the HFV LTR and internal promoter elements.
55 een the 5' long terminal repeat (LTR) and an internal promoter for the neomycin (neo) gene, so that t
56 sion of a short PAX6 isoform derived from an internal promoter in a multicopy YAC transgenic line res
57 native transcript is due to activation of an internal promoter in chondrocytes and have identified a
58        Transcripts 3 and 4 originate from an internal promoter in intron 2 and either include or lack
59 The chick type III collagen gene contains an internal promoter in intron 23 in addition to the promot
60                        It is encoded from an internal promoter in the ATX1 locus as an isoform contai
61           The biological significance of the internal promoter in the eIF4G mRNA might lie in the pro
62 on could have been due to the presence of an internal promoter in the fliF gene or in the Tn5G transp
63 nt (PRE) linked to the IAB8 enhancer, and an internal promoter in the iab-8 domain, which transcribes
64 sactivation of the simian foamy virus type 1 internal promoter in which Tas interacts directly with t
65 criptional terminators and identifies active internal promoters in this normally highly conserved clu
66 er in the long terminal repeat (LTR) and the internal promoter (IP) located within the env gene of th
67 g three consensus AP-1 binding sites, and an internal promoter (IP) within the env gene.
68 cond promoter within the env gene termed the internal promoter (IP).
69 e MIE promoter, the distal promoter, and the internal promoter, iP2, are dependent upon AP-1 recruitm
70 tic explanation for the observation that the internal promoter is activated significantly earlier tha
71                                          The internal promoter is located in an intron removed from t
72 ter and enhancer elements indicates that the internal promoter is not regulated in a manner similar t
73                       We show below that the internal promoter is regulated by an activation element
74 ocated immediately 5' to the TATA box in the internal promoter, is required for transactivation by Ta
75                                      Another internal promoter lay in the secG-yvaK intercistronic re
76 pts and showed that they were produced by an internal promoter located at the 5' boundary of coding e
77 transposition requires transcription from an internal promoter located within its 5'-untranslated reg
78 ong terminal repeat and the newly discovered internal promoter located within the env gene.
79  the viral structural proteins, and a second internal promoter, located towards the 3' end of the env
80 trength, number, and positioning of operons' internal promoters might have evolved to compensate for
81               Additionally, TFIIIA binds the internal promoter of the 5S RNA gene and supports assemb
82 IIIA) to its cognate DNA sequence within the internal promoter of the gene.
83 ated and characterized both the upstream and internal promoters of this gene and tested their ability
84 ce element insertions that activated cryptic internal promoters or provided new promoters, and large
85 , we conducted sequence analysis of the LTR, internal promoter, ORF-1, and ORF-2 on a tissue culture
86 c operon, whereas EcaR directly activates an internal promoter (P(wecE)) to induce downstream gene ex
87                              A non-canonical internal promoter, P2, was found in the first intron tha
88  contexts, we highlight a mechanism by which internal promoters participate in Itga2b regulation.
89 d sequence in intron 5 of Tcf7l2 conceals an internal promoter region that, when activated by Vax2, d
90 in human tRNA isodecoder genes occurs in the internal promoter regions for RNA polymerase III.
91                          The activity of the internal promoter relies on the integrity of a polypyrim
92 terized nas operon promoter but also from an internal promoter residing between the nasC and nasD gen
93 endent on a combination of both external and internal promoter sequence elements.
94 ons in the D arm were mutated to generate an internal promoter sequence, and the mutRNA(UCA)(Trp) gen
95 s in transcription linked to the creation of internal promoter sites.
96            Surprisingly, the wild-type SFV-1 internal promoter Tas DNA binding site fails to conform
97    This region functions as a Vax2-activated internal promoter that drives the expression of dnTcf7l2
98 , we report that the IL-1R1 gene contains an internal promoter that drives the transcription of a sho
99 traditionally studied organisms rely on gene-internal promoters that precisely position the initiatio
100                    The vectors used included internal promoters that substantially improved proviral
101  vectors almost universally use heterologous internal promoters to express transgenes.
102 a (which use an enhancer-independent cryptic internal promoter) translocations.
103  transcript resulting from activation of the internal promoter turns over relatively rapidly; thus, t
104 moter upstream of the operon and by a second internal promoter upstream of the salKRZ genes.
105                                 We annotated internal promoter usage in operons using SL1 and SL2 dat
106 promoter preceded ilvB-ilvN, and a potential internal promoter was found upstream of ilvN.
107         In addition, a potential alternative internal promoter was revealed to initiate at least two
108 e stem cell virus long terminal repeat as an internal promoter was subsequently assessed during in vi
109 sertion, and relocation, but the presence of internal promoters was not found to facilitate operon lo
110                                              Internal promoters were detected using the 5' rapid ampl
111                                          The internal promoter, which is used preferentially in cultu
112 e promoter in the long terminal repeat or an internal promoter, which we believe indicates that many
113  showed that BMRF2 is expressed from a novel internal promoter within the BMRF1 coding region.
114 A transcription was occurring, suggesting an internal promoter within the operon.
115 lding on our recent discovery of a conserved internal promoter within the Titin gene, we sought to de

 
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