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1 ved in cells endogenously overexpressing the antisense gene.
2 iral vector construct containing the RIalpha antisense gene.
3 cible system to express ectopically the WAK4 antisense gene.
4 ted silencing of pmeu1 by a heterologous PME antisense gene.
5 re detected, 257 of which were classified as antisense genes.
6 IO3 gene may lie within the structure of the antisense gene, a complex arrangement often observed in
7 As also significantly associate with natural antisense genes-again, this feature is not observed in l
8 plicating HIV-1-derived vector expressing an antisense gene against the HIV envelope.
9                        Plants expressing the antisense gene also had high endogenous salicylic acid l
10 T1080 cells stably transfected with the HPR1 antisense gene but was decreased in the cells overexpres
11                  The protein product of this antisense gene, called ASP, is poorly characterized, and
12           No transcript corresponding to the antisense gene construct was detected in any of the alfa
13 ients during early plant development, a VspA antisense gene construct was used to create transgenic p
14 es of GS1 genes in alfalfa, we have utilized antisense gene constructs aimed specifically at the 3'UT
15 stitutive expression of a fruit-specific PME antisense gene does not affect the level of pmeu1 transc
16 ion raises the possibilities that additional antisense genes exist and that the antisense arrangement
17                   The discovery of a pair of antisense genes expressed during productive infection ra
18 resistant clones were isolated which contain antisense gene fragments of the translation initiation f
19 al and sexual reproduction by regulating its antisense gene GzmetE through RNAi pathway.
20                          The majority of the antisense genes had a similar effect sizes in an indepen
21                In this article, we show that antisense genes have significantly shorter introns than
22                                    We tested antisense gene inhibition by LNAs and LNA-DNA chimeras c
23  "cross-check" siRNA and other approaches to antisense gene inhibition that rely on oligomers with ph
24          Here we examine the rules governing antisense gene inhibition within cells by oligonucleotid
25  Simultaneous expression of paired sense and antisense genes is an essential step and an important in
26 rapeutic strategies targeting both sense and antisense genes may be required for efficacy in HD patie
27 ports our proposal that the short introns of antisense genes might be functionally important and inte
28 mal response time ('nimble' genes), and that antisense genes might be prime candidates for such nimbl
29 ervation of functional human and murine EMX2 antisense genes, of overlap between the sense and the an
30 s strikingly with that induced by endogenous antisense gene overexpression.
31 interactions between a plasmid encoded sense-antisense gene pair (RNAI and RNAII).
32  be a CT-coding gene/CT-ncRNA pair, or sense-antisense gene pair involved in regulatory interactions.
33 sis that may be applied to other natural cis-antisense gene pairs in eukaryotic genomes.
34          In this study, protein-coding sense-antisense gene pairs were analyzed with a particular foc
35 lso deregulated in 42% of the observed sense-antisense gene pairs.
36 ibited by the product of a small overlapping antisense gene previously believed to encode an excision
37 nsgenic Arabidopsis plants expressing a PEI1 antisense gene produced white seeds in which embryo deve
38 his finding also makes it possible to assess antisense gene regulation efficiency of these brush-DNA
39           The induced expression of the WAK4 antisense gene resulted in a significant decrease of WAK
40 c potato plants constitutively expressing an antisense gene sequence for myo-inositol 3-phosphate syn
41                              The adoption of antisense gene silencing as a novel disinfectant for pro
42 complexes with PPAA-g-PAO copolymers enhance antisense gene silencing effects in A2780 human ovarian
43 ization of off-targets may be beneficial for antisense gene silencing in prokaryotic organisms.
44  off-targets hybrids and the efficacy of the antisense gene silencing, suggesting that the minimizati
45 sly characterized HTLV-3- and HTLV-4-encoded antisense genes, termed APH-3 and APH-4, respectively, w
46                        Mammalian APeg3 is an antisense gene that is localized within the 3'-untransla
47 ports future clinical evaluation of TGF-beta antisense gene therapy for TGF-beta-expressing tumors.
48 e would be a prerequisite in considering the antisense gene therapy for the control of hypertension a
49 tor in the efficacy of oligonucleotide-based antisense gene therapy.
50 which maps to the RP11-634B7.4 gene, a novel antisense gene to three olfactory receptor genes.
51  potential of antisense RNA transcribed from antisense genes to interfere with HBV replication.
52 ion units, including a substantial amount of antisense gene transcription, and 40 genes within the ge
53                                          The antisense gene Tsix determines X chromosome choice and r
54                We have hypothesized that the antisense gene, Tsix, controls Xist expression.
55              Xist action is repressed by the antisense gene, Tsix, whose full-length RNA product is c
56 -specific transcript), and is blocked by the antisense gene, Tsix.
57 one of the marker genes codelivered with the antisense gene, was found to be expressed only in the ab
58 ants constitutively expressing a prosystemin antisense gene were approximately 3 times higher than gr
59      Sense genes expressed opposite of these antisense genes were also deregulated in 42% of the obse
60                 Transgenic plants containing antisense genes were generated to decipher E6 function.