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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
9 T1080 cells stably transfected with the HPR1 antisense gene but was decreased in the cells overexpres
11 ients during early plant development, a VspA antisense gene construct was used to create transgenic p
12 es of GS1 genes in alfalfa, we have utilized antisense gene constructs aimed specifically at the 3'UT
13 stitutive expression of a fruit-specific PME antisense gene does not affect the level of pmeu1 transc
14 ion raises the possibilities that additional antisense genes exist and that the antisense arrangement
16 resistant clones were isolated which contain antisense gene fragments of the translation initiation f
20 "cross-check" siRNA and other approaches to antisense gene inhibition that rely on oligomers with ph
22 Simultaneous expression of paired sense and antisense genes is an essential step and an important in
23 rapeutic strategies targeting both sense and antisense genes may be required for efficacy in HD patie
24 ports our proposal that the short introns of antisense genes might be functionally important and inte
25 mal response time ('nimble' genes), and that antisense genes might be prime candidates for such nimbl
26 ervation of functional human and murine EMX2 antisense genes, of overlap between the sense and the an
30 nsgenic Arabidopsis plants expressing a PEI1 antisense gene produced white seeds in which embryo deve
31 his finding also makes it possible to assess antisense gene regulation efficiency of these brush-DNA
33 c potato plants constitutively expressing an antisense gene sequence for myo-inositol 3-phosphate syn
35 complexes with PPAA-g-PAO copolymers enhance antisense gene silencing effects in A2780 human ovarian
37 off-targets hybrids and the efficacy of the antisense gene silencing, suggesting that the minimizati
38 sly characterized HTLV-3- and HTLV-4-encoded antisense genes, termed APH-3 and APH-4, respectively, w
40 ports future clinical evaluation of TGF-beta antisense gene therapy for TGF-beta-expressing tumors.
41 e would be a prerequisite in considering the antisense gene therapy for the control of hypertension a
45 ion units, including a substantial amount of antisense gene transcription, and 40 genes within the ge
50 one of the marker genes codelivered with the antisense gene, was found to be expressed only in the ab
51 ants constitutively expressing a prosystemin antisense gene were approximately 3 times higher than gr
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