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1 s affected only by downregulation of RORC by RNA-mediated interference.
2 les and loss-of-function screening by way of RNA-mediated interference.
3 cell cycle functions after gene silencing by RNA-mediated interference.
4 gous to vertebrate endocytosis factors using RNA-mediated interference.
5 or (AHR) or the transcription factor RORC by RNA-mediated interference affected IL-22 production, whe
6 pressing dCBP and reduced by double-stranded RNA-mediated interference against dCBP.
7             Depletion of endogenous CHO1 via RNA-mediated interference also affected the formation of
8 x to bacterial internalization was tested by RNA-mediated interference and identified known component
9 es of functional genomics data gathered from RNA-mediated interference and yeast two-hybrid analyses
10                   Furthermore, delta-catenin RNA-mediated interference can block the induction of den
11  is an essential gene, since inactivation by RNA-mediated interference causes worms to arrest early i
12 1-overexpressing clones using PELP1-specific RNA-mediated interference compromised the susceptibility
13  macrophages in which TREX1 was inhibited by RNA-mediated interference, cytosolic HIV DNA accumulated
14                       Silencing myosin Vb by RNA-mediated interference decreased the expression of wi
15            Functional characterization using RNA-mediated interference demonstrated that over forty o
16 pressed with GLD-1; (2) they can have mutant/RNA-mediated interference depletion phenotypes indicatin
17 by either pharmacologic inhibition of Src or RNA-mediated interference-directed knockdown leads to a
18                                              RNA-mediated interference experiments in C. elegans show
19                                              RNA-mediated interference experiments indicated that a c
20                                              RNA-mediated interference has been one major approach fo
21 s in which Hck expression was silenced using RNA-mediated interference (Hck shRNA).
22 g C10orf22 in HepG2/C3A cells was reduced by RNA-mediated interference, hypotaurine production decrea
23                                              RNA-mediated interference in C. elegans embryos shows th
24 ch and that removal of kuzbanian activity by RNA-mediated interference in Drosophila tissue culture c
25                       Inhibition of SOCS1 by RNA-mediated interference in the HTLV-1-transformed cell
26  that of TFH cells, and depletion of Id2 via RNA-mediated interference increased the frequency of TFH
27                                              RNA-mediated interference indicates a requirement for nh
28 cies produces a single homolog of FOG-3, and RNA-mediated interference indicates that FOG-3 functions
29     We show that a decrease in SPP levels by RNA-mediated interference inhibits heavy-chain dislocati
30                  miRNAs are processed by the RNA-mediated interference machinery.
31 ction; specifically, gene ablation of CBP by RNA-mediated interference markedly reduces the E3 ubiqui
32 acking nanos function were derived either by RNA-mediated interference (nos-1 and nos-2) or by use of
33                                              RNA-mediated interference of Ce-grh-1 results in embryon
34                 Here, we use double-stranded RNA-mediated interference of gene expression to reveal t
35      Murr1 was detected in CD4+ T cells, and RNA-mediated interference of Murr1 in primary resting CD
36 ved inhibitor of p53; inhibition of iASPP by RNA-mediated interference or antisense RNA in C. elegans
37  opposite to the known roles of Piwi and the RNA-mediated interference pathway in epigenetic silencin
38 d so far, possesses components of a putative RNA-mediated interference pathway, telomere-associated t
39 e RNA processing is fundamental to all small RNA-mediated interference pathways.
40            Disruption of AIR-2 expression by RNA- mediated interference produces entire broods of one
41                           In contrast, Hsp27 RNA-mediated interference promoted Akt inactivation duri
42     In contrast, Hsp27 down-regulation using RNA-mediated interference promoted Bax activation, incre
43                  Loss of HCP-4 expression by RNA-mediated interference resulted in a failure to gener
44 s associated histone-modifying activities by RNA-mediated interference resulted in alterations of his
45 -4A biosynthesis by ectopic expression or by RNA-mediated interference resulted in alterations of the
46                     Inactivation of etr-1 by RNA-mediated interference resulted in embryonic lethalit
47 tment, and reduction of Syk expression using RNA-mediated interference results in a specific and mass
48       Inhibition of elt-5 and -6 function by RNA-mediated interference results in penetrant late embr
49              Disruption of son-1 function by RNA-mediated interference results in the same spicule de
50                                Here, we used RNA mediated interference (RNAi) to determine the functi
51 s-6 activity caused by a genetic mutation or RNA-mediated interference (RNAi) affects normal DNA degr
52 dence has demonstrated that the mechanism of RNA-mediated interference (RNAi) can be exploited to ach
53                                         This RNA-mediated interference (RNAi) can be inherited for mo
54 ells in G1, while reducing cki-1 activity by RNA-mediated interference (RNAi) causes extra larval cel
55                              Double-stranded RNA-mediated interference (RNAi) has recently emerged as
56                                              RNA-mediated interference (RNAi) inactivation of a repre
57                                              RNA-mediated interference (RNAi) is a conserved mechanis
58                                              RNA-mediated interference (RNAi) is a recently discovere
59                                     Although RNA-mediated interference (RNAi) is a widely conserved p
60  demonstrate the efficacy of double-stranded RNA-mediated interference (RNAi) of gene expression in g
61 nction by dominant-negative LINGO-1, LINGO-1 RNA-mediated interference (RNAi) or soluble human LINGO-
62                                              RNA-mediated interference (RNAi) reveals the GLHs are cr
63               Here we describe a genome-wide RNA-mediated interference (RNAi) screen for genes that m
64                          Using a genome-wide RNA-mediated interference (RNAi) screen, we identified t
65 ed by gene knockout, ribozyme, antisense, or RNA-mediated interference (RNAi) technologies.
66 h plants or Caenorhabditis elegans could use RNA-mediated interference (RNAi) technology to gain insi
67                                 We have used RNA-mediated interference (RNAi) to analyze the phenotyp
68                                     By using RNA-mediated interference (RNAi) to disrupt the expressi
69  have relied on non-conditional mutations or RNA-mediated interference (RNAi) to inactivate AIR-2.
70 nd embryonic polarity in C. elegans, we used RNA-mediated interference (RNAi) to inhibit cdc-42 activ
71 he genome of Caenorhabditis elegans and used RNA-mediated interference (RNAi) to investigate their ro
72 the spindle and the cleavage furrow, we used RNA-mediated interference (RNAi) to study the effects of
73                            Here we have used RNA-mediated interference (RNAi) to target nearly 90% of
74 ional components in the MES pathway, we used RNA-mediated interference (RNAi) to test candidate genes
75                                           In RNA-mediated interference (RNAi), double-stranded RNAs (
76                                           In RNA-mediated interference (RNAi), externally provided mi
77  silencing of the dominant disease allele by RNA-mediated interference (RNAi), for the arrest--and po
78                        Using double-stranded RNA-mediated interference (RNAi), the role of protein ph
79                          Here we describe an RNA-mediated interference (RNAi)-based approach to disco
80                                The advent of RNA-mediated interference (RNAi)-based functional genomi
81 ree Arls (Arl-1, Arl-2, and Arl-3) by use of RNA-mediated interference (RNAi).
82 argets by precise complementarity and elicit RNA-mediated interference (RNAi).
83                   We performed a genome-wide RNA-mediated interference screen in a Drosophila cell li
84 esponse events with a high-content multiplex RNA-mediated interference screen of chromatin-modifying
85  chemoattractant-guided migration, we did an RNA-mediated interference screen that identified several
86                                     Using an RNA-mediated interference screen, we identified phosphol
87                                     Using an RNA-mediated interference screen, we identified the WNK1
88  in combination with data from a genome-wide RNA-mediated interference screen.
89  studies have taken advantage of genome-wide RNA-mediated interference screening in drosophila cells,
90 tion of endogenous Cdc42 expression by using RNA-mediated interference (short hairpin RNA [shRNA]) se
91                          I have used a novel RNA-mediated interference technique to interfere specifi
92  the expression of CDC-25.1 was disrupted by RNA-mediated interference, the anterior cortical membran
93                                      We used RNA-mediated interference to demonstrate that fog-3 is i
94 ly, depletion of nematode beta-G spectrin by RNA-mediated interference to undetectable levels does no
95                                              RNA-mediated interference was applied to inactivate indi
96                                        Using RNA-mediated interference, we demonstrate modulation of
97 ng a new fly tau loss-of-function allele and RNA-mediated interference, we found that endogenous Tau