ライフサイエンスコーパス: RNA-mediated interference

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 recently discovere

58 Although RNA-mediated interference (RNAi) is a widely conserved p

59 demonstrate the efficacy of double-stranded RNA-mediated interference (RNAi) of gene expression in g

60 nction by dominant-negative LINGO-1, LINGO-1 RNA-mediated interference (RNAi) or soluble human LINGO-

61 RNA-mediated interference (RNAi) reveals the GLHs are cr

62 Here we describe a genome-wide RNA-mediated interference (RNAi) screen for genes that m

63 Using a genome-wide RNA-mediated interference (RNAi) screen, we identified t

64 ed by gene knockout, ribozyme, antisense, or RNA-mediated interference (RNAi) technologies.

65 h plants or Caenorhabditis elegans could use RNA-mediated interference (RNAi) technology to gain insi

66 We have used RNA-mediated interference (RNAi) to analyze the phenotyp

67 By using RNA-mediated interference (RNAi) to disrupt the expressi

68 have relied on non-conditional mutations or RNA-mediated interference (RNAi) to inactivate AIR-2.

69 nd embryonic polarity in C. elegans, we used RNA-mediated interference (RNAi) to inhibit cdc-42 activ

70 he genome of Caenorhabditis elegans and used RNA-mediated interference (RNAi) to investigate their ro

71 the spindle and the cleavage furrow, we used RNA-mediated interference (RNAi) to study the effects of

72 Here we have used RNA-mediated interference (RNAi) to target nearly 90% of

73 ional components in the MES pathway, we used RNA-mediated interference (RNAi) to test candidate genes

74 In RNA-mediated interference (RNAi), double-stranded RNAs (

75 In RNA-mediated interference (RNAi), externally provided mi

76 silencing of the dominant disease allele by RNA-mediated interference (RNAi), for the arrest--and po

77 Using double-stranded RNA-mediated interference (RNAi), the role of protein ph

78 Here we describe an RNA-mediated interference (RNAi)-based approach to disco

79 The advent of RNA-mediated interference (RNAi)-based functional genomi

80 ree Arls (Arl-1, Arl-2, and Arl-3) by use of RNA-mediated interference (RNAi).

81 argets by precise complementarity and elicit RNA-mediated interference (RNAi).

82 We performed a genome-wide RNA-mediated interference screen in a Drosophila cell li

83 esponse events with a high-content multiplex RNA-mediated interference screen of chromatin-modifying

84 chemoattractant-guided migration, we did an RNA-mediated interference screen that identified several

85 Using an RNA-mediated interference screen, we identified phosphol

86 Using an RNA-mediated interference screen, we identified the WNK1

87 in combination with data from a genome-wide RNA-mediated interference screen.

88 studies have taken advantage of genome-wide RNA-mediated interference screening in drosophila cells,

89 tion of endogenous Cdc42 expression by using RNA-mediated interference (short hairpin RNA [shRNA]) se

90 I have used a novel RNA-mediated interference technique to interfere specifi

91 the expression of CDC-25.1 was disrupted by RNA-mediated interference, the anterior cortical membran

92 We used RNA-mediated interference to demonstrate that fog-3 is i

93 ly, depletion of nematode beta-G spectrin by RNA-mediated interference to undetectable levels does no

94 RNA-mediated interference was applied to inactivate indi

95 Using RNA-mediated interference, we demonstrate modulation of