ライフサイエンスコーパス: run-off

1 hrough volatilization, leaching, and surface run off.

2 d microbial contaminations through rainwater run-off.

3 he entire coronary length and its peripheral run-off.

4 tion, leaching, denitrification, and surface run-off.

5 hen these pools are washed out during spring run-off.

6 nevitably reach water bodies via leaching or run-off.

7 At the unfamiliar test site, naive ants ran off a longer portion of their vector from path integ

8 source (feeder) to unfamiliar terrain, ants run off a portion of the homeward vector or its entirety

9 The Australian desert ant Melophorus bagoti runs off a smaller portion of its vector if the test sit

10 m2 promoter-reporter gene assays and nuclear run-off analyses of nascent mdm2 transcripts showed that

11 Results from nuclear run-off analysis and mRNA stability studies established

12 nscriptional activity as measured by nuclear run-off analysis at specific stages of spermatogenesis.

13 Nuclear run-off analysis established transcriptional up-regulati

14 o inhibition of transcription, since nuclear run-off analysis showed an approximately 80% decrease in

15 l as to coastal acidification driven by land run off and rising sea level.

16 ntly associated with proximity to freshwater run-off and collection during the wet season.

17 hich will escalate the amount of terrestrial run-off and mechanical disruption affecting coastal ecos

18 ts for elongation factors, allowing ribosome run-off and orderly translation shutdown.

19 scored with modified Rutherford weighting of run-off arteries.

20 These are not formed through replication run off, as we show that mitomycin C or cisplatin-induce

21 anscriptional level as determined by nuclear run-off assay and blocking of the Bt2cAMP-dependent indu

22 The nuclear run-off assay and semiquantitative RT-PCR shows that PCB

23 Using an in vitro replication run-off assay under physiological conditions, the antige

24 A nuclear run-off assay utilizing the unique properties of the DNA

25 As assessed by nuclear run-off assay, CaN19 transcription increased rapidly in

26 nce Correlation Spectroscopy (FCS), ribosome Run-Off Assays (ROA) after Harringtonine application, an

27 Nuclear run-off assays and half-life studies showed that accumul

28 ics, such as cycloheximide, both in ribosome run-off assays and in in vivo experiments.

29 Nuclear run-off assays and transient transfections with a human

30 Nuclear run-off assays and Western immunoblot showed low levels

31 Nuclei run-off assays demonstrated that p16 expression induced

32 Luciferase and nuclear run-off assays demonstrated that p21WAF1/CIP1 is, in par

33 Nuclear run-off assays indicate that this induction is at least

34 RNA stability studies and nuclear run-off assays indicated that acute treatment with FGF-2

35 Nuclear run-off assays revealed increased rates of COX-2 transcr

36 Northern blot analysis and nuclear run-off assays revealed maximum DOR mRNA level and trans

37 Nuclear run-off assays showed that COX-2 transcription rate was

38 Nuclear run-off assays showed that the sGC activator protoporphy

39 g ribonuclease protection assays and nuclear run-off assays, we further determined that PDGF did not

40 Using in vitro transcription run-off assays, we present biochemical evidence that Car

41 lex was highly functional in transcriptional run-off assays.

42 er-luciferase reporter construct and nuclear run-off assays.

43 d salinity in coastal water due to increased run-off can make intertidal bivalves more susceptible to

44 Contamination of surface waters due to run-off, coupled with its moderate solubility in water,

45 ive of 13 colorectal cell lines, and nuclear run-off data indicated reduced transcription was a major

46 were not due to unprocessed transcriptional run-off events.

47 60 fold lower than those reported for urban run-off exhibited significantly longer burrowing times,

48 onse to nicotinic stimulation, and a nuclear run-off experiment indicated that the response occurred

49 anscription activity was observed in nuclear run off experiments, indicating that the increased mRNA

50 Nuclear run-off experiments indicate that enhancement of iNOS by

51 Transient transfection assays and nuclear run-off experiments showed that PMA increased EGF recept

52 By contrast, nuclear run-off experiments using nuclei obtained from Dex-stimu

53 ed that can screen for glyphosate in produce run-off/extract.

54 tressors (for example, sediment and nutrient run-off from agriculture, sewage discharges, dredging, d

55 Run-off from farms and wastewater treatment plant overfl

56 s of MMP-9 promoter activation and a nuclear run-off indicated that neuropeptide induction of MMP-9 e

57 Diastolic run off into the pulmonary circulation and labile corona

58 exogenous agents (e.g. pesticides, nutrient run-off, introduced fishes) might be interacting with Ri

59 synthesis at permissive temperatures, slows run-off of polyribosomes, and reduces binding to eEF1A.

60 rops, with prairie strips arranged to arrest run-off on slopes.

61 socosms, indicating that other components of run-off or other storm effects likely exert a larger inf

62 from the adjacent shelf sea with terrestrial run-off playing a secondary role.

63 7 RNA polymerase synthesizes, in addition to run-off products of precise length, transcripts with an

64 The enzyme predominantly used for in vitro run-off RNA synthesis is bacteriophage T7 RNA polymerase

65 cantly associated with an increased risk for run-off-road crashes (RR, 1.55; 95% CI, 1.21-2.00).

66 eep on weekend nights increased the risk for run-off-road crashes and crashes occurring in the late-n

67 vehicles), crash characteristics (rollover, run-off-road incidents, collisions with trees), temporal

68 Median run-off scores were 5.3 (range, 3-8) and 6.6 (range, 3-9

69 second intron of the nestin gene and nuclear run-off studies show that increases in N-Myc protein up-

70 ciferase reporter gene construct and nuclear run-off studies.

71 Once mobile, the branch point can run off the end of the junction.

72 hich encircles the leading strand template, "runs off" the end of the DSB.

73 slowdown occurs, on average, when a critical run-off threshold of about 1.4 centimetres a day is exce

74 hannel drainage modes is consistent with the run-off threshold, fast-flow periods, and later-summer s

75 rimers both linked to T7 polymerase in vitro run off transcription.

76 Run-off transcription analyses showed that the rate of t

77 ion and to stimulate ackA transcription in a run-off transcription assay.

78 in vitro as judged by lacZ reporter fusions, run-off transcription assays and nucleotide resolution s

79 transcriptional activation as determined by run-off transcription assays and VEGF promoter-luciferas

80 In vitro run-off transcription assays revealed FUS-enhanced RNA p

81 Results of nuclear run-off transcription assays showed that melanocyte-stim

82 Using in-vitro run-off transcription assays, the affinity purified RNA

83 and protruding templates, promoter-initiated run-off transcription by RNA polymerase II generates dis

84 in vivo by reporter studies, and in vitro by run-off transcription experiments.

85 hod to identify additional target promoters: run-off transcription followed by macroarray analysis (R

86 xigenin-labeled cRNA probes were prepared by run-off transcription from plasmids containing cDNAs for

87 A choice of cloning and run-off transcription linearisation restriction enzyme s

88 on of single and multiple rounds of in vitro run-off transcription suggested that the inhibitory effe

89 While in vitro run-off transcription using purified SigN on the Bacillu

90 Nuclear run-off transcription with nuclei from germline transfor

91 f DNA libraries, assembly of gene cassettes, run-off transcription, site-directed mutagenesis and foo

92 When prepared directly by in vitro run-off transcription, we show here that the predominant

93 Addition of the remaining NTPs resulted in run-off transcription, with an efficiency that was promo

94 neral and salt-sensitive (250 mM) feature of run-off transcription.

95 have exploited a newly developed technique, run-off transcription/microarray analysis (ROMA) to defi

96 Nuclear run-off transcriptions demonstrated that Spi-1 transcrip

97 On 5'-overhung templates the extended run-off transcripts appear to be retained within an RNA-

98 t recombinant p50 enhanced the production of run-off transcripts from the bcl-2 P1 promoter.

99 Run-off transcripts on a blunt-ended template were initi

100 Unexpectedly, approximately 4% of the run-off transcripts were, depending on the repeat sequen

101 A major difference is the precise run-off transcripts with homogeneous 3'-termini synthesi

102 t either BPDE isomer to generate full-length run-off transcripts.

103 In addition, polysome run-off translation assays demonstrated an increase in P

104 e drugs had a significant effect in vitro on run-off translation of isolated polysomes.