ライフサイエンスコーパス: run-off

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

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

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

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

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

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

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

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

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

10 Nuclear run-off analysis established transcriptional up-regulati

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

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

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

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

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

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

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

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

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

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

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

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

23 Nuclei run-off assays demonstrated that p16 expression induced

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

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

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

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

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

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

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

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

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

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

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

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

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

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

38 60 fold lower than those reported for urban run-off exhibited significantly longer burrowing times,

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

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

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

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

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

44 Run-off from farms and wastewater treatment plant overfl

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

46 Diastolic run off into the pulmonary circulation and labile corona

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

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

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

50 7 RNA polymerase synthesizes, in addition to run-off products of precise length, transcripts with an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

74 Nuclear run-off transcription with nuclei from germline transfor

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

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

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

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

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

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

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

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

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

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

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

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

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

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