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3 sed from such chimeras were able to activate hut transcription in a purified system in vitro, as were
6 C activates transcription of operons such as hut (histidine utilization) and ure (urea utilization),
7 ty tested: (i) it activates transcription at hut and ure; (ii) it competes with the lysine-sensitive
10 required for amino acid regulation of either hut induction or the expression of proline oxidase, the
13 ll substrates in laboratory and experimental hut studies against pyrethroid-resistant malaria vectors
15 nalyses of bioassay studies and experimental hut trials are used to characterise how pyrethroid resis
16 aying product (VECTRON T500) in experimental hut trials against pyrethroid-resistant vector populatio
17 that mosquito data collected in experimental hut trials can be used to parameterize mechanistic model
18 ito abundance data collected in experimental hut trials indicates these dynamics are likely to exist
23 meterized by an analysis of the experimental hut data and used to predict the epidemiological impact
24 sistant An. gambiae sl entering experimental huts in Cove, Benin treated with VECTRON T500 was simila
25 e demonstrate, using semi-field experimental huts, that CYP6P9b-mediated resistance associates with r
26 l IRS with pirimiphos-methyl in experimental huts and houses in a village-wide trial was evaluated ag
27 evaluated as IRS treatments in experimental huts in an area of Benin where the mosquitoes Anopheles
30 ic 300CS (pirimiphos-methyl) in experimental huts when partially sprayed against wild, free-flying po
33 or bottom half of the walls of experimental huts were sprayed, with or without also spraying the cei
36 ilar studies using the NAC-binding site from hut showed that two mutations in the promoter proximal h
37 rophobic residue activate transcription from hut and ure promoters, but fail to repress gdhA expressi
39 y generated inside the screened and grounded huts, the birds again lost their magnetic orientation ca
40 he same order as NAC(WT) (ure > gdhA > nac > hut); (v) it induces the same slight bend as dimers of N
52 strate that the mfd mutation relieves CCR of hut and gnt expression at the cis-acting cre sequences l
54 crh mutation individually had any affect on hut CCR but that hut CCR was abolished in a ptsH1 crh do
58 in electrically grounded, aluminium-screened huts, which attenuated electromagnetic noise in the freq
59 85.8] for the bottom half + ceiling sprayed huts and 76.9% [76.6, 77.3] for the top half + ceiling s
60 2.9, 84.5] for bottom half + ceiling sprayed huts and 81.3% [79.6, 83.0] for the top half + ceiling s
64 de was compared monthly to the fully sprayed huts over the study period with a non-inferiority margin
65 [81.5, 89.7] was recorded for fully sprayed huts, 83.7% [82.9, 84.5] for bottom half + ceiling spray
66 ity was 86.7% [85.3, 88.1] for fully sprayed huts, 85.6% [85.4, 85.8] for the bottom half + ceiling s
67 iod was 88.5% [87.7, 89.3] for fully sprayed huts, 88.3% [85.1, 91.4] for bottom half + ceiling spray
69 reverse transcriptase PCR analyses show that hut locus transcription is subject to hemin-responsive r
70 gainst formation of AH meltglass in thatched hut fires at 1100 degrees -1200 degrees C, and low value
71 dhA; (iii) it binds to the same sites at the hut, ure, nac, and gdhA promoters as NAC(WT); (iv) the r
72 The protein Pa3175 is dislocated from the hut operon and was shown to catalyze the hydrolysis of N
73 phily (premature exit of mosquitoes from the hut), deterrence, time to 50% or 95% knock-down, and per
79 eld and Actellic, this was true only for the huts with the bottom half + ceiling, reflecting the rest
82 to density and resting behavior in unsprayed huts, after which two treatments of partial indoor resid
83 ential locus dedicated to hemin utilization (hut) encoding a putative hemin receptor, HutA; a TonB-li
84 ion of the CCR of the histidine utilization (hut) enzymes in cells grown in minimal medium showed tha
85 transcription of the histidine utilization (hut) operon and to repress transcription of the glutamat
86 cid repression of the histidine utilization (hut) operon were isolated by transposon mutagenesis.
87 ocated in both of the histidine utilization (hut) operons were upregulated in both QS and flhDC mutan
88 omagnetic noise present in unscreened wooden huts at the University of Oldenburg campus, they could n