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1 and phorate) and one pyrethroid insecticide (permethrin).
2 ion, and the emerging adults were exposed to permethrin.
3 and cypermethrin but not to chlorpyrifos or permethrin.
4 th cotton fibers that have been treated with permethrin.
5 t with commercial products of bifenthrin and permethrin.
6 e binding site with the active isomer 1R-cis-permethrin.
7 ed to either deltamethrin (0.3 - 3 mg/kg) or permethrin (1 - 100 mg/kg) followed by collection of cor
8 ely needs to be metabolically activated, and permethrin (190-fold) and lindane (63-fold), compounds a
10 richness and two insecticides, carbaryl and permethrin, also altered the microbial community structu
11 IIS6, reduced the binding affinity of 1S-cis-permethrin, an inactive isomer that shares the same bind
12 ower sensitivity to the synthetic pyrethroid permethrin and a approximately 2-fold increased sensitiv
13 ncentrations correlated with both the parent permethrin and bifenthrin concentrations in the tissues
15 techniques to predict the bioavailability of permethrin and bifenthrin to two benthic invertebrates (
16 d that this protein metabolized both type I (permethrin and bifenthrin) and type II (deltamethrin and
17 cides 2,4-D and glyphosate, the insecticides permethrin and carbaryl, and the rodenticide warfarin.
18 Compared with their cis- counterparts, trans-permethrin and cypermethrin were hydrolyzed 22- and 4-fo
19 ed pesticides were pyrethroids, particularly permethrin and cypermethrin with average concentrations
21 the honeybee's channel is also sensitive to permethrin and fenvalerate, respectively type I and type
23 ic ability of CYP9M10/CPR and CYP6AA7/CPR to permethrin and its metabolites, including 3-phenoxybenzo
24 rotoxic compound acting via sodium channels (permethrin) and a compound requiring metabolic activatio
25 for indoor use (carbaryl, cypermethrin, and permethrin) and DDT did not change over time in our stud
27 ng our study period (carbaryl, cypermethrin, permethrin, and propoxur) and four that are no longer so
31 ly decreased resistance of the mosquitoes to permethrin but also repressed the expression of four ins
33 zed by their levels of tolerance to specific permethrin concentrations within and among the mosquito
35 , endosulfan, iprodione, lambda-cyhalothrin, permethrin, cypermethrin, and deltamethrin) in lettuce.
36 tigmine bromide (PB) and pesticides DEET and permethrin during the war has been proposed as one of th
39 olachlor (p = 0.01), trifluralin (p = 0.05), permethrin (for animal application) (p = 0.02), and toxa
41 5% CI, 14 to 50), from 24.6% to 11.4% in the permethrin group (relative reduction, 54%; 95% CI, 35 to
42 [CI], 37 to 60), from 41.7% to 15.8% in the permethrin group (relative reduction, 62%; 95% CI, 49 to
44 otype was significantly more frequent in the permethrin group than in the placebo group (73% vs 45%,
45 e group), mass administration of permethrin (permethrin group), or mass administration of ivermectin
50 rsons were randomly assigned to receive 0.4% permethrin-impregnated underwear or an identical-appeari
51 ignificantly more homeless persons receiving permethrin-impregnated underwear than homeless persons r
53 to low doses of GWIR chemicals PB, DEET, and permethrin induced depressive- and anxiety-like behavior
56 roids (bifenthrin, cyfluthrin, cypermethrin, permethrin, lambda-cyhalothrin, fluvalinate, fenvalerate
58 and three insecticides (malathion, carbaryl, permethrin) on microbial communities of container aquati
61 standard-care group), mass administration of permethrin (permethrin group), or mass administration of
63 te insensitivity and are the major source of permethrin resistance but that other genes dispersed thr
64 Mujeres, Mexico, that had been selected for permethrin resistance for two generations and a referenc
67 sponds with a SNP previously associated with permethrin resistance in the para sodium channel gene an
68 er detoxification genes also up-regulated in permethrin resistant mosquitoes included a glucuronosylt
73 ns and their combinations in other field and permethrin selected Culex mosquitoes, finding that the c
74 ains of the field parental strains and their permethrin selected offspring, 3 nonsynonymous (A(109)S,
75 between field parental mosquitoes and their permethrin selected offspring, and among different mosqu
76 nations presented across different field and permethrin selected populations in response to high leve
77 parental mosquito strain HAmCq(G0) and their permethrin-selected high resistant offspring HAmCq(G8) w
78 ated genes in HAmCq(G8) mosquitoes following permethrin selection, suggesting a homeostatic response
81 Quantitative trait loci (QTL) controlling permethrin survival in Ae. aegypti were mapped in an F(3
82 sistance for two generations and a reference permethrin-susceptible strain originally from New Orlean
83 tandard care involving the administration of permethrin to affected persons and their contacts (stand
84 d repellents are applied in combination with permethrin-treated clothing, protection against bites of
87 uito feeding in human subjects above that of permethrin-treated uniform fabric worn on the arm of the
88 s oocytes and the effects of the pyrethroids permethrin (type I) and deltamethrin (type II) on Na+ cu
90 , the (-)enantiomer of cis-bifenthrin or cis-permethrin was preferentially degraded, resulting in rel
91 ption of PCB-52, PCB-153, bifenthrin and cis-permethrin were isotropic, validating the assumption for
92 congeners as well as some pesticides (e.g., permethrin) were determined from the subtropical eucalyp
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