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1 e highly resistant to DDT but susceptible to deltamethrin.
2 Bioassays showed no resistance to deltamethrin.
3 site overlapping with those of both BTX and deltamethrin.
4 ive analog DAP 1855 antagonize the action of deltamethrin.
5 ng voltage-gated sodium channels targeted by deltamethrin.
6 ovirus metabolizes deltamethrin to 4-hydroxy deltamethrin.
7 rethroids examined, including permethrin and deltamethrin.
8 20-fold less sensitive than the wild-type to deltamethrin.
9 trasted resistance levels to the insecticide deltamethrin.
10 artially reversed the channel sensitivity to deltamethrin.
11 in sensitivity to a pyrethroid insecticide, deltamethrin.
12 ither alpha-scorpion toxin or the pyrethroid deltamethrin.
13 than 3% of total Na(+) channels modified by deltamethrin.
14 6, rendered the channel greatly resistant to deltamethrin.
15 pmental exposure to the pyrethroid pesticide deltamethrin.
21 while, they were 7x for cypermethrin, 6x for deltamethrin and 5x for imidacloprid within the Asia-II-
23 own adjacent kdr mutation at position L785F, deltamethrin and BTX were probably situated next to each
25 e I (permethrin and bifenthrin) and type II (deltamethrin and Lambda-cyhalothrin) pyrethroids but not
26 acological blockers of CN (cyclosporin A and deltamethrin) and peptide inhibitors of CN [the Xenopus
28 gate whether domestic livestock treated with deltamethrin (applied by a sponging method) would prove
30 del yielded a complex in which a pyrethroid (deltamethrin) binds between the linker helix IIL45 and t
34 nophenoxy)ethane-N,N,N',N'-tetraacetic acid, deltamethrin, cyclosporin A, and okadaic acid each alone
35 Mice exposed to the pyrethroid pesticide deltamethrin during development exhibit several features
40 n D2:S4-S5 cytoplasmic linker), enhanced the deltamethrin-induced maintained current by approximately
41 In this regard, the calcineurin inhibitor deltamethrin inhibited the Ca2+ ionophore-induced dephos
42 r residual spraying (IRS) with a pyrethroid (deltamethrin) insecticide in the first year and a carbam
44 ca were exposed to similar concentrations of deltamethrin on electrostatic netting or a standard long
45 ses at 2 Hz further augmented the effects of deltamethrin on Nav1.4-I687M mutant channels so that app
46 ryptophan reduced the channel sensitivity to deltamethrin only by 3- to 10-fold, indicating that an a
52 a P450 gene responsible for the majority of deltamethrin resistance observed in the QTC279 strain of
53 n the brain-specific insect P450 involved in deltamethrin resistance shed new light on the understand
54 activity were significantly associated with deltamethrin resistance, with monooxygenase activity pla
56 ant, Nav1.4-I687M/N784K, exhibited a partial deltamethrin-resistant phenotype but was completely resi
57 ore than a 200-fold higher expression in the deltamethrin-resistant QTC279 strain when compared with
58 n this study, we found that three additional deltamethrin-sensing residues in IIIS6, Ile(3i12), Gly(3
64 The Na+ channels deactivated slowly after deltamethrin treatment, the resultant "tail" currents be
65 s of the pyrethroids permethrin (type I) and deltamethrin (type II) on Na+ currents were investigated
66 osquito strains when a 15-fold lower dose of deltamethrin was applied and when the exposure time was
69 itivity of the double mutant M918T+L1014F to deltamethrin was similar to that of M918T alone, whereas
71 zuron, emamectin benzoate, cypermethrin, and deltamethrin were measured in water, sediment, and biota
72 secticide susceptibility to 4% DDT and 0.05% deltamethrin WHO-impregnated papers was determined with
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