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1  mg/m(2) for clothianidin and 25 mg/m(2) for deltamethrin).
2 re than 22 times compared to the side panel (deltamethrin).
3  2 ng L(-1), revealing a high sensitivity to deltamethrin.
4 ted high sensitivity and selectivity towards deltamethrin.
5 trasted resistance levels to the insecticide deltamethrin.
6 pmental exposure to the pyrethroid pesticide deltamethrin.
7 e highly resistant to DDT but susceptible to deltamethrin.
8            Bioassays showed no resistance to deltamethrin.
9  site overlapping with those of both BTX and deltamethrin.
10 ive analog DAP 1855 antagonize the action of deltamethrin.
11 ng voltage-gated sodium channels targeted by deltamethrin.
12 ovirus metabolizes deltamethrin to 4-hydroxy deltamethrin.
13 rethroids examined, including permethrin and deltamethrin.
14 20-fold less sensitive than the wild-type to deltamethrin.
15 artially reversed the channel sensitivity to deltamethrin.
16  in sensitivity to a pyrethroid insecticide, deltamethrin.
17 ither alpha-scorpion toxin or the pyrethroid deltamethrin.
18  than 3% of total Na(+) channels modified by deltamethrin.
19 6, rendered the channel greatly resistant to deltamethrin.
20 ne bags and a pesticide treatment containing deltamethrin 0.13% and fenitrothion 1% while Sitotroga c
21          Rats were acutely exposed to either deltamethrin (0.3 - 3 mg/kg) or permethrin (1 - 100 mg/k
22 application with performance better than the deltamethrin (29.88%).
23 S product Fludora Fusion (clothianidin 50% + deltamethrin 6.25% WP-SB).
24          Comparison of the actions of NA and deltamethrin, a calcineurin antagonist and potent inhibi
25 fected with C alpha-PKA is blocked by 800 nM deltamethrin, a calcineurin inhibitor.
26  was observed with only 1% mortality against deltamethrin, a high LD(50) (96.57 ug/ml), and a high LT
27                                 In contrast, deltamethrin, a specific protein phosphatase type 2B inh
28                      The Hill slope of 2 for deltamethrin action on the wild-type channel and the mut
29                               Pharmaceutical deltamethrin (Alpha Max), used as delousing treatments i
30 l sensitivities to permethrin and DDT versus deltamethrin among these mutants as well as contrasting
31 while, they were 7x for cypermethrin, 6x for deltamethrin and 5x for imidacloprid within the Asia-II-
32 . pomonella sensitivity to two insecticides, deltamethrin and azinphos methyl.
33  from multiple S6 segments were critical for deltamethrin and BTX actions.
34 own adjacent kdr mutation at position L785F, deltamethrin and BTX were probably situated next to each
35                                              Deltamethrin and cypermethrin were not detected above th
36 e I (permethrin and bifenthrin) and type II (deltamethrin and Lambda-cyhalothrin) pyrethroids but not
37     We observed high resistance intensity to deltamethrin and malathion in Ae. aegypti mosquitoes Res
38 resistant An. stephensi upon 1-h exposure to deltamethrin and malathion insecticides, compared to the
39 s were employed to determine the response to deltamethrin and malathion.
40   Furthermore, gste2-T154S was implicated in deltamethrin and permethrin resistance but susceptibilit
41 otyped for resistance to alpha-cypermethrin, deltamethrin and permethrin, with and without pre-exposu
42  resistance to two widely used insecticides: deltamethrin and pirimiphos-methyl, using sequencing dat
43 .83, 15.03, 33.05, 72.7 and 160 mg a.i./L of deltamethrin and the control (distilled water) with 10 r
44 s of livestock treatments containing copper, deltamethrin and triclabendazole on invertebrate density
45 sion 56.25WP-SB (mixture of clothianidin and deltamethrin) and Actellic 300CS (pirimiphos-methyl) in
46 acological blockers of CN (cyclosporin A and deltamethrin) and peptide inhibitors of CN [the Xenopus
47              Permethrin was less potent than deltamethrin, and its binding to all channel types was n
48 esticides (thiamethoxam, lambda-cyhalothrin, deltamethrin, and metalaxyl) and their metabolites in Ra
49 cals (pyrene, phenanthrene, 4-n-nonlyphenol, deltamethrin, and methoxychlor) in this model and compar
50 gate whether domestic livestock treated with deltamethrin (applied by a sponging method) would prove
51 tropolymerization of o-phenylenediamine with deltamethrin as a template molecule.
52 ound increasing resistance to permethrin and deltamethrin as the number of IC haplotypes increased.
53                                              Deltamethrin at 10 microM elicited weak gating changes i
54  containing acetamiprid, lambda-cyhalothrin, deltamethrin, benzovindiflupyr, and prothioconazole, at
55 del yielded a complex in which a pyrethroid (deltamethrin) binds between the linker helix IIL45 and t
56 eonicotinoid clothianidin and the pyrethroid deltamethrin (brand name Fludora Fusion) as a new vector
57            An. gambiae s.l. was resistant to deltamethrin but susceptible to clothianidin and broflan
58 a-cyhalothrin, fluvalinate, fenvalerate, and deltamethrin) by APCI were studied.
59 y discovered kdr mutations and predicted new deltamethrin-channel contacts.
60                       PermaNet Dual is a new deltamethrin-chlorfenapyr net developed by Vestergaard S
61 trostatic netting or a standard long-lasting deltamethrin-coated bednet (PermaNet 2.0).
62 r mechanisms of resistance to the pyrethroid deltamethrin (commonly used in bednets) and PM (widespre
63 10 OD insecticide containing thiacloprid and deltamethrin, commonly used in the OSR fields.
64 ly a few minutes, the commercially available deltamethrin crystals, form I, melt and crystallize upon
65 nophenoxy)ethane-N,N,N',N'-tetraacetic acid, deltamethrin, cyclosporin A, and okadaic acid each alone
66 986*/+)) mouse line exposed to the pesticide deltamethrin (DM) from conception to postnatal day 22.
67                                              Deltamethrin (DM) is a widely used insecticide that has
68                               The pyrethroid deltamethrin (DM) is broadly used for insect control.
69 ence of P. elaeisis were also reduced by the deltamethrin doses lower than the commercially recommend
70  5.57% were obtained for pyriproxyfen (PPX), deltamethrin (DTM) and etofenprox (ETF), respectively.
71  5.57% were obtained for pyriproxyfen (PPX), deltamethrin (DTM) and etofenprox (ETF), respectively.
72                               The pyrethroid deltamethrin (DTM) is used to treat Atlantic salmon (Sal
73     Mice exposed to the pyrethroid pesticide deltamethrin during development exhibit several features
74     In one group livestock were treated with deltamethrin during the malaria transmission seasons of
75 , and 95.0%, of azoxystrobin, cyproconazole, deltamethrin, epoxiconazole, kresoxim-methyl and pencona
76  significantly associated with resistance to deltamethrin following PBO-pre-exposure, warranting func
77 in, cyfluthrin, permethrin, cypermethrin and deltamethrin from fresh chili, chili flakes, and curry p
78  high resistance intensity to the pyrethroid deltamethrin (> 1,500-fold), and mortality following exp
79                  Calmodulin, 200 nM Ca2+ and deltamethrin have no effect on Po,peak in the absence of
80  recovery of susceptibility was observed for deltamethrin in 2021.
81 n with pyrethroids such as a-cypermethrin or deltamethrin in insecticide treated bednets (ITNs) to co
82 a-cyhalothrin, permethrin, cypermethrin, and deltamethrin) in lettuce.
83 ribolium castaneum developed in metal silos, deltamethrin-incorporated polypropylene bags and a pesti
84 ase calcineurin with either cyclosporin A or deltamethrin increases the rundown.
85 n D2:S4-S5 cytoplasmic linker), enhanced the deltamethrin-induced maintained current by approximately
86    In this regard, the calcineurin inhibitor deltamethrin inhibited the Ca2+ ionophore-induced dephos
87 r residual spraying (IRS) with a pyrethroid (deltamethrin) insecticide in the first year and a carbam
88 cide molecules-malathion (K(D) 6.43 muM) and deltamethrin (K(D) 46.7 muM) were demonstrated using MD
89 nce of thiamethoxam, lambda-cyhalothrin, and deltamethrin metabolites in plants exposed to these subs
90  probit analysis estimates for cypermethrin, deltamethrin, monocrotophos and imidacloprid.
91 n exposure to the roof of PermaNet3.0 (PBO + deltamethrin) more than 22 times compared to the side pa
92 ca were exposed to similar concentrations of deltamethrin on electrostatic netting or a standard long
93 ses at 2 Hz further augmented the effects of deltamethrin on Nav1.4-I687M mutant channels so that app
94 ryptophan reduced the channel sensitivity to deltamethrin only by 3- to 10-fold, indicating that an a
95   Similarly, the 24-hour mortality rate with deltamethrin-only LLINs was very low and not significant
96              Similarly, 24-hour mortality to deltamethrin-only LLINs was very low and not significant
97       Furthermore, intracellular dialysis of deltamethrin or cyclosporin A, the specific calcineurin
98                 The initial concentration of deltamethrin, penconazole, kresoxim-methyl, cyproconazol
99 lic health insecticides, namely pyrethroids (deltamethrin, permethrin, and alpha-cypermethrin), Carba
100               After deployment of the ITNs a deltamethrin persistence of 9 months was observed despit
101 nce to both type I (permethrin) and type II (deltamethrin) pyrethroids.
102                      We hypothesize that the deltamethrin receptor and the BTX receptor are situated
103                                              Deltamethrin reduced parasitism and the emergence rates
104  on biological parameters of the insecticide deltamethrin, registered for the control of defoliator c
105 dy presents the first phenotypic testing for deltamethrin resistance and the first whole genome seque
106 rongest and most consistent association with deltamethrin resistance came from Cyp6aa1, this was base
107                   In this study, we examined deltamethrin resistance in An. sinensis from China and i
108                        This study identified deltamethrin resistance in the Anopheles gambiae sensu l
109 p to 33-fold) and correlated positively with deltamethrin resistance intensity across villages (r(2)
110  a P450 gene responsible for the majority of deltamethrin resistance observed in the QTC279 strain of
111 n the brain-specific insect P450 involved in deltamethrin resistance shed new light on the understand
112  activity were significantly associated with deltamethrin resistance, with monooxygenase activity pla
113 ila melanogaster showed that CYP6BQ9 confers deltamethrin resistance.
114                               Similarly, for deltamethrin, resistance was strongly associated with a
115 ant, Nav1.4-I687M/N784K, exhibited a partial deltamethrin-resistant phenotype but was completely resi
116 ore than a 200-fold higher expression in the deltamethrin-resistant QTC279 strain when compared with
117                             Through repeated deltamethrin selection in adult mosquitoes from a field
118                                              Deltamethrin selection led to the rapid enrichment of th
119 n this study, we found that three additional deltamethrin-sensing residues in IIIS6, Ile(3i12), Gly(3
120  Synergist bioassays significantly recovered deltamethrin susceptibility implicating CYP450s (mortali
121 ain when compared with its expression in the deltamethrin-susceptible Lab-S strain.
122  properties, progesterone, pyriproxyfen, and deltamethrin that may be present in the chicken egg.
123 e for DDT, lambdacyhalothrin, bendiocarb and deltamethrin the mortality rate ranged from 1.63-3.29%.
124 nexpensive method to improve the efficacy of deltamethrin, the most active and most commonly used pyr
125  enzyme expressed in baculovirus metabolizes deltamethrin to 4-hydroxy deltamethrin.
126 oids and PBO pre-exposure partially restored deltamethrin toxicity but not permethrin.
127 y, but a contribution of ABC transporters to deltamethrin toxicity is suspected.
128          This study assessed the effect of a deltamethrin-treated net (100 mg/m(2)) attached to a one
129                                          The deltamethrin-treated net significantly reduced (nearly t
130 ated net; C - with cattle and protected by a deltamethrin-treated net; D - no cattle and no net.
131    The Na+ channels deactivated slowly after deltamethrin treatment, the resultant "tail" currents be
132 ificantly reduced by the triclabendazole and deltamethrin treatments in both years and by as much as
133 s of the pyrethroids permethrin (type I) and deltamethrin (type II) on Na+ currents were investigated
134 osquito strains when a 15-fold lower dose of deltamethrin was applied and when the exposure time was
135             The resistance of A. funestus to deltamethrin was monitored using bioassays.
136 stance intensity against both permethrin and deltamethrin was recorded.
137         The rate of internalization of (14)C deltamethrin was significantly slower in a resistant str
138 itivity of the double mutant M918T+L1014F to deltamethrin was similar to that of M918T alone, whereas
139                                         When deltamethrin was used for IRS, incidence rates in the LL
140  molitor pupae exposed to 15.03 mg a.i./L of deltamethrin, was higher.
141 h enhanced the inhibition of nerve firing by deltamethrin, was observed using a Drosophila central ne
142     Cadusafos, chlorpyrifos, permethrin, and deltamethrin were found in at least one sample of the 15
143 zuron, emamectin benzoate, cypermethrin, and deltamethrin were measured in water, sediment, and biota
144 secticide susceptibility to 4% DDT and 0.05% deltamethrin WHO-impregnated papers was determined with
145  imprinted polymer (MIP) technique to detect deltamethrin with high sensitivity and selectivity.
146                  Challenging mosquitoes with deltamethrin, with or without ABC transporter modulators

 
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