ライフサイエンスコーパス: permethrin

1 and phorate) and one pyrethroid insecticide (permethrin).

2 imilarly resistant to alpha-cypermethrin and permethrin.

3 kg and when contraindicated substituted with permethrin.

4 oss-resistance to malathion, bendiocarb, and permethrin.

5 s comparable for MDA based on ivermectin and permethrin.

6 PADs) for real-time and on-site detection of permethrin.

7 ially restored deltamethrin toxicity but not permethrin.

8 ion, and the emerging adults were exposed to permethrin.

9 and cypermethrin but not to chlorpyrifos or permethrin.

10 th cotton fibers that have been treated with permethrin.

11 t with commercial products of bifenthrin and permethrin.

12 e binding site with the active isomer 1R-cis-permethrin.

13 The method can quantify levels >= 0.0015% permethrin, 0.00045% alpha-cypermethrin and 0.00025% pyr

14 ed to either deltamethrin (0.3 - 3 mg/kg) or permethrin (1 - 100 mg/kg) followed by collection of cor

15 ctin (11.8%; 95% CI, 8.4%-15.4%) and topical permethrin (10.8%; 95% CI, 7.5%-14.5%).

16 ely needs to be metabolically activated, and permethrin (190-fold) and lindane (63-fold), compounds a

17 ng and synthetic agrochemicals (for example, permethrin 2)(5,6).

18 DA (IVM-1), or screen and treat with topical permethrin 5% for individuals with scabies and their hou

19 Chlorpyrifos (98.7%), cis- and trans-permethrin (97.5%), bifenthrin (59.3%), and 3PBA (98.7%)

20 iptomic shifts across time after exposure to permethrin, a 3'Tag-Seq analysis was employed on samples

21 Permethrin adulticidal spraying, which targets the volta

22 richness and two insecticides, carbaryl and permethrin, also altered the microbial community structu

23 IIS6, reduced the binding affinity of 1S-cis-permethrin, an inactive isomer that shares the same bind

24 ower sensitivity to the synthetic pyrethroid permethrin and a approximately 2-fold increased sensitiv

25 gambiae after PBO synergist assays for both permethrin and alpha-cypermethrin and total recovery of

26 ncentrations correlated with both the parent permethrin and bifenthrin concentrations in the tissues

27 ed to be 2.4 x 10(3) to 1.1 x 10(5) L/kg for permethrin and bifenthrin on these solids.

28 techniques to predict the bioavailability of permethrin and bifenthrin to two benthic invertebrates (

29 d that this protein metabolized both type I (permethrin and bifenthrin) and type II (deltamethrin and

30 cides 2,4-D and glyphosate, the insecticides permethrin and carbaryl, and the rodenticide warfarin.

31 ncidence of insecticides such as cyfluthrin, permethrin and cyhalothrin was typical for these samples

32 Compared with their cis- counterparts, trans-permethrin and cypermethrin were hydrolyzed 22- and 4-fo

33 ed pesticides were pyrethroids, particularly permethrin and cypermethrin with average concentrations

34 We identify differential sensitivities to permethrin and DDT versus deltamethrin among these mutan

35 observed between silicone sampler levels of permethrin and DEET with their corresponding urinary met

36 plication and found increasing resistance to permethrin and deltamethrin as the number of IC haplotyp

37 while high resistance intensity against both permethrin and deltamethrin was recorded.

38 ally diverse pyrethroids examined, including permethrin and deltamethrin.

39 the honeybee's channel is also sensitive to permethrin and fenvalerate, respectively type I and type

40 CYP9M10 and CYP6AA7 in the detoxification of permethrin and its metabolites PBOH and PBCHO.

41 ic ability of CYP9M10/CPR and CYP6AA7/CPR to permethrin and its metabolites, including 3-phenoxybenzo

42 This study examines resistance patterns to permethrin and malathion in West Nile virus vectors, Cx.

43 entally relevant concentrations of atrazine, permethrin and malathion will mediate a shift in the mos

44 of hydrocarbon jet fuel, dioxin, pesticides (permethrin and methoxychlor), plastics, and herbicides (

45 spectrum antiparasitic drugs (mainly topical permethrin and oral ivermectin) have been widely availab

46 useful for the synthesis of the insecticide permethrin and other natural products.

47 ent study, efficacy of blankets treated with permethrin and piperonyl butoxide (PBO) was evaluated ag

48 rotoxic compound acting via sodium channels (permethrin) and a compound requiring metabolic activatio

49 for indoor use (carbaryl, cypermethrin, and permethrin) and DDT did not change over time in our stud

50 ese genes confers resistance to both type I (permethrin) and type II (deltamethrin) pyrethroids.

51 ecticides, namely pyrethroids (deltamethrin, permethrin, and alpha-cypermethrin), Carbamates (bendioc

52 Cadusafos, chlorpyrifos, permethrin, and deltamethrin were found in at least one

53 amples exposed to malathion, intermediate in permethrin, and lowest in controls.

54 ng our study period (carbaryl, cypermethrin, permethrin, and propoxur) and four that are no longer so

55 re 2,4-D, atrazine, chlorpyrifos, malathion, permethrin, and propoxur.

56 Cyhalothrin, cypermethrin, permethrin, and resmethrin were detected much less frequ

57 ch as 1,3-Dichloro-2-propanol, imidacloprid, permethrin, are attributed to the inactivation of AMPK.

58 stereoisomer of the commonplace insecticide permethrin as well as a range of cyclopropane-based inse

59 d topically with fluralaner in comparison to permethrin at 48 h and orally with fluralaner in compari

60 In contrast to earlier studies with permethrin, biotransformation of bifenthrin to estrogeni

61 efugee camps where LLINs cannot be used, PBO-permethrin blankets may provide protection against resis

62 ly decreased resistance of the mosquitoes to permethrin but also repressed the expression of four ins

63 Fluralaner outperformed permethrin by > 2-fold for the horn flies but underperfo

64 2-fold for the horn flies but underperformed permethrin by > 45-fold for stable flies at 24 h.

65 Permethrin caused 100% mortality in C. furens in field a

66 Copper, permethrin, chromium, triclosan, and lead were also impo

67 zed by their levels of tolerance to specific permethrin concentrations within and among the mosquito

68 4 days apart using weight-based bands, or 5% permethrin cream 7-14 days apart if ivermectin was contr

69 Permethrin cream and oral ivermectin are first-line trea

70 npropathrin, lambda-cyhalothrin, cyfluthrin, permethrin, cypermethrin and deltamethrin from fresh chi

71 tion (Na(+)channel-interfering insecticides; permethrin, cypermethrin).

72 , endosulfan, iprodione, lambda-cyhalothrin, permethrin, cypermethrin, and deltamethrin) in lettuce.

73 al environmental contaminants interfere with permethrin detection, confirming its high selectivity.

74 or the first rapid, sensitive, and selective permethrin detection.

75 tigmine bromide (PB) and pesticides DEET and permethrin during the war has been proposed as one of th

76 associated with mosquito survival following permethrin exposure (Prevalence Ratio; PR = 1.92, CI = 1

77 Following a 1-hr permethrin exposure, 439 F(3) adult mosquitoes were phen

78 ecovery and survival of mosquitoes following permethrin exposure.

79 uding gamma-hexachlorocyclohexane, propoxur, permethrin, fipronil, mecoprop, prochloraz, and carbenda

80 olachlor (p = 0.01), trifluralin (p = 0.05), permethrin (for animal application) (p = 0.02), and toxa

81 equently in the ivermectin group than in the permethrin group (15.6% vs. 6.8%).

82 5% CI, 14 to 50), from 24.6% to 11.4% in the permethrin group (relative reduction, 54%; 95% CI, 35 to

83 [CI], 37 to 60), from 41.7% to 15.8% in the permethrin group (relative reduction, 62%; 95% CI, 49 to

84 ermethrin-resistant haplotype was 51% in the permethrin group and 44% in the placebo group.

85 otype was significantly more frequent in the permethrin group than in the placebo group (73% vs 45%,

86 e group), mass administration of permethrin (permethrin group), or mass administration of ivermectin

87 were in the standard-care group, 532 in the permethrin group, and 716 in the ivermectin group.

88 Nests directly fumigated with permethrin had fewer parasites and fledged more offsprin

89 Permethrin-impregnated clothing for the prevention of ti

90 Permethrin-impregnated underwear is more efficient than

91 rsons were randomly assigned to receive 0.4% permethrin-impregnated underwear or an identical-appeari

92 ignificantly more homeless persons receiving permethrin-impregnated underwear than homeless persons r

93 trains and not significantly less toxic than permethrin in a susceptible strain and a mildly pyrethro

94 nce between topically applied fluralaner and permethrin in all five insecticide-resistant strains tes

95 methrin may have increased the resistance to permethrin in body lice and thus must be avoided.

96 cal fluralaner was 6- to 28-fold as toxic as permethrin in four pyrethroid-resistant strains and not

97 he present sensor can quantitatively analyze permethrin in real samples.

98 niques significantly decreased resistance to permethrin in resistant mosquitoes.

99 to low doses of GWIR chemicals PB, DEET, and permethrin induced depressive- and anxiety-like behavior

100 The decays of permethrin-induced tail currents were exclusively monoph

101 Permethrin is a pyrethroid pesticide and insect repellen

102 Permethrin is an insecticide used to suppress Ae. aegypt

103 roids (bifenthrin, cyfluthrin, cypermethrin, permethrin, lambda-cyhalothrin, fluvalinate, fenvalerate

104 The use of permethrin may have increased the resistance to permethr

105 ected in >70% of silicone samplers including permethrin, N,N-diethyl-meta-toluamide (DEET), and chlor

106 hrin (Olyset(R) Net), 1% pyriproxyfen and 2% permethrin (Olyset(R) Duo), or 0.55% pyriproxyfen and 0.

107 th 1% pyriproxyfen (pyriproxyfen-LLIN) or 2% permethrin (Olyset(R) Net), 1% pyriproxyfen and 2% perme

108 and three insecticides (malathion, carbaryl, permethrin) on microbial communities of container aquati

109 contributions of fipronil, imidacloprid, and permethrin originating from a pet groomer, with elevated

110 7/CPR increased the cell line's tolerance to permethrin, PBOH, and PBCHO.

111 of levoglucosan and some pesticides such as permethrin peaked during the smoldering phase.

112 cals associated with GWI are the insecticide permethrin (PER) and the nerve gas prophylactic pyridost

113 , zeta-cypermethrin (ZCY), cyfluthrin (CYF), permethrin (PER), esfenvalerate (ESF) and tetraconazole

114 standard-care group), mass administration of permethrin (permethrin group), or mass administration of

115 up); or the synergist piperonyl butoxide and permethrin (piperonyl butoxide group).

116 h pyridostigmine bromide (PB) 1.3 mg/kg/day, permethrin (PM) 0.13 mg/kg/day (skin), DEET 40 mg/kg/day

117 nce in genotype distribution associated with permethrin resistance [OR = 4.69 (CI:1.53-14.35, chi(2)

118 N physical integrity and bioefficacy, and no permethrin resistance among local mosquitoes.

119 te2-T154S was implicated in deltamethrin and permethrin resistance but susceptibility to alpha-cyperm

120 te insensitivity and are the major source of permethrin resistance but that other genes dispersed thr

121 Mujeres, Mexico, that had been selected for permethrin resistance for two generations and a referenc

122 Permethrin resistance in Cx. pipiens was influenced by k

123 as indeed correlated with the high levels of permethrin resistance in mosquitoes.

124 Mutations associated with permethrin resistance in the body lice were also identif

125 sponds with a SNP previously associated with permethrin resistance in the para sodium channel gene an

126 One strain had its naturally high permethrin resistance levels maintained by periodic trea

127 terase and oxidase levels were predictive of permethrin resistance while beta-esterase and insensitiv

128 e changes in gene expression associated with permethrin resistance, exome-capture gDNA deep sequencin

129 Permethrin resistance, however, is a growing problem and

130 a network of heritable features determining permethrin resistance.

131 -miR-33 that was genetically associated with permethrin resistance; resulting isoforms had structural

132 er detoxification genes also up-regulated in permethrin resistant mosquitoes included a glucuronosylt

133 the roles of key P450 genes overexpressed in permethrin resistant mosquitoes that confer insecticide

134 VGSC protein levels were lower in the permethrin resistant strain than in the related permethr

135 At baseline, the prevalence of the permethrin-resistant haplotype was 51% in the permethrin

136 On day 45, the permethrin-resistant haplotype was significantly more fr

137 highly overexpressed (>50-fold; q < 0.01) in permethrin-resistant mosquitoes.

138 npropathrin (RR = 4.36; 95% CI, 1.09-17.50); permethrin (RR = 1.57; 95% CI, 1.02-2.42); OPs as a clas

139 5N for survival to DDT (M form P = 0.03) and permethrin (S form P = 0.003).

140 ns and their combinations in other field and permethrin selected Culex mosquitoes, finding that the c

141 ains of the field parental strains and their permethrin selected offspring, 3 nonsynonymous (A(109)S,

142 between field parental mosquitoes and their permethrin selected offspring, and among different mosqu

143 nations presented across different field and permethrin selected populations in response to high leve

144 We compared the gut microbiota of permethrin-selected (PS) strain of Aedes aegypti relativ

145 parental mosquito strain HAmCq(G0) and their permethrin-selected high resistant offspring HAmCq(G8) w

146 ated genes in HAmCq(G8) mosquitoes following permethrin selection, suggesting a homeostatic response

147 ptome analysis of Culex mosquitoes following permethrin selection.

148 t multiple genes are involved in response to permethrin selection.

149 Quantitative trait loci (QTL) controlling permethrin survival in Ae. aegypti were mapped in an F(3

150 formulated adulticide efficacy, to evaluate permethrin susceptibility in the widely distributed coas

151 sistance for two generations and a reference permethrin-susceptible strain originally from New Orlean

152 methrin resistant strain than in the related permethrin-susceptible strain.

153 tandard care involving the administration of permethrin to affected persons and their contacts (stand

154 of overexpression of pre-miR-33 isoforms on permethrin toxicological phenotypes, VGSC transcript abu

155 wo IC haplotypes compromised the efficacy of permethrin treated fabrics.

156 Strong pyrethroid IR and the failure of permethrin treated uniforms have been linked to the pres

157 who had access to bed nets, maternal use of permethrin-treated baby wraps significantly reduced the

158 d repellents are applied in combination with permethrin-treated clothing, protection against bites of

159 Nests with permethrin-treated cotton had significantly fewer P. dow

160 rol, and about 50% reduction compared to the permethrin-treated fabric control.

161 uito feeding in human subjects above that of permethrin-treated uniform fabric worn on the arm of the

162 were randomly assigned in a 1:1 ratio to use permethrin-treated wraps (intervention group) or sham-tr

163 s oocytes and the effects of the pyrethroids permethrin (type I) and deltamethrin (type II) on Na+ cu

164 similar clearance rates by week 2 (74% with permethrin vs 68% with ivermectin; relative risk, 0.91;

165 mples collected from beef cattle feed yards, permethrin was detected most frequently at >67% of parti

166 Permethrin was less potent than deltamethrin, and its bi

167 , the (-)enantiomer of cis-bifenthrin or cis-permethrin was preferentially degraded, resulting in rel

168 ption of PCB-52, PCB-153, bifenthrin and cis-permethrin were isotropic, validating the assumption for

169 congeners as well as some pesticides (e.g., permethrin) were determined from the subtropical eucalyp

170 ith the lowest mortality (0.97%) reported to permethrin, while for DDT, lambdacyhalothrin, bendiocarb

171 ance to alpha-cypermethrin, deltamethrin and permethrin, with and without pre-exposure to the synergi