ライフサイエンスコーパス: lepidopteran

1 oper (Trichoplusia ni), a generalist-chewing lepidopteran.

2 elds might adversely affect nearby nontarget lepidopterans.

3 corn fields and cause mortality in nontarget lepidopterans.

4 ticularly common in amphibians, reptiles and lepidopterans.

5 eders and specialists on 'soft' prey such as lepidopterans.

6 ers, proposed to be mediators of toxicity in lepidopterans.

7 (b) predict an important role of learning in lepidopteran agricultural pests.

8 physiological actions of 5HT observed in the lepidopteran AL.

9 cial biotechnology solutions for controlling lepidopteran and coleopteran insect pests on crops depen

10 ave been used successfully for management of lepidopteran and coleopteran pest species, the sap-sucki

11 s by the Ultrabithorax (Ubx) gene product in Lepidopteran and Dipteran hindwings.

12 e family in insects before the divergence of lepidopteran and dipteran lineages.

13 hosphatases (ALPs, EC 3.1.3.1) isolated from lepidopteran and dipteran species are identified as rece

14 IPD072Aa leaves several lepidopteran and hemipteran insect species unaffected bu

15 a significant evolutionary distance between lepidopteran and orthopteran viruses.

16 silk fibroins share many elements with other lepidopteran and trichopteran fibroins, such as conserve

17 tantly, this approach could be used in other lepidopterans and "nonmodel" insects, thus opening new a

18 etic sex chromosome systems (ZZ/ZW) found in lepidopterans and birds promote the evolution of exagger

19 ly large investment in mushroom bodies for a lepidopteran, and indeed rank highly compared to other i

20 his is the first YXFGLamide to be found in a lepidopteran, and there are indications that additional

21 cannibalistic species were coleopterans and lepidopterans, and the cannibals often were juveniles th

22 s work contributes to the elucidation of the lepidopteran antiviral response against infection of seg

23 Among the lepidopterans at high potential risk from this technolog

24 lights the unusual evolutionary stability of lepidopteran autosomes; in contrast, higher rates of int

25 ge evolutionary distance between CuniNPV and lepidopteran baculoviruses.

26 ttle conservation relative to the genomes of lepidopteran baculoviruses.

27 uence similarity to previously characterized lepidopteran betaGRPs from hemolymph, but unlike these i

28 ce during the mid-Cretaceous, in addition to lepidopteran body-fossil evidence from Early Cretaceous

29 eolytic activation step occurs in the gut of lepidopteran but not coleopteran herbivores, and is cata

30 hat occurs at the end of the larval stage in lepidopteran (butterflies and moths) insects.

31 vates JH synthesis in adult, but not larval, lepidopteran CA.

32 ive toxin binding region similar to those in lepidopteran cadherin B. thuringiensis receptors.

33 g function in BT-R1 as well as in homologous lepidopteran cadherins.

34 Here we report that lepidopterans can still fly when their hindwings are cut

35 combinant CR3, and we show here that another lepidopteran cell line, Trichoplusia niTN-5B1-4 (High-Fi

36 progeny production in NPV-infected, cultured lepidopteran cells.

37 ricted in their replication after entry into Lepidopteran cells.

38 finer taxonomic scales showed that different lepidopteran clades select hosts based on different defe

39 Yponomeutoids were one of the earliest lepidopteran clades to evolve external feeding and to ex

40 efenses of Inga to phylogenies for the major lepidopteran clades.

41 ugiperda ascovirus, a DNA virus that attacks lepidopterans, codes for an executioner caspase synthesi

42 ome accessible to the general biological and lepidopteran communities, we established MonarchBase.

43 rovide effective and economic control of the lepidopteran complex on rice with less risk to the envir

44 lated juvenile hormone biosynthesis in adult lepidopteran corpora allata and was subsequently shown t

45 ae of corn earworm (Helicoverpa armigera), a lepidopteran crop pest, by affinity chromatography on im

46 rties of HP1, we expressed Drosophila HP1 in lepidopteran cultured cells using a recombinant baculovi

47 and have differential rates of processing by lepidopteran digestive enzymes.

48 Although the lepidopteran ESP/YP2s are related to lipoprotein lipases

49 ding motif as an anchor, to demonstrate that lepidopteran ESP/YP2s, higher-dipteran YPs, and lipoprot

50 gulation of an AS-C gene was modified during Lepidopteran evolution to promote scale cell formation.

51 importance, and its value for tracing early lepidopteran evolution, the biodiversity and phylogeny o

52 or patterns and were a key innovation during Lepidopteran evolution.

53 e resulting advances in our understanding of lepidopteran evolution.

54 ome of 157 kbp, which attacks species of the lepidopteran family Noctuidae.

55 his result holds true whether calculated per lepidopteran family or for a caterpillar assemblage as a

56 % are specialized predators, indicating that lepidopteran feeding habits are highly constrained.

57 s may be the chief adaptive asset derived by lepidopterans from possession of oversize hindwings.

58 Here we exploited the biphasic nature of Lepidopteran genetic linkage to map this gene in diamond

59 s the evolutionary rate of rearrangements in lepidopteran genomes appears to be one of the fastest am

60 resent ButterflyBase, a unified resource for lepidopteran genomics.

61 MsEPV and lepidopteran genus B EPVs lack genome colinearity and ex

62 Bias level shifts within the lepidopteran genus Papilio are most likely a result of p

63 Lepidopteran green- and red-sensitive visual pigments fo

64 ion of TD2 to the extreme environment of the lepidopteran gut.

65 r the first time a NMR structure of SCP-2 in lepidopteran H. armigera and reveals its important funct

66 Here we show that larvae of the specialized lepidopteran herbivore Heliothis subflexa reduce their v

67 by infestation with larvae of the generalist lepidopteran herbivore Spodoptera littoralis.

68 tryptophan, reduced growth of the generalist lepidopteran herbivore Trichoplusia ni (cabbage looper)

69 t is polyphagous while the majority of other lepidopteran herbivores are specialist.

70 questions using the tree genus Inga and its lepidopteran herbivores in the Amazon.

71 emporally different volatile blends and that lepidopteran herbivores use induced plant signals releas

72 mite herbivory resembled those observed for lepidopteran herbivores.

73 tion related to Thr catabolism in the gut of lepidopteran herbivores.

74 each other than to any previously sequenced lepidopteran hexamerin or arthropod hemocyanin.

75 gs suggest that rather than protecting their lepidopteran host from viral infection, Wolbachia instea

76 pressed and their products function to alter lepidopteran host physiology, enabling endoparasitoid de

77 of SfIAP, the principal cellular IAP of the lepidopteran host Spodoptera frugiperda.

78 Ai-mediated silencing of an immune gene in a lepidopteran host Spodoptera littoralis, leaving the mid

79 es and developmental cascades in parasitized lepidopteran hosts of C. sonorensis.

80 ) can infect and kill a wide range of larval lepidopteran hosts, but the dosage required to achieve m

81 ly different from those found in terrestrial lepidopteran hosts.

82 ly unrecognized motifs that are not found in lepidopteran IAPs.

83 ontrolling Bt Cry1Ac toxin resistance in two lepidopterans, implying that this protein plays a critic

84 The lepidopteran innate immune response against RNA viruses

85 e report the crystal structure of PPO from a lepidopteran insect at a resolution of 1.97 A, which is

86 egenerate PCR approach was used to isolate a lepidopteran insect cDNA encoding a beta4-galactosyl-tra

87 and expression of foreign genes in cultured lepidopteran insect cells and insects.

88 In summary, this study demonstrated that lepidopteran insect cells encode and express a beta4-N-a

89 the generation of paucimannosidic glycans in lepidopteran insect cells has not been identified.

90 the glycoprotein processing capabilities of lepidopteran insect cells.

91 mbrane-targeted receptors, in Drosophila and lepidopteran insect cells.

92 Lepidopteran insect larvae have a high K+ and a low Na+

93 ), whose gene product shows activity against lepidopteran insect larvae including black cutworm (Agro

94 ichia coli insecticidal activity against the lepidopteran insect larvae mentioned above.

95 ts a novel class of proteins insecticidal to lepidopteran insect larvae.

96 l for effective control of several different lepidopteran insect pests in genetically modified tobacc

97 lants were bioassayed for resistance to five lepidopteran insect pests.

98 na benthamiana plants to study its effect on lepidopteran insect pests.

99 sgenic glyphosate resistance (CP4 EPSPS) and lepidopteran insect resistance (Cry1Ac).

100 MNPV) in the cell line Sf9, derived from the lepidopteran insect Spodoptera frugiperda, stimulated a

101 tity of the gene encoding this enzyme in the lepidopteran insect, Spodoptera frugiperda.

102 byx mori is also a useful model organism for lepidopteran insect.

103 s, biological lepidopteran insecticides, non-lepidopteran insecticides and fungicides.

104 The use of chemical lepidopteran insecticides might be associated with hepat

105 phosate, non-glyphosate herbicides, chemical lepidopteran insecticides, biological lepidopteran insec

106 emical lepidopteran insecticides, biological lepidopteran insecticides, non-lepidopteran insecticides

107 XptA2 had only modest oral toxicity against lepidopteran insects but as a complex with co-produced X

108 model substrate, biochemical assays in large Lepidopteran insects demonstrated that low levels of l-D

109 folded XptA1 can pass through the midgut of Lepidopteran insects susceptible to the insecticidal tox

110 Lepidopteran insects use sex pheromones derived from fat

111 ed with the wasp egg during oviposition into lepidopteran insects, enabling the survival and developm

112 Hemolin, a plasma protein from lepidopteran insects, is composed of four immunoglobulin

113 erstand the potential role of lipid rafts in lepidopteran insects, we isolated and analyzed the prote

114 tructurally unrelated to hemolymph JHBP from lepidopteran insects.

115 equired for the successful parasitization of lepidopteran insects.

116 orhabditis briggsae KT0001 and a pathogen of lepidopteran insects.

117 ich is necessary for lethal toxicity against lepidopteran insects.

118 ir effect via the secretion of bombyxin, the lepidopteran insulin-like hormone.

119 her evidence that ascoviruses evolved from a lepidopteran iridovirus.

120 itiated photoaffinity analogs of the natural lepidopteran juvenile hormones, JH I and II [epoxy[3H]bi

121 over, its close resemblance to the ancestral lepidopteran karyotype (n=31) makes it a useful referenc

122 chromosomes, we conclude that the ancestral lepidopteran karyotype has been n=31 for at least 140 My

123 examined whether nucleocapsids interact with lepidopteran kinesin-1 motor molecules and are potential

124 Lepidopteran larvae (caterpillars) synthesize silk prote

125 ured the community composition and traits of lepidopteran larvae (caterpillars).

126 supposedly exocrine structures recorded for lepidopteran larvae is reviewed.

127 in leaf damage, diversity, and abundance of lepidopteran larvae on two widely distributed host speci

128 t tissues than do well-studied insects (e.g. lepidopteran larvae or aphids).

129 rypsin, are the primary digestive enzymes in lepidopteran larvae, and are also involved in Bacillus t

130 ansport of Hv1a across the gut epithelium in lepidopteran larvae, GNA is also capable of delivering H

131 ons as a synergist of Cry1A toxicity against lepidopteran larvae.

132 Baculovirus infection can also induce ELA in lepidopteran larvae.

133 ike P74, are essential for oral infection of lepidopteran larval hosts of Autographa californica M nu

134 posits, suggests that the radiation of major lepidopteran lineages probably occurred during the Late

135 icating an important role for cholesterol in lepidopteran lipid rafts structure.

136 In this study, we investigated the role of lepidopteran microtubule transport using coimmunoprecipi

137 We have cloned this protein from a larval lepidopteran midgut (Manduca sexta) cDNA library.

138 Lepidopteran midgut aminopeptidases N (APNs) are phyloge

139 on the solution structures of undelipidated lepidopteran moth PBPs determined thus far.

140 premetamorphic male larvae of two different Lepidopteran moth species.

141 t stimulated sex pheromone biosynthesis in a lepidopteran moth.

142 We discovered that lepidopteran (moth and butterfly) IAPs, which are degrad

143 This lepidopteran (moth) retroelement contains gag and pol ge

144 Pheromone-binding proteins (PBPs) in lepidopteran moths selectively transport the hydrophobic

145 Lepidopterans (moths) produce Vg as the major yolk prote

146 notable improvements in our understanding of lepidopteran navigation strategies, including the hither

147 genus Granulovirus (GVs), the group I and II lepidopteran nucleopolyhedroviruses (NPVs), and the dipt

148 ranching to the hymenopteran NeseNPV and the lepidopteran nucleopolyhedroviruses and granuloviruses.

149 ngiensis is the most used MCA for control of lepidopteran orchard pests.

150 rotein sequences, along with other published lepidopteran PBPs, to investigate the evolutionary relat

151 duced no adverse effects in the recalcitrant lepidopteran pest Helicoverpa armigera.

152 Plutella xylostella has become the major lepidopteran pest of Brassica owing to its strong abilit

153 selection experiments with eight species of lepidopteran pests indicates that some cross-resistance

154 Previous estimates for lepidopteran pests targeted by Bt crops seem to meet thi

155 d reduction in pesticide application against lepidopteran pests(2-9).

156 s (Bt G. hirsutum) that confer resistance to lepidopteran pests, is extensively cultivated worldwide.

157 the Cry1Ab protein (Bt corn) is resistant to lepidopteran pests.

158 based screening of resistance to Bt crops in lepidopteran pests.

159 bserved with highly potent Bt toxins against lepidopteran pests.

160 ) insecticides are very selectively toxic to lepidopteran pests.

161 acillus thuringiensis (Bt) control important lepidopteran pests.

162 uringiensis (Bt rice) is highly resistant to lepidopteran pests.

163 in the generation of structural diversity in lepidopteran pheromone biosynthesis as a result of the d

164 These lepidopteran pheromones are used extensively for pest co

165 They constitute a second major class of lepidopteran pheromones, different from the C10-C18 acet

166 ed HP1 from bacterial (unphosphorylated) and lepidopteran (phosphorylated) cells has similar secondar

167 Here we summarize progress on lepidopteran phylogeny since 1975, emphasizing the super

168 the most comprehensive molecular analysis of lepidopteran phylogeny to date, focusing on relationship

169 analyses will be necessary to fully resolve lepidopteran phylogeny.

170 is also compromised in resistance toward the lepidopteran predator Manduca sexta (tobacco hornworm).

171 galeae, which constitute the characteristic lepidopteran proboscis, and the tentacle suggest that th

172 The database supports many needs of the lepidopteran research community, including molecular mar

173 transgenic plants, compared with 20% on the lepidopteran-resistant breeding line GatIR81-296, and mo

174 Using RNAi screening, we show that Lepidopteran RNAi, Nuclear Factor-kappaB, and ubiquitin-

175 in the expanded state in which they occur in lepidopterans seem to contribute in an essential way to

176 Transient expression of rpr in the lepidopteran SF-21 cell line induced apoptosis displayin

177 that transient overexpression of RPR in the lepidopteran SF-21 cell line induces apoptosis and that

178 The lepidopteran sounds have previously been shown to alert

179 pplied to recent empirical work in different lepidopteran species and (b) predict an important role o

180 Yet many mite and lepidopteran species can thrive on plants defended by cy

181 In contrast, the Lepidopteran species show polyphyletic relationships for

182 oth compounds are registered for use against lepidopteran species such as the diamondback moth, Plute

183 ) lines, resistant to feeding by a number of lepidopteran species, rapidly mobilize a unique 33-kDa c

184 n pheromone glands of adult females of eight lepidopteran species.

185 me functions of per may be conserved in this lepidopteran species.

186 D. melanogaster hobo element to transpose in lepidopteran species.

187 ion of a genetic transformation system for a lepidopteran species.

188 Wild-type Cry1Ac, a three-domain, lepidopteran-specific toxin, bound purified gypsy moth (

189 genetic complexity of host plant use in the Lepidopteran subfamily Heliothinae suggest that architec

190 Gracillariidae, a member of the most derived lepidopteran suborder, the Ditrysia.

191 ns seem to contribute in an essential way to lepidopteran survival.

192 des with major wing-patterning loci in other lepidopteran systems, suggesting the existence of basal

193 ost interactions in experimentally-tractable Lepidopteran systems.

194 Among rare eastern North American lepidopterans, the (mostly indirect) consequences of the

195 insects and 116 rare eastern North American lepidopterans to determine the importance of invasive sp

196 r and Pieris rapae), hindwing removal causes lepidopterans to incur a loss in both linear and turning

197 We describe specific improvements to the lepidopteran transposon piggyBac and the P element that

198 human dihydrofolate reductase, added to the lepidopteran transposon piggyBac, transformed parasites

199 cell lines, namely, High Five cells from the lepidopteran Trichoplusia ni and S2 cells from the dipte

200 that nucleocapsid AC141 associates with the lepidopteran Trichoplusia ni KLC and kinesin-1 heavy cha

201 d stable transformation of the medfly with a lepidopteran vector represents transposon function over

202 NA viruses with circular genomes that attack lepidopterans, where they produce large, enveloped virio

203 Lepidopteran wing colour patterns are a key innovation,

204 Lepidopteran wing scales are the individual units of win

205 One of the more striking features of lepidopteran wing scales are the longitudinal ridges tha

206 t bristles and hairs, longitudinal ridges in lepidopteran wing scales gain new significance for their

207 nd dynamic expression of Notch in developing lepidopteran wings suggests that this signalling pathway

208 colors create the patterns that characterize lepidopteran wings.