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1 A and mE75B, were reported in Manduca sexta (Lepidoptera).
2 males are primary endoparasitoids of eggs of Lepidoptera.
3 f sex pheromone biosynthetic pathways in the Lepidoptera.
4 ecropin before the divergence of Diptera and Lepidoptera.
5 y factor for the host's antiviral defense in Lepidoptera.
6 rred from bacteria to phytophagous mites and Lepidoptera.
7 ns Cry1Ab, Cry1Ac or both in four species of Lepidoptera.
8 erves as a resource for melanism research in Lepidoptera.
9 panded to the other insect groups except for Lepidoptera.
10 iation of moths and butterflies in the order Lepidoptera.
11 l, mechanism for diversification of tropical Lepidoptera.
12 y undescribed duplication of this gene among Lepidoptera.
13 orted as functional Cry1A toxin receptors in Lepidoptera.
14 ed to morphological diversity in Diptera and Lepidoptera.
15 cific biological example: oviposition in the Lepidoptera.
16 s, particularly as natural enemies of larval Lepidoptera.
17 and detoxification compared with specialist Lepidoptera.
18 llelochemicals and synthetic insecticides in Lepidoptera.
19 common in the Lycaenidae compared with other Lepidoptera.
20 losely related taxa, such as Trichoptera and Lepidoptera (Amphiesmenoptera), differ greatly in sperm
22 ing of neuropeptidergic signaling systems in Lepidoptera and aid in the design of peptidomimetics, ps
27 suggest that this mechanism is common within Lepidoptera and that cortex has become a major target fo
28 the profound differences in responses of the Lepidoptera and the Diptera to juvenile hormone (JH).
29 ng the evolution of sexual dimorphism in the Lepidoptera, and alternative hypotheses have been neglec
31 a, Isoptera, Hemiptera, Coleoptera, Diptera, Lepidoptera, and Hymenoptera), GABA-like immunoreactive
34 ural predator of eggs of Utetheisa ornatrix (Lepidoptera, Arctiidae), a moth that sequesters pyrroliz
39 Here we show that larval diets of tropical Lepidoptera are more specialized than those of their tem
41 The wing patterns of butterflies and moths (Lepidoptera) are diverse and striking examples of evolut
42 taining Novartis event 176 on two species of Lepidoptera, black swallowtails and monarch butterflies,
45 importance of resident microbiomes in larval Lepidoptera (caterpillars) is lacking, despite the fact
46 ing diverse insect orders including Diptera, Lepidoptera, Coleoptera, and Hymenoptera as well as in d
47 genetic analyses of Nymphalidae and of other Lepidoptera, combined with orthologue-level comparisons
49 of the early-diverging lineages of ditrysian Lepidoptera, comprise about 1,800 species worldwide, inc
50 ecticidal activity against neonate larvae of Lepidoptera (Diatraea saccharalis), causing 60% mortalit
51 structural database covering the Coleoptera, Lepidoptera, Diptera and Lepidoptera/Diptera specificity
52 ncluding 39 viruses from hosts of the orders Lepidoptera, Diptera, and Hymenoptera, was reconstructed
56 p represented in this study, the leaf-mining Lepidoptera, exhibits a wide range of subordinal taxonom
62 composition of species-rich geometrid moth (Lepidoptera: Geometridae) assemblages in the mature temp
64 ies have reported that chromosome synteny in Lepidoptera has been well conserved, yet the number of h
68 stemin-mediated resistance to Manduca sexta (Lepidoptera) herbivory, demonstrating that MPK1 and MPK2
69 pical skipper butterfly Perichares philetes (Lepidoptera, Hesperiidae), described in 1775, which barc
70 ovarian cells of three different species of lepidoptera, i.e. B. mori (silkmoth), Samia cynthia rici
71 st an evolutionary split between Diptera and Lepidoptera in how the ecdysone biosynthetic pathway is
73 ately promote the species diversification of Lepidoptera in temperate forests with respect to escape
74 ura antennal unigenes had high homology with Lepidoptera insects, especially genes of the genus Spodo
75 (NomegaV), a T=4 icosahedral virus infecting Lepidoptera insects, were produced in insect cells using
78 in the thoracic and subesophageal neurons of Lepidoptera larvae and may be absent in a subset of the
80 n that populations of moths and butterflies (Lepidoptera) may be particularly susceptible to populati
82 s by comparing host specialization in larval Lepidoptera (moths and butterflies) at eight different N
83 t specificity and beta diversity in tropical Lepidoptera (moths and butterflies) from New Guinea and
84 ewing), Hymenoptera (bees, ants, and wasps), Lepidoptera (moths), and Diptera (flies and mosquitoes).
91 to a phylogeny revealed two instances within Lepidoptera of convergently evolved L photopigment linea
92 tic XY system in Drosophila to ZW systems in Lepidoptera or mobile genes determining sex as found in
95 Cabbage White Butterfly [Pieris rapae (L.) (Lepidoptera: Pieridae)], which feeds on cruciferous host
97 redominantly midgut-expressed gene from many Lepidoptera possess key residues shown to be part of the
102 ales of the lesser waxmoth Achroia grisella (Lepidoptera: Pyralidae) produce ultrasonic advertisement
104 mitochondrial cytochrome c oxidase I from 28 Lepidoptera species and 1,359 individuals across four ho
105 t Survey shows that parasitism of particular Lepidoptera species is strongly host-plant-dependent, th
106 is structurally more closely similar to the Lepidoptera-specific Cry1Aa than the Coleoptera-specific
107 tagged databases have been used to discover Lepidoptera-specific genes, provide evidence for horizon
108 E75 activation by JH, in both Diptera and Lepidoptera, suggests a conserved function in the JH sig
109 timated there are over 100,000 moth species (Lepidoptera) that produce sex pheromones comprising comm
112 Until recently, deep-level phylogeny in Lepidoptera, the largest single radiation of plant-feedi
114 tted fireworm moth, Choristoneura parallela (Lepidoptera: Tortricidae) were characterized and assayed
116 om Antiquan germ plasm that are resistant to Lepidoptera, we have demonstrated that a unique 33-kD cy
117 y, alpha-amylases from Helicoverpa armigera (Lepidoptera) were not inhibited by AhAI while Tribolium
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