ライフサイエンスコーパス: dipteran

1 brate divergence is almost twice that of the dipteran.

2 age-specific glycosphingolipid expression in dipterans.

3 alization has not been investigated in other dipterans.

4 are robust and conserved in many species of dipterans.

5 ood and that their vectors were non-mosquito dipterans.

6 Drosophila species, as well as in some other Dipterans.

7 able prospect of the method working in other dipterans.

8 Hox3 duplication and is only found in higher dipterans.

9 tripe enhancers in the eve loci of different dipterans.

10 olution, we identified kek1 orthologs within dipterans.

11 is role during the evolution of more-derived dipterans.

12 embryogenesis appears to be unique to higher dipterans.

13 In both cases (on removal of a dipteran and a coleopteran leaf-miner species) we found

14 ble conservation of required factors between dipteran and human hosts.

15 at most of the dumpy gene has evolved in the dipteran and other insect orders by purifying selection

16 e drive strategy can be satisfied in a model dipteran and that there is a reasonable prospect of the

17 gone considerable evolutionary change in the dipterans and that similar patterns of pair-rule gene ex

18 xual phenotypes also determines sex in other dipterans and the silk moth, while the upstream genes va

19 , which is pervasive in Drosophila and other dipterans (and has a homologous position as an intron fo

20 soforms are present in the distantly-related Dipteran Anopheles gambiae, suggesting that the properti

21 these technologies need to be validated for dipterans as the members of this clade play important ec

22 te difference exists between vertebrates and dipterans, because the percentage difference between the

23 thereby adjust gene activity to a variety of dipteran blastoderm cytoarchitectures.

24 r3 plants exhibited strong resistance to the dipteran Bradysia impatiens and the fungus Alternaria br

25 glycosylation pattern, specifically that of dipteran cells, to inhibit dsRNA-induced cytokine produc

26 ani ring (BR) genes in polytene cells in the dipteran Chironomus tentans.

27 LSP-1 calliphorin and LSP-2 form a distinct dipteran clade whose members are more similar to each ot

28 previously been interpreted to suggest that dipteran crop contractions do not include a neural compo

29 The N-terminal leader of dipteran DIAP1 also conferred virus-induced IAP depletio

30 It is apparent that the higher dipterans did not requisition a lipoprotein lipase to re

31 understand the structure of the head of the Dipteran Drosophila melanogaster have joined the discour

32 pteran Trichoplusia ni and S2 cells from the dipteran Drosophila melanogaster.

33 ebrates estimate that vertebrates split from dipterans (Drosophila) approximately 900 million years a

34 Studies performed on the Dipteran, Drosophila melanogaster, indicate that this is

35 The dipteran DVHFs had 82 readily recognizable human homolog

36 biofilms at day 21 and increased cumulative dipteran emergence by 65% and 89% during the first and t

37 anogaster transcript annotations and 666,153 dipteran EST sequences we have identified 44 putative co

38 male form is the default, arose during early dipteran evolution.

39 la melanogaster, which serves as a "typical" dipteran example without eye stalks.

40 Higher dipterans exist in all freshwater wetland types, are mic

41 de between mammals ( approximately 70 My) or Dipteran families ( approximately 100 My), animal phyla

42 d remains the same between mammals (17.2) or Dipteran families (15.9), but it becomes much slower bet

43 Unexpectedly, several species within the dipteran family Drosophilidae were found to contain two

44 Dipteran flies are amongst the smallest and most agile o

45 These tradeoffs are best studied in Dipteran flies in which rapid mechanosensory feedback to

46 terans), as well as hemipterans (true bugs), dipterans (flies), and hymenopterans (wasps and ants), a

47 Comparative analyses revealed that dipterans follow similar codon usage and nucleotide bias

48 t for the exclusion of acalyptrate and other dipterans from wetlands ecology studies.

49 ct Loqs-PD in Ae. aegypti; analysis of other dipteran genomes demonstrated that this isoform is not c

50 In contrast, we show here that several dipteran genomes encode two novel, highly related, micro

51 nogaster become fixed via epistasis in other Dipteran genomes.

52 The systematic position of this dipteran has remained enigmatic due to the absence of re

53 horax (Ubx) gene product in Lepidopteran and Dipteran hindwings.

54 pororida and use a variety of vertebrate and dipteran hosts worldwide.

55 enome assembly of an extremophile, the first dipteran in the family Chironomidae, and the first Antar

56 e oligosaccharide differs from that of other dipterans in the linkage at a single glycosidic bond, a

57 In contrast, H1 isoforms are not present in Dipterans, including D. melanogaster, except for an embr

58 underwent a fission event in some Brachycera dipterans, including Drosophila species, creating two in

59 a recently derived trait, and that in other dipterans, including the medically important mosquitoes,

60 The other AGT is a typical dipteran insect AGT and is specific for converting glyox

61 tor Anopheles gambiae, to determine how this dipteran insect maintains its chromosome ends.

62 e encoding a LSP-1-like protein from a lower dipteran insect, the malaria mosquito Anopheles gambiae.

63 eral-directional motion of a Drosophila-like dipteran insect, which may then be used to estimate the

64 ing protein which is lethal to the larvae of Dipteran insects and broadly cytolytic in vitro.

65 The halteres of dipteran insects are essential sensory organs for flight

66 In this review, we use the wing veins of dipteran insects as potential models for understanding t

67 The halteres of Dipteran insects play an important role in flight contro

68 Because dipteran insects such as D. melanogaster lack glutathion

69 Because dipteran insects such as Drosophila melanogaster lack gl

70 During the last larval instar, dipteran insects synthesize two hexamerins rich in aroma

71 ated into the diets of three coleopteran and dipteran insects that have acidic gut lumen, recombinant

72 nomes (such as Caenorhaditis elegans and the Dipteran insects) and those that methylate their genomes

73 te-life mortality plateau in both humans and dipteran insects, seemingly at odds with both prior data

74 In dipteran insects, the lobula plate neuropil provides a m

75 ductase-1 (DmTrxR-1) is a key flavoenzyme in dipteran insects, where it substitutes for glutathione r

76 y manipulate than other mosquito species and dipteran insects.

77 s the largest transcription factor family in dipteran insects.

78 of longitudinal hovering flight dynamics for dipteran insects.

79 ion in both olfactory and visual pathways in Dipteran insects; these genes may prove useful in the de

80 Thus, HFR1 is an antinutrient to dipteran larvae and may play a significant role in deter

81 s in a representative of a basally diverging dipteran lineage, the moth midge Clogmia albipunctata.

82 for the developmental hourglass model in the dipteran lineage.

83 ts before the divergence of lepidopteran and dipteran lineages.

84 whereas the mature Crz is identical in other dipteran members.

85 d verified the utility of 454 sequencing for dipteran mitochondrial genomes.

86 s the utility of 454 sequencing approach for dipteran mtgenomic research.

87 Antibody to the dipteran myosuppressin peptide, dromyosuppressin, TDVDHV

88 teran nucleopolyhedroviruses (NPVs), and the dipteran NPV, CuniNPV.

89 demonstrate that in Drosophila, as in other dipterans, optic glomeruli are involved in further recon

90 /site/year when comparisons are made between dipterans or between mammals, but only 5 x 10(-10) when

91 Myiasis, which is the dipteran parasitism of living vertebrates, occurs in sev

92 We conclude that more intensive study of dipteran parasitoids is required before we can understan

93 cuses on several aspects of the bionomics of dipteran parasitoids that have received little comprehen

94 n fly (Mayetiola destructor) larvae, a major dipteran pest of this crop.

95 se of RNA interference (RNAi) to control two dipteran pests, Musca domestica and Delia radicum, by di

96 Here we show that the dipteran rate of molecular evolution is similar to other

97 -adapted species (i.e., snails and predatory dipterans) relative to small-bodied, cold-adapted taxa (

98 Within dipterans, Schizophora represents a recent radiation of

99 ne dehydrogenase in 37 species, including 31 dipterans sequenced by us.

100 foliar herbivores), their parasitoids, and a dipteran species (root herbivore).We tested the hypothes

101 , EC 3.1.3.1) isolated from lepidopteran and dipteran species are identified as receptors for Cry1Ac

102 cellular localisation of mRNAs from multiple dipteran species both in situ and by injection into Dros

103 ed to the coding region of bicoid from three dipteran species in transgenic Drosophila embryos using

104 n of different domains of the dsx gene in 29 dipteran species showed that, over short evolutionary ti

105 arable expression patterns observed in other dipteran species suggest conserved regulatory mechanisms

106 are essentially the same in closely related dipteran species with embryos of very different size.

107 A major difference between dipteran species, however, is the size of the embryo, wh

108 - and cold stress-responsive gene in diverse dipteran species.

109 a three-dimensional domain-swapped dimer in dipteran species.

110 s established largely by the activity of the dipteran-specific Bicoid (Bcd) morphogen gradient, which

111 and that its role has been reduced in higher dipterans such as Drosophila.

112 In dipterans such as the fruitfly Drosophila melanogaster (

113 ions are associated with behaviors unique to dipterans, such as regurgitation (or bubbling), nuptial

114 The myrmecophile larva of the dipteran taxon Nothomicrodon Wheeler is rediscovered, al

115 the dorsal ectoderm in two highly divergent dipterans, the fruitfly Drosophila melanogaster and the

116 amplified by two primers designed from other dipteran transferrin sequences.

117 (Haemosporida), with diverse life cycles and dipteran vectors that infect other vertebrates.

118 parasitism, and in one case (removal of the dipteran) we found significantly higher abundance a year

119 nterior development in Drosophila and higher dipterans, which is not conserved.

120 nd robo3 exist as distinct genes only within dipterans, while other insects, like the flour beetle Tr

121 to obtain complete mitochondrial genomes for dipterans without the aid of conventional molecular tech

122 ectly demonstrate their homology with higher-dipteran YPs were unsuccessful.

123 monstrate that lepidopteran ESP/YP2s, higher-dipteran YPs, and lipoprotein lipases are indeed homolog