ライフサイエンスコーパス: Hymenoptera

1 sex determination mechanism of Chalcidoidea (Hymenoptera).

2 differences between major groups within the Hymenoptera.

3 tists working on insect species of the order Hymenoptera.

4 a, Coleoptera, and Neuroptera but not in the Hymenoptera.

5 complete metamorphosis) and were lost in the Hymenoptera.

6 >200,000 species of the entire insect order Hymenoptera.

7 ut to the mushroom body's calyx in different Hymenoptera.

8 ation (CSD), which is common in haplodiploid Hymenoptera.

9 differ markedly from those known from other Hymenoptera.

10 those found in the better studied parasitic Hymenoptera.

11 in the olfactory pathways of these eusocial Hymenoptera.

12 ifferences in mating biology relative to the Hymenoptera.

13 helytoky, is particularly common in solitary Hymenoptera.

14 ing, and social behavior within the stinging Hymenoptera.

15 europil essential for learning and memory in Hymenoptera.

16 animal groups, most notably in the aculeate Hymenoptera, a clade comprising ants, bees, and stinging

17 How the males of the insect order Hymenoptera acquire centrosomes is a mystery, as they or

18 The stinging wasps (Hymenoptera: Aculeata) are an extremely diverse lineage

19 We recruited 134 patients with Hymenoptera allergy and 76 healthy control subjects for

20 mic mastocytosis (SM) may be associated with hymenoptera allergy.

21 mately 200 million years in the phylogeny of Hymenoptera, allowing researchers to leverage genetic, g

22 de the basis for a natural classification of Hymenoptera and allow for future comparative analyses of

23 ally dimorphic sensory systems are common in Hymenoptera and are considered to result from sex-specif

24 room bodies are particularly large in social Hymenoptera and are thought to be involved in the contro

25 site in many insect groups such as Diptera, Hymenoptera and Coleoptera, and frugivorous vertebrates

26 or describing AL compartmentalization across Hymenoptera and discuss possible evolutionary scenarios.

27 rgic rhinitis, and to prevent anaphylaxis to hymenoptera and fire ant stings.

28 as many families of Coleoptera, Diptera, and Hymenoptera and on poorly sampled parts of the world.

29 Hymenoptera and Psocodea have greatly elevated rates of

30 that this population of LNs arose within the Hymenoptera and underwent extensive morphological modifi

31 ancestral among bees, ants, and wasps (Order Hymenoptera), and the close relatedness that it generate

32 In eusocial Hymenoptera (ants, bees and wasps), queen and worker adu

33 In some eusocial Hymenoptera (ants, bees and wasps), workers can produce

34 ism database for insect species of the order Hymenoptera (ants, bees and wasps).

35 from female only, in taxa such as the social Hymenoptera (ants, bees, and wasps) [1], to an unbiased

36 mparatively less focus than the haplodiploid Hymenoptera (ants, bees, and wasps); however, they are t

37 In the Hymenoptera (ants, bees, wasps), there have been many tr

38 structed a linkage map of Bombus terrestris (Hymenoptera, Apidae) phase unknown.

39 Thus, all eusocial species of Hymenoptera are contained within two major groups, chara

40 luding Diptera, Lepidoptera, Coleoptera, and Hymenoptera as well as in diapauses that occur in differ

41 he extensive fossil record of other aculeate Hymenoptera as well as that of ants.

42 cestral form of sex determination within the Hymenoptera because members of the most basal taxa have

43 tera (beetles), Neuroptera (green lacewing), Hymenoptera (bees, ants, and wasps), Lepidoptera (moths)

44 ion techniques on three species of parasitic Hymenoptera (Braconidae), and test the effects of body s

45 Toxoneuron nigriceps (Hymenoptera, Braconidae) is an endophagous parasitoid of

46 of the aphid parasitoid Binodoxys communis (Hymenoptera: Braconidae) and herein we build upon those

47 t that the parasitic wasp Diachasma alloeum (Hymenoptera: Braconidae) has formed new incipient specie

48 the parasitic wasp Bracon sp. near hebetor (Hymenoptera: Braconidae) is based upon a single locus or

49 The parasitoid wasp Cotesia glomerata (L.) (Hymenoptera: Braconidae) parasitizes early instar larvae

50 s canaliculatus, and Diachasmimorpha mellea (Hymenoptera: Braconidae), that attack Rhagoletis pomonel

51 m body growth comparable to that in foraging Hymenoptera, but also identifies plasticity in several o

52 ytokous parthenogenesis is widespread in the Hymenoptera, but its genetic underpinnings have been des

53 nd divergence times of all major lineages of Hymenoptera by analyzing 3,256 protein-coding genes in 1

54 cuticular morphology in Nasonia vitripennis (Hymenoptera; Chalcidoidea).

55 he presence of DNA methylation, which in non-Hymenoptera correlates with CpG depletion.

56 f the gall wasp Antistrophus rufus Gillette (Hymenoptera: Cynipidae) feed within inconspicuous galls

57 ect host, the oak gallwasp Biorhiza pallida (Hymenoptera: Cynipidae).

58 Oak gall wasps (Hymenoptera: Cynipidae, Cynipini) are characterized by p

59 fects the European pine sawfly, N. sertifer (Hymenoptera: Diprionidae), was sequenced and analyzed.

60 parasitoid virulence in Asecodes parviclava (Hymenoptera: Eulophidae) when attacking three closely re

61 d risk factors for severe anaphylaxis due to Hymenoptera field stings with an emphasis on details rel

62 al complexity has been confined primarily to Hymenoptera (for example, ants and bees).

63 Ants (Hymenoptera, Formicidae) represent one of the most succe

64 (Hymenoptera: Formicidae) use directed aerial descent to

65 large-scale molecular phylogeny of the ants (Hymenoptera: Formicidae), based on 4.5 kilobases of sequ

66 esent the sister lineage to all extant ants (Hymenoptera: Formicidae).

67 ptera, Coleoptera, Diptera, Lepidoptera, and Hymenoptera), GABA-like immunoreactive neurons within a

68 The Hymenoptera Genome Database (HGD) is a comprehensive mod

69 We report an update of the Hymenoptera Genome Database (HGD), a model organism data

70 In the haplodiploid Hymenoptera, haploid males arise from unfertilized eggs,

71 d males from unfertilized haploid eggs, some Hymenoptera have a secondary system called complementary

72 The Hymenoptera have arrhenotokous haplodiploidy in which ma

73 Social Hymenoptera have played a leading role in development an

74 eins also supports a reclassification of the Hymenoptera in relation to Diptera and Coleoptera.

75 The Hymenoptera, in particular, have evolved life-histories

76 and allow for future comparative analyses of Hymenoptera, including their genomes, morphology, venoms

77 disorders with KIT mutations may present as Hymenoptera-induced or idiopathic anaphylaxis.

78 d ancestral mode of sex determination in the Hymenoptera is arrhenotokous parthenogenesis, in which d

79 -understood mode of sex determination in the Hymenoptera is complementary sex determination (CSD), in

80 Relatedness within colonies of social Hymenoptera is often significantly lower than the outbre

81 nce owes to the haplodiploid genetics of the Hymenoptera leading to females being relatively more rel

82 unatus), Orthoptera (Schistocerca gregaria), Hymenoptera (Lysiphlebus testaceipes), and Hemiptera (To

83 In the Hymenoptera, males develop as haploids from unfertilized

84 uggest that sex determination systems in the Hymenoptera may be evolutionary labile.

85 fication and key evolutionary transitions of Hymenoptera, most notably from phytophagy to parasitoidi

86 luded 65 species of Dasymutilla velvet ants (Hymenoptera: Mutillidae).

87 micry complex in North American velvet ants (Hymenoptera: Mutillidae).

88 , ants, bees, and other insects in the order Hymenoptera, only uniparental haploid males that arise f

89 with diversification in others (Coleoptera, Hymenoptera, Orthoptera).

90 As parasitoids, predators, and pollinators, Hymenoptera play a fundamental role in virtually all ter

91 Nasonia longicornis (Hymenoptera: Pteromalidae) has an A supergroup and two c

92 Nasonia (Hymenoptera: Pteromalidae) is a genus of parasitoid wasp

93 In addition, the calyces of Hymenoptera receive substantial direct input from the op

94 The complex social organization of eusocial Hymenoptera relies on sophisticated olfactory communicat

95 onships among the major lineages of aculeate Hymenoptera remain contentious [6-12].

96 Although most Hymenoptera reproduce via arrhenotokous haplodiploidy, t

97 Hymenoptera (sawflies, wasps, ants, and bees) are one of

98 this reproductive strategy is common to all Hymenoptera, sex-determination is not strictly specified

99 ciated miRNAs from outside advanced eusocial Hymenoptera, so providing evidence for caste-associated

100 g of the biology of agriculturally important Hymenoptera species through genomics.

101 Cross-reactivity between hymenoptera species varies according to the different al

102 Our analyses suggest that extant Hymenoptera started to diversify around 281 million year

103 -three patients with allergic reaction after Hymenoptera sting (11 wasp and 12 honeybee) were treated

104 First-line treatment for Hymenoptera sting anaphylaxis is intramuscular adrenalin

105 An anaphylactic reaction due to a Hymenoptera sting is a clinical emergency, and patients,

106 r (n = 152), MIMA and age at the most recent Hymenoptera sting were independent predictors for HVAn (

107 history of an anaphylactic reaction after a hymenoptera sting were tested.

108 atients seen at our mastocytosis center with Hymenoptera sting-induced anaphylaxis, documented hypote

109 Twenty-two patients with Hymenoptera sting-induced anaphylaxis, without skin lesi

110 in patients with severe reactions caused by Hymenoptera stings and increased serum basal tryptase (S

111 Hymenoptera stings and natural rubber latex are the comm

112 ols without history of systemic reactions to Hymenoptera stings and no sIgE to whole venoms.

113 Hymenoptera stings can cause severe anaphylaxis in untre

114 on symptoms, including anaphylaxis following Hymenoptera stings or other triggers.

115 ticaria or angioedema in severe reactions to Hymenoptera stings with hypotension might represent the

116 patients with systemic allergic reactions to Hymenoptera stings, 76 with double positivity of serum-s

117 s who present with anaphylactic reactions to Hymenoptera stings, as well as to recognize and treat th

118 is has been described particularly following hymenoptera stings, but also occasionally after the inta

119 -medication of anaphylactic reactions due to Hymenoptera stings, to inform healthcare staff about app

120 ubset of patients with systemic reactions to Hymenoptera stings.

121 astocytosis and 52 had reactions to previous hymenoptera stings.

122 risk factor for severe systemic reactions to hymenoptera stings.

123 otherapy is recommended only for OcAn due to Hymenoptera stings.

124 ective in preventing future anaphylaxis from hymenoptera stings.

125 children who experience severe reactions to hymenoptera stings.

126 unrecognized major radiation of phytophagous Hymenoptera that did not lead to wood-dwelling and paras

127 y aposematic species (such as members of the hymenoptera, the lepidoptera, and amphibia) are highly m

128 beetle relative and the early divergence of Hymenoptera; the recognition of hexapods as a crustacean

129 compare them with similar data for eusocial Hymenoptera, to better identify commonalities and differ

130 an help explain the apparent ease with which Hymenoptera transition between sexual and asexual reprod

131 ns, minute Trichogramma evanescens Westwood (Hymenoptera: Trichogrammatidae) parasitic wasps scale br

132 fic immunotherapy (AIT) is very efficient in hymenoptera venom (HV)-allergic patients, long-term outc

133 Detection of IgE to recombinant Hymenoptera venom allergens has been suggested to improv

134 silonRI cross-linking or by stimulation with hymenoptera venom allergens, were significantly reduced

135 llergens improve the diagnostic precision in Hymenoptera venom allergy (HVA), in particular in patien

136 Diagnostic tests in patients with Hymenoptera venom allergy are frequently positive to ven

137 ergen immunotherapy (AIT) in respiratory and Hymenoptera venom allergy are well established; however,

138 Severe anaphylaxis in Hymenoptera venom allergy has been associated with a num

139 Hymenoptera venom allergy is a potentially life-threaten

140 Anaphylaxis caused by hymenoptera venom allergy is associated with elevation o

141 prevalence of mastocytosis in patients with Hymenoptera venom allergy is high, and thus the disease

142 ding to current guidelines, skin testing for hymenoptera venom allergy should be performed in a stepw

143 ur hypothesis in 847 patients with confirmed hymenoptera venom allergy.

144 omatic sensitization and clinically relevant Hymenoptera venom allergy.

145 ested to improve the diagnostic precision in Hymenoptera venom allergy.

146 vere anaphylactic reactions in patients with hymenoptera venom allergy.

147 lent systemic mastocytosis with a history of Hymenoptera venom exposure after age 15 years or greater

148 t group, irrespective of disease subtype and Hymenoptera venom exposure, HVAn prevalence gradually in

149 eeded to avoid otherwise undetectable IgE to hymenoptera venom extracts in about 8% of such patients.

150 Additionally, hymenoptera venom has for a long time been claimed to mo

151 t-resolved diagnosis (CRD) are promising for Hymenoptera venom or food allergy.

152 Sensitization to Hymenoptera venom without systemic sting reactions (SSRs

153 at induce life-threatening anaphylaxis (e.g. Hymenoptera venom).

154 Api m 10 was found at a similar frequency in hymenoptera venom-allergic patients with and without ele

155 zation pattern and diagnostic sensitivity in hymenoptera venom-allergic patients with elevated sBT le

156 levels are a well-described risk factor for Hymenoptera venom-induced anaphylaxis (HVAn) in patients

157 ood sample identifies SM among patients with hymenoptera venom-induced anaphylaxis in whom the diagno

158 Thirteen SM patients presented with Hymenoptera venom-induced anaphylaxis, no skin lesions,

159 nts with acute anaphylaxis, predominantly to Hymenoptera venom.

160 d anaphylaxis (HVAn) in patients allergic to Hymenoptera venom.

161 Twenty-two Hymenoptera-venom allergic patients with sIgE antibodies

162 imultaneously injected concentrations of two hymenoptera venoms is safe and permits the investigator

163 Although sensitization to Hymenoptera venoms was common, the risk of SSRs in sensi

164 sBT tryptase level and systemic reactions to hymenoptera venoms were analyzed for their IgE reactivit

165 Social wasps (Hymenoptera: Vespidae) forage for water, pulp, carbohydr

166 osts of the orders Lepidoptera, Diptera, and Hymenoptera, was reconstructed based on sequences from t

167 y eusocial honeybee Apis mellifera and other Hymenoptera, we identify deeply conserved similarities,

168 To counteract this, Hymenoptera with traits that promote inbreeding, such as

169 has appeared several times independently in Hymenoptera, within different families such as Apidae (b