ライフサイエンスコーパス: Hymenoptera

1 sex determination mechanism of Chalcidoidea (Hymenoptera).

2 helytoky, is particularly common in solitary Hymenoptera.

3 ing, and social behavior within the stinging Hymenoptera.

4 europil essential for learning and memory in Hymenoptera.

5 differences between major groups within the Hymenoptera.

6 tists working on insect species of the order Hymenoptera.

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

8 complete metamorphosis) and were lost in the Hymenoptera.

9 >200,000 species of the entire insect order Hymenoptera.

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

11 despread in insects, especially the aculeate Hymenoptera.

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

13 differ markedly from those known from other Hymenoptera.

14 those found in the better studied parasitic Hymenoptera.

15 a major influence on diversification rate in Hymenoptera.

16 t there is considerable variation within the Hymenoptera.

17 ition to the genomic resources available for Hymenoptera.

18 in the olfactory pathways of these eusocial Hymenoptera.

19 ifferences in mating biology relative to the Hymenoptera.

20 leoptera (95 species), Diptera (54 species), Hymenoptera (21 species), and Neuroptera (11 species).

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

22 port an instance of sexual divergence in the Hymenoptera, a sexually reproducing group that lacks sex

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

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

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

26 We prospectively recruited 374 patients with Hymenoptera allergy and no overt signs of mastocytosis w

27 ty, dysautonomia, flushing and pruritus, and hymenoptera allergy have variably been described in prio

28 ike asthma, allergic rhinitis, food allergy, hymenoptera allergy, or atopic dermatitis are highly pre

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

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

31 t secondary metabolite detoxification in the Hymenoptera, an order that contains numerous highly bene

32 meters, performed best, localising 91.21% of Hymenoptera and 80.69% of Diptera individuals.

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

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

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

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

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

38 Social parasites are common among eusocial Hymenoptera and exhibit a wide range of distinct life hi

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

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

41 Hymenoptera and Psocodea have greatly elevated rates of

42 ectively), partly due to Syrphidae mimicking Hymenoptera and the challenge of detecting smaller, blur

43 elationships between 2,352 pairs of stinging Hymenoptera and their Syrphidae mimics based on a large-

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

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

46 Diptera, Hymenoptera, and Coleoptera had their greatest abundance

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

48 Monogenic reproduction is well documented in Hymenoptera (ants, bees and wasps), where it is associat

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

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

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

52 Hymenoptera (ants, bees, and wasps) played an important

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

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

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

56 s of color pattern variation in bumble bees (Hymenoptera, Apidae, Bombus), a group that has undergone

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

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

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

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

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

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

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

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

65 g parasitic wasp Cotesia sesamiae (Cameron) (Hymenoptera: Braconidae) attraction to volatiles collect

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

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

68 onnative parasitoid Heterospilus prosopidis (Hymenoptera: Braconidae) on the intraspecific interferen

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

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

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

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

73 dominant strategy since the Late Triassic in Hymenoptera, but was not an immediate driver of diversif

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

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

76 The majority of pollinators, especially Hymenoptera, choose plant species on which they had high

77 e lower trophic level, exemplified by larger Hymenoptera connecting networks of different habitats an

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

79 Beewolves, a group of solitary digger wasps (Hymenoptera: Crabronidae), provide their brood cells wit

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

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

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

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

84 xa.(5)(,)(6)(,)(7) Our results indicate that Hymenoptera diversification is multifaceted and lineage-

85 ants.(3)(,)(4) However, our understanding of Hymenoptera diversification remains limited by a lack of

86 The evolution of eusociality in Hymenoptera-encompassing bees, ants, and wasps-is charac

87 sitoids Anagyrus cachamai and A. lapachosus (Hymenoptera: Encyrtidae), two candidate neoclassical bio

88 systemic anaphylaxis, most notably caused by Hymenoptera envenomation.

89 Chouioia cunea Yang (Hymenoptera: Eulophidae) has been widely used for biolog

90 Tetrastichus planipennisi (Hymenoptera: Eulophidae) is a gregarious, koinobiont end

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

92 id Palmistichus elaeisis Delvare et LaSalle (Hymenoptera: Eulophidae), are preferable.

93 We demonstrate that Hymenoptera experienced successive replacements during t

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

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

96 ucture of the tentorium of the genus Lasius (Hymenoptera, Formicidae) and its minor variation among s

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

98 Stings of certain ant species (Hymenoptera: Formicidae) can cause intense, long-lasting

99 aining colonies of imported fire ants (IFA) (Hymenoptera: Formicidae) in the laboratory are crucial f

100 (Hymenoptera: Formicidae) use directed aerial descent to

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

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

103 s to barcode various Solenopsidini ant taxa (Hymenoptera: Formicidae: Myrmicinae), including the thie

104 rentiate harmful "model" organisms (stinging Hymenoptera) from harmless "mimics" (hoverflies, Diptera

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

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

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

108 We report an update of the Hymenoptera Genome Database, a genomic database of hymen

109 By analyzing the composition of 124 Hymenoptera genomes, spread over the diversity of this c

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

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

112 The Hymenoptera have arrhenotokous haplodiploidy in which ma

113 Social Hymenoptera have played a leading role in development an

114 t orders Diptera, Ephemeroptera, Coleoptera, Hymenoptera, Hemiptera, Odonata, and Trichoptera.

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

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

117 We found that all sequenced Hymenoptera, including sister lineages, possess the non-

118 are their genomes with those of other social Hymenoptera, including the northern giant hornet Vespa m

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

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

121 Allergic reactions to Hymenoptera insect stings remain a major global clinical

122 The origin of eusociality in the Hymenoptera is a question of major interest.

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

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

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

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

127 estimated the origin and diversification of Hymenoptera lineages, considering changes in preservatio

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

129 n nesting strategies observed among solitary Hymenoptera makes them an excellent model to comparative

130 In the Hymenoptera, males develop as haploids from unfertilized

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

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

133 The venom of velvet ants (Hymenoptera: Mutillidae) is notoriously painful.

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

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

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

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

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

139 pragmatic, by considering other insects (eg Hymenoptera), provision of a written action plan and sel

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

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

142 native parasitoid Anisopteromalus calandrae (Hymenoptera: Pteromalidae).

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

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

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

146 orders (Coleoptera, Lepidoptera, Diptera and Hymenoptera) represented 96.7% of all studied specimens.

147 Although most Hymenoptera reproduce via arrhenotokous haplodiploidy, t

148 leoptera (beetles), Lepidoptera (moths), and Hymenoptera (sawflies).(3)(,)(4) Based on the occurrence

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

150 The egg parasitoid Telenomus remus (Hymenoptera: Scelionidae) has been investigated for clas

151 he egg parasitoid Hadronotus pennsylvanicus (Hymenoptera: Scelionidae), a prospective biocontrol agen

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

153 The genus Sirex (Hymenoptera: Siricidae) consists of 29 species including

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

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

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

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

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

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

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

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

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

163 ho had (1) moderate to severe anaphylaxis to Hymenoptera sting, (2) 20% + 2 ng/mL increase in tryptas

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

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

166 , followed by unspecified causes (20.7%) and hymenoptera stings (5.6%).

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

168 Hymenoptera stings and natural rubber latex are the comm

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

170 viduals with large local reactions (LLRs) to Hymenoptera stings and with asymptomatic sensitization t

171 Hymenoptera stings can cause severe anaphylaxis in untre

172 Large local reaction to Hymenoptera stings is usually defined as a swelling >10

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

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

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

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

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

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

179 children who experience severe reactions to hymenoptera stings.

180 astocytosis and 52 had reactions to previous hymenoptera stings.

181 ubset of patients with systemic reactions to Hymenoptera stings.

182 risk factor for severe systemic reactions to hymenoptera stings.

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

184 ective in preventing future anaphylaxis from hymenoptera stings.

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

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

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

188 led the largest time-calibrated phylogeny of Hymenoptera to date and investigated the origin and poss

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

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

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

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

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

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

195 Diagnosis of Hymenoptera venom allergy (HVA) is straightforward in th

196 1319 individuals with Hymenoptera venom allergy (HVA) who needed VIT from refe

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

198 ia is more frequent in patients with SM with Hymenoptera venom allergy and severe mediator-related sy

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

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

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

202 Hymenoptera venom allergy is a potentially life-threaten

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

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

205 Hymenoptera venom allergy ranks among the top three caus

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

207 T(D816V) who displayed HalphaT, anaphylaxis, hymenoptera venom allergy, bone disease, pruritus, flush

208 ociated with severe reactions in adults with Hymenoptera venom allergy, systemic mastocytosis, and id

209 vere anaphylactic reactions in patients with hymenoptera venom allergy.

210 t of allergic rhinitis, allergic asthma, and Hymenoptera venom allergy.

211 omatic sensitization and clinically relevant Hymenoptera venom allergy.

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

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

214 Mastocytosis is a risk factor for Hymenoptera venom anaphylaxis (HVA).

215 rome (MMAS), represent an increased risk for Hymenoptera venom anaphylaxis (HVA).

216 Subcutaneous Hymenoptera venom and alum injections induce IL-33 relea

217 cremental cost-effectiveness ratio (ICER) of Hymenoptera venom depot immunotherapy (HVDI) compared to

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

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

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

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

222 Hymenoptera venom hypersensitivity reactions and severe

223 nse, we investigated the effect of IL-33 and Hymenoptera venom on MC cytokine profiles under VIT-like

224 uman skin MCs were stimulated with IL-33 and Hymenoptera venom or Compound 48/80, with or without IL-

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

226 Sensitization to Hymenoptera venom without systemic sting reactions (SSRs

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

228 immunotherapy (VIT) in patients allergic to Hymenoptera venom, a leading cause of anaphylaxis in adu

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

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

231 ished diagnostic tool for risk assessment in Hymenoptera venom-allergic patients.

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

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

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

235 unknown cause(s) are associated with severe Hymenoptera venom-triggered anaphylaxis (HVA).

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

237 role of MCs for the type of response towards Hymenoptera venom.

238 nts with acute anaphylaxis, predominantly to Hymenoptera venom.

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

240 Most common triggers were Hymenoptera venoms in cutaneous mastocytosis (CM) and in

241 HR are mainly triggered by Hymenoptera venoms in patients with CM and ISM and by dr

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

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

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

245 We analyzed potential triggers (Hymenoptera venoms, food, drug, inhalant and others) and

246 tings and with asymptomatic sensitization to Hymenoptera venoms.

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

248 ld's largest hornet, Vespa mandarinia Smith (Hymenoptera: Vespidae), which occurs naturally in the In

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

250 The order Hymenoptera (wasps, ants, sawflies, and bees) represents

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

252 upergroup B, while infections in Diptera and Hymenoptera were dominated by A-type Wolbachia.

253 We then survey Hymenoptera with more specialised morphological castes,

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

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