ライフサイエンスコーパス: pupae

1 grammed cell death (PCD) and arrest as early pupae.

2 entral brain region of late-stage Drosophila pupae.

3 id not affect the incidence of nondiapausing pupae.

4 ol-operated larvae developed into diapausing pupae.

5 operated larvae developed into nondiapausing pupae.

6 neurons in cultures from OK107-GAL4;UAS-GFP pupae.

7 e pupae significantly more rapidly than male pupae.

8 tHex-1.2) is only found in female larvae and pupae.

9 rentiation of many cell types in embryos and pupae.

10 CNS of third instar larvae, and die as early pupae.

11 Most flies lacking tiggrin die as larvae or pupae.

12 larvae (L4) and disappears abruptly in early pupae.

13 ult development when injected into debrained pupae.

14 Da protein in larvae and a 53-kDa protein in pupae.

15 r ants seem to do so only in the presence of pupae.

16 t-feeding on the water-rich hemolymph of SWD pupae.

17 ation and mitochondrial energy generation in pupae.

18 laid by females that emerged from irradiated pupae.

19 vae and adults but were absent from eggs and pupae.

20 ignificantly higher than that from 4-day-old pupae.

21 any non-MB NBs from decommissioning in early pupae.

22 cted deposits of chitin fibers in Drosophila pupae.

23 ndosomal sorting of Notch and Spdo in living pupae.

24 ecdysone-dependent transition from larvae to pupae.

25 bility in severing their larval dendrites in pupae.

26 le> larvae> worker pupae approximately alate pupae.

27 transcript during development, especially in pupae.

28 ntaining a number of brood cells occupied by pupae.

29 o as to maintain conditions that benefit the pupae.

30 U(M) within the same 10 neuronal clusters in pupae.

31 e significantly lower than that of 4-day-old pupae (10.3%).

32 ) gin traps of tenebrionid and scarab beetle pupae,(11)(,)(12) or abdominal tracheal gills of mayfly

33 ergence of adult females from 0 to 2-day-old pupae (120.2-142.3 per pupa) was significantly higher th

34 eggs/female) than those from 0 and 1-day-old pupae (178.4-178.9 eggs/female).

35 reds of species of tropical caterpillars and pupae-26 examples of which are displayed here from the d

36 ant-negative Orai in dopaminergic neurons of pupae abolished flight.

37 aegypti larvae over the total of larvae and pupae adjusted for daily rainfall when compared to tires

38 mbles that of escl, with expression in early pupae, adult females, and male testes.

39 cript in unfertilized eggs, embryos, larvae, pupae, adult head and thorax, ovary, testis, and S2 tiss

40 lcarata across developmental stages (larvae, pupae, adults) and different landscape environments (con

41 Although wild-type larvae transition to pupae after 5 days, arrested third instar (ATI) larvae p

42 flicted prepupae metamorphosed to white-eyed pupae, all wound scars disappeared with the exuviae.

43 Diapausing pupae also clear anaerobic by-products and regenerate ma

44 t, cellular immunity indices were highest in pupae and adult females, while the sixth instar (L6) and

45 y, yielding hyperproliferative phenotypes in pupae and adult flies.

46 bservation that it regulates the size of the pupae and adult flies.

47 nable interaction proteomics from developing pupae and adult flies.

48 ophila olfactory projection neurons (PNs) in pupae and adults revealed global downregulation of wirin

49 er analyzed canB2 expression and function in pupae and adults.

50 lly all tissues that normally express per in pupae and adults.

51 nd differential localisation and dynamics in pupae and adults.

52 and the production of large (giant) larvae, pupae and adults.

53 P in specific tissues of living prepupae and pupae and compiled images of these animals into time-lap

54 ated that MdBV replication begins in stage 2 pupae and continues in adults.

55 d from the developing thoracic legs of early pupae and cultured in the presence of neurons assumed a

56 cone dynamics in developing brains of intact pupae and data-driven computational modeling.

57 Some developmental abnormalities of the pupae and emerging moths were noted.

58 initially isolated from Hyalophora cecropia pupae and have since been isolated and identified in var

59 2 mRNA accumulates only in female larvae and pupae and is expressed at very low levels in adult femal

60 l fluid that lies between the metamorphosing pupae and its pupal case.

61 induced at the transcriptional level in mid-pupae and maintained into adulthood, and this response i

62 alpha and burs beta are expressed in larvae, pupae and newly emerged adults.

63 using the same selectable markers, the white pupae and temperature-sensitive lethal genes.

64 The larvae had metamorphosed into pupae and then to pharate adults but did not complete ad

65 ae live a normal life span, they do not form pupae and thus do not give rise to eclosed flies.

66 ve compounds (PhACs) was examined in larvae, pupae, and (sub)adults of three groups of aquatic insect

67 es isolated from libraries of 0-4-h embryos, pupae, and adult heads from Drosophila melanogaster has

68 , 2nd, 3rd, and 4th instar larvae, prepupae, pupae, and adult.

69 nd tissue-specific per expression in larvae, pupae, and adults are present in the CRS and that the pe

70 easured telomere length in larvae, prepupae, pupae, and adults of two species of solitary bees, Osmia

71 nt in the peritracheal Inka cells in larvae, pupae, and adults, Ap, PC2, Fur1, PAL2, and dDA1 are not

72 em-specific fluorescence in embryos, larvae, pupae, and adults.

73 st1alpha are expressed in A. gambiae larvae, pupae, and adults.

74 1 resulted in a reduction in size of larvae, pupae, and adults.

75 were undetectable in 3rd+4th instars, worker pupae, and alate (mixed sex) pupae; readily detectable i

76 was undetectable in 3rd+4th instars, worker pupae, and alate pupae; low in male and female alates an

77 because the host-feeding process killed the pupae, and because wasps that engaged in greater host-fe

78 Caterpillars, pupae, and foodplants offer better distinguishing charac

79 rtant foods such as mango, seafood, silkworm pupae, and natto.

80 This evidence can include eggs, larvae, pupae, and puparial casings.

81 PRs were fluorescently labeled in larvae and pupae, and the number of indistinguishably close anatomi

82 Many of these individuals died as mature pupae, and those that eclosed showed poor locomotion and

83 e> alate (winged adult) male> larvae> worker pupae approximately alate pupae.

84 Silkworm pupae are highly valuable as edible insects due to their

85 ngesting water and that it host-feeds on SWD pupae as a water-intake strategy.

86 the bioactive compounds present in silkworm pupae (Bombyx mori).

87 Homozygous mutant animals die as pupae, but lethality is rescued by the mini-GAL4-driven

88 vn mutants die as white undifferentiated pupae, but the rescued individuals showed global differe

89 The removal of mite-infested pupae by worker bees, Varroa Sensitive Hygiene (VSH), le

90 ting the bioactive compounds within silkworm pupae can provide useful information for advanced proces

91 Adult females emerging from 2-day-old pupae carried significantly more eggs (258.2 eggs/female

92 sed a tobit model for Ae. aegypti larvae and pupae count data, type and count of aquatic habitats, an

93 Experimental removal of mice, which eat moth pupae, demonstrated that moth outbreaks are caused by re

94 l survival; if the secretion is not removed, pupae develop fungal infections and die.

95 Mite-infested pupae developed into adults with either normal or deform

96 cting and developmentally staging Drosophila pupae, dissecting fly eyes at defined stages of developm

97 n resulted in embryos, larvae, and enclosing pupae drowning, underfed, or desiccating.

98 of adult emergence were conducted until all pupae either emerged or died.

99 Lycaenid larvae and pupae employ complex chemical and acoustical signals to

100 erge and when it emerges on a nest with more pupae (even though worker-brood relatedness tends to be

101 xpression of the X-linked gene yellow in the pupae exactly foreshadows the adult melanization pattern

102 of this parasitoid, emerged from T. molitor pupae exposed to 15.03 mg a.i./L of deltamethrin, was hi

103 we reveal that unlike solitary insects, ant pupae extrude a secretion derived from the moulting flui

104 Examination of pupae following ablation showed that migrating PTCs from

105 was also significantly (p < 0.05) reduced in pupae following injection causing 30% and 42% knockdown

106 An. stephensi eDNA, derived from emergent pupae for 24 h, was remarkably stable, and still detecta

107 ch provided valuable information to optimize pupae for the mass rearing of C. cunea on host T. molito

108 Indirect flight muscles of late pupae from each mutant displayed disrupted myofibril ass

109 Mutants of importin-beta11 died as late pupae from neuronal defects, and neuronal importin-beta1

110 curs in capped brood cells and mite-infested pupae from these cells usually have high levels of DWV.

111 on and eclosion and to arrest development of pupae in a concentration dependent fashion.

112 iads and garbage cans had significantly more pupae in relation to larvae when compared to tires, trad

113 tly increases preference for Protocalliphora pupae in the introgression line relative to the recessiv

114 sequencing, we identified VDV1 in honey bee pupae in the US.

115 inal discs in living Drosophila melanogaster pupae in vivo and over time.

116 erties, to raise their broods (larvae and/or pupae) in advantageous thermal conditions.

117 a novel pairing between worm embryo and fly pupae, in addition to the embryo-to-embryo and larvae-to

118 Mosquito larvae and pupae, including from field Aedes aegypti can acquire ZI

119 e latter cause may result from the fact that pupae-laden nests are especially likely to survive, and

120 While females from unirradiated pupae laid a total of 43,142 eggs, no egg was laid by fe

121 sis in the heminotal epithelia of Drosophila pupae leading to thorax closure corresponds with spatiot

122 rthermore, topical methoprene application to pupae leads to the ectopic accumulation of JhI-1 and JhI

123 s to severe neurodegeneration as revealed by pupae lethality; the latter effect could be rescued by H

124 fly, Ceratitis capitata) associated with the pupae life stage and timepoints immediately following ad

125 in 3rd+4th instars, worker pupae, and alate pupae; low in male and female alates and queens; and inc

126 (st) and 2(nd) instar larvae, mature larvae, pupae, male and female adults.

127 ability of females that emerged from treated pupae mated with their siblings were evaluated using blu

128 % of the attacks (0.9% of all available host pupae) more than one mite was involved and behaved as pa

129 Nasonia are parasitic wasps that utilize fly pupae; Nasonia vitripennis is a generalist that parasiti

130 hosts and developmental time of C. cunea in pupae of different ages.

131 nd adult fertility of C. cunea on T. molitor pupae of different ages.

132 ected from fifth instar larvae and 1-day-old pupae of Heliothis virescens after injection of prepupae

133 Our findings indicated that 2-day-old pupae of T. molitor were most suitable to rear C. cunea.

134 led water) with 10 replications, each with a pupae of the alternative host Tenebrio molitor Linnaeus

135 ral cDNAs isolated from brains of diapausing pupae of the flesh fly, Sarcophaga crassipalpis, show ex

136 multispinosus develop as ectoparasitoids of pupae of the invasive ant Paratrechina longicornis.

137 By consecutively moving butterfly pupae of the species Pieris napi from several different

138 l emergence was significantly delayed and no pupae or adult workers were produced.

139 ession and localisation in ovaries, embryos, pupae or adults by stainings and live imaging approaches

140 ient for the true ATM ortholog, dATM, die as pupae or eclose with eye and wing abnormalities.

141 ct or synthetic Mas-ETH into pharate larvae, pupae, or adults initiates preecdysis within 2 to 10 min

142 mperature-shift experiments in which larvae, pupae, or adults were shifted for blocks of time from on

143 hat possess weak who mutations either die as pupae, or survive as adults with defects in wing positio

144 Application of mild ICPD treatment for Eri pupae powder production enhance its functionality over c

145 dy explores the tailoring opportunity of Eri pupae powder properties using instant controlled pressur

146 or, density, and antioxidant activity of Eri pupae powder were studied.

147 from only one fly species, yet evidence from pupae (preadult emergence samples) show that most Bellop

148 4.6% of the 52 nests containing cocoons) but pupae prevalence was low (4.0%, n = 1401 cocoons).

149 We first found that diapausing flesh fly pupae primarily use anaerobic glycolysis during metaboli

150 instars, worker pupae, and alate (mixed sex) pupae; readily detectable in male and female alates; inc

151 g during maturation of the flight circuit in pupae reduces Tyrosine Hydroxylase (TH) expression in th

152 Pupae rendered acyclic with a JHA application consume O(

153 we collected 3636 flowers yielding 1478 fly pupae representing 14 Blepharoneura fly species, 18 para

154 xpected product of ADC, into dsTcADC-treated pupae rescued the pigmentation phenotype, resulting in n

155 strated that cannibalization of DWV-infected pupae resulted in high levels of this virus in worker be

156 in adult males directly after emerging from pupae revealed larval fungal exposure significantly decr

157 , and developmental stages (egg, larvae, and pupae), revealing that although SiOBPs were expressed in

158 ere identified in mosquito eggs, larvae, and pupae sampled from aquatic environments.

159 Observations of embryos, larvae, and pupae show that GFP-moe is also useful for labeling the

160 expression of WntA and fz2 in WntA crispant pupae show that they are under positive and negative fee

161 Live imaging in lepidopteran pupae shows that SOP cells undergo two asymmetric divisi

162 ral stages of larvae but did retrieve female pupae significantly more rapidly than male pupae.

163 dly, rbf null mutants can develop until late pupae stage when the activity of dE2F1 is reduced, and c

164 ansition from the third instar larvae to the pupae stage.

165 utations in optix result in lethality at the pupae stage.

166 gene leads to the rapid generation of white pupae strains in C. capitata and B. tryoni.

167 Locally high proportions of parasitized host pupae suggest that M. multispinosus could serve as a bio

168 hermal range (0-36 degrees C) for A. ipsilon pupae that acts as the precursor for adult (moth) migrat

169 ERR) directs a transcriptional switch in mid-pupae that promotes glucose oxidation and lipogenesis in

170 ly after completion of bristle elongation in pupae, the actin bundles break down as the bristle surfa

171 When dsTcDDC was injected into young pupae, the resulting adults had abnormally dark brown bo

172 ns, developmental transitions from larvae to pupae to adults act as a switch for whether the effect i

173 ndings that injection of 20E into developing pupae to delay the fall in 20E delayed APR(4) death.

174 the exuvial fluid decreases the survival of pupae to microbial challenges, and the isolated apocrine

175 oideus vindemiae, to exploit Drosophila host pupae under different temporal variability treatments, e

176 laying by females that emerged from treated pupae was considered the treatment endpoint.

177 Steady-state RNA isolated from early pupae was examined, as this developmental stage critical

178 ons, however, the incidence of nondiapausing pupae was higher (51%, n = 41) than that of the intact (

179 host) that emerged from 0, 1, and 2-day-old pupae was significantly higher than that from 4-day-old

180 t the microbiome of post-feeding larvae (pre-pupae) was similar to that of the brood cell walls and n

181 wing the morphogenesis of arista laterals in pupae, we have determined that the branched laterals are

182 unds injected into developing Junonia coenia pupae, we identified several specific sulfated polysacch

183 aging of GFP-expressing myoblasts in vivo in pupae, we observed that despite denervation, the migrati

184 lytra abnormalities found in TcCHT7-silenced pupae were also manifest in the ensuing adults.

185 active compounds in male and female silkworm pupae were analyzed using chemometrics.

186 fested hosts containing a total of 9578 late pupae were considered unirradiated controls.

187 d cherries containing a total of 37,489 late pupae were irradiated with a maximum absorbed dose of 80

188 e adult brain as well as those of larvae and pupae were revealed.

189 es constructed from the RNA of nondiapausing pupae were selected for further screening.

190 Heterozygotes for either mutant die as pupae when raised at 29 degrees , but are normally viabl

191 The genus Comamonas was most abundant in pupae whereas completely absent in adults.

192 ates the recycling of phosphorylated Rh1* in pupae whereas it regulates the deactivation in adult.

193 und in 2-day-old (1.2%) and 3-day-old (1.4%) pupae, which were significantly lower than that of 4-day

194 ve degeneration of imaginal discs and die as pupae, while other genotypes survive to adulthood after

195 pRNAi entails injecting pupae with double-stranded RNA, allowing the injected wa

196 n, was detected only in mites collected from pupae with high DWV levels but not in the passaged mites

197 e Hygiene (VSH), leads to cannibalization of pupae with high DWV loads, thereby offering an alternati

198 er 8 additional days of passage on honey bee pupae with low viral loads, the DWV load dropped by 29-f

199 ith partially-rescued phenotype and 68.2% of pupae with partially- or fully-rescued phenotype, respec

200 bitor 3-iodo-tyrosine (3-IT) resulted in 20% pupae with partially-rescued phenotype and 68.2% of pupa

201 Zeugodacus cucurbitae, a key phenotype white pupae (wp) has been used for decades to selectively remo