ライフサイエンスコーパス: pupae

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

2 ult development when injected into debrained pupae.

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

4 cted deposits of chitin fibers in Drosophila pupae.

5 ndosomal sorting of Notch and Spdo in living pupae.

6 ecdysone-dependent transition from larvae to pupae.

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

8 bility in severing their larval dendrites in pupae.

9 le> larvae> worker pupae approximately alate pupae.

10 transcript during development, especially in pupae.

11 ntaining a number of brood cells occupied by pupae.

12 o as to maintain conditions that benefit the pupae.

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

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

15 entral brain region of late-stage Drosophila pupae.

16 id not affect the incidence of nondiapausing pupae.

17 ol-operated larvae developed into diapausing pupae.

18 operated larvae developed into nondiapausing pupae.

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

20 e pupae significantly more rapidly than male pupae.

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

22 rentiation of many cell types in embryos and pupae.

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

24 Most flies lacking tiggrin die as larvae or pupae.

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

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

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

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

29 nable interaction proteomics from developing pupae and adult flies.

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

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

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

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

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

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

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

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

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

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

40 2 mRNA accumulates only in female larvae and pupae and is expressed at very low levels in adult femal

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

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

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

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

45 , 2nd, 3rd, and 4th instar larvae, prepupae, pupae, and adult.

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

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

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

49 1 resulted in a reduction in size of larvae, pupae, and adults.

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

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

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

53 Caterpillars, pupae, and foodplants offer better distinguishing charac

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

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

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

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

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

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

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

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

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

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

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

65 Examination of pupae following ablation showed that migrating PTCs from

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

92 Pupae rendered acyclic with a JHA application consume O(

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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