ライフサイエンスコーパス: eclosion

1 arkness (DD1), albeit with a delayed peak of eclosion.

2 plays extensive sleep-dependent growth after eclosion.

3 rom the TM-AChE transgene died shortly after eclosion.

4 dogenous circadian rhythms of locomotion and eclosion.

5 cell death (PCD) within 24 hours after adult eclosion.

6 fects a locus previously implicated in pupal eclosion.

7 ent and normally eliminated immediately post-eclosion.

8 omplete, processive clearance within days of eclosion.

9 s, TC004091, resulted in the arrest of adult eclosion.

10 Drosophila undergo pronounced changes after eclosion.

11 anning as well as wing expansion after adult eclosion.

12 ansion of integumentary structures and adult eclosion.

13 al complex from days 1 and 7 to day 14 after eclosion.

14 to pharate adults but did not complete adult eclosion.

15 r larval-larval molting, pupation, and adult eclosion.

16 itinolytic activity but contributed to adult eclosion.

17 temporal manner in adult flies shortly after eclosion.

18 ELISA and reached a maximum at 3 days after eclosion.

19 for cuticle tanning and wing expansion after eclosion.

20 cadian rhythms in rest:activity behavior and eclosion.

21 , contains a functional clock at the time of eclosion.

22 ed by the environment or by experience after eclosion.

23 inal disc and resulted in lethality prior to eclosion.

24 rapid and dramatic eye-stalk inflation after eclosion.

25 cle, and undergo apoptosis within 2 hours of eclosion.

26 nervate the optic lobes and are required for eclosion.

27 tere cells continue to secrete cuticle after eclosion.

28 at mediates the temporal regulation of adult eclosion.

29 stes fuscatus disappear within a few days of eclosion.

30 adian clock output pathway controlling adult eclosion.

31 ments of the clock output pathway regulating eclosion.

32 However, during adult eclosion, ~70% of the adults were unable to shed their e

33 3) adult flies survive up to 24 hr following eclosion, a phenotype reminiscent of mice, where Sod2-/-

34 direct flight muscle (IFM) groups soon after eclosion, accompanied by apoptosis.

35 s survive through the pupal stage and die at eclosion (adult emergence).

36 allozymes correlate with the timing of adult eclosion, an event dependent on the duration of the over

37 oral deficits, including slow, uncoordinated eclosion and an insensitivity to ecdysis-triggering horm

38 neurodegeneration in fruit flies, impairing eclosion and decreasing life span.

39 led to 100% mortality within two weeks after eclosion and increased larval susceptibilities to antich

40 resulted in improved survival of HD flies to eclosion and prolonged adult life compared with intrabod

41 nd to lower the success rate of pupation and eclosion and to arrest development of pupae in a concent

42 e patterns of which may be related to larval eclosion and water uptake necessary for eggshell rupture

43 We find that, between eclosion and wing expansion, the epithelia within the fo

44 terestingly, the most severe failure seen at eclosion appeared to be in a function required for abdom

45 minus including the TAD exhibited arrhythmic eclosion behavior.

46 al ecdysis, whereas larval ecdysis and adult eclosion behaviors showed only subtle defects.

47 hich encodes a related semaphorin, die after eclosion, but no responsible abnormality is evident.

48 were not in better condition at the time of eclosion, but they were in better condition 7-11 days af

49 tly, we present evidence suggesting that the eclosion defect previously attributed to the Mtd locus m

50 Following adult eclosion, electrophysiological recordings were made from

51 We examined post-eclosion elimination of the Drosophila wing epithelium i

52 eclosion rhythms, the daily distribution of eclosion events (i.e., gating) was abnormal.

53 f APPL and Tau resulted in adults that, upon eclosion, failed to expand wings and harden the cuticle,

54 dfxr mutants also display strong eclosion failure and circadian rhythm defects.

55 Following eclosion from the pupal case, wings of the immature adul

56 re of cuticle synthesized some 30 h prior to eclosion from the pupal case.

57 Moreover, 8 days after adult eclosion, glial cells no longer responded to brain injur

58 der flies, between 6 and 50 days after adult eclosion, glial division was scarcely observed in the in

59 MP (cGMP) when exposed to the insect peptide eclosion hormone (EH) before pupal ecdysis.

60 The neuropeptide eclosion hormone (EH) is a key regulator of insect ecdys

61 Eclosion hormone (EH) is an integral component in the ca

62 immunoreactive to an antiserum specific for eclosion hormone (EH), a neuropeptide regulator of molti

63 hormones: ecdysis triggering hormone (ETH), eclosion hormone (EH), and crustacean cardioactive pepti

64 s neuropeptides including kinin, FMRFamides, eclosion hormone (EH), crustacean cardioactive peptide (

65 uropeptides implicated in ecdysis, including Eclosion hormone (EH), Crustacean cardioactive peptide (

66 f ETH is stimulated by a brain neuropeptide, eclosion hormone (EH).

67 ing expansion and tanning, whereas synthetic eclosion hormone induces only wing expansion.

68 s neurons within the brain that then release eclosion hormone within the CNS.

69 7 of Tribolium), adipokinetic hormone (AKH), eclosion hormone, and insulin-like peptide.

70 CRF-like diuretic hormones (DHs) 41 and 30, eclosion hormone, kinins, myoinhibitory peptides (MIPs),

71 or regulating prothoracicotropic hormone and eclosion hormone, two neurohormones under circadian cont

72 rvous system responds to Mas-ETH, but not to eclosion hormone, with patterned motor bursting correspo

73 thought to be initiated by the brain peptide eclosion hormone.

74 with shorter latency than that reported for eclosion hormone.

75 ssociated differences in the timing of adult eclosion, host fruit odor preference and avoidance behav

76 Circadian rhythms of locomotor activity and eclosion in Drosophila depend upon the reciprocal autore

77 ring hatching--an event that is analogous to eclosion in insects.

78 placed in primary cell culture 4 days before eclosion in medium containing 1 microg/ml 20E.

79 usly to exhibit either aperiodic or rhythmic eclosion in separate studies.

80 death of intersegmental muscles after adult eclosion in the tobacco hornworm moth, Manduca sexta.

81 transgene rescue of developmental delay and eclosion lethal phenotypes.

82 Whereas PCD soon after eclosion occurred in eiger mutants as in the wild type,

83 TH results in delayed larval development and eclosion of larger flies with more cells.

84 Knocking down expression after adult eclosion of the nuclear hormone receptor Hr39, a master

85 DPTP69D during the mid- to late-pupal stage, eclosion requires DPTP69D during the early to mid-larval

86 ne, to the allatectomized females just after eclosion rescued both the male courtship and the mating

87 The knockouts lacked the lights-on eclosion response despite having a normal circadian eclo

88 on of the NMJs during the first 5 days after eclosion revealed four major findings: 1) type I boutons

89 utput functions because the clock-controlled eclosion rhythm is normal in DCO mutants.

90 n response despite having a normal circadian eclosion rhythm.

91 rest:activity rhythms, the cellular basis of eclosion rhythms is less well understood.

92 However, both the PG clock function and eclosion rhythms require the presence of LNs.

93 ough CCAP KO populations exhibited circadian eclosion rhythms, the daily distribution of eclosion eve

94 from LNs, is necessary for the PG clock and eclosion rhythms.

95 w that the LN clock is insufficient to drive eclosion rhythms.

96 This clock is required for normal eclosion rhythms.

97 nged mothers were dissected within 24 h post-eclosion, SGH(+) was observed to increase from 4.5% in t

98 p growth rates, offspring mass and offspring eclosion success, relative to high larval-density or mix

99 At eclosion, the imago of C. whitei goes through a pumping

100 latitudinal clines, associations with adult eclosion time, and within-generation responses to select

101 e Drosophila adults do not grow larger after eclosion, timing of feeding cessation during the third a

102 estore memory at all ages, from one-day post-eclosion to thirty-day-old flies, proving their ability

103 hetic odorless medium were transferred after eclosion to three different media: (i) a synthetic mediu

104 based differences in host preference, adult eclosion under the "correct" host species, and allochron

105 After pupal development and adult eclosion, unilateral (with one antennal disc left intact

106 PR(4)s is triggered by the decline in 20E at eclosion was supported by findings that injection of 20E

107 n Mef2 RNAi was induced in muscles following eclosion, we found no adverse effects of attenuating Mef

108 s and nondiapausing counterparts after adult eclosion were fed with three different carbohydrate sour

109 hey were in better condition 7-11 days after eclosion, with females also being in better condition th