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1 bon dioxide (CO(2)) closes within 48 h after eclosion.
2 adian clock output pathway controlling adult eclosion.
3 ments of the clock output pathway regulating eclosion.
4 rom the TM-AChE transgene died shortly after eclosion.
5 al complex from days 1 and 7 to day 14 after eclosion.
6 dogenous circadian rhythms of locomotion and eclosion.
7 d followed by recovery within 24 h following eclosion.
8 e and timepoints immediately following adult eclosion.
9 men fails to fill normally with gas prior to eclosion.
10 sient skeletal muscles that are required for eclosion.
11 evelopment and extends into the prosoma post-eclosion.
12 plays extensive sleep-dependent growth after eclosion.
13 cell death (PCD) within 24 hours after adult eclosion.
14 fects a locus previously implicated in pupal eclosion.
15 ent and normally eliminated immediately post-eclosion.
16 omplete, processive clearance within days of eclosion.
17 s, TC004091, resulted in the arrest of adult eclosion.
18  Drosophila undergo pronounced changes after eclosion.
19 anning as well as wing expansion after adult eclosion.
20 ansion of integumentary structures and adult eclosion.
21 to pharate adults but did not complete adult eclosion.
22 r larval-larval molting, pupation, and adult eclosion.
23 itinolytic activity but contributed to adult eclosion.
24 temporal manner in adult flies shortly after eclosion.
25  ELISA and reached a maximum at 3 days after eclosion.
26 for cuticle tanning and wing expansion after eclosion.
27 cadian rhythms in rest:activity behavior and eclosion.
28 , contains a functional clock at the time of eclosion.
29 ed by the environment or by experience after eclosion.
30 inal disc and resulted in lethality prior to eclosion.
31 arkness (DD1), albeit with a delayed peak of eclosion.
32 rapid and dramatic eye-stalk inflation after eclosion.
33 cle, and undergo apoptosis within 2 hours of eclosion.
34 nervate the optic lobes and are required for eclosion.
35 tere cells continue to secrete cuticle after eclosion.
36 at mediates the temporal regulation of adult eclosion.
37 stes fuscatus disappear within a few days of eclosion.
38                        However, during adult eclosion, ~70% of the adults were unable to shed their e
39 3) adult flies survive up to 24 hr following eclosion, a phenotype reminiscent of mice, where Sod2-/-
40 direct flight muscle (IFM) groups soon after eclosion, accompanied by apoptosis.
41 s survive through the pupal stage and die at eclosion (adult emergence).
42 allozymes correlate with the timing of adult eclosion, an event dependent on the duration of the over
43 oral deficits, including slow, uncoordinated eclosion and an insensitivity to ecdysis-triggering horm
44 tellogenesis (yolk accumulation) begins upon eclosion and continues through the process of sexual mat
45  neurodegeneration in fruit flies, impairing eclosion and decreasing life span.
46 led to 100% mortality within two weeks after eclosion and increased larval susceptibilities to antich
47 nitiation of vitellogenesis that occurs post-eclosion and its re-initiation post-mating.
48 ther glia or neurons causes severely reduced eclosion and longevity.
49 resulted in improved survival of HD flies to eclosion and prolonged adult life compared with intrabod
50 nd to lower the success rate of pupation and eclosion and to arrest development of pupae in a concent
51 e patterns of which may be related to larval eclosion and water uptake necessary for eggshell rupture
52                        We find that, between eclosion and wing expansion, the epithelia within the fo
53 chronizes daily activities, such as feeding, eclosion, and mating to diurnal light:dark cycles, while
54 atively impacting egg load, oviposition, and eclosion, and promoting an increase in egg reabsorption.
55 terestingly, the most severe failure seen at eclosion appeared to be in a function required for abdom
56 ypes of neurons and glia that are diploid at eclosion, become polyploid in the adult Drosophila brain
57 minus including the TAD exhibited arrhythmic eclosion behavior.
58 al ecdysis, whereas larval ecdysis and adult eclosion behaviors showed only subtle defects.
59 hich encodes a related semaphorin, die after eclosion, but no responsible abnormality is evident.
60  were not in better condition at the time of eclosion, but they were in better condition 7-11 days af
61 tly, we present evidence suggesting that the eclosion defect previously attributed to the Mtd locus m
62 utants exhibit late pupal lethality or pupal eclosion defects.
63        EB exposure for the first 2 days post-eclosion drives large-scale reductions in glomerular vol
64 tern of emergence by allowing or stimulating eclosion during certain windows of time and inhibiting e
65 y, rhythms (for instance in gene expression, eclosion, egg-laying, and feeding) tend to be low amplit
66                              Following adult eclosion, electrophysiological recordings were made from
67                             We examined post-eclosion elimination of the Drosophila wing epithelium i
68  eclosion rhythms, the daily distribution of eclosion events (i.e., gating) was abnormal.
69 f APPL and Tau resulted in adults that, upon eclosion, failed to expand wings and harden the cuticle,
70             dfxr mutants also display strong eclosion failure and circadian rhythm defects.
71                                    Following eclosion from the pupal case, wings of the immature adul
72 re of cuticle synthesized some 30 h prior to eclosion from the pupal case.
73                 Moreover, 8 days after adult eclosion, glial cells no longer responded to brain injur
74 der flies, between 6 and 50 days after adult eclosion, glial division was scarcely observed in the in
75                                              Eclosion hormone (EH) and bursicon originated prior to t
76 MP (cGMP) when exposed to the insect peptide eclosion hormone (EH) before pupal ecdysis.
77                             The neuropeptide eclosion hormone (EH) is a key regulator of insect ecdys
78                                              Eclosion hormone (EH) is an integral component in the ca
79  immunoreactive to an antiserum specific for eclosion hormone (EH), a neuropeptide regulator of molti
80  hormones: ecdysis triggering hormone (ETH), eclosion hormone (EH), and crustacean cardioactive pepti
81 uropeptides implicated in ecdysis, including Eclosion hormone (EH), Crustacean cardioactive peptide (
82 s neuropeptides including kinin, FMRFamides, eclosion hormone (EH), crustacean cardioactive peptide (
83 f ETH is stimulated by a brain neuropeptide, eclosion hormone (EH).
84 ing expansion and tanning, whereas synthetic eclosion hormone induces only wing expansion.
85 s neurons within the brain that then release eclosion hormone within the CNS.
86 7 of Tribolium), adipokinetic hormone (AKH), eclosion hormone, and insulin-like peptide.
87  CRF-like diuretic hormones (DHs) 41 and 30, eclosion hormone, kinins, myoinhibitory peptides (MIPs),
88 or regulating prothoracicotropic hormone and eclosion hormone, two neurohormones under circadian cont
89 rvous system responds to Mas-ETH, but not to eclosion hormone, with patterned motor bursting correspo
90 thought to be initiated by the brain peptide eclosion hormone.
91  with shorter latency than that reported for eclosion hormone.
92 ssociated differences in the timing of adult eclosion, host fruit odor preference and avoidance behav
93 s had a negative effect on both pupation and eclosion in both control and park(25) flies, with a grea
94  Circadian rhythms of locomotor activity and eclosion in Drosophila depend upon the reciprocal autore
95 ring hatching--an event that is analogous to eclosion in insects.
96 placed in primary cell culture 4 days before eclosion in medium containing 1 microg/ml 20E.
97  development) facilitates synchronous spring eclosion in nature; cold microclimates where diapause pr
98 usly to exhibit either aperiodic or rhythmic eclosion in separate studies.
99  death of intersegmental muscles after adult eclosion in the tobacco hornworm moth, Manduca sexta.
100                                     At adult eclosion JH hemolymph titer was low, increased in 1-day
101  transgene rescue of developmental delay and eclosion lethal phenotypes.
102                       Whereas PCD soon after eclosion occurred in eiger mutants as in the wild type,
103 TH results in delayed larval development and eclosion of larger flies with more cells.
104         Knocking down expression after adult eclosion of the nuclear hormone receptor Hr39, a master
105 n previtellogenic (PVG) stage (2-7 days post-eclosion) of female adult Aedes aegypti.
106 ty), larval survival, larval stage duration, eclosion rates, and sex-ratios of the progeny were recor
107 er of eggs deposited, larval stage duration, eclosion rates, and sex-ratios were not significantly di
108 cluding shorter development times and higher eclosion rates.
109 DPTP69D during the mid- to late-pupal stage, eclosion requires DPTP69D during the early to mid-larval
110 ne, to the allatectomized females just after eclosion rescued both the male courtship and the mating
111           The knockouts lacked the lights-on eclosion response despite having a normal circadian eclo
112 on of the NMJs during the first 5 days after eclosion revealed four major findings: 1) type I boutons
113 utput functions because the clock-controlled eclosion rhythm is normal in DCO mutants.
114 n response despite having a normal circadian eclosion rhythm.
115 rest:activity rhythms, the cellular basis of eclosion rhythms is less well understood.
116      However, both the PG clock function and eclosion rhythms require the presence of LNs.
117 ough CCAP KO populations exhibited circadian eclosion rhythms, the daily distribution of eclosion eve
118  from LNs, is necessary for the PG clock and eclosion rhythms.
119 w that the LN clock is insufficient to drive eclosion rhythms.
120            This clock is required for normal eclosion rhythms.
121 nged mothers were dissected within 24 h post-eclosion, SGH(+) was observed to increase from 4.5% in t
122 p growth rates, offspring mass and offspring eclosion success, relative to high larval-density or mix
123                                           At eclosion, the imago of C. whitei goes through a pumping
124 ry sensory neurons (OSNs) are silenced after eclosion; thus, OSN activity is required for closing the
125  latitudinal clines, associations with adult eclosion time, and within-generation responses to select
126 e Drosophila adults do not grow larger after eclosion, timing of feeding cessation during the third a
127 estore memory at all ages, from one-day post-eclosion to thirty-day-old flies, proving their ability
128 hetic odorless medium were transferred after eclosion to three different media: (i) a synthetic mediu
129  based differences in host preference, adult eclosion under the "correct" host species, and allochron
130            After pupal development and adult eclosion, unilateral (with one antennal disc left intact
131 PR(4)s is triggered by the decline in 20E at eclosion was supported by findings that injection of 20E
132 n Mef2 RNAi was induced in muscles following eclosion, we found no adverse effects of attenuating Mef
133 injected diapause-destined female post-adult eclosion were fed for 7 days with 10% glucose containing
134 s and nondiapausing counterparts after adult eclosion were fed with three different carbohydrate sour
135 hey were in better condition 7-11 days after eclosion, with females also being in better condition th

 
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