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1 istically with thyroid hormone to accelerate metamorphosis).
2 ation of larval insects into the adult form (metamorphosis).
3 ammals (puberty) and holometabolous insects (metamorphosis).
4 for 7 days and depurated until completion of metamorphosis.
5 leads to tadpole lethality at the climax of metamorphosis.
6 omorphic species, which undergo differential metamorphosis.
7 mations via a process we term macromolecular metamorphosis.
8 become integrated into the mature SEZ during metamorphosis.
9 from microbial infection during molting and metamorphosis.
10 or to the induction of larval settlement and metamorphosis.
11 nes adult morphogenesis in the hemimetabolan metamorphosis.
12 y system undergoes massive remodeling during metamorphosis.
13 to morphological changes upon initiation of metamorphosis.
14 -embryonic developmental transitions such as metamorphosis.
15 nitors at four stages, from embryogenesis to metamorphosis.
16 hanges of the Xenopus olfactory organ during metamorphosis.
17 d that they are eventually eliminated during metamorphosis.
18 based one (adult mode) as it transits beyond metamorphosis.
19 or on a novel one invented by the newt after metamorphosis.
20 hanges of the Xenopus olfactory organ during metamorphosis.
21 its regenerative ability of the limbs after metamorphosis.
22 lose their ability to regenerate limbs after metamorphosis.
23 ctivate circadian oscillator function during metamorphosis.
24 dpoles and led to tadpole lethality prior to metamorphosis.
25 histoblast nests to the hormonal control of metamorphosis.
26 and the organisation of pigment cells during metamorphosis.
27 y contributing to the correct culmination of metamorphosis.
28 nd the factors they produce stimulate animal metamorphosis.
29 ion in Dicer-1 knockdown individuals rescues metamorphosis.
30 terocyte identity during a defined window of metamorphosis.
31 nderstanding of the molecular basis of adult metamorphosis.
32 be specified twice, during embryogenesis and metamorphosis.
33 e same regulatory mechanism to promote adult metamorphosis.
34 nregulation of all three miRNAs seen late in metamorphosis.
35 e a reduced ability to successfully complete metamorphosis.
36 and begin to reform in the months following metamorphosis.
37 sults in eyeless animals, and is lethal peri-metamorphosis.
38 t a role for awd in ACP wing development and metamorphosis.
39 ntestinal progenitors that take place during metamorphosis.
40 ded to have lower infection prevalence after metamorphosis.
41 emoval of obsolete larval neurons during CNS metamorphosis.
42 erant (Met), plays a critical role in insect metamorphosis.
43 opmental stages but loses the ability during metamorphosis.
44 (DEOM) which occurs during the first 24h of metamorphosis.
45 olt timer that establishes a minimal time to metamorphosis.
46 horacicotropic hormone (PTTH) that initiates metamorphosis.
47 ryogenesis, larval development, and juvenile metamorphosis.
48 al stage and form the adult intestine during metamorphosis.
49 es acting downstream of JH and Met in insect metamorphosis.
50 idal to the eponymous stellate shape, during metamorphosis.
51 and 81.5% of P. regilla were infected after metamorphosis.
52 to recover from Bd infection as they undergo metamorphosis.
53 loses its bile ducts and gallbladder during metamorphosis.
54 ster molecular genetic tools to study insect metamorphosis.
55 the rod loss phenotype was not obvious after metamorphosis.
56 e ecdysteroid molting hormones that regulate metamorphosis.
57 al changes in X. tropicalis intestine during metamorphosis.
58 it is required broadly for patterning during metamorphosis.
59 e to produce MACs are capable of stimulating metamorphosis.
60 xillary and labial appendages, are formed at metamorphosis.
61 uired for adult intestinal stem cells during metamorphosis.
62 h of the pentaradial adult rudiment prior to metamorphosis.
63 increases in osmoregulatory capacity during metamorphosis.
64 es without affecting axons during Drosophila metamorphosis.
65 gateway for the tissue development preceding metamorphosis.
66 cle exit and terminal differentiation during metamorphosis.
67 that the mif1 gene is required for inducing metamorphosis.
68 formation of the larva into the adult during metamorphosis.
69 to new morphologies driven by macromolecular metamorphosis.
70 ms can lead to fates as diverse as death and metamorphosis.
71 the remodeling of cartilage tissue, prior to metamorphosis.
72 een in the shift from incomplete to complete metamorphosis.
73 P reconstitution, ensuring the completion of metamorphosis.
74 aevis before, during, and after TH-dependent metamorphosis.
75 into the different processes involved during metamorphosis.
76 o control Drosophila wing development during metamorphosis.
77 through metamorphosis) or during T3-induced metamorphosis.
78 mation of adult intestinal stem cells during metamorphosis.
81 meostatic adjustment to starvation but start metamorphosis 4 d after feeding onset, regardless of lar
82 small amounts of cardiac glycosides through metamorphosis, a trait that has been optimized in monarc
84 d mitigation strategies need to consider how metamorphosis affects the movement of materials between
86 rus infection decreased survival and delayed metamorphosis, although chronic corticosterone exposure
87 tion underlying differences in the timing of metamorphosis among three spadefoot toads with different
88 o interpret, as larval neurons degenerate at metamorphosis and a tripartite nervous system differenti
89 that account for effects of contaminants on metamorphosis and adult insect emergence for the develop
92 eroid-dependent program at the initiation of metamorphosis and are the primary phagocytic cell type i
93 larval secondary lineage projections through metamorphosis and bfy identifying each neuroglian-positi
96 , could be linked with biological effects on metamorphosis and gonadal phenotypes, respectively, that
97 In Rhodnius prolixus, both the physiology of metamorphosis and its hormonal control are known in deta
98 rowth and development of the tadpoles during metamorphosis and leads to tadpole lethality at the clim
102 arval bacteriome dissociates at the onset of metamorphosis and releases bacteriocytes that undergo en
103 ls were significantly elevated by stage 5 of metamorphosis and remained elevated through stage 7, whe
105 dentify bacterial cues that stimulate animal metamorphosis and test hypotheses addressing their mecha
106 3 target genes during natural and T3-induced metamorphosis and that Dot1L is itself a T3 target gene.
107 te that GHR and PRLR may both participate in metamorphosis and that GHR may mediate SW acclimation.
108 posed to 17alpha-ethynylestradiol throughout metamorphosis and the early postmetamorphic period.
109 conservation between MB axon pruning during metamorphosis and the refinement of ectopic larval neuro
110 nge) (LT) or 21-22 degrees C (range) (HT) to metamorphosis and then transferred to 21-22 degrees C.
111 P. luteoviolacea from inducing settlement or metamorphosis and three MAPK inhibitors, we established
112 d hormone (the primary morphogen controlling metamorphosis) and corticosterone (a stress hormone acti
114 nica with an miR-2 inhibitor, which impaired metamorphosis, and by treating Dicer-1-depleted individu
116 in tadpoles from the pond of origin, across metamorphosis, and in toadlets via microbial fingerprint
119 ages, stressful and stochastic events during metamorphosis, and stressful environmental conditions at
121 ependent transcription factor that represses metamorphosis, and that depletion of Kr-h1 expression in
122 xposure mortality in the larval stage and at metamorphosis, and very strongly reduced adult lifespan.
123 r key innovations, such as wings or complete metamorphosis are usually invoked as potential evolution
124 rent larval activities (e.g., attachment and metamorphosis) are under the control of different neural
125 ue degeneration and remodeling during anuran metamorphosis as a mechanism for altering tissue-specifi
127 tinal remodeling during T3-dependent Xenopus metamorphosis as a model for organ maturation and format
129 can induce tubeworm and coral metamorphosis; Metamorphosis-Associated Contractile structures (MACs) a
130 producing ordered arrays of phage tail-like metamorphosis-associated contractile structures (MACs).
131 teoviolacea initiate cilia loss and activate metamorphosis-associated transcription; finally, signali
134 ntify a location on the sea floor to undergo metamorphosis based on the presence of specific bacteria
135 cation on the seafloor to settle and undergo metamorphosis based on the presence of specific surface-
138 Lipid stores are consumed shortly after metamorphosis but contribute little to energy metabolism
139 lier breeding and larval survival or mass at metamorphosis, but earlier breeding was associated with
140 abolous insects suggests that holometabolous metamorphosis combines patterning processes of both late
145 nction of Hox genes and Tc-hth/Tc-exd during metamorphosis did not match predictions based on embryon
146 ticularly sensitive due to the potential for metamorphosis-driven mobilization, which could transfer
148 tants have severe defects in pupariation and metamorphosis due to a lack of activation of ecdysone-re
150 tional checkpoints, which inhibit precocious metamorphosis during nutrient restriction in undersized
153 ion of a number of processes associated with metamorphosis, either in the less modified hemimetabolan
154 us, adaptive developmental plasticity during metamorphosis enables spinal CPG-driven extraocular moto
157 n of flight initiated the trajectory towards metamorphosis, favoring enhanced differences between juv
158 aquatic larval stage, a brief and pronounced metamorphosis, followed by a terrestrial adult stage.
159 iator complex, causing them to shrink during metamorphosis, followed by nuclear accumulation of Prosp
160 helial stem cell proliferation at the end of metamorphosis (for the few that survive through metamorp
161 a complex life history marked by a dramatic metamorphosis from a benthic filter-feeding ammocoete la
163 y variable affecting the timing of amphibian metamorphosis from tadpoles to tetrapods, through the pr
165 ng hypochord-induced loss of the tail during metamorphosis has enabled the evolution of the unique an
167 e presynaptic and become apparent only after metamorphosis, highlighting a delayed response to a sign
170 ntact with surface-bound bacteria to undergo metamorphosis; however, the mechanisms that underpin thi
172 sponse variables, including size and mass at metamorphosis in A. maculatum, but at a reduced strength
175 We studied the regulation of molting and metamorphosis in bed bugs with a goal to identify key pl
177 3 is the key determinant that promotes adult metamorphosis in both hemimetabolous and holometabolous
180 suggests that mechanisms of bacteria-induced metamorphosis in Hydroides may have conserved features i
181 o zinc and warming before, during, and after metamorphosis in Ischnura elegans damselflies from high-
182 lignaria We demonstrate that starvation cues metamorphosis in O. lignaria and that a critical weight
183 unveil a remarkable potential for structural metamorphosis in proteins and demonstrate key principles
184 re we show that hdc is expressed just before metamorphosis in sensory neurons that undergo remodeling
185 oroaniline (3,4-DCA) on thyroid function and metamorphosis in tadpoles of Lithobates catesbeianus.
187 T3 directly activated the c-Myc gene during metamorphosis in the intestine via binding of the T3 rec
189 bility in streams decreases survival through metamorphosis in the salamander Gyrinophilus porphyritic
190 ing thyroid hormone (T3)-dependent amphibian metamorphosis in two highly related species, the pseudo-
192 ave characterized a period during behavioral metamorphosis in which zebrafish are highly reactive to
194 of tadpoles and the inverse of their size at metamorphosis) in our tadpole-parasitic cercarial (trema
195 Hox is initiated in the late larva prior to metamorphosis, in preparation for the transition to the
196 s cultripes and Spea multiplicata accelerate metamorphosis, increase standard metabolic rate (SMR), a
199 The first JH was described in 1934 as a "metamorphosis inhibitory hormone" in Rhodnius prolixus b
201 its brief journey as a larva to its radical metamorphosis into adult form-and relate these features
203 opolymer or hyperbranched polymer undergoes 'metamorphosis' into comb, star and hydrophobic block cop
205 polysulfide dissolution by understanding the metamorphosis is essential for realizing stable and high
212 arbons (PAHs) were predominantly lost during metamorphosis leading to approximately 2 to 125-fold hig
213 ingomyelin-rich cells undergoes a structural metamorphosis, leading to the assembly of nanopores at t
214 Toxicity included stunted growth, delayed metamorphosis, malformations, organ pathology, and DNA d
216 These results support the hypothesis that metamorphosis may be a survival bottleneck, particularly
217 he nerve-associated progenitors lasting into metamorphosis may have facilitated the evolution of adul
218 y factors that can induce tubeworm and coral metamorphosis; Metamorphosis-Associated Contractile stru
219 gent, insight into the triggers of Hydroides metamorphosis might lead to practical strategies for fou
221 either the development of flight or complete metamorphosis nor the Cretaceous Terrestrial Revolution
222 Pt-Sb platform supports the fluoride-induced metamorphosis of a stiboranyl X ligand into a stiborane
226 activity during the N-terminal to C-terminal metamorphosis of FPPase to CPPase, with product selectiv
230 ributed marine bacterium that stimulates the metamorphosis of marine animal larvae, an important bact
235 olacea biofilms producing MACs stimulate the metamorphosis of the tubeworm Hydroides elegans, TBP bio
237 t the larva must surpass before it can enter metamorphosis on a normal schedule, and the inhibitory a
238 for only 12-24 h was sufficient to result in metamorphosis on day 4, regardless of further feeding or
243 decisions of when and where animals undergo metamorphosis, optimizing conditions for adult developme
246 flatfish and transcriptomic analyses during metamorphosis point to a role for thyroid hormone and re
247 gument were compared during the larval-pupal metamorphosis process of the S. exigua wild type (SEW) a
248 d explore why, the developmental decision of metamorphosis relies on cues from environmental bacteria
251 uring thyroid hormone (T3)-dependent Xenopus metamorphosis resembles postembryonic intestinal maturat
253 nique molecular switch occurs during lamprey metamorphosis resulting in distinct gill carbonic anhydr
254 ounding functional constraints on variation, metamorphosis seems to have promoted the morphological e
255 ably expressed markers, differentiate during metamorphosis, sending terminal axonal and dendritic bra
258 d ca18 and protein expression in gill across metamorphosis show that the ca19 levels are highest in a
259 of genes known to be involved in molting and metamorphosis showed high levels of Kruppel homolog 1 [K
260 ommodation of endocrine pathways controlling metamorphosis, showing how phenotypic plasticity within
261 roendocrine signaling cascade that initiates metamorphosis, similar to the way in which their mammali
262 larval newt, but this changes abruptly after metamorphosis so that the formation of anterior and post
264 s and staining intensity further change over metamorphosis, suggesting compositional rearrangement.
265 n larvae fed ad libitum eventually underwent metamorphosis, suggesting that some secondary mechanism
266 etween the start of feeding and the onset of metamorphosis suggests that larvae possess a molt timer
268 mammalian immune system may be linked to the metamorphosis that allows them to transfer from mammals
272 itially concentrated in the gut; however, by metamorphosis, the majority were found in other tissues.
273 ure with regard to carry-over effects across metamorphosis: their dependence on hatching period, and
274 s, quantified settlement success and size at metamorphosis, then outplanted juveniles to Tomales Bay,
277 ling of lineage tracts disappearing early in metamorphosis, they were unable extend the identificatio
281 transformations that occur during amphibian metamorphosis to show that PNNs can be highly dynamic in
283 y during summers influences survival through metamorphosis, using capture-mark-recapture data from Me
288 mechanisms by which bacteria promote animal metamorphosis, we begin to illustrate how, and explore w
289 larvae taken prior to observed mortality at metamorphosis, we found that exposure to OSS and exogeno
290 amining Drosophila tracheal outgrowth during metamorphosis, we show that progenitors follow a stereot
291 ding delayed development and reduced size at metamorphosis, were associated with elevated metalloid e
292 Purified Mif1 is sufficient for triggering metamorphosis when electroporated into tubeworm larvae.
293 ting that some secondary mechanism regulates metamorphosis when provisions are not completely consume
295 ogrammed cell death occurs during Drosophila metamorphosis, when most of the larval tissues are destr
296 re highest in ammocoetes and decrease during metamorphosis while ca18 shows the opposite pattern with
297 iched by approximately 1 per thousand during metamorphosis, while delta(13)C used to estimate diet, w
299 only during the larval stage but also after metamorphosis, yet notably only in low-latitude damselfl