ライフサイエンスコーパス: hatching

1 ed larval herring abundance (an index of egg hatching).

2 rvae spontaneously expressing GFP days after hatching.

3 findings about ion versus "nano" effects on hatching.

4 ukosis and hemangiomas within 2 months after hatching.

5 o in the likelihood of maternal, matricidal, hatching.

6 partner(s) with fidelity following birth or hatching.

7 trieved from fresh feces and survived beyond hatching.

8 ne and in the inner ear from >2 months after hatching.

9 latively late, at the same time as embryonic hatching.

10 early stage embryo mortalities and premature hatching.

11 fates in the third larval stage, a day after hatching.

12 mortality only for the first few days after hatching.

13 opment and reduced female egg-laying and egg hatching.

14 ns were not altered by commensal microbes or hatching.

15 ryonic stages before becoming coordinated at hatching.

16 llum) finish their neuronal expansion before hatching.

17 pts for uxs1 localize to skeletal domains at hatching.

18 30-40% of primary neurons around the time of hatching.

19 s were treated during the first 25 days post-hatching.

20 taging zone for their migration after larval hatching.

21 atching and, for the parakeets, 1 week after hatching.

22 g preference for the familiar call following hatching.

23 a preference for the familiar call following hatching.

24 ands surgically removed at 3 to 6 days after hatching.

25 nging was positively correlated with earlier hatching.

26 r concentration declined precipitously after hatching.

27 Tissue was collected on the day of hatching.

28 r bimodal (audiovisual) stimulation prior to hatching.

29 er uptake necessary for eggshell rupture and hatching.

30 es-specific perceptual preferences following hatching.

31 ed and should kill host offspring soon after hatching.

32 to bobwhite maternal Calls A or B following hatching.

33 I(DS) defined electrophysiologically around hatching.

34 ain during late embryonic development and at hatching.

35 atively high egg mortality would favor early hatching.

36 ith a pulsating light in the period prior to hatching.

37 rrest of clk-1 larvae fed a Q-less diet from hatching.

38 ginning at either 1 week or 2 weeks prior to hatching.

39 off between predation risks before and after hatching.

40 tive to negative isoforms around the time of hatching.

41 t terminally differentiated neurons prior to hatching.

42 ns of CR-IR were achieved about a week after hatching.

43 sis, which remains uniformly expressed until hatching.

44 c bursa, cell death increases markedly after hatching.

45 ntiation with Sk-Tmod replacing E-Tmod after hatching.

46 ic day, [E] 8.5) to about 900 at the time of hatching.

47 tage, and decreased subsequent to blastocyst hatching.

48 one day after hatching and three days after hatching.

49 epared to develop rapidly and robustly until hatching.

50 e to arrested gonadogenesis following embryo hatching.

51 out any association with a genetic parent at hatching.

52 generation of forces required for blastocyst hatching.

53 re capable of identifying parental odours at hatching.

54 n during a limited time period shortly after hatching.

55 ion, increase in heart rate, and accelerated hatching.

56 nch farm population at 10 and 15 months post-hatching.

57 d during embryogenesis and was strong around hatching.

58 e involved in a cascade of events leading to hatching.

59 e slowly inactivating mechano-current before hatching.

60 rly displaced distribution of VNC neurons at hatching.

61 effector genes were also up-regulated during hatching.

62 bryo but levels fully recover by the time of hatching.

63 at this individual weighed ~3.4 kilograms at hatching.

64 yo during the last three or four days before hatching [5] [6].

65 esulted in a significant delay in blastocyst hatching, a developmental step facilitating implantation

66 inbred lines, a locus that affects maternal hatching, a phenotype closely linked to dietary restrict

67 Here, using the chick embryo close to hatching, a well-accepted model for dioxin toxicity, we

68 ality than C-IVF in terms of cell number and hatching ability.

69 tures, Hinfp-null embryos exhibit a delay in hatching, abnormal growth, and loss of histone H4 gene e

70 at gastric gland development occurs close to hatching, accompanied by the onset of gastric proton pum

71 Emerging evidence suggests that assisted hatching (AH) techniques may improve clinical pregnancy

72 After hatching, alligators were raised under controlled labora

73 Plasticity in hatching allows embryos to use immediate, local informat

74 embryogenesis and exit from quiescence after hatching, although how they do so is unknown [3].

75 e neuropeptides during this period or during hatching--an event that is analogous to eclosion in inse

76 egg exposure to desiccation before inducing hatching and allowing surviving larvae to compete for 59

77 is observed in birds as young as 47 d after hatching and also in adult birds but not in younger bird

78 From the day of hatching and before attaining sustained aerial flight, d

79 time of implantation, as blastocysts exhibit hatching and blastocyst outgrowth defects upon in vitro

80 ral blood island (VBI), cranial ganglia, and hatching and cement glands.

81 Starting shortly after hatching and continuing through adulthood, ground birds

82 Assisted hatching and diagnosis of ovulation disorder were margin

83 P-null blastocysts are viable and capable of hatching and forming both an inner cell mass and a troph

84 e are important causes of variability in egg hatching and larva survival.

85 At 6 months, the percentage hatching and larval survival rates were greatest in the

86 G. strigosum by showing higher rates of egg hatching and larval survival.

87 For other phenotypes (egg-hatching and male fertility), however, one gene shows fu

88 how soil moisture contributes to successful hatching and particularly how it shapes nest site choice

89 perimental conditions on the third day after hatching and raised for 3 weeks.

90 of the zona pellucida to minimize precocious hatching and reduced fecundity.

91 the imitation of a song model 80-90 d after hatching and retain it with little change for the rest o

92 pulation on the stress response, spontaneous hatching and swim activity at different stages of develo

93 that GCs play key roles in stress response, hatching and swim activity during early development.

94 Spontaneous hatching and swim activity were significantly affected b

95 ake instantaneous behavioral decisions about hatching and the accompanying shift from arboreal to aqu

96 The injected embryos were incubated until hatching and then sacrificed; cells from these embryos w

97 a and Robusta maculata) within one day after hatching and three days after hatching.

98 that HB-EGF promotes blastocyst growth, zona-hatching and trophoblast outgrowth.

99 quail at several stages of embryogenesis, at hatching and, for the parakeets, 1 week after hatching.

100 centrations restored blastocyst development, hatching, and cell number.

101 a result of reduced levels of egg laying and hatching, and developing egg chambers display defects in

102 >30 ng/L each during the period of spawning, hatching, and development for resident fishes.

103 riables as oocyte batch, blastocyst quality, hatching, and length of time in culture.

104 ndistinguishable glomeruli formed only after hatching, apparently by segregating from five larger pre

105 ed gene sequences (e.g., beta-adult and beta-hatching) are no more sensitive than the nearby constitu

106 hasic uptake pattern with slow uptake before hatching (around 48 hpf) and faster uptake thereafter.

107 Animals that survive to hatching arrest as misshapen larvae that occasionally ex

108 e normal lymphocytes actively emigrate after hatching, as measured by BrdU pulse-chase labeling and i

109 ve hierarchies while gaining the benefits of hatching asynchrony.

110 Zebrafish embryos were incubated until hatching at control temperature (T(E) = 27 degrees C) or

111 incubate for 8-9 months before synchronously hatching at the onset of the following rainy season.

112 ntifiable glomeruli already developed before hatching, at 72 h after fertilization, in configurations

113 scribed in adults are in place shortly after hatching, at a time when zebrafish are accessible to a b

114 ges of embryonic development between E16 and hatching, at about E21.

115 Our results show that EcR is required for hatching, at each larval molt, and for the initiation of

116 silateral to the eye exposed to light before hatching became essential for recall of imprinting memor

117 modulation of neural signaling that controls hatching behavior by producing specific neuropeptides in

118 larvae show a greatly reduced frequency of a hatching behavior of wild-type Drosophila in which larva

119 , dPC2 (amontillado), is required for normal hatching behavior, and immunoblotting data indicate that

120 cted within the apical plate ectoderm of the hatching blastula and are confined to the apical organ a

121 Soon after the hatching blastula stage, BMP2/4 transcripts can be detec

122 yos remain immobilized in rosettes until the hatching blastula stage.

123 r adults and that C displays were present at hatching, but A and B displays appeared to emerge gradua

124 chicks leave the paraventricular zone after hatching, but a pool of neurons stays in the vicinity of

125 Inhibition of Siah2 or Drp1 in hatching C. elegans reduces their life span.

126 manipulating the occurrence of pre- or post-hatching care, we show that the offspring of three buryi

127 f larvae on parental feeding, but not on pre-hatching care.

128 It consists of a deeply impressed cross-hatching carved into the bedrock of the cave that has re

129 Dark-rearing from hatching causes correlated spontaneous activity to persi

130 ccumbed to epitheliocystis from 21 days post hatching, causing mortality in a quarter of the hosts.

131 At postnatal day 0 (P0), right after hatching, ChAT-immunoreactivity was present in the gangl

132 Late-hatching chicks suffer higher mortality only for the fir

133 ins in phasic (gizzard) smooth muscle around hatching coincided with the switch from exon inclusion t

134 emerge, to slow and narrow a few days before hatching, coinciding with the emergence of excitatory GA

135 s that the telencephalon of zebra finches at hatching contains a thick proliferative subventricular z

136 as independent of copper uptake, while after hatching, copper uptake was increased under hypoxia, cor

137 nic bursa, and decreased significantly after hatching, correlating inversely with apoptosis.

138 h (Danio renio) eleutheroembryos (72 h after hatching, corresponding to 144 h post fertilization, hpf

139 : -1.435, -1.132) were negatively related to hatching date.

140 raits, and (ii) be strongly modulated by egg hatching dates.

141 dimorphic expression of these genes at post-hatching day 25, and documented that the sex differences

142 treated with E2 or control vehicle from post-hatching days 3 through 25, at which time norepinephrine

143 injecting BrdU, a cell birth marker, on post-hatching days 61-65 and killing the animals 30 d later.

144 During post-hatching developmental ages (P) 18-23, quantitative anal

145 "Resurrection Ecology" (hatching dormant resting eggs deposited in the past) rec

146 hree primary questions: First, how does post-hatching E2 treatment affect HSD17B4 mRNA expression in

147 ass spectrometry to demonstrate that the pre-hatching embryo changes ULF composition in vivo.

148 adaptation to a fluctuating normoxia-anoxia hatching environment by increasing embryo survival under

149 cing irregularly fluctuating normoxia-anoxia hatching environments failed to evolve randomizing mater

150 hibits the proteolytic activity of Zebrafish Hatching Enzyme 1 and thereby delay or impair hatching s

151 muM dissolved Cu in the environment reduces hatching enzyme activity by 50%.

152 ikely to be preparatory for secretion of the hatching enzyme during the following cleavage cycle.

153 riptional regulator of the sea urchin embryo hatching enzyme gene, SpHE.

154 embryonic morphogenesis, egg laying, and egg hatching even in mutants lacking the Gr63a neuronal CO(2

155 , UCN3 mRNA levels tended to increase toward hatching, except for caudal brainstem, where a gradual d

156 rvae lacking all mxp function die soon after hatching, exhibiting strong transformations of maxillary

157 is commonly found in arthropods and induces hatching failure of eggs from crosses between Wolbachia-

158 However, most of the observed failures were hatching failures, which were not explained by albumen [

159 r condition despite older females laying and hatching fewer eggs.

160 Hatching from eggs is a shift in niche and in life histo

161 A (gRNA) target design, embryo injection and hatching, germ-line transmission and for minimizing off-

162 Zic1 are necessary and sufficient to promote hatching gland and preplacodal fates, respectively, wher

163 embryos caused cyclopia, mislocalization of hatching gland tissue, and duplication or splitting of t

164 ired for the terminal differentiation of the hatching gland, a specialized secretory organ whose spec

165 GP96 RNA is localized within the floorplate, hatching gland, and in the cells of the otic placode and

166 ion, Pax3 is expressed in progenitors of the hatching gland, and Zic1 is detected in the preplacodal

167 nd retina as well as the immature notochord, hatching gland, enveloping cell layer, and fin by exposi

168 ral crest, the preplacodal ectoderm, and the hatching gland.

169 e olfactory vesicles, the stomodeum, and the hatching gland.

170 clude that sex differentiation starts before hatching, goes through an all-male stage for both sexes

171 s fire a single spike, whereas shortly after hatching (H) the vast majority fire repetitively on depo

172 lity that chicks recognise parental odour at hatching has been completely overlooked, despite the fac

173 show that this organelle forms rapidly after hatching in a process that involves vesicle fusion and n

174 pulatory motoneurons, assessed on the day of hatching in both experiments, were not dimorphic in size

175 lly, expression of IgT is present 4 d before hatching in developing embryos.

176 n first appeared at about the time of larval hatching in dorsal cells of the posterior trunk.

177 bryonic growth and development shortly after hatching in response to monomethyl branched-chain fatty

178 ermal relationships affect the match between hatching in sandeel and egg production of its copepod pr

179 Shortly after hatching in the absence of food, L1 larvae arrest their

180 ogenesis, HyBra1 is expressed shortly before hatching in the region that will form the apical end of

181 velopmental rate, survival, and body size at hatching in two populations of sockeye salmon (Oncorhync

182 arausius morosus, where retinal growth after hatching is accompanied by a diurnal-to-nocturnal shift

183 a virulent egg parasite and that this early hatching is induced by water-borne cues emitted from inf

184 enotypically plastic, i.e., early or delayed hatching is likely to be inducible.

185 models, one would predict that the timing of hatching is, to some degree, phenotypically plastic, i.e

186 At hatching, it is expressed in several head neurons, the p

187 etics describe the impact of dissolved Cu on hatching; it is estimated that indefinitely long exposur

188 After hatching, juveniles of most sea turtle species undertake

189 well as changes in these parameters in post-hatching larvae of 3, 4, and 5 days post fertilisation (

190 The hatching larval brain contains six groups of primary DA

191 cally process peptide hormones that regulate hatching, larval growth, and larval ecdysis.

192 Bones record rapid growth rates and hatching lines, indicating that this individual weighed

193 in the halibut brain already at the time of hatching, long before the eyes are functional.

194 spinal cord of halibut larvae at the time of hatching may be primary sensory cells or interneurons re

195 s well as its coincidence with the moment of hatching, may be explained by a dynamic economical model

196 Numerous subgroup analyses stratified by hatching method, conception mode, extent of AH, embryos

197 t fail to exit cellular quiescence at larval hatching (milou and eif4(1006)) have a DNA replication b

198 arrest as partially elongated embryos or as hatching, misshapen L1 larvae.

199 a spontaneous behaviour appropriate to drive hatching movements, but has only minor effects on evoked

200 by manipulating both egg TH levels and post-hatching nest temperature in wild pied flycatchers (Fice

201 Across the months, the first day of hatching occurred earlier in warmer conditions suggestin

202 from the flagellar membrane for post-mitotic hatching of daughters from the mother cell wall.

203 n the oocyte development, egg production and hatching of eggs laid.

204 red 2 days after myogenesis, just before the hatching of fully formed cydippid larvae.

205 t has a substantial inhibitory impact on egg hatching of G. pallida.

206 Knockdown of ABC-C6 inhibits egg hatching of Meloidogyne and Globodera spp., relative to

207 Knockdown of ABC-G33 has no impact on egg hatching of Meloidogyne spp. but has a substantial inhib

208 hoosing a nest site that promotes successful hatching of offspring, especially in animals that do not

209 bation, whereby coots specifically delay the hatching of parasitic eggs, improves the reliability of

210 affect cellular differentiation but blocked hatching of the blastocysts from the zona pellucida.

211 g grounds, early arrival is favoured so that hatching of young can coincide with the peak of food qua

212 ops and evaluates a mechanistic model of the hatching of zebrafish eggs that were exposed to CuO engi

213 However, earlier-hatching offspring are now exposed to inclement weather

214 Larvae hatching on a plant that is already attacked by conspeci

215 ies of these insects must be functional from hatching onward, while thousands of new neurons are adde

216 g per day, orally, from day 2 to day 9 after hatching) or corn oil vehicle (VEH) with or without mono

217 However, learning based on hatching order is reliable in naturally parasitized coot

218 mutants is that while they die shortly after hatching owing to an obstructed gut passage, they nevert

219 4E and Ptp10D display synthetic lethality at hatching owing to respiratory failure.

220 d limb proportions which may, influence post-hatching performance.

221 ts across metamorphosis: their dependence on hatching period, and the lack of studies quantifying adu

222 Eight days after hatching (PHD) CB staining clearly delineated Area X.

223 or in developmental arrest immediately post-hatching-phenotypes that are fully suppressed by materna

224 analysis shows that the Drosophila brain at hatching possesses a large fraction of developmentally a

225 it was unrecognized previously that the pre-hatching, pre-implantation bovine embryo also engages in

226 rcial value and are culled immediately after hatching, raising concerns for animal welfare.

227 s are attacked by snakes, tadpoles escape by hatching rapidly and falling into the water below.

228 es accelerated egg development and increased hatching rate and larval survival in response to accumul

229 ine accelerated early development, increased hatching rate and produced larger larvae at 5 days post

230 posure to three pellets (330 mg) reduced the hatching rate of females and decreased the acrosome inte

231 In addition, the reproduction and hatching rate of R. similis isolated from the Rs-cps tra

232 arameters important for mass rearing such as hatching rate, adult emergence and sex ratio were compar

233 xicological end points, including mortality, hatching rate, and heart rate were recorded.

234 rol female reduced population growth and egg hatching rate, but did not influence gender ratio.

235 addition to a dose-dependent effect of Cd on hatching rate, DNA fragmentation was observed in embryos

236 erall fitness cost was closely linked to egg hatching rate, fecundity, emergence rate, larval surviva

237 The phenotype, the hatching time, the hatching rate, the sex ratio, the presence of own germ c

238 signalling is essential for oviposition and hatching rate.

239 rement is damage-free and barely affects the hatching rate.

240 e longer, produce more eggs, and have higher hatching rates in compatible crosses.

241 nted with 50 mug of E2 on the third day post-hatching showed a significant increase in the density of

242 us embryos which get resorbed or shed before hatching, similar to those of geckos.

243 High metabolic rates combined with small hatching size in ammonoids as opposed to lower metabolic

244 In asynchronously hatching species, parents are thought to either adjust b

245 ulated craniofacial elements of several post-hatching specimens of the non-avian dinosaur Hypacrosaur

246 han 50% of embryos and always around the pre-hatching stage.

247 pmental structures from early embryo to post-hatching stages.

248 21(st) century, potential impacts on future hatching success (the number of hatched eggs in a nest)

249 system characterized by low population mean hatching success (usually < 10%) of unfertilized eggs fr

250 in which they incubate, including effects on hatching success and hatchling viability (hatchling prod

251 Heartbeat, hatching success and swimming behavior of F1 embryos wer

252 ditions were projected for Sandy Point where hatching success has already declined over time along wi

253 -specific changes in reproductive timing and hatching success in response to noise exposure were expl

254 tic response to rising temperatures, in that hatching success increased up to some critical temperatu

255 tified embryonic mortality, infertility, and hatching success of each clutch, and assessed all hatchl

256 complete picture of how mothers can promote hatching success through adjustments in nest site choice

257 at Hg in eggs was negatively correlated with hatching success, and this effect was driven by both inc

258 Hatching success, heartbeat, and swimming activity were

259 ) was the single most important predictor of hatching success, more so than regional sea surface temp

260 We analyzed the effects on hatching success, offspring survival, and physiology.

261 ad minnow embryos assessing five end points (hatching success, time to hatch, length, deformities, an

262 atching Enzyme 1 and thereby delay or impair hatching success.

263 nd perfluorododecanoate was related to lower hatching success.

264 that mate only with siblings have decreased hatching success.

265 roductive output, produced eggs with reduced hatching success.

266 t, maturation of audition around the time of hatching suggested that synaptic transmission in the coc

267 ammed elimination of bursal stem cells after hatching, suggesting that Nr13 plays a role in maintaini

268 lly rescue hypercapnia-induced delays in egg hatching, suggesting that Zfh2's role in mediating respo

269 ther tetrapods, grew more quickly just after hatching than later in life.

270 polysis of the embryonic cuticle, so that at hatching the embryo displays the final adult number of l

271 The final step is perforation, where (after hatching) the primary mouth opens.

272 Until hatching, the innervation continued to increase in densi

273 lays its eggs on the seeds themselves; after hatching, the larvae burrow into and develop inside the

274 Around hatching there is a large increase in the ability of bla

275 ir counterparts in chickens remain thin from hatching through adulthood.

276 , we test the hypothesis that G changes from hatching through reproductive maturation.

277 The phenotype, the hatching time, the hatching rate, the sex ratio, the pre

278 arvae at high spatiotemporal resolution from hatching to adulthood ( approximately 3 days).

279 effects of deafferentation on the bulb from hatching to adulthood.

280 at Mussaurus rapidly grew from about 60 g at hatching to ~7 kg at one year old, reaching >1000 kg at

281 enetic effects ranged from 13% (for internal hatching) to 46% (for population growth).

282 lecular events involved in cyst dormancy and hatching, two key steps of their development.

283 ined in a regular 12-h light/dark cycle from hatching until 4 weeks of age, whereas dark-reared turtl

284 recognition by delaying parasitic eggs from hatching until after the first host eggs.

285 at experienced 10 min/hr of Call A or B from hatching until testing preferred the familiar call at Da

286 s without the diagnosis, and use of assisted hatching was associated with birth defects among singlet

287 ecrease in pupation, adult emergence and egg hatching was enhanced in the combined treatments.

288 Around hatching, waves gradually become stationary patches, whe

289 velopmental rate but body length and mass at hatching were largely insensitive to temperature.

290 ides We found that offspring were smaller at hatching when females laid eggs in presence of a male, s

291 of both CHH and CCAP were seen during larval hatching, when compared to the adult moult, and cell-spe

292 oincides closely with the observed moment of hatching, when development switches metamorphically from

293 ery bright signal upon photoactivation after hatching, which allowed us to examine cell coupling in l

294 om the 8- and 15-day hypoxia treatment still hatching while no non-arribada eggs hatched after more t

295 crawling-like sequences until shortly before hatching, while other reflexes also mature.

296 sed predation on larvae) would favor delayed hatching, while relatively high egg mortality would favo

297 having little effect on time to and size at hatching (whole-organism responses).

298 rest development just prior to or just after hatching with a pharynx that appears fully formed but is

299 Upon hatching, young turtles migrate offshore and are rarely

300 s from serial sections in embryonic and post-hatching zebra finches.