ライフサイエンスコーパス: hatch

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

2 e the number of taste buds over stages after hatch.

3 improved rapidly between days 1 and 14 post-hatch.

4 howed a brief up-regulation around 50 h post-hatch.

5 ed protein response and apoptosis to reduced hatch.

6 2- to 3-fold, respectively, and they fail to hatch.

7 after 10 days, and larvae were collected at hatch.

8 es in Bd one, three, and five days after egg hatch.

9 eduction (90%) of this drug in the embryo at hatch.

10 nal diet groups were fed the same diet after hatch.

11 00 detected sources were from tank vents and hatches.

12 roceed for a further 10 days, before the egg hatches.

13 rvae spontaneously expressing GFP days after hatching.

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

15 e slowly inactivating mechano-current before hatching.

16 rly displaced distribution of VNC neurons at hatching.

17 effector genes were also up-regulated during hatching.

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

19 at this individual weighed ~3.4 kilograms at hatching.

20 trieved from fresh feces and survived beyond hatching.

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

22 ukosis and hemangiomas within 2 months after hatching.

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

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

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

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

27 early stage embryo mortalities and premature hatching.

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

29 mortality only for the first few days after hatching.

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

31 ns were not altered by commensal microbes or hatching.

32 ryonic stages before becoming coordinated at hatching.

33 llum) finish their neuronal expansion before hatching.

34 pts for uxs1 localize to skeletal domains at hatching.

35 one day after hatching and three days after hatching.

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

37 epared to develop rapidly and robustly until hatching.

38 e to arrested gonadogenesis following embryo hatching.

39 out any association with a genetic parent at hatching.

40 generation of forces required for blastocyst hatching.

41 re capable of identifying parental odours at hatching.

42 n during a limited time period shortly after hatching.

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

44 d during embryogenesis and was strong around hatching.

45 ertile eggs were injected with virus, and 35 hatched (13%); 23 of these potential founders (F0) were

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

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

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

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

50 nt still hatching while no non-arribada eggs hatched after more than four days in hypoxia.

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

52 After hatching, alligators were raised under controlled labora

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

54 data showing localized reduction of both egg hatch and adult female numbers.

55 uM selenomethionine (SeMet) decreased embryo hatch and depleted glutathione in Japanese medaka embryo

56 In this issue, Hatch and Hetzer show that actin fibers constrict the nu

57 larval survival, time to 50% hatch, size at hatch and post-larval growth rates.

58 xtracted from the parent fish, these embryos hatched and grew to adulthood.

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

60 Assisted hatching and diagnosis of ovulation disorder were margin

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

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

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

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

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

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

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

68 Spontaneous hatching and swim activity were significantly affected b

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

70 individual juveniles (fry, four months post hatch) and characterised them by Illumina high-throughpu

71 er resulted in 89.8% +/- 3.91-86.7% +/- 3.87 hatch, and no significant increase in deformities.

72 ocapsules (>/= 800 mg/L) cause inhibition of hatch, and we suggest that a low pH environment may expl

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

74 >30 ng/L each during the period of spawning, hatching, and development for resident fishes.

75 at three early life stages: embryonic; post-hatch; and post-larval, to a high energy water accommoda

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

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

78 ing embryos which successfully developed and hatched as active larvae at about four and a half months

79 ve hierarchies while gaining the benefits of hatching asynchrony.

80 peratures and produce smaller eggs that both hatch at lower rates and produce smaller larvae than fem

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

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

83 in embryos as they developed from morula to hatched blastocysts by a progressive increase in the lac

84 mbryos undergo caspase-mediated apoptosis as hatched blastocysts, but not as morulae or blastocysts.

85 of foxN2/3 mRNA begins in micromeres at the hatched blastula stage and then is lost from micromeres

86 lthough it is well established that the last hatched/born offspring in a brood or litter often show r

87 ect and brood their eggs until the juveniles hatch, but to date there is little published information

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

89 . from 0.0002 to 0.13), while body weight at hatch (BW1), 35 days-of-age (BW35), and 41 days-of-age (

90 Newly hatched C. elegans larvae (L1s) halt development in "L1

91 We show that exposing newly hatched C. elegans to pathogenic bacteria results in per

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

93 Newly hatched Caenorhabditis elegans respond to food deprivati

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

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

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

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

98 cross tissues during both embryonic and post-hatch chick development.

99 and introduced this mutant pool into day-of-hatch chicks.

100 ing experiments confirm that coots use first-hatched chicks in a brood as referents to learn to recog

101 d parasite, uses cues learned from the first-hatched chicks of each brood to recognize and reject par

102 In recently hatched chicks, baseline fecal corticosterone metabolite

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

104 er control conditions, the embryonic to post-hatch comparison (first transition) had a greater number

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

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

107 staining to existing bone structures, cross hatch damage and a single crack extending from the notch

108 Hatch date and breeding success also varied with a pair'

109 ts of annual reproductive performance, brood hatch date and breeding success, differed between reside

110 concentrations in eggs increased with later hatch date, independent of lipid content which also incr

111 text of multilayered factors including year, hatch date, weather and location, confirming that this e

112 rst breeding year correlates positively with hatch date; hence, early-hatched individuals experience

113 : -1.435, -1.132) were negatively related to hatching date.

114 rounds, pair formation, nest initiation, and hatch dates all showed significant delays ranging from 9

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

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

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

118 ns created from controlled variations in the hatch distance within the same part.

119 erlying sequences of visual stimuli in newly hatched domestic chicks using filial imprinting, suggest

120 Newly hatched domesticated mallards that were briefly exposed

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

122 Novel PFAS were confirmed in chicks hatched downstream of a fluoropolymer production site in

123 tion were exposed to EDCs until 21 days post hatch (dph), reared to adulthood in clean water at eleva

124 rested at the blastocyst stage and failed to hatch due to defective TE development.

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

126 Also, T. retortaeformis hatched earlier than G. strigosum.

127 over effect was only present in females that hatched early in the season, and was not mediated by met

128 ts on future hatching success (the number of hatched eggs in a nest) were predicted using the climati

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

130 d, and the number of morphologically intact, hatched embryos was increased from approximately 24 to 7

131 ion of immunity and host protection in newly hatched embryos.

132 , and induced teratogenesis in 100% +/- 0 of hatched embryos.

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

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

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

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

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

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

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

140 ur early life history stages; eyed egg, post hatch, first feeding and three weeks post first feeding

141 Juvenile squid and octopods hatch from the egg already swimming in this inertial reg

142 Importantly, adult brine flies, which hatched from aquatic larva, bioaccumulated the highest S

143 We used D. galeata clones hatched from ephippia 10 to 60 years old, which were fir

144 ring in X. ramesis, while P. chephrenis that hatched from larger clutches survived for less time unde

145 ecognize parasitic offspring after they have hatched from the egg, even when the host and parasitic c

146 d a reduction in the proportion of eggs that hatched from trpm germ-line knockout mutant females, alt

147 hree or four-day androgen treatment of newly hatched fry, but not by estrogens, mineralocorticoids, g

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

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

150 ife commences when rains fill the pool: fish hatch, grow rapidly and mature in as few as two weeks, a

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

152 rsa and periphery in the absence of Ag after hatch; however, intrabursal injection of PE prolonged su

153 rity, in which a 'vestigial' egg is laid and hatches immediately(7).

154 When C. elegans hatch in a food-free environment, postembryonic growth a

155 nlight and WAF significantly reduced percent hatch in mahi-mahi embryos.

156 tiated by ingestion of infective eggs, which hatch in the intestine.

157 clutch size is driven by a decline with date hatched in the ability of offspring to recruit.

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

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

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

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

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

163 tes positively with hatch date; hence, early-hatched individuals experience colder conditions at arri

164 ncluding an egg within an ovary and possible hatched individuals, are here described from rocks of th

165 ience colder conditions at arrival than late-hatched individuals.

166 s of gravel-scouring flows on eggs and newly hatched individuals.

167 gotic null embryos from null mothers fail to hatch into first instar larvae.

168 cestral mode of development in which embryos hatch into first nymphs that resemble miniature adults.

169 wild-type counterparts, but the eggs do not hatch into larvae.

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

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

172 sion of PCN transcriptomes from dry cysts to hatched juveniles using RNA-Seq.

173 After hatching, juveniles of most sea turtle species undertake

174 additionally increased mortality of recently hatched larvae by 22%.

175 s in alcohol-laden food sources that protect hatched larvae from infection.

176 species exhibits a life cycle whereby newly hatched larvae must find suitable intermediate hosts (fr

177 ly development and increased its toxicity in hatched larvae.

178 ompromised somatic cells and arrest of newly hatched larvae.

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

180 The hatching larval brain contains six groups of primary DA

181 ant 'growing days' in the spring relative to hatch led to similar results.

182 g five end points (hatching success, time to hatch, length, deformities, and heart rate).

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

184 nd intersegmental vessel area within freshly hatched live embryos.

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

186 concentrations in down feathers of recently hatched (<3 days) and blood of older (15-37 days) Forste

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

203 We found that all hatched offspring from the chimera GE hens were derived

204 res provisioning of an egg meal to the newly hatched offspring.

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

206 ), but no infection was found in individuals hatched on Aride, Denis or Fregate.

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

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

209 n chicks and then discriminate against later-hatched parasitic chicks in the same brood.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

228 signalling is essential for oviposition and hatching rate.

229 y, transgenic CinA can rescue defects in egg-hatch rates when expressed in females.

230 er, if parasitic eggs are among the first to hatch, recognition cues are confounded and parents then

231 LE, ALARMc, BASE-AF2, CHADS2, CHA2DS2VASc or HATCH score (AUC 0.716, 0.671, 0.648, 0.552, 0.519 and 0

232 Newly hatched sea turtles exposed to artificially generated ma

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

234 The percentage of embryos hatched significantly increased following prednisolone t

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

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

237 mbryo survival, larval survival, time to 50% hatch, size at hatch and post-larval growth rates.

238 r power, 1250 mm/s scanning speed, and 80 um hatch spacing without, any post-process heat treatments.

239 eters such as laser power, laser scan speed, hatch spacing, and powder layer thickness were optimized

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

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

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

243 eather disease virus (BFDV) were revealed on hatch success, but these effects were remarkably short-l

244 to E2beta did not adversely impact survival, hatch success, growth, or genotypic ratios.

245 21(st) century, potential impacts on future hatching success (the number of hatched eggs in a nest)

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

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

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

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

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

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

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

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

254 Hatching success, heartbeat, and swimming activity were

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

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

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

258 roductive output, produced eggs with reduced hatching success.

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

260 nd perfluorododecanoate was related to lower hatching success.

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

262 The late-hatched survivors can equal or exceed their older siblin

263 imal, we significantly reduced the number of hatched T. muris eggs.

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

265 Until hatching, the innervation continued to increase in densi

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

267 y strategy such that resident-resident pairs hatched their broods 12 days earlier than migrant-migran

268 Individual resident males and females hatched their broods 6 days earlier and fledged 0.2 more

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

270 pid droplet formation may provide an "escape hatch" through which misfolded proteins, toxins, and vir

271 While sandeel hatch time was found to be related to the rate of season

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

273 One QTL for hatch timing was associated with the marker, Omm1241.

274 to SeMet and hypersalinity decreased embryo hatch to 3.7% +/- 1.95, and induced teratogenesis in 100

275 ss deficits, and then reared larvae from egg hatch to adulthood under diurnally variable regimens inc

276 ne pathways than the second transition (post-hatch to post-larval).

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

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

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

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

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

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

283 ed was 136 from 1970 to the enactment of the Hatch-Waxman Act in 1984; 284 from 1985 to the enactment

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

285 All eggs from heterozygous queens failed to hatch when they did not inherit this haplotype.

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

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

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

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

290 erized by retinal dystrophy and blindness at hatch, with secondary globe enlargement and loss of corn

291 Within treatments, populations hatched within 1 day of each other, on average, and amon

292 When Caenorhabditis elegans larvae hatch without food, they arrest development in the first

293 Hatch-year female survival was also density dependent.

294 n Model for the Earth Simulator, we generate hatch-year trajectories for loggerhead turtles emanating

295 As a result, hatch-year trajectories remain mostly below 35 degrees N

296 ion distance, or breeding season, 13 species hatched young earlier over time with most advancing >3 d

297 val in the recruitment year were high, early-hatched young had a higher recruitment probability than

298 Upon hatching, young turtles migrate offshore and are rarely

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

300 how that colonization by commensals in newly hatched zebrafish primes neutrophils and induces several