ライフサイエンスコーパス: hatch

1 increasing with D-BLUP (b=0.32+/-0.15 deaths/hatch).

2 incompatibility (that is, elimination of egg hatch).

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

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

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

6 ed protein response and apoptosis to reduced hatch.

7 2- to 3-fold, respectively, and they fail to hatch.

8 e and development rate quantified as time to hatch.

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

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

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

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

13 00 detected sources were from tank vents and hatches.

14 n during a limited time period shortly after hatching.

15 ukosis and hemangiomas within 2 months after hatching.

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

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

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

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

20 early stage embryo mortalities and premature hatching.

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

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

23 mortality only for the first few days after hatching.

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

25 ns were not altered by commensal microbes or hatching.

26 ryonic stages before becoming coordinated at hatching.

27 llum) finish their neuronal expansion before hatching.

28 e to arrested gonadogenesis following embryo hatching.

29 pts for uxs1 localize to skeletal domains at hatching.

30 d during embryogenesis and was strong around hatching.

31 30-40% of primary neurons around the time of hatching.

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

33 taging zone for their migration after larval hatching.

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

35 g preference for the familiar call following hatching.

36 a preference for the familiar call following hatching.

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

38 nging was positively correlated with earlier hatching.

39 out any association with a genetic parent at hatching.

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

41 e slowly inactivating mechano-current before hatching.

42 rly displaced distribution of VNC neurons at hatching.

43 effector genes were also up-regulated during hatching.

44 generation of forces required for blastocyst hatching.

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

46 at this individual weighed ~3.4 kilograms at hatching.

47 re capable of identifying parental odours at hatching.

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

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

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

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

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

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

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

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

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

57 ozygous Pdp1(p205) embryos develop normally, hatch and become viable larvae.

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

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

60 lutein and zeaxanthin were examined in newly hatched and 28-day-old WHAM chicks compared with control

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

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

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

64 Assisted hatching and diagnosis of ovulation disorder were margin

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

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

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

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

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

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

71 Spontaneous hatching and swim activity were significantly affected b

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

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

74 ecreasing with C-BLUP (b=-0.06+/-0.15 deaths/hatch) and increasing with D-BLUP (b=0.32+/-0.15 deaths/

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

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

77 >30 ng/L each during the period of spawning, hatching, and development for resident fishes.

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

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

80 ve hierarchies while gaining the benefits of hatching asynchrony.

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

82 After the eggs have hatched at 3 dpf, an aphidicolin-resistant polymerase, p

83 In mite-infested nests, male nestlings hatched at larger sizes, completed growth earlier, and h

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

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

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

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

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

89 -PMCA and Sp-SERCA mRNA begin at the 18 hour hatched blastula stage and peak 4-5-fold higher by 25 h

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

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

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

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

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

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

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

97 When newly hatched Caenorhabditis elegans larvae are starved, their

98 Newly hatched Caenorhabditis elegans respond to food deprivati

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

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

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

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

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

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

105 pYA3658 were used to orally immunize day-of-hatch chicks, colonization of the bursa, spleen, and liv

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

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

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

109 In recently hatched chicks, baseline fecal corticosterone metabolite

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

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

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

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

114 ly available for research purposes at http://hatch.cpmc.columbia.edu/highresmrs.html

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

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

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

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

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

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

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

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

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

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

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

126 resolved in meso, (ii) residues 57-62 in the hatch domain and residues 574-581 in loop 21-22 are diso

127 14-stranded beta-barrels with an N-terminal hatch domain blocking the barrel interior.

128 lasmic space does not require removal of the hatch domain from the barrel.

129 crystal forms, as have residues 86-96 in the hatch domain, and (v) the conformation of residues 6 and

130 is contiguous with a passageway through the hatch domain, lined by both hydrophobic and polar or cha

131 t to the periplasm via a channel through the hatch domain.

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

133 Newly hatched domesticated mallards that were briefly exposed

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

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

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

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

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

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

140 may become infected by ingesting a recently hatched egg clutch or become parasitized by individuals

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

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

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

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

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

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

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

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

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

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

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

152 e built a digital nuclear atlas of the newly hatched, first larval stage (L1) of the wild-type hermap

153 om of the groove, which represents an escape hatch for long lipids from mycobacterial pathogens.

154 mal, adult BER occurs fully when the embryos hatch from the chorionic membrane and encounter normal o

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

156 When Caenorhabditis elegans larvae hatch from the egg case in the absence of food, their de

157 These embryos do not hatch from the zona pellucida in vitro, fail to grow in

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

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

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

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

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

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

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

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

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

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

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

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

173 C. elegans larvae hatch in a developmentally arrested state (L1 arrest) an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

197 ompromised somatic cells and arrest of newly hatched larvae.

198 ly development and increased its toxicity in hatched larvae.

199 The hatching larval brain contains six groups of primary DA

200 multiple catalytic domains, prevented embryo hatch, larval molting, pupation, and adult metamorphosis

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

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

203 nd intersegmental vessel area within freshly hatched live embryos.

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

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

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

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

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

209 The regression of percentage of mortality on hatch number was significantly different between methods

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

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

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

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

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

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

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

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

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

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

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

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

222 4E and Ptp10D display synthetic lethality at hatching owing to respiratory failure.

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

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

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

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

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

228 s not detected in the vast majority of newly hatched planarians or in small tissue fragments that wil

229 lly parasitized coot nests because host eggs hatch predictably ahead of parasite eggs.

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

231 pt the disulfide bond have a very low embryo hatch rate compared with wild-type controls, indicating

232 nificant differences are observed in the egg hatch rate resulting from incompatible crosses, providin

233 dent rescue of the maternal effect on embryo hatch rate.

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

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

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

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

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

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

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

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

242 signalling is essential for oviposition and hatching rate.

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

244 viability, as measured by reduced embryonic hatch rates and larval lethality.

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

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

247 Newly hatched sea turtles exposed to artificially generated ma

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

249 The percentage of embryos hatched significantly increased following prednisolone t

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

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

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

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

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

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

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

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

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

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

260 Hatching success, heartbeat, and swimming activity were

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

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

263 nd perfluorododecanoate was related to lower hatching success.

264 roductive output, produced eggs with reduced hatching success.

265 ales exhibit disorganized nuclei and fail to hatch, suggesting strongly that a maternal contribution

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

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

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

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

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

271 Until hatching, the innervation continued to increase in densi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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