ライフサイエンスコーパス: hatching

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

2 e to arrested gonadogenesis following embryo hatching.

3 mortality only for the first few days after hatching.

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

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

6 ns were not altered by commensal microbes or hatching.

7 ryonic stages before becoming coordinated at hatching.

8 llum) finish their neuronal expansion before hatching.

9 pts for uxs1 localize to skeletal domains at hatching.

10 30-40% of primary neurons around the time of hatching.

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

12 taging zone for their migration after larval hatching.

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

14 g preference for the familiar call following hatching.

15 a preference for the familiar call following hatching.

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

17 d during embryogenesis and was strong around hatching.

18 nging was positively correlated with earlier hatching.

19 r concentration declined precipitously after hatching.

20 Tissue was collected on the day of hatching.

21 r bimodal (audiovisual) stimulation prior to hatching.

22 er uptake necessary for eggshell rupture and hatching.

23 es-specific perceptual preferences following hatching.

24 ed and should kill host offspring soon after hatching.

25 to bobwhite maternal Calls A or B following hatching.

26 I(DS) defined electrophysiologically around hatching.

27 ain during late embryonic development and at hatching.

28 atively high egg mortality would favor early hatching.

29 out any association with a genetic parent at hatching.

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

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

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

33 off between predation risks before and after hatching.

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

35 tive to negative isoforms around the time of hatching.

36 t terminally differentiated neurons prior to hatching.

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

38 sis, which remains uniformly expressed until hatching.

39 c bursa, cell death increases markedly after hatching.

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

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

42 tage, and decreased subsequent to blastocyst hatching.

43 ct an individual's subsequent survival after hatching.

44 trigeminal sensorimotor circuits present at hatching.

45 ffect the maintenance of CR expression after hatching.

46 o affect cell adhesion or muscle function at hatching.

47 s makes up the entire serotonergic system by hatching.

48 n and die late in embryogenesis before or at hatching.

49 urons of NL have many short dendrites before hatching.

50 ircuit is formed but immature at the time of hatching.

51 e slowly inactivating mechano-current before hatching.

52 rly displaced distribution of VNC neurons at hatching.

53 effector genes were also up-regulated during hatching.

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

55 generation of forces required for blastocyst hatching.

56 at this individual weighed ~3.4 kilograms at hatching.

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

58 re capable of identifying parental odours at hatching.

59 ukosis and hemangiomas within 2 months after hatching.

60 n during a limited time period shortly after hatching.

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

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

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

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

65 early stage embryo mortalities and premature hatching.

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

67 d with a full complement of sensillae before hatching; 2) the infolding and rotations that form the d

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

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

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

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

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

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

74 At hatching about 40 to 50 glial cells are present along th

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

76 By 12 days after hatching all of the major adult ganglia were discernible

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

78 hicks were reared in 1 of 3 conditions after hatching: altered tactile, auditory, or visual experienc

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

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

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

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

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

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

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

86 Assisted hatching and diagnosis of ovulation disorder were margin

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

88 proximately 18 boutons on muscles 7 and 6 by hatching and grow to approximately 180 boutons by third

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

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

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

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

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

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

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

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

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

98 Spontaneous hatching and swim activity were significantly affected b

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

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

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

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

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

104 >30 ng/L each during the period of spawning, hatching, and development for resident fishes.

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

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

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

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

109 embryogenesis, but they die within 2 days of hatching as first instar larvae.

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

111 ve hierarchies while gaining the benefits of hatching asynchrony.

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

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

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

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

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

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

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

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

120 ecular basis of the circadian control of egg hatching behavior in the silkmoth Antheraea pernyi.

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

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

123 istently abolishes the circadian gate of egg hatching behavior.

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

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

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

127 y developed and possess normal morphology at hatching but fail to respond to light stimulation.

128 ther induced by song playbacks 30 days after hatching but not at 20 days nor in juveniles reared in s

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

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

131 nstem circuits grow in the first month after hatching, but are not yet mature at the time the head re

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

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

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

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

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

137 The barn owl's head grows after hatching, causing interaural distances to more than doub

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

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

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

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

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

143 (including specimens 6, 8, and 12 days after hatching), competent, and metamorphosing larvae with pos

144 reatment of pharate larvae on the day before hatching consistently abolishes the circadian gate of eg

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

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

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

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

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

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

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

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

153 ick contentment calls in the period prior to hatching demonstrated prenatal auditory learning, whethe

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

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

156 en shown to play critical roles in embryonic hatching, dorsal/ventral patterning, and early developme

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

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

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

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

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

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

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

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

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

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

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

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

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

170 al axial mesodermal derivatives, such as the hatching gland and notochord, are largely spared.

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

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

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

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

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

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

177 ic shield region, showing descendants in the hatching gland, head mesoderm, notochord, somitic mesode

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

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

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

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

182 the inhibition of estrogen synthesis before hatching had a small but significant effect in demasculi

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

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

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

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

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

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

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

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

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

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

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

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

195 Egg hatching is rhythmically gated, persists under constant

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

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

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

199 ility [II (stP36) and V (stP6)] and internal hatching [IV (stP5)] were also mapped in these crosses.

200 The hatching larval brain contains six groups of primary DA

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

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

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

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

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

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

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

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

209 ng the first 36 or the first 72 hr following hatching modified chicks' preferential responding to spe

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

211 e as late embryos because they lack vigorous hatching movements.

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

213 We also observed a reduced rate of zona-hatching of blastocysts in vitro in the presence of anan

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

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

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

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

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

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

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

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

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

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

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

225 4E and Ptp10D display synthetic lethality at hatching owing to respiratory failure.

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

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

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

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

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

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

232 nder UV-B shields had a significantly higher hatching rate and fewer deformities, and developed more

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

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

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

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

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

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

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

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

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

242 signalling is essential for oviposition and hatching rate.

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

244 , both fitness, as measured by fertility and hatching rates of eggs, and genetic diversity declined s

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

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

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

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

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

250 We monitored hatching success and development in long-toed salamander

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

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

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

256 Hatching success, heartbeat, and swimming activity were

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

258 that mate only with siblings have decreased hatching success.

259 roductive output, produced eggs with reduced hatching success.

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

261 nd perfluorododecanoate was related to lower hatching success.

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

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

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

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

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

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

268 Until hatching, the innervation continued to increase in densi

269 In larvae 6 days after hatching, the neuropil had already appeared in the apica

270 y stop bursting spontaneously 2-4 weeks post-hatching, the time when receptive-field areas reach adul

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

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

273 rse of vocal development in budgerigars from hatching to about 4 weeks postfledging (approximately 85

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

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

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

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

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

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

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

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 Around hatching, waves gradually become stationary patches, whe

284 ropic effects on mean life span and internal hatching were found linked to stP5.

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

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

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

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

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

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

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

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

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

294 auditory midbrain of tadpoles shortly after hatching, with higher rates of synchronous neural activi

295 Upon hatching, young turtles migrate offshore and are rarely

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