ライフサイエンスコーパス: egg

1 olism is essential for making a high-quality egg.

2 T are able to successfully introduce dietary egg.

3 major component secreted by live schistosome eggs.

4 play a role by feeding on adults, chicks or eggs.

5 se AAs were directly routed from muscle into eggs.

6 oceratops and basal sauropodomorph Mussaurus eggs.

7 for example, maternally-derived steroids in eggs.

8 en from seemingly passive structures such as eggs.

9 he high fertilization treatment laid lighter eggs.

10 e segregation to the production of aneuploid eggs.

11 tivation-induced zinc release compared to WT eggs.

12 s and the steroids mothers transfer to their eggs.

13 vation similar to that observed in zip9(-/-) eggs.

14 eetle reproductive success by eating blowfly eggs.

15 and determine where the female fly lays her eggs.

16 partellus (Swinhoe) (Lepidoptera: Crambidae) eggs.

17 >= 0.35 kU(A) /L) varied by food: milk 5.7%, egg 4.0%, and peanut 7.9%.

18 er, but parasitic eggs are usually the first eggs a female lays.

19 for proper zinc modulation during zebrafish egg activation and presents the first evidence of zinc m

20 the first evidence of zinc modulation during egg activation in a non-mammalian species.

21 Despite occurring hours earlier, egg activation mediates clearance of these proteins thro

22 al oocyte development, chorion formation and egg activation.

23 Egg adaptation likely did not substantially affect our R

24 e analyze antibody responses elicited by the egg-adapted 3c3.A H3N2 vaccine strain in ferrets and hum

25 Here, we find that the egg-adapted H3N2 component of the 2019 Southern Hemisphe

26 We completed neutralization assays using an egg-adapted H3N2 virus, a cell-based H3N2 virus, wild-ty

27 itive patients had greater nAb titers to the egg-adapted vaccine virus compared to the cell-grown vac

28 ed exclusively in cell culture, thus lacking egg adaptive changes.

29 ved IIVs provide opportunities to assess how egg-adaptive substitutions influence HA immunogenicity.

30 iters against H3 HA-pseudoviruses containing egg-adaptive substitutions T160K and L194P were high, bu

31 All vaccines boosted titers to HA with egg-adaptive substitutions, suggesting boosting from pas

32 Non-breeders began to care for eggs after male removal and further increased parental c

33 Wines fined with egg albumin and plant-based proteins from potato, pea, a

34 effectiveness to reduce wine turbidity than egg albumin but modified in different way the phenolic c

35 ntire sequence of ovomucoid, in plasma of 38 egg-allergic and 6 atopic children.

36 Egg-allergic children had lower esIgA(1) (P = .010) and

37 e and huFcepsilonRIalpha/F709 mice that were egg-allergic with anti-FcepsilonRIalpha mAbs safely remo

38 Egg allergy affects almost 1 in 10 Australian infants.

39 early egg introduction and (b) did not have egg allergy at 12 months.

40 ound in mice to be responsible for different egg allergy risk.

41 essions were used to compare groups based on egg allergy status and comorbidities.

42 rved in PBMCs from individuals with milk and egg allergy.

43 cts contaminated at 5 mug g(-1) for milk and egg and 10 mug g(-1) for soy and crustaceans.

44 With egg and peanut OIT, a limited remission, or sustained un

45 anisms starts with the fusion of the haploid egg and sperm gametes to form the genome of a new diploi

46 their breeding grounds, where they mate, lay eggs and die.

47 an immortal cell lineage that gives rise to eggs and/or sperm each generation.

48 n and sensitization to specific foods (milk, egg, and peanut).

49 nsumed cereal and staples, 57.9% meats, 4.7% eggs, and 0.5% nuts and seeds.

50 matrix that surrounds all mammalian oocytes, eggs, and early embryos and plays vital roles during oog

51 be propagated in goslings, embryonated goose eggs, and primary goose embryo fibroblasts, and is thus

52 PCs are released from insect eggs, and they induce salicylic acid and H(2)O(2) accumu

53 Egg- and cell-derived 2018-2019 season influenza vaccine

54 Egg- and cell-derived IIVs elicited responses similar to

55 d on antibody response to S. mansoni soluble egg antigen (SEA) with stool-based measures of infection

56 t IgG antibodies against Schistosoma mansoni egg antigens (SmSEA) cross-react with allergens in natur

57 by an extract from schistosome eggs (soluble egg antigens) and culture supernatants of live schistoso

58 s model, we find that only mature S. mansoni eggs are shed into the feces of mice and humans.

59 Eggs are suspended in a gel of unknown composition that

60 ition in the egg-laying order, but parasitic eggs are usually the first eggs a female lays.

61 s where to build a nest or where to lay your eggs, are critical for the offspring's fitness and survi

62 d to assess the role of the gel encasing the eggs, as well as the impact of stress on reproductive bi

63 predators, but information on the nature of egg-associated elicitors is scarce.

64 The finding of PCs as egg-associated molecular patterns (EAMPs) illustrates th

65 amino acids during embryo development in the egg at no cost of reduced sulfur.

66 een proposed that zinc released by mammalian eggs at fertilization may block additional sperm from en

67 of relevance for managing parent flocks and eggs at the hatchery in case of Salmonella infection in

68 ock is detected and destroyed, including the eggs at the hatchery.

69 Among 12 777 214 beneficiaries, the egg-based adjuvanted (RVE, 7.7%; 95% confidence interval

70 stent with prior research, we found that the egg-based adjuvanted and HD vaccines were slightly more

71 ded egg-based high-dose trivalent (HD-IIV3), egg-based adjuvanted trivalent (aIIV3), egg-based standa

72 Exposures included egg-based high-dose trivalent (HD-IIV3), egg-based adjuv

73 as not significantly more effective than the egg-based quadrivalent vaccine (RVE, 2.5%; 95% CI, -2.4%

74 ccines were slightly more effective than the egg-based quadrivalent vaccines.

75 ines were marginally more effective than the egg-based quadrivalent vaccines.

76 V3), egg-based adjuvanted trivalent (aIIV3), egg-based standard dose (SD) quadrivalent (IIV4), cell-b

77 tigens may undergo adaptive mutations during egg-based vaccine production.

78 r the cell-cultured vaccine compared with SD egg-based vaccines.

79 zone (egg-based, n = 23), Fluzone High-Dose (egg-based, n = 16), Flublok (recombinant protein-based,

80 responses in humans vaccinated with Fluzone (egg-based, n = 23), Fluzone High-Dose (egg-based, n = 16

81 nt geochemical signature than those from the egg-bearing layers described in Auca Mahuevo.

82 Externally deposited eggs begin development with an immense cytoplasm and a s

83 hormones, fecundity, sperm and egg quality, egg biochemical composition and fads2 expression were st

84 Among children allergic to unbaked egg but tolerant to BE, those treated with egg OIT were

85 egg OIT in participants allergic to unbaked egg but tolerant to BE.

86 ated PBMCs from children allergic to milk or egg, but not peanut, were significantly lower compared t

87 a urchin spermatozoa towards the conspecific egg by a spatially and temporally orchestrated series of

88 uction is polyspermy, or fertilization of an egg by multiple sperm.

89 that transcriptome abundance doubles in the egg cell and increases approximately 1.6-fold in the cen

90 Fertilization of an egg cell by more than one sperm cell can produce viable

91 when double fertilization precedes maternal (egg cell) genome loss.

92 s, causing their preferential segregation to egg cells in a process known as meiotic drive.

93 distributions of small RNAs in the sperm and egg cells of rice.

94 ead across heterochromatic regions, while in egg cells, 24-nt siRNAs were concentrated at a smaller n

95 and hindsight during Drosophila melanogaster egg chamber development.

96 y for establishing the posterior fate of the egg chamber, we show that it is not sufficient to determ

97 sistance concentrated near the center of the egg chamber.

98 The information from the egg chemoattractant concentration field is decoded into

99 ulture supernatants of live schistosome egg (egg-conditioned medium), and in particular by IPSE/alpha

100 show no overall association between moderate egg consumption and risk of T2D.

101 Egg consumption was assessed every 2-4 y using a validat

102 Illegally collected clutches of turtle eggs containing a decoy transmitter enabled us to track

103 ing a negative binomial regression fitted to egg count data, we found that every percentage point inc

104 We carried out 1,977 faecal egg counts (FECs) across five years to estimate nematode

105 simultaneously detect the presence of milk, egg, crustaceans and soy.

106 menogenesis and forms the primed pluripotent egg cylinder, which is able to generate the embryonic ti

107 BMI, lifestyle, and dietary confounders, a 1-egg/d increase was associated with a 14% (95% CI: 7%, 20

108 Each 1 egg/d was associated with higher T2D risk among US studi

109 ants; 41,248 incident T2D cases), for each 1 egg/d, the pooled RR of T2D was 1.07 (95% CI: 0.99, 1.15

110 arily as an animal feed in the production of eggs, dairy, pork and chicken.

111 The lutein bio-accessibility in enriched eggs decreased after GI digestion except in RIR fried sa

112 stosomiasis is caused by immune responses to eggs deposited in the bladder wall.

113 ccurred, and 25 645 occurred in the standard egg-derived IIV4 group.

114 ccIIV4 vs egg-derived quadrivalent vaccines (egg-derived IIV4) for that season.

115 cord of ccIIV4 and 1 261 675 had a record of egg-derived IIV4.

116 rived inactivated influenza vaccine (IIV) to egg-derived IIVs provide opportunities to assess how egg

117 ional bio-nanocomposite comprised largely of egg-derived polymers and cellulose nanomaterials as a co

118 ive vaccine effectiveness (rVE) of ccIIV4 vs egg-derived quadrivalent vaccines (egg-derived IIV4) for

119 may have greater effectiveness than standard egg-derived vaccines.

120 ly, insect eggs trigger defenses that impede egg development or attract predators, but information on

121 in differentiated cells is nonessential for egg development.

122 ion of THg transferred from females to their eggs differed among bird taxa and with maternal THg expo

123 Here we report a new type of egg discovered in nearshore marine deposits from the Lat

124 Strikingly, immature eggs do not recruit macrophages, revealing that the eggs

125 and culture supernatants of live schistosome egg (egg-conditioned medium), and in particular by IPSE/

126 nase that may function as a receptor for the egg elicitor and other genes implicated in early plant d

127 The calcified, hard-shelled dinosaur egg evolved independently at least three times throughou

128 Using Xenopus egg extract and in vitro reconstitution systems, here we

129 ombine our in vitro reconstitution assay and egg extract experiments with computational modeling to s

130 ein interactions in cell-free Xenopus laevis egg extract identified the dimeric histone chaperone fac

131 microfluidics, hydrogels, and Xenopus laevis egg extract to investigate the mechanics of aster moveme

132 Using Xenopus egg extracts and biochemical reconstitution, we found th

133 We showed in both Xenopus laevis egg extracts and mammalian cells that a conserved cystei

134 t by dynein and actomyosin forces in Xenopus egg extracts and observed outward co-movement of MTs, en

135 nerated by encapsulating cytoplasmic Xenopus egg extracts into cell-sized 'water-in-oil' droplets.

136 Using frog egg extracts that recapitulate NHEJ, we show that end pr

137 monstrate biochemically using Xenopus laevis egg extracts that the Cdk1-counteracting phosphatase PP2

138 ignal that triggers CMG unloading in Xenopus egg extracts using single-molecule and ensemble approach

139 se spindles in Haemanthus endosperm and frog egg extracts.

140 determine their repair mechanism in Xenopus egg extracts.

141 eggshell trigger granulomas that facilitate egg extrusion into the environment.

142 e, or Punica granatum, a PunA source, on the egg fatty acid profile.

143 oduce sperm with defects in capacitation and egg fertilization.

144 sumption of animal foods (animal fat, dairy, eggs, fish/seafood, meat).

145 diameter, presence of distended oviducts or eggs for females, and testes length and sperm activity i

146 steak, butter, canned tuna, catfish, cheese, eggs, french fries, fried chicken, ground beef, ground p

147 rs were placed alone in a novel aquarium and eggs from an established spawning pair were introduced.

148 arly disrupts early embryonic development in eggs from diverse phyla, including Cnidaria, Echinoderma

149 that a fundamental strategy protecting human eggs from fertilization by multiple sperm may have evolv

150 The material consisted of eggs from hens fed with a mixture without oil and with t

151 Eggs from larp6b single mutant females showed minor chor

152 d site and a reference site, and a subset of eggs from the reference site were treated with estradiol

153 nsity, prevalence of heavy infections (>=400 eggs/gram of feces), and total prevalence being particul

154 both assays, and study 2, performed with an egg-grown adjuvanted quadrivalent influenza vaccine (aQI

155 quadrivalent influenza vaccine (aQIVe) using egg-grown target virus.

156 number of eggs laid, duration of egg laying, egg hatchability, and adult longevity in P. pseudoinsula

157 prevent these supernumerary fertilizations, eggs have evolved multiple mechanisms.

158 cuses on how biochemical studies of the frog egg helped identify the cyclin-based mitotic oscillator

159 pecialised cells: the sperm in males and the egg in females, each carrying the genetic inheritance of

160 eproductive tract and from the layers of the egg in order to complete their fertilization journey.

161 s ater), a brood parasite that commonly lays eggs in blackbird nests.

162 nses to bladder-wall-injected S. haematobium eggs in Il4ra(-/-) versus wild-type mice.

163 g that it is best to avoid 'putting all your eggs in one basket'.

164 ms are solely based on the detection of worm eggs in stool.

165 ha, BRD0705, also inhibited fertilization of eggs in vitro.

166 It exceeds all nonavian dinosaur eggs in volume and differs from them in structure.

167 us genome, only 3 are present in the chicken egg, including the egg-specific avian beta-defensin 11 (

168 Total mercury (THg) concentrations in eggs increased with maternal blood THg concentrations; h

169 study explored the use of spent hen, a major egg industry byproduct, as the starting material for pre

170 type (concentrated, baked), and quantity of egg ingested in the long term.

171 S. haematobium egg injection triggered significant urothelial prolifera

172 perm protein, TMEM95, is necessary for sperm-egg interaction.

173 s only observed in infants who (a) had early egg introduction and (b) did not have egg allergy at 12

174 , called chemoattractants, released from the egg investments in a process known as chemotaxis.

175 Although the elephant bird egg is slightly larger, its eggshell is roughly five tim

176 Eggs laid by hens receiving SBP had linearly (P < 0.01)

177 wed minor chorion defects, but chorions from eggs laid by larp6a;larp6b double mutant females were mo

178 g success, pre-oviposition period, number of eggs laid, duration of egg laying, egg hatchability, and

179 Mating and egg laying are tightly cooordinated events in the reprod

180 we identify the neural circuitry that links egg laying to mating status in Drosophila melanogaster.

181 piRNA production commenced shortly after egg laying, and inactivation of the more abundant piRNA

182 ons (oviDNs) is necessary and sufficient for egg laying, and is equally potent in virgin and mated fe

183 Since taste is essential to feeding, egg laying, and mating decisions in insects, improved un

184 ion period, number of eggs laid, duration of egg laying, egg hatchability, and adult longevity in P.

185 ior of the roundworm Caenorhabditis elegans, egg laying, to perform a behavior-based screen for natur

186 animals prolong the duration of reproductive egg laying, which may enable the subsequent development

187 rwise associated with <20% reduction in post-egg-laying breeding success.

188 nsmitter GPCR expression and function in the egg-laying circuit provides a model for understanding GP

189 t on the timing of breeding, being higher if egg-laying commenced before the median date, and substan

190 ified assumptions that (1) workers take over egg-laying following queen death and (2) productivity in

191 ject via the anterior commissure, similar to egg-laying monotreme mammals.

192 ck coloration increases with position in the egg-laying order, but parasitic eggs are usually the fir

193 flies, geosmin is not aversive but mediates egg-laying site selection.

194 role for dopamine in coupling locomotion and egg-laying together across states.

195 erformance, egg quality, blood chemistry and egg lipid peroxidation was studied.

196 Egg lipids suggest these different reproductive outcomes

197 tely 54% and 44% of the respective adult and egg mass populations were observed within the first 15 m

198 Egg-mass bearing females were exposed to a 5 h heat ramp

199 ces released from tissue-trapped schistosome eggs may be important factors contributing to the develo

200 As gravid females burrow, their eggs may bioaccumulate PAHs from contaminated sediments,

201 ryos developed from MTH1 knock-out zebrafish eggs microinjected with N6-methyl-dATP compared with non

202 Tardigrade egg morphology shows a diverse appearance, and it is kno

203 ant role, but only highly resistant diapause eggs of killifish have been found to survive passage thr

204 trolled feeding experiment, where developing eggs of two cosmopolitan, invasive cyprinids (common car

205 1%) versus 10 of 23 participants assigned to egg OIT (43.5%) (P = .009).

206 f participants who are BE-reactive underwent egg OIT and identical double-blind, placebo-controlled f

207 th sustained unresponsiveness after extended egg OIT are able to successfully introduce dietary egg.

208 y and efficacy of BE ingestion compared with egg OIT in participants allergic to unbaked egg but tole

209 d egg but tolerant to BE, those treated with egg OIT were significantly more likely to achieve SU tha

210 who are BE-tolerant was similar with BE and egg OIT, but more frequent in participants who are BE-re

211 activation decreased similarly after BE and egg OIT.

212 ves when both vector stages were reared from eggs on infected plants.

213 ization to milk (OR 1.7, 95% CI 1.2-2.1) and egg (OR 1.4, 95% CI 1.01-1.9), but not peanut (OR 0.98,

214 their parents at the start of OIT for milk, egg, peanut, sesame, or tree nuts, at the end of up-dosi

215 Six allergenic ingredients (milk, egg, peanut, soybean, hazelnut, and almond) were incurre

216 th worm counts (p = 0.023) and the number of eggs per gram (epg) counts (p < 0.001).

217 This evidence suggests that egg pigmentation could play an important role in thermor

218 ologically sustained elevation of zinc in WT eggs prior to activation resulted in abnormal chorion el

219 heir activity, feeding behavior, metabolism, egg production and gene expression.

220 skewed sex ratios, ovarian atresia, reduced egg production, and altered gene expression.

221 eal from humans, which they use to stimulate egg production.

222 ost plants, good flying capability, and high egg production.

223 Egg proteins also influenced viscoelastic properties of

224 es substantial economic losses by diminished egg quality and increased morbidity and mortality of inf

225 lp (SBP) in laying hen diets on performance, egg quality, blood chemistry and egg lipid peroxidation

226 reproductive hormones, fecundity, sperm and egg quality, egg biochemical composition and fads2 expre

227 well as measures of maternal investment and egg quality.

228 face proteins that are responsible for sperm-egg recognition, binding, and fusion.

229 lbendazole arms also revealed higher CRs and egg reduction rates against hookworm than the monotherap

230 MT) asters in Xenopus laevis and other large eggs remains unclear.

231 ze) and performance (ingestion rate (IR) and egg reproduction rate (EPR)) of the numerically dominant

232 latworm parasites that feed on blood and lay eggs, resulting in pathology.

233 c composition of these soft-shelled dinosaur eggs, revealing a stratified arrangement resembling turt

234 te juvenile instars and is not involved with egg sac construction.

235 xtract fluoroquinolones from honey, milk and egg samples and satisfactory extraction recoveries were

236 zip9(-/-) eggs showed abnormal cortical vesicle development and ha

237 hundreds of fertilized H. symbiolongicarpus eggs simultaneously with minimal embryo death and no lon

238 nship between pH levels and traits (body and egg size) and performance (ingestion rate (IR) and egg r

239 ival and growth, we estimated the effects of egg size, timing of breeding, inter- and intra-annual va

240 ric and symmetric lipid vesicles composed of egg SM, cholesterol, and either unsaturated dioleoyl PC

241 were induced by an extract from schistosome eggs (soluble egg antigens) and culture supernatants of

242 well-established that food proteins, such as egg, soya, cow's milk and wheat, are detectable in breas

243 ferentially targeted between populations, as egg-specific and birch pollen-specific IgE was more comm

244 re present in the chicken egg, including the egg-specific avian beta-defensin 11 (Gga-AvBD11).

245 Our experiment shows that egg spraying with pesticides should be considered as a r

246 e an epithelial sheet around the ellipsoidal egg surface during a gastrulation process known as epibo

247 Only 0.2% of ingested eggs survived gut passage, yet, given the abundance, die

248 ome variation between the different types of eggs tested in these experiments, especially with regard

249 evel mycotoxins were detected in most of the eggs tested.

250 survival and physiology by manipulating both egg TH levels and post-hatching nest temperature in wild

251 susceptible mosquitoes (CYP6P9a-SS) lay more eggs than heterozygote (OR = 2.04: P = 0.01) and homozyg

252 ound day 21 after inoculation with infective eggs that is transcriptionally characterized by markers

253 dern crocodilians and birds lay hard-shelled eggs, this eggshell type has been inferred for non-avian

254 15) N(Pro-Phe) was similar across muscle and egg tissue in previously published data for income-breed

255 were transaminated during their routing into egg tissue.

256 ure of red-legged partridge (Alectoris rufa) eggs to an herbicide (2,4-D) and a fungicide (tebuconazo

257 ical and complex fluid that carries sperm to eggs to initiate the fertilization process.

258 Egg-to-adult D. suzukii survival was also 12% lower on C

259 ost results from granulomas that form around eggs trapped in the liver and gut.

260 Similarly, insect eggs trigger defenses that impede egg development or att

261 value of production and sales from broilers, eggs, turkeys, and chicks was $42.8 billion.

262 mediated dispersal ability of soft-membraned eggs undergoing active development.

263 al vesicles of males, resulting in decreased egg viability when these males inseminate nonmated femal

264 ed a reproductive response in later seasons: Egg volume and nestling survival were higher in subseque

265 diapsids, revealing that the first dinosaur egg was soft-shelled.

266 The accumulation of PunA in eggs was largely higher than that of alpha-ESA.

267 In cell-free extracts of Xenopus laevis eggs, we find that nuclei define such pacemakers by conc

268 ast three omega-3-PUFA enriched (or control) eggs/week, for 6 months.

269 Alligators eggs were collected from a contaminated site and a refer

270 % CI: 0.15, 0.88; P = .006), number of times eggs were consumed in the previous 24 hours (beta coeffi

271 Fertilized chicken eggs were incubated and divided randomly into control (C

272 the reproductive season progressed; smaller eggs were laid earlier, larger eggs were laid later.

273 ssed; smaller eggs were laid earlier, larger eggs were laid later.

274 ed that substances released from schistosome eggs were responsible for the observed effects.

275 Eggs were subjected to quality assessment.

276 nd maternally deposited gene in Nile tilapia eggs which is known to play a role in repression of tran

277 Chicken egg white (CEW) was applied as the crude feedstock of ly

278 has been developed to detect pig gelatin and egg white in experimental five-year aged Nebbiolo-based

279 rcial ELISA kit was instead unable to detect egg white in the same samples.

280 solution at a dose rate of 40.3 MGy/s on hen egg white lysozyme (HEWL) crystals at RT and cryotempera

281 erved in young pigs rendered allergic to hen egg white protein (HEWP).

282 Our aim was to characterise egg white protein digestion products and study their abi

283 This method allowed both gelatin and egg white proteins to be detected and quantified in aged

284 on for purification of lysozyme from chicken egg white was investigated.

285 Egg white-specific IgE, skin testing, and basophil activ

286 ple application in honey, cocos nucifera and egg white.

287 The embryo was found in an egg with thicker eggshell and a partly different geochem

288 However, larp6a mutant females produced eggs with chorions that failed to elevate fully and were

289 roportion of maternal THg was transferred to eggs with increasing female THg concentrations.

290 iate material in poultry nutrition to enrich eggs with PUFA.

291 Nuclear c-Jun staining pattern around lodged eggs without ambient immune reaction, and directionally

292 ids, metabisotopomics of triacylglycerols in egg yolk allowed the multivariate classification of samp

293 s) in endogenous stores (e.g. muscle) and in egg yolk and albumen reflect the nutrient sourcing that

294 A granule fraction (G(in)) produced by egg yolk centrifugation was pressure-treated at 400 and

295 ncrease was observed in the n3 FA content in egg yolk in experimental groups, as well as all PUFA (po

296 clusion of SBP linearly (P < 0.01) decreased egg yolk malondialdehyde, cholesterol, and triglyceride,

297 od was developed for multi-class analysis of egg yolk using a dilute/precipitate, centrifuge, and sho

298 To this end, egg yolk was taken as a model matrix.

299 P. granatum seed oil both accumulated RmA in egg yolk, indicating an efficient conversion from the al

300 In WT eggs, zinc was detected in cortically-localized vesicles