ライフサイエンスコーパス: yolk

1 e PE and PI species are mostly absent in the yolk.

2 microstructure of granule fractions from egg yolk.

3 nfirmed in samples of SOD extracted from egg yolk.

4 ibutors to the antioxidant properties of egg yolk.

5 carotenoid, and malondialdehyde (MDA) in egg yolk.

6 x mobility in fresh and freeze-thawed gelled yolk.

7 formation of an epithelial sheet around the yolk.

8 all carotenoid absorption via lipid-rich egg yolk.

9 memade matrix-matched standards based on egg yolk.

10 and 49% in 74 hpf embryos were found in the yolk.

11 oncentration in albumen, but only for 13% in yolk.

12 the nascent epithelium and three-dimensional yolk.

13 bryos by reducing varying amounts of vegetal yolk.

14 roinjecting CR leachate into the air cell or yolk.

15 e prepared with control yolks or soy control yolks.

16 fed breakfast doses of 0, 1, 2, 4, or 6 egg yolks.

17 NOR) for their quantification in poultry egg-yolks.

18 Residues of Sudan I were detected in egg yolks (0.29+/-0.03microg/kg, mean+/-SD) only after the a

19 ses 1 and 2 (mug kg(-)(1)): 6521 and 7329 in yolk, 1370 and 1539 in white.

20 ghest SigmaOP concentration, followed by egg yolk (14.8+/-2.4 ng/g ww) approximately egg albumen (14.

21 tive to standard control and LA-rich control yolks, (2) compare the rheological properties of mayonna

22 both doses (mug kg(-)(1)): 5920 and 9453 in yolk; 4831 and 6050 in white, in doses 1 and 2, respecti

23 Paint layers of egg yolk adhesive (E) and lead white tempera (E + LW) were e

24 ar role in the unwanted gel formation of egg yolk after conventional freezing.

25 MM dropped below the LOD (1.9 mug kg(-1)) in yolk after day 16 and 19 for doses 1 and 2.

26 metabisotopomics of triacylglycerols in egg yolk allowed the multivariate classification of samples

27 extracellular space into oocytes along with yolk and accumulates in punctate structures within embry

28 (Larus argentatus; n=8) and the separate egg yolk and albumen of their entire clutches of eggs (n=16)

29 n endogenous stores (e.g. muscle) and in egg yolk and albumen reflect the nutrient sourcing that dist

30 r penguin Delta(15) N(Pro-Phe) was higher in yolk and albumen than in muscle, reflecting the mobiliza

31 rophic' AA) had higher delta(15) N values in yolk and albumen than in muscle, suggesting that they we

32 ealization of painted and gilded areas, i.e. yolk and albumen, respectively.

33 oning, we separated embryonic cells from the yolk and allowed them to develop as spherical aggregates

34 o different foodstuffs, sour cream, egg, egg yolk and chicken nuggets.

35 ction spend roughly half their body mass for yolk and egg production; following mass spawning, the pa

36 Egg yolk and its main component, low-density lipoproteins (L

37 e eye lens, with lower levels in the retina, yolk and other tissues.

38 les like phosvitin and lipovitellin from egg yolk and phospholipids/phosphopeptides from human serum.

39 o co-protein effect with soy glycinin or egg yolk and positive co-protein effects with bovine serum a

40 tting of Au, which is sandwiched between the yolk and shell, leads to the desired nanocup morphology.

41 plied for the determination of cobalt in egg yolk and Vitamin B12 and the recovery results were found

42 posed for the determination of cobalt in egg yolk and Vitamin B12 at trace levels.

43 es in the SMM and TMP concentrations between yolk and white in post treatment period were found.

44 ethoxine (SMM) and trimethoprim (TMP) in egg yolk and white was measured during and after administrat

45 Effects of freeze-dried egg white, yolk and whole egg enrichment on water behaviour in fres

46 Additionally, egg yolks and human milk appear to be bioavailable sources.

47 Carotenoids accumulated in the egg yolk are of importance for two reasons.

48 nted for 25% of the SigmaOP concentration in yolk, but was not detected in albumen.

49 der, poppy, sunflower and pumpkin seeds, egg yolk, carum, hazel nuts and amaranth) on the morphologic

50 sing maternal shRNA technology we found that yolk catabolism depends on the Tor pathway and on the au

51 Yolk catabolism initiates at cellularization in Drosophi

52 rved Tor metabolic sensing pathway regulates yolk catabolism, similar to Tor-dependent metabolic regu

53 n, autophagy was not required for initiating yolk catabolism.

54 ts showed that CR leachate injected into the yolk caused mild to severe developmental malformations,

55 ctin and microtubule cytoskeleton within the yolk cell and defects in the outer enveloping cell layer

56 ess in which the blastoderm spreads over the yolk cell.

57 A granule fraction (G(in)) produced by egg yolk centrifugation was pressure-treated at 400 and 600

58 owever, obtained from ANN analysis where the yolk coefficient, air cell height, thick albumen height,

59 nd mass, and improved feed conversion ratio, yolk color core and Haugh unit.

60 ika, used in animal husbandry to enhance egg yolk colour.

61 ngth, eggshell thickness, albumen height and yolk colour.

62 y, a non-destructive technique, can identify yolk components and detect changes in the matrix.

63 ion times of proton pools representing major yolk constituents.

64 ll type and not differences in pigmentation, yolk content, cell size, or position in the embryo.

65 eductions of ovary size, egg production, and yolk deposition in mature oocytes.

66 dation and also from the accumulation of the yolk-derived and newly synthesized lipids from carbohydr

67 Together, these data suggest that yolk-derived E2 sets the ventral boundary of hemogenic v

68 and then on fresh and dried egg albumen and yolk down to 2.10(^4) and 1.10(^5) dilution factors, res

69 Changes in SOD activity of the egg yolk during its storage for 200days were also described.

70 od samples that include vegetable salad, egg yolk, egg white, whole egg and minced pork meat has vali

71 Raman spectra of the yolk extracts were recorded in the range from 3100 to 99

72 Raman spectra of the yolk extracts were recorded in the range from 3100 to 99

73 rgic (71.3%): 29 reacted to CE, seven to egg yolk (EY) and 22 to egg white (EW) and 38 reacted to RE.

74 his included different concentrations of egg yolk (EY; 5, 10 or 15%) and glycerol (2, 5 or 10%), dilu

75 ere measured above LOD (0.3 mug kg(-)(1)) in yolk for both doses on day 37 post-treatment.

76 laevis embryos at the 50-cell stage (~200 ng yolk free protein/blastomere) generated 20 943 unique pe

77 e change: +5.69% +/- 9.9%) compared with the yolk-free egg treatment (-3.69% +/- 5.3%) (P < 0.01), bu

78 rize the effects of whole eggs compared with yolk-free eggs on HDL function and composition in overwe

79 (~2) whole eggs compared with 100 g of (~2) yolk-free eggs per day, separated by a 4-wk washout.

80 When the mass of yolk-free proteins in single blastomeres decreased from

81 Hen egg yolk from chicken eggs were examined for their mycotoxin

82 ubule forces that probe blastomere shape and yolk gradients, biased by cortical polarity domains, may

83 However, increasing yolk granule size did not slow their velocity, and the F

84 fer of folic acid and phosvitin from the egg yolk granule to the plasma fraction.

85 e (1) compare the FA composition of CLA-rich yolk granules and plasma, relative to standard control a

86 of the embryo from the meiotic spindle while yolk granules are transported throughout the embryo by k

87 ganelles were transported as a unit with the yolk granules, resulting in sperm DNA within 2 microm of

88 eir velocity, and the F-actin moved with the yolk granules.

89 Cu,Zn-SOD isolated from egg yolk had an optimum at pH 6.

90 A stability test indicated that yolk had varied matrix mobility within the same sample a

91 e compared with the soybean (SL) and hen egg yolk (HL) lecithin in sunflower-fish oil O/W emulsion sy

92 tides from casein variants, nonfat milk, egg yolk, human serum and HeLa cell extract.

93 PC molecular species are present inside the yolk in addition to the blastodisc, while PE and PI spec

94 ase was observed in the n3 FA content in egg yolk in experimental groups, as well as all PUFA (polyun

95 Haugh unit, albumin pH, thick albumin ratio, yolk index, air cell size, and S-ovalbumin content of UC

96 ranatum seed oil both accumulated RmA in egg yolk, indicating an efficient conversion from the alpha-

97 Catabolism of yolk is initiated by acidification of the yolk platelet,

98 ified as Phacellophora camtschatica (the egg-yolk jelly).

99 Concurrent with the appearance of "egg-yolk lesions," the OCT showed a cleft in the outer retin

100 However, the yolk lipid extract successfully classified the eggs of t

101 100% accuracy by UV-VIS-NIR spectrum of the yolk lipid extract with the QDA statistical analysis.

102 d to intense lipid burden from high rates of yolk-lipid oxidation and also from the accumulation of t

103 d 94% at 35 degrees C when compared with egg yolk lipids extract.

104 Egg yolk lipids were extracted with food grade ethanol and e

105 the CLnA concentrations, but also CLA in egg-yolk lipids.

106 secondary structure of a newly developed egg yolk livetin formulation and its components alpha-liveti

107 Egg yolk low density lipoprotein (LDL)/polysaccharide nanoge

108 ion of SBP linearly (P < 0.01) decreased egg yolk malondialdehyde, cholesterol, and triglyceride, whi

109 CLA-yolk mayonnaise was more viscous, had greater storage mo

110 nd (3) compare the emulsion stability of CLA-yolk mayonnaise.

111 1200ngg(-1) in individual egg white and egg yolk, measured over 2days.

112 est demonstrated high repeatability of fresh yolk measurements, but significant differences (p<0.05)

113 Here we show that when injected into the yolk of a 2 day-post-fertilization (dpf) embryo of Tg (f

114 phore-tagged sialic acid and fucose into the yolk of zebrafish embryos at the one-cell stage enables

115 Yolks of 80 eggs were analysed as aliquots by the three

116 alues that did not differ between muscle and yolk or albumen, suggesting that most of these AAs were

117 red in delta(13) C values between muscle and yolk or between muscle and albumen, suggesting de novo s

118 relative to mayonnaise prepared with control yolks or soy control yolks.

119 n egg presence in the extract, i.e. albumen, yolk, or their co-presence in the matrix.

120 osensor to simultaneously recognize albumen, yolk, or their mixtures in HVPD extracts.

121 Incorporation of ferulic acid (FA) into egg-yolk phosphatidylcholine (PC) in a lipase-catalyzed acid

122 in saline by sonication, using 5% (w/v) egg yolk phospholipid as an emulsifier.

123 ch studied the enzymatic modification of egg yolk phospholipids and its effect on physicochemical pro

124 Egg yolk phosvitin is of particular interest due to its func

125 However, the fatty acid (FA) composition of yolk plasma and granule fractions are unreported.

126 s between the forming basal membrane and the yolk plasmalemma.

127 of yolk is initiated by acidification of the yolk platelet, leading to the activation of Cathepsin-li

128 cked into membrane-bound compartments called yolk platelets.

129 oxidative stability of control and enriched yolk powders as revealed by a moderate increase of the q

130 rnesoate suppresses transcript levels of the yolk precursor Vitellogenin both in cell culture and in

131 Vitellogenin, the egg yolk precursor, is a well-known biomarker of endocrine d

132 enormous size because of a massive uptake of yolk precursors such as very low density lipoprotein and

133 p- and down-regulation of female-specific Ds-Yolk protein 1 (Ds-Yp1) gene expression by temperature s

134 oocytes and the synthesis and deposition of yolk protein [10, 11].

135 reducing E2-dependent vitellogenin (VTG; egg yolk protein precursor) synthesis, (b) VTG-dependent egg

136 we obtained the entire mRNA sequence of the yolk protein precursor, vitellogenin, and monitored its

137 at body and subsequent accumulation of these yolk protein precursors by developing oocytes.

138 Yolk provides an important source of nutrients during th

139 Y are selected as analytes for egg white and yolk recognition, respectively.

140 ally arrested larvae that produce sperm from yolk reserves.

141 Embryonic large molecule derived from yolk sac (ELYS) is a constituent protein of nuclear pore

142 denocarcinoma (PDAC) originate from both the yolk sac (YS) and bone marrow.

143 ro MF-depletion strategy and fate-mapping of yolk sac (YS) and fetal liver (FL) hematopoiesis.

144 ly validate the use of gestational sac (GS), yolk sac (YS) diameter, crown-rump length (CRL), and emb

145 The putative progenitors of trMacs, yolk sac (YS) erythromyeloid progenitors, did not expres

146 lose association in the blood islands of the yolk sac (YS).

147 rom erythromyeloid progenitors (EMPs) in the yolk sac and develop in the forming CNS.

148 ing development, MCs enter the skin from the yolk sac and embryonic liver and are later mixed with ce

149 CNS, originate during embryogenesis from the yolk sac and enter the CNS quite early (embryonic day 9.

150 ion of cancer cells after injection into the yolk sac and extravasation of cancer cells into tissues

151 hematopoietic progenitors located within the yolk sac and fetal liver as well as definitive hematopoi

152 mouse macrophages derived from the embryonic yolk sac and from fetal liver.

153 ilarities with microglial progenitors in the yolk sac and immature microglia in early embryos.

154 rated through primitive hematopoiesis in the yolk sac and migrate into the brain rudiment after estab

155 ively from precursors originating within the yolk sac and migrate to the CNS under development, witho

156 ainly from progenitor cells generated in the yolk sac and of 'passenger' or 'transitory' myeloid cell

157 rom primitive hematopoiesis in the embryonic yolk sac and self-renew throughout life.

158 that the brain vasculature, like that of the yolk sac and the eye choriocapillaris and hyaloid vascul

159 The function of the primary yolk sac and the origin of extraembryonic mesoderm remai

160 scuss the intricate relationship between the yolk sac and the primate embryo and highlight the pivota

161 We demonstrate that DPFCs originate in the yolk sac and then rapidly migrate to other extra- and in

162 embryo and highlight the pivotal role of the yolk sac as a multifunctional hub for haematopoiesis, ge

163 EMPs develop in the yolk sac at embryonic day (E) 8.5, migrate and colonize

164 otential in vitro have been described in the yolk sac before emergence of HSCs, and fetal macrophages

165 the hemangioblast as the cell of origin for yolk sac blood and endothelium.

166 sites of embryonic hematopoiesis such as the yolk sac by way of blood flow.

167 tion, bilaminar disc formation, amniotic and yolk sac cavitation, and primordial germ cell-like cell

168 ion, bi-laminar disc formation, amniotic and yolk sac cavitation, and trophoblast diversification.

169 ly 140,000 liver and 74,000 skin, kidney and yolk sac cells, we identify the repertoire of human bloo

170 heir mutagenesis in mice impaired neural and yolk sac ciliogenesis, leading to morphogenetic anomalie

171 ts; for example, most tissue macrophages are yolk sac derived, monocytes and macrophages follow a mul

172 embryogenesis is hallmarked by two phases of yolk sac development.

173 However F4/80(HI) macrophages from the yolk sac did not respond to LPS treatment.

174 , which is rapidly superseded by a secondary yolk sac during gastrulation.

175 increase in the incidence of pericardial and yolk sac edema relative to controls.

176 n dilbit WAF-exposed embryonic zebrafish but yolk sac edema was similar in all exposures.

177 erm cell tumor predominantly consisting of a yolk sac element (Fig 1).

178 identify, in the fetal liver, a sequence of yolk sac EMP-derived and HSC-derived haematopoiesis, and

179 and HSC-derived haematopoiesis, and identify yolk sac EMPs as a common origin for tissue macrophages.

180 Yolk sac erythro-myeloid progenitors (EMP) contribute su

181 tissue-resident macrophages are derived from yolk sac erythromyeloid progenitors and fetal liver prog

182 i, the exocoelomic cavity, and the secondary yolk sac function together as a physiological equivalent

183 OX7 is broadly expressed across the RUNX1(+) yolk sac HE population compared with SOX17.

184 ly well studied, the molecular regulation of yolk sac HE remains poorly understood.

185 Embryonic SSMs originated from yolk sac hematopoiesis and were replaced by a postnatal

186 specification in the dorsal aorta, enhanced yolk sac hematopoiesis, and exuberant cardiac blood isla

187 show that TRPM6 activity in the placenta and yolk sac is essential for embryonic development.

188 The yolk sac is phylogenetically the oldest of the extraembr

189 e species indicates that the human secondary yolk sac likely performs key functions early in developm

190 In a chicken yolk sac membrane model, under the same ultrasound param

191 and TC-(57)CoB12 accumulated in the visceral yolk sac of KO mice where megalin is expressed and provi

192 progenitors (EMPs) that first appear in the yolk sac of the early developing embryo.

193 st compounds into the embryonic body and the yolk sac of the zebrafish embryo using TK experiments, a

194 (0)-resins can be carefully implanted in the yolk sac of zebrafish embryos and display excellent bioc

195 y give rise to chorio-allantoic and visceral yolk sac placentae, respectively.

196 Resident macrophages are derived from yolk sac precursors and seed the liver during embryogene

197 resident macrophages originally derived from yolk sac precursors.

198 tiple progenitor pools, microglia arise from yolk sac progenitors and are widely considered to be equ

199 ng early embryogenesis, microglia arise from yolk sac progenitors that populate the developing centra

200 pothesise that the hypoblast-derived primary yolk sac serves as a source for early extraembryonic mes

201 endoderm (PrE), which forms extra-embryonic yolk sac tissues.

202 associated with worse outcome, whereas pure yolk sac tumor (YST) was associated with better outcome,

203 s differentiated derivatives, teratoma (TE), yolk sac tumor (YST), and choriocarcinoma.

204 my, which revealed a 5-cm tumor that was 95% yolk sac tumor and 5% embryonal carcinoma, and retroperi

205 ixed germ cell tumor with 85% embryonal, 10% yolk sac tumor, and 5% mature teratoma histologies.

206 of Mexican-born mothers had a higher risk of yolk sac tumors (HR, 1.46; 95% CI, 0.99-2.17), while chi

207 ial lipodystrophy and a history of childhood yolk sac tumour.

208 Several of these mutants also display yolk sac vascular defects, suggesting a role for thrombi

209 N629D/N629D yolk sac vessels and aorta consist of sinusoids without

210 ses precursor cells of the embryo proper and yolk sac(1).

211 hen the blastoderm begins to spread over the yolk sac, a process involving coordinated epithelial sur

212 n leads to vascular defects in the placenta, yolk sac, and embryo proper, as well as abnormal neural

213 ascular abnormalities in the lung, placenta, yolk sac, and retina.

214 ion of target transcripts in placenta and/or yolk sac, and that some of these would be important for

215 xposed animals (whole larvae, as well as the yolk sac, brain, and heart).

216 ut the same in both WT and KO mouse visceral yolk sac, brain, and spinal column.

217 or erythro-myeloid progenitors (EMPs) in the yolk sac, but it decreased the expression of alpha4-inte

218 e products of transient hematopoiesis in the yolk sac, dorsal aorta, and developing heart tube functi

219 y in multiple anatomical sites including the yolk sac, dorsal aorta, and heart tube.

220 primitive endoderm (PE), which will form the yolk sac, is a crucial developmental decision.

221 lial cells termed haemogenic, present in the yolk sac, placenta and aorta, through an endothelial-to-

222 ptor 2(+) macrophages derived from primitive yolk sac, recombination activating gene 1(+) lymphomyelo

223 ells, identifying the earliest stages in the yolk sac, throughout embryonic development and in all ad

224 into the extra-embryonic region to form the yolk sac, umbilical cord and placenta.

225 The human embryo retains a yolk sac, which goes through primary and secondary phase

226 hypoblast gives rise to a transient primary yolk sac, which is rapidly superseded by a secondary yol

227 Functionally, yolk sac-derived chemokine (C-C motif) receptor 2(-) mac

228 with different ontogenetic origins: prenatal yolk sac-derived Kupffer cells and peripheral blood mono

229 , red pulp macrophages, a discrete subset of yolk sac-derived macrophages, were found to be altered i

230 Whereas yolk sac-derived microglia reside in the brain, blood-de

231 The recent paradigm shift that microglia are yolk sac-derived, not hematopoietic-derived, is reshapin

232 protein is a rodent-specific, placenta- and yolk sac-specific member of the tristetraprolin (TTP) fa

233 oid progenitors (EMPs) present in the murine yolk sac.

234 y in trophoblast giant cells in the parietal yolk sac.

235 omic data for the coelomic fluid bathing the yolk sac.

236 he placenta, and the epithelial cells of the yolk sac.

237 lood vessel formation in the embryo body and yolk sac.

238 om Mesp1-Cre(+) cells in both the embryo and yolk sac.

239 Predominant histology was yolk sac.

240 m which is derived the embryo proper and the yolk sac.

241 r and innate lymphoid cell precursors in the yolk sac.

242 xtensively self-renew and can be seeded from yolk sac/foetal liver progenitors with little input from

243 Genetic fate mapping revealed that yolk-sac and fetal monocyte progenitors gave rise to the

244 cells that develop during organogenesis from yolk-sac erythro-myeloid progenitors (EMPs) distinct fro

245 in European sea bass (Dicentrarchus labrax) yolk-sac larvae was explored.

246 Cx3cr1(+) yolk-sac macrophage descendants resided in the adult spl

247 Yolk-sac macrophages of EMP origin produced neonatal ost

248 ty of organs in which substantial numbers of yolk-sac macrophages persisted in adulthood.

249 cing (RNA-seq) data for the human and murine yolk sacs and compare those data with data for the chick

250 Aggf1+/- KO caused defective angiogenesis in yolk sacs and embryos.

251 nt, have aberrant vasculogenesis in embryos, yolk sacs and placentas, and die between embryonic day 1

252 In the absence of Eng, yolk sacs inappropriately express the cardiac marker, Nk

253 leaved caspase-3 were abnormally abundant in yolk sacs of Ripk1(D325A/D325A) embryos.

254 cripts, whereas there were few changes in KO yolk sacs.

255 For all egg yolk samples and all NaCl-containing LDL samples, the si

256 ) subtype avian influenza virus (AIV) in egg yolk samples, and 45% had antibodies against different A

257 ifferences (p<0.05) were found within gelled yolk samples.

258 phase in oil-in-water emulsions, from which yolk-shell and dual-shell hollow SiNPs@C composites are

259 rate Sb-based nanofibers composed of bunched yolk-shell building units as a significantly improved an

260 Taken together, the yolk-shell Fe3 O4 @Au NPs can be regarded as an ideal ma

261 Here by making yolk-shell nanocomposite of aluminium core (30 nm in dia

262 Yolk-shell nanostructures (YSNs) composed of a core with

263 Hollow and yolk-shell nanostructures have been used to increase the

264 such as porous solid spheres, core-shell and yolk-shell particles as well as single-shell and multi-s

265 t thermal reduction is proposed to fabricate yolk-shell Sb@C nanoboxes embedded in carbon nanofibers

266 ed by the cup-shaped void space created by a yolk-shell silica template that spontaneously takes an e

267 Pd-FeO(x) NPs are transformed into a porous yolk-shell structure along with the formation of SMSIR u

268 To circumvent this issue, yolk-shell structured MPHNs comprising a Fe3 O4 core wit

269 he shell is continuous, but it transforms to yolk-shell, with neither sacrificial template nor core e

270 To address such issues, well-designed yolk-shelled carbon@Fe3 O4 (YSC@Fe3 O4 ) nanoboxes as hi

271 pective to design a carbon/metal-oxide-based yolk-shelled framework as a high sulfur-loading host for

272 framework-67/Ni-Co layered double hydroxides yolk-shelled structures are first synthesized and then t

273 r phosvitin transfer and recovery in the egg yolk soluble fraction.

274 on (2 M methanol + 0.1 M trehalose + 10% egg yolk solution) was employed.

275 ol + 5.5 M Me(2)SO + 0.5 M sucrose + 10% egg yolk solution) was selected for Experiment 2.

276 oyloleoylphosphatidylcholine (POPC)) and egg-yolk sphingomyelin (EYSM) lipids, and allowed us to extr

277 nalizing the endoderm until they meet at the yolk stalk (umbilicus in mammals)(1,6).

278 quantitatively identify carotenoids from egg yolk such as spectrophotometric methods described by AOA

279 ], and the release of Nodal signals from the yolk syncytial layer (YSL) [9-12].

280 ween the enveloping cell layer (EVL) and the yolk syncytial layer (YSL) in the gastrulating zebrafish

281 Here, we show that the zebrafish yolk syncytial layer (YSL) secretes a ventralizing signa

282 A1 is expressed mostly in the extraembryonic Yolk Syncytial Layer (YSL) starting before shield stage

283 an being attracted to their destination, the yolk syncytial layer, cells appear to migrate away from

284 nfirming the capability to differentiate egg-yolk tempera from other kind of tempera binders as well

285 fat, which appears to derive from unconsumed yolk that was produced for reproduction.

286 Between the nuclear layer and the yolk, the cytoplasm was homogeneous and viscously domina

287 We used an N-glycan isolated from hen egg yolk together with the Nbz linker for Fmoc chemistry sol

288 ve tool to determine total carotenoid of egg yolk under laboratory-independent conditions with little

289 as developed for multi-class analysis of egg yolk using a dilute/precipitate, centrifuge, and shoot p

290 C50 values, and sublethal effects on growth, yolk utilization, and pancreas and liver development.

291 Average SOD activity in egg yolk was 98.5+/-19.5U.g(-1) while in egg white reached 6

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

293 olk, whereas the hardness of hard-boiled egg yolks was not affected.

294 egg powder and its fractions (egg white and yolk) was developed by combining microwave-induced combu

295 To determine egg yolk we focus here on the determination of immunoglobuli

296 Cu,Zn-SOD derived from hen egg white and egg yolk were determined, and compared with those of enzymes

297 FA profile and cholesterol content in yolks were determined.

298 valbumin, egg white, whole egg, defatted egg yolk, wheat albumins and wheat globulins were detected.

299 d positive impact on the colour of the eggs' yolk, whereas the hardness of hard-boiled egg yolks was

300 metes, but support is gathering for maternal yolk, which is deposited into ooctyes, as an extranuclea