ライフサイエンスコーパス: chick

1 ability of a laid egg resulting in a fledged chick.

2 from epiblast to defined neural lineages in chick.

3 M, occur at equivalent stages in the emu and chick.

4 ocytes that eliminate apoptotic cells in the chick.

5 ces misshapen or fused sensory organs in the chick.

6 al ganglion cells project their axons in the chick.

7 ion and cell cycle analyses in the embryonic chick.

8 to a potential predator attack than control chicks.

9 d apply it to posthatch zebra finch songbird chicks.

10 r of species studied, parents ignore begging chicks.

11 ome and metabolome of developing young layer chicks.

12 e infections and complementation analysis in chicks.

13 more, and parents preferentially feed those chicks.

14 mass recession occurred in 73% of all study chicks.

15 lection at 1, 3, and 9 days postinfection in chicks.

16 d higher body weight gain than the untreated chicks.

17 wing inoculation of SE in two-week-old layer chicks.

18 ts with more wormwood leaves produce heavier chicks.

19 tapping into parental choice for ornamented chicks.

20 cks were duller (less red) than nonparasitic chicks.

21 ikely to share paternity when they sired any chicks.

22 7-day old chicks (10 birds/group) were either untreated or they re

23 almost 20%) among common tern Sterna hirundo chicks, a well-studied species long-established as growi

24 Maternal FO consumption enriched chick adipose tissue in EPA and DHA and reduced adiposit

25 Conversely Lmx1a (or cLmx1b in the chick) allows sensory organ segregation by antagonizing

26 Use of the chick also allowed us to merge histological, immunochemi

27 amic morphoskeletons in wild-type and mutant chick and fly embryos, we find that they capture the ear

28 ell migration at three progressive stages in chick and identify and establish hierarchical relationsh

29 n of cNCCs to mature cardiomyocytes in fish, chick and mice, as well as their role in the regeneratio

30 Using frog, chick and mice, we analyzed the regulation of Prdm12 and

31 Through experiments conducted in both chick and mouse embryos we have developed a model explai

32 il factors and Zeb2 fulfil a similar role in chick and mouse in directly repressing ectodermal cadher

33 al actin cable and adherens-junctions within chick and mouse neuroepithelial cells.

34 nd their comparison with counterparts in the chick and mouse pretectum.

35 ression patterns evolved differently between chick and mouse.

36 of the morphogen Sonic hedgehog (SHH) in the chick and zebra finch, two species that differ in size d

37 Recent lineage-tracing experiments in chick and zebrafish embryos have shown that cNCCs can al

38 ons, determining food availability for their chicks and consequent breeding success.

39 ayed start of breeding with lighter eggs and chicks and lower breeding success the following breeding

40 ith that of sternal cartilage development in chicks and mice.

41 y and vestibular nuclei develop in embryonic chicks and mice.

42 Corticosterone-implanted chicks and their siblings were faster in responding to a

43 ed for Salmonella to colonize and persist in chicks and were not previously associated with this abil

44 accessibility in Muller glia from zebrafish, chick, and mice in response to different stimuli.

45 on to form multinucleated myotubes in mouse, chick, and zebrafish.

46 perienced babies and human fetuses, domestic chicks, and monkeys exhibit a preference for faces and f

47 ously known to be needed during infection in chicks, and one of these (STM1297) suggests an important

48 water colony, being detected among 34-38% of chicks annually.

49 re of the radioactive Mr 27,000 band by anti-chick apolipoprotein A-I antibodies confirmed its identi

50 tic birds [2,3,7], which might also occur in chick appearances when arms races escalate.

51 Day-old domestic chicks approach the larger of two groups of identical ob

52 ratio values in the offspring suggests that chicks are more capable to deal with potential stressful

53 Using the chick as a model organism, we show that vertebrate Pax6

54 Using the chick as a model, we found a precise and dynamic express

55 vidual mixed lineage progenitor cells in the chick as these cells offer a window into the cell fate d

56 Here, using domestic chicks as a model predator, we manipulated the degree of

57 f the zebra finch (Taeniopygia guttata) from chick at posthatch day (d) 8 to adult (up to 147 d) in f

58 y, however the UAV detected up to 52.4% more chicks because chicks were camouflaged and invisible to

59 families, chick coloration predicts whether chicks become "favorites" when parents begin control ove

60 In our first experiment, chicks begged significantly longer in response to the od

61 hypothalamus, pons, and medulla of posthatch chick brains, but not in some areas that are among the m

62 bryo corresponds to Snail2/P-cadherin in the chick, but both Snail factors and Zeb2 fulfil a similar

63 n of orexin system in the liver of 9-day old chicks, but did not affect feed intake.

64 aluate the role of SPI-1 in the infection of chicks by Salmonella, we created and utilized strains ha

65 This indicates that chicks can extract the common proportional value shared

66 We treat embryonic chick cardiac cells with a potassium channel blocker, wh

67 Chick cardiac crest ablation results in failure of this

68 In isolated chick cardiomyocytes and sections from canine heart, we

69 lion cells, our transcriptomes of developing chick cells also contained representation from multiple

70 n NE and bacterial dynamics and functions in chicks challenged with C. perfringens.

71 In the chick chorioallantoic membrane (CAM) assay used to measu

72 In a Chick Chorioallantoic Membrane (CAM) in vivo model, linc

73 tivity of HT C6 was confirmed in vivo in the chick chorioallantoic membrane assay.

74 The chick cochlear nucleus, nucleus magnocellularis (NM), ex

75 related homeobox 1 (PROX1) in the developing chick colon.

76 Deltaape1 was also impaired for chick colonization and adhesion, invasion, intracellular

77 We show that neonatal chick colonization with Salmonella enterica serovar Ente

78 xplained by color variation within families: Chick coloration increases with position in the egg-layi

79 However, within families, chick coloration predicts whether chicks become "favorit

80 Maternal effects influence chick coloration, but coot females do not use this mecha

81 However, the chick corneal stromal structure is remarkably complex in

82 layer, and anterior stroma were generated in chick corneas on embryonic day 7.

83 Then chicks could choose between two identical, left or right

84 itism is common in coots and brood parasitic chicks could manipulate hosts by tapping into parental c

85 rived from alcohol-exposed neural fold-stage chick crania, wherein alcohol causes facial deficits rec

86 P) antagonist we detected by analysis of the chick cranial mesoderm.

87 three groups and reared with (i) commercial chick crumb, (ii) crumb plus 1% live mealworm or (iii) c

88 the regulation of muscle progenitors during chick development has not been investigated.

89 tor (a rapidly expanding, looming stimulus), chicks displayed a fast escape response.

90 spatially distinct subpopulations within the chick dorsal neural tube.

91 veloped force apparatus, we demonstrate that chick dorsal root ganglion axons exhibit a tension buffe

92 able of targeted migration in the developing chick embryo and extensive colonization of the adult mou

93 effects of sildenafil on the fetus using the chick embryo and hypothesised that sildenafil also prote

94 In vivo chick embryo angiogenesis assay again confirms the antia

95 e also tested a four-channel device on fixed chick embryo Brainbow samples and identified individual

96 cumulated in different tumor xenografts in a chick embryo CAM model.

97 current, INa, based on 30 year old data from chick embryo cell aggregates).

98 cline on the antibody response to a purified chick embryo cell vaccine, given on a postexposure proph

99 tly reduced HepG2 tumor growth in a modified chick embryo chorioallantoic membrane (CAM) assay, assoc

100 sent study we tested the hypothesis that the chick embryo chorioallantoic membrane (CAM) can be used

101 of mouse aortic rings and neoangiogenesis in chick embryo chorioallantoic membrane.

102 Here, using the chick embryo close to hatching, a well-accepted model fo

103 Using the chick embryo model, here we show that sildenafil treatme

104 ng a 3R compliant cost effective preclinical chick embryo model.

105 o maintain their ability to metastasize in a chick embryo model.

106 e recombination experiments performed in the chick embryo provide evidence that signals operating dur

107 intrinsically disordered phosphoprotein, in chick embryo skeletal development, and using circular di

108 hat synaptic upscaling could be triggered in chick embryo spinal motoneurons by complete blockade of

109 spensions and ventricular tissue from day 16 chick embryo were collected and analyzed for comparison

110 Here, we show that in the chick embryo, E-cadherin is weakly expressed in the epib

111 tect against fetal growth restriction in the chick embryo, supporting the idea that the protective ef

112 In early chick embryo, we found that inducing high glucose levels

113 Using the chick embryo, we uncover novel genes in the gene regulat

114 g early morphogenesis of the gut tube in the chick embryo.

115 n of the foregut and heart tube in the early chick embryo.

116 tgrowth of neurites from both PC12 cells and chick embryonic dorsal root ganglia (DRG) bodies, as wel

117 s from both PC12 multicellular spheroids and chick embryonic dorsal root ganglia bodies.

118 ets, including human fetal echocardiography, chick embryonic heart ultrasound images, and zebrafish e

119 ression of alternative codon-derived DPRs in chick embryonic spinal cord confirmed in vitro data, rev

120 aggregation both in vitro and in vivo in the chick embryonic spinal cord.

121 Day 10 chick embryonic ventricular CM (3.5 x 10(4) cell cluster

122 Chick embryos (n = 11 per group) were incubated in normo

123 ss diverse contexts, including cell culture, chick embryos and adult mouse brain tissue.

124 o a pathway for sulfur metabolism present in chick embryos but not in mammals.

125 ocations and orientations in the epiblast of chick embryos in the early stages of primitive streak fo

126 Zebrafish, Xenopus and chick embryos largely show consistent requirements for s

127 Inhibition of Ssdp1/2 activity in mouse and chick embryos suppresses the generation of motor neurons

128 Here, we combine experiments on chick embryos with computational modeling to explore a n

129 in vitro (cultured dorsal spinal neurons of chick embryos) and in vivo (developing chick spinal comm

130 Notably, upon implantation into chick embryos, adult NC cells behaved similar to their e

131 Finally, in chick embryos, blocking the Wnt5a function in the caudal

132 In chick embryos, skeletal muscle formation is initiated by

133 Here we describe a new approach, using chick embryos, to discover organizers based on a common

134 of the cranial versus trunk neural crest in chick embryos, we identified and characterized regulator

135 engrafted on the chorioallantoic membrane of chick embryos, we observed a reduction of tumour cell pr

136 Using chick embryos, we show that the hypoxic cellular respons

137 required for NC delamination in Xenopus and chick embryos, whereas they do not affect the motile pro

138 ts engraft and adopt a metastatic program in chick embryos.

139 tor expression in the neural plate border of chick embryos.

140 m quails that are grafted into the coelom of chick embryos.

141 ound August and that the rapid growth of the chicks enabled them to reach a robust size before the au

142 target gene expression in mouse embryos and chick ex vivo assays.

143 Human neonates and domestic chicks exhibit several similarities in the predispositio

144 is were markedly up-regulated in choroids of chick eyes during the recovery from induced myopia, and

145 In Experiment 2, while chicks failed to spontaneously use a striped wall in a s

146 ish and carrion), analysis of delta(15) N in chick feathers identified a three-guild community struct

147 However, delta(15) N in chick feathers, which reflected trophic (level) speciali

148 eed and dimethylarsinic acid in breasts from chicks fed the SHC-containing diet.

149 ine was the major metabolite in breasts from chicks fed the UL-containing diet.

150 study used an ex vivo [embryonic day (E)18] chick femur defect model to examine the bone regenerativ

151 mm-drill defects in the mid-diaphysis of E18 chick femurs and cultured organotypically for 10 d.

152 It is unknown whether the chick fetal wound healing is capable of recapitulating t

153 We previously demonstrated that chick fetal wound healing shows a regenerative phenotype

154 etrin-1 (NTN1) is precisely expressed in the chick fissure margin during fusion but is immediately do

155 spiracles (ems)] RGCs in mouse neocortex and chick forebrain and found evidence for both sequential a

156 nts of active motors and clutches: embryonic chick forebrain neurons (ECFNs; optimum approximately 1

157 Chicks from both maternal diet groups were fed the same

158 Chicks from cross-fostered eggs responded significantly

159 genes to dissect the function of TIM4 in the chick (Gallus gallus).

160 We trained 3-day-old chicks (Gallus gallus) on a given numerical magnitude (5

161 Here we trained 4-day-old domestic chicks (Gallus gallus) to respond to stimuli depicting m

162 Indeed, the extra insects fed to urban chicks greatly reduced the significant differences in su

163 lised suburban and urban areas more as their chicks grew and appeared to use diverse foraging strateg

164 On high-LCPUFA diets, chicks grew faster, were in better condition, and had gr

165 ironmental changes: Adult body condition and chick growth rate were negatively linked to SIC and merc

166 and recorded their foraging behaviour during chick guarding.

167 normal chicks, the highly myopic-astigmatic chicks had significantly higher expression of all three

168 ing contact repulsion at the cell surface in chick half-somites.

169 reduced rainfall - but the mean body mass of chicks has not changed.

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

171 tein localisation and phenotypic evidence in chick, humans, mice and zebrafish that Netrin-1 has an e

172 In Experiment 2, chicks identified a specific proportion (2:1) from eithe

173 Biotinylated rabbit polyclonal to chick IgY (rIgPxcIgY) and phosphorylthioate-modified oli

174 We used a chick in vivo model to investigate nuclear factor kappa

175 uantity and quality of food for Tree Swallow chicks in a full factorial design.

176 alternative to the culling of 1-day-old male chicks in laying hen production.

177 streaked shearwater (Calonectris leucomelas) chicks in semi-field conditions resulted in the accumula

178 increased proportion of large prey items to chicks in the nest and spent less time flying while fora

179 The chicks in treatment groups consistently displayed higher

180 In predictable and good environments, chicks in worse condition beg more, and parents preferen

181 optic fissure closure (OFC) in the embryonic chick, including evidence for roles of apoptosis and epi

182 Gene expression in chick indicates that this non-neural origin of pineal pr

183 with this prediction, analysis of developing chick inner ear revealed that ligand-producing hair cell

184 A nest of begging chicks invites an intuitive explanation: needy chicks wa

185 erential gene expression in infected primary chick kidney cells indicated that the host cell response

186 amine the linkage between these processes in chick limb cartilage.

187 correlated with some long-chain PFAS in CFRE chick livers.

188 ntial toxicity of PCB enantiomers to newborn chicks may be different from that of adults.

189 integrin beta-1 (CA*beta1) in the embryonic chick mesencephalon, enhances neurogenesis and increases

190 ates from this second clade were tested in a chick model of infection and exhibited a reduced coloniz

191 the investigations reported here, we used a chick model system to assess the threshold duration of e

192 Here, we use mouse and chick models to show that dorsal ventricular layer (dVL)

193 similar but a close to significant increase (chick mortality 24% higher than controls).

194 ay with tebuconazole significantly increased chick mortality, which was 26% higher than that of contr

195 scular junctions (NMJs) when cocultured with chick myofibers for several weeks.

196 ous experience, we investigated responses of chicks naive to movement.

197 Here, we have used chick neural crest (NC) cells, a highly migratory stem c

198 ging and molecular perturbation of migrating chick neural crest cells in vivo.

199 to specification and maintained in migrating chick neural crest cells.

200 and compared its output to the growth of the chick neuroepithelium to assess the interplay between IN

201 By cross-fostering chicks of different age between nests, we successfully p

202 developmental fusion defects, and show that chick OFC is a powerful model for epithelial fusion rese

203 nd lower basal metabolic rates compared with chicks on both low LCPUFA diets.

204 Finally, no chick or adult was recaptured away from its natal site a

205 s may also play a role by feeding on adults, chicks or eggs.

206 ood distribution, implicating a role for the chick ornamentation in the parental life-history strateg

207 we found that overexpression of Ntn1 in the chick otic vesicle prevented canal fusion by inhibiting

208 f signaling pathway regulators to developing chick otocysts, we show that BMP signaling regulates the

209 wheat, spelt and rye) and four gluten-free (chick pea, lupin, buckwheat, amaranth) flours were used

210 migrant-migrant pairs, and fledged 0.7 more chicks per year on average.

211 r broods 6 days earlier and fledged 0.2 more chicks per year than migrant males and females on averag

212 position was more important for Tree Swallow chick performance than food quantity.

213 When objects were all identical, chicks performed randomly, as expected (Experiment 1).

214 ation defect of cNCCs, resulting in abnormal chick pharyngeal arch development.

215 the associative learning ability of pheasant chicks, Phasianus colchicus, then released them into the

216 esistance against S. Enteritidis in neonatal chicks, phenocopying germ-free mice associated with adul

217 xplore natural patterns of variation in coot chick plumage color, both within and between families, t

218 The resulting Ran-SPION-rIgPxcIgY carries chick polyclonal to microtubule-associated protein 2 (MA

219 Chicks preferentially retained LCPUFA in brain and muscl

220 Chick premigratory cranial neural crest cells reduce Cad

221 Chicks reared with 7 objects were presented with the ope

222 s, and during the incubation period (but not chick rearing), bolder individuals were more site-faithf

223 re changes in habitat suitability during the chick-rearing period based on historic satellite observa

224 competition between these species during the chick-rearing period by comparing their foraging behavio

225 longed or shortened by approximately 25% the chick-rearing period of 42 breeding pairs.

226 Yet, the possibility that chicks recognise parental odour at hatching has been com

227 uption of ZBP1 function in vivo in mouse and chick resulted in commissural axon guidance errors.

228 to produce somatic mutations of OTX2 in the chick retina and identified similar phenotypes to those

229 omes from individual cells isolated from the chick retina throughout retinogenesis.

230 s with electrophysiology and in vitro CSD in chick retina with intrinsic optical imaging, we addresse

231 glia-derived progenitor cells (MGPCs) in the chick retina.

232 dulator selective for NR2A, at 3 muM, in the chick retina.

233 ing influences the formation of MGPCs in the chick retina.

234 nes, RGC axons from goldfish, zebrafish, and chick retinal explants avoided rat M1-4 but freely cross

235 pocampal neurons and goldfish, zebrafish and chick retinal explants.

236 In chick retinal ganglion cells (RGCs), downregulation of A

237 e specific cell types from mouse, human, and chick retinas, as well as from Drosophila midguts.

238 Thus, the paradigmatic chick retinotectal projection, due to its neighborhood p

239 owing SCI in various animal models (lamprey, chick, rodents, nonhuman primates), different forms of s

240 strategy, perhaps as a reliable signal of a chick's size or age.

241 Again, at test, chicks selectively responded to the previously reinforce

242 e dense material, and docked mitochondria in chick sensory and Aplysia bag cell neurons growing rapid

243 the fission of mitochondria along embryonic chick sensory axons driven by combined PI3K and Mek-Erk

244 Here we show that in the embryonic chick, Shh is expressed transiently in prechordal mesode

245 ly, the number and tightness of loops in the chick small intestine can be increased or decreased dire

246 Next, focusing on the developing chick small intestine, we determined that Bmp2 expressed

247 We found that although chicks solely relied on geometry, rats navigated based o

248 ns of chick embryos) and in vivo (developing chick spinal commissural axons and rat callosal axons) f

249 Using dorsal patterning of the chick spinal cord we found that Daam2 promotes Wnt signa

250 and not EphB receptor signaling in mouse and chick spinal motor axons.

251 Focussing largely on mouse and chick studies, we concentrate on the positioning of the

252 Chicks succeeded when those features were differently or

253 gh contact with treated soils did not affect chick survival but altered some biochemical parameters p

254 ct availability has a considerable impact on chick survival: Even a single inclement weather event ca

255 ates and the likelihood that their nests and chicks survived during the subsequent breeding season.

256 These factors reduce chick survivorship as they cannot metabolize saline wate

257 Here, we use chick sympathetic neuroblasts to examine the normal func

258 by MYCN/ALK cooperation, we used cultures of chick sympathetic neuroblasts.

259 Here we show that Zebra Finch chicks (Taeniopygia guttata) are capable of identifying

260 ior-posterior and medial-lateral axes of the chick tectum using microarray based transcriptional prof

261 We show in chick that two different tissues, namely the lateral hea

262 eg more, and preferentially feed the biggest chicks that beg less.

263 parents in some species even neglect smaller chicks that beg more, and preferentially feed the bigges

264 change prior to fledging for 313 common tern chicks that successfully fledged from two discrete popul

265 Chicks that were provisioned at higher rates were more l

266 nly apparent for individuals who had fledged chicks the year before.

267 In chick, the driver of cluster pattern is tensile force fr

268 Unlike the well-studied chick, the mouse cornea had no acellular primary stroma.

269 Thus, unlike in chick, the murine villus patterning system is independen

270 In zebrafish and chick, the transition from quiescence to reactivity is e

271 We found that, compared to normal chicks, the highly myopic-astigmatic chicks had signific

272 les do not use this mechanism to benefit the chicks they lay as parasites.

273 s after the onset of incubation, and newborn chick tissues.

274 CBs 95, 132, and 149 occurred in the newborn chick tissues.

275 Exposing chicks to one hour of light during the night disrupts th

276 All birds cared for chicks until normal fledging age, resulting in birds wit

277 In Experiment 1, we found that both rats and chicks used environmental geometry to compute locations

278 of visual stimuli in newly hatched domestic chicks using filial imprinting, suggesting that statisti

279 neous navigation task with rats and domestic chicks, using a single prominent featural cue (a striped

280 icks invites an intuitive explanation: needy chicks want to be fed and parents want to feed them.

281 and sales from broilers, eggs, turkeys, and chicks was $42.8 billion.

282 te enantioselectivity for PCB 135 in newborn chicks was observed.

283 The Chick-Watson inactivation kinetic model, based on integr

284 The extension of the Chick-Watson model, in the ICT domain, described well th

285 Chicks were assigned to a Control diet and BEOs diet (Co

286 UAV detected up to 52.4% more chicks because chicks were camouflaged and invisible to ground observer

287 However, counter to expectation, parasitic chicks were duller (less red) than nonparasitic chicks.

288 total of 576 (19 days old) Cobb 500 broiler chicks were fed eight finisher diets consisting of 4 con

289 We found that the chicks were less likely to approach and eat prey with hi

290 f miR-203 inhibits neural crest migration in chick, whereas its functional inhibition using a 'sponge

291 1 pellet (110 mg) produced heavier eggs and chicks, whereas males exposed to 1 pellet presented an i

292 In their offspring, those chicks whose parents were exposed to CHS showed higher i

293 Regarding the H/L ratio, chicks whose parents were supplemented showed lower H/L

294 nt of Sonic hedgehog (Shh) signalling in the chick wing bud specifies cells with three antero-posteri

295 c hedgehog (Shh) signalling in the embryonic chick wing bud specifies positional information required

296 h)-expressing polarising region cells of the chick wing bud.

297 ion of Shh signalling at a specific stage of chick wing development results in a pattern of four digi

298 we electroporated granule cell precursors in chick with plasmids encoding fluorescent proteins and pr

299 age is favored by strong parental choice for chicks with more extreme ornamentation but left unresolv

300 Prior chick work indicated that digit phalanges and their asso