ライフサイエンスコーパス: chicken

1 A expression profiles in mouse, opossum, and chicken.

2 the connectivity between ICX and TeO in the chicken.

3 acs and compare those data with data for the chicken.

4 to chicken) and/or lard supplemented beef or chicken.

5 eef, horsemeat, duck meat, ostrich meat, and chicken.

6 t dog or cat, cattle, and poultry other than chicken.

7 in mice, and against Campylobacter jejuni in chicken.

8 wild species that gave rise to the domestic chicken.

9 rotein oxidation in the impaired quality PSE chicken.

10 pathology and extrapulmonary virus spread in chickens.

11 HT1080 and HeLa, and remained attenuated in chickens.

12 on is partially compensated between sexes in chickens.

13 reconstruct in vitro the microbiota of feral chickens.

14 rom normally slaughtered and dead on arrival chickens.

15 ion in gut lesions and mortality in infected chickens.

16 ion of the median lethal dose in two-day old chickens.

17 do not know how piRNAs co-evolve with TEs in chickens.

18 imism could be a useful welfare indicator in chickens.

19 ene conferred extrapulmonary virus spread in chickens.

20 es not produce piRNAs in undomesticated wild chickens.

21 that have putatively been under selection in chickens.

22 t an easy way to visualize all taste buds in chickens.

23 ly divergent LD patterns found in commercial chickens.

24 ion products were found in live but not dead chickens.

25 in five purebred lines of commercial broiler chickens.

26 documented consequence of chronic stress in chickens.

27 in primary chicken embryonic fibroblasts and chickens.

28 tinal tract of free-range, broiler and feral chickens.

29 f a midbrain network to visual perception in chickens.

30 iruses that can cause a rising prevalence in chickens.

31 re able to infect and be transmitted between chickens.

32 tion characteristics and transmissibility in chickens.

33 ll positives (384/602) and 81.2% of positive chickens (359/442).

34 05) when it was blended with fish (7.1%) and chicken (4.9%), however it was unaffected by beef.

35 coli isolates were likely to originate from chickens (56%) or from pigs (32%).

36 In contrast to chicken, a visually foraging bird, the majority of duck

37 nes have been used widely to protect village chickens against Newcastle disease, due to their decreas

38 --based on simulations with the K237E mutant chicken alpha-actinin--and evaluate the mechanism of alp

39 direct projection from ICX to the TeO in the chicken, although this is small and only to the deeper l

40 m the ceca within the production lifetime of chickens, although is involved in clearance from the sma

41 The method enabled detection of 1%(w/w) of chicken and 1%(w/w) pork in a mixture of the meat of thr

42 ere are wildlife species as sensitive as the chicken and demonstrates how using predictive genotyping

43 s of xDP, xFP, and waDP were administered to chicken and double-crested cormorant hepatocytes to dete

44 being impacted, two avian ToxChip PCR arrays-chicken and double-crested cormorant-were utilized, and

45 ociated non-coding variants are faced with a chicken and egg problem - such variants cannot be easily

46 The chicken and fish protein groups had lower GSH and higher

47 uring and detecting S. typhimurium in ground chicken and ground beef.

48 tance genes and the shared resistome of pig, chicken and human fecal samples.

49 We showed that in chicken and mouse embryos, PAPC expression is tightly re

50 Using chicken and mouse models, we show that the identity, not

51 a common prosensory domain in the embryonic chicken and mouse otocyst.

52 ved expression during canal morphogenesis in chicken and mouse.

53 study of functional immunity to C. jejuni in chicken and shows antibody is ineffective in clearing C.

54 rban and agricultural development, including chicken and turkey litter leachate, wastewater treatment

55 n the waterfowl reservoir and the commercial chicken and turkey populations, with the ultimate goal o

56 We first exploited differences between chicken and zebra finch gut morphology to identify the B

57 on computational and experimental data from chicken and zebra finch, and acts to equalize male-to-fe

58 tomics to comparatively examine resistant-AS chickens and AS controls.

59 leling detection of IAV in H9N2-infected SPF chickens and chickens from LBM showed that pan-IAV FRET-

60 f humans, nematodes, drosophilids, platypus, chickens and leishmania.

61 thogenicity of the H7N2 viruses by infecting chickens and mice.

62 s, are the largest contributors, followed by chickens and pigs.

63 LV-J, a retrovirus that causes infections in chickens and serious economic losses in the poultry indu

64 re able to infect and be transmitted between chickens and showed increased binding to human-like rece

65 ation to other gallinaceous species, such as chickens and turkeys.

66 e later outbreaks affected mostly commercial chickens and turkeys.

67 ed upon the consumption of beef (compared to chicken) and/or lard supplemented beef or chicken.

68 This suggests that the roles of UCN3 in chicken, and perhaps sauropsids in general, are not all

69 rent types of restructured meat (pork, beef, chicken, and turkey) was developed using six tryptic mar

70 enes encoding C/EBPalpha in humans, rodents, chickens, and frogs and is also present in the promoters

71 ence of single-stranded DNA viruses, such as chicken anemia virus (CAV) and porcine circovirus 2 (PCV

72 oading properties and tapasin involvement in chicken are fixed in duck alleles and suggest tapasin in

73 e previously shown that Kauai Island's feral chickens are a highly variable and admixed population.

74 Eimeria species that infect chickens are most significant, with Eimeria tenella amon

75 he strategies used by Salmonella to colonize chickens are poorly understood.

76 ude that changes in corticosterone levels in chickens are sufficient to cause a specific change in de

77 genotyped using the 60K SNP Illumina iSelect chicken array.

78 s largely untested, and the relevance of the chicken as an ecological model is uncertain.

79 In the chicken as well as in the turtle (from data in the liter

80 b sites for many human, mouse, zebrafish and chicken assemblies to support the Genome Reference Conso

81 ced vibrations within the apical half of the chicken basilar papilla in vivo and found broadly-tuned

82 rther contrast to BCO1, purified recombinant chicken BCO2 also catalyzes the oxidative cleavage of 9-

83 We have expressed recombinant chicken BCO2 in the strain E. coli BL21-Gold (DE3) and p

84 genotype is the replacement of the earlier A/chicken/Beijing/1/1994 (BJ/94)-like M gene with the A/qu

85 No new interactions were found for chicken BetaM and human Na,K-ATPase beta1, beta2 and bet

86 pale, soft and exudative (PSE) condition in chicken breast are studied.

87 uated and reproduced by utilizing a boneless chicken breast as a phantom.

88 By embedding a TSPN-containing tube in chicken-breast tissue, an imaging depth of more than 5 c

89 earch on the genomic characteristics of this chicken breed as well as others.

90 Thirty meat mixtures containing beef, chicken, camel, rabbit, goat and sheep with varying perc

91 hat normally slaughtered and dead on arrival chicken can be differentiated based on the metabolic pro

92 and 3) compare microbial communities between chicken carcass rinsates and recovered bacteria from med

93 PSE was induced by incubation of post-mortem chicken carcasses at 37 degrees C for 200min.

94 identify microbial compositional changes on chicken carcasses during processing, 2) determine the an

95 saccharides were successfully extracted from chicken cartilage and skin.

96 Our results show that chicken cathelicidin-2 kills E. coli by permeabilizing t

97 In this article, we show that chicken cathelicidin-2 kills Escherichia coli in an immu

98 vation on a Marek's disease lymphoma-derived chicken cell line, MDCC-MSB1.

99 s induction of the IFN signalling pathway in chicken cells and can potentiate virus replication.

100 ied gene expression and protein synthesis in chicken cells infected with the important poultry pathog

101 Chicken cells lacking Rnf4 are hypersensitive to hyroxyu

102 ensuring transmission to rodent, human, and chicken cells lacking the appropriate receptor.

103 ne folate derivatives kills human, mouse and chicken cells that cannot detoxify formaldehyde or that

104 ng radiation-induced DSB repair in human and chicken cells.

105 uni strains and the impact on fitness during chicken colonisation, survival in houseflies and under n

106 ays reduced virulence in vivo, in a model of chicken colonization.

107 ing 68 animal manure pooled samples of cats, chickens, cows, dogs, ducks, pigs, and pigeons.

108 at five regions of the cornea and sclera in chickens developing high myopia and astigmatism induced

109 mic absorption spectrometry quantified Cu in chicken dialyzable fraction.

110 study we determined that two inbred lines of chicken differing in their genetic background , Lines 0

111 eukosis virus (ALV) has endogenized prior to chicken domestication, remains infectious, and threatens

112 regulated by ancient CELF family homologs in chicken, Drosophila, and Caenorhabditis elegans suggests

113 oil used continuously for deep-fat frying of chicken drumsticks.

114 TRPM7-deficient chicken DT40 B lymphocytes exhibit a strongly impaired S

115 whole-genome sequencing of multiple isogenic chicken DT40 cell clones to precisely determine the cons

116 We report the use of the BU-1 locus of chicken DT40 cells to screen for small molecules able to

117 0 new, heat-stable peptide markers unique to chicken, duck and goose were identified, with significan

118 Faecal contamination of meat, especially chicken, during processing represents a key route of tra

119 The target of one chicken egg (60g) was reached on the 18(th) day.

120 thod is validated using calorimetry data for chicken egg lysozyme, mutated Protein A, three wild-type

121 reatment, consisting of the ingestion of one chicken egg per day; no allergic symptoms have been obse

122 e tripeptide LWL and subsequently applied to chicken egg white lysozyme, in which one biotinylated el

123 s@ew) with bright photoluminescence by using chicken egg white proteins as starting materials to reac

124 atients could eat foods containing half of a chicken egg.

125 Contaminated chicken/egg products are major sources of human salmonel

126 oyed chorioallantoic membranes of fertilized chicken eggs as host.

127 Using the nascent skin of the developing chicken embryo as a model system, we find that morpholog

128 genomic imprinting has been reported in the chicken embryo as a whole, we interrogated the existence

129 By using the chicken embryo as an animal model, science has been able

130 levating miR-16 significantly inhibited DF-1 chicken embryo cell proliferation, consistent with a rol

131 of different tissues into the periphery of a chicken embryo elicit different responses: Hensen's node

132 is rapidly replacing its progenitor primary chicken embryo fibroblasts (CEFs) for studies on avian v

133 we summarise studies that have exploited the chicken embryo model to determine the effects on prenata

134 In contrast to mammals, in the chicken embryo the effects on the developing cardiovascu

135 ence of genomic imprinting in the 12-day-old chicken embryonic brain and liver by examining ASE in F1

136 nfection severity and infectivity in primary chicken embryonic fibroblasts and chickens.

137 ced in a developmentally regulated manner in chicken embryonic retinal pigment epithelium (RPE)/choro

138 Gain and loss of function of PAPC in chicken embryos disrupted somite segmentation by alterin

139 al RCAS vector system to generate transgenic chicken embryos that constitutively and stably expressed

140 pa defines the antiviral state in developing chicken embryos, we used replication-competent retrovira

141 colysis in the posterior region of mouse and chicken embryos.

142 ular target, are teratogenic when exposed to chicken embryos.

143 ncreased the survival rate of virus-infected chicken embryos.

144 ITIES to single cell expression data of T2EC chicken erythrocytes pointed to BATF as a candidate nove

145 he time of meso-zeaxanthin production during chicken eye development, and we present evidence that ov

146 ition of meso-zeaxanthin biosynthesis during chicken eye development.

147 id microextraction of doxycycline (DOC) from chicken fat.

148 ere isolated from the case patients and from chicken fecal samples collected at the live bird markets

149 were identified on an assembled scaffold of chicken feces, and are carried by human pathogens.

150 ASA was the only As species detected in chicken feed samples, with a concentration between 0.72

151 otal arsenic in selected food samples (beef, chicken, fish, milk, cheese, egg, rice, rice-based produ

152 Chicken from a particular poultry supplier was identifie

153 A total of 565 chickens from five commercial purebred lines, including

154 ion of IAV in H9N2-infected SPF chickens and chickens from LBM showed that pan-IAV FRET-PCR had a hig

155 In chickens (Gallus gallus), NL is a well-studied model sys

156 In chickens (Gallus gallus), three pathways arise from nucl

157 distribution of UCN3 mRNA in a sauropsid-the chicken, Gallus gallus.

158 exhibit cooperative behavior in two types of chicken games (the hawk-dove game and the snowdrift game

159 eration can be exhibited by the poor in some chicken games.

160 4-hydroxy-3-nitrophenyl)acetyl conjugated to chicken gamma globulin and found a similar effect.

161 tantial regions are missing from the current chicken genome assembly.

162 itive-sequence content was identified in the chicken genome but without indicating its genomic positi

163 regions spanning approximately 1.45 % of the chicken genome in each line were detected by consensus o

164 ould be resolved in future assemblies of the chicken genome.

165 Here we reported that all active TEs in the chicken germ line are targeted by piRNAs, and as TEs los

166 sing order of CML concentration: beef, bacon>chicken > fish>dairy products>grain products>fruits/vege

167 short turnover cycle, our data suggest that chicken gustatory tissue provides an ideal system for mu

168 nderstand the transcriptomic architecture of chicken gustatory tissues.

169 ns that are not typically retrieved from the chicken gut.

170 A radiation hybrid panel of chicken-hamster Wg3hCl2 cells was used to map the genome

171 molecules varies as much as 10-fold between chicken haplotypes and is inversely correlated with dive

172 The chicken has long been considered uniquely sensitive to D

173 Chicken NK-lysin (cNK-lysin), the chicken homologue of human granulysin, is a cationic amp

174 against A/Hong Kong/G9/97 (H9N2), and 36% A/chicken/Hong Kong/SF4/01 (H6N1).

175 isolate of HFMG is greatly attenuated in the chicken host relative to the index isolate, notably demo

176 Here we report the characterization of chicken IFN-kappa (chIFN-kappa) near the type I IFN locu

177 viruses that caused countrywide outbreaks in chickens in China during 2010 to 2013, which led to the

178 of H9N2 viruses in countrywide outbreaks in chickens in China, which was responsible, through reasso

179 ntribution to the rising virus prevalence in chickens in China.IMPORTANCE We recently described the c

180 ed scan is implemented in a diverse panel of chickens including 72 distinct breeds genotyped at 538 2

181 we identified 137 genes that are missing in chicken, including the long-sought-after nephrin and tum

182 ghly contagious T-cell lymphoid neoplasia of chicken induced by Marek's disease virus (MDV).

183 iments, RNA was isolated from tracheas of 20 chickens infected with M. gallisepticum Rlow and 20 mock

184 s that were preferentially bound by IgY from chickens infected with Salmonella Typhimurium or S.

185 Anserine was found to be specific for chicken intake, whereas trimethylamine-N-oxide showed go

186 both normal and stimulated conditions using chicken interferon-alpha (chIFN-alpha) and the attenuate

187 for efficient C. jejuni colonization of the chicken intestine.

188 tably demonstrating a virulence phenotype in chickens inversely related to that in the finch host.

189 patterns in the embryonic brain of mouse and chicken is being essential for understanding pallial org

190 In chicken, lateral plate mesoderm (LPM) adjacent to occipi

191 Misidentification of the chicken leptin gene has hampered research of leptin sign

192 s was used to map the genome location of the chicken leptin gene.

193 The high GC-content observed for the chicken leptin syntenic group suggests that other simila

194 Mapping chicken leptin together with a cluster of five syntenic

195 me mapping and sequence characteristics, the chicken leptin was not located on a microchromosome, whi

196 n F1 reciprocal crosses of two highly inbred chicken lines (Fayoumi and Leghorn).

197 ined on livers of high-weight and low-weight chicken lines by microarray.

198 DOM fluorescence (EEM-PARAFAC) indicated the chicken litter contained a biologically reactive fluores

199 analysis of variance (RM-ANOVA) showed that chicken litter leachate stimulated phytoplankton growth

200 ing the observed phytoplankton growth in the chicken litter leachate treatments.

201 ith tissue-mimicking phantoms and an ex vivo chicken liver through 2D/3D imaging.

202 ast food and full-fat dairy, fish, red meat, chicken, low-fat milk, and legumes.

203 rocessed food samples [chicken sausages (2), chicken luncheon (2), turkey meat loaf, milk chocolate w

204 clear whether TLR3 has same function against chicken lymphoma.

205 model of Cox-2 over-expression driven by the chicken lysozyme locus (cLys-Cox-2), which directs integ

206 peptides modulate the immune response in the chicken macrophage cell line HD11 and in chicken primary

207 The chicken major histocompatibility complex (MHC) has stron

208 linc-GALMD3 might be a critical regulator in chicken MD and could be used as a candidate-promising ma

209 Patients with food allergy to fish and chicken meat (n = 29) or chicken meat only (n = 7) were

210 ost realistic scenario assayed (i.e., spiked chicken meat analysis), only 13% of the AgNPs present in

211 Consumption of chicken meat and eating out were the most important risk

212 In this study, a chicken meat containing AgNPs (candidate reference mater

213 allergy to fish and chicken meat (n = 29) or chicken meat only (n = 7) were recruited.

214 analysing the colour change when tested with chicken meat spiked with the three pathogenic bacteria.

215 The target DNA spiked food matrix (chicken meat) is also successfully detected at a concent

216 for the detection of fraudulently processed chicken meat.

217 to reduce Campylobacter load, especially on chicken meat.

218 uld differentiate pork from beef, chevon and chicken meat.

219 ell culture and 1000-fold more virulent in a chicken model than other strains; accordingly, the isola

220 Chicken Na(+)/H(+) exchanger type I (chNHE1), a multispa

221 Chicken NK-lysin (cNK-lysin), the chicken homologue of h

222 and VA2013 in their levels of virulence for chickens; notably, this difference correlated inversely

223 In contrast, ectopic expression of the same chicken Ntn1 in the mouse otic vesicle, where apoptosis

224 n acrylamide content of French Fries, chips, chicken nuggets, onions rings, breakfast cereals, biscui

225 nt foodstuffs, sour cream, egg, egg yolk and chicken nuggets.

226 We used the layered chicken optic tectum to model cortical development, and

227 ockdown of MCT8 in neural progenitors of the chicken optic tectum, a layered structure that shares ma

228 esent evidence that overexpression of either chicken or human RPE65 in cell culture leads to the prod

229 significantly stimulated axonal growth from chicken or rat dorsal root ganglia (DRGs).

230 res moving in their typical bipedal (man and chicken) or quadrupedal mode (crawling-baby and cat).

231 nal proof for its identification as the true chicken ortholog.

232 We demonstrated with chicken OVA-specific TCR-transgenic mice that the same t

233 rotein via hepatic nuclear factor 4alpha and chicken ovalbumin upstream promoter transcription factor

234 that female mouse embryos lacking Coup-tfII (chicken ovalbumin upstream promoter transcription factor

235 Chicken ovalbumin upstream promoter-transcription factor

236 nanoclusters, which were mainly composed of chicken ovalbumin-encapsulated AuNCs, can recognize rici

237 presence of Galbeta(1-->4)GlcNAc ligands on chicken ovalbumin.

238 tor family, was identified from an embryonic chicken pancreatic cDNA library in a screen for secreted

239 Chicken parvalbumin and two new allergens, aldolase and

240 of xDP, xFP, and waDP, respectively, using a chicken PCR array comprising 27 AhR-related genes.

241 n of well-established methods (i.e., CEH and chicken PCR array) to the double-crested cormorant demon

242 Wnt signaling enhances the proliferation of chicken PGCs via the stabilization of beta-catenin and a

243 In DDX4 knockout chickens, PGCs are initially formed but are lost during

244 As animal sources we considered chicken, pig, pet dog or cat, cattle, and poultry other

245 urfold larger carbonyl content determined in chicken, pork and beef (2.8, 3.6 and 3.1 nmol/mg of prot

246 trol), and proteins isolated from soy, fish, chicken, pork and beef.

247 We attribute the dampened seasonal cycles in chicken pox information-seeking behavior to VZV vaccine-

248 Priming of chicken primary fibroblasts and tracheal organ cultures

249 the chicken macrophage cell line HD11 and in chicken primary monocytes by evaluating the induction of

250 of the Wnt/beta-catenin signaling pathway in chicken primordial germ cells (PGCs) in vitro.

251 porter construct to the DDX4 (vasa) locus in chicken primordial germ cells (PGCs).

252 d stress hormone, corticosterone, in broiler chickens produced a pessimistic judgment bias.

253 muscle dystrophy are observed in commercial chicken products, but the muscle physiological causes fo

254 IgE-reactive chicken proteins were identified (Edman, MS analysis) an

255 0 subjects consumed increasing quantities of chicken, red meat, processed meat, and fish over 3 succe

256 house finch, was significantly attenuated in chickens relative to VA1994, displaying less-severe path

257 Whether genomic imprinting exists in chickens remains debatable, as previous studies have rep

258 enome-wide association study (GWAS) in an F2 chicken resource population.

259 ches, displayed significant virulence in the chicken respiratory tract.

260 Pharmacological immobilisation of embryonic chickens revealed that altered motility, independent of

261 zes the essential steps in understanding the chicken Rous sarcoma virus (RSV) genome association with

262 ic lesions in the midbrain severely impair a chicken's ability to discriminate orientations.

263 sulfaquinoxaline (151.4-1196.7 mug kg(-1) in chicken samples) and sulfadiazine (109.8 mug kg(-1) in a

264 ted pork DNA in nine processed food samples [chicken sausages (2), chicken luncheon (2), turkey meat

265 Metabolomic evaluation of chicken serum using ultra-performance liquid chromatogra

266 In mouse, but not opossum and chicken, sex bias is coordinated across tissues such tha

267 Raman signals of the scaffolds and HA (fresh chicken skin used as a top layer).

268 recent cryo-electron microscopy structure of chicken Slo2.2, the ion permeation pathway of the channe

269 filament model obtained by rigidly docking a chicken smooth muscle myosin structure to the reconstruc

270 We report the full-length sequence of two chicken source influenza A (H7N9) viruses found in Guang

271 This research establishes that chicken sulfated GAG polysaccharides can enhance iron up

272 al phenomenon is proposed to be termed 'fish-chicken syndrome' with cross-reactive allergens involved

273 e first report about the function of TLR3 in chicken T-cell lymphoma, especially in signal pathway.

274 Combined with other features of chicken taste buds, e.g., uniquely patterned array and s

275 In chicken, the TeO is organized in 15 layers where visual

276 tal of 14,326 gene transcripts were found in chicken thrombocytes across all ligand exposures.

277 and biochemical pathways reveal the role of chicken thrombocytes in proinflammatory responses linked

278 lymphocytes in response to C. jejuni in the chicken through depletion of the B lymphocyte population

279 lts suggest that IAV(H7N9) viruses evolve in chickens through antigenic drift to include a signature

280 the catbird is at least as sensitive as the chicken to DLCs, based on both embryotoxicity and mRNA i

281 s evaluated after submitting beef, pork, and chicken to five different thermal treatments.

282 We trained young chickens to discriminate a stimulus (paper cone) placed

283 n the midbrain stimulus selection network-in chickens trained to perform an orientation discriminatio

284 dered to be adapted to gallinaceous species (chickens, turkeys, quail, etc.) and less likely to infec

285 Mature chicken UCN3 is predicted to be a 40-amino acid peptide

286 tube-shaped taste buds were observed in the chicken using 2-photon microscopy.

287 re taste buds than previously appreciated in chickens using molecular markers to stain oral epithelia

288 Stronger activity for man and chicken versus baby and cat was found in the right pSTS

289 Unlike other sequenced sex chromosomes, the chicken W chromosome did not acquire and amplify genes s

290 opose that, like the human Y chromosome, the chicken W chromosome is essential for embryonic viabilit

291 We sequenced the chicken W chromosome, compared its gene content with our

292 f human C. jejuni isolates to originate from chickens was highest (74%), whereas pigs were a negligib

293 MRSA1679a, a strain isolated from chicken, was observed to be highly virulent, in cell cul

294 Specific Pathogen-Free (SPF) layer chickens were infected with ALV-J or maintained as non-i

295 Broiler chickens were used because they are obesity-prone, and b

296 In chicken, which has a Z/W sex chromosome system, expressi

297 Both in chicken with an age of 21 and 31days, respectively, pect

298 mmon cause of lameness in commercial broiler chickens worldwide.

299 The similarities of CSF-c cells in chicken, Xenopus, and zebrafish suggest that these chara

300 mpare the organization of the CSF-c cells in chicken, Xenopus, and zebrafish, by analyzing the expres

301 In a chicken yolk sac membrane model, under the same ultrasou