ライフサイエンスコーパス: hen

1 We identified 851 and 2816 hen's egg and cow's milk articles respectively.

2 Cs were performed with cow's milk (n = 633), hen's egg (n = 456), wheat (n = 265) and/or soy (n = 317

3 Trait data from a total of 772 hens in 67 sire families from one generation of the pedi

4 e for peanut (n = 135), cow's milk (n = 93), hen's egg (n = 53), hazelnut (n = 28), and cashew nut (n

5 otoreceptor retinoid-binding promoter, and a hen egg lysozyme-specific CD4(+) TCR transgene.

6 ecipient mice immunized with pDNA encoding a hen egg lysozyme (HEL)-IgFc fusion protein (JwHEL)+JwIL4

7 Using primary B cells that express a hen egg lysozyme (HEL)-specific BCR, we found that oligo

8 models, one in which T cells specific for a hen-egg white lysozyme (HEL) peptide were injected into

9 Using a hen egg lysozyme double-transgenic model, we further dem

10 An animal model using adult hens was implemented for the in vivo experiments.

11 transfected with I-Ak genes and the model Ag hen egg white lysozyme targeted to the endoplasmic retic

12 ., exposure of CD4 cells to their target Ag, hen egg lysozyme [HEL] and APCs).

13 approached by a bi-specific antibody against hen egg lysozyme consisting of scFv fragments of D1.3 an

14 -old infants who were not sensitized against hen's egg, as determined based on specific serum antibod

15 m in which naive CD4 cells, specific against hen egg lysozyme (HEL), are injected into recipient mice

16 polarized Th1 or Th17 cells specific against hen egg lysozyme induce ocular inflammation in recipient

17 transgenic CD4 murine cells specific against hen egg lysozyme.

18 l and B cell responses to three protein Ags: hen egg white lysozyme, OVA, and listeriolysin O.

19 tering of solutions of bovine serum albumin, hen egg white ovalbumin, hen egg white ovomucoid, and bi

20 ude of fertilized eggs laid by high altitude hens also restricted fetal growth, but to a lesser exten

21 vel of fertilized eggs laid by high altitude hens not only restored, but enhanced, fetal growth relat

22 talline (alphaBc), bovine serum albumin, and hen egg-white lysozyme (HEWL) in aqueous solution.

23 that SIC binds to SLPI and to both human and hen egg lysozyme (HEL) but not to lactoferrin.

24 Using the Ig and hen egg lysozyme double transgenic mouse model, we demon

25 Studies in B cell knockout and hen egg lysozyme Ig transgenic mice revealed that B cell

26 ast to family members (human lactoferrin and hen ovotransferrin), both lobes are almost equally open:

27 Cow's milk and hen's egg were prevalent elicitors in the first 2 years,

28 Using OVA and hen egg lysozyme in crisscross fashion, we confirmed the

29 the model Ags pigeon cytochrome c (PCC) and hen egg lysozyme (HEL).

30 trast, two other antigens, phycoerythrin and hen egg lysozyme, were not captured by these cells.

31 significant threat to poultry production and hen health in many parts of the world.

32 conserved across lytic transglycosylases and hen egg white lysozyme, and this differentiating asparta

33 common with both lytic transglycosylases and hen egg white lysozyme.

34 serotype Kentucky received 10 exp9 CFU, and hens injected with serotype Enteritidis received 10 exp7

35 eople (>30,000 cases of human paralysis) and hens (the best animal model for this demyelinating disea

36 iological form on egg quality parameters and hens performance was investigated.

37 active B cells expressing high affinity anti-hen egg lysozyme (HEL) Ag receptors exposed in vivo to m

38 an anti-ovalbumin T-cell receptor or an anti-hen egg lysozyme B-cell receptor were studied.

39 ch during B cell ontogeny, autoreactive anti-hen egg lysozyme MD4 Ig transgene B cells are negatively

40 ion, we have studied the development of anti-hen egg lysozyme MD4 Ig transgene B cells while systemat

41 ived from an affinity-matured series of anti-hen egg white lysozyme (HEL) mouse IgG1, were constructe

42 splenic B lymphocytes from wild-type or anti-hen egg lysozyme BCR transgenic mice, and on a mature mo

43 mature, respond to antigen, and secrete anti-hen egg lysozyme antibodies.

44 ded our findings to another TCR system (anti-hen egg lysozyme [HEL] TCR/HEL mice) where similarly ext

45 c models of B cell self-reactivity, the anti-hen egg lysozyme BCR transgenic strain and the AM14 rheu

46 characterize the interface between the anti-hen egg white lysozyme (HEL) antibody HyHEL-63 and HEL.

47 ells stimulated via the BCR with the antigen hen egg lysozyme, or surrogate for antigen anti-IgM, dem

48 Allogeneic RBCs expressing the HOD antigen (hen egg lysozyme [HEL]-ovalbumin-human transmembrane Duf

49 in the presence and absence of its antigen, hen egg-white lysozyme.

50 not limited to Smith Ag-specific B cells as hen egg lysozyme- and p-azophenylarsonate-specific B cel

51 es to Ags containing disulfide bonds such as hen egg lysozyme (HEL).

52 demonstrated that globular proteins, such as hen egg lysozyme in phosphate buffered saline at room te

53 determination of Lys in real samples such as hen egg white.

54 Salt bridges between self-associating hen egg white (HEW) lysozyme and bovine insulin molecule

55 with hen's egg or cow's milk allergy; baked hen's egg or cow's milk intervention with or without a c

56 roposed that the frequent ingestion of baked hen's egg or cow's milk accelerates the resolution of he

57 determine whether the introduction of baked hen's egg or cow's milk into the diet of children with h

58 s the hypothesis that the ingestion of baked hen's egg or cow's milk results in more patients outgrow

59 genic foods: cow's milk, peanut, hard-boiled hen's egg, sesame, whitefish (cod), and wheat; the stand

60 Both hen egg-white lysozyme and protein L are found to underg

61 how that the denaturing temperatures of both hen egg white lysozyme and ribonuclease A are sensitive

62 expressing either soluble or membrane-bound hen egg lysozyme (sHEL or mHEL, respectively) under cont

63 e B10.BR mice transfused with membrane-bound hen egg lysozyme antigen-transgenic RBCs also demonstrat

64 at display a cell surface Ag, membrane-bound hen egg lysozyme, strongly activate Ag-specific B cells.

65 hydrations, the low frequency conformational hen egg white lysozyme dynamics can be described by a di

66 se of air puff (CN); air puff to conspecific hen (APC); air puff to observer hen (APH).

67 urs after intentional hen's egg consumption, hen's egg protein levels were significantly increased in

68 nd protein and hydration dynamics of crowded hen egg white lysozyme (HEWL) labeled with a metal-carbo

69 t(R) HRT was useful as a means of diagnosing hen's egg allergy and predicting severity of induced sym

70 measured for turkey ovomucoid third domain, hen lysozyme, Bacillus circulans xylanase, and human and

71 ucted a similar experiment in which domestic hens were exposed to the mild distress of unrelated, but

72 is related to the storage stability of dried hen egg white (DEW) and its hydrolysates (HEW) in an IMF

73 nvestigated the efficacy and safety of early hen's egg introduction at age 4 to 6 months to prevent h

74 e target compounds in various types of eggs (hen, quail and duck) and honey samples (flower, forest,

75 uinone-2,6-disulfonate (AQDS(2-)) and either hen egg white lysozyme (HEWL) or bovine serum albumin (B

76 ive in rickettsiae isolated from embryonated hen egg yolk sacs.

77 e parental recombinant strain in embryonated hen eggs, in MDCK cells, or in vivo in a mouse model.

78 In embryonated hen's eggs and leucopenic mice, the outcome of invasive

79 usion with RBCs expressing a B-cell epitope (hen egg lysozyme [HEL]) fused to (OVA)(323-339).

80 ely transferred into recipients that express hen egg lysozyme in the lens of the eye.

81 nsgenic (Tg) strains were created expressing hen egg-white lysozyme (HEL) in a pancreas-specific fash

82 o-self-antigen in transgenic mice expressing hen egg lysozyme (HEL) under a retina-specific promoter.

83 the state of tolerance in Tg mice expressing hen egg lysozyme (HEL) under control of the rhodopsin pr

84 adoptively transferred into mice expressing hen egg lysozyme in their eyes, both Th1 and Th17 induce

85 ar inflammation in recipient mice expressing hen egg lysozyme in their eyes.

86 generated double-transgenic mice expressing hen egg lysozyme, under the retinal interphotoreceptor r

87 vitamin D-enhanced eggs (produced by feeding hens at the maximum concentration of vitamin D3 or serum

88 h the more highly charged surfaces of folded hen egg white lysozyme (HEWL) and bovine serum albumin (

89 or peanut, 1.1 mg for cow's milk, 1.5 mg for hen's egg, 7.4 mg for cashew nut, and 0.29 mg for hazeln

90 boxylase (GAD) 206-220 or GAD 524-538 or for hen egg lysozyme 11-25 as a control in NOD, NOD-scid, an

91 s expressed in B cells that are specific for hen egg lysozyme (E/HEL-Tg).

92 nsgenic mice that express a BCR specific for hen egg lysozyme (IgHEL).

93 CR-transgenic Th1 or Th17 cells specific for hen egg lysozyme induce ocular inflammation in recipient

94 In contrast, 3A9 T cells (specific for hen egg lysozyme(46-61)/I-A(k)) are completely eliminate

95 hemical gradient of presentation of the four hen egg-white lysozyme epitopes observed in cell lines e

96 al characteristics of Cu,Zn-SOD derived from hen egg white and egg yolk were determined, and compared

97 We used an N-glycan isolated from hen egg yolk together with the Nbz linker for Fmoc chemi

98 Lysozyme from hen egg white (HEWL) was covalently immobilized on spher

99 ability to release antioxidant peptides from hen egg white and protease P was selected based on the a

100 presenting MHC class II bound peptides from hen egg white lysozyme (HEL) injected intravenously.

101 We quantitated the amounts of peptides from hen egg-white lysozyme presented by I-A(k) molecules in

102 model, we took a segment of polypeptide from hen egg lysozyme that in the native protein forms the bi

103 ive and recombinant allergenic proteins from hen's egg and cow's milk were spotted on silicon chips c

104 was detected in R. prowazekii purified from hen egg yolk sacs, and G3PDH activity was assayable in R

105 se interactions we imaged B cells (TgB) from hen egg lysozyme (HEL) transgenic mice and DC pulsed wit

106 f shell eggs were processed: one issued from hens fed with a standard diet and another receiving a di

107 n were significantly greater than those from hens that were not treated with melatonin.

108 Egg weights from hens treated with melatonin were significantly greater t

109 promised neither the formation of functional hen egg lysozyme-specific IgM nor the secretion of free

110 Among 406 screened infants, 23 (5.7%) had hen's egg-specific IgE before randomization.

111 4; P = .24), and 2.1% were confirmed to have hen's egg allergy versus 0.6% in the placebo group (rela

112 nheated hen's egg in 71.6% and 69.6%; heated hen's egg in 54.2% and 54.8%; milk in 23.0% and 23.3%; p

113 In 8 of 8 households, hen's egg was detectable in dust samples of eating area

114 ality of a commercial spray-dried hydrolysed hen egg white powder (HEW).

115 groups of hens were treated as follows: (i) hens were inoculated orally with Kentucky and injected i

116 pansion of Tregs did not occur in BAFF-Tg/Ig hen egg lysozyme BCR chimeras, demonstrating a requireme

117 cularly 2 weeks later with Enteritidis, (ii) hens were contact infected with Kentucky and then with E

118 th Kentucky and then with Enteritidis, (iii) hens were injected with Enteritidis only, and (iv) hens

119 nsor proposed was able to detect antibody in hen serum diluted up to 7 x 10(7)-fold.

120 thodology has been successfully validated in hen eggs, obtaining method detection limits in the range

121 ier state and through the onset of laying in hens were determined.

122 ndicating enantiomer-selective metabolism in hens.

123 common with OP-induced delayed neuropathy in hens and people but differs in the neuropathological sig

124 Contact infected hens were kept in rooms with deliberately infected hens.

125 ere kept in rooms with deliberately infected hens.

126 cteria from reproductive tissues of infected hens are packaged into the eggs and persist inside the h

127 A small fraction of i.v. injected hen egg-white lysozyme rapidly entered the thymus into t

128 Forty-eight hours after intentional hen's egg consumption, hen's egg protein levels were sig

129 ether levels are increased after intentional hen's egg consumption.

130 ere injected with Enteritidis only, and (iv) hens were contact infected with Enteritidis only.

131 observed in the bioaerosols of pig and layer hen confinement than the turkey confinement buildings an

132 Male birds of egg-laying hen strains have no commercial value and are culled imme

133 e culling of 1-day-old male chicks in laying hen production.

134 strain UMN179, isolated from an Iowa laying hen with peritonitis.

135 ncriminated as the causative agent of laying hen peritonitis, Gallibacterium anatis are frequently is

136 Laying hens often experience unbalanced calcium utilization whi

137 Forty Isa Brown laying hens (26weeks old) were equally subjected to 4 dietary t

138 otal of 150 18weeks old Lohmann Brown laying hens were housed in cages and fed with basal diet and fo

139 edness of 71 isolates from commercial laying hens in Iowa and 18 international reference isolates.

140 with prevalence data of Salmonella in laying hens (P < .001), broilers (P < .001), and slaughter pigs

141 istration of a SMM/TMP combination in laying hens in doses of 8 g l(-)(1) and 12 g l(-)(1) in drinkin

142 s utilizes to colonize and persist in laying hens, we used selective capture of transcribed sequences

143 ent of peritonitis and salpingitis in laying hens.

144 cycline (DC) is forbidden compound in laying hens.

145 lorum causes persistent infections in laying hens.

146 Ninety-six brown Lohmann laying hens, were equally assigned into three groups.

147 A group of laying hens (n=18) received feed contaminated with Sudan I at t

148 nitis is the major disease problem of laying hens in commercial table egg and parent stock operations

149 sca, were supplemented to the diet of laying hens in order to increase the level of omega-3 long-chai

150 olism so we supplemented the diets of laying hens using two biofortified maize varieties with distinc

151 f punicic acid (CLnA) in the diets of laying hens, on the physicochemical properties of eggs.

152 intestinal and reproductive tract of laying hens, resulting in contaminated poultry products.

153 r, albumen height) and performance of laying hens.

154 The laying hens received feed containing 0.27 +/- 0.034 mg/kg of se

155 ggs by addition of linseed oil to the laying hens' diet has been evaluated in terms of production par

156 r its unintentional administration to laying hens.

157 ltitude of fertilized eggs laid by sea level hens markedly restricted fetal growth.

158 er extent compared to eggs laid by sea level hens.

159 f response to the related homologue of ML-M, hen eggwhite lysozyme, was similar in these two groups o

160 When Clara cell secretory protein-membrane hen egg lysozyme/hemoglobin transgenic mice were crossed

161 tively diagnosed food allergy to cow's milk, hen's egg, and/or wheat were recruited at an outpatient

162 t treatment was designed to produce modified hen's egg with reduced allergenic potential.

163 ed out for both the wild-type and the mutant hen lysozyme (TRP62GLY) to study the single mutation eff

164 ognizing antigens that are (insulin) or not (hen egg lysozyme; HEL) expressed by ss-cells have proven

165 Each observer hen was exposed to two replicates of four conditions, in

166 conspecific hen (APC); air puff to observer hen (APH).

167 empathy-like responses previously, observer hens showed no behavioural or physiological responses to

168 During each test, the observer hens' behaviour and physiology were measured throughout

169 The peptide spanning residues 48-61 of hen egg white lysozyme (HEL) presented by I-A(k) gives r

170 The peptide spanning residues 48-62 of hen egg white lysozyme presented by I-A(k) molecules giv

171 in, first identified as a minor component of hen egg white and found to be antimicrobial against Esch

172 ss a chimeric membrane protein consisting of hen egg lysozyme and a hemoglobin epitope tag under the

173 We found no evidence that consumption of hen's egg starting at 4 to 6 months of age prevents hen'

174 Thermally induced transition curves of hen egg-white lysozyme were measured in the presence of

175 erport(R) HRT is useful for the diagnosis of hen's egg allergy, and may also aid in predicting the se

176 of the Allerport(R) HRT in the diagnosis of hen's egg allergy.

177 In vivo, a low dose of hen egg lysozyme (1 microg) induced significant CD83 but

178 rnative to current sources for enrichment of hen eggs.

179 type B TCR recognizing the 48-62 epitope of hen egg white lysozyme (HEL) presented by I-A(k).

180 to citrullinated variants of two epitopes of hen egg-white lysozyme, a major and a minor one, bound t

181 d and real art samples for the evaluation of hen egg presence in the extract, i.e. albumen, yolk, or

182 nic (Tg) mice that express a soluble form of hen egg lysozyme (HEL) and in which B cell tolerance to

183 e-regulated expression of a secreted form of hen egg lysozyme, tagged with a murine hemoglobin (Hb) e

184 and timing of exposure to different forms of hen egg lysozyme as a self-Ag.

185 simulation, for the surprising misfolding of hen egg-white lysozyme caused by a single mutation (W62G

186 emonstrated the electrochemical nitration of hen egg white lysozyme to be at Tyr23 initially, followe

187 o examine MHC class I and II presentation of hen egg-white lysozyme (HEL) in different forms, soluble

188 or cow's milk accelerates the resolution of hen's egg or cow's milk allergy.

189 Dielectric response of hen egg white lysozyme is measured in the far infrared (

190 Two samples of hen eggs bought at supermarkets and one of quail eggs we

191 croseconds molecular dynamics simulations of hen lysozyme generated on BlueGene/L.

192 protein that binds the acidic active site of hen egg lysozyme and inhibits the enzyme.

193 The early stages of hen egg white lysozyme (HEWL) fibrillation were quantita

194 obes and water on eight static structures of hen egg white lysozyme (HEWL) in various conformational

195 We applied FTMap to nine structures of hen egg-white lysozyme (HEWL), whose hot spots have been

196 probe covalently attached to the surface of hen egg white lysozyme dissolved in D(2)O/glycerol solut

197 lectrochemical adsorption and voltammetry of hen-egg-white-lysozyme (HEWL) was studied at an array of

198 mpact of additional vitamin D in the diet of hens on the resulting egg vitamin D content, the effect

199 d into the human food supply through eggs of hens that appear healthy.

200 d with those of enzymes from erythrocytes of hens and SOD standard.

201 To explore this issue, 4 groups of hens were treated as follows: (i) hens were inoculated o

202 Conversely, egg shell mass of hens treated with melatonin was significantly lower than

203 atonin was significantly lower than those of hens not treated with melatonin.

204 (HH26) are specific for the same epitope on hen egg white lysozyme (HEL), and share >90% sequence ho

205 tical structurally characterized epitopes on hen egg white lysozyme (HEL).

206 ffect of the altered level of linseed oil on hens laying performance, fatty acid content and composit

207 by exposing female C57BL/6 wild-type mice or hen egg lysozyme B-cell receptor transgenic mice to desi

208 vine serum albumin, hen egg white ovalbumin, hen egg white ovomucoid, and binary mixtures of these th

209 Parents and health staff perceive hen's egg allergy (HEA) as a common food allergy in earl

210 introduction at age 4 to 6 months to prevent hen's egg allergy in the general population.

211 gg starting at 4 to 6 months of age prevents hen's egg sensitization or allergy.

212 r a membrane-bound form of the model protein hen egg white lysozyme (HEL).

213 in acidic solutions, using the model protein hen egg-white lysozyme.

214 chemically dominant peptide from the protein hen egg white lysozyme (HEL) generates different conform

215 We show here that processing of the protein hen egg-white lysozyme (HEL) resulted in citrullination

216 slationally modified peptides of the protein hen egg-white lysozyme (HEL), consisting of nitration of

217 on dynamics than a mesophilic model protein, hen egg white lysozyme (HEWL), at all measured temperatu

218 escent probes attached to a typical protein, hen egg-white lysozyme (HEWL).

219 terminus of beta-catenin, the model proteins hen egg lysozyme and streptavidin, and immunoglobulins f

220 successfully demonstrated using the proteins hen egg-white lysozyme (HEWL) and porcine pepsin.

221 shifts of Trp C(gamma) in several proteins, hen egg white lysozyme, horse myoglobin, horse heart cyt

222 f pH and ionic strengths for three proteins: hen egg white lysozyme (HEWL), chymotrypsinogen, and T4

223 in recipient mice expressing eye-restricted hen egg lysozyme, we found important differences in the

224 mon waveguide resonance (PWR) studies showed hen egg phosphatidyl choline (PC) bilayers produce amphi

225 were crossed with mice that express soluble hen egg lysozyme and whose B cells bear receptors specif

226 mice that are double-transgenic for soluble hen egg lysozyme (HEL) and an Ig that recognizes HEL wit

227 duction in response to low levels of soluble hen egg lysozyme (HEL) both in vivo and in vitro as dete

228 After immunization with soluble hen egg lysozyme, both MZ and FO B cells captured Ag and

229 tor of anaphylaxis in children, specifically hen's egg, cow's milk, and nuts.

230 chemical and rheological properties of spent hen proteins recovered by acid and alkaline extraction h

231 on on lipid oxidation of refrigerated stored hen eggs enriched with very long-chain n-3 fatty acids,

232 Cs from transgenic mHEL mice express surface hen egg lysozyme (HEL) as a transmembrane protein.

233 vaccinia virus (a smallpox virus surrogate), hen egg lysozyme, cholera toxin, ricin, and staphylococc

234 I molecules possessing a beta-chain-tethered hen egg lysosome peptide lack the Ia.2 epitope and fail

235 he second-order elastic moduli of tetragonal hen egg-white lysozyme crystals were determined as a fun

236 lysozyme auto-Ag-specific B cells in Ig(Tg) hen egg lysozyme (HEL) transgenic mice inhabit the splee

237 mounts of rHEL-C3d3 were more effective than hen egg lysozyme alone in up-regulating c-FLIP levels an

238 We previously found that hen egg white lysozyme, homologous to the disease-relate

239 Our previous research has demonstrated that hens show clear behavioural and physiological responses

240 These results indicate that hens mainly mobilized visceral fat for egg formation and

241 al and physiological response indicates that hens show no basis for emotional empathy in this context

242 The hen has long held promise as a low-cost, high-yield bior

243 ds in terms of distribution in the feed, the hen's livers and the eggs.

244 generally larger than those observed in the hen egg white lysozyme (HEWL) ortholog, which shares 61%

245 These results support the potential of the hen as a bioreactor for the production of commercially v

246 gence of xenopatients and the utility of the hen model to study OvCa prevention, tumorigenesis, metas

247 without a comparator; and resolution of the hen's egg or cow's milk allergy as determined by food ch

248 These promising findings indicate that the hen is close to becoming a competitive manufacturing pla

249 to the embryo can be manipulated through the hen diet.

250 or 10% of control unmodified soy oil to the hen's diet.

251 Using the hen egg lysozyme transgenic system, we show that IgM(hig

252 Immunization with the hen egg-white lysozyme (HEL) protein induces T cells to

253 After 12weeks of feeding the hens, eggs collection began.

254 or affecting the cholesterol content was the hens age (P<0.0001).

255 lk results in more patients outgrowing their hen's egg or cow's milk allergy respectively.

256 The polymers were conjugated to thiolated hen egg white lysozyme and purified.

257 P does not diminish Ag presentation of three hen egg white lysozyme epitopes.

258 Only three hen's egg and three cow's milk studies fulfilled our pre

259 6-month-old infants were already allergic to hen's egg.

260 or children with histories of anaphylaxis to hen's eggs.

261 g-term desensitization in treated animals to hen OVA via a dexamethasone-dependent tolerogenic mechan

262 The algorithm has been applied to hen egg-white lysozyme and to thermolysin, interacting w

263 shown that fusing complement fragment C3d to hen egg lysozyme (HEL) enhanced the immunogenicity of HE

264 children undergoing open food challenges to hen's egg or cow's milk, either fresh or extensively hea

265 established delayed-type hypersensitivity to hen OVA were immunized with an OVA-derived, MHC II-restr

266 pe and CD72-deficient B cells in response to hen egg lysozyme Ag stimulation.

267 migrated to T cell areas in the response to hen egg lysozyme.

268 The primary outcome was sensitization to hen's egg (increased specific serum IgE levels) by age 1

269 rgy to chicken meat without sensitization to hen's eggs.

270 ells, whereas a VLR:Tmu receptor specific to hen egg lysozyme (a self-antigen with respect to chicken

271 in which TCR-transgenic Th cells specific to hen egg lysozyme (HEL) are adoptively transferred to rec

272 4 cells from TCR transgenic mice specific to hen egg lysozyme (HEL) are polarized with IL-6/TGF-beta

273 that B cells, which express BCRs specific to hen egg lysozyme (HEL) display diminished responsiveness

274 in which naive transgenic cells specific to hen egg lysozyme are adoptively transferred into recipie

275 productive tract are phenomena restricted to hens, indicating that such changes are likely to be rela

276 ng range of the silicon microarray for total hen's egg-specific IgE was comparable to the range of 0.

277 >150 mg, respectively) in eggs of transgenic hens.

278 other animals, we examined whether treating hens with melatonin would affect eggshell thickness and

279 , selected physicochemical properties of two hen egg white powders (with and without hydrolysis) were

280 13 and 2014, respectively, included unheated hen's egg in 71.6% and 69.6%; heated hen's egg in 54.2%

281 To address this question, we used hen egg lysozyme-specific BCR transgenic mice to elucida

282 Using hen egg-white lysozyme, the effect of blood proteins on

283 Finally, by using hen egg lysozyme double transgenic mice, we demonstrated

284 A mouse model utilizing hen egg lysozyme (HEL) "anergic" B cells was studied.

285 es against His6-H5 HA in serum of vaccinated hen using serial 10-fold dilutions of serum.

286 5.6% of the children in the verum group were hen's egg sensitized versus 2.6% in the placebo group (p

287 research is necessary to investigate whether hen's egg allergen in house and bed dust plays a role in

288 ilot study, we wanted to investigate whether hen's egg allergen is detectable in house dust collected

289 or cow's milk into the diet of children with hen's egg or cow's milk allergies respectively leads to

290 on (8.4 +/- 1.5 days; n = 18), compared with hen egg lysozyme-immunized C57BL/6 (13.3 +/- 2.2 days; n

291 Structure determination in complex with hen egg white lysozyme revealed an extended VH binding i

292 of the type I IgNAR V domain in complex with hen egg-white lysozyme (HEL) reveals a minimal antigen-b

293 ructed homodimeric receptors in complex with hen-egg white lysozyme demonstrate how nanomolar affinit

294 eptide, p524-543, but not, for example, with hen egg white lysozyme.

295 sma VLRB responses of lamprey immunized with hen egg lysozyme and beta-galactosidase (beta-gal), demo

296 o antigen, E/HEL-Tg mice were immunized with hen egg lysozyme.

297 ty VLRA isolated from lamprey immunized with hen egg white lysozyme (HEL) in unbound and antigen-boun

298 f principle, we demonstrate this method with hen egg lysozyme that shows at least two kinetic phases

299 e observed when crossing STAT5b-CA mice with hen egg lysozyme (HEL) H chain transgenic mice.

300 ohort studies; children aged 0-18 years with hen's egg or cow's milk allergy; baked hen's egg or cow'