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

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

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

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

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

8 Adult hens were kept in control conditions or exposed to UCMS

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

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

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

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

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

14 transgenic CD4 murine cells specific against hen egg lysozyme.

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

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

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

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

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

20 ty of 4 (rice, finger millet, mung bean, and hen egg) commonly consumed complementary foods in childr

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

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

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

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

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

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

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

28 (WL) were compared with the soybean (SL) and hen egg yolk (HL) lecithin in sunflower-fish oil O/W emu

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

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

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

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

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

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

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

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

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

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

39 date PMD using a well-characterized antigen, hen egg white lysozyme, then demonstrate the utility of

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

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

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

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

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

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

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

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

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

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

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

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

52 Eggs laid by hens receiving SBP had linearly (P < 0.01) greater prote

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

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

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

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

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

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

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

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

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

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

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

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

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

66 passage of a virulent strain on embryonated hen's eggs until attenuation; however, little is known a

67 ants with T/E segment 3 grown in embryonated hens' eggs.

68 itional value has been enhanced by enriching hen's diet with bioactive compounds, but factors influen

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

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

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

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

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

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

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

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

77 Focal hens with severe KBFs at 3-4 weeks prior to sampling (n

78 rons in the hippocampal formation than focal hens with minimal fractures (n = 9).

79 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

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

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

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

83 regulation classifies egg production in four hen housing systems: organic, free range, barn and cages

84 Crossing of domestic fowl hens with Guinea fowl male resulted in lower fertility,

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

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

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

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

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

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

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

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

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

94 The material consisted of eggs from hens fed with a mixture without oil and with the additio

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

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

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

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

99 at all hatched offspring from the chimera GE hens were derived from the donor rare heritage breed bro

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

101 4; P = .24), and 2.1% were confirmed to have hen's egg allergy versus 0.6% in the placebo group (rela

102 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

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

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

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

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

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

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

109 Dietary inclusion of SBP could improve hen performance, health, egg quality, and egg shelf life

110 -)C5ar1(-/-) , and Daf1(-/-) B2 cells and in hen egg lysozyme-immunized muMT recipients of MD4 B2 cel

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

112 Those produced in hen egg, Madin-Darby canine kidney (MDCK), and insect (S

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

114 ndicating enantiomer-selective metabolism in hens.

115 Northern fowl mites significantly increased hen preening behaviour and resulted in increased skin le

116 lts suggested that after 10 and 100 infected hens were seeded, the likelihood of detecting an infecte

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

118 ere kept in rooms with deliberately infected hens.

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

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

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

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

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

124 inese institutions, as well as from a laying hen spontaneous ovarian cancer model.

125 s blood biomarkers for both human and laying hen ovarian cancer.

126 udies were verified in both human and laying hen ovarian cysts and tumor specimens.

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

128 of including sugar beet pulp (SBP) in laying hen diets on performance, egg quality, blood chemistry a

129 elevated in cancer versus control in laying hen plasma samples, consistent with the fact that endome

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

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

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

133 and histopathologic findings and the laying hen model support the long-standing incessant ovulation

134 Laying hens fed SBP had lower (P < 0.01) serum total lipids, ch

135 Laying hens often experience unbalanced calcium utilization whi

136 Laying hens were provided feed spiked with five technical mixtu

137 A total of 200 laying hens were randomly assigned into 4 groups and were offer

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

139 ned longitudinally from Lohmann Brown laying hens housed in a commercial multi-tier aviary were used

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

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

142 ed oil (LO) added to feed mixture for laying hens upon the quality characteristics of table eggs, the

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

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

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

146 ent of peritonitis and salpingitis in laying hens.

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

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

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

150 n of CP transfer from feed to eggs of laying hens exposed over 91 days.

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

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

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

154 In commercial flocks of laying hens, keel bone fractures (KBFs) are prevalent and assoc

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

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

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

158 evaluated the impact of supplementing laying hens' feeds with flaxseeds combined with oil derived fro

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

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

161 r its unintentional administration to laying hens.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

180 This study investigated the effect of hen breed, diet enrichment, and cooking methods in modul

181 rnative to current sources for enrichment of hen eggs.

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

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

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

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

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

187 oint was associated with increased levels of hen's egg white and peanut sIgE independent of eczema se

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

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

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

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

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

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

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

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

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

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

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

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

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

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

202 ereas egg was labeled through oral dosing of hens with a uniformly 2H-labeled amino acid mixture.

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

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

205 efore, during, and after mite infestation of hens using animal-based welfare metrics.

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

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

208 he impact of mites or other ectoparasites on hen behaviour or welfare is not well studied.

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

210 m resolution at a dose rate of 40.3 MGy/s on hen egg white lysozyme (HEWL) crystals at RT and cryotem

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

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

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

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

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

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

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

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

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

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

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

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

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

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

225 d to individual birds to continuously record hen movement before, during, and after infestation with

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

227 ite Leghorn (WLH) and Rhode Island Red (RIR) hens were fed a corn-soybean-based diet enriched with fl

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

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

230 Spent hen muscle protein hydrolysate prepared by thermoase (SP

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

232 The study explored the use of spent hen, a major egg industry byproduct, as the starting mat

233 ur study supports the potential use of spent hens as antihypertensive functional food ingredients and

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

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

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

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

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

239 We conclude that hen harriers in Britain suffer elevated levels of mortal

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

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

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

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

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

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

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

247 ract successfully classified the eggs of the hen housing system.

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

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

250 r disappearances of a protected species, the hen harrier, are associated with grouse moors, which are

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

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

253 e classification of samples according to the hen breed, to the farming system and origin.

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

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

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

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

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

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

260 observed in young pigs rendered allergic to hen egg white protein (HEWP).

261 6-month-old infants were already allergic to hen's egg.

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

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

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

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

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

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

271 4 cells from TCR transgenic mice specific to hen egg lysozyme (HEL) are polarized with IL-6/TGF-beta

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

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

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

275 Using data from 58 satellite tracked hen harriers, we show high rates of unexpected tag failu

276 >150 mg, respectively) in eggs of transgenic hens.

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

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

279 13 and 2014, respectively, included unheated hen's egg in 71.6% and 69.6%; heated hen's egg in 54.2%

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

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

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

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

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

285 5.6% of the children in the verum group were hen's egg sensitized versus 2.6% in the placebo group (p

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

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

288 ) cell numbers on an individual level, while hens that acquired fractures earlier in their lives had

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

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

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

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

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

297 examine the performance of this method with hen egg lysozyme as a model system, reproducing its well

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'