ライフサイエンスコーパス: wild-type mice

1 lb/c mice without disruption of these genes (wild-type mice).

2 mbed more frequently to HSV-1 infection than wild type mice.

3 e not different in IL-1R2(-/-) compared with wild type mice.

4 o secondary lymphoid organs was monitored in wild type mice.

5 mass ratio at advanced ages than age-matched wild type mice.

6 M173, is less effective in mHAQ mice than in wild type mice.

7 total body knockout female mice compared to wild type mice.

8 ed recovery after peripheral nerve injury in wild type mice.

9 ificantly reduced in Nlrp3 deficient than in wild type mice.

10 o the vasculature or diluted into blood from wild type mice.

11 1R2(-/-) mice were created and compared with wild type mice.

12 proterenol-challenged heart than age-matched wild type mice.

13 mage, and photocarcinogenesis as compared to wild type mice.

14 ate sodium for 7 days and were compared with wild-type mice.

15 ferent in Ormdl3(Delta2-3/Delta2-3)/CC10 and wild-type mice.

16 xalate levels 2.5-fold greater than those of wild-type mice.

17 thin Ab-deficient DHLMP2A mice compared with wild-type mice.

18 y higher (1.7-fold) in Slco1a/1b(-/-) versus wild-type mice.

19 ric conduction in the peri-infarct zone than wild-type mice.

20 K, pGSK3b, and Hh activity, as compared with wild-type mice.

21 ned epidermal barrier function compared with wild-type mice.

22 treatment transiently increases hepcidin in wild-type mice.

23 from the lungs of fungal allergen-challenged wild-type mice.

24 roid progenitors in the spleen compared with wild-type mice.

25 er-matched controls, global BK knockout, and wild-type mice.

26 ompared to that of macrophages isolated from wild-type mice.

27 containing 3 inflammasome when compared with wild-type mice.

28 consumed greater quantities of nicotine than wild-type mice.

29 f AngII (400 ng/kg per minute) in APA-KO and wild-type mice.

30 was accelerated in PTPA(+/gt) compared with wild-type mice.

31 reduced phagocytosis at all ages compared to wild-type mice.

32 re leaner and more sensitive to insulin than wild-type mice.

33 profoundly impaired in Fmr1-KOs relative to wild-type mice.

34 typeable Haemophilus influenzae, relative to wild-type mice.

35 ceiving PD146176 were undistinguishable from wild-type mice.

36 to systemic infection by S Typhimurium than wild-type mice.

37 ron)-gamma-producing NK cells, compared with wild-type mice.

38 ls were lower in CCL7-deficient mice than in wild-type mice.

39 hepcidin expression similarly as observed in wild-type mice.

40 oes it ameliorate post-MI dysfunction, as in wild-type mice.

41 th intraperitoneal delivery of VEGF-A165b to wild-type mice.

42 reater percentage of affected limbs than the wild-type mice.

43 s of Zip14 KO mice compared with young adult wild-type mice.

44 ting in total IgG levels that are similar to wild-type mice.

45 om Nrf-2(-/-) mice than in chondrocytes from wild-type mice.

46 proved vasorelaxation both in Sirt3(-/-) and wild-type mice.

47 of muscle tissues in Irf1 (-/-) mice than in wild-type mice.

48 w increased rate of cell death compared with wild-type mice.

49 iled to infect TgEq but retained tropism for wild-type mice.

50 ttractant CXCL1 in their lungs compared with wild-type mice.

51 ed left ventricular remodeling compared with wild-type mice.

52 ce are less than 50% of that in the brain of wild-type mice.

53 onse of PV-cells with reduced CS compared to wild-type mice.

54 riasis-associated cytokines as compared with wild-type mice.

55 oxalate secretion than intestinal tissue of wild-type mice.

56 inflammatory infiltrates, and fibrosis than wild-type mice.

57 the hippocampus of DN-DISC mice, but not in wild-type mice.

58 8(+) T cells in miR-31-deficent mice than in wild-type mice.

59 -7 in the eye increased laser-induced CNV in wild-type mice.

60 Six-week-old male C57BL/6 wild-type mice.

61 n DGKzeta-deficient (DGKzeta(-/-)) mice than wild-type mice.

62 higher viral genome copies in skin than did wild-type mice.

63 compared with a large increase (58-fold) in wild-type mice.

64 yte-specific iPLA2gamma transgenic mice, and wild-type mice.

65 pensable for physiological NHEJ in otherwise wild-type mice.

66 ntiation was markedly impaired in parabiotic wild-type mice.

67 ignificantly different between GPVI(-/-) and wild-type mice.

68 apoptosis and ATP depletion than cells from wild-type mice.

69 CD4(+) or CD8(+) T cells from late-pregnant wild-type mice.

70 noticed significant local mucosal injury in wild-type mice.

71 n levels and alpha-cell expansion similar to wild-type mice.

72 shed differentiation potential compared with wild-type mice.

73 in lifespan in PTPA(+/gt) mice compared with wild-type mice.

74 icant decrease in Tfh cells compared with in wild-type mice.

75 s mimicked by a selective Vps34 inhibitor in wild-type mice.

76 e more resistant to bacterial infection than wild-type mice.

77 rse was significantly attenuated compared to wild-type mice.

78 oduction and sperm motility in knock-out and wild-type mice.

79 of PKA were increased by glucocorticoids in wild-type mice.

80 -treated mutant but not in similarly treated wild-type mice.

81 e-primed reinstatement in OCT3-deficient and wild-type mice.

82 eta- and GLAST-dependent synaptopathy in EAE wild-type mice.

83 aller cerebral infarct volumes compared with wild-type mice.

84 express low NR2E3 relative to the livers of wild-type mice.

85 cantly greater cell loss in Gba1-mutant than wild-type mice.

86 during cold exposure (15 degrees C) in male wild-type mice.

87 e were found in the brains of the parabiotic wild-type mice.

88 Ox deposition and tubular damage observed in wild-type mice.

89 ved a pulmonary challenge that was lethal to wild-type mice.

90 umococci into the bloodstream, compared with wild-type mice.

91 odelling and less markers of senescence than wild-type mice.

92 e exhibited worse renal tubular lesions than wild-type mice.

93 ogenesis as compared with those implanted in wild-type mice.

94 scription 5 (GH-Stat5) signaling compared to wild-type mice.

95 ttenuated intestinal pathology compared with wild-type mice.

96 a significant increase in AHR compared with wild-type mice.

97 lls from Ncr1(iCre)R26R(lsl-)(DTA) , Noe, or wild-type mice.

98 olarization after TBI compared with C3H/OuJ (wild-type) mice.

99 enhances spatial memory formation in normal (wild-type) mice.

100 coupling (PAC) in stg/stg, stg/+, tg/tg and wild-type (+/+) mice.

101 uring the diurnal cycle in the livers of (1) wild-type mice, (2) arrhythmic Arntl knockout mice, (3)

102 +/- 0.5 days) was much shorter than that in wild-type mice (27.5 +/- 1.6 days).

103 ing monocytes is increased 9-fold by feeding wild-type mice a Western diet or by applying topical TLR

104 as impaired (>80%) in AMPKalpha2(-/-) versus wild-type mice, a phenotype reproduced in mice lacking A

105 In wild-type mice, a small-molecule AOC3 inhibitor treatmen

106 also show that high-speed liver cytosol from wild-type mice activates CerS3 activity, whereas cytosol

107 In wild-type mice, administration of an IL-36R antagonist a

108 ed GlcCer and GlcSph levels in the brains of wild-type mice after administration of the GCase inhibit

109 ice developed an identical disease course to wild-type mice after challenge with MOG35-55 Single-cell

110 matically more severe disease phenotype than wild-type mice after intranasal inoculation of RABV.

111 the left ventricle and in the circulation of wild-type mice after MI.

112 a(p21(CIP/WAF1))-/-, earlier than at 24 h in wild-type mice after TBI.

113 in albuminuria not observed in AngII-treated wild-type mice along with increased segmental and global

114 mpairment of tumor cell growth compared with wild-type mice, along with decreased mitogen-activated p

115 entally breaching immunological tolerance in wild-type mice also leads to the production of tier 2 HI

116 amin D) each increased serum FGF23 levels in wild-type mice and in mice with global deficiency of the

117 or [(11)C]-12 and [(18)F]-17 in the lungs of wild-type mice and in the myocardium of transgenic mice

118 n between OS phagocytosis and ketogenesis in wild-type mice and mice with defects in phagosome matura

119 ues from 2-months and 2-years-old CalpTG and wild-type mice and performed high throughput RNA-Sequenc

120 ation, and programmed cell death observed in wild-type mice and promoted epithelial recovery, which a

121 type 1 R192Q missense mutation as well as in wild-type mice and rats.

122 ) significantly increased survival (>50%) of wild-type mice and reduced hypothermia and bacterial tit

123 biotic consortium plus L. plantarum CUL66 in wild-type mice and supports further assessment in human

124 e investigated CYCLO effects on autophagy in wild-type mice and TgCRND8 mice-an Alzheimer's Disease (

125 mice normalized plasma PPi levels to that of wild-type mice and, consequently, completely prevented e

126 These cells myelinate fewer axons than in wild-type mice and, in corpus callosum, the myelin is th

127 nce distribution was estimated in 8-week-old wild type mice, and stochastically varied for each condi

128 mage at doses that caused minimal effects in wild-type mice, and adoptive transfer of gammadelta T ce

129 ve, orally available, and brain-penetrant in wild-type mice, and confirmation of target engagement wa

130 circulation and accumulated in the brains of wild-type mice, and formed cerebral amyloid angiopathy a

131 fferent human cell lines, in liver tumors in wild-type mice, and in mice that carried a hepatitis B s

132 romising brain uptake and rapid clearance in wild-type mice, and initial microPET imaging studies of

133 ngs and spleen of fungal allergen-challenged wild-type mice are capable of prolonged survival ex vivo

134 uated fibrotic response to UUO compared with wild-type mice, as demonstrated by reduced collagen abun

135 by analyzing naturally switched B cells from wild-type mice, as well as by engineering polyclonal Igh

136 We found that B cells from wild-type mice, as well as Ighgamma1/gamma1 and Ighepsil

137 , and eotaxin were reduced in ROCK2(+/-) vs. wild-type mice, as were airway hyperresponsiveness and m

138 were lower in Brd4 heterozygous mice than in wild-type mice at 21 days after birth.

139 transgene alone; however, when compared with wild-type mice, both groups developed glucose intoleranc

140 s, and facilitated GABAergic transmission in wild type mice but not in transgenic mice with reduced T

141 ments rapidly restore oculomotor function in wild-type mice but are profoundly impaired in BK channel

142 had reduced survival upon TAC compared with wild-type mice but exhibited no mortality when undergoin

143 sked by depression, which can be revealed in wild-type mice but is absent in Syt7 knockout mice.

144 injection of AM 404 reduced hyperalgesia in wild-type mice but not in CB1(-/-) mice.

145 ANKL expression in mesenchymal stem cells of wild-type mice but not in STAT5a knockout mice.

146 and GolT, was found to decrease infection in wild-type mice but not in the Atp7a(LysMcre) mice.

147 ys-SSH and GSSH are produced in the brain of wild-type mice but not in those of 3MST-KO mice.

148 er 5 of the motor cortex, which is strong in wild-type mice but weak in humans, may be explained by F

149 elongation and increased light scattering in wild-type mice, but not in mice lacking the rod G-protei

150 -fat-diet-induced diabetic hyperglycaemia in wild-type mice, but not in Trpm5(-/-) mice.

151 erexpression of IFN-beta in the CNS of adult wild-type mice, but not of mice lacking IFN-I receptor o

152 E concentrations of Cyp27b1-KO compared with wild-type mice, but not those of IgG1 or IgA.

153 t but significant reduction as compared with wild type mice by 8 to 12 wk.

154 in ovariectomized mice and were increased in wild-type mice by estrogen administration, whereas lung

155 A mice, which could only be recapitulated in wild-type mice by glutathione dialysis.

156 s in dorsal hippocampus of otherwise normal (wild-type) mice by microinjecting before training a sing

157 Compared to wild-type mice, Ces1/Ces1g (-/-) mice had reduced plasma

158 Compared with wild-type mice, Cftr(-/-) mice showed reduced expression

159 In wild-type mice, citric acid stimulation evoked significa

160 lanar cell polarity genes Vangl2 and Ptk7 In wild-type mice, collagen-fibril bundles appear within a

161 er beta-catenin expression compared with PKC wild-type mice, consistent with an altered phenotype of

162 mice recovered from clinical disease, while wild-type mice continued to show signs of disease.

163 In vivo soft tissue infection in wild-type mice demonstrated that Exserohilum provokes ro

164 RABV antibody responses in SAP-deficient and wild-type mice, demonstrating that BAFF modulated immuni

165 Kalpha2(DeltaMC) mice was lower than that in wild-type mice despite being higher after 24 hours.

166 When fed an oxalate-rich diet, wild-type mice developed progressive CKD, whereas Tnfr1-

167 P2X-dbl KO mice, like wild-type mice, did exhibit acid-induced c-Fos activity

168 he differential CT responses in IgA(-/-) and wild-type mice disappeared after intestinal microbiota e

169 NK cells from STAT3 wild-type mice downregulate NKG2D in response to VPA, bu

170 mportantly, these changes were replicated in wild-type mice during hyperglycemia.

171 fic overexpression of IL-10 (M(IL10)) and in wild-type mice during hyperinsulinemic-euglycemic clampi

172 were readily hydrolyzed in mitochondria from wild-type mice during oxidative stress.

173 e ILC2 and ILC3, respectively, compared with wild-type mice during RSV infection.

174 yed less organ atrophy and fibrosis than did wild-type mice during the chronic phases (2 and 6 wk pos

175 gressively increased in kidneys of nephritic wild-type mice during the course of NTN, indicating thei

176 Moreover, diabetic wild-type mice exhibited functional deficiencies in visu

177 rfusion injury, THP(-/-) mice, compared with wild-type mice, exhibited aggravated injury and an impai

178 ron gamma in the small intestine compared to wild-type mice exposed to smoke.

179 In wild-type mice fed an unsupplemented ad libitum diet, ag

180 levels were compared in claudin-18 null and wild-type mice following aspergillus sensitization.

181 locomotor deficits in open-field tests than wild-type mice following low oral rotenone doses given t

182 one marrow-derived mononuclear cells rescued wild-type mice from cecal ligation and puncture-induced

183 = 4) mice, and these mice were compared with wild-type mice given control saline (n = 5) by using PET

184 stent peritonitis surgery, we observed that wild type mice had significantly elevated proinflammator

185 acute and chronic HDM-driven models, whereas wild-type mice had a purely TH2-mediated eosinophilic in

186 However, mutant and wild-type mice had similar plasma vasopressin and solute

187 In normoglycemic wild-type mice, hepatic expression of Ad36E4ORF1 lowered

188 Compared with wild-type mice, heterozygous and homozygous R607H knocki

189 mic neutrophil depletion was found to render wild-type mice highly sensitive to respiratory F. tulare

190 glycemia and raised plasma ghrelin levels in wild-type mice, hyperglycemia was averted in similarly t

191 ces were observed between GPR55 knockout and wild type mice in either development or maintenance of n

192 l also exists in vivo, as we discovered that wild-type mice in the fed state increased their expressi

193 During the learning process, wild-type mice increased the number of CD4(+) T cells in

194 In wild-type mice, increasing task difficulty by introducin

195 Wild-type mice initially learnt, but with prolonged trai

196 , which are devoid of gammadelta T cells, or wild-type mice injected IP with control isotype IgG or g

197 Furthermore, wild-type mice injected with anti-mLAMalpha3 F(ab')2 wer

198 In wild-type mice, interaction of ICOS/ICOSL results in ADA

199 As compared with wild-type mice intestinal gene expression, loss of Ret i

200 Compared to wild-type mice, IRAK-M-deficient mice showed reduced tub

201 train, passage of GPI-anchorless prions into wild type mice led to the emergence of a novel strain wi

202 Anti-CD4 depletion in Ldlr/wild-type mice led to a decrease of serum IgG1 and IgG2c

203 in combination with low-dose IL-33 to naive wild-type mice, led to synergistic increases in airway T

204 Wild-type mice made septic via cecal ligation and punctu

205 eosinophils from fungal allergen-challenged wild-type mice maintain a distinct cytokine profile, and

206 Compared with wild-type mice, MAP3K14 activity-deficient aly/aly (MAP3

207 agonist N-methyl LTC4 to allergen sensitized wild-type mice markedly boosted ILC2 expansion and IL-5/

208 ODS AND We studied ventricular myocytes from wild-type mice, mice with alpha1A and alpha1B knockin re

209 Indeed, compared with wild-type mice, MLKL knockout mice displayed more severe

210 tably, when Alk4 was down-regulated in adult wild-type mice, muscle mass decreased even more.

211 owed less neurological deficit compared with wild-type mice (n=6).

212 Compared with wild-type mice, NgR123-null mice had a sharp increase in

213 Similar to wild-type mice, Nhe8(-/-) mice generated Golgi-derived v

214 Compared with wild-type mice, normal, or uremic mice lacking Cyp27b1 h

215 -MPO antibody transfer for NCGN induction in wild-type mice or mice expressing the CCR2 promoter-cont

216 , membrane bound as in brain microsomes from wild-type mice or purified GPI-anchorless amyloid fibril

217 In wild-type mice, oxaliplatin treatment produced cold allo

218 izygous Tg-TBK1 mice and 20% fewer RGCs than wild-type mice (P = 1.9 x 10-5) at 6 months of age.

219 In wild-type mice, p-Creb marked nephron progenitors (NP),

220 nificantly decreased on pressure overload in wild-type mice, paralleling a decreased oxidative metabo

221 In wild-type mice, patch-clamp electrophysiological studies

222 In wild-type mice, pharmacologic treatment with the GR anta

223 s antibody sharply reduces adipose tissue in wild-type mice, phenocopying genetic haploinsufficiency

224 TRAF3IP2 expression and myocardial injury in wild type mice post-I/R.

225 Moreover, overexpression of DLST in wild-type mice protected against cardiac hypertrophy and

226 In wild-type mice, PTEN reduction occurred after TRAS forma

227 increased serum glycolate concentrations in wild-type mice, rats, and nonhuman primates.

228 Wild-type mice received saline before challenge.

229 nd to assess prophylactic benefits, 3xTg and wild-type mice received tau immunization from 2-6 months

230 R blocker treatment was confirmed in healthy wild-type mice receiving metoprolol.

231 ctive overexpression of Tmem18 in the PVN of wild-type mice reduced food intake and also increased en

232 otal) administration of recombinant Gal-3 to wild-type mice resulted in a dose-dependent reduction in

233 phagocytic cells by clodronate liposomes in wild-type mice resulted in a reduction of gastric H. pyl

234 and striatal micropunches from Brd1(+/-) and wild-type mice revealed differential expression of genes

235 Wild-type mice showed increased myocilin expression in t

236 Wild-type mice subjected to IL-17A neutralization and IL

237 effects were observed in IL-10(-/-), but not wild type, mice, suggesting that IL-10 deficiency predis

238 wall adhesions between age-grouped PV-KO and wild-type mice, suggesting a delay in microglial activat

239 lengthening under constant light compared to wild-type mice, suggesting an increased sensitivity to l

240 d clearance was reduced by 40% compared with wild-type mice, suggesting Oatp1b transporters are impor

241 expression caused no significant changes in wild-type mice, suggesting that Hjv is not a limiting fa

242 In ovariectomized wild-type mice, tamoxifen significantly reduced food int

243 ogical model of Abeta containing deposits in wild-type mice that recapitulates major retinal pathophy

244 Compared with wild-type mice, the cell surface levels of Cav1.2 in the

245 In wild-type mice, there was persistent postnatal expressio

246 ebral injection into tau transgenic (Tg) and wild-type mice, thereby modeling human tau pathology.

247 V-Cre, and in NBQX- and rapamycin-pretreated wild-type mice, these compounds blocking alpha-amino-3-h

248 s were decreased in transgenic compared with wild-type mice; these changes were present at postnatal

249 ofoundly reduced rapid eye movement sleep in wild-type mice; these effects were eliminated in Taar1 k

250 Compared with wild-type mice, THP(-/-) mice had markedly fewer MPCs in

251 neration of the Dnajb1-Prkaca fusion gene in wild-type mice to be sufficient to initiate formation of

252 ssessment of responses of GPR55 knockout and wild-type mice to mechanical and thermal (heat, cold) st

253 Allergic asthma was induced in C57BL/6 J wild-type mice, Toll-like receptor (TLR) 4 knockout (Tlr

254 ined from Cbx3/HP1gamma-insufficient mice or wild type mice treated with Cbx3/HP1gamma-insufficient C

255 Wild type mice treated with rhCD55 immediately after rep

256 2 innate lymphoid cells (ILC2), and C57BL/6 wild-type mice treated with anti-IL5 antibody.

257 not observed in Ig-treated Rag1(-/-) mice or wild-type mice treated with anti-type I IFNR alone.

258 sponse element of Gpr64 gene in the uteri of wild-type mice treated with P4.

259 ly, both the renal injury and dysfunction in wild-type mice undergoing iAKI is significantly ameliora

260 CaMK4 showed increased survival compared to wild-type mice upon infection with C. neoformans This in

261 knock-out and heterozygous mice compared to wild-type mice using RNA-seq; and (iii) morphological an

262 Compared with UUO-treated wild-type mice, UUO-treated IL-36 knockout mice exhibite

263 ke phenotype can be transferred to syngeneic wild-type mice via Tgfbr2(Myeko) bone marrow transplant

264 observed in cortical pyramidal neurons from wild type mice was conspicuously reduced in TASK(-/-) mi

265 y of D2 receptor desensitization observed in wild type mice was not recapitulated with this method of

266 Fibrosis development in wild-type mice was associated with a time-dependent depo

267 ally, the administration of exogenous NGF to wild-type mice was found to significantly increase load-

268 Adoptive transfer of ILC2s from wild-type mice was performed in wild-type and PKC-theta-

269 nia, we found that goal-oriented learning in wild-type mice was supported by stable spatial maps and

270 In wild-type mice, we show that a small molecule inhibitor

271 Age-matched nBmp2NLS(tm) and wild type mice were analyzed by immunohistochemistry, be

272 Moreover, Morris water maze-trained wild-type mice were able to increase astrocyte-produced

273 expression changes elicited by tamoxifen in wild-type mice were abrogated in ERalpha-AF1-deficient m

274 -wave and oscillatory potentials of diabetic wild-type mice were also absent in REDD1-deficient mice.

275 fibrosis, AEC mtDNA damage, and apoptosis in wild-type mice were amplified in Sirt3(-/-) animals.

276 Higher levels of colonization in wild-type mice were associated with increased presence o

277 monas species directly impair wound healing, wild-type mice were infected with Pseudomonas aeruginosa

278 toward either M1 or M2 macrophages in vivo, wild-type mice were injected with gamma interferon (IFN-

279 Wild-type mice were inoculated with either trimannose-co

280 [KO]), iNOS-deficient (iNOS KO), and C57BL/6 wild-type mice were orally infected with A. actinomycete

281 ROCK2-haploinsufficient (ROCK2(+/-) ) and wild-type mice were sensitized with ovalbumin (OVA).

282 Malat1 knock-out and wild-type mice were subjected to 1 h of middle cerebral

283 -Taar1(tm1(NLSLacZ)Blt) (Taar1 knockout) and wild-type mice were surgically implanted to record elect

284 In this study, Ehmt1(+/-) and wild-type mice were tested on several cognitive tests in

285 lso sufficient to improve these behaviors in wild-type mice, when circulating levels of OCN decline a

286 stine of C57BL/6.IgA(-/-) mice compared with wild-type mice, which was further amplified with cholera

287 easured after exercise decreases upon HFD in wild type mice while p66shc(-/-) animals are protected.

288 Treatment of wild type mice with paroxetine, a chemical inhibitor of

289 Gal-1 in mice lacking Gal-1 or treatment of wild-type mice with a neutralizing anti-Gal-1 mAb confir

290 We challenged juvenile Scnn1b-Tg and wild-type mice with Aspergillus fumigatus and house dust

291 Daily intranasal treatment of wild-type mice with C3a beginning 7 days after stroke in

292 was significantly reduced after treatment of wild-type mice with CSP, and uPA-deficient mice were unr

293 atine administration into Gamt-deficient and wild-type mice with demyelinating injury reduced oligode

294 t survive sepsis, whereas treatment of naive wild-type mice with IL-33 induces immunosuppression.

295 IL-6R by CD4(+) T cells and by treatment of wild-type mice with neutralizing anti-IL-6 mAb.

296 ing the peripheral macrophage populations of wild-type mice with Nrp1-depleted bone marrow-derived ma

297 on of 25 pmol of 12 increased tear volume in wild-type mice with sustained action for 8 h and was wit

298 t- and anxiolytic-like behavioral effects in wild-type mice, with a concurrent increase in plasma adi

299 ene C4 synthase-deficient mice compared with wild-type mice, with increased retention of eosinophils

300 e was compared to an adjuvant-based model in wild-type mice (WT-OVA/alum).