ライフサイエンスコーパス: wild-type mice

1 wever, ADMA treatment had no such effects on wild type mice.

2 REDD1 knockouts were expanded compared with wild type mice.

3 ld margin between 5-month-old 5xFAD mice and wild type mice.

4 nger life-span when compared with littermate wild type mice.

5 xpression and delayed extinction compared to wild type mice.

6 DUSP11-deficient mice compared with those of wild-type mice.

7 reinfection with C. rodentium compared with wild-type mice.

8 ted S. haematobium eggs in Il4ra(-/-) versus wild-type mice.

9 om Gpr81-null mice compared with tumors from wild-type mice.

10 ncreased in DeltaNC16A mice as compared with wild-type mice.

11 alloresponses after skin transplantation in wild-type mice.

12 (+)CD8alphaalpha(+) cells in comparison with wild-type mice.

13 tumor cells had worse outcomes compared with wild-type mice.

14 burden or airway neutrophilia compared with wild-type mice.

15 on, and reduced circulating C3 compared with wild-type mice.

16 tion of dextran sodium sulfate compared with wild-type mice.

17 ration of carbon tetrachloride compared with wild-type mice.

18 ime, and higher NREMS delta density than the wild-type mice.

19 proliferate and differentiate into cDC1s in wild-type mice.

20 with lineage-negative bone marrow cells from wild-type mice.

21 mRNA were induced by dietary iron loading in wild-type mice.

22 ic lamina propria macrophages, compared with wild-type mice.

23 ibrosis and kidney malfunction compared with wild-type mice.

24 OR signaling in epididymal adipose tissue in wild-type mice.

25 ctivation is reversed in both cell lines and wild-type mice.

26 in infected Stat3(SA/SA) mice compared with wild-type mice.

27 changes in joint inflammation compared with wild-type mice.

28 less efficient in the humanized mice than in wild-type mice.

29 oclasts in PolgA(mut/mut) mice compared with wild-type mice.

30 organotypic hippocampal slice cultures from wild-type mice.

31 re all significantly reduced relative to the wild-type mice.

32 0-fold higher than that from the age-matched wild-type mice.

33 acerbated in Iqgap1(-/-) mice as compared to wild-type mice.

34 g had lower levels of lung inflammation than wild-type mice.

35 ce after intradermal IL-23 treatment than in wild-type mice.

36 laries almost doubled compared with diabetic wild-type mice.

37 suppressed in Gpr81-null mice compared with wild-type mice.

38 in suppression in Huh7 hepatoma cells and in wild-type mice.

39 se of muscle wasting that impairs fitness of wild-type mice.

40 sed melanoma metastasis patterns to those of wild-type mice.

41 o-resistant areas of the aortic arch even in wild-type mice.

42 AV-specific CD4 T cell responses compared to wild-type mice.

43 oughout the vascular network was observed in wild-type mice.

44 bacteria in Grhl2 KO mice compared with the wild-type mice.

45 e volar keratinocytes or in vivo footpads of wild-type mice.

46 s switching to IgG1 in both transnuclear and wild-type mice.

47 neys of Gsr (-/-) mice but were not found in wild-type mice.

48 hile almost no dissemination was observed in wild-type mice.

49 d to adult dorsal root ganglion neurons from wild-type mice.

50 in the brain by 32% compared to age-matched wild-type mice.

51 se in portal hypertension compared to BDL in wild-type mice.

52 critical for LPS-induced endotoxic shock in wild-type mice.

53 muscle was decreased by 20-25% compared with wild-type mice.

54 am(KO/KO) mouse, were indistinguishable from wild-type mice.

55 ated 5-HT production, compared with infected wild-type mice.

56 3R(+)) Treg cells develop as are observed in wild-type mice.

57 eptor-deficient mice compared to age-matched wild-type mice.

58 orce in limb muscles compared to age-matched wild-type mice.

59 tards development of diet induced obesity in wild-type mice.

60 had reduced DSPP expression, compared to the wild-type mice.

61 susceptible to lethal VSV disease than were wild-type mice.

62 marked increase in foot swelling compared to wild-type mice.

63 E-specific, isotype-switched plasmablasts as wild-type mice.

64 re not altered in the dKO mice compared with wild-type mice.

65 s of MLN increased IL-12/23p40 compared with wild-type mice.

66 are less susceptible to superinfection than wild-type mice.

67 ound that atherogenesis was enhanced in aged wild-type mice.

68 ce was knocked in, as compared with injected wild-type mice.

69 spiratory infection with vaccinia virus than wild-type mice.

70 T cells from CD83(flox/flox)/CD4-cre(wt/wt) wild-type mice.

71 profiles to those seen in the plasma DNA of wild-type mice.

72 ted kidney injury in Gstm1 knockout, but not wild-type mice.

73 the GCP-rCpa1 vaccine compared with those of wild-type mice.

74 s more severe in Lpar2(-/-) mice compared to wild-type mice.

75 sions in the Ahr knockout in comparison with wild-type mice.

76 in the brains of 5xFAD mice versus those of wild-type mice.

77 ng a norovirus small animal disease model in wild-type mice.

78 oidosis mouse model (APP/PS1-21 mice) and in wild-type mice.

79 cells, compared with healthy individuals or wild-type mice.

80 ntly elevated in knock-in mice compared with wild-type mice.

81 gh-fat diet-fed RBP4-overexpressing mice vs. wild-type mice.

82 e more resistant to apoptosis than GCPs from wild-type mice.

83 and cartilage destruction was comparable to wild-type mice.

84 ina propria of Gitr(-/-) mice as compared to wild-type mice.

85 odes (RLN) were analyzed in TNFRp55(-/-) and wild-type mice.

86 tologic evidence of acute kidney injury than wild-type mice.

87 Intraperitoneal POL5551 injections in wild-type mice (8 mg/kg at 2, 4, 6, and 8 days) enhanced

88 In wild-type mice, a significant age-related decrease in k

89 Compared with wild-type mice, ablation of the miR-17-92 cluster signif

90 were acutely secreted in the blood serum of wild-type mice after 15 Gy radiation dose, inducing a ga

91 chemic brain injury and improved survival in wild-type mice after CA/CPR (81.8% in SPL-334.1 versus 3

92 uced significantly less serum IFN-alpha than wild-type mice after injection of TLR9 agonist, and BCAP

93 mes and worse neurological deficits than the wild-type mice after ischemia.

94 of both GPR119 and CD36 were upregulated in wild-type mice after VSG.

95 seizure activity in these mice with those of wild type mice and Kcnt1(-/-) mice.

96 s was assessed for systemic delivery in both wild type mice and the NSG-PiZ transgenic mouse model of

97 Both juvenile wild-type mice and adult mice lacking ngr1 in L4 display

98 However, wild-type mice and all existing humanized mouse models c

99 In wild-type mice and ApoE(-/-) mice on a Western diet, ult

100 resistant to growth of various cancers than wild-type mice and are more responsive to anti-PD-1 immu

101 iate wheat-induced intestinal dysfunction in wild-type mice and exacerbate inflammation to gluten in

102 81-negative) implanted in mammary fat pad of wild-type mice and Gpr81-null mice.

103 nd Ctss mRNA transcripts compared with young wild-type mice and greater age-related changes at 12 to

104 ped more severe T-cell transfer colitis than wild-type mice and had an increased burden of bacteria i

105 red that similar astrocytes appeared in aged wild-type mice and in aging human brains, suggesting the

106 hibit worsened clinical symptoms relative to wild-type mice and increased expression of S100A9 and S1

107 MAP4K1(KO) mice, tumors grow slower than in wild-type mice and infiltrating T cells are less exhaust

108 transplanted from Il1rl2(-/-) to irradiated wild-type mice and intestinal tissues were analyzed.

109 cells and in vivo studies in mice, including wild-type mice and knockout mice deficient in peptidylpr

110 etagenomic sequencing analyses of feces from wild-type mice and mice with defects in TGFB signaling (

111 ty in the DCT and NCC expression/activity in wild-type mice and mice with kidney-specific knockout of

112 vector recapitulated these complications in wild-type mice and restored the survival period in Fgf21

113 ntotemporal dementia (FTD) as well as in the wild-type mice and tau knock-out and P301L tau mouse mod

114 We derived intestinal organoids from wild-type mice and Tgr5(-/-) mice, incubated them with B

115 consume greater quantities of nicotine than wild-type mice and that knock-down of Chrna3 gene transc

116 ansplanted bone marrow from knockout mice to wild-type mice and vice versa to dissect cell type-depen

117 pts were expressed at very low levels in the wild-type mice and were significantly upregulated in the

118 ificantly smaller in TRPV1(-/-) mice than in wild-type mice, and almost completely abolished after a

119 ed protocols for inducing chronic uveitis in wild-type mice, and demonstrate a predominant memory Th1

120 ein, and Il10 and Tgfb1 mRNAs, compared with wild-type mice, and fewer T-regulatory cells.

121 serotypes were injected intrathymically into wild-type mice, and gene transfer efficiency was monitor

122 C/MS, in normal small intestines of C57BL/6J wild-type mice, and in normal and tumour samples from Ap

123 miR-146a expression declined in old wild-type mice, and loss of miR-146a promoted premature

124 intestine and were shed less in the feces of wild-type mice, and such defects were rescued in Rnasel

125 mice succumbed to fulminant disease whereas wild-type mice, and those engineered to express only tra

126 In wild-type mice, Ang II increased susceptibility to AF in

127 ccupancy in the liver of fasted versus refed wild-type mice are largely confined to low and intermedi

128 Wild-type mice are resistant to CCHFV infection, and typ

129 he theta and gamma frequency bands, which in wild-type mice are tightly linked to running speed, was

130 er severity of AKI in knockout compared with wild-type mice, as demonstrated by semiquantitative inju

131 In wild-type mice, ascending aortic constriction caused myo

132 l enhancement in transgenic mice relative to wild type mice at all dose levels.

133 fully functional: upon transfer to congenic, wild type mice at controlled frequencies, such B cells c

134 ntly neutralized mouse-adapted SARS-CoV-2 in wild-type mice at a dose as low as 2 mg/kg and exhibited

135 S100-knockout mice weighed 21% more than wild-type mice at age 8 weeks and a higher proportion de

136 ight loss, and disease activity index in the wild-type mice but not EPCR(-/-) mice.

137 dian Hedgehog expression in growth plates of wild-type mice but not in HN overexpressing mice or HN-t

138 eight gain in response to a high-fat diet in wild-type mice but not in mice lacking GDF15 or its rece

139 posure acutely suppresses BAT temperature in wild-type mice but not in Opn5-null mice.

140 o 42.7 kDa) conjugates induced a response in wild-type mice but not in T cell-deficient mice, suggest

141 )-PAF caused preterm labor and fetal loss in wild-type mice but not in TLR4-deficient mice.

142 ed these effects in BLA pyramidal neurons in wild-type mice but not in Tmem74(-/-) mice.

143 us show comparable influenza virus titres to wild type mice, but display increased morbidity accompan

144 f potassium inactivated NCC within 1 hour in wild-type mice, but had no effect in knockin mice.

145 Transfer of Tregs from oxazolone-sensitized wild-type mice, but not Dock8(-/-) mice, reduced the CHS

146 We also found that the gut microbiota from wild-type mice, but not from Crtam(-/-) mice, induces CR

147 ophils to the peritoneum and the synovium in wild-type mice, but not in GEF-H1(-/-) mice.

148 ination are attenuated in human cells and in wild-type mice, but not in live mosquitoes.

149 LCMV infection is self-limited in wild-type mice, but Prf1-/- mice develop prolonged virem

150 AS model mice kindled similarly to wild-type mice, but they displayed a markedly increased

151 of TREM2 in primary microglial cultures from wild type mice by using siRNA to decrease Trem2 expressi

152 ecreased in PPARalpha (-/-) mice relative to wild-type mice by 21 months of age.

153 aspects of this metabolic profile in PRs of wild-type mice by activation of the mammalian target of

154 eveloped and characterized in two strains of wild-type mice by modifying interphotoreceptor retinoid-

155 eptin sensitivity that is similar to that of wild-type mice by multiple measures.

156 and vitamin A supplementation (VAS) model in wild-type mice (C57BL/6) and established AD model on bot

157 VU0119498 treatment of wild-type mice caused a significant increase in plasma i

158 uscle injury to tibialis anterior muscles of wild-type mice caused ICAM-1 to be expressed by a popula

159 h MuPyV, we found that MuPyV encephalitis in wild-type mice causes an encephalopathy, which is marked

160 Holo- or apo-RBP4 injection in wild-type mice causes insulin resistance and elevates PG

161 Compared with wild-type mice, CD38 knockout (KO) mice showed reduced m

162 Neutrophil depletion in wild-type mice conferred protection from ischemic stroke

163 ntly inhibited tumor cell adhesion to HEC in wild-type mice confirming that Notch controls hepatic me

164 lating Edn1, we studied four groups of mice: wild-type mice, connecting tubule/collecting duct-specif

165 died mice with knockout of CDC42 or RAC1 and wild-type mice (controls).

166 Our findings comparing 5XFAD versus wild-type mice correlate well with histology, showing pr

167 In vivo studies with wild-type mice demonstrated significant pharmacologic ef

168 f expression of a Bcl2 transgene) than in B6 wild-type mice despite the lower serum BAFF levels in th

169 te (AOM/DSS) exposure, both Xist-deleted and wild-type mice develop gastrointestinal tumors.

170 Following C. muridarum inoculation, wild-type mice develop robust hydrosalpinx, but OT1 mice

171 Wild-type mice develop significant kidney injury, protei

172 We found that in wild-type mice, diabetes reduced PMo in the general circ

173 gical suppression of BACE1 activity in adult wild-type mice did not reproduce the hearing deficit or

174 While antibiotic-treated wild-type mice display diminished macrophage responses t

175 -/-) mice had better long-term survival than wild-type mice during chronic infection.

176 ping a baseline mRNA expression catalogue of wild-type mice during early embryogenesis (4-36 somites)

177 thermore, melanopsin-activated astrocytes in wild-type mice enhanced the firing rate of cortical neur

178 D4(+) T cells from B cell-deficient, but not wild-type, mice enhanced susceptibility to infection, fu

179 ides-infected lungs compared with vaccinated wild-type mice, especially Th17 cells.

180 of mice given GDNF were similar to those of wild-type mice except for Bacteroides.

181 After IL-23 gene transfer, wild-type mice exhibited concurrent skin and joint chang

182 nic in wild-type (TG), or KO background, and wild-type mice exposed to TAC.

183 rom Hol(Tg/Tg) mice compared with feces from wild-type mice; fecal microbiomes of mice given GDNF wer

184 Compared with feces from wild-type mice, feces from mice with defects in TGFB sig

185 early and persistently in AT and AT MDCs of wild-type mice fed a high-fat diet (HFD).

186 of YAP is significantly increased in KCs of wild-type mice fed a high-fat diet (HFD).

187 gly, we detected trivial FGF13 in adipose of wild-type mice fed normal chow and no obesity in adipose

188 Wild-type mice fed normal chow exhibited dysbiosis after

189 cantly inhibited hydrosalpinx development in wild-type mice following an intravaginal inoculation wit

190 ir TG but many fewer LAT-positive cells than wild-type mice from day 7 to day 30 but that after day 3

191 Depletion of neutrophils protected wild-type mice from skin and joint disease without suppr

192 Analysis of nearly 10,000 wild-type mice from two large-scale experiments revealed

193 Aged wild-type mice had elevated acoustic thresholds and syna

194 C57BL/6J wild-type mice had offspring exhibiting similar malforma

195 Compared with wild-type mice, IL-1R(-/-) mice have more severe liver a

196 In wild-type mice, IL-33 or OVA induced similar airway hype

197 ey are abolished in SIRT3-deficient mice and wild type mice in which SIRT3 is selectively depleted fr

198 evelop in the aorta and brain vasculature of wild-type mice in an age-dependent manner.

199 easured the cochlear blood flow of salsa and wild-type mice in response to loud sound (120 dB SPL, 30

200 1 showed altered distributions compared with wild-type mice, in both ongoing and visually evoked acti

201 the onset of rod degeneration compared with wild type mice, including reduction of key photoreceptor

202 ce escaped several complications observed in wild-type mice, including augmentation of blood pressure

203 histone mark H3K9me3 in mdx mice compared to wild-type mice, indicating a chromatin conformation less

204 taining in CH24H-knockout mice compared with wild-type mice, indicating a specificity of soticlestat

205 duration of infection (3 versus 10 weeks) in wild-type mice, indicating that the within-host immune p

206 inflammatory pathology compared with that in wild-type mice, indicating that type III IFN exacerbates

207 e analysis revealed that aortic challenge in wild-type mice induced the DNA damage response, the infl

208 mized female GPR30(-/-) , ERalpha(-/-) , and wild-type mice injected intramuscularly with the potent

209 ng was blocked, both in Il21r KO mice and in wild-type mice injected with IL-21R-Fc fusion-protein.

210 In wild-type mice injected with melanoma cells, we show tha

211 To determine whether the cochlea of adult wild-type mice is susceptible to AD treatment-like suppr

212 jected into the mPFC or lateral ventricle of wild-type mice, it reverses chronic unpredictable stress

213 In wild-type mice, iTreg cells suppressed lung allergic res

214 el intensity and subcellular distribution in wild-type mice, knockout mice, and receptor-positive and

215 jection of two antisense oligonucleotides in wild-type mice leads to a dose-dependent increase in pro

216 ated deletion of Inpp5a in the cerebellum of wild-type mice leads to Purkinje cell degeneration, and

217 Here, we find that physiological aging in wild-type mice leads to telomere shortening and a reduce

218 Wild type mice lost significant muscle and bone mass dur

219 oscopy, we demonstrate in adult male C57BL/6 wild-type mice marked differences between MC versus S1 P

220 Compared with nontransgenic wild-type mice, mice with neuronal Mfn2 overexpression a

221 In wild-type mice, most bacteria are within iNOS(+) granulo

222 In healthy retinas of wild-type mice, Muller glial cells phagocytosed cell bod

223 nt with SOL muscle abnormalities in R58Q vs. wild-type mice, myosin ATPase staining revealed a decrea

224 Compared with wild type mice, Nlrc4(-/-) mice controlled H. pylori bet

225 in the peripheral nervous system and CNS of wild-type mice of either sex and protected in vitro sens

226 on of anti-IL11 or anti-IL11RA antibodies to wild-type mice on the HFMCD or WDF, or to db/db mice on

227 ed by the NWAs Junin and Tacaribe virus than wild-type mice or cells are.

228 Naive T cells were isolated from wild-type mice or cord blood from healthy donors and sub

229 tion of modified Sia in cells and tissues of wild-type mice or in mice lacking CMP-N-acetylneuraminic

230 In wild-type mice, oral metformin increased circulating GDF

231 icant macrothrombocytopenia as compared with wild-type mice (Pdk1fl/fl).

232 ng tumor cells with mirn23a (-/-) BMDMs into wild-type mice phenocopied tumor growth in mirn23a (-/-)

233 In aging wild-type mice, phospholemman was hypophosphorylated, an

234 educed in HIF-2alpha(mye/-) mice compared to wild-type mice post-APAP challenge.

235 eNAD exposed to colonic muscularis of wild-type mice produced eADPR, eAMP and eADO.

236 y predicted the onset of SD in both FHM2 and wild-type mice, providing a novel mechanism in migraine

237 verexpress human A53T protein and littermate wild-type mice received a single injection of LPS (2 mg/

238 KI and wild-type mice received PPIs or PBS intraperitoneally an

239 epatic ChREBP activity to levels observed in wild-type mice receiving AAV8-scrambled short hairpin RN

240 HDAC10(-/-) but not wild-type mice receiving fully MHC-mismatched cardiac tr

241 /-) mice treated with G-1 compared to 10% in wild-type mice receiving no G-1.

242 dministration of 1,25(OH)(2) vitamin D(3) to wild-type mice resulted in the expected increase in acti

243 tretch in both, BEAS-2B cells and ventilated wild-type mice, resulted in TRPV4 activation and reduced

244 een and mesenteric lymph nodes compared with wild-type mice; sCYLD/SMAD7 mice had even larger increas

245 ively active Rap1a (CARap1a) into the RPE of wild type mice, self-complementary AAV2 (scAAV2) vectors

246 In contrast, wild-type mice showed no RPE degeneration after blue lig

247 e accumulation was higher in TAAR1-KO versus wild-type mice, suggesting a negative feedback mechanism

248 ts and greater axonal and myelin injury than wild-type mice, suggesting that endogenously expressed t

249 ponses that were comparable in magnitudes to wild-type mice, suggesting that this B cell response was

250 We subjected wild-type mice, Sult1e1 knockout mice, and Sult1e1 knock

251 Remarkably, wild-type mice survived asymptomatically with pbgA-lpxC

252 ic acid, and xanthurenic acid were higher in wild-type mice than in Abcg2(-/-) mice.

253 ant Lm-infected GNLY-transgenic mice than in wild-type mice that lack GNLY.

254 Compared with wild-type mice, the double-knockout mice displayed inhib

255 val rates of infected ILC-deficient mice and wild-type mice, there was significantly reduced survival

256 tabotropic) signaling through NMDARs, and in wild-type mice this structural plasticity required activ

257 ve transport of phosphate only in jejunum of wild-type mice, though NaPi-IIb protein expression was u

258 ed fat and collagen deposition compared with wild-type mice, thus also supporting Myoc as a regulator

259 Here, we subjected adult, wild-type mice to distinct chronic jet-lag paradigms, wh

260 Gsdmd(-/-) mice were more susceptible than wild-type mice to intranasal infection with Burkholderia

261 The inherent resistance of wild-type mice to SARS-CoV-2, combined with a wealth of

262 Here, we use immunocompetent wild-type mice to show that hNSC-derived EV treatment ad

263 d to compare single-cell transcriptomes from wild-type mice to those of mice with a collecting duct-s

264 optive transfer of monocyte/macrophages from wild-type mice trafficked to wounds with restoration of

265 ment on cardiac performance was abolished in wild-type mice transplanted with bone marrow derived fro

266 eutrophils in competitive chimera models and wild-type mice treated with IL-4.

267 We also used wild-type mice treated with the SULT1E1 inhibitor triclo

268 PHx in wild-type mice triggered rapid intrahepatic coagulation,

269 thetized and ventilated adult female C57BL/6 wild-type mice underwent a 4, 8, 12, or 16-minute potass

270 Materials and Methods Twenty-eight female wild-type mice underwent focused ultrasound treatment af

271 AnxA1 knockout (AnxA1(-/-)) and wild-type mice underwent MI induced by ligation of the l

272 tant TBP in different brain regions in adult wild-type mice via stereotaxic injection of adeno-associ

273 ery, and the transient steatosis observed in wild type mice was virtually absent in mice lacking both

274 Similarly, KLK-5-induced inflammation in wild-type mice was also ameliorated when treated with SO

275 In contrast to wild-type mice, WD-fed TCRdelta-deficient and CCR6-defic

276 The KO mice and their matched wild-type mice were challenged with chronic-plus-binge a

277 Wild-type mice were exposed to the carcinogen, 4-nitroqu

278 Mice genetically engineered to lack Ccr2 and wild-type mice were treated +/-CCR2 antagonist RS102895

279 Wild-type mice were treated by FUSIN delivery of near-in

280 lated factor 2 (Nrf2)(-/-) and corresponding wild-type mice were used at 2 to 3 and 12 to 13 months o

281 s and macrophages from SerpinB2 knockout and wild-type mice were used for functional studies and tran

282 n (-/-) mice, which are about twice those of wild type mice, were largely maintained during spaceflig

283 utrophils, and increased CXCL1 compared with wild-type mice, whereas deletion of STAT2 did not change

284 f)/Tie2-Cre knockout compared to EphA4f.(/f) wild type mice, which coincided with altered mRNA transc

285 h pregnenolone 16alpha-carbonitrile (PCN) in wild-type mice, which greatly reduced the severity of Tc

286 ponsiveness to methacholine as compared with wild-type mice, which were independent of inflammation a

287 nt with FGF23 increased testicular weight in wild-type mice, while mice with global loss of either FG

288 itecture and turnover in an ageing series of wild type mice with that of the PolgA(mut/mut) mitochond

289 ress this question, we colonized germfree or wild-type mice with a model intestinal commensal strain

290 Treating wild-type mice with an anti-CCL2 mAb attenuated the seve

291 Cotreating wild-type mice with Ang II and the NPR-C agonist cANF do

292 Notably, treatment of infected wild-type mice with apoptotic cells significantly increa

293 to blunt the increase in HVR that occurs in wild-type mice with CH.

294 Fecal oxalate excretion was enhanced in wild-type mice with CKD.

295 sely, IL-2 complex-induced Treg expansion in wild-type mice with established lung fibrosis completely

296 We experimentally infected wild-type mice with MuAstV isolated from immunocompromis

297 -4 receptor-alpha knockout (Il4ra(-/-) ) and wild-type mice with S. haematobium eggs.

298 l muscle from global Zip14 knockout (KO) and wild-type mice (WT).

299 In contrast to wild-type mice, Ythdf1-deficient mice show an elevated a

300 In pregnant wild-type mice, ZIKV I1404 increased the magnitude and r