ライフサイエンスコーパス: mice exposed to

1 is-N7G-BD adduct amounts in liver tissues of mice exposed to 0.5, 1.0, and 1.5 ppm BD for 2 weeks wer

2 ide (TG) levels, were higher in conventional mice exposed to 1 ppm arsenic, while arsenic exposure di

3 ere assessed, an acute lung injury model and mice exposed to 10% O2 for 3 weeks.

4 Wild-type (WT) mice exposed to 100 ppm Cl2 for 5 min had airway neutrop

5 ith controls and 4 to 8-fold higher in Bmpr2 mice exposed to 16alphaOHE 1.25 mug/h for 4 weeks.

6 r-activated receptor-gamma and CD36 in those mice exposed to 16alphaOHE and protein derived from HPAH

7 y and used it to isolate RGCs from wild type mice exposed to 2 weeks of IOP elevation generated by th

8 quantify TETS concentration in the serum of mice exposed to 2x LD50 dose of TETS and to monitor kine

9 ory changes and lung histology of Mmp28(-/-) mice exposed to 3 and 6 months of cigarette smoke.

10 the diabody mixture protected almost all the mice exposed to 3 LD(50) s.c. of venom.

11 d pulmonary vascular remodeling in wild-type mice exposed to 3 weeks of hypoxia; this beneficial acti

12 Heart tissue from mice exposed to 3% CO exhibited a 42 +/- 19% reduction i

13 Mice exposed to 37d of spaceflight displayed elevated li

14 in the spleen of adult male and female CD-1 mice exposed to 4 to 40,000 mug/kg/day BPA or 0.02 to 2

15 ounced effects were seen in 2.7-3.2-year-old mice exposed to 40% caloric restriction starting at 0.3

16 parenchyma and the bronchoalveolar space of mice, exposed to 48 hours of hyperoxia together with nor

17 ously demonstrated that PHDi prevents OIR in mice exposed to 5 days of sustained 75% oxygen followed

18 trically in male, female, and ovariectomized mice exposed to 6 months of cigarette smoke.

19 ciated sepsis caused high mortality rates in mice exposed to 6-9 Gy of gamma-rays.

20 e (1,N(6)-HMHP-dA), in tissues of laboratory mice exposed to 6.25-625 ppm BD.

21 In this study, the mortality of mice exposed to 7 Gy of gamma-rays (7 Gy GIARS mice) was

22 , arterial blood gases, and blood glucose in mice exposed to 8% O2 for 2 or 6 h.

23 well as the brain and blood transcriptome in mice exposed to 9 weeks of unpredictable chronic mild st

24 wborn severe combined immunodeficiency-beige mice exposed to 90% O2 from birth; sham controls receive

25 High-dose i.p. MSC administration to newborn mice exposed to 90% O2 resulted in the restoration of no

26 Wood mice exposed to a 0.9 to 5 MHz frequency sweep changed t

27 Here we report that mice exposed to a conspecific receiving electrical foots

28 ary damage and inflammation in Cftr-knockout mice exposed to a dextran sodium sulfate-induced portal

29 n-1, by human airway epithelial cells and in mice exposed to A fumigatus spores or secreted fungal fa

30 body weight gain and glucose intolerance in mice exposed to a high-fat diet.

31 Male mice exposed to a methylating agent exhibited a reduced

32 and CAST/EiJ, both in unexposed mice and in mice exposed to a model DNA-damaging chemical, 1,3-butad

33 cells in the dentate gyrus (DG) and CA3 than mice exposed to a novel context.

34 encing, we characterized lung neutrophils in mice exposed to a pro-allergic low dose of lipopolysacch

35 Mice exposed to a prolonged day length of 16- and 24-h l

36 recordings of single units in behaving male mice exposed to a rat to investigate the encoding of pre

37 d mainly inhibitory action in SCN neurons of mice exposed to a short-day photoperiod.

38 ver, did not delay melanoma onset in TN(61R) mice exposed to a single neonatal dose of UVB.

39 the colonic mucosa-associated microbiota in mice exposed to a social stressor (called social disrupt

40 ented the acquisition of social avoidance in mice exposed to a social threat, but did not affect a pr

41 lly induced demyelination is enhanced in old mice exposed to a youthful systemic milieu through heter

42 spectrometry, in liver and kidney tissues of mice exposed to AA-I, at doses ranging from 0.001 to 1 m

43 e, miR-146a delivery or Akt2 silencing in WT mice exposed to acid resulted in suppression of iNOS in

44 We examined memory formation in mice exposed to acute hypoxia.

45 were continuously measured for three days in mice exposed to ad libitum and restricted feeding condit

46 Although disease modeling in mice exposed to AGAbs indicates that complement-mediated

47 n protein of the BAFF-receptor, BAFFR-Fc, in mice exposed to air or CS for 24 weeks and evaluated sev

48 administration of anti-CXCL13 antibodies in mice exposed to air or CS for 24 weeks, and several hall

49 ere compared with aged-matched 3xTgAD and WT mice exposed to air or desflurane alone.

50 e examination of adenosine receptor-knockout mice exposed to AKI demonstrated that renal protection b

51 One group of WT mice exposed to alcohol received recombinant human FGF21

52 fected social recognition in adulthood: only mice exposed to all three hits showed deficits in this a

53 Infantile mice exposed to alpha-, gamma-, or CM-HBCD demonstrated

54 In mice exposed to alpha-HBCD, four hydroxylated metabolite

55 basis for these effects, we determined that mice exposed to an HFD combined with MGF exhibited a sub

56 ments were performed using NZM and apoE(-/-) mice exposed to an IFNalpha-containing or empty adenovir

57 Using C57BL/6 mice exposed to an LD(50-80/30) of (60)Co TBI (7.75-7.9

58 However, VSG mice exposed to antibiotics, regardless of their specifi

59 We showed that mice exposed to antigen through the skin, in the presenc

60 Parkin knockout mice exposed to aortic constriction-induced cardiac pres

61 Leishmania donovani was serially passaged in mice exposed to arsenic in drinking water at environment

62 After five monthly passages in mice exposed to arsenic, isolated parasites were found t

63 As mice exposed to avirulent C. difficile spores ingested i

64 cells and in bronchoalveolar lavage fluid of mice exposed to B20 were approximately 20-30% higher tha

65 on was observed in both livers and hearts of mice exposed to BDL.

66 ges in vascular remodeling were monitored in mice exposed to bleomycin in conjunction with genetic re

67 amined in the lungs of patients with IPF and mice exposed to bleomycin.

68 epithelial cells of patients with IPF and in mice exposed to bleomycin.

69 and no evidence of PH compared with control mice exposed to BLM.

70 d marked induction of p53 in ATII cells from mice exposed to BLM.

71 Mice exposed to brief uncontrollable stress showed impai

72 However, exercised mice exposed to bright light had 2 times greater retinal

73 ction and photoreceptor nuclei than inactive mice exposed to bright light.

74 TcdB) in sera and body fluids of piglets and mice exposed to C. difficile to investigate the relation

75 mined the F2 generation and F3 generation of mice exposed to caffeine from E10.5-13.5, as this coinci

76 l ventricle dilation) preferentially in male mice exposed to CAPs, and it persisted through young adu

77 Mice exposed to CASPR2-IgG, compared with control-IgG in

78 sitization, and fibrosis in airways of naive mice exposed to cat dander.

79 le and immune related gene sets in Lcn2(-/-) mice exposed to CCl(4), along with decrease in Timp1 and

80 r the colonization of pneumococcus in BALB/c mice exposed to cholera toxin 4 weeks prior to challenge

81 ngly, the reduced plasma insulin in M4K4 iKO mice exposed to chronic (16 weeks) HFD was not observed

82 ne the role of FGF21 in hepatic steatosis in mice exposed to chronic alcohol treatment and to discern

83 MS/MS quantification of the hepatic ECM from mice exposed to chronic carbon tetrachloride (CCl4); rec

84 t CS exposure.Measurements and Main Results: Mice exposed to chronic CS or to elastase, and patients

85 C57BL/6J mice exposed to chronic CS, BMAL1 knockout (KO) mice and

86 In this study, we found that mice exposed to chronic HA (5000 m for 12 weeks) exhibit

87 hypoxia-pulmonary arterial hypertension, and mice exposed to chronic hypoxia expressed increased StAR

88 Mice exposed to chronic hypoxia for 7 days manifest an e

89 vo in miR-143-/- and anti-miR-143-3p-treated mice exposed to chronic hypoxia in both preventative and

90 d distal pulmonary artery muscularization in mice exposed to chronic hypoxia or SU5416/hypoxia.

91 developed less severe PH than did wild-type mice exposed to chronic hypoxia, with less distal pulmon

92 a(2+)](i), pH, and RV pressure that occur in mice exposed to chronic hypoxia.

93 Mice exposed to chronic intermittent ethanol (CIE) vapor

94 leukin-6, and tumor necrosis factor-alpha in mice exposed to chronic mild stress.

95 s depression-like behaviors and anhedonia in mice exposed to chronic restraint stress.

96 ulated in mDCs of smokers with emphysema and mice exposed to chronic smoke.

97 ook an unbiased plasma proteomic analysis of mice exposed to chronic social stress and observed dysre

98 Moreover, angiotensin II-infused mice exposed to chronic stress exhibited greater blood p

99 trol subjects (n = 19/group) and of C57BL/6J mice exposed to chronic stress or control conditions (n

100 Finally, LAC had no effect on mGlu2 knockout mice exposed to chronic unpredictable stress, and a sing

101 ffect in Flinders Sensitive Line rats and in mice exposed to chronic unpredictable stress, which, res

102 brotic environment and pulmonary fibrosis in mice exposed to chrysotile.

103 Mice exposed to cigarette smoke developed emphysema with

104 NOD2-deficient mice exposed to cigarette smoke developed ileitis, chara

105 Mice exposed to cigarette smoke for 4 weeks demonstrated

106 The development of emphysema in humans and mice exposed to cigarette smoke is promoted by activatio

107 d the expression and function of miR-135b in mice exposed to cigarette smoke or nontypeable Haemophil

108 Importantly, NTHI-specific T cells from mice exposed to cigarette smoke produced lower levels of

109 mphysema-associated lung volume expansion in mice exposed to cigarette smoke.

110 e lungs of emphysematous chronic smokers and mice exposed to cigarette smoke.

111 atory and pro-resolving effects in cells and mice exposed to cigarette smoke.

112 ApoE-KO and ApoE-p50-DKO mice exposed to CIH for 30 and 9 weeks, respectively, di

113 ly ameliorated acute renal tubular damage in mice exposed to cisplatin insult, associated with enhanc

114 Mice exposed to cNIC exhibited long-term potentiation in

115 , developed by Celldex Therapeutics Inc., in mice exposed to Co-60 gamma total body irradiation (TBI)

116 tine on the metabolic profiles in tissues of mice exposed to cobalt-60 total-body gamma-radiation.

117 structure, and these were most pronounced in mice exposed to cocaine during adolescence.

118 these effects were again more pronounced in mice exposed to cocaine during adolescence.

119 amine corticostriatal activity in adolescent mice exposed to cocaine in utero.

120 Mice exposed to cold fare considerably better at 05:00 (

121 Mice exposed to cold temperatures had increased levels o

122 ighly induced ATFs in thermogenic tissues of mice exposed to cold temperatures or treated with the be

123 s increased in the circulation of humans and mice exposed to cold.

124 Male ApoE(-/-) mice exposed to constant light had increased serum chole

125 cell and spinal cord slice cultures, and in mice exposed to control or EndoS-treated NMO-IgG.

126 C1q-Flox mice exposed to cranial RT showed no cognitive deficits

127 Neither CD4(+) nor CD8(+) T cells from donor mice exposed to CS alone are sufficient to cause inflamm

128 was acetylated and degraded in the lungs of mice exposed to CS and in patients with chronic obstruct

129 ze the activation of 2'-5' OAS in lungs from mice exposed to CS and viral pathogen-associated molecul

130 sGCalpha1(-/-) mice exposed to CS exhibited bronchial hyperresponsivene

131 (AM) obtained from RAGE null and C57BL/6 WT mice exposed to CS for one week or four months.

132 nd conventional natural killer (NK) cells in mice exposed to CS over 4 days and examined the contribu

133 Compared to wild-type mice exposed to CS, the number of total inflammatory cel

134 icroglia isolated from the frontal cortex of mice exposed to CUS show elevated CSF1 receptor expressi

135 were produced quickly in the lungs of naive mice exposed to cysteine proteases, such as bromelain an

136 on were evaluated in wild-type and Mdr2(-/-) mice exposed to darkness or melatonin treatment or in ma

137 ive abnormalities were prevented in DN-DISC1 mice exposed to Delta(9)-THC by simultaneous adolescent

138 Offspring of mice exposed to DEPs were hypersensitive to OVA, as indi

139 Mice exposed to desiccating stress showed hyperprolifera

140 s, eyelids from normal young and old mice or mice exposed to desiccating stress were evaluated by imm

141 mbrane conductance regulator (Cftr) knockout mice exposed to dextran sodium sulfate and in vitro in p

142 Beclin 1(+/-) mice exposed to doxorubicin were protected in terms of s

143 livers of long-lived Snell dwarf mice and in mice exposed to drugs that have been shown to extend lif

144 aily PZ-235 treatment of filaggrin-deficient mice exposed to dust mite allergens for 8 weeks signific

145 For instance, mice exposed to E. coli as neonates had increased locomo

146 ed histopathological signs of lung injury in mice exposed to E. coli.

147 We found that mice exposed to ECS for 54 wk developed lung adenocarcin

148 pocampal BDNF was detected in APPSWE /PS1dE9 mice exposed to EE, however, no changes were detected in

149 ole-genome microarray analysis of lungs from mice exposed to either 24 hours hypoxia or normoxia.

150 tent antidepressant-like effect in Ghsr-null mice exposed to either CSDS or caloric restriction, whil

151 Compared to HDM or DEP alone, mice exposed to either dose of DEP together with HDM dem

152 ree lung lavage were increased compared with mice exposed to either hyperthermia or LPS alone.

153 ned the effects of spontaneous withdrawal in mice exposed to either nicotine (6.3 or 18 mg/kg/day) or

154 rozygotes and wild type (Hhip (+/+)) C57/BL6 mice exposed to either room-air or CS for six months.

155 We found that mice exposed to either SE or LE showed persistent expans

156 donovani parasites were serially passaged in mice exposed to environmentally relevant concentrations

157 Our data indicate that female mice exposed to ES display a behavioral and physiologic

158 When compared with control mice, female mice exposed to ES displayed decreased social behavior a

159 eneration and adult synaptic dysfunctions in mice exposed to ethanol at P7.

160 icity and novel object recognition memory in mice exposed to ethanol at P7.

161 s potential role in synaptic dysfunctions in mice exposed to ethanol during early brain development i

162 onse curves were generated in naive mice and mice exposed to ethanol in a model of voluntary consumpt

163 on abnormalities in the neocortex of newborn mice exposed to ethanol in utero.

164 erefore the development of obesity in female mice exposed to excess fat energy.

165 eficient in IL-1beta and increased plaque in mice exposed to excess IL-1beta.

166 a was endogenously increased) and from young mice exposed to exogenous TNF-alpha exhibited significan

167 All CCL2(-/-)CX3CR1(GFP/GFP) mice exposed to extra-light ( approximately 800lux, 6 h/

168 Sidt2-deficient mice exposed to extracellular dsRNA, encephalomyocarditi

169 Tumors from Apc(Min/+) mice exposed to F. nucleatum exhibit a proinflammatory e

170 ects of ACVR2B/Fc on muscle and bone mass in mice exposed to Folfiri.

171 y study in which samples were collected from mice exposed to gamma radiation was analyzed.

172 In contrast, fecal extracts from mice exposed to gamma-HBCD contained multiple isomers of

173 s responsible for reduced longevity of dwarf mice exposed to GH treatment early in life.

174 In vivo, mice exposed to GMT, SB431542, and XAV939 for 2 weeks af

175 in insulin receptor mutant (Insr(P1195L/+)) mice exposed to HFD (Insr(P1195L/+)/HFD mice) revealed i

176 Gipr(-/-) offspring of mice exposed to HFD during IU/L became insulin resistant

177 RF1 in vivo and in vitro, whereas MuRF1(-/-) mice exposed to high CO2 did not develop muscle atrophy.

178 Mice exposed to high CO2 had decreased skeletal muscle w

179 Mice exposed to high levels of arsenic in utero have inc

180 dative cytosine modification accumulation in mice exposed to high-fat diet (HFD), injected with strep

181 Mice exposed to HOCl developed a diffuse cutaneous SSc w

182 Mice exposed to hours-long restraint or loud noise were

183 characterize the microbiota in intestines of mice exposed to hyperbaric oxygen, human rectal biopsy a

184 of autophagy in smooth muscle cells of young mice exposed to hyperlipidemia led to increased aortic P

185 ly, we reported that 14-week-old young adult mice exposed to hyperoxia as newborns had spatial and le

186 Nrf2-sufficient (wild type) newborn mice exposed to hyperoxia develop hypoalveolarization, w

187 a, and endothelial apoptosis in the lungs of mice exposed to hyperoxia.

188 significantly increased in lungs of neonatal mice exposed to hyperoxia.

189 revented alveolar simplification in neonatal mice exposed to hyperoxia.Conclusions: Cell therapy invo

190 d in human PAH, and the deletion of Arrb1 in mice exposed to hypoxia led to worse PAH with a loss of

191 ival curves and organ pathology in Ndufs4 KO mice exposed to hypoxia or hyperoxia.

192 terine arteries (UtA) isolated from pregnant mice exposed to hypoxia or normoxia from gestational day

193 ulation, miR410 is downregulated in lungs of mice exposed to hypoxia-induced pulmonary hypertension (

194 increased expression of miR-145 in wild-type mice exposed to hypoxia.

195 In SCD mice exposed to hypoxia/reoxygenation, oral administrati

196 did not affect BAL parameters alone in young mice exposed to i.t.

197 lls was drastically reduced in LCMV-infected mice exposed to IAP antagonists.

198 d to apoE(-/-) mice, while NZM and apoE(-/-) mice exposed to IFNalpha developed accelerated thrombosi

199 Control mice exposed to inhaled OVA showed no evidence of pulmon

200 ng injury and cellular apoptosis in C57BL/6J mice exposed to intratracheal LPS for 24 h.

201 In addition, female mice exposed to LAN increased central tendency in the op

202 Mice exposed to LAN on three consecutive nights increase

203 otection following BBT-059 administration in mice exposed to lethal and supralethal doses of total bo

204 n antisense morpholino increases survival of mice exposed to lethal total body irradiation.

205 lucose tolerance was measured in (nocturnal) mice exposed to light-dark stimulus patterns simulating

206 olated from wild-type and from Cftr-knockout mice exposed to lipopolysaccharide.

207 Patients, coworkers, and mice exposed to liquefied brain tissue had an autoantibo

208 nses in wild-type BALB/c and Il21r-deficient mice exposed to local airway challenge with house dust m

209 ven water with a high salinity compared with mice exposed to long days.

210 with their wild-type littermates, BAP1(+/-) mice exposed to low-dose asbestos fibers showed signific

211 e also measured these markers in midbrain of mice exposed to maternal immune activation (MIA) during

212 In vivo, using mice exposed to mechanical ventilation, we found that th

213 performed a global analysis on the brains of mice exposed to MeHg by magnetic resonance imaging, an i

214 ency and decreases in threshold in the IC of mice exposed to MeHg for 4 weeks compared with vehicle m

215 ion increased in skeletal muscles from young mice exposed to metabolic stress and in muscles from hea

216 : group 1, untreated mice (n = 15); group 2, mice exposed to metformin treatment (750 mg/kg/d) for th

217 In vivo, mice exposed to MI released IL-1alpha in the plasma, and

218 Mice exposed to microbes typically exhibit characterized

219 cortex (PFC) and nucleus accumbens (NAc) of mice exposed to multimodal chronic restraint stress.

220 label proteins, mostly expressed in BALf of mice exposed to nanoparticles.

221 ponsiveness in vivo among juvenile and adult mice exposed to neonatal hyperoxia.

222 at uric acid was increased in the airways of mice exposed to NO2 and that administration of uricase i

223 nvestigated colitis development in Il10(-/-) mice exposed to normal or 3SL-deficient milk during lact

224 Consistent with these effects, male mice exposed to nPM displayed alterations in the express

225 Additionally, mice exposed to OSPM exhibited significant decreases in

226 the risk of acute and subchronic toxicity to mice exposed to OSPW-OF at environmentally relevant conc

227 s infiltrating the respiratory epithelium of mice exposed to OVA or HDM.

228 In IL-1R KO mice exposed to OVA+SEB, attraction of CD4+ cells and pr

229 lammation was studied in IL-1R knockout (KO) mice exposed to OVA+SEB.

230 S1P levels remain unchanged in MC-deficient mice exposed to OVA.

231 of STAT6 to the promoter region of Muc5ac in mice exposed to OVA.

232 etion and levels of the muc5ac transcript in mice exposed to ovalbumin (OVA).

233 Mice exposed to ozone, a source of oxidative stress, had

234 BMDM from low fat-fed mice exposed to palmitate (PA) for 18 h ex vivo also sho

235 uring weight gain or loss in male and female mice exposed to PCB-77.

236 Mice exposed to phthalates in utero exhibit MNG inductio

237 We observed similar data in pregnant mice exposed to PI-based cART.

238 Coupled with increased FR response rates, mice exposed to postnatal CAPS displayed increased FR re

239 Mice exposed to ppDIO did not show altered mRNA expressi

240 We show that SNAP-25 deficient mice exposed to prenatal nicotine exhibit hyperactivity

241 Pancreata of KC mice exposed to radiation had a higher frequency of adva

242 Pancreata from mice exposed to radiation had fewer CD8(+) T cells than

243 Mice exposed to radiation plus PBS had increased interst

244 u-P responses were seen in WT and CRFR2 null mice exposed to repeated stress, which were sustained at

245 t, and very few differences were observed in mice exposed to rmTBI compared to controls.

246 g also caused slower weight gain compared to mice exposed to room air.

247 Mice exposed to S. pneumoniae prior to IAV do not mainta

248 In mice exposed to S. pneumoniae prior to IAV, the initial

249 in body weight between days 4 and 9, whereas mice exposed to SEB and also treated with abatacept show

250 ected in TNFR KO mice as well as in C57BL/6J mice exposed to SF but treated with TNF-alpha neutralizi

251 In addition, mice exposed to short days had higher VO(2) values when

252 Mice exposed to short, winter-like, light cycles showed

253 We recently showed that mice exposed to short-term (12 wk) E-cig smoke (ECS) sus

254 ysema and antigen-presenting cells (APCs) of mice exposed to smoke or nanoparticulate carbon black (n

255 n of interferon gamma, compared to wild-type mice exposed to smoke.

256 1c(+) lung antigen presenting cells (APC) of mice exposed to smoke.

257 in the small intestine compared to wild-type mice exposed to smoke.

258 ally identified DRN GABA and 5-HT neurons in mice exposed to social defeat, a model that induces long

259 ocial behavior in male and female California mice exposed to social defeat.

260 (15 nM) previously measured in the serum of mice exposed to social stress significantly increased pr

261 or antagonist, is antihyperalgesic in primed mice exposed to spinal administration of a D1/D5 agonist

262 When compared with control mice, mice exposed to stress displayed increased susceptibilit

263 behavioral and neurophysiological studies in mice exposed to stress or to intracerebroventricular inj

264 in the nucleus accumbens was reduced in all mice exposed to stress, whereas decreased myelin thickne

265 Mice exposed to TAC demonstrated a significant, longitud

266 d-type (TG), or KO background, and wild-type mice exposed to TAC.

267 ctic countermeasure and a mitigator in CD2F1 mice exposed to TBI.

268 systematically characterize CIPN recovery in mice exposed to the antitubulin cancer drugs eribulin, i

269 e alone, was significantly reduced by 22% in mice exposed to the combination.

270 ons of socially isolated versus group-housed mice exposed to the contextual fear conditioning test, e

271 tihistamine-resistant scratching behavior in mice exposed to the haptens, oxazolone and urushiol, the

272 hFVIII-specific antibodies and inhibitors in mice exposed to the live-attenuated measles-mumps-rubell

273 agmentation and increased sleep duration for mice exposed to the more robust light-dark pattern.

274 early demonstrated that P2X(7)(-/-) mice and mice exposed to the P2X(7) antagonist, brillian blue G,

275 Mice exposed to the pyrethroid pesticide deltamethrin du

276 In contrast, mice exposed to the same infection dose of ST306 or a pn

277 Mice exposed to the stressor had different microbial com

278 our bases and using DNA from liver tissue of mice exposed to the tobacco-specific nitrosamine 4-(meth

279 ne loss did not occur in homecage mice or in mice exposed to the training context alone.

280 the fate of CD8 T cells from transgenic TCR mice exposed to their cognate Ags as self or in the cont

281 pared to H(2)O and a novel odorant, vanilla, mice exposed to TMT in the home cage showed increased av

282 cotinine concentrations in serum samples of mice exposed to tobacco smoke for 12 or 24 weeks and fou

283 othesized that metabolites in the urine from mice exposed to total body radiation (TBI) would predict

284 e the auditory pathology of adult male CBA/J mice exposed to traumatic noise (2-20 kHz; 106 dB; 2 h).

285 T8-deficient hepatocytes and GLUT8-deficient mice exposed to trehalose resisted trehalose-induced AMP

286 showed that great-great-grandsons of female mice exposed to tributyltin (TBT) throughout pregnancy a

287 (DPOAE) to assess hearing recovery in FVB/nJ mice exposed to two different noise levels.

288 quencing to characterize DCs from skin LN of mice exposed to two different Th2 stimuli: the helminth

289 eolar lavage fluids (BALf) from male C57BL/6 mice exposed to ultrafine carbon black nanoparticles, a

290 Mice exposed to unpaired shocks showed a generalized red

291 h uninfected OVA-treated mice or OVA-treated mice exposed to UV-inactivated RSV.

292 two etiologically distinct models of autism: mice exposed to valproic acid in utero and Fmr1 knockout

293 zed lipidomics to analyze serum samples from mice exposed to various percentages of neutrons and X-ra

294 These lesions were extremely rare in mice exposed to vehicle control or filtered air.

295 detected, approximately 50% were altered in mice exposed to viable vs. HIC 48 h postexposure.

296 d increased Il4, Il13 and Il33 expression in mice exposed to viable vs. HIC.

297 c analysis was performed on lung tissue from mice exposed to virulent (Francisella tularensis ssp tul

298 imals and increased dramatically in allergic mice exposed to virus.

299 At 6 months, Abcc6(-/-) mice exposed to vitamin D and calcium supplementation de

300 on and assessed tumor formation in humanized mice exposed to wild-type virus and a viral mutant (Delt