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

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

4 By 67 weeks of age, mice exposed to 100% oxygen between postnatal days 1 to

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

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

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

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

11 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

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

13 illary acidic protein (GFAP)-EGFP transgenic mice exposed to 48 h of 80% oxygen from postnatal day 6

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

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

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

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

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

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

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

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

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

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

24 CXCR2 knockout mice exposed to a median lethal dose of acetaminophen ha

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

26 These responses were not observed in mice exposed to a nonassociative learning procedure.

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

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

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

30 We hypothesized that mice exposed to a similar diet would develop NASH with f

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

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

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

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

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

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

37 Mice exposed to acute levels of cigarette smoke exhibite

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

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

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

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

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

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

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

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

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

47 O(2)(.-) in SCG neurons from caspase 3-null mice exposed to an apoptotic stimulus.

48 we report that group V sPLA(2) (Pla2g5)-null mice exposed to an extract of house dust mite Dermatopha

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

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

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

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

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

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

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

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

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

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

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

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

61 Analysis of skin from wild-type and DKO mice exposed to BP for 6, 12, or 24 hours revealed a rel

62 Male deer mice exposed to BPA or ethinyl estradiol (EE) through ma

63 Mice exposed to brief uncontrollable stress showed impai

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

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

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

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

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

69 Furthermore, CCR2 knockout mice exposed to chitin had diminished reactive oxygen sp

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

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

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

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

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

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

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

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

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

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

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

81 Mice exposed to chronic intermittent ethanol (CIE) vapor

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

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

84 locked the expression of social avoidance in mice exposed to chronic social defeat and concurrently p

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

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

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

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

89 Gene expression profiling of Rora-null mice exposed to cigarette smoke demonstrated enrichment

90 Mice exposed to cigarette smoke developed emphysema with

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

92 Mice exposed to cigarette smoke for 4 weeks demonstrated

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

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

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

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

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

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

99 in human emphysematous lungs and in lungs of mice exposed to cigarette smoke.

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

101 al Na(+) channels (ENaC) by measuring AFC in mice exposed to Cl(2) (0-500 ppm for 30 min) and Na(+) a

102 Mice exposed to cNIC exhibited long-term potentiation in

103 Islet allografts from donor mice exposed to CO are protected from immune rejection a

104 TCRalpha(-/-) mice exposed to CO or treated with the pharmacologic HO-

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

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

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

108 trating increased monocyte transmigration in mice exposed to cocaine, which was attenuated by pretrea

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

110 Mice exposed to cold temperatures had increased levels o

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

112 lls were measured in the peripheral blood of mice exposed to concentrated particles from ambient air

113 s studies, we detected increased toxicity in mice exposed to continuous light.

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

115 Mice exposed to CPZ for 2 and 3 weeks displayed more cli

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

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

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

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

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

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

122 xaggerated inflammatory response in lungs of mice exposed to CS.

123 ve pulmonary disease, as well as in lungs of mice exposed to CS.

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

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

126 of Notch1 signaling in vivo was validated in mice exposed to DAPT, which failed to demonstrate barrie

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

128 TG mice exposed to DDC for 4 weeks followed by 2 days of no

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

130 Mice exposed to desiccating stress showed hyperprolifera

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

132 noclonal antibody to sclerostin (Scl-AbI) in mice exposed to dexamethasone (DEX).

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

134 Similarly, colonic mucosal tissues from mice exposed to dextran sulfate sodium showed histone H3

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

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

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

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

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

140 creased in silica-exposed mice compared with mice exposed to either Al(2)O(3) or saline beginning 3 w

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

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

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

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

145 cteria up to 5 days after infection, whereas mice exposed to elastase, LPS, or PBS cleared all bacter

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

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

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

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

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

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

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

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

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

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

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

157 Sidt2-deficient mice exposed to extracellular dsRNA, encephalomyocarditi

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

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

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

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

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

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

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

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

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

167 Mice exposed to high CO2 had decreased skeletal muscle w

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

169 pathy (OIR) was used to analyze retinas from mice exposed to high oxygen or room air to evaluate the

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

171 Mice exposed to HOCl developed a diffuse cutaneous SSc w

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

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

174 o, and in alveolar macrophages isolated from mice exposed to hyperoxia (100% oxygen).

175 Similarly, adult mice exposed to hyperoxia as neonates display alveolar s

176 Alveolar macrophages isolated from Nrf2(-/-) mice exposed to hyperoxia displayed persistent oxidative

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

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

179 would improve survival in P. murina-infected mice exposed to hyperoxia.

180 Fas-Fas ligand pathway in P. murina-infected mice exposed to hyperoxia.

181 smooth muscle cells of pulmonary vessels of mice exposed to hypoxia and rats challenged with MCT in

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

183 In NY1DD mice exposed to hypoxia-reoxygenation, treatment with AT

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

185 d pulmonary fibrosis seen in A(2B)R knockout mice exposed to i.p. bleomycin.

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

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

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

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

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

191 To this end, Balb/c mice exposed to light damage were treated with rapamycin

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

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

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

195 ation increase dramatically in the hearts of mice exposed to load-induced cardiac stress.

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

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

198 rs of DNA damage and DNA damage responses in mice exposed to low dose-rate radiation to reveal potent

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

200 rkdc/SCID) (severe combined immunodeficient) mice exposed to low-dose radiation.

201 phage-specific LITAF-deficient (macLITAF-/-) mice exposed to LPS have a delayed onset in the serum le

202 were observed in airway epithelial cells of mice exposed to LPS or cigarette smoke and of patients w

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

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

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

206 Mice exposed to microbes typically exhibit characterized

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

208 irway epithelium and was reduced in lungs of mice exposed to neonatal hyperoxia.

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

210 a suggest that loss of BMP signaling in aged mice exposed to neonatal oxygen is associated with a sho

211 pho-Smad1/5/8 were reduced in lungs of aging mice exposed to neonatal oxygen.

212 In addition, DC subsets isolated from mice exposed to nicotine produced significantly less cyt

213 Strikingly, adult mice exposed to NIMA accepted permanently K(b+) heart al

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

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

216 Additionally, mice exposed to OSPM exhibited significant decreases in

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

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

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

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

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

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

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

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

225 al barrier, and this effect was abrogated in mice exposed to PDGF-BB neutralizing antibody, thus unde

226 Treatment of mice exposed to phototoxic doses of light with NACA main

227 Mice exposed to phthalates in utero exhibit MNG inductio

228 rdiopulmonary resuscitation (CA/CPR) in male mice exposed to physiological vs. pharmacological doses

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

230 Surprisingly, we find that knockout mice exposed to PO induced by thoracic aortic constricti

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

232 ink was further confirmed in MMP-9-deficient mice exposed to PPARalpha or PPARgamma agonist and injec

233 Mice exposed to ppDIO did not show altered mRNA expressi

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

235 wild-type mice in basal conditions, knockout mice exposed to pressure overload developed less hypertr

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

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

238 Mice exposed to radiation plus PBS had increased interst

239 long-term repopulating activity of HSCs from mice exposed to recombinant NXPH1.

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

241 e in hippocampus was dramatically reduced in mice exposed to repeated swim, a stimulus known to activ

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

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

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

245 In mice exposed to septic stress induced by cecal ligation

246 trate that Saa3 is expressed in the lungs of mice exposed to several mixed Th2/Th17-polarizing allerg

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

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

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

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

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

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

253 1c(+) lung antigen presenting cells (APC) of mice exposed to smoke.

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

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

256 (15 nM) previously measured in the serum of mice exposed to social stress significantly increased pr

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

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

259 nt (Nrf2(-/-)) but not wild-type (Nrf2(+/+)) mice exposed to sublethal hyperoxia succumbed to death d

260 ymorphonuclear leukocytes recovered from the mice exposed to SWCNT and MWCNT (1.2 x 10(6) +/- 0.52 an

261 Mice exposed to TAC demonstrated a significant, longitud

262 Conversely, we observed that mice exposed to the 2009 H1N1 virus were protected again

263 uoxetine or desipramine restores learning in mice exposed to the aberrant light cycle, suggesting tha

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

265 hils from vitamin D sufficient and deficient mice exposed to the chemoattractants, KC/CXCL1 and C5a,

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

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

268 yocytes from Kv1.3(/) mice or from wild-type mice exposed to the Kv1.3 blocker margatoxin completely

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

270 n neutropenic animals than in nonneutropenic mice exposed to the microorganism.

271 Gstp(-/-)/Tg.AC mice exposed to the proinflammatory phorbol ester 12-O-t

272 Mice exposed to the pyrethroid pesticide deltamethrin du

273 However, polysomnographic recording in mice exposed to the shifting schedule revealed no sleep

274 Mice exposed to the stressor had different microbial com

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

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

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

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

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

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

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

282 we recorded mPFC and hippocampal activity in mice exposed to two anxiogenic arenas.

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

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

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

286 Mice exposed to unpaired shocks showed a generalized red

287 the rhythmicity of repair rate, we find that mice exposed to UV radiation (UVR) at 4:00 AM display a

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

289 Using skin tissue from C57BL/6 mice exposed to UVB radiation, we demonstrate that MnSOD

290 ncer (invasive squamous cell carcinoma) than mice exposed to UVR at 4:00 PM.

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

292 ive PDAC (P < .005, chi2 test; compared with mice exposed to vehicle).

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

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

295 mmatory markers were found in hypothyroid WT mice exposed to VILI compared with euthyroid mice, indic

296 Mice exposed to VILI recapitulated the serum TH findings

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 epithelial cell proliferation in tongues of mice exposed to whole-body irradiation.

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