ライフサイエンスコーパス: mice inoculated with

1 ble to growth shift caused 100% mortality in mice inoculated with 10 parasites.

2 The majority of RHAbeta-/- mice inoculated with 10(4) PFU of attenuated Mengo virus

3 doses, but day 3 titers in the pancreases of mice inoculated with 10(4) PFU were reduced.

4 Within 72 h all mice inoculated with 10(6) CFU of the parental C. albica

5 The majority of mice inoculated with 10(8) CFU of S. aureus maintained n

6 routinely observed in RNase L(-/-) PKR(-/-) mice inoculated with 10(8) PFU of VVDeltaE3L, with a dis

7 In nude mice inoculated with 1205 Lu melanoma cells, a preventiv

8 ected (100%) from rotavirus challenge, while mice inoculated with 2/6-VLPs mixed with CT showed a mea

9 All mice inoculated with 2/6-VLPs mixed with LT and LT-R192G

10 Mice inoculated with 2/6-VLPs with LT produced significa

11 from wild-type and anchorless PrP transgenic mice inoculated with 22L, 79A and/or RML scrapie strains

12 In vivo studies on mice inoculated with 32D-T315I cells and treated with 2j

13 , CpG ODN alone had no effect on survival of mice inoculated with 38C13 cells.

14 trating leukocytes (TIL) in all but 5 of 148 mice inoculated with 39 different biopsy tissue specimen

15 etastasis to the lung, liver, and sternum of mice inoculated with 4T07 cells in vivo.

16 MSC levels remain elevated in mice inoculated with 4T1/IL-1beta even after the primary

17 In mice inoculated with 5 x 10(5) IFU, spread of C. pneumon

18 sessed in a syngeneic murine model (C57BL/6J mice inoculated with 5 x 10(6) ID8-Luc cells/mouse).

19 In a prospective study, mice inoculated with a B. burgdorferi clinical isolate g

20 2 or IFN-gamma cleared rVV more rapidly than mice inoculated with a control rVV and developed only lo

21 we demonstrate that germ-free adult pregnant mice inoculated with a gut microbial community shaped by

22 ivered it directly into the lungs of C57BL/6 mice inoculated with a lethal dose of Klebsiella pneumon

23 with trophic forms compared to responses in mice inoculated with a mixture of trophic forms and cyst

24 Mice inoculated with a nontarget microRNA control ZIKV d

25 Mice inoculated with a single dose of rVSV-VP1 through i

26 In vivo experiments with Ab94 in K18-hACE2 mice inoculated with a stringent dose of 100,000 PFU of

27 d melanocyte destruction only in the skin of mice inoculated with a vaccinia virus encoding mouse TRP

28 Most importantly, mice inoculated with a VACV expressing the IFN-gamma gen

29 ckdown by free uptake in cell culture and in mice inoculated with A431 tumor xenografts (EGFR amplifi

30 eta amyloid plaques in the brains of bigenic mice inoculated with Abeta42 prions prepared in the pres

31 ed in severe combined immunodeficient (SCID) mice inoculated with activated hPBMCs in Matrigel.

32 is comparable to the 60% survival rate among mice inoculated with an attenuated rabies vaccine strain

33 e mouse colonization model, only 1 out of 23 mice inoculated with an SOD-deficient mutant of a mouse-

34 use model of GBS vaginal colonization, where mice inoculated with an Srr-1-deficient mutant exhibited

35 We show that mice inoculated with attenuated plasmid-cured strains of

36 fied recombinant YajC protein indicated that mice inoculated with B. abortus 19 or 2308 or B. meliten

37 nd deformation of the tails were observed in mice inoculated with B. abortus S19 but not in those ino

38 In contrast, mice inoculated with B. abortus S19DeltavjbR did not sho

39 K18-hACE2 transgenic mice inoculated with B.1.617.2 and receiving intranasall

40 -105972 treatment increased the life span of mice inoculated with B16 melanoma, P388 leukemia, and Ad

41 nsferred OT-1 CD8(+) T cells in the VPLNs of mice inoculated with B16-OVA TP-DCs.

42 e formation of tumor nodules in the lungs of mice inoculated with B16BL6 melanoma or Lewis lung carci

43 ides significantly increased the survival of mice inoculated with B16F10, TC-1, or MC38 tumors, respe

44 r substantially extended the survival of the mice inoculated with BaF3/NPM-ALK WT cells but not those

45 All lethally irradiated BALB/c mice inoculated with BCL1 cells and T-cell-depleted bone

46 pulmonary metastasis in BF10 mice or in BF1 mice inoculated with BF10-Th2 cells decreased to the lev

47 iod of approximately 100 d, whereas the same mice inoculated with brain homogenates from spontaneousl

48 e of interleukin (IL)-4 and IL-10, or normal mice inoculated with burn-associated type 2 T cells.

49 d with the IL-4/IL-10 mixture, and d) normal mice inoculated with burn-associated type 2 T cells.

50 deer mice and all hamsters and Swiss Webster mice inoculated with CA9 seroconverted.

51 n sections of lung and trachea from rats and mice inoculated with CAR bacillus isolates known to cont

52 erythema (rash) in comparison with humanized mice inoculated with cell culture medium only.

53 Mice inoculated with chimeric L1-CCR5 particles generate

54 e response was observed in all the groups of mice inoculated with chlamydial antigens.

55 In addition, after mating, the mice inoculated with COMC were found to have fertility r

56 and microvessel density was also reduced in mice inoculated with constitutively overexpressing PEDF

57 inflammatory cytokine production compared to mice inoculated with control ZIKV.IMPORTANCE Myeloid cel

58 s detected in the brains and spinal cords of mice inoculated with coronavirus and sacrificed at 4, 42

59 However, all SCIDbgMN mice inoculated with CP-PMN alone or resident Mphi alone

60 (C3H-scid) mice, but not immunocompetent C3H mice, inoculated with cultured B. burgdorferi, tick-born

61 Mice inoculated with CVB3-PL2-Ad2L1 demonstrated a brief

62 l of CVB3-binding serum immunoglobulin G1 in mice inoculated with CVB3-PL2-mIL4/46.

63 pathic CVB3 was also isolated from hearts of mice inoculated with CVB3.

64 of susceptible SJL/J (H-2s) and B10.S (H-2s) mice inoculated with DAL*-1.

65 Mice inoculated with live, but not mice inoculated with dead, chlamydial organisms produced

66 The survival rate of mice inoculated with Deltagra2 was significantly higher;

67 In contrast, sera from mice inoculated with DNA expressing Env-C3d protein trim

68 , mortality was reduced by more than half in mice inoculated with E. coli exposed to cranberry proant

69 ole cecal tissue and of isolated crypts from mice inoculated with E. histolytica.

70 and, blood specimens serially collected from mice inoculated with E. risticii Ohio 380, and blood and

71 159V were significantly higher than those of mice inoculated with EgCME-WT.

72 and gammadelta T cells prolonged survival of mice inoculated with either human bladder cancer or fibr

73 PrP(Sc)) in the skeletal muscle of wild-type mice inoculated with either the Me7 or Rocky Mountain La

74 tes recovered from gamma interferon knockout mice inoculated with emergent tachyzoites grew at a slow

75 likely to become systemically infected than mice inoculated with environmental strains (P < 0.01).

76 Mice inoculated with epidemic strains were significantly

77 hu-HSC-transplanted NOD/SCID/gamma(c)(null) mice inoculated with equivalent high-titer HIV-1(JR-CSF)

78 In contrast, mice inoculated with GFP alone or a combination of wild-

79 Furthermore, mice inoculated with Gli2-Rep-expressing cells exhibited

80 observed in all less-than-48-hour-old BALB/c mice inoculated with greater than 2 x 10(5) R7 focus-for

81 HIF-1(Deltamyel) mice inoculated with H. pylori for 6 mo presented with a

82 Mice inoculated with H7 parasites formed significantly f

83 asally inoculated with HA-KO/PspA virus, and mice inoculated with HA-KO/PspA virus were completely pr

84 Although mice inoculated with hamster scrapie do not develop clin

85 ter cross-species infection using a model of mice inoculated with hamster scrapie strain 263K.

86 Healthy chimeras (SCID mice inoculated with healthy donor PBMC) treated with an

87 C57BL/6 mice inoculated with Helicobacter felis develop gastriti

88 Cecal, but not colonic, pathology in C57BL/6 mice inoculated with Helicobacter hepaticus plus anti-IL

89 We report that Nod2-deficient mice inoculated with Helicobacter hepaticus, an opportun

90 s 6 h after infection did not differ between mice inoculated with hemolysin-expressing strains and th

91 omparisons were made between male and female mice inoculated with herpes simplex virus type 1 (HSV-1)

92 Accelerated tumour growth over 28 days in mice inoculated with hFcRn-expressing HT-29 human colore

93 viruses caused weight loss and death in some mice inoculated with high virus doses.

94 viremia and HIV infection in thy/liv-SCID-hu mice inoculated with HIV-1(59) was inhibited by acute tr

95 in the prevention of bilateral retinitis in mice inoculated with HSV-1 through the anterior chamber

96 In a tumor xenograft model using SCID mice inoculated with Huh7 cells, administration of GANT6

97 nts metastasis, and prolongs the survival of mice inoculated with human prostate cancer cell lines an

98 Nude mice inoculated with human prostate tumor cells secretin

99 Histological examination of tissues from mice inoculated with HVP2nv isolates showed extensive ne

100 ant against the infection, although the same mice inoculated with irradiated mouse MLNM (I-MLNM) died

101 We find no instances of reversion in mice inoculated with K33S rCan.

102 In vivo antitumor efficacy studies using mice inoculated with KB cells demonstrate significantly

103 100% of mice inoculated with KFV101 survive, compared with 20% o

104 mproved survival and reduced tumor growth in mice inoculated with KIR3DL2(+) tumors.

105 other proinflammatory, type 1 cytokines than mice inoculated with L. major alone within the first 48

106 s of lung tissue demonstrated that while A/J mice inoculated with L. pneumophila alone develop multif

107 survival of severe combined immunodeficiency mice inoculated with LCLs.

108 quence of virus recovered from brain of SCID mice inoculated with LGT mutants identified sites in the

109 s also detected in brain tissue of ovine PrP mice inoculated with limiting dilutions (endpoint titrat

110 Wild-type mice inoculated with Listeria monocytogenes intravenousl

111 day 42, RSV RNA remained detectable only in mice inoculated with live or UV light-treated RSV.

112 tivity (AHR) were significantly increased in mice inoculated with live RSV.

113 culture and PCR were significantly higher in mice inoculated with live RSV.

114 Mice inoculated with live, but not mice inoculated with

115 ere performed on thymocytes from preleukemic mice inoculated with M-MuLV and Mo+PyF101 M-MuLV.

116 edius-inoculated mice (P < 10-6), and 75/104 mice inoculated with M. oralis mixed with S. intermedius

117 mmunoglobulin G was detectable in all of the mice inoculated with M. pneumoniae and was inversely cor

118 At 530 days, however, 78% of the mice inoculated with M. pneumoniae demonstrated abnormal

119 recombinant viruses, immunocompetent BALB/c mice inoculated with mammary adenocarcinoma exhibited pr

120 ombined GITR and IL23R antibody treatment of mice inoculated with MC38 tumors resulted in robust and

121 Mice inoculated with MDA-MB-231 cells developed osteolyt

122 strated significant in vivo efficacy in nude mice inoculated with MiaPaCa-2, a human pancreatic tumor

123 nd mtrE mutants, but not a farB mutant, from mice inoculated with mutant or wild-type gonococci was r

124 Mice inoculated with mutant parasites were not protected

125 bone marrow DCs isolated from Tlr9-deficient mice inoculated with Mycobacterium antigen expressed low

126 Severely immunodeficient mice inoculated with myeloid-restricted ZIKV did not dem

127 Mice inoculated with myeloid-restricted ZIKV had a decre

128 pecific DO11.10 T cells in recipient IL-4-/- mice inoculated with N. brasiliensis plus OVA.

129 Relative to mice inoculated with nontransduced dendritic cells, sple

130 Irradiated mice inoculated with normal mouse MLN macrophages (M) we

131 STAT5-DNM survived significantly longer than mice inoculated with NPM/ALK+ cells infected with the em

132 Infant Swiss Webster mice, inoculated with NVAV by the intraperitoneal route,

133 e-causing PrP isoforms in Tg(BoPrP)Prnp(0/0) mice inoculated with nvCJD and BSE brain extracts were i

134 heart, liver, and lungs were collected from mice inoculated with one of three C. albicans strains (S

135 comparable between OX40L(+/+) and OX40L(-/-) mice inoculated with OVA and H. polygyrus.

136 of IL-4 and IL-5, but inhibited IFN-gamma in mice inoculated with ova.

137 Mice inoculated with ovalbumin served as a negative cont

138 culture, while 83% (40 of 48) of the control mice inoculated with ovalbumin were culture positive (P

139 rage number of IFU per mouse detected in the mice inoculated with ovalbumin, CpG, and alum.

140 ponses to P. aeruginosa We found that female mice inoculated with P. aeruginosa died earlier and show

141 For mice inoculated with P. carinii, an ELISPOT assay was us

142 iNOS(-/-) mice inoculated with P. gingivalis developed skin lesion

143 V-infected human volunteers, as well as from mice inoculated with packaged Venezuelan equine encephal

144 tension of lifespan in transgenic human PRNP mice inoculated with pathogenic human prion isolates rep

145 e; iNOS mRNA was comparable in scid mice and mice inoculated with PBS but was 6-fold higher in CD4 ce

146 ctively reduced PCa tumor size and weight in mice inoculated with PC3 PCa cells.

147 ic micrometastasis were compared between the mice inoculated with PEDF-overexpressing tumor cells and

148 id (severe combined immunodeficiency [SCID]) mice inoculated with peripheral blood lymphocytes from E

149 All of SCIDbgMN mice inoculated with peritoneal macrophages (PMphi) from

150 tomorphometry was 9-fold greater in chow-fed mice inoculated with Pg than in noninoculated mice (P<0.

151 C are present in the draining lymph nodes of mice inoculated with PGE(2) receptor agonists, compared

152 Bronchoalveolar lavage fluids from mice inoculated with phosphate-buffered saline (PBS) or

153 in severe combined immunodeficiency disease mice inoculated with phytohemoagglutinin-activated human

154 ted pathogen spread systemically in the same mice inoculated with PMN from thermally injured mice (TI

155 th E. faecalis or MRSA, whereas all SCIDbgMN mice inoculated with PMphi from mild SIRS mice survived

156 BALB/c mice inoculated with pmrA and pmrHFIJKLM mutant strains

157 Gnotobiotic mice inoculated with PSC-derived microbiota exhibited T

158 The mortality of CF mice inoculated with Pseudomonas-laden beads was signifi

159 ed immunosorbent assay, and NMR studies that mice inoculated with PVY develop antibodies that bind to

160 Synthetic prions recovered from transgenic mice inoculated with recPrP amyloid displayed structural

161 with cyclosporine, prolonged the survival of mice inoculated with renal cancer cells or T24 human bla

162 We confirmed these findings in mice inoculated with reovirus, as well as in donor-deriv

163 with which they were immunized, but only the mice inoculated with replicon particles expressing the G

164 E. faecalis spread systemically in SCIDbgMN mice inoculated with resident Mphi and TI-PMN, while all

165 In contrast, cells from C57BL/6 mice inoculated with rhsp60 responded to all fragments b

166 Retinal samples from mice inoculated with RML scrapie were collected at 30, 6

167 ion, we measured their levels in brains from mice inoculated with Rocky Mountain Laboratory (RML) pri

168 gic changes was similar to that found in FVB mice inoculated with Rocky Mountain Laboratory (RML) pri

169 In contrast, mice inoculated with rVSV-G1670A and -G1672A, which are

170 Moreover, we demonstrated that mice inoculated with rVSV-VP1 triggered a comparable lev

171 Importantly, gammadelta T cell-deficient mice inoculated with S. aureus and treated with a single

172 Mice inoculated with S. aureus strains containing the pu

173 h of SAFV-2 in rodent cells in vitro, BALB/c mice inoculated with SAFV-2 showed antibody titers of >1

174 Mice inoculated with samples from the affected patients

175 elity was maintained in Tg(HuPrP,V129,A224V) mice inoculated with sCJD VV2 or MM1 prions, despite the

176 C57BL10 and IRW mice inoculated with scrapie brain developed clinical sc

177 Tg(C1) mice inoculated with scrapie prions remain healthy and d

178 IL-1Ra-deficient or overexpressor transgenic mice inoculated with scrapie, neither loss nor overexpre

179 ation of the antibody was accelerated in the mice inoculated with sgp120-mC3d(3)-DNA.

180 wed a delayed mammary tumor growth in Balb/c mice inoculated with sh-a2 4T-1 cells compared with cont

181 Ascended infection occurred in 17 to 20% of mice inoculated with strain FA1090.

182 uppressive phenotype in vitro, mirn23a (-/-) mice inoculated with syngeneic tumor cells had worse out

183 Administration of 1 to Balb/C mice inoculated with syngenic meth/A cells demonstrated

184 All mice inoculated with the A12-P1 deopt mutant developed a

185 Mice inoculated with the Arctic AD sample exhibited a pa

186 After infection mice inoculated with the CAM/RB strain developed hind li

187 Hamsters and K18-hACE2 transgenic mice inoculated with the complementation-derived virions

188 culation, there was a difference between the mice inoculated with the control IgG-treated inoculum an

189 ed with KFV101 survive, compared with 20% of mice inoculated with the ctxAB mutant.

190 However, mice inoculated with the Deltacahk1 null strain survived

191 e lung tissue appeared essentially normal in mice inoculated with the Deltalpp mutant of CO92 and giv

192 tion of Ad.DF3.BAX was also assessed in nude mice inoculated with the DF3-positive 36M2 human ovarian

193 rtality and delay in the onset of illness in mice inoculated with the double-mutant strain, which was

194 Mice inoculated with the formyl peptide-producing wild-t

195 ulation and persisted for at least 5 days in mice inoculated with the highest dose of virus (10(7) PF

196 sed to treat severe combined immunodeficient mice inoculated with the human prostate cancer line PC-3

197 tly, in vivo administration of IGF-I in SCID mice inoculated with the OPM-2 line led to approximately

198 Strikingly, mice inoculated with the ORF3null virus displayed no fec

199 olitis, and death were noted in 12-month-old mice inoculated with the palm civet HC/SZ/61/03 strain o

200 colonize mouse stomachs, whereas 78% of the mice inoculated with the parent strain became H. pylori

201 Within 72 h all mice inoculated with the parental C. albicans strain had

202 and tissue virus burdens resembling those of mice inoculated with the parental SPYF-MN virus.

203 However, mice inoculated with the prfA mutant did not exhibit sys

204 Mice inoculated with the recombinant virus were unaffect

205 In mice inoculated with the RML strain of prions, anle138b

206 BALB/c EP2 knockout mice inoculated with the spontaneously metastatic BALB/c

207 a pathology that could be distinguished from mice inoculated with the Swedish or sporadic AD samples,

208 lls, C57Bl/KaLwRij immunocompetent syngeneic mice inoculated with the VLA4-null clones showed prolong

209 diated immune responses were detected in the mice inoculated with the vortexed MOMP.

210 suffered from fewer neoplastic lesions than mice inoculated with the wild type form of E. coli NC101

211 Of 12 mice inoculated with the wild type, all contained H. pyl

212 on of the spleen and liver, as was noted for mice inoculated with the wild-type parent strain.

213 ecame H. pylori positive, while 15 out of 17 mice inoculated with the wild-type strain were shown to

214 synovial tissue was significantly higher in mice inoculated with the wild-type strain.

215 Fewer mice inoculated with the wild-type virus survived in com

216 hile <20 colonies were detected in mice (BF1 mice) inoculated with the same number of B16F1 cells.

217 Moreover, mice inoculated with these detoxified strains were prote

218 , and neuropathological analysis showed that mice inoculated with these samples maintained strain-spe

219 Antibodies from mice inoculated with these strains recapitulated the spe

220 onses previously observed in immunocompetent mice inoculated with trophic forms compared to responses

221 High levels of human Ig in the sera of mice inoculated with tumor biopsy tissue are associated

222 In mice inoculated with tumor cells intraperitoneally (ip),

223 Injection of human apoA1 into A1KO mice inoculated with tumor cells remarkably reduced both

224 rthritis was observed in only 25 of 60 (42%) mice inoculated with two of these B. burgdorferi strains

225 Studies of mice inoculated with UTI89, a sequenced isolate, have re

226 Immunodeficient SCID mice inoculated with VACVs not expressing IFN-gamma demo

227 ivative) were assayed using splenocytes from mice inoculated with various BCG recombinants.

228 ng infection, or nasal carriage in nonimmune mice inoculated with virulent pneumococci.

229 nfection using wild-type and IL-10-deficient mice inoculated with virulent serotype 2 of the RF spiro

230 titers and greater weight loss compared with mice inoculated with virus alone.

231 Mice inoculated with virus containing an arginine at thi

232 In the present study, BALB/cJ mice inoculated with virus-containing plasma from affect

233 ed to high levels in thymic lymphocytes from mice inoculated with virus.

234 Mice inoculated with VRP-NV2 elicited reduced systemic a

235 BALB/c mice inoculated with VV at sites of Th2-biased allergic

236 at 21 weeks postinoculation, the livers from mice inoculated with wild type exhibited moderate lobula

237 In contrast, C3H mice inoculated with wild-type Ad recognized an epitope

238 rred normally during the primary response in mice inoculated with wild-type or SpA-deficient S. aureu

239 l immune responses were detected in infected mice inoculated with wild-type SS1, but not with SS1::08

240 ent furanoallocolchicinoid 10c using C57BL/6 mice inoculated with Wnt-1 tumor cells indicated signifi

241 serum collected at various time points from mice inoculated with WNV.

242 ere identified in the CNS of SJL/J and B10.S mice inoculated with wt-DA.

243 ecreased bone metastases and tumor burden in mice inoculated with ZR-75-1 cells.