ライフサイエンスコーパス: inoculation

1 erent carbon sources in comparison to single inoculation.

2 when delivered to the oviduct by intrabursal inoculation.

3 t to three partial thickness wounds prior to inoculation.

4 wheat bran particles after 20 and 40 h post inoculation.

5 ted hemoglobin (P = 0.004) by MSOT 2 d after inoculation.

6 matode infected plants at 0, 3, 7 days after inoculation.

7 d a >100-fold increase in VA1 RNA 72 h after inoculation.

8 f SIV (mac239) infection 48 hr after vaginal inoculation.

9 ble in rodents and primates by intracerebral inoculation.

10 24 hours before and 2 hours after each virus inoculation.

11 l activation or T cell homing to the site of inoculation.

12 duced infectivity in C3H/HeN mice via needle inoculation.

13 wing either intraperitoneal or intramuscular inoculation.

14 and dry weight) were measured 35 days after inoculation.

15 ever, Treg cell numbers collapsed after LCMV inoculation.

16 ted hemoglobin (P = 0.004) by MSOT 2 d after inoculation.

17 educed water-soaking symptoms at the site of inoculation.

18 ephalitis in Irf2(-/-) mice after peripheral inoculation.

19 macaques 3 days following an intrarectal SIV inoculation.

20 5.2(b) expression is induced after bacterial inoculation.

21 e donors for 24 hours during days 3-10 after inoculation.

22 ice were euthanized 6 wk after the last oral inoculation.

23 opulation of neurons following sciatic nerve inoculation.

24 ower genital tract following an intravaginal inoculation.

25 large, as is the case with direct intranasal inoculation.

26 and 35 days after experimental pneumococcal inoculation.

27 uniformly fatal disease following intranasal inoculation.

28 le in determining the plant response to PGPR inoculation.

29 noculated barley plants 4 weeks after fungal inoculation.

30 addition of polyethylene glycol (PEG) during inoculation.

31 d with S. intermedius (P < 10-6) 7 days post-inoculation.

32 astrointestinal tract following intravaginal inoculation.

33 aximal decrease in FEV1 during 10 days after inoculation.

34 18)F-FDS or (18)F-FDG from days 1 to 4 after inoculation.

35 following experimental oral or intracranial inoculation.

36 25] = -5.98% [SE, 8.56%]) or symptoms after inoculation.

37 inobenzidine (DAB) stain 72h after bacterial inoculation.

38 placebo (n = 4) groups, respectively, after inoculation.

39 issemination to distant tissues after needle inoculation.

40 ly but replicate well following intracranial inoculation.

41 <0.05) between co-inoculation and sequential inoculation.

42 (SA) in the SV-treated plants after pathogen inoculation.

43 letely inhibited teratoma formation from ESC inoculations.

44 emphasized potential sources of endovascular inoculations.

45 infection by mosquito bite than needle-based inoculations.

46 ith a disruption in avrBs2 gene was used for inoculations.

47 an +/- SD) vs. 0.58 +/- 0.51; P < 0.001) and Inoculation (6.7 +/- 5.1 vs. 0.92 +/- 0.39; P < 0.001) g

48 and wild-type (WT) C57Bl6-B.129 mice by oral inoculation 9 times with 10(9) colony-forming units of P

49 Following intravaginal inoculation, a C. muridarum strain deficient in plasmid-

50 Six or 7 d after virus inoculation, a dynamic (11)C-PBR28 or (R)-(11)C-PK11195

51 Two weeks after tumor inoculation, a dynamic (18)F-FHNP PET scan with arterial

52 By 24 hr following inoculation, a proinflammatory signature that lacked ant

53 ngly, treating plants with putrescine before inoculation accelerated wilt symptom development and R.

54 Groups of thirty whiteflies given a 24 h of inoculation access period (IAP) to inoculate CCYV on cuc

55 the leaves of plants 3h after the E. cloacae inoculation, according to a mechanism involving endogeno

56 Aside from delivering fixed N, how does inoculation affect legume N concentrations?

57 Five to six weeks after inoculation, all mice were scanned with small-animal PET

58 The inoculation amount had a positive influence on the pheno

59 More inoculation amount leads to faster ethanol formation and

60 cal practices (temperature, flipping and the inoculation amount of newly selected yeast F-78 from thi

61 nance (MR) images were obtained 9 days after inoculation and 2 hours and 5 days after treatment.

62 ginsenoside Ro followed by HT29 intravenous inoculation and 40-day oral ginsenoside Ro significantly

63 nts of the inflammasome, both at the site of inoculation and at early sites of distal virus spread.

64 collected serial blood samples shortly after inoculation and daily for 8 days.

65 ividually substituted segments after in vivo inoculation and found no mutations, suggesting that PH1N

66 creased P. gingivalis colonization following inoculation and increased periodontal disease susceptibi

67 nti-C5 i.p. on day 3 or 6 after intragastric inoculation and monitored for clinical signs of disease

68 the remaining 2 vials received no C albicans inoculation and no antifungal supplementation (negative

69 ues at 1, 3, 7, and 14 days after penile SIV inoculation and quantified the levels of unspliced SIV R

70 not differ significantly (p<0.05) between co-inoculation and sequential inoculation.

71 Analysis (PCA), the inoculation sequence (co-inoculation and sequential) has impacts on volatile comp

72 accumulation already displayed 4 weeks after inoculation and shoot biomass deficiency, which is detec

73 wed noticeable lung infection on day 2 after inoculation and significantly greater infection on day 3

74 that showed a positive response to bacterial inoculation and was amenable to genetic and molecular re

75 e slightly down-regulated 2-6 days after Pgt inoculation and were not affected by temperature.

76 protect against mucosal as well as systemic inoculation are needed.

77 routes, such as subcutaneous or intradermal inoculations are rare, even though the sharing of needle

78 e plasma cells in lymph nodes following oral inoculation as compared with young mice.

79 unity experienced a complex change after B16 inoculation, as determined through marked differences in

80 ZIKV inoculation at E10 causes placental inflammation, placen

81 Intrauterine inoculation at embryonic day (E) 10, but not E14, with A

82 Maternal inoculation at embryonic day 6.5 (E6.5) or E7.5 resulted

83 Under identical experimental conditions, inoculation at low infection multiplicities resulted in

84 Following a single intranasal inoculation, both animal species shed the vaccine viruse

85 By 6 hours after inoculation, brain- and PMCAb-derived PrP(Sc) were found

86 induction of disease symptoms at the site of inoculation but reduced spread through the vasculature.

87 ease in Colony Forming Units (CFU) upon soil inoculation but this behavior is not well-understood.

88 e virus in blood 7 weeks following the first inoculation, but viral-RNA persistence, low-level viral

89 thin bacterial populations, implying initial inoculation by multiple individual cells with distinct g

90 We demonstrated that this method of inoculation can achieve a transduction rate of >90% of t

91 After intramuscular inoculation, CE(NiP)DeltaP2-5 caused significantly lower

92 ions of goethite and redox mediator, and the inoculation cell density all affect the characteristics

93 er parasite burdens at the cutaneous site of inoculation compared with wild-type controls, whereas NL

94 of phenanthrene degradation genes 4 h after inoculation, compared to the inoculum suspension concomi

95 c mice following VACV infection or poly(I-C) inoculation, consistent with differences in innate immun

96 groups also received a single oral bacterial inoculation consisting of twelve cultured Enterococcus s

97 Transmission was observed until day 5 after inoculation, corresponding to high culture titers and po

98 Because the inoculation culture process can take between 24 and 48h

99 icantly shorter duration of shedding in post-inoculation day 10 subgroup and lower cumulative sheddin

100 mitted by needle sharing during subcutaneous inoculation, despite the absence of visible blood contam

101 he gastrointestinal tract since intragastric inoculation did not rescue the mutants' colonization.

102 ne with the chronic wasting disease agent by inoculation directly into the brain (intracranially) or

103 sity in the resulting microbiota and, at low-inoculation doses, can result in hosts that remain uncol

104 lected at 30, 60, 90, 105, and 120 days post inoculation (dpi) or at the onset of clinical signs of d

105 days (cohort 2) before CHMI by direct venous inoculation (DVI) of 3200 aseptic, purified, cryopreserv

106 Inoculation experiments confirmed that fungi affected se

107 Inoculation experiments show that EMF communities are cr

108 Inoculation experiments suggested plant local adaptation

109 Using dual inoculation experiments, we further show active exclusio

110 6 days or euthanized between days 0 and 4 of inoculation for analysis of the inflammatory response an

111 ial groups are shared with roots, suggesting inoculation from soil.

112 ial growth, site-directed mutagenesis, mouse inoculation (from cultured cells and after cohabitation)

113 Transcervical inoculation further confirmed the correlation between C.

114 group compared with Mdr1a (-/-) mice in the Inoculation group (P = 0.25), nor was there any differen

115 ere fed AIN-76A rodent diet, and mice in the Inoculation groups also received a single oral bacterial

116 a and KC/GRO) was observed at two hours post-inoculation; however, cytokines returned to baseline lev

117 cord was observed after direct intracranial inoculation, Ifitm3 likely functions as an antiviral pro

118 fetal brain lesions after Zika virus (ZIKV) inoculation in a pregnant pigtail macaque.

119 vivo challenge study, prior Embp intranasal inoculation in chickens suppressed the viral titres and

120 receptor 3, CNTO3157, on experimental HRV-16 inoculation in healthy subjects and asthmatic patients.

121 UBI-29-41 was observed at sites of S. aureus inoculation in infected mice (ratio of target to nontarg

122 ization (IVSC) at four critical stages after inoculation in J 11 (resistant) and JL 24 (susceptible)

123 H3N8 CIV challenge with a single intranasal inoculation in mice.

124 Intranasal inoculation in postnatal day 14 mice with VSVDeltaG-CHIK

125 valuated at different time points after cell inoculation in vivo.

126 ted Lyme disease (12 to 13 months after tick inoculation) in doxycycline-treated (28 days; 5 mg/kg, o

127 ne conidia were harvested, and then used for inoculations, in their dry condition; secondly, cultures

128 administration to mice before low dose oral inoculation increases L. monocytogenes growth in the int

129 nhances viral dissemination from the site of inoculation independently of interferon regulatory facto

130 different androstenone level and salmonella inoculation indicated that the functional usage of PAS m

131 It was evident that the periodic inoculation induced higher corrosion losses of the concr

132 total staff time with the adoption of tissue inoculation into blood culture bottles compared to conve

133 c agars and thioglycolate broth) compared to inoculation into blood culture bottles.

134 Novosphingobium sp. LH128 was examined after inoculation into phenanthrene spiked soil.

135 rain LH128-GFP enters a VBNC-like state upon inoculation into soil but is metabolically active and th

136 Following inoculation into the bladders of C3H/HEN and C3H/HeOuJ m

137 evelop an animal model utilizing direct ZIKV inoculation into the uterine wall of pregnant, immunocom

138 cerebral beta-amyloidosis upon intracerebral inoculation into young APP tg mice.

139 Virus inoculation led to recruitment and infection of Langerha

140 so three types of pest damage: tree pathogen inoculation, mass accumulation on susceptible hosts, and

141 CMV was constructed, and a vascular puncture inoculation method utilizing Agrobacterium was optimized

142 methods performed poorly compared to direct inoculation methods, negating the need for the broth enr

143 ella cucumerina (P. cucumerina) vary between inoculation methods.

144 metabolic defense signatures upon different inoculation methods.

145 rrets following traditional or aerosol-based inoculation methods.

146 After tail vein inoculation, most luciferase-generated bioluminescence s

147 d to one of two treatment groups (Control or Inoculation, n = 12 per group).

148 c cancer cell lines and a spleen subcapsular inoculation nude mouse model were also used.

149 Intracranial inoculation of 1-d-old immunocompetent CD-1 mice with 1

150 Conventional intratracheal inoculation of a liquid suspension of H5N1 influenza vir

151 treatment with exogenous MMP-3.Intracameral inoculation of AAV-2/9 containing a CMV-driven MMP-3 gen

152 l-1,2,3,6-tetra-hydropyridine or intranigral inoculation of aggregated toxic alpha-SYN.

153 Our study shows that the inoculation of Al-10Si braze alloy with these compounds

154 We assessed immunization by direct venous inoculation of aseptic, purified, cryopreserved, non-irr

155 Inoculation of bone marrow/liver/thymus (BLT) mice with

156 Intriguingly, inoculation of control monocytes together with Lewis lun

157 We performed systemic inoculation of control or Runx2 knockdown invasive MDA-M

158 y, the effect of simultaneous and sequential inoculation of cultures in moromi fermentation models, w

159 likelihood of prion shedding in saliva; oral inoculation of deer with CWD-positive saliva resulted in

160 Biocontrol efficacy could be improved by co-inoculation of different microorganisms.

161 In particular, the inoculation of DTMUV into rhesus monkeys did not result

162 Here, we performed intracerebral inoculation of embryonic mouse brains with dengue virus

163 Using intracerebral inoculation of embryonic mouse brains, we found that ZIK

164 rmal ductal outgrowth resulted from a single inoculation of ESCs and mECM.

165 Consistently, inoculation of GABA enhanced arboviral infection, indica

166 ing and assessed infectivity by means of the inoculation of hamsters and the subsequent examination f

167 etween day 4 and day 8 after intraperitoneal inoculation of high- and low-dose challenges, respective

168 ce daily) prophylactically before intranasal inoculation of highly pathogenic H5N1 virus (A/Indonesia

169 Surprisingly, after peripheral inoculation of immunocompetent mice on the day of birth,

170 e infection resulting from atraumatic rectal inoculation of Indian rhesus macaques with low doses of

171 In experiments involving inoculation of individual isogenic derivatives of NTHi s

172 A single intranasal/intratracheal inoculation of juvenile baboons with BPZE1 resulted in t

173 ion-resistant (tier 2) 16055 virus following inoculation of liposome-arrayed trimers.

174 Inoculation of maize and wheat with Pf-5 X940 largely im

175 Transcervical inoculation of medroxyprogesterone-treated HLA-DR4 trans

176 Intranasal (i.n.) inoculation of mice represents an experimental approach

177 Intestinal inflammation is attenuated after inoculation of mice with three Lactobacillus strains cap

178 een in vivo in the murine model of BA, where inoculation of mice with TRTRVSRLY peptide significantly

179 Following inoculation of mice, KLKI MHV68 established and maintain

180 Following corneal inoculation of mice, the mutant was not significantly di

181 Tumor-xenografts derived from orthotopic-inoculation of MYB-overexpressing PC cells exhibited far

182 a, the rat model has relied on intratracheal inoculation of organisms because of safety and equipment

183 After inoculation of P. flocculosa, the tripartite interaction

184 Inoculation of p13Bri in mice elicited antibodies to the

185 Importantly, intraperitoneal inoculation of pancreatic homogenates containing IAPP ag

186 Furthermore, inoculation of pancreatic IAPP aggregates into the brain

187 le interval, 77 to 100%), whereas when using inoculation of periprosthetic tissues into blood culture

188 Soil bioaugmentation involves the inoculation of pollutant-degrading bacteria to accelerat

189 Periodontitis was induced by oral inoculation of Porphyromonas gingivalis and Fusobacteriu

190 we first assessed the safety of intravenous inoculation of predatory bacteria in rats.

191 , survival of ALS mice was not changed after inoculation of preformed fibrils.

192 Our results show that a prophylactic inoculation of prion-infected animals with an anti-prion

193 Inoculation of PS19 transgenic tau (P301S) mice with the

194 enotype than wild-type mice after intranasal inoculation of RABV.

195 Intrabronchial inoculation of rhesus macaques with simian varicella vir

196 Inoculation of rice with H. rubrisubalbicans increased t

197 pulations and highlighting the impact of the inoculation of selected exogenous strains on natural str

198 metastases was determined after intravenous inoculation of syngeneic 9801L pancreas carcinoma cells.

199 Inoculation of Tg(GPPrP) mice with BSE and vCJD prions r

200 A retro-orbital vein inoculation of the C. muridarum organisms at a lower dos

201 ype 1 interferon response (IFNR(-/-)), after inoculation of the eye, the initial majority of infected

202 After inoculation of the MG with a mastitis-causing E. coli st

203 We found that inoculation of the same animal with two strains can resu

204 Intraperitoneal inoculation of the thermally injured mice, bypassing the

205 f H2O2 produced in A. tequilana leaves after inoculation of their endophytic bacteria (Enterobacter c

206 cination regime was used with the sequential inoculation of three different inactivated FMDV serotype

207 Inoculation of three-week-old piglets showed that A2MC2-

208 Co-inoculation of two entomopathogenic fungi (Beauveria bas

209 Experimental inoculation of viable Plasmodium falciparum sporozoites

210 ntal infection of ruminants by either direct inoculation of virus, or through blood feeding by infect

211 apies, and vaccines, but they rely on needle inoculation of virus: the effects of mosquito-borne infe

212 The inoculation of viruses into mosquito bite sites is an im

213 Inoculation of WNV-NS5-E218A, a WNV with a mutant NS5(E2

214 increased resistance to BPH only at 3 d post-inoculation of Xoo, while the Xoo infection did not affe

215 In this study, intrarectal inoculations of Sprague-Dawley rats with predatory bacte

216 ess of treatment, but there was no effect of inoculation on body weight (P > 0.25).

217 cally investigated the impacts of wastewater inoculation on the corrosion of concrete in sewers.

218 mptoms, and pathogen spread from the site of inoculation over time for strains with mutations in avrB

219 d in all groups in response to P. gingivalis inoculation (P < 0.01), whereas bone remodeling markers

220 s C, intensive flipping (5-6 times/24h), and inoculation quantity 3-4% and a fermentation on 20 degre

221 grees C, medium flipping (3-4 times/24h) and inoculation quantity 3-4% for production of commercial,

222 ission (human biting rates and entomological inoculation rates [EIRs]) was studied using a multivaria

223 intensity that correlate with entomological inoculation rates but lack precision in settings where s

224 expression or sham and intratracheal E. coli inoculation, rats underwent 4 hours of mechanical ventil

225 1 human volunteer subjects under 4 different inoculation regimes (HRV, RSV, H1N1, H3N2).

226 This, together with the inoculation results, suggests that coevolutionary and co

227 ring of needles is common practice for these inoculation routes in the veterinary sector.

228 nown, or following non-biologically relevant inoculation routes.

229 g to Principal Component Analysis (PCA), the inoculation sequence (co-inoculation and sequential) has

230 After traumatic cutaneous inoculation, several fungi can cause neglected mycoses s

231 Baseline imaging before inoculation showed no focal areas of lung consolidation

232 sponse that can limit VSV spread at both the inoculation site and among synaptically connected neuron

233 rized by an edema that retained virus at the inoculation site and an inflammatory influx of neutrophi

234 enhancement of viral dissemination from the inoculation site and in disease severity.

235 understanding plant defense pathways at the inoculation site and systemically in uninoculated tissue

236 NS1 Abs reduced viral Ag expression at skin inoculation sites and shortened DENV-induced prolonged b

237 At 7 days after inoculation, SIV had disseminated to the blood, systemic

238 y, we determined that, by day 7 after penile inoculation, SIV has moved first to the inguinal lymph n

239 Four hours after inoculation, strain LH128-GFP showed about 99% reduction

240 s tested in a pilot system as an alternative inoculation strategy to the use of free suspended cells

241 Mucosal inoculation successfully induced immune tolerance to col

242 Here, we used an oral inoculation system for CVB3, which follows the natural r

243 evised a minimally invasive surgical bladder inoculation technique that yields reproducible upper and

244 of established methods, including different inoculation techniques, bacterial mutant strains, and as

245 confirmed infected grasses as hosts using re-inoculation tests.

246 After peripheral inoculation, the virus entered the CNS in all mice teste

247 After mono-inoculation, there was no significant difference in colo

248 ation of Pip in leaves distal to P. syringae inoculation, they display a considerable systemic acquir

249 f H. uvarum/S. cerevisiae; inoculum size and inoculation time of S. cerevisiae; fermentation time and

250 was much less efficient, requiring a longer inoculation time to reach its maximal infectivity.

251 imes consistently decreased (3 to 2 ns) with inoculation time.

252 ly, feces were collected for seven days post-inoculation to determine the effect on gut bacterial div

253 eptible S. arcanum accessions upon A. solani inoculation to unravel metabolic dynamics during differe

254 and CT images were acquired 10 d after tumor inoculation, to establish baseline distribution and upta

255 fect on memory; this occurred only in the co-inoculation treatment.

256 G. arboreum plants were infested by graft inoculation using a CLCuD infected scion of G. hirsutum.

257 T was performed on days 0, 1, 2, and 3 after inoculation using either (18)F-FDS or (18)F-FDG (n = 12

258 t genotype on growth response to mycorrhizal inoculation was investigated in a panel of diverse maize

259 Restriction of infection via apical inoculation was overcome by disruption of intercellular

260 ct murine models of IPA on days 2 and 3 post inoculation when infection is established and active dis

261 s exhibited respiratory clinical signs after inoculation, which were more severe and of longer durati

262 al T cells shortly after a high-dose mucosal inoculation, while not preventing infection altogether,

263 of TaADF4 mRNA was diminished in response to inoculation with a virulent race, CYR31.

264 nferred in vivo Our studies demonstrate that inoculation with Ad5-poIRF7/3(5D) completely protects sw

265 0 maize lines was evaluated with and without inoculation with arbuscular mycorrhizal fungi.

266 rease in callose responsiveness following co-inoculation with both microbes.

267 7 and nod+ E5, E6, F487A, and PI262090 after inoculation with Bradyrhizobium sp.

268 erent concentrations of amphotericin B after inoculation with Candida albicans in light-exposed and l

269 The results therefore demonstrate that inoculation with col(V) can successfully ameliorate the

270 ion shedding in saliva compared to that from inoculation with CWD-positive brain.

271 Inoculation with different viral loads led to different

272 lene levels also increased in rice roots but inoculation with H. rubrisubalbicans impaired growth of

273 showed a significant reduction in FGS after inoculation with Heterobasidion parviporum compared to t

274 the MAbs and were then challenged by corneal inoculation with HSV-1 had reduced eye disease, shedding

275 Inoculation with M. canis also decreased major histocomp

276 ificantly shifted 11 days after experimental inoculation with M. gallisepticum.

277 Upon inoculation with MERS-CoV, human DPP4 knockin (KI) mice

278 oduction increased as early as 6 hours after inoculation with Mesorhizobium loti This ethylene respon

279 lls of mice or hamsters following extranasal inoculation with mock-infected brain homogenate, differe

280 After the inoculation with P. subcapitata, TA-DOM aromaticity (ind

281 with altered localization of PEN3-GFP after inoculation with powdery mildew fungi.

282 Similarly, we showed that corneal inoculation with rAAV vectors in the rabbit efficiently

283 We hypothesized that footpad or ocular inoculation with rAAV8 would result in transduction of d

284 Inoculation with rfaG, waaL, wzzE, and wzyE mutants show

285 Following inoculation with rhizobia, mtlax2 roots developed fewer

286 After 6 wk post-inoculation with Rhizophagus irregularis, root developme

287 reduced alcohol wine when used in sequential inoculation with Saccharomyces cerevisiae.

288 We investigated whether oral inoculation with specific intestinal bacteria increased

289 Following inoculation with the ureolytic bacteria, Sporosarcina pa

290 he passaging process, (ii) direct intranasal inoculation with the viral stock resulted in a selective

291 dysbiosis induced by antifungal treatment or inoculation with typically rare fungi results in exagger

292 BSD) was conducted using RNASeq, after graft inoculation with Ugandan cassava brown streak virus (UCB

293 Inoculation with virulent and avirulent strains of the b

294 However, co-inoculation with wildtype rescued DeltaspeC growth, indi

295 ils by comparing various peripheral sites of inoculations with different alphaS protein preparations.

296 Single inoculations with R. irregularis or P. putida had differ

297 ing of chitosan-induced callose after single inoculations with R. irregularis or P. putida, only the

298 ramatically within days to weeks after tumor inoculation, with CD11b(+)Gr1(hi)Ly6C(-) cells having th

299 were significantly more prominent 7 d after inoculation, with increased mean signal intensity of oxy

300 Following subcutaneous inoculation, ZIKV RNA is detected in plasma 1 day post i