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4 course of the infection, a group of animals was inoculated with 10(6) IFU/mouse (20 times the ID(50)
5 aw milk samples from a known noninfected cow were inoculated with 10(2) to 10(8) CFU/ml of live M. av
8 man challenge study, 310 university students were inoculated with 10(4) colony-forming units of N. la
11 am-vaccinated dams for up to 8 h before they were inoculated with 10(6) CFU of a Shiga toxin-negative
13 ere combined immunodeficiency (SCID animals) were inoculated with 10(6) IFU/mouse (20 times the ID(50
17 lanoma development and metastasis, nude mice were inoculated with 1205Lu melanoma cells into the left
28 geenan-treated phagocytic cell-depleted mice were inoculated with 4T1 and assessed for primary tumor
30 ) iNOS(-/-) mice or C57BL/6 (wild-type) mice were inoculated with 5 x 10(4) PFU of MCMV K181 strain (
31 vectored antigens in humans, six volunteers were inoculated with 5 x 10(7) to 8 x 10(7) CFU of phoP/
36 ultures, at the appropriate stage of growth, are inoculated with A. tumefaciens containing the binary
39 ed for pustule formation, six human subjects were inoculated with a CDT mutant and parent at multiple
40 o circumvent this problem, three chimpanzees were inoculated with a genetically defined stock of cell
42 n in colonial bat species, little brown bats were inoculated with a homologous RABV or one of two het
44 oseltamivir was given 4 h before the ferrets were inoculated with a lethal dose of A/Vietnam/1203/04
45 tcompeted by the wild-type strain when birds were inoculated with a low dose (10(5) CFU per bird).
50 chimpanzee with AIDS (C499), two chimpanzees were inoculated with a plasma-derived isolate termed hum
51 fectivity of this isolate, 3 Macaca sylvanus were inoculated with a pool of M. fascicularis serum and
52 ating microcosms that were producing benzene were inoculated with a previously described enriched met
54 with recombinant poliovirus, immunized mice were inoculated with a recombinant poliovirus expressing
56 days of preexposure measurements, volunteers were inoculated with a rhinovirus and monitored for 14 d
58 sol was more pronounced (P < 0.04) when mice were inoculated with a sublethal dose of C. albicans.
60 purifications, and during P2 to P13 the pigs were inoculated with a tissue filtrate from the correspo
61 zole (BTH) for 7 d, and these exposed plants were inoculated with a tumorigenic Agrobacterium strain.
63 tine facility, healthy volunteers ("donors") were inoculated with A/Wisconsin/67/2005 (H3N2) influenz
66 t brain extracts from APP null mice that had been inoculated with Abeta seeds up to 6 months previous
67 d be delayed for at least 6 days when cattle were inoculated with Ad5-boIFN-lambda3 and challenged 24
68 dge) on a Mueller-Hinton agar plate that had been inoculated with an S. aureus isolate; the plate was
70 stem cells [human immune system (HIS) mice] were inoculated with an AML cell line or patient-derived
72 pe (WT) control mice and IFNgammaR(-/-) mice were inoculated with an attenuated form of Mycobacterium
73 rrets specific pathogen free for H. mustelae were inoculated with an Hsr-deficient mutant strain or t
77 In this study, B. burgdorferi-negative dogs were inoculated with B. turicatae, and seroconversion wa
78 In control experiments in which the surface was inoculated with bacteria but no neutrophils were add
83 tin or pea (Pisum sativum) seed lectin (PSL) were inoculated with Bradyrhizobium japonicum or Rhizobi
84 xpressing low levels of MoPrP(C)(P101L) that were inoculated with brain extracts from ill Tg2866 mice
86 nhuman primates to CWD, two squirrel monkeys were inoculated with brain tissue from a CWD-infected mu
87 label cells in S-phase division, all animals were inoculated with bromodeoxyuridine 24 h prior to sam
90 orm and sepsis developed in normal mice that were inoculated with burned-mouse infection site tissue
92 ver, mouse models in which the vaginal vault is inoculated with C. trachomatis do not recapitulate th
97 sing an excised-leaf-assay, the three points were inoculated with C. sublineola, and pathogenicity le
103 addition, when leaf disks from 'Ogy' plants were inoculated with conidia of the poplar pathogenic fu
110 d female Long Evans rats (Rattus norvegicus) were inoculated with doses of Seoul virus ranging from 1
111 the 50% infectious dose (ID(50)), male mice were inoculated with doses ranging from 10(2) to 10(6) i
112 cross of C3H/HeJ and (BALB/cxC3H/HeJ)F1 mice were inoculated with E. coli, and the number of E. coli
117 endent challenges, in which bladders of mice were inoculated with either a single mutant or the wild
119 er these preliminary studies, SCID mice that were inoculated with either HIV-infected or uninfected h
120 ied corneas of 6-week-old female BALB/c mice were inoculated with either HSV-1 17Syn(+) (high phenoty
125 , a reservoir containing reconstituted blood was inoculated with Enterococcus faecalis and hemofilter
126 ely unrelated, clonally propagated genotypes were inoculated with F. circinatum microconidia and lesi
127 ed a continuous-flow anaerobic culture which was inoculated with fecal samples from healthy volunteer
133 of tobacco, tomato, soybean and Arabidopsis were inoculated with Fusarium conidia and this resulted
135 y 10 mg/kg/day) adult male rhesus recipients were inoculated with GP120 protein antigen on day -28 an
138 without 0.2 ppm Se, and after 5 weeks, they were inoculated with H. bakeri infective third-stage lar
139 (2) H. pylori infected group (HP): the rats were inoculated with H. pylori (10(8-) 10(10) CFU/mL; 1
145 severe combined immunodeficient [SCID]) mice were inoculated with H. pylori strain SS1 or SS1::0826ka
146 y-six C57BL/6, Helicobacter-free female mice were inoculated with H. pylori Sydney strain 1, and 16 m
147 growing hydroponically in Hoagland's medium were inoculated with H. seropedicae and incubated for 3
148 H1N1 infection in early life, infant monkeys were inoculated with H1N1 by upper airway administration
155 y this issue, the eyes of Swiss-Webster mice were inoculated with HSV-1 (KOS), and 37-47 days later t
159 velop any spontaneous neurological phenotype were inoculated with (i) brain extracts containing PrP(T
162 oculated negative controls, group 2 (n = 19) was inoculated with Ingelvac PRRS MLV vaccine, group 3 (
163 n total, 317 Arabidopsis thaliana accessions were inoculated with its natural Turnip mosaic virus (Tu
165 field isolate 98-37120, and group 6 (n = 20) was inoculated with known high-virulence PRRSV isolate A
167 LCMV infection, in which developing rat pups were inoculated with LCMV at a series of postnatal ages,
168 lack mangabeys (BkMs) (Lophocebus aterrimus) were inoculated with lepromatous tissue that had been se
172 f biofilms in equine endometritis, six mares were inoculated with lux-engineered Pseudomonas aerugino
176 /-) C57BL/6 mice, and wild-type C57BL/6 mice were inoculated with MCMV k181 by way of the supraciliar
177 Chronic treatment of nude mice, which had been inoculated with MDA-MB-231 cells, with inhibitor 38
178 ator of the tumor response to TGF-beta, mice were inoculated with MDA-MB-231 breast cancer cells expr
179 diated osteolysis in vivo, athymic nude mice were inoculated with MDA-MB-231 cells stably expressing
182 ns from wild-type and ceacam1a knockout mice were inoculated with MHV to determine the extent to whic
183 How do we initially realize that we have been inoculated with microbes, and how is the immune res
184 r pylori infection in infants, suckling mice were inoculated with mixtures of strains that preferenti
185 In the present study, M. spicilegus neonates were inoculated with Moloney ecotropic MLV (MoMLV).
186 lethal dose of C. parvum survived after they were inoculated with Mphi from SCIDbg mice exposed to C.
188 Sprague-Dawley rats (n = 45; age, 12 weeks) were inoculated with N1S1 HCC cells in the liver, and 8
189 A total of 11 Macaca nemestrina macaques were inoculated with NC mutant SIV expressing DNA, intra
190 mutants was assessed previously in mice that were inoculated with needle and syringe and was found to
194 (MEs) of wild-type (WT) and MyD88(-/-) mice were inoculated with nontypeable Haemophilus influenzae
195 Healthy, genetically susceptible adults were inoculated with NV Lot 001-09NV and monitored for i
198 Aerobic/F and BacT/Alert FA Plus BC bottles were inoculated with one of two isolates (1 meropenem su
201 these experiments, immunodeficient scid mice were inoculated with P. carinii and were heavily infecte
203 o immunosuppressed rats, beginning when rats were inoculated with P. carinii, caused 85 and 99.88% re
204 targeted mice (GM-/-) depleted of CD4+ cells were inoculated with P. carinii, the intensities of infe
206 rticipants (Study 1, n = 2; Study 2, n = 24) were inoculated with P. vivax-infected red blood cells t
208 After an i.d. challenge, 15 of 16 mice who were inoculated with phosphate-buffered saline developed
210 2(-/-) or wild-type hematopoietic cells that were inoculated with Plasmodium berghei ANKA, a murine m
211 intact and gonadectomized (gdx) C57BL/6 mice were inoculated with Plasmodium chabaudi AS-infected ery
212 ator controlled study, in which participants were inoculated with Plasmodium falciparum induced blood
214 ate, Dacron polyester, or rayon-tipped swabs were inoculated with pneumococci or were immersed in nas
215 However, when immunocompetent BALB/c mice were inoculated with Pneumocystis, a vigorous Th2-like p
217 Diabetic (db/db) and control (db/+) mice were inoculated with Porphyromonas gingivalis, a pathoge
218 model, cohorts of naive immunocompetent mice were inoculated with primary murine APL cells from a fro
219 RSV field isolate 98-38803, group 5 (n = 19) was inoculated with PRRSV field isolate 98-37120, and gr
221 For biofouling tests, wastewater effluent was inoculated with Pseudomonas aeruginosa and artificia
222 The inner parts of five implants, per group, were inoculated with Pseudomonas aeruginosa suspension a
223 ing simulated herbivory but also when leaves were inoculated with Pseudomonas syringae pv tomato DC30
230 In an efficacy trial, Holstein Friesian cows were inoculated with S. aureus and treated intramammaril
231 adenovirus (Ad), while one additional animal was inoculated with saline intranasally as a control.
232 ced cells that bound SARS-CoV S glycoprotein were inoculated with SARS-CoV, and increases in subgenom
233 known exometabolites of marine phytoplankton were inoculated with seawater bacterial assemblages, and
234 To test this hypothesis, male Norway rats were inoculated with Seoul virus and regulatory T cells
239 , but is expressed in root systems that have been inoculated with Sinorhizobium meliloti and are deve
242 n pair-housed, juvenile male rhesus macaques were inoculated with SIVmac239 and, 4 wk postinoculation
245 In this study, four lactating rhesus monkeys were inoculated with SIVmac251 and monitored for SIV env
248 soluble JRFL gp140 trimers, and control NHPs were inoculated with soluble JRFL protein trimers withou
249 ntigen (STAg), wild-type and TRAF6(-/-) mice were inoculated with STAg, and the production of IL-12(p
252 roductive infection in vivo, rhesus macaques were inoculated with strains of single-cycle SIV (scSIV)
254 C57BL/6) and TLR2-deficient (TLR2(-/-)) mice were inoculated with Streptococcus pneumoniae (1 x 10(6)
256 large grit, acid-etched (SLA) titanium disks were inoculated with subgingival dental plaque and cultu
261 Ingelvac PRRS MLV vaccine, group 3 (n = 20) was inoculated with the parent strain of the vaccine (AT
267 and IFN-gamma-deficient (IFN-gamma gko) mice were inoculated with the JHM strain of murine coronaviru
269 s and virulence, groups of juvenile macaques were inoculated with the molecular clone SIVmac239 with
271 esponse, B cell-deficient and wild-type mice were inoculated with the nematode parasite, Nippostrongy
274 ild-type and TLR7-deficient (TLR7(-/-)) mice were inoculated with the rodent-specific pathogen pneumo
276 tes progression to AIDS, pig-tailed macaques were inoculated with the simian counterparts, SIV and ST
277 ravenously with swine HEV, 19 pigs (group 2) were inoculated with the US-2 strain of human HEV, and 1
281 dependent challenges in which mouse bladders were inoculated with the wild type or a fimbrial mutant
282 s this, pregnant and nonpregnant BALB/c mice were inoculated with the wild-type pH1N1 strain A/Califo
293 the vaccine (ATCC VR2332), group 4 (n = 19) was inoculated with vaccine-like PRRSV field isolate 98-
294 al immune responses in vivo, rhesus macaques were inoculated with variants of rhesus cytomegalovirus
297 loading) to schwertmannite suspensions which were inoculated with wetland sediment and suspended in N