1 of the three isolates that did not form IBCs
when inoculated alone were able to do so when coinoculat
2 When inoculated alone, both bacteria colonized the roots
3 nsport system were able to infect the kidney
when inoculated as a pure culture but were unable to eff
4 When inoculated as xenografts in nude mice, PPARdelta -/
5 Conversely, strain-DK1, even
when inoculated at a dose 4 logs greater than the parent
6 sigma1s is essential for reovirus virulence
when inoculated at a site that requires systemic spread
7 and 90.3, 100, 100 and 97.6%, respectively,
when inoculated at bedside.
8 of disease, viremia, or virus shedding even
when inoculated at doses 100-fold higher than those requ
9 Finally, the delta(glnA-ntrC) strain,
when inoculated at doses as low as 10 organisms, provide
10 When inoculated at the same multiplicity of infection an
11 re required for growth in the mammalian host
when inoculated by peripheral routes.
12 magnitude less virulent than wild-type virus
when inoculated directly into the brain.
13 susceptible to bacterial colonization, even
when inoculated ex vivo to exclude tear fluid effects.
14 vaccines are immunogenic in gnotobiotic pigs
when inoculated i.n. and that the adjuvant mLT enhanced
15 a pmrA null mutant is actually hypervirulent
when inoculated i.p. into C3H/HeN mice.
16 India 7124, produced uniform acute lethality
when inoculated i.v. in high doses (10(9) plaque-forming
17 than AhR heterozygous (AhR(+/-)) littermates
when inoculated i.v. with log-phase Listeria monocytogen
18 d cells, fail to induce FAE destruction and,
when inoculated in LB, are attenuated for M-cell invasio
19 ) in vitro but replicated only to low levels
when inoculated in rhesus monkeys.
20 and induced a rapidly fatal disease process
when inoculated in secondary recipient mice.
21 When inoculated in sheep by the intranasal or intraderma
22 nificantly less prone to develop bone tumors
when inoculated in the arterial circulation with human p
23 When inoculated individually by soaking the soil, both n
24 ces increased current in response to arsenic
when inoculated into a BES.
25 When inoculated into athymic mice, calreticulin inhibite
26 When inoculated into athymic mice, vasostatin significan
27 CLC) growth in vitro as well as tumor growth
when inoculated into athymic mice.
28 When inoculated into BALB/c mice by intragastric gavage,
29 When inoculated into BALB/c mice, both vectors induced a
30 ontrols and reduced the parasite load 3-fold
when inoculated into BALB/c mice.
31 MRSA strains grew rapidly
when inoculated into cecal mucus in vitro but were unabl
32 When inoculated into chickens, the wild-type strain colo
33 Like other epizootic VEEV strains,
when inoculated into guinea pigs and mice, the Mexican i
34 When inoculated into hamsters, both of these types of sy
35 two Arf alleles can initiate lympholeukemias
when inoculated into immunocompetent, syngeneic recipien
36 When inoculated into immunodeficient mice, thioredoxin-t
37 human tumor lines do not form visible tumors
when inoculated into immunosuppressed mice.
38 When inoculated into juvenile pig-tailed macaques, the P
39 When inoculated into macaque monkeys, SHIV(MD14) carryin
40 However,
when inoculated into macaques, the virus failed to repli
41 ins replicated at significantly lower levels
when inoculated into mice immunized with VSV-C/E1/E2 or
42 When inoculated into mice, the recombinant virus induced
43 When inoculated into microcosms containing legumes or gr
44 When inoculated into naive rhesus monkeys, SHIV-89.6P ca
45 When inoculated into naive wild-type (WT) mice, this per
46 ple retrovirus that induces T-cell lymphomas
when inoculated into neonatal mice.
47 Polyoma virus is a potent oncogenic pathogen
when inoculated into newborn mice of particular H-2(k) s
48 , the Pt-tropic HIV-1 was rapidly controlled
when inoculated into newborn Pt macaques, although it tr
49 opment of the hypersensitivity response (HR)
when inoculated into Nicotiana benthamiana; however, it
50 se epithelioid-appearing, transfected cells,
when inoculated into nude mice, form progressively growi
51 een reported to cause bone formation in vivo
when inoculated into nude mice.
52 cytes in cultures and acute PBj-like disease
when inoculated into pig-tailed macaques.
53 Importantly,
when inoculated into pigs, PRRSV-CON confers significant
54 d a rapid and severe CD4(+) T-cell depletion
when inoculated into rhesus macaques.
55 When inoculated into rhesus monkeys, NYVAC-Pf7 was safe
56 in vitro but were deficient in producing LPD
when inoculated into SCID mice.
57 When inoculated into severe combined immunodeficient mic
58 this strain induces severe hemolytic anemia
when inoculated into specific-pathogen-free-derived cats
59 fectivity in cell culture and produced virus
when inoculated into suckling mice.
60 When inoculated into susceptible day-old chicks, all vir
61 d MalDeltaNL disease and virulence phenotype
when inoculated into swine.
62 the delta5 Sal transfectant was not rejected
when inoculated into syngeneic hosts.
63 alities, and were capable of forming nodules
when inoculated into the abdominal subcutaneous tissue o
64 When inoculated into the bladder of a mouse, ASN-conditi
65 Yet,
when inoculated into the brains of HSV-1-sensitive A/J m
66 When inoculated into the eyes of mice, the AAV-expressin
67 When inoculated into transgenic mice, these amyloid fibr
68 When inoculated intracerebrally into the appropriate tra
69 7 of 14 type C isolates were lethal, whereas
when inoculated intraduodenally, these strains were all
70 Most MAb RB6-8C5-treated mice died
when inoculated intragastrically with as few as 4 x 10(4
71 ix isolates were of low infectivity to ticks
when inoculated intramuscularly into hosts.
72 h the H3N2 human and the H7N1 avian viruses:
when inoculated intranasally at a high dose, only the An
73 When inoculated intranasally into hamsters, there was es
74 Studies presented here show that
when inoculated intranasally into mice, rM51R-M virus wa
75 When inoculated intranasally into mice, the SH-minus vir
76 When inoculated intraperitoneally (i.p.), the Vero cell-
77 rain was nearly as virulent as the wild type
when inoculated intraperitoneally in the mouse model.
78 er, unlike FECV-RM, they readily induced FIP
when inoculated intraperitoneally into specific-pathogen
79 When inoculated intraperitoneally, a route that results
80 ic when used to inoculate mice s.c., but not
when inoculated intraperitoneally.
81 SIVsmE543-3 was infectious and induced AIDS
when inoculated intravenously into pig-tailed macaques (
82 om controls, remained dormant for up to 5 mo
when inoculated on CAMs.
83 japonicum cultures showed the same activity
when inoculated on to soybean roots.
84 xpression and induced decreased tumor burden
when inoculated s.c. with Lewis lung carcinoma cells.
85 licate poorly in the brains of infected mice
when inoculated subcutaneously but replicate well follow
86 s and display enhanced vascular permeability
when inoculated subcutaneously in the nude mouse.
87 n infections was significantly less virulent
when inoculated subcutaneously into mice.
88 In contrast,
when inoculated subcutaneously only the GerH receptor wa
89 the psn or irp2 gene were avirulent in mice
when inoculated subcutaneously.
90 ually capable of replicating in neurons, but
when inoculated together, neurons selected for the viral
91 When inoculated twice with Ad vectors lacking both E1A a
92 of rovA increases the LD(50) of the organism
when inoculated using the oral route.
93 ral loads than those vaccinated with dSIV(R)
when inoculated with a recombinant vaccinia virus expres
94 When inoculated with a transplantable lymphoma cell line
95 a cell line, L3055, formed solid tumors only
when inoculated with an FDC line, HK.
96 pes4), that displays severe disease symptoms
when inoculated with avirulent strains of Pseudomonas sy
97 ple transgenes exhibited accelerated disease
when inoculated with disease-associated mutant PrP, Tg m
98 When inoculated with either of two biologically differen
99 taking PSFC measurements of macrophage cells
when inoculated with enhanced green fluorescent protein
100 Surprisingly,
when inoculated with equal infectious doses (PFU), even
101 We found that seedlings grew similarly
when inoculated with local vs foreign microbial communit
102 howed that CD40L(-/-) mice control infection
when inoculated with low numbers of parasites and that c
103 When inoculated with LPS, IRF-1 gene knockout (IRF-1 KO)
104 K cell group 2D (NKG2D) ligand RAE-1beta, or
when inoculated with metastatic melanoma, prostate carci
105 ed immunodeficiency disease remained healthy
when inoculated with MVA at 1,000 times the lethal dose
106 vere loss of CD4+ cells within 1 month, even
when inoculated with only a single animal infectious dos
107 When inoculated with P. carinii, both wild-type (wt) and
108 When inoculated with P. s. tomato without avrPto, all th
109 When inoculated with Rocky Mountain Laboratory (RML) pri
110 and led to significantly reduced nodulation
when inoculated with S. meliloti.
111 verexpressed HRT produced micro-HRs or no HR
when inoculated with TCV and were resistant to infection
112 When inoculated with the ME49 strain, PCC-Tg animals exh
113 o have the visible plant cell death response
when inoculated with the non-xopX-expressing strains Xcv
114 imb inoculation with sigma1s-null virus than
when inoculated with wild-type virus.