ライフサイエンスコーパス: when inoculated

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 three genera, colonized roots endophytically when inoculated as spores under drought stress, whereas

5 When inoculated as xenografts in nude mice, PPARdelta -/

6 Conversely, strain-DK1, even when inoculated at a dose 4 logs greater than the parent

7 kinetics in MDCK, A549, and RAW 264.7 cells when inoculated at a multiplicity of infection (MOI) of

8 sigma1s is essential for reovirus virulence when inoculated at a site that requires systemic spread

9 and 90.3, 100, 100 and 97.6%, respectively, when inoculated at bedside.

10 of disease, viremia, or virus shedding even when inoculated at doses 100-fold higher than those requ

11 Finally, the delta(glnA-ntrC) strain, when inoculated at doses as low as 10 organisms, provide

12 ) HAD(50)) and remains completely attenuated when inoculated at high doses (10(6) HAD(50)), demonstra

13 When inoculated at the same multiplicity of infection an

14 re required for growth in the mammalian host when inoculated by peripheral routes.

15 plants with the highest microbial densities when inoculated did not have the highest microbial densi

16 magnitude less virulent than wild-type virus when inoculated directly into the brain.

17 susceptible to bacterial colonization, even when inoculated ex vivo to exclude tear fluid effects.

18 vaccines are immunogenic in gnotobiotic pigs when inoculated i.n. and that the adjuvant mLT enhanced

19 a pmrA null mutant is actually hypervirulent when inoculated i.p. into C3H/HeN mice.

20 India 7124, produced uniform acute lethality when inoculated i.v. in high doses (10(9) plaque-forming

21 than AhR heterozygous (AhR(+/-)) littermates when inoculated i.v. with log-phase Listeria monocytogen

22 d cells, fail to induce FAE destruction and, when inoculated in LB, are attenuated for M-cell invasio

23 ) in vitro but replicated only to low levels when inoculated in rhesus monkeys.

24 and induced a rapidly fatal disease process when inoculated in secondary recipient mice.

25 When inoculated in sheep by the intranasal or intraderma

26 nificantly less prone to develop bone tumors when inoculated in the arterial circulation with human p

27 When inoculated individually by soaking the soil, both n

28 ces increased current in response to arsenic when inoculated into a BES.

29 When inoculated into athymic mice, calreticulin inhibite

30 When inoculated into athymic mice, vasostatin significan

31 CLC) growth in vitro as well as tumor growth when inoculated into athymic mice.

32 When inoculated into BALB/c mice by intragastric gavage,

33 When inoculated into BALB/c mice, both vectors induced a

34 ontrols and reduced the parasite load 3-fold when inoculated into BALB/c mice.

35 MRSA strains grew rapidly when inoculated into cecal mucus in vitro but were unabl

36 When inoculated into chickens, the wild-type strain colo

37 ts in immunity associated with delivery mode when inoculated into germ-free mice.

38 Like other epizootic VEEV strains, when inoculated into guinea pigs and mice, the Mexican i

39 When inoculated into hamsters, both of these types of sy

40 two Arf alleles can initiate lympholeukemias when inoculated into immunocompetent, syngeneic recipien

41 When inoculated into immunodeficient mice, thioredoxin-t

42 human tumor lines do not form visible tumors when inoculated into immunosuppressed mice.

43 When inoculated into juvenile pig-tailed macaques, the P

44 When inoculated into macaque monkeys, SHIV(MD14) carryin

45 However, when inoculated into macaques, the virus failed to repli

46 ins replicated at significantly lower levels when inoculated into mice immunized with VSV-C/E1/E2 or

47 When inoculated into mice, the recombinant virus induced

48 When inoculated into microcosms containing legumes or gr

49 ler tumors that elicited decreased allodynia when inoculated into mouse paws.

50 ntaining HAV RNA demonstrated no infectivity when inoculated into naive mice but contained neutralizi

51 When inoculated into naive rhesus monkeys, SHIV-89.6P ca

52 When inoculated into naive wild-type (WT) mice, this per

53 ple retrovirus that induces T-cell lymphomas when inoculated into neonatal mice.

54 Polyoma virus is a potent oncogenic pathogen when inoculated into newborn mice of particular H-2(k) s

55 , the Pt-tropic HIV-1 was rapidly controlled when inoculated into newborn Pt macaques, although it tr

56 opment of the hypersensitivity response (HR) when inoculated into Nicotiana benthamiana; however, it

57 se epithelioid-appearing, transfected cells, when inoculated into nude mice, form progressively growi

58 een reported to cause bone formation in vivo when inoculated into nude mice.

59 cytes in cultures and acute PBj-like disease when inoculated into pig-tailed macaques.

60 Importantly, when inoculated into pigs, PRRSV-CON confers significant

61 d a rapid and severe CD4(+) T-cell depletion when inoculated into rhesus macaques.

62 When inoculated into rhesus monkeys, NYVAC-Pf7 was safe

63 in vitro but were deficient in producing LPD when inoculated into SCID mice.

64 When inoculated into severe combined immunodeficient mic

65 this strain induces severe hemolytic anemia when inoculated into specific-pathogen-free-derived cats

66 fectivity in cell culture and produced virus when inoculated into suckling mice.

67 When inoculated into susceptible day-old chicks, all vir

68 d MalDeltaNL disease and virulence phenotype when inoculated into swine.

69 the delta5 Sal transfectant was not rejected when inoculated into syngeneic hosts.

70 alities, and were capable of forming nodules when inoculated into the abdominal subcutaneous tissue o

71 When inoculated into the bladder of a mouse, ASN-conditi

72 Yet, when inoculated into the brains of HSV-1-sensitive A/J m

73 When inoculated into the eyes of mice, the AAV-expressin

74 When inoculated into transgenic mice, these amyloid fibr

75 , aged mice failed to transmit this syndrome when inoculated intracerebrally into further recipient a

76 When inoculated intracerebrally into the appropriate tra

77 d subcutaneously but remaining neurovirulent when inoculated intracranially.

78 7 of 14 type C isolates were lethal, whereas when inoculated intraduodenally, these strains were all

79 Most MAb RB6-8C5-treated mice died when inoculated intragastrically with as few as 4 x 10(4

80 ix isolates were of low infectivity to ticks when inoculated intramuscularly into hosts.

81 h the H3N2 human and the H7N1 avian viruses: when inoculated intranasally at a high dose, only the An

82 When inoculated intranasally into hamsters, there was es

83 Studies presented here show that when inoculated intranasally into mice, rM51R-M virus wa

84 When inoculated intranasally into mice, the SH-minus vir

85 When inoculated intranasally, mCoV is pneumotropic and r

86 When inoculated intraperitoneally (i.p.), the Vero cell-

87 rain was nearly as virulent as the wild type when inoculated intraperitoneally in the mouse model.

88 er, unlike FECV-RM, they readily induced FIP when inoculated intraperitoneally into specific-pathogen

89 When inoculated intraperitoneally, a route that results

90 ic when used to inoculate mice s.c., but not when inoculated intraperitoneally.

91 SIVsmE543-3 was infectious and induced AIDS when inoculated intravenously into pig-tailed macaques (

92 om controls, remained dormant for up to 5 mo when inoculated on CAMs.

93 japonicum cultures showed the same activity when inoculated on to soybean roots.

94 xpression and induced decreased tumor burden when inoculated s.c. with Lewis lung carcinoma cells.

95 ing lower viral loads in the serum and brain when inoculated subcutaneously but remaining neurovirule

96 licate poorly in the brains of infected mice when inoculated subcutaneously but replicate well follow

97 s and display enhanced vascular permeability when inoculated subcutaneously in the nude mouse.

98 n infections was significantly less virulent when inoculated subcutaneously into mice.

99 In contrast, when inoculated subcutaneously only the GerH receptor wa

100 the psn or irp2 gene were avirulent in mice when inoculated subcutaneously.

101 ually capable of replicating in neurons, but when inoculated together, neurons selected for the viral

102 When inoculated twice with Ad vectors lacking both E1A a

103 of rovA increases the LD(50) of the organism when inoculated using the oral route.

104 ral loads than those vaccinated with dSIV(R) when inoculated with a recombinant vaccinia virus expres

105 e nodule organogenesis from nodule infection when inoculated with a subcompatible Rhizobium strain.

106 When inoculated with a transplantable lymphoma cell line

107 a cell line, L3055, formed solid tumors only when inoculated with an FDC line, HK.

108 pes4), that displays severe disease symptoms when inoculated with avirulent strains of Pseudomonas sy

109 ple transgenes exhibited accelerated disease when inoculated with disease-associated mutant PrP, Tg m

110 When inoculated with either of two biologically differen

111 taking PSFC measurements of macrophage cells when inoculated with enhanced green fluorescent protein

112 Surprisingly, when inoculated with equal infectious doses (PFU), even

113 disease symptoms and bacterial accumulation when inoculated with foliar bacterial pathogens P. syrin

114 al blood mononuclear cells in the mice that, when inoculated with HIV in cell culture, were resistant

115 Plants delayed flowering under stress only when inoculated with live microbial communities, and thi

116 We found that seedlings grew similarly when inoculated with local vs foreign microbial communit

117 howed that CD40L(-/-) mice control infection when inoculated with low numbers of parasites and that c

118 When inoculated with LPS, IRF-1 gene knockout (IRF-1 KO)

119 K cell group 2D (NKG2D) ligand RAE-1beta, or when inoculated with metastatic melanoma, prostate carci

120 ed immunodeficiency disease remained healthy when inoculated with MVA at 1,000 times the lethal dose

121 vere loss of CD4+ cells within 1 month, even when inoculated with only a single animal infectious dos

122 When inoculated with P. carinii, both wild-type (wt) and

123 When inoculated with P. s. tomato without avrPto, all th

124 When inoculated with Rocky Mountain Laboratory (RML) pri

125 and led to significantly reduced nodulation when inoculated with S. meliloti.

126 verexpressed HRT produced micro-HRs or no HR when inoculated with TCV and were resistant to infection

127 When inoculated with the ME49 strain, PCC-Tg animals exh

128 o have the visible plant cell death response when inoculated with the non-xopX-expressing strains Xcv

129 ween GTC-d11- and HepG2.2.15-derived viruses when inoculated with the same genome equivalents.

130 When inoculated with TuMV, loss-of-function mutant plant

131 imb inoculation with sigma1s-null virus than when inoculated with wild-type virus.