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1 ectious virus produced by RPE cells (10(6.5) TCID50/0.1 ml) significantly surpassed levels produced b
3 han when given at the regular dose, 10(7.26) TCID50 (40 participants); as a control, a placebo vaccin
4 ncentrations ranging from 10(1.4) to 10(4.4) TCID50/5 microliters were capable of inducing both infla
5 the highest concentration of virus (10(4.4) TCID50/5 microliters) in CD-1 mice resulted in only the
6 CTL response when given at a dose of 10(8.0) TCID50 (60 participants) than when given at the regular
7 from 0.01 50% tissue culture infective dose (TCID50) and were able to detect at least 1 TCID50 of ent
8 nts treated at high-dose levels (10(8)-10(9) TCID50), and their median overall survival of 26.5 month
12 to 10(9) 50% tissue culture infective doses (TCID50) consistently infected all the animals, and many
15 immunodeficiency virus type 1 (HIV-1) and <1 TCID50 for simian immunodeficiency virus isolated from a
16 ml in the blood and between 10(6) and 10(10) TCID50/g tissue in the intestines, kidney, lungs, brain,
17 .5 log10 50% tissue culture infectious dose [TCID50]) in nasal wash viral titers and inflammation res
18 Viral antigen-specific ELISAs, qRT-PCR and TCID50 infectious assays were utilized to determine anti
21 ingle high doses ranging from 10(7) to 10(9) TCID50 Mahoney type 1 virus were infected, and many of t
22 urine blood (EBOV concentration of 1 x 10(7) TCID50 . ml(-1)) at 4:1 vol/vol buffer/sample ratios.
23 issue culture infective dose per milliliter [TCID50 . ml(-1)]) and murine blood (EBOV concentration o
25 4 x 10(2) 50% tissue culture infective dose (TCID50)/ml, as well as the no-virus negative-control sam
28 50/mL, for a saturation value of ~4.801x10(3)TCID50/mL, with good repeatability and excellent specifi
31 gative adults randomly received either 106.8 TCID50 of ALVAC-CMV(gB) or 106.8 TCID50 of ALVAC-RG, exp
32 ) vector expressing HIV-1MN gp160 or 10(5.5) TCID50 of ALVAC-rabies virus glycoprotein control at 0 a
33 ither 106.8 TCID50 of ALVAC-CMV(gB) or 106.8 TCID50 of ALVAC-RG, expressing the rabies glycoprotein,
34 tion against experimental challenge with 107 TCID50 of attenuated H1N1 (vaccine strain) by intranasal
36 ho were randomized to receive 10(6) or 10(7) TCID50 of canarypox (ALVAC) vector expressing HIV-1MN gp
37 (TCID50) and were able to detect at least 1 TCID50 of enterovirus in cerebrospinal fluid, stool, or
38 nuclear cells (PBMC) were challenged with 10 TCID50 of HIV-1MN or HIV-1BaL, titered in PBMC from norm
39 ety and immunogenicity of two doses of 10(7) TCID50 of live, attenuated cold-adapted (ca) influenza A
44 s received a single intranasal dose (10(6.2) TCID50) of ca A/Kawasaki/9/86 (H1N1) or ca A/Los Angeles
45 10(7) median tissue culture infective doses (TCID50) of MVA-BN, 10 subjects received vaccine containi
46 in 10(6) 50% tissue culture infective doses (TCID50) of SHRV/ml, and adult zebrafish were susceptible
47 ID50) per 0.05 mL], medium dose [7.5 x 10(4) TCID50 per 0.25 mL], or high dose [3.0 x 10(5) TCID50 pe
48 ID50 per 0.25 mL], or high dose [3.0 x 10(5) TCID50 per 1.0 mL]), or the active comparator-Priorix.
49 10(4) median tissue culture infection doses (TCID50) per 0.05 mL], medium dose [7.5 x 10(4) TCID50 pe
51 l dose (LD50) was determined to be 0.015 50% TCID50 (tissue culture infective dose) of MARV/Ang-MA in
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