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1 e response to that elicited by the IpaB/IpaD combination vaccine.
2 o be the highest dose level of 3.0 mg of the combination vaccine.
3 ween monovalent RSV cpts-248/404 vaccine and combination vaccine.
4 sponsiveness of the env DNA component in the combination vaccine.
5 strains in humans could be rectified by this combination vaccine.
8 s received a separate consistency lot of the combination vaccine, and 1 group received separate but c
13 ating the potential for the development of a combination vaccine consisting of Invaplex and other imm
18 ages 2, 3, and 4 months until 2004, when new combination vaccines containing inactivated poliovirus w
21 acterization of a recombinant hypoallergenic combination vaccine for specific immunotherapy of HDM al
25 ved as the number of doses of the DTaP/PRP-T combination vaccine increased (P<.02 and P=.01, respecti
26 ears of life has increased, and although new combination vaccines may eventually simplify the schedul
29 gella is endemic, protection studies using a combination vaccine of Shigella sonnei vaccine strain WR
32 PIV3 vaccine; 16 (76%) of 21 children given combination vaccine shed PIV3-cp45 versus 11 (92%) of 12
33 se results demonstrate the potential of this combination vaccine strategy and suggest that vaccine pr
34 using the chimpanzee model to investigate a combination vaccine strategy involving sequential primin
37 nes cell envelope proteinase, we developed a combination vaccine that is highly effective in blocking
38 he UK has coincided with the distribution of combination vaccines that contain acellular pertussis (D
39 B vaccine (Engerix-B), and hepatitis A and B combination vaccine (Twinrix) were studied using the VAE
42 e level of protection afforded by WRSd1 in a combination vaccine was lower than the protection elicit
45 similar across immunization types, including combination vaccines when compared with single-dose vacc
46 or receptor (HER2) extracellular domain in a combination vaccine with a promiscuous T-cell epitope (i
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