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1 future development of diagnostic assays and vaccine preparations.
2 fied and/or contaminating TLR ligands in PPS vaccine preparations.
3 prove to be essential components of malaria vaccine preparations.
4 e of such strains or synthetic constructs in vaccine preparations.
6 0 (40 participants); as a control, a placebo vaccine preparation also was administered (10 participan
7 l pathogenesis and host protective immunity, vaccine preparation and characteristics, stimulated host
9 nd that immunization of rabbits with an rD15 vaccine preparation conferred partial protection against
10 HER-2/neu-overexpressing cancers received a vaccine preparation consisting of putative HER-2/neu hel
12 ce with formalin-inactivated influenza virus vaccine preparations containing disparate HA and NA prot
13 ogic materials that come in contact with the vaccine preparation during production to prevent the int
14 more, inclusion of NA in addition to HA in a vaccine preparation for chickens may not enhance the hig
15 nactivated respiratory syncytial virus (RSV) vaccine preparations have been shown to cause enhanced d
18 5) vectors both expressing Ag85A in a single vaccine preparation is able to reduce anti-vector immuni
21 een treated clinically with crude or defined vaccine preparations or cytokines, such as IFN-gamma and
22 nt out the importance of cell substrates for vaccine preparation since the virus may change during pa
23 prior infection and 2 Aspergillus fumigatus vaccine preparations (sonicate and filtrate) administere
24 aride (LPS) and assessed the ability of each vaccine preparation to protect mice against pulmonary ch
26 rticipants and study staff not involved with vaccine preparation were masked to the randomisation gro
27 terns of mutations present at a low level in vaccine preparations were characteristic of seed viruses
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