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1 uggesting that rV10 may serve as an improved plague vaccine.
2 lla flagellin as an adjuvant in an acellular plague vaccine.
3 ndidate for development of an effective anti-plague vaccine.
4 ve antigen proposed for inclusion in subunit plague vaccines.
5 but should not be exposed to live-attenuated plague vaccines.
6 YopE could be a valuable addition to subunit plague vaccines and provide a new animal model in which
8 e human immune response to a new recombinant plague vaccine, comprising recombinant F1 (rF1) and rV a
9 Mice delivered with a single dose of F1-V plague vaccine containing both gene and protein in the T
14 tis challenge, and we suggest that pneumonic plague vaccines should aim to induce mixed type 1 and ty
15 These observations strongly suggest that plague vaccines should strive to maximally prime both ce
16 rongly suggest that development of pneumonic plague vaccines should strive to prime both CD4 and CD8
17 ar Typhi strain to create a bivalent mucosal plague vaccine that produces both the protective F1 caps
18 aid the development of a safe and effective plague vaccine, we are investigating roles for T cells d
19 As a first step in formulating an improved plague vaccine, we developed a simple purification strat
20 a part of a project to develop a plant-made plague vaccine, we expressed our model antigen, the Yers
21 a part of a project to develop a plant-made plague vaccine, we expressed the Yersinia pestis F1-V an
22 development of safe and effective pneumonic plague vaccines, we are deciphering mechanisms used by t
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