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1 potency to non-disease-inducing Ags using a bacterial vaccine.
2 emic or mucosal immunizations with viral and bacterial vaccines.
3 ing the use of MIP antigens for inclusion in bacterial vaccines.
4 kable improvement in the development of live bacterial vaccines.
5 , and it is now being used for several other bacterial vaccines.
6 ustained following vaccination with a killed bacterial vaccine adjuvanted with aluminum hydroxide and
7 hetic CpG-ODNs but not with the DNA of mixed bacterial vaccine and were shown to be phosphorothioate
9 crobial origin and to an orally administered bacterial vaccine, and plasma-derived IgG Abs to systemi
11 e present uncertainty of which live viral or bacterial vaccines can be given to immunodeficient patie
12 ation may be potentially applied to numerous bacterial vaccine candidates, and irradiated bacteria co
13 alysis of 6 civilian studies of mixed killed bacterial vaccines containing pneumococci identified sig
14 stematic review and reanalysis of studies of bacterial vaccine efficacy (VE) in preventing pneumonia
16 size and nanometer size), we have designed a bacterial vaccine form that exhibits improved efficacy o
17 to multiple pneumococcal serotypes and that bacterial vaccines may play a role in preventing influen
18 e humoral immunity induced by many viral and bacterial vaccines mediates protection that is maintaine
20 ing mutations into candidate live attenuated bacterial vaccines offers a promising approach for the d
21 rt of the World Health Organization Invasive Bacterial-Vaccine Preventable Diseases (IB-VPD) surveill
22 ion of immature/T1 B cells by TLR ligands or bacterial vaccine rapidly induces T1 cells to divide, pr
23 a, as well as stockpiling of antibiotics and bacterial vaccines, should also be high priorities for p
25 rradiated Listeria monocytogenes as a killed bacterial vaccine, testing the hypothesis that irradiati
26 e elicited by oral delivery of a recombinant bacterial vaccine, tetanus toxin fragment C (TTFC) was e
27 ecular patterns found in attenuated viral or bacterial vaccines that function as Toll-like receptor (
28 A new target strategy in the development of bacterial vaccines, the induction of antibodies to micro
30 sistance marker-free DNA vaccines as well as bacterial vaccine vectors devoid of engineered antibioti
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