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1 f the human CCKB/gastrin receptor coupled to diphtheria toxoid.
2  those who had received at least one dose of diphtheria toxoid.
3 ached to protein carriers such as tetanus or diphtheria toxoids.
4 eness of one, two, or three or more doses of diphtheria toxoid against diphtheria among 40- to 49-yea
5 ination coverage with three or more doses of diphtheria toxoid among adults and children.
6 mmunogenicity and safety of a single dose of diphtheria toxoid among adults, blood samples for detect
7 the complete primary vaccination series with diphtheria toxoid and adults 40-49 years of age were the
8  reduced the interval since the last dose of diphtheria toxoid and improved protection against diphth
9  in the infants and their immune response to diphtheria toxoid and pneumococcal vaccination.
10 nd did not affect infant immune responses to diphtheria toxoid and pneumococcal vaccination.
11 Control and Prevention recommend tetanus and diphtheria toxoids and acellular pertussis (Tdap) vaccin
12 ids and acellular pertussis, and tetanus and diphtheria toxoids and acellular pertussis vaccines are
13 us, meningococcal conjugate, and tetanus and diphtheria toxoids and acellular pertussis vaccines.
14 al immunization with tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis (Tdap) vaccin
15 recommended that the tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis vaccine (Tdap
16 single dose of Tdap (tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis vaccine).
17       In 2012, Tdap (tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis) vaccine was
18  (eg, meningococcal; tetanus toxoid, reduced diphtheria toxoid, and reduced acellular pertussis; and
19                   In contrast, the mean anti-diphtheria toxoid antibody response increased with incre
20 nt meningococcal conjugate vaccine that uses diphtheria toxoid as the protein carrier (MCV4-DT).
21 ted a panel of diverse hMAbs that recognized diphtheria toxoid, as well as a variety of recombinant p
22 d W-135) meningococcal vaccine conjugated to diphtheria toxoid at 1 of 3 doses and were monitored for
23 alled in January 1999 because of a subpotent diphtheria toxoid component.
24 ter vaccination with either PRP alone or the diphtheria toxoid conjugate of PRP.
25 he A, C, Y, and W-135 Neisseria meningitidis-diphtheria toxoid conjugate vaccine, when given to healt
26  a C. neoformans serotype D strain 24067 GXM-diphtheria toxoid conjugate.
27 this and other studies, low effectiveness of diphtheria toxoid-containing vaccine was suspected to be
28 e produce a single antigenic type of DT, and diphtheria toxoid continues to be an effective vaccine f
29 ere then conjugated with the carrier protein diphtheria toxoid cross-reactive material (CRM) 197 (DT)
30 otein, including keyhole limpet hemocyanion, diphtheria toxoid cross-reactive material (CRM) 197 (DT)
31 P13 was conjugated to tetanus toxoid (TT) or diphtheria toxoid (DT) and administered subcutaneously i
32 tion) were conjugated to the carrier protein diphtheria toxoid (DT) and used to immunize animals.
33 ), pertactin (Prn), tetanus toxoid (TT), and diphtheria toxoid (DT) were measured using commercially
34 w DC pulsed in vitro with an intact protein (diphtheria toxoid (DT)) produce exosomes that induce, in
35 onjugated to an immunogenic carrier protein, diphtheria toxoid (DT), and formulated in a nanoparticul
36 uvants that have activity on the skin, using diphtheria toxoid (DTx) and tetanus toxoid as model anti
37 han microparticles with two antigens (TT and diphtheria toxoid) entrapped simultaneously.
38  infection, required at least three doses of diphtheria toxoid for reliable protection against diseas
39 ning only 12 aa from GAS, when conjugated to diphtheria toxoid, has been shown to protect mice agains
40 dred fifty samples were studied by ELISA for diphtheria toxoid IgG antibodies to assess the utility o
41    This study suggests that one dose of 2 Lf diphtheria toxoid is highly effective in raising DAT to
42                    However, S2 conjugated to diphtheria toxoid is highly immunogenic and induces Abs
43  30 days after immunization with Td (tetanus-diphtheria toxoids; manufactured by Serum Institute of I
44 ]) and to have a time since the last dose of diphtheria toxoid of 3-4 years (3.1 [1.1-9.1]) or 5-7 ye
45 ng Ag derived from allografts, we used CD11c-diphtheria toxoid receptor mice to conditionally ablate
46 egies, the immunogenicity of the tetanus and diphtheria toxoids (Td) vaccine was assessed.
47 idered eligible for vaccination with tetanus-diphtheria toxoids (Td).
48 s documented; (6) neonatal immunization with diphtheria toxoid, tetanus toxoid, and acellular pertuss
49 ria toxoid-tetanus toxoid-pertussis (DTP) or diphtheria toxoid-tetanus toxoid (DT) vaccine, 1 to 3 do
50  Previous studies suggested that tetanus and diphtheria toxoids (TTD and DTD, respectively) contain "
51 f maintaining high levels of age-appropriate diphtheria toxoid vaccination, surveillance, accessible
52 r dose of V-TT CV (n=22) or licensed tetanus-diphtheria toxoid vaccine (Td) (n=10; double-masked desi
53 ings, which showed that protection by the J8-diphtheria toxoid vaccine is Ab-mediated and suggest tha
54 sive adult coverage rates for first doses of diphtheria toxoid vaccine, communication interventions e
55  (92%) had received three or more doses of a diphtheria toxoid vaccine, compared with 72% of case-pat
56 trol strategies, immunogenicity of a tetanus-diphtheria toxoids vaccine (Td) containing 2 limits of f
57                            A booster dose of diphtheria-toxoid vaccine given to children in the Russi
58 ontrols had received at least three doses of diphtheria-toxoid vaccine.
59 Td) containing 2 limits of flocculation (Lf) diphtheria toxoid was evaluated.
60  diphtheria toxin reacted with formaldehyde (diphtheria toxoid) was compared to that of diphtheria to
61  coadministered antigens such as tetanus and diphtheria toxoids when applied to the skin.
62 47%) controls had received a booster dose of diphtheria toxoid within the previous 2 years.

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