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1 tug of war for iron may provide a new way to vaccinate.
2 ed toxins against which the patient could be vaccinated.
3 e used to adjust for the likelihood of being vaccinated.
4 ls within the labor-sending communities were vaccinated.
5 eptibility was detected among the repeatedly vaccinated.
6 ia is common and almost all children are BCG-vaccinated.
7 zing antibodies than naive subjects who were vaccinated.
8 nt women and infants who are too young to be vaccinated.
9 but fewer than half of these travelers were vaccinated.
10 ding similar levels of efficiency per person vaccinated.
11 21, 2013, and Jan 11, 2016, we enrolled and vaccinated 101 participants with 306 doses of mRNA (80-6
13 cRCTs in which preschool-aged children were vaccinated: 22% (95% CI, 1%-38%; I2 = 0%; N = 1903) agai
15 s also significantly reduced among HPV-16/18-vaccinated (4.1%) compared with unvaccinated subjects (1
17 communities where school-aged children were vaccinated: 60% (95% confidence interval [CI], 41%-72%;
18 However, ILI incidence was similar between vaccinated (7.6% and 10.8%) and nonvaccinated (4.2% and
19 9.6% (CI, 8.4% to 10.8%) of candidates were vaccinated, 7.5% (CI, 6.4% to 8.6%) had no documented va
22 sfer of antisera or CD4(+) T cells from PhtD-vaccinated adult mice led to a nonsignificant reduction
25 , there have been no recurrences in patients vaccinated after receiving trastuzumab as part of standa
26 Best Practice Advice 1: Clinicians should vaccinate against hepatitis B virus (HBV) in all unvacci
33 iduals, who had given informed consent, were vaccinated and followed up for 21 days under good clinic
36 d declines in rotavirus infection and AGE in vaccinated and unvaccinated age groups within 1 year of
37 illomavirus (HPV) prevalence among HPV-16/18-vaccinated and unvaccinated Finnish male adolescents par
38 No differences were detected between the vaccinated and unvaccinated groups in risk for inpatient
39 ere used to compare disease severity between vaccinated and unvaccinated patients, adjusting for timi
40 cine immediately; vaccination protected both vaccinated and unvaccinated people in those clusters.
41 s (IRRs) of suspected and confirmed cases in vaccinated and unvaccinated populations were estimated w
43 e, 2151 consented, and 2119 were immediately vaccinated) and 4557 contacts and contacts of contacts i
45 pe HPV (HPV-6, -11, -16, and -18) among all, vaccinated, and unvaccinated women at waves 1, 2, and 3,
46 uman donors with natural HCMV infection or a vaccinated animal, we mapped eight sites on the dominant
48 d markedly lower influenza titers than RD-Ad-vaccinated animals after challenge with influenza A/PR/8
51 position of C3d in the corneal epithelium of vaccinated animals following challenge and delayed viral
52 nasopharyngeal virulent bacterial burden of vaccinated animals was substantially reduced (0.002%) co
54 connected individuals are more likely to get vaccinated, as are people who are exposed to friends who
55 ing of viral nucleic acids from the stool of vaccinated, asymptomatic children and their close contac
59 cancer varied from 55% (53-56%) among women vaccinated at age 9 years to 6% (range: 6-7%) among wome
60 Of the MMR-eligible, 3477 (53%) were not vaccinated at the visit; of these, 1689 (48%) were not v
62 at the visit; of these, 1689 (48%) were not vaccinated because of traveler refusal, 966 (28%) becaus
63 increasingly evident, especially among girls vaccinated before HPV exposure in countries with high va
64 ns exemplify a complex, coupled system where vaccinating behavior and disease dynamics influence one
65 sults support the hypothesis that population vaccinating behavior near the disease elimination thresh
75 cremental cost-effectiveness ratio (ICER) of vaccinating boys was euro9134/LY (95% credible interval
76 Because of the high risk of reinfection, vaccinating boys who have not yet been exposed may be cr
78 most likely arose from unvaccinated or under-vaccinated canines, not from a novel CPV strain incapabl
79 d occurred by 10 days postinfection (dpi) in vaccinated cattle and by 21 dpi in nonvaccinated animals
81 eloping and refining approaches to reach and vaccinate children and other vulnerable populations in c
82 ncidences decreased between 2005 and 2016 in vaccinated children (by 68.5%), and in the whole populat
85 influenza A or B virus in all participants (vaccinated children and persons who did not receive the
86 eactive T-cell response in 14 trivalent LAIV-vaccinated children using the fluorescent immunospot ass
87 s the many well-trained polio staff who have vaccinated children, conducted surveillance, tested stoo
92 iterature on "herd"/indirect protection from vaccinating children aged 6 months to 17 years against i
93 better quantify the indirect protection from vaccinating children for different settings/endpoints.
95 trial, with rates of increase for six orally vaccinated chimpanzees very similar to four intramuscula
96 cell responses were also detected in Triplex-vaccinated CMV-seronegatives, and in DryVax-vaccinated s
100 s of circulating CXCL13 were higher in those vaccinated compared with controls, mirroring an increase
101 itis cases declined by 57% (95% CI 55-59) in vaccinated compared with unvaccinated populations, with
102 Adjusted vaccine effectiveness for confirmed vaccinated compared with unvaccinated women was 95.93% (
104 re after randomisation among all immediately vaccinated contacts and contacts of contacts versus 23 c
109 fected animals, which may lead to disease in vaccinated dogs that are also infectious to sand flies.
111 as also lower for participants consecutively vaccinated during both the current and prior seasons (41
114 easons (41%; 95% CI, 18%-57%) than for those vaccinated during the current season only (75%; 95% CI,
115 ram (RWHAP), 12.5% (CI, 11.1% to 13.9%) were vaccinated during the surveillance period versus 3.7% (C
116 g a 5-year period in California in an cohort vaccinated exclusively with acellular pertussis (aP) vac
117 ntly we reported a vaccine-induced sex bias: vaccinated female but not male rhesus macaques exhibited
121 2.3.4.4), whereas antisera from dk/Hok/69 ca-vaccinated ferrets cross-reacted with clade 2.3.4.4 and
125 vel decreases in CIN among cohorts partially vaccinated for HPV may be considered when clinical pract
128 T by neutralising antibody assay in the H5N2 vaccinated group (1395.85 [1040.79-1872.03]) was also si
129 ition antibodies in the previously LAIV H5N2 vaccinated group (566.89 [95% CI 436.97-735.44]) were si
132 rgeted vaccination programs could be used to vaccinate habituated great apes but also human populatio
133 sponses could be elicited in humans requires vaccinating human subjects with a fibroblast-adapted mut
134 h immune sera and monoclonal antibodies from vaccinated humans showed not only high-level ADCC and AD
135 SAT-6 and Ag85B, in Mtb-infected mice and in vaccinated humans with and without underlying Mtb infect
136 y, transfection with long dsRNA specifically vaccinates IFN-deficient cells against infection with vi
140 timated to be 51% (95% CI, 45%-57%) in those vaccinated in both the current and previous season, comp
141 17 and April 21, 2016, 1510 individuals were vaccinated in four rings in Guinea, including 303 indivi
142 y assigned contacts and contacts of contacts vaccinated in immediate clusters versus 16 cases (7 clus
145 ver, the protection was lower in individuals vaccinated in the current season after >2 prior doses (3
146 s was not statistically lower in individuals vaccinated in the current season only (52%) or in those
147 season, compared with 33% (95% CI, 17%-47%) vaccinated in the current season only and 35% (95% CI, 2
148 nce interval, 49%-78%) was observed in those vaccinated in the current season who had received 1-2 pr
149 children were unvaccinated, 349 mothers were vaccinated in the first trimester, and 5962 mothers were
153 eed for high vaccination coverage to protect vaccinated individuals and chemoprophylaxis for close co
154 dence of Ebola virus disease in eligible and vaccinated individuals assigned to immediate vaccination
155 nst Ebola virus disease, with no cases among vaccinated individuals from day 10 after vaccination in
157 s, but their use potentially will predispose vaccinated individuals to infection by the related Dengu
159 onships at equilibrium among the fraction of vaccinated individuals, the population size, the basic r
162 vaccinees were present in 43% of MF59/rgp120-vaccinated infants but only in 12% of the vaccinated adu
163 he effect was caused by herd immunity, since vaccinated infants were more likely to be surrounded by
164 utaneously, which is the preferred route for vaccinating infants, who may develop nasal congestion as
165 , bone marrow, and mesenteric lymph nodes of vaccinated infected, unvaccinated infected, and uninfect
170 CD4(+) T cells from bacillus Calmette-Guerin-vaccinated mice and show that high-quality microarrays c
171 16-ova-Melanoma) protection in around 40% of vaccinated mice and significantly delayed tumor progress
177 t epitopes caught up with the conventionally vaccinated mice, and analysis of the breadth of the CD8(
178 in PhtD-vaccinated adult mice, but not PCV13-vaccinated mice, caused a loss of vaccine-induced protec
183 Initiative has made substantial progress in vaccinating millions of children worldwide, including th
189 f two unvaccinated controls, two of the four vaccinated monkeys showed no detectable viral RNA sequen
190 immune deficiency syndrome, enabling 50% of vaccinated monkeys to clear a subsequent virulent simian
191 ries of heroin challenges over six months in vaccinated monkeys, drug-sequestering antibodies caused
192 ible adverse effects in offspring of A(H1N1)-vaccinated mothers beyond the perinatal period and into
194 s, antibody responses among children born to vaccinated mothers were reduced based on earlier adminis
197 eling to estimate the added effectiveness of vaccinating multiple cohorts of females (12-26 years) in
199 nd RIG-I-like helicase signaling, whereas in vaccinated MyD88(-/-) mice the adjuvant effect was reduc
200 ted by the absence of the adjuvant effect in vaccinated MyD88(-/-)Cardif(-/-) mice, which are devoid
202 re people who are exposed to friends who get vaccinated or are exposed to friends who get the flu.
203 ed with different H1N1 isolates before being vaccinated or infected with another influenza virus.
204 pen-label trial was done in which previously vaccinated participants (40 from LAIV H5N2 group and 20
205 reactions, and 50 (78%) of 64 intradermally vaccinated participants and 29 (78%) of 37 intramuscular
206 st vaccination, 60 (94%) of 64 intradermally vaccinated participants and 36 (97%) of 37 intramuscular
207 ticipants and 36 (97%) of 37 intramuscularly vaccinated participants reported solicited injection sit
208 ticipants and 29 (78%) of 37 intramuscularly vaccinated participants reported solicited systemic adve
210 strategy to improve on the effects of BCG in vaccinated people living in tuberculosis-endemic countri
212 make it easier to see when friends have been vaccinated (personalized vaccination campaigns) and when
213 (IIV) in providing both direct protection in vaccinated persons and herd protection in unvaccinated p
216 s cytology-screened women in Australia's HPV-vaccinated population (by 2014, resident women </=33 yea
217 and how these could be applied to reach and vaccinate populations in other settings across the world
222 rstanding and refining current approaches to vaccinating populations in conflict and humanitarian eme
225 on this cocktail approach by simultaneously vaccinating rabbits with a combination of plasmids encod
226 monthly decreases in the number of children vaccinated ranging from -419 (95% CI -683 to -155; p=0.0
227 ere individuals can dynamically adjust their vaccinating strategies and their payoffs depend nonlinea
230 efficacy study, a group of sheep (n = 5) was vaccinated subcutaneously with the glycoprotein-based su
235 in other young children too old to have been vaccinated suggest additional benefit through indirect p
237 genetically modified virus, we were able to vaccinate swine and protect them from developing ASF.
238 es were unable to secure sufficient doses to vaccinate the entire at-risk population-approximately 1
242 jects with preexisting immunity to DENV were vaccinated, they developed higher levels of neutralizing
246 women, with 2-fold fewer women needing to be vaccinated to prevent SDI (4; 95% CI, 3-8) than PCR-CI (
248 analyze the antibody repertoire in subjects vaccinated two years in a row with either identical vacc
249 urse of a more chronic viral infection, mice vaccinated using the vaccine targeting subdominant epito
250 6/11 infections was significantly reduced in vaccinated versus unvaccinated individuals (0.11% v 1.61
251 6/11 infections was significantly reduced in vaccinated versus unvaccinated men (0.0% v 2.13%; Padj =
252 s ratios (ORs) comparing disease outcomes in vaccinated versus unvaccinated participants via multivar
256 unization, nine (64%) of 14 (95% CI, 35-87%) vaccinated volunteers remained without parasitemia compa
257 mal cervical cytology result was lower among vaccinated vs unvaccinated females (hazard ratio [HR], 0
258 stment, stillbirth was 51% less likely among vaccinated vs unvaccinated mothers (aHR, 0.49; 95% confi
259 Most MMR-eligible travelers who were not vaccinated were evaluated in the South (2262 travelers [
260 y infants aged 6 weeks, not previously polio vaccinated, were allocated after computer-generated rand
262 d vaccination strategy, in which miners were vaccinated while in the mines, with that of a community-
264 ubjects were randomized 2:2:2:2:1; 1194 were vaccinated with 1 dose of 1 of 3 lots of rVSVDeltaG- ZEB
267 these studies, we found that when mice were vaccinated with a combination of CPS-CRM197 and Hcp1, 10
269 ly, ferrets infected with the 1986 virus and vaccinated with a single dose of the COBRA HA VLP vaccin
270 blood mononuclear cells (PBMCs) from donors vaccinated with a tetravalent DLAV vaccine (TV005) with
271 ior and durable B-cell responses in macaques vaccinated with an occluded CD4 binding site on the HIV
273 possesses the glycosylation site) and humans vaccinated with baculovirus-expressed H3 antigens (that
274 erved a marked increase in skin Treg in mice vaccinated with Ccl22, with repetitive vaccination suffi
276 lung pathology was observed only in animals vaccinated with FI-RSV, but not in animals vaccinated wi
277 mmunized with GP-alone or GP-alpha-syn, mice vaccinated with GP+RAP or GP+RAP/alpha-syn displayed inc
279 ) of 40 participants who had previously been vaccinated with LAIV H5N2 had an increase in haemaggluti
280 anticoagulated blood from 12 healthy adults vaccinated with meningococcal serogroup B and serogroup
285 at monoclonal antibodies derived from humans vaccinated with the HVEM binding domain of HSV-1 gD (i)
286 of people worldwide, most of whom have been vaccinated with the partially effective Mycobacterium bo
287 e the CD8 T cell responses of human subjects vaccinated with two fibroblast-adapted HCMV vaccines.
288 s vaccinated with FI-RSV, but not in animals vaccinated with unadjuvanted or adjuvanted RSV-G vaccine
289 HA VLP vaccines than COBRA preimmune ferrets vaccinated with VLP vaccines expressing wild-type HA pro
290 challenged newborn mice born to female mice vaccinated with VSVm-ZENV containing the transmembrane d
293 d the antibody responses in girls previously vaccinated with zero, 1, 2, or 3 doses of quadrivalent H
294 ulticenter study, adults >/=65 years of age, vaccinated with ZVL >/=5 years previously (HZ-PreVac), w
296 rios that offer less intensive screening for vaccinated women and more on increasing coverage and inc
298 significantly lower (0.61%) among confirmed-vaccinated women than among those who self-reported vacc
299 fectiveness of the bivalent vaccine in these vaccinated women who attended for routine cervical scree
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