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1 matode stages released from infected snails (cercariae).
2  in vivo early postinfection with S. mansoni cercariae.
3 ties of infected snails and human-infectious cercariae.
4 t rhesus macaques were exposed to S. mansoni cercariae.
5 -/-) mice were also infected with S. mansoni cercariae.
6  animals were exposed to Schistosoma mansoni cercariae.
7 mph nodes of mice vaccinated with irradiated cercariae.
8 as associated with the presence of trematode cercariae.
9 ercariae tentatively identified as virgulate cercariae.
10 ted, with the highest concentration found in cercariae.
11 animals previously immunized with irradiated cercariae.
12 various times postinfection with schistosome cercariae.
13 ors did not, however, enhance infectivity of cercariae.
14  (24.4%) of the snails shedding schistosomes cercariae.
15 rasites involve their clonal parthenitae and cercariae.
16 ) were infected with 500 Schistosoma mansoni cercariae.
17  after repeated immunization with irradiated cercariae.
18  in humans from nonspecific skin-penetrating cercariae.
19 ly owing to the resource subsidy provided by cercariae.
20 formation of a swimming aggregate of several cercariae adjoined together by their tails.(4) Through t
21 how that this compound paralyzes schistosome cercariae and prevents infection and does so more effect
22 sistently 50 to 80% carried a combination of cercariae and sporocysts of digenetic virgulate trematod
23 documenting the diversity of parthenitae and cercariae and why researchers who do describe them give
24 ts showed differential responses to egg- and cercariae-antigens.
25 ral selection should favour the evolution of cercariae-avoidance behaviours.
26 , is driven by the production of free-living cercariae by snail populations.
27              Extracts of Schistosoma mansoni cercariae caused increased vascular permeability and ede
28 o repeated doses (4x) of Schistosoma mansoni cercariae, compared to a single dose (1x), results in CD
29 Baboons vaccinated with radiation-attenuated cercariae develop high levels of protection against schi
30                          Schistosoma mansoni cercariae display specific behavioral responses to abiot
31 aling reduces a minnows' risk of exposure to cercariae, either directly via detection of cercariae in
32                                              Cercariae exposed to various light/temperature regimens
33 xposures with water (weeks 0 and 9) prior to cercariae exposure (week 18).
34 of an artificial shoal reduced their risk of cercariae exposure compared with those along peripheral
35 were percutaneously infected with S. mansoni cercariae, followed by i.v. injection of eggs.
36           Given that infected snails release cercariae for 3-4 months a year, the pond trematode comm
37              Minnows distinguished infective cercariae from other potential aquatic threats and respo
38 t after a single vaccination with irradiated cercariae in double cytokine-deficient vs wild-type mice
39 ansform rapidly from free-swimming infective cercariae in freshwater to endoparasitic schistosomules.
40  of such stimulants on signaling pathways of cercariae in relation to host finding and invasion.
41  cercariae, either directly via detection of cercariae in the water column followed by behavioural av
42 oma mansoni sporocysts capable of generating cercariae in vitro.
43 ed between 14 and 1660 free-swimming larvae (cercariae) infected snail(-1) 24 h(-1) in mid-summer.
44 he transformation of free-living, infectious cercariae into schistosomula and coincides with the appe
45 sporocysts that give rise to human-infective cercariae larvae.
46 le provides new directions for understanding cercariae motility and new strategies for preventing sch
47  Pacific treefrogs (Hyla regilla) exposed to cercariae of a trematode parasite (Ribeiroia sp.).
48     Repeated CHI with sequential exposure to cercariae of different sexes (male-female-male) revealed
49 ole of NO in mice vaccinated with irradiated cercariae of S. mansoni.
50 vaccinated with 15- or 50-kilorad-irradiated cercariae of S. mansoni.
51     Mice immunized with radiation-attenuated cercariae of Schistosoma mansoni display resistance to c
52 ficant quantities of PGE(2) were produced by cercariae of Schistosoma mansoni following incubation wi
53 C57BL/6 mice vaccinated once with irradiated cercariae of Schistosoma mansoni, is mediated by CD4+ T
54 ice vaccinated a single time with attenuated cercariae of Schistosoma mansoni, the protection induced
55  a supposedly prey-mimetic colony comprising cercariae of two distinct morphotypes.
56                              Aquatic larvae (cercariae) of the trematode parasite Schistosoma mansoni
57 oaling in fathead minnows exposed to larvae (cercariae) of two of their most common species of tremat
58 , and adult worms, but is not present in the cercariae or ciliated miracidia.
59  3 exposures (weeks 0, 9, and 18) to 20 male cercariae, or to the infection control group, which rece
60                  Percutaneous infection with cercariae over the skin site at which cercarial homogena
61 -IG) predators that only consume free-living cercariae (parasitic trematodes) reduced metacercarial i
62       True eDNA was detected in as few as 10 cercariae per liter of water in laboratory experiments.
63 (IgE deficient), were infected by S. mansoni cercariae percutaneously.
64 ory products released by Schistosoma mansoni cercariae rapidly produce IL-10 as a result of MyD88-med
65 occupational exposure to Schistosoma mansoni cercariae revealed that some individuals develop resista
66 sphorylated (activated) CaMKII is present in cercariae, schistosomula and adult worms, and show that
67  each schistosome life stage examined (eggs, cercariae, schistosomula, adult males and females).
68 entional snail surveys (snail collection and cercariae shedding) with eDNA (water samples) showed 71%
69                               Post-treatment cercariae-specific responses were also more proinflammat
70 -spined sticklebacks towards the free-living cercariae stages of two common freshwater trematode para
71 e 22 degrees C the snails released trematode cercariae tentatively identified as virgulate cercariae.
72  developmental stages (eggs, sporocysts, and cercariae) that do not possess the specialized double me
73 roduce a water-soluble factor that paralyzes cercariae, the life cycle stage infecting humans.
74  cages in outdoor mesocosms, exposed them to cercariae, then compared mean worm numbers in grouped vs
75 e S. japonicum life cycle, especially during cercariae transformation, which enables parasites to sur
76  structure and behavior.(1)(,)(2) One of the cercariae transmission strategies is to attain a prey-li
77 e recommence formally naming parthenitae and cercariae using an improved naming scheme.
78 tral issue by using the radiation-attenuated cercariae vaccine in mice genetically engineered to exhi
79           We conclude that in the irradiated-cercariae vaccine model, C57BL/6J and CBA/J mice produce
80  The process of skin invasion by Schistosoma cercariae was reviewed in a recent Trends Research Updat
81 ollowing three immunizations with irradiated cercariae was similar in the two groups.
82 t O-glycans and glycosphingolipid glycans of cercariae were observed.
83 tive sera of mice vaccinated with irradiated cercariae were shown to recognize carbohydrate epitopes
84 atedly vaccinated with 15-kilorad-irradiated cercariae, which also achieve the highest levels of prot
85 up Digenea (flukes) have free-living larvae, cercariae, which are remarkably diverse in structure and
86  showing increased production of schistosome cercariae with greater access to food resources.
87 ential role of fish as biocontrol agents for cercariae with similar dispersion strategies, in instanc