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1 ease caused by trematode flukes of the genus Schistosoma.
2 ection with parasitic helminths of the genus Schistosoma.
3 on caused by various trematodes of the genus Schistosoma.
4 the first report of lethal gene silencing in Schistosoma.
5 disease caused by blood flukes of the genus Schistosoma.
6 The coevolution of blood flukes of the genus Schistosoma and their human hosts is paradigmatic of lon
8 ned from Mali with a Schistosoma haematobium-Schistosoma bovis hybrid infection, confirmed by DNA seq
10 iased immune responses in mice infected with Schistosoma, but the precise mechanism remains to be elu
12 ponses during Schistosoma mansoni infection, Schistosoma egg antigen (SEA) immunization, and house du
14 ternal transcribed spacer) DNA data from the Schistosoma eggs or miracidia recovered from the infecte
16 eta-induced pulmonary vascular disease after Schistosoma exposure, and targeted inhibition of this pa
22 young adults were recruited from areas where Schistosoma haematobium (S.h) infections were high or lo
23 aran Africa show that genital infection with Schistosoma haematobium [corrected] may increase the ris
24 compared patterns of recognition of defined Schistosoma haematobium adult worm antigens by serum ant
26 the distribution of Schistosoma mansoni and Schistosoma haematobium and the incidence of schistosomi
27 sthorchis viverrini, Clonorchis sinensis and Schistosoma haematobium are classified as Group 1 biolog
28 thorchis viverrini, Clonorchis sinensis, and Schistosoma haematobium are classified as group 1 biolog
31 d 7-12-y-old anemic children with documented Schistosoma haematobium infection (n = 224 for AGP, CRP,
32 s consistent with observed field patterns of Schistosoma haematobium infection and antibody responses
33 assessed whether bladder pathology in human Schistosoma haematobium infection is related to the bala
39 trongly associated with increasing levels of Schistosoma haematobium worm IgG1, with adolescents with
41 es urinary tract coinfection by bacteria and Schistosoma haematobium worms, the etiologic agent of ur
43 , in turn, reduces morbidity is proposed for Schistosoma haematobium, a parasite of major public heal
45 osomiasis, caused by the parasitic trematode Schistosoma haematobium, affects over 112 million people
46 Urogenital schistosomiasis, infection with Schistosoma haematobium, is linked to increased risk for
48 lated from 12 patients showed infection with Schistosoma haematobium, S haematobium-Schistosoma bovis
49 Africa, 112 million people are infected with Schistosoma haematobium, with the most intense infection
51 eins recognized by pooled serum samples from Schistosoma haematobium-exposed Zimbabweans were determi
52 recently published study, which included 163 Schistosoma haematobium-infected individuals and 183 mat
55 Belgian travelers returned from Mali with a Schistosoma haematobium-Schistosoma bovis hybrid infecti
61 py despite the presence of SULT orthologs in Schistosoma hematobium and Schistosoma japonicum The rea
62 previously demonstrated that infection with Schistosoma hematobium was associated with protection ag
63 giardia (in 5.7%), trichuris (in 5.0%), and schistosoma (in 1.8%); among 5575 Southeast Asian refuge
65 -/-) or IL-13(-/-) mice, were protected from Schistosoma-induced PH, with decreased right ventricular
67 on driven by IL-4 and IL-13 is necessary for Schistosoma-induced TGF-beta-dependent vascular remodeli
68 pression in resting splenic macrophages from Schistosoma-infected mice and in wild-type lamina propri
71 The proportion of children infected with Schistosoma japonicum (15.6%, P = .03) and hookworm (22.
73 d transcriptomic profiles of male and female Schistosoma japonicum across eight time points throughou
75 d both prepatent and patent infections using Schistosoma japonicum DNA isolated from serum, urine, sa
76 among 99 pregnant women living in an area of Schistosoma japonicum endemicity in the Philippines.
77 nates born to mothers residing in an area of Schistosoma japonicum endemicity was assessed for these
79 -sectional relation between the intensity of Schistosoma japonicum infection, hemoglobin concentratio
82 human pathogens that cause schistosomiasis, Schistosoma japonicum is the only one that is endemic in
83 omiasis, the indirectly transmitted helminth Schistosoma japonicum remains endemic, partly because of
84 e relationship between cytokine responses to Schistosoma japonicum soluble adult worm extract (SWAP),
85 asts were placed in culture and treated with Schistosoma japonicum soluble egg antigens (SEA) or plas
86 SULT orthologs in Schistosoma hematobium and Schistosoma japonicum The reason for this species-specif
88 who were otherwise healthy but infected with Schistosoma japonicum were enrolled and randomly assigne
90 differences between Schistosoma mansoni- and Schistosoma japonicum-induced hepatic granuloma are also
92 ne candidates rSj97, rSj67, and rSj22 from a Schistosoma japonicum-infected cohort in Leyte, the Phil
95 t study in Leyte, the Philippines, among 611 Schistosoma japonicum-infected participants 7-30 years o
99 fect that multiple percutaneous exposures to Schistosoma larvae has on the development of early CD4+
100 e hookworm (45%), Mansonella perstans (21%), Schistosoma mansoni (18%), and Plasmodium falciparum (11
102 in a Ca(v)beta subunit of the human parasite Schistosoma mansoni (beta(Sm)), a motif that does not oc
103 Here, we express SMDR2, a Pgp homologue from Schistosoma mansoni (Platyhelminthes), in Chinese hamste
104 e Ags from the eggs of the helminth parasite Schistosoma mansoni (schistosome egg Ag (SEA)) leads to
106 opeptidases (legumains) from the bloodfluke, Schistosoma mansoni (SmAE), and the hard tick, Ixodes ri
107 The taurocyamine kinase from the blood fluke Schistosoma mansoni (SmTK) belongs to the phosphagen kin
110 ic disease caused by the parasitic trematode Schistosoma mansoni after deposition of eggs in the live
112 glycoprotein (VSVG) for the transduction of Schistosoma mansoni and delivery of reporter transgenes
114 on, a cohort of 163 Ugandans coinfected with Schistosoma mansoni and HIV-1 was treated with praziquan
117 co-infection model in C57BL/6 mice involving Schistosoma mansoni and Leishmania donovani, two importa
118 wed much less mortality after infection with Schistosoma mansoni and much more susceptibility to Nipp
119 -21R-/- mice with the Th2-inducing pathogens Schistosoma mansoni and Nippostrongylus brasiliensis and
120 in mice infected with the helminth parasite Schistosoma mansoni and observed an upregulation of CD14
121 exposed EC2 domain from Sm-TSP-2, a TSP from Schistosoma mansoni and one of the better prospects for
125 nevitably influence both the distribution of Schistosoma mansoni and Schistosoma haematobium and the
128 e, we demonstrate that somatic stem cells in Schistosoma mansoni are biased towards generating a popu
130 The blood flukes Schistosoma japonicum and Schistosoma mansoni are the first major human platyhelmi
136 to excretory/secretory products released by Schistosoma mansoni cercariae rapidly produce IL-10 as a
137 vy and quantifiable occupational exposure to Schistosoma mansoni cercariae revealed that some individ
138 t exposure of mice to repeated doses (4x) of Schistosoma mansoni cercariae, compared to a single dose
142 ucture of a hammerhead ribozyme derived from Schistosoma mansoni containing the rate-enhancing periph
143 to determine whether children infected with Schistosoma mansoni develop protection-related immune re
145 C57BL/6 mice infected with the helminth Schistosoma mansoni develop small hepatic granulomas aro
146 weight, although a recent treatment trial in Schistosoma mansoni did not detect this association.
147 ted, pathogen-derived Ag (soluble extract of Schistosoma mansoni egg [SEA]) that induces type 2 immun
149 egulated in response to the helminth soluble Schistosoma mansoni egg Ag, which conditions DCs to indu
150 cteria bovis purified protein derivative and Schistosoma mansoni egg antigen challenge indicating an
152 nt were confirmed by in vivo studies using a Schistosoma mansoni egg-challenged mouse model, a well-s
153 obese mice with recombinant helminth-derived Schistosoma mansoni egg-derived omega1 (omega1), a poten
154 signaling participates in the development of Schistosoma mansoni egg-induced CD4(+) Th2 responses, it
157 osylated T2 ribonuclease (RNase) secreted by Schistosoma mansoni eggs and abundantly present in solub
159 sensitized and subsequently challenged with Schistosoma mansoni eggs developed pulmonary hypertensio
160 responses against Trichuris muris worms and Schistosoma mansoni eggs do not develop in mice with IRF
161 ch the mice were sensitized with inactivated Schistosoma mansoni eggs followed by S. mansoni egg Ag c
163 le egg antigens (SEA; a soluble extract from Schistosoma mansoni eggs) inhibit the activation of DCs
165 After exposure to bleomycin (BLM), but not Schistosoma mansoni eggs, IL-17A produced by CD4(+) and
172 onal study, examining children infected with Schistosoma mansoni from 6 schools in Uganda that had pr
174 ta, a natural host for the human blood fluke Schistosoma mansoni Granulins are growth factors that dr
175 esolution crystal structure of a full-length Schistosoma mansoni hammerhead ribozyme that permits us
176 ferring immunity to the intestinal trematode Schistosoma mansoni Here, we report that abrogation of I
177 amates were prepared as potent inhibitors of Schistosoma mansoni histone deacetylase 8 (smHDAC8).
180 fection of mammals by the parasitic helminth Schistosoma mansoni induces antibodies to glycan antigen
182 mmunopathological characteristics, caused by Schistosoma mansoni infection in IL-4 receptor alpha-def
183 t helminthic parasites using the established Schistosoma mansoni infection model in 2 novel mouse mod
184 aecal slides over three consecutive days for Schistosoma mansoni infection simultaneously by age grou
187 thin cDCs impaired Th2 cell responses during Schistosoma mansoni infection, Schistosoma egg antigen (
198 resistance of B. glabrata to infection with Schistosoma mansoni or Echinostoma paraensei, and functi
200 as evident in DCs responding to the helminth Schistosoma mansoni or the allergen house dust mite (HDM
205 ome worm antigens were associated with lower Schistosoma mansoni reinfection intensity, while no asso
210 crystal structures of the GTPase domain of a Schistosoma mansoni septin (SmSEPT10), one bound to GDP
211 ilonRI coaggregation mediated by HIVgp120 or Schistosoma mansoni soluble egg Ag accelerated maximal C
213 earch identified Schistosoma haematobium and Schistosoma mansoni surveys done in, respectively, 9318
215 tigens, including the allergen-like proteins Schistosoma mansoni tegumental-allergen-like 1 protein (
218 ant public health problem and infection with Schistosoma mansoni the major cause of liver disease.
219 egrated QSAR-based virtual screening (VS) of Schistosoma mansoni thioredoxin glutathione reductase (S
220 ova in mice infected with the human parasite Schistosoma mansoni through mechanisms that are currentl
221 levels in 177 Ugandans (aged 7-50) in a high Schistosoma mansoni transmission area, both before and 7
223 ucture of a hammerhead ribozyme derived from Schistosoma mansoni under conditions that permit detaile
226 irst description of an SCP/TAPS gene family (Schistosoma mansoni venom allergen-like (SmVALs)) in the
227 dent folding of the hammerhead ribozyme from Schistosoma mansoni was monitored with double electron-e
232 f dmd-1 exhibits male-specific expression in Schistosoma mansoni, a derived, dioecious flatworm.
233 ized a new member of the cyclase family from Schistosoma mansoni, a member of the Platyhelminthes phy
235 During infection with the helminth parasite Schistosoma mansoni, Ab regulates hepatic inflammation,
237 nyl PZQ derivatives was tested against adult Schistosoma mansoni, and values in the micromolar range
238 f double-stranded RNA interference (RNAi) in Schistosoma mansoni, appraises delivery systems for tran
240 Infections with helminth parasites, such as Schistosoma mansoni, are often chronic and characterized
241 y parasite ova during natural infection with Schistosoma mansoni, but the role of TGF-beta is less cl
242 a glabrata is an intermediate snail host for Schistosoma mansoni, one of the important schistosomes i
244 -wide preventive chemotherapy strategies for Schistosoma mansoni, spatial scan statistics were used t
245 t work we assessed the lncRNAs complement of Schistosoma mansoni, the blood fluke that causes schisto
246 In infection with the trematode helminth Schistosoma mansoni, the severity of CD4 T cell-mediated
247 ociation was observed between infection with Schistosoma mansoni, Trichuris, or Strongyloides species
248 ed by relatively recent empirical studies on Schistosoma mansoni, we use a mathematical model to inve
249 d antibodies in sera from mice infected with Schistosoma mansoni, which revealed the presence of both
252 is both necessary and sufficient to prevent Schistosoma mansoni-infected mice from developing severe
254 inflammation was analyzed in offspring from Schistosoma mansoni-infected mothers mated during the TH
255 oma haematobium-Plasmodium falciparum versus Schistosoma mansoni-P. falciparum) has produced conflict
281 morbidity due to Opisthorchis viverrini and Schistosoma mekongi infections in 243 individuals in Lao
284 ors, including IgG antibodies to malaria and schistosoma parasites, heterophile antibodies, and rheum
288 first step to reducing the global burden of Schistosoma-related disease; however, they might not dra
291 prevalence ratios for intestinal nematodes, schistosoma species, giardia, and entamoeba were calcula
293 n to levels of circulating anodic antigen, a Schistosoma-specific antigen that is steadily secreted b
294 -resolution risk estimates of infection with Schistosoma spp and of the number of doses of praziquant
296 nts of this disease are trematode flatworms (Schistosoma) that live and lay eggs within the vasculatu
299 One representative example is the trematode Schistosoma, which causes schistosomiasis, an infectious
300 aryotic parasites and multicellular metazoan Schistosoma worms have lost the spermidine biosynthetic
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