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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
7 luding Clonorchis, Opistorchis, Paragonimus, Schistosoma, and Dicrocoelium.
8 ned from Mali with a Schistosoma haematobium-Schistosoma bovis hybrid infection, confirmed by DNA seq
9  with Schistosoma haematobium, S haematobium-Schistosoma bovis hybrids, and S bovis.
10 iased immune responses in mice infected with Schistosoma, but the precise mechanism remains to be elu
11 t least 1 genital specimen test positive for Schistosoma by PCR.
12 ponses during Schistosoma mansoni infection, Schistosoma egg antigen (SEA) immunization, and house du
13                                              Schistosoma eggs and their secretions have been studied
14 ternal transcribed spacer) DNA data from the Schistosoma eggs or miracidia recovered from the infecte
15  and sufficient for the development of PH in Schistosoma-exposed mice.
16 eta-induced pulmonary vascular disease after Schistosoma exposure, and targeted inhibition of this pa
17                                    Following Schistosoma exposure, TSP-1 levels in the lung increase,
18 mental pulmonary hypertension (PH) caused by Schistosoma exposure.
19 creted proteins with sequences unique to the Schistosoma genera.
20                                              Schistosoma genomes provide a comprehensive resource for
21 ted tropical disease, caused by flatworms of Schistosoma genus.
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
25             The literature search identified Schistosoma haematobium and Schistosoma mansoni surveys
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
29                              The blood fluke Schistosoma haematobium causes urogenital schistosomiasi
30                                              Schistosoma haematobium egg excretion rates showed a med
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
34                                              Schistosoma haematobium infection was positively associa
35 f FGS in women with different intensities of Schistosoma haematobium infection.
36 hildren with afebrile malaria, hookworm, and Schistosoma haematobium infection.
37                      Among the schistosomes, Schistosoma haematobium is responsible for the most infe
38                                              Schistosoma haematobium is responsible for two-thirds of
39 trongly associated with increasing levels of Schistosoma haematobium worm IgG1, with adolescents with
40                  Urogenital schistosomiasis, Schistosoma haematobium worm infection, afflicts million
41 es urinary tract coinfection by bacteria and Schistosoma haematobium worms, the etiologic agent of ur
42              Schistosoma mansoni (and rarely Schistosoma haematobium) intestinal infection is also no
43 , in turn, reduces morbidity is proposed for Schistosoma haematobium, a parasite of major public heal
44                                              Schistosoma haematobium, a parasitic flatworm that infec
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
47        Urogenital schistosomiasis, caused by Schistosoma haematobium, is the most prevalent form of s
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
50                         Venous blood from 72 Schistosoma haematobium-exposed participants was culture
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
53                     A Nigerian cohort of 168 Schistosoma haematobium-infected individuals and 192 hea
54            Research into human coinfections (Schistosoma haematobium-Plasmodium falciparum versus Sch
55  Belgian travelers returned from Mali with a Schistosoma haematobium-Schistosoma bovis hybrid infecti
56  (IPTp)-is known to exhibit activity against Schistosoma haematobium.
57 arlier compared with Schistosoma mansoni and Schistosoma haematobium.
58                            Thus, the natural Schistosoma hammerhead ribozyme is almost as efficient a
59 e ligation than the cleavage activity of the Schistosoma hammerhead ribozyme.
60 ibrium between cleavage and ligation for the Schistosoma hammerhead.
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
64                       Mice with experimental Schistosoma-induced PH had evidence of increased IL-4 an
65 -/-) or IL-13(-/-) mice, were protected from Schistosoma-induced PH, with decreased right ventricular
66 king Smad3 were significantly protected from Schistosoma-induced pulmonary hypertension.
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
69                    Hookworm, Plasmodium, and Schistosoma infections contribute to anemia, but their i
70      We found that young age, Plasmodium and Schistosoma infections, cellular iron deficiency, and st
71     The proportion of children infected with Schistosoma japonicum (15.6%, P = .03) and hookworm (22.
72                The pathology associated with Schistosoma japonicum (S. japonicum) infection in humans
73 d transcriptomic profiles of male and female Schistosoma japonicum across eight time points throughou
74                             The blood flukes Schistosoma japonicum and Schistosoma mansoni are the fi
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
78 label-free self-catalyzed immobilization for Schistosoma japonicum GST.
79 -sectional relation between the intensity of Schistosoma japonicum infection, hemoglobin concentratio
80 2L in hepatic granuloma pathology induced by Schistosoma japonicum infection.
81                     Among the three species, Schistosoma japonicum is remarkable at conserving energy
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
87                          Based on studies of Schistosoma japonicum transmission in irrigated agricult
88 who were otherwise healthy but infected with Schistosoma japonicum were enrolled and randomly assigne
89             The main disease-causing agents, Schistosoma japonicum, S. mansoni and S. haematobium, ar
90 differences between Schistosoma mansoni- and Schistosoma japonicum-induced hepatic granuloma are also
91                           In a cohort of 580 Schistosoma japonicum-infected 7- to 30-year-old patient
92 ne candidates rSj97, rSj67, and rSj22 from a Schistosoma japonicum-infected cohort in Leyte, the Phil
93                               We treated 611 Schistosoma japonicum-infected Filipinos with praziquant
94            In a cross-sectional study of 641 Schistosoma japonicum-infected individuals in Leyte, Phi
95 t study in Leyte, the Philippines, among 611 Schistosoma japonicum-infected participants 7-30 years o
96 hronic infection with Schistosoma mansoni or Schistosoma japonicum.
97 e candidate for both Schistosoma mansoni and Schistosoma japonicum.
98 s from individuals chronically infected with Schistosoma japonicum.
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
101                                              Schistosoma mansoni (and rarely Schistosoma haematobium)
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
105                         After challenge with Schistosoma mansoni (Sm) eggs, Retnla(-/-) mice develope
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
108                   Using data from a study of Schistosoma mansoni (trematode) infections in Biomphalar
109 ighest activity (IC(5)(0): 0.3 muM) on adult Schistosoma mansoni .
110 ic disease caused by the parasitic trematode Schistosoma mansoni after deposition of eggs in the live
111 ulation in a Th2-mediated immune response to Schistosoma mansoni Ags.
112  glycoprotein (VSVG) for the transduction of Schistosoma mansoni and delivery of reporter transgenes
113         Our results show that the genomes of Schistosoma mansoni and Drosophila melanogaster lack det
114 on, a cohort of 163 Ugandans coinfected with Schistosoma mansoni and HIV-1 was treated with praziquan
115 is in Ugandan schoolchildren coinfected with Schistosoma mansoni and hookworm.
116  treatment of schoolchildren coinfected with Schistosoma mansoni and hookworm.
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
122 cerbated where there is transmission of both Schistosoma mansoni and Plasmodium falciparum.
123                          After adjusting for Schistosoma mansoni and Plasmodium infection, we estimat
124 lowing extensive searching of the genomes of Schistosoma mansoni and S. japonicum.
125 nevitably influence both the distribution of Schistosoma mansoni and Schistosoma haematobium and the
126 site sooner and mature earlier compared with Schistosoma mansoni and Schistosoma haematobium.
127 dely studied as a vaccine candidate for both Schistosoma mansoni and Schistosoma japonicum.
128 e, we demonstrate that somatic stem cells in Schistosoma mansoni are biased towards generating a popu
129                  Hepatitis C virus (HCV) and Schistosoma mansoni are major causes of chronic liver di
130   The blood flukes Schistosoma japonicum and Schistosoma mansoni are the first major human platyhelmi
131 ein digestion, using the parasitic helminth, Schistosoma mansoni as an experimental model.
132                 Sm-p80, the large subunit of Schistosoma mansoni calpain, is a leading antigen candid
133               We sought to determine whether Schistosoma mansoni causes experimental PH associated wi
134        Infection with the parasitic helminth Schistosoma mansoni causes significant liver fibrosis an
135                                              Schistosoma mansoni cercariae display specific behaviora
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
139 only controls; eight animals were exposed to Schistosoma mansoni cercariae.
140 control group (n = 3) were infected with 500 Schistosoma mansoni cercariae.
141 responses have previously been observed with Schistosoma mansoni coinfection.
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
144        CBA/J mice infected with the helminth Schistosoma mansoni develop severe CD4 T cell-mediated h
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
148 cteria bovis purified protein derivative- or Schistosoma mansoni egg Ag (SEA)-coated beads.
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
151 cteria bovis purified protein derivative- or Schistosoma mansoni egg antigen-coated beads.
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
155             The IL-4-inducing principle from Schistosoma mansoni eggs (IPSE/alpha-1), the major secre
156 A protein in CFA, aluminum salts (Alum), and Schistosoma mansoni eggs (Sm Egg).
157 osylated T2 ribonuclease (RNase) secreted by Schistosoma mansoni eggs and abundantly present in solub
158                                              Schistosoma mansoni eggs contain factors that trigger po
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
162 nt portion of the variation in the number of Schistosoma mansoni eggs per gram of fecal matter.
163 le egg antigens (SEA; a soluble extract from Schistosoma mansoni eggs) inhibit the activation of DCs
164                        Following exposure to Schistosoma mansoni eggs, a model of Th2 cytokine-mediat
165   After exposure to bleomycin (BLM), but not Schistosoma mansoni eggs, IL-17A produced by CD4(+) and
166               After intravenous injection of Schistosoma mansoni eggs, IL-31Ralpha(-/-) mice develope
167 Th2 cytokine production when challenged with Schistosoma mansoni eggs.
168 ntly challenged with lung granuloma-inducing Schistosoma mansoni eggs.
169                         People in regions of Schistosoma mansoni endemicity slowly acquire immunity,
170                           The human pathogen Schistosoma mansoni exhibits a highly evolved and intric
171                                              Schistosoma mansoni exposure results in prototypical typ
172 onal study, examining children infected with Schistosoma mansoni from 6 schools in Uganda that had pr
173       The recent release of version 3 of the Schistosoma mansoni genome assembly has made a wealth of
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).
178 ssess the eudysmic ratios of 1 and 2 against Schistosoma mansoni in vitro.
179       To analyze the reproductive biology of Schistosoma mansoni in-depth we isolated complete ovarie
180 fection of mammals by the parasitic helminth Schistosoma mansoni induces antibodies to glycan antigen
181                   Praziquantel treatment for Schistosoma mansoni infection enhances Th2 responsivenes
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
185                    We used a murine model of Schistosoma mansoni infection to further investigate whe
186                   During the patent phase of Schistosoma mansoni infection, Foxp3(+) Treg cells are a
187 thin cDCs impaired Th2 cell responses during Schistosoma mansoni infection, Schistosoma egg antigen (
188  to screen migrants from endemic regions for Schistosoma mansoni infection.
189 ibrosis that develops in response to chronic Schistosoma mansoni infection.
190                                      As with Schistosoma mansoni infections, the pathology of urogeni
191                                The larvae of Schistosoma mansoni invade their mammalian host by utili
192                  The intravascular trematode Schistosoma mansoni is a causative agent of schistosomia
193                                              Schistosoma mansoni is a parasitic fluke that infects mi
194                                The trematode Schistosoma mansoni is one of the etiological agents of
195                                              Schistosoma mansoni is responsible for the neglected tro
196                 The hammerhead ribozyme from Schistosoma mansoni is the best characterized of the nat
197                              The blood fluke Schistosoma mansoni is the causative agent of the intest
198  resistance of B. glabrata to infection with Schistosoma mansoni or Echinostoma paraensei, and functi
199 isease results from a chronic infection with Schistosoma mansoni or Schistosoma japonicum.
200 as evident in DCs responding to the helminth Schistosoma mansoni or the allergen house dust mite (HDM
201          We determined the responsiveness to Schistosoma mansoni over a 2-year period, when reinfecti
202                                              Schistosoma mansoni parasites of both sexes recovered fr
203 liver reporter transgenes into the genome of Schistosoma mansoni parasites.
204                    Here, we characterize two Schistosoma mansoni products, tyrosinase 1 and tyrosinas
205 ome worm antigens were associated with lower Schistosoma mansoni reinfection intensity, while no asso
206        A recombinant antigen vaccine against Schistosoma mansoni remains elusive, in part because the
207        Infection with the trematode parasite Schistosoma mansoni results in a distinct heterogeneity
208        Infection with the trematode helminth Schistosoma mansoni results in a parasite egg-induced, C
209                 In the mouse, infection with Schistosoma mansoni results in an egg-producing infectio
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
212             We previously suggested that the Schistosoma mansoni spliced leader AUG might contribute
213 earch identified Schistosoma haematobium and Schistosoma mansoni surveys done in, respectively, 9318
214 y (SmCalp1 and SmCalp2) are expressed in the Schistosoma mansoni tegument.
215 tigens, including the allergen-like proteins Schistosoma mansoni tegumental-allergen-like 1 protein (
216                      The digenetic trematode Schistosoma mansoni that causes the form of schistosomia
217                We have targeted a protein of Schistosoma mansoni that plays an important role in the
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
222 ren from 2 villages with different levels of Schistosoma mansoni transmission.
223 ucture of a hammerhead ribozyme derived from Schistosoma mansoni under conditions that permit detaile
224         Similar to other metazoan pathogens, Schistosoma mansoni undergoes transcriptional and develo
225                  In vitro studies with adult Schistosoma mansoni using several substrates suggest tha
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
228                                 Emergence of Schistosoma mansoni with reduced sensitivity to praziqua
229 resistance evolved in the human blood fluke (Schistosoma mansoni) in Brazil in the 1970s.
230 soides sigmodontis, a filarial nematode, and Schistosoma mansoni, a blood fluke.
231                                              Schistosoma mansoni, a causative agent of schistosomiasi
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
234                The micro-exon genes (MEG) of Schistosoma mansoni, a parasite responsible for the seco
235  During infection with the helminth parasite Schistosoma mansoni, Ab regulates hepatic inflammation,
236 diated by soluble egg Ag (SEA) obtained from Schistosoma mansoni, and by RA.
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
239            Parasitic helminth worms, such as Schistosoma mansoni, are endemic in regions with a high
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
243         In the case of the human blood fluke Schistosoma mansoni, responsible for intestinal bilharzi
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
250                                              Schistosoma mansoni- and Mycobacterium tuberculosis-spec
251                      The differences between Schistosoma mansoni- and Schistosoma japonicum-induced h
252  is both necessary and sufficient to prevent Schistosoma mansoni-infected mice from developing severe
253 , we isolated eosinophils from the livers of Schistosoma mansoni-infected mice.
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
256 on of liver granulomas in mice infected with Schistosoma mansoni.
257 e hosts for the digenetic trematode parasite Schistosoma mansoni.
258 tion of neoblast-like cells in the trematode Schistosoma mansoni.
259 ll trafficking in response to challenge with Schistosoma mansoni.
260 anctuary staff, were naturally infected with Schistosoma mansoni.
261 ced exclusively by the eggs of the trematode Schistosoma mansoni.
262 llowing infection with the helminth parasite Schistosoma mansoni.
263 aneous infections with the helminth parasite Schistosoma mansoni.
264  Th2 response against the parasitic helminth Schistosoma mansoni.
265  characterized eIF4E from the human parasite Schistosoma mansoni.
266 against the blood-feeding trematode parasite Schistosoma mansoni.
267 tal in transmission of the human blood fluke Schistosoma mansoni.
268 , intermediate host of the human blood fluke Schistosoma mansoni.
269 e hard tick Ixodes ricinus, and the flatworm Schistosoma mansoni.
270 igmosomoides polygyrus, Trichuris muris, and Schistosoma mansoni.
271  tissues of mice infected with the trematode Schistosoma mansoni.
272 ing cells when these mice were infected with Schistosoma mansoni.
273 e identified in the Platyhelminth trematode, Schistosoma mansoni.
274 potent activity against pathogenic trematode Schistosoma mansoni.
275 exacerbated in Batf3(-/-) mice infected with Schistosoma mansoni.
276 in-13 overexpression or after infection with Schistosoma mansoni.
277 me released by the cercarial larvae stage of Schistosoma mansoni.
278 transferase (SULT) in the parasitic flatworm Schistosoma mansoni.
279 (+/-) mice were infected percutaneously with Schistosoma mansoni.
280 rom the smooth muscles of the human parasite Schistosoma mansoni.
281  morbidity due to Opisthorchis viverrini and Schistosoma mekongi infections in 243 individuals in Lao
282              Forty-two percent of women with Schistosoma-negative urine specimens had at least 1 geni
283                                              Schistosoma ova were identified exclusively among Africa
284 ors, including IgG antibodies to malaria and schistosoma parasites, heterophile antibodies, and rheum
285                                              Schistosoma PCR may give an indication of the diagnosis.
286                                              Schistosoma PCR was done on urine, biopsy, cervicovagina
287 arrow transplantation also protected against Schistosoma-PH.
288  first step to reducing the global burden of Schistosoma-related disease; however, they might not dra
289 olates and an isolate of the closely-related Schistosoma rodhaini, which infects rodents.
290                In areas where Plasmodium and Schistosoma species are both endemic, coinfections are c
291  prevalence ratios for intestinal nematodes, schistosoma species, giardia, and entamoeba were calcula
292 but no association between P. falciparum and Schistosoma species.
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
295 0 million people worldwide are infected with Schistosoma spp.
296 nts of this disease are trematode flatworms (Schistosoma) that live and lay eggs within the vasculatu
297                                     With few Schistosoma vaccine candidates in clinical trials, unexp
298              A marker for the parasitic worm Schistosoma was used in this study.
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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