ライフサイエンスコーパス: Schistosoma

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