ライフサイエンスコーパス: Schistosoma

1 disease caused by blood flukes of the genus Schistosoma.

2 ease caused by trematode flukes of the genus Schistosoma.

3 ection with parasitic helminths of the genus Schistosoma.

4 on caused by various trematodes of the genus Schistosoma.

5 The coevolution of blood flukes of the genus Schistosoma and their human hosts is paradigmatic of lon

6 luding Clonorchis, Opistorchis, Paragonimus, Schistosoma, and Dicrocoelium.

7 data for the prevalence of Strongyloides or Schistosoma antibodies in serum or the prevalence of lar

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 IPSE (Interleukin-4-inducing principle from Schistosoma eggs), a schistosome-derived host modulatory

16 and sufficient for the development of PH in Schistosoma-exposed mice.

17 eta-induced pulmonary vascular disease after Schistosoma exposure, and targeted inhibition of this pa

18 Following Schistosoma exposure, TSP-1 levels in the lung increase,

19 mental pulmonary hypertension (PH) caused by Schistosoma exposure.

20 creted proteins with sequences unique to the Schistosoma genera.

21 Schistosoma genomes provide a comprehensive resource for

22 ted tropical disease, caused by flatworms of Schistosoma genus.

23 young adults were recruited from areas where Schistosoma haematobium (S.h) infections were high or lo

24 aran Africa show that genital infection with Schistosoma haematobium [corrected] may increase the ris

25 compared patterns of recognition of defined Schistosoma haematobium adult worm antigens by serum ant

26 The literature search identified Schistosoma haematobium and Schistosoma mansoni surveys

27 the distribution of Schistosoma mansoni and Schistosoma haematobium and the incidence of schistosomi

28 sthorchis viverrini, Clonorchis sinensis and Schistosoma haematobium are classified as Group 1 biolog

29 thorchis viverrini, Clonorchis sinensis, and Schistosoma haematobium are classified as group 1 biolog

30 The blood fluke Schistosoma haematobium causes urogenital schistosomiasi

31 Schistosoma haematobium egg excretion rates showed a med

32 d 7-12-y-old anemic children with documented Schistosoma haematobium infection (n = 224 for AGP, CRP,

33 s consistent with observed field patterns of Schistosoma haematobium infection and antibody responses

34 al profiles in people with or without active Schistosoma haematobium infection and to determine wheth

35 Although Schistosoma haematobium infection has been reported to b

36 assessed whether bladder pathology in human Schistosoma haematobium infection is related to the bala

37 Schistosoma haematobium infection was positively associa

38 f FGS in women with different intensities of Schistosoma haematobium infection.

39 hildren with afebrile malaria, hookworm, and Schistosoma haematobium infection.

40 Schistosoma haematobium is a parasitic helminth which ca

41 Among the schistosomes, Schistosoma haematobium is responsible for the most infe

42 Schistosoma haematobium is responsible for two-thirds of

43 how the cervical environment is impacted by Schistosoma haematobium or Schistosoma mansoni infection

44 ur change interventions for the reduction of Schistosoma haematobium prevalence and infection intensi

45 ter as an effective control strategy against Schistosoma haematobium transmission.

46 trongly associated with increasing levels of Schistosoma haematobium worm IgG1, with adolescents with

47 Urogenital schistosomiasis, Schistosoma haematobium worm infection, afflicts million

48 n urogenital schistosomiasis, infection with Schistosoma haematobium worms, remains poorly understood

49 es urinary tract coinfection by bacteria and Schistosoma haematobium worms, the etiologic agent of ur

50 Schistosoma mansoni (and rarely Schistosoma haematobium) intestinal infection is also no

51 , in turn, reduces morbidity is proposed for Schistosoma haematobium, a parasite of major public heal

52 Schistosoma haematobium, a parasitic flatworm that infec

53 osomiasis, caused by the parasitic trematode Schistosoma haematobium, affects over 112 million people

54 Urogenital schistosomiasis, infection with Schistosoma haematobium, is linked to increased risk for

55 Urogenital schistosomiasis, caused by Schistosoma haematobium, is the most prevalent form of s

56 lated from 12 patients showed infection with Schistosoma haematobium, S haematobium-Schistosoma bovis

57 cted tropical disease caused by the parasite Schistosoma haematobium, which resides in the vasculatur

58 Venous blood from 72 Schistosoma haematobium-exposed participants was culture

59 recently published study, which included 163 Schistosoma haematobium-infected individuals and 183 mat

60 A Nigerian cohort of 168 Schistosoma haematobium-infected individuals and 192 hea

61 Schistosoma haematobium-infected schoolchildren were stu

62 Research into human coinfections (Schistosoma haematobium-Plasmodium falciparum versus Sch

63 Belgian travelers returned from Mali with a Schistosoma haematobium-Schistosoma bovis hybrid infecti

64 (IPTp)-is known to exhibit activity against Schistosoma haematobium.

65 py despite the presence of SULT orthologs in Schistosoma hematobium and Schistosoma japonicum The rea

66 giardia (in 5.7%), trichuris (in 5.0%), and schistosoma (in 1.8%); among 5575 Southeast Asian refuge

67 Schistosoma spindale and Schistosoma indicum are ruminant-infecting trematodes of

68 cum are ruminant-infecting trematodes of the Schistosoma indicum group that are widespread across Sou

69 Mice with experimental Schistosoma-induced PH had evidence of increased IL-4 an

70 -/-) or IL-13(-/-) mice, were protected from Schistosoma-induced PH, with decreased right ventricular

71 king Smad3 were significantly protected from Schistosoma-induced pulmonary hypertension.

72 on driven by IL-4 and IL-13 is necessary for Schistosoma-induced TGF-beta-dependent vascular remodeli

73 contact patterns can affect the dynamics of Schistosoma infection and the success of control interve

74 Schistosoma infection has been associated with altered i

75 dapted an established transmission model for Schistosoma infection that couples local human and snail

76 Hookworm, Plasmodium, and Schistosoma infections contribute to anemia, but their i

77 We found that young age, Plasmodium and Schistosoma infections, cellular iron deficiency, and st

78 The proportion of children infected with Schistosoma japonicum (15.6%, P = .03) and hookworm (22.

79 The pathology associated with Schistosoma japonicum (S. japonicum) infection in humans

80 d transcriptomic profiles of male and female Schistosoma japonicum across eight time points throughou

81 The blood flukes Schistosoma japonicum and Schistosoma mansoni are the fi

82 d both prepatent and patent infections using Schistosoma japonicum DNA isolated from serum, urine, sa

83 among 99 pregnant women living in an area of Schistosoma japonicum endemicity in the Philippines.

84 nates born to mothers residing in an area of Schistosoma japonicum endemicity was assessed for these

85 label-free self-catalyzed immobilization for Schistosoma japonicum GST.

86 2L in hepatic granuloma pathology induced by Schistosoma japonicum infection.

87 human pathogens that cause schistosomiasis, Schistosoma japonicum is the only one that is endemic in

88 omiasis, the indirectly transmitted helminth Schistosoma japonicum remains endemic, partly because of

89 asts were placed in culture and treated with Schistosoma japonicum soluble egg antigens (SEA) or plas

90 SULT orthologs in Schistosoma hematobium and Schistosoma japonicum The reason for this species-specif

91 Based on studies of Schistosoma japonicum transmission in irrigated agricult

92 who were otherwise healthy but infected with Schistosoma japonicum were enrolled and randomly assigne

93 The main disease-causing agents, Schistosoma japonicum, S. mansoni and S. haematobium, ar

94 differences between Schistosoma mansoni- and Schistosoma japonicum-induced hepatic granuloma are also

95 ne candidates rSj97, rSj67, and rSj22 from a Schistosoma japonicum-infected cohort in Leyte, the Phil

96 We treated 611 Schistosoma japonicum-infected Filipinos with praziquant

97 s from individuals chronically infected with Schistosoma japonicum.

98 hronic infection with Schistosoma mansoni or Schistosoma japonicum.

99 e candidate for both Schistosoma mansoni and Schistosoma japonicum.

100 fect that multiple percutaneous exposures to Schistosoma larvae has on the development of early CD4+

101 e hookworm (45%), Mansonella perstans (21%), Schistosoma mansoni (18%), and Plasmodium falciparum (11

102 Lower LDL-c levels were associated with Schistosoma mansoni (2.37 vs 2.80 mmol/L; -0.25 [95% CI,

103 Schistosoma mansoni (and rarely Schistosoma haematobium)

104 in a Ca(v)beta subunit of the human parasite Schistosoma mansoni (beta(Sm)), a motif that does not oc

105 Here, we express SMDR2, a Pgp homologue from Schistosoma mansoni (Platyhelminthes), in Chinese hamste

106 e Ags from the eggs of the helminth parasite Schistosoma mansoni (schistosome egg Ag (SEA)) leads to

107 After challenge with Schistosoma mansoni (Sm) eggs, Retnla(-/-) mice develope

108 Schistosoma mansoni (Sm) infection has been linked with

109 ped IgE fine specificity among Ugandan rural Schistosoma mansoni (Sm)-endemic communities, proximate

110 roarray technology among Ugandans from rural Schistosoma mansoni (Sm)-endemic islands (n = 209), and

111 In cross-sectional surveys in Ugandan rural Schistosoma mansoni (Sm)-endemic islands, and in nearby

112 opeptidases (legumains) from the bloodfluke, Schistosoma mansoni (SmAE), and the hard tick, Ixodes ri

113 The taurocyamine kinase from the blood fluke Schistosoma mansoni (SmTK) belongs to the phosphagen kin

114 Using data from a study of Schistosoma mansoni (trematode) infections in Biomphalar

115 ighest activity (IC(5)(0): 0.3 muM) on adult Schistosoma mansoni .

116 ic disease caused by the parasitic trematode Schistosoma mansoni after deposition of eggs in the live

117 ulation in a Th2-mediated immune response to Schistosoma mansoni Ags.

118 glycoprotein (VSVG) for the transduction of Schistosoma mansoni and delivery of reporter transgenes

119 Our results show that the genomes of Schistosoma mansoni and Drosophila melanogaster lack det

120 ween these 2 major liver-residing pathogens, Schistosoma mansoni and hepatitis B virus (HBV), is bare

121 is in Ugandan schoolchildren coinfected with Schistosoma mansoni and hookworm.

122 treatment of schoolchildren coinfected with Schistosoma mansoni and hookworm.

123 wed much less mortality after infection with Schistosoma mansoni and much more susceptibility to Nipp

124 in mice infected with the helminth parasite Schistosoma mansoni and observed an upregulation of CD14

125 exposed EC2 domain from Sm-TSP-2, a TSP from Schistosoma mansoni and one of the better prospects for

126 cerbated where there is transmission of both Schistosoma mansoni and Plasmodium falciparum.

127 After adjusting for Schistosoma mansoni and Plasmodium infection, we estimat

128 nevitably influence both the distribution of Schistosoma mansoni and Schistosoma haematobium and the

129 dely studied as a vaccine candidate for both Schistosoma mansoni and Schistosoma japonicum.

130 e, we demonstrate that somatic stem cells in Schistosoma mansoni are biased towards generating a popu

131 Hepatitis C virus (HCV) and Schistosoma mansoni are major causes of chronic liver di

132 The blood flukes Schistosoma japonicum and Schistosoma mansoni are the first major human platyhelmi

133 is approach by targeting omega-1 (omega1) of Schistosoma mansoni as proof of principle.

134 ity in mice infected with juvenile and adult Schistosoma mansoni by incorporating a weak base functio

135 Sm-p80, the large subunit of Schistosoma mansoni calpain, is a leading antigen candid

136 We sought to determine whether Schistosoma mansoni causes experimental PH associated wi

137 Infection with the parasitic helminth Schistosoma mansoni causes significant liver fibrosis an

138 Schistosoma mansoni cercariae display specific behaviora

139 to excretory/secretory products released by Schistosoma mansoni cercariae rapidly produce IL-10 as a

140 t exposure of mice to repeated doses (4x) of Schistosoma mansoni cercariae, compared to a single dose

141 only controls; eight animals were exposed to Schistosoma mansoni cercariae.

142 control group (n = 3) were infected with 500 Schistosoma mansoni cercariae.

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 weight, although a recent treatment trial in Schistosoma mansoni did not detect this association.

146 fficiently detect DNA traces of the parasite Schistosoma mansoni directly in the aquatic environment,

147 ted, pathogen-derived Ag (soluble extract of Schistosoma mansoni egg [SEA]) that induces type 2 immun

148 egulated in response to the helminth soluble Schistosoma mansoni egg Ag, which conditions DCs to indu

149 ave shown that rabbit IgG antibodies against Schistosoma mansoni egg antigens (SmSEA) cross-react wit

150 nt were confirmed by in vivo studies using a Schistosoma mansoni egg-challenged mouse model, a well-s

151 obese mice with recombinant helminth-derived Schistosoma mansoni egg-derived omega1 (omega1), a poten

152 signaling participates in the development of Schistosoma mansoni egg-induced CD4(+) Th2 responses, it

153 The IL-4-inducing principle from Schistosoma mansoni eggs (IPSE/alpha-1), the major secre

154 A protein in CFA, aluminum salts (Alum), and Schistosoma mansoni eggs (Sm Egg).

155 osylated T2 ribonuclease (RNase) secreted by Schistosoma mansoni eggs and abundantly present in solub

156 Schistosoma mansoni eggs contain factors that trigger po

157 sensitized and subsequently challenged with Schistosoma mansoni eggs developed pulmonary hypertensio

158 responses against Trichuris muris worms and Schistosoma mansoni eggs do not develop in mice with IRF

159 nt portion of the variation in the number of Schistosoma mansoni eggs per gram of fecal matter.

160 le egg antigens (SEA; a soluble extract from Schistosoma mansoni eggs) inhibit the activation of DCs

161 Following exposure to Schistosoma mansoni eggs, a model of Th2 cytokine-mediat

162 After exposure to bleomycin (BLM), but not Schistosoma mansoni eggs, IL-17A produced by CD4(+) and

163 After intravenous injection of Schistosoma mansoni eggs, IL-31Ralpha(-/-) mice develope

164 People in regions of Schistosoma mansoni endemicity slowly acquire immunity,

165 To this end, the targeting of Schistosoma mansoni epigenetic enzymes, which regulate t

166 Schistosoma mansoni exposure results in prototypical typ

167 onal study, examining children infected with Schistosoma mansoni from 6 schools in Uganda that had pr

168 ta, a natural host for the human blood fluke Schistosoma mansoni Granulins are growth factors that dr

169 ferring immunity to the intestinal trematode Schistosoma mansoni Here, we report that abrogation of I

170 amates were prepared as potent inhibitors of Schistosoma mansoni histone deacetylase 8 (smHDAC8).

171 pecies on transmission of the human parasite Schistosoma mansoni in Kenya.

172 ssess the eudysmic ratios of 1 and 2 against Schistosoma mansoni in vitro.

173 To analyze the reproductive biology of Schistosoma mansoni in-depth we isolated complete ovarie

174 fection of mammals by the parasitic helminth Schistosoma mansoni induces antibodies to glycan antigen

175 nt is impacted by Schistosoma haematobium or Schistosoma mansoni infection by quantifying gene expres

176 mmunopathological characteristics, caused by Schistosoma mansoni infection in IL-4 receptor alpha-def

177 Intensive MDA reduced Schistosoma mansoni infection intensity: the prevalence

178 aecal slides over three consecutive days for Schistosoma mansoni infection simultaneously by age grou

179 We used a murine model of Schistosoma mansoni infection to further investigate whe

180 During the patent phase of Schistosoma mansoni infection, Foxp3(+) Treg cells are a

181 thin cDCs impaired Th2 cell responses during Schistosoma mansoni infection, Schistosoma egg antigen (

182 atocellular activation of c-Jun and STAT3 by Schistosoma mansoni infection.

183 to screen migrants from endemic regions for Schistosoma mansoni infection.

184 Traditionally, human Schistosoma mansoni infections have been detected using

185 As with Schistosoma mansoni infections, the pathology of urogeni

186 dentify sensitive new serological markers of Schistosoma mansoni infections, we have compiled a recom

187 The larvae of Schistosoma mansoni invade their mammalian host by utili

188 The intravascular trematode Schistosoma mansoni is a causative agent of schistosomia

189 Schistosoma mansoni is a parasitic fluke that infects mi

190 The trematode Schistosoma mansoni is one of the etiological agents of

191 Schistosoma mansoni is responsible for the neglected tro

192 Schistosoma mansoni is the causative agent of intestinal

193 The blood fluke Schistosoma mansoni is the causative agent of the intest

194 resistance of B. glabrata to infection with Schistosoma mansoni or Echinostoma paraensei, and functi

195 e analyzed according to schistosome species (Schistosoma mansoni or S. haematobium), number of treatm

196 isease results from a chronic infection with Schistosoma mansoni or Schistosoma japonicum.

197 as evident in DCs responding to the helminth Schistosoma mansoni or the allergen house dust mite (HDM

198 We determined the responsiveness to Schistosoma mansoni over a 2-year period, when reinfecti

199 Schistosoma mansoni parasites of both sexes recovered fr

200 liver reporter transgenes into the genome of Schistosoma mansoni parasites.

201 As an example, the human blood fluke Schistosoma mansoni produces highly fucosylated glycan s

202 ome worm antigens were associated with lower Schistosoma mansoni reinfection intensity, while no asso

203 A recombinant antigen vaccine against Schistosoma mansoni remains elusive, in part because the

204 Infection with the trematode parasite Schistosoma mansoni results in a distinct heterogeneity

205 Infection with the trematode helminth Schistosoma mansoni results in a parasite egg-induced, C

206 In the mouse, infection with Schistosoma mansoni results in an egg-producing infectio

207 crystal structures of the GTPase domain of a Schistosoma mansoni septin (SmSEPT10), one bound to GDP

208 ilonRI coaggregation mediated by HIVgp120 or Schistosoma mansoni soluble egg Ag accelerated maximal C

209 nsitized and challenged intratracheally with Schistosoma mansoni soluble egg antigens (SEAs) to induc

210 earch identified Schistosoma haematobium and Schistosoma mansoni surveys done in, respectively, 9318

211 y (SmCalp1 and SmCalp2) are expressed in the Schistosoma mansoni tegument.

212 tigens, including the allergen-like proteins Schistosoma mansoni tegumental-allergen-like 1 protein (

213 The digenetic trematode Schistosoma mansoni that causes the form of schistosomia

214 cale RNA interference (RNAi) screen in adult Schistosoma mansoni that examined the function of 2216 g

215 We have targeted a protein of Schistosoma mansoni that plays an important role in the

216 egrated QSAR-based virtual screening (VS) of Schistosoma mansoni thioredoxin glutathione reductase (S

217 ova in mice infected with the human parasite Schistosoma mansoni through mechanisms that are currentl

218 ren from 2 villages with different levels of Schistosoma mansoni transmission.

219 ucture of a hammerhead ribozyme derived from Schistosoma mansoni under conditions that permit detaile

220 Similar to other metazoan pathogens, Schistosoma mansoni undergoes transcriptional and develo

221 In vitro studies with adult Schistosoma mansoni using several substrates suggest tha

222 irst description of an SCP/TAPS gene family (Schistosoma mansoni venom allergen-like (SmVALs)) in the

223 Schistosoma mansoni was associated with lower total chol

224 dent folding of the hammerhead ribozyme from Schistosoma mansoni was monitored with double electron-e

225 Emergence of Schistosoma mansoni with reduced sensitivity to praziqua

226 resistance evolved in the human blood fluke (Schistosoma mansoni) in Brazil in the 1970s.

227 soides sigmodontis, a filarial nematode, and Schistosoma mansoni, a blood fluke.

228 f dmd-1 exhibits male-specific expression in Schistosoma mansoni, a derived, dioecious flatworm.

229 The micro-exon genes (MEG) of Schistosoma mansoni, a parasite responsible for the seco

230 n identifying novel stem cell populations of Schistosoma mansoni, a prevalent parasite that infects h

231 During infection with the helminth parasite Schistosoma mansoni, Ab regulates hepatic inflammation,

232 diated by soluble egg Ag (SEA) obtained from Schistosoma mansoni, and by RA.

233 nyl PZQ derivatives was tested against adult Schistosoma mansoni, and values in the micromolar range

234 f double-stranded RNA interference (RNAi) in Schistosoma mansoni, appraises delivery systems for tran

235 Parasitic helminth worms, such as Schistosoma mansoni, are endemic in regions with a high

236 Infections with helminth parasites, such as Schistosoma mansoni, are often chronic and characterized

237 y parasite ova during natural infection with Schistosoma mansoni, but the role of TGF-beta is less cl

238 a glabrata is an intermediate snail host for Schistosoma mansoni, one of the important schistosomes i

239 In the case of the human blood fluke Schistosoma mansoni, responsible for intestinal bilharzi

240 -wide preventive chemotherapy strategies for Schistosoma mansoni, spatial scan statistics were used t

241 t work we assessed the lncRNAs complement of Schistosoma mansoni, the blood fluke that causes schisto

242 In infection with the trematode helminth Schistosoma mansoni, the severity of CD4 T cell-mediated

243 ociation was observed between infection with Schistosoma mansoni, Trichuris, or Strongyloides species

244 omphalaria snails, the intermediate host for Schistosoma mansoni, using Illumina MiSeq sequencing of

245 ed by relatively recent empirical studies on Schistosoma mansoni, we use a mathematical model to inve

246 d antibodies in sera from mice infected with Schistosoma mansoni, which revealed the presence of both

247 The differences between Schistosoma mansoni- and Schistosoma japonicum-induced h

248 is both necessary and sufficient to prevent Schistosoma mansoni-infected mice from developing severe

249 , we isolated eosinophils from the livers of Schistosoma mansoni-infected mice.

250 inflammation was analyzed in offspring from Schistosoma mansoni-infected mothers mated during the TH

251 oma haematobium-Plasmodium falciparum versus Schistosoma mansoni-P. falciparum) has produced conflict

252 A sequencing on two-day old schistosomula of Schistosoma mansoni.

253 (+/-) mice were infected percutaneously with Schistosoma mansoni.

254 rom the smooth muscles of the human parasite Schistosoma mansoni.

255 e hosts for the digenetic trematode parasite Schistosoma mansoni.

256 tion of neoblast-like cells in the trematode Schistosoma mansoni.

257 ll trafficking in response to challenge with Schistosoma mansoni.

258 anctuary staff, were naturally infected with Schistosoma mansoni.

259 ced exclusively by the eggs of the trematode Schistosoma mansoni.

260 llowing infection with the helminth parasite Schistosoma mansoni.

261 aneous infections with the helminth parasite Schistosoma mansoni.

262 Th2 response against the parasitic helminth Schistosoma mansoni.

263 characterized eIF4E from the human parasite Schistosoma mansoni.

264 , intermediate host of the human blood fluke Schistosoma mansoni.

265 e hard tick Ixodes ricinus, and the flatworm Schistosoma mansoni.

266 igmosomoides polygyrus, Trichuris muris, and Schistosoma mansoni.

267 transferase (SULT) in the parasitic flatworm Schistosoma mansoni.

268 tive against various developmental stages of Schistosoma mansoni.

269 on of liver granulomas in mice infected with Schistosoma mansoni.

270 against the blood-feeding trematode parasite Schistosoma mansoni.

271 tal in transmission of the human blood fluke Schistosoma mansoni.

272 exacerbated in Batf3(-/-) mice infected with Schistosoma mansoni.

273 in-13 overexpression or after infection with Schistosoma mansoni.

274 me released by the cercarial larvae stage of Schistosoma mansoni.

275 morbidity due to Opisthorchis viverrini and Schistosoma mekongi infections in 243 individuals in Lao

276 Forty-two percent of women with Schistosoma-negative urine specimens had at least 1 geni

277 Schistosoma ova were identified exclusively among Africa

278 ors, including IgG antibodies to malaria and schistosoma parasites, heterophile antibodies, and rheum

279 Schistosoma PCR may give an indication of the diagnosis.

280 Schistosoma PCR was done on urine, biopsy, cervicovagina

281 arrow transplantation also protected against Schistosoma-PH.

282 olates and an isolate of the closely-related Schistosoma rodhaini, which infects rodents.

283 itors on parasite survival and reproduction, Schistosoma sirtuins were postulated as potential therap

284 In areas where Plasmodium and Schistosoma species are both endemic, coinfections are c

285 prevalence ratios for intestinal nematodes, schistosoma species, giardia, and entamoeba were calcula

286 but no association between P. falciparum and Schistosoma species.

287 nt risk factors for asIgE sensitization were Schistosoma-specific antibody levels and helminth infect

288 n to levels of circulating anodic antigen, a Schistosoma-specific antigen that is steadily secreted b

289 ersely associated with bathing in lakewater, Schistosoma-specific IgG4 and Sm infection.

290 modifier for risk factors including Sm- and Schistosoma-specific IgG4.

291 Schistosoma spindale and Schistosoma indicum are ruminan

292 -resolution risk estimates of infection with Schistosoma spp and of the number of doses of praziquant

293 0 million people worldwide are infected with Schistosoma spp.

294 nts of this disease are trematode flatworms (Schistosoma) that live and lay eggs within the vasculatu

295 vement on the long-term burden reduction for Schistosoma transmission control, and we identified the

296 Seasonal variation makes Schistosoma transmission less sustainable and easier to

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