ライフサイエンスコーパス: Schistosoma mansoni

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

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

3 aneous infections with the helminth parasite Schistosoma mansoni.

4 Th2 response against the parasitic helminth Schistosoma mansoni.

5 characterized eIF4E from the human parasite Schistosoma mansoni.

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

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

8 igmosomoides polygyrus, Trichuris muris, and Schistosoma mansoni.

9 tissues of mice infected with the trematode Schistosoma mansoni.

10 ing cells when these mice were infected with Schistosoma mansoni.

11 e identified in the Platyhelminth trematode, Schistosoma mansoni.

12 potent activity against pathogenic trematode Schistosoma mansoni.

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

14 nt intermediate hosts of the human pathogen, Schistosoma mansoni.

15 rganization of the cathepsin D gene locus of Schistosoma mansoni.

16 infection with the type 2-promoting pathogen Schistosoma mansoni.

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

18 ed a cDNA encoding PHM in the human parasite Schistosoma mansoni.

19 t baseline and in response to infection with Schistosoma mansoni.

20 e fibrosis induced by the parasitic helminth Schistosoma mansoni.

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

22 sponse development to the parasitic helminth Schistosoma mansoni.

23 in the life cycle of the trematode pathogen Schistosoma mansoni.

24 ilk and on the Th2 driving helminth parasite Schistosoma mansoni.

25 hemokines in experimental mouse models using Schistosoma mansoni.

26 mice to survive infection with the parasite Schistosoma mansoni.

27 l intermediate host of the human blood fluke Schistosoma mansoni.

28 ria glabrata to infection with the trematode Schistosoma mansoni.

29 sensitization with soluble egg Ags (SEA) of Schistosoma mansoni.

30 ting a protein library of the human parasite Schistosoma mansoni.

31 chronic infection with the helminth parasite Schistosoma mansoni.

32 ve collagen deposition during infection with Schistosoma mansoni.

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

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

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

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

37 e hosts for the digenetic trematode parasite Schistosoma mansoni.

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

39 ll trafficking in response to challenge with Schistosoma mansoni.

40 anctuary staff, were naturally infected with Schistosoma mansoni.

41 against the blood-feeding trematode parasite Schistosoma mansoni.

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

43 llowing infection with the helminth parasite Schistosoma mansoni.

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

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

46 Schistosoma mansoni, a causative agent of schistosomiasi

47 uence tag data base of the helminth parasite Schistosoma mansoni, a causative agent of schistosomiasi

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

49 g the role of B. glabrata in transmission of Schistosoma mansoni, a digenean parasite that infects ne

50 ized a new member of the cyclase family from Schistosoma mansoni, a member of the Platyhelminthes phy

51 Schistosoma mansoni, a multicelluar eukaryotic blood flu

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

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

54 Two of the five genes identified in Schistosoma mansoni account for over 90% of the activity

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

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

57 Schistosoma mansoni, an intravascular parasite, has evol

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

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

60 Two populations with differing histories of Schistosoma mansoni and hepatitis C infection were compa

61 on, a cohort of 163 Ugandans coinfected with Schistosoma mansoni and HIV-1 was treated with praziquan

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

63 treatment of schoolchildren coinfected with Schistosoma mansoni and hookworm.

64 We show that Ugandan adults coinfected with Schistosoma mansoni and human immunodeficiency virus typ

65 co-infection model in C57BL/6 mice involving Schistosoma mansoni and Leishmania donovani, two importa

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

67 -21R-/- mice with the Th2-inducing pathogens Schistosoma mansoni and Nippostrongylus brasiliensis and

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

69 d two Ca(2+) channel beta subunits, one from Schistosoma mansoni and one from Schistosoma japonicum.

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

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

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

73 lowing extensive searching of the genomes of Schistosoma mansoni and S. japonicum.

74 omologues from two other schistosome species-Schistosoma mansoni and Schistosoma bovis, which are imp

75 nt humoral responses in humans infected with Schistosoma mansoni and Schistosoma haematobium and cons

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

77 site sooner and mature earlier compared with Schistosoma mansoni and Schistosoma haematobium.

78 The blood flukes Schistosoma mansoni and Schistosoma japonicum inflict im

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

80 strated that mice concurrently infected with Schistosoma mansoni and Toxoplasma gondii undergo accele

81 Schistosoma mansoni (and rarely Schistosoma haematobium)

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

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

84 Schistosoma mansoni- and Mycobacterium tuberculosis-spec

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

86 nsiveness (AHR) and tissue eosinophilia in a Schistosoma mansoni antigen-sensitized and airway-challe

87 humoral immune response to crude and defined Schistosoma mansoni antigens aggregates within families.

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

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

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

91 o infective larvae of the parasitic helminth Schistosoma mansoni are poorly understood, but here for

92 The eggs of Schistosoma mansoni are strong inducers of a Th2 respons

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

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

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

96 ein digestion, using the parasitic helminth, Schistosoma mansoni as an experimental model.

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

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

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

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

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

102 Schistosoma mansoni cercariae display specific behaviora

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

104 vy and quantifiable occupational exposure to Schistosoma mansoni cercariae revealed that some individ

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

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

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

108 Subjects with HCV/Schistosoma mansoni coinfection have a more rapid progre

109 nts with acute HCV hepatitis with or without Schistosoma mansoni coinfection, a parasitic infection w

110 responses have previously been observed with Schistosoma mansoni coinfection.

111 ucture of a hammerhead ribozyme derived from Schistosoma mansoni containing the rate-enhancing periph

112 The genome of Schistosoma mansoni contains a proviral form of a retrov

113 that B cell-deficient (muMT) mice exposed to Schistosoma mansoni develop augmented tissue pathology a

114 Mice infected with Schistosoma mansoni develop polarized Th2 responses in w

115 to determine whether children infected with Schistosoma mansoni develop protection-related immune re

116 CBA/J mice infected with the helminth Schistosoma mansoni develop severe CD4 T cell-mediated h

117 C57BL/6 mice infected with the helminth Schistosoma mansoni develop small hepatic granulomas aro

118 Mice infected with Schistosoma mansoni develop Th2 cytokine-mediated granul

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

120 nized with radiation-attenuated cercariae of Schistosoma mansoni display resistance to challenge infe

121 g and the adult worm developmental stages of Schistosoma mansoni during chronic infections with the p

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

123 cteria bovis purified protein derivative- or Schistosoma mansoni egg Ag (SEA)-coated beads.

124 onstrated that induction of Th2 responses by Schistosoma mansoni egg Ag is largely due to carbohydrat

125 A recently cloned major Schistosoma mansoni egg Ag p38 induced and elicited stro

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

127 nulomas elicited with Mycobacterium bovis or Schistosoma mansoni egg Ag-coated beads, respectively.

128 cobacteria bovis protein Ags and helminthic, Schistosoma mansoni egg Ags elicited multiple chemokines

129 cteria bovis purified protein derivative and Schistosoma mansoni egg antigen challenge indicating an

130 pe (induced by the pulmonary embolization of Schistosoma mansoni egg antigen-coated beads in mice sen

131 cteria bovis purified protein derivative- or Schistosoma mansoni egg antigen-coated beads.

132 mycobacterial purified protein derivative or Schistosoma mansoni egg antigens.

133 The granuloma that surrounds the Schistosoma mansoni egg is the cause of pathology in mur

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

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

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

137 Using a Schistosoma mansoni egg-induced granuloma model, we exam

138 Schistosoma mansoni egg-induced lung pathology requires

139 Schistosoma mansoni egg-induced pulmonary granuloma form

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

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

142 cytokine responses and granulomata, we used Schistosoma mansoni eggs (SME).

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

144 model, mice are sensitized with inactivated Schistosoma mansoni eggs and are subsequently challenged

145 We developed a mouse model using Schistosoma mansoni eggs and cytokine-deficient mice to

146 Schistosoma mansoni eggs contain factors that trigger po

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

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

149 ch the mice were sensitized with inactivated Schistosoma mansoni eggs followed by S. mansoni egg Ag c

150 d by the intrapulmonary embolization of live Schistosoma mansoni eggs into S. mansoni-sensitized mice

151 The injection of Schistosoma mansoni eggs into the footpads of mice resul

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

153 nsitivity pulmonary granulomas by embolizing Schistosoma mansoni eggs to the lungs of osteopontin-def

154 condary pulmonary granulomata in response to Schistosoma mansoni eggs was blunted in MCP-1(-/-) mice,

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

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

157 optimal Th2 responses following exposure to Schistosoma mansoni eggs, a potent and natural Th2-induc

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

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

160 Th2 cytokine production when challenged with Schistosoma mansoni eggs.

161 ntly challenged with lung granuloma-inducing Schistosoma mansoni eggs.

162 itial lung granulomas induced by antigens of Schistosoma mansoni eggs.

163 effective TH2 responses when challenged with Schistosoma mansoni eggs.

164 erium bovis or soluble antigens derived from Schistosoma mansoni eggs.

165 by embolization of beads coated with Ags of Schistosoma mansoni eggs.

166 obacterium bovis or soluble Ags derived from Schistosoma mansoni eggs.

167 Mice sensitized with SCHISTOSOMA: mansoni eggs and IL-12 develop liver granul

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

169 The human pathogen Schistosoma mansoni exhibits a highly evolved and intric

170 Schistosoma mansoni exposure results in prototypical typ

171 ties of PGE(2) were produced by cercariae of Schistosoma mansoni following incubation with linoleic a

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 In infection with Schistosoma mansoni, hepatic granuloma formation is medi

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

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

179 The Schistosoma mansoni homologue (SmSmad2) was overexpresse

180 Results: Schistosoma mansoni, hookworm, Strongyloides stercoralis

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

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

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

184 Levels of Schistosoma mansoni-induced interleukin (IL)-4 and IL-5

185 Infection with the helminth parasite Schistosoma mansoni induces a pronounced Th2-type respon

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

187 hal forms of liver pathology that develop in Schistosoma mansoni infected mice polarized for type-1 a

188 mune reactions after praziquantel therapy in Schistosoma mansoni-infected fishermen working in an are

189 s derived from the spleens and granulomas of Schistosoma mansoni-infected mice during the course of t

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

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

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

193 Schistosoma mansoni-infected wild-type (WT) mice develop

194 Hepatic fibrosis is the hallmark of Schistosoma mansoni infection and often results in porta

195 Praziquantel treatment for Schistosoma mansoni infection enhances Th2 responsivenes

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

197 Schistosoma mansoni infection is highly endemic in parts

198 The hallmark of Schistosoma mansoni infection is the formation of liver

199 t helminthic parasites using the established Schistosoma mansoni infection model in 2 novel mouse mod

200 Schistosoma mansoni infection resulted in a significantl

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

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

203 IL-13) characterize the host response after Schistosoma mansoni infection, and recent studies have i

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

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

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

207 ibrosis that develops in response to chronic Schistosoma mansoni infection.

208 in IL-13-dependent liver fibrosis caused by Schistosoma mansoni infection.

209 major role in the immunopathology induced by Schistosoma mansoni infection.

210 CBA/J male mice with chronic Schistosoma mansoni infections display either moderate s

211 Experimental Schistosoma mansoni infections of mice lead to a dynamic

212 In murine Schistosoma mansoni infections, schistosome-specific cro

213 As with Schistosoma mansoni infections, the pathology of urogeni

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

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

216 h coinfection of hepatitis B virus (HBV) and Schistosoma mansoni is a frequent event in humans, littl

217 Schistosoma mansoni is a parasitic fluke that infects mi

218 The biology of the helminth parasite Schistosoma mansoni is closely integrated with that of i

219 evelopment among mouse strains infected with Schistosoma mansoni is not known.

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

221 Schistosoma mansoni is responsible for the neglected tro

222 The hammerhead ribozyme from Schistosoma mansoni is the best characterized of the nat

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

224 ence of interleukin-4 (IL-4), infection with Schistosoma mansoni leads to a severe fatal disease rath

225 leavage of a trans-cleaving construct of the Schistosoma mansoni natural hammerhead ribozyme.

226 During infection with Schistosoma mansoni, NO production increases following t

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

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

229 ferent regions of Kenya, 1 each with endemic Schistosoma mansoni or Schistosoma haematobium.

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

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

232 th either the Th2 response-inducing parasite Schistosoma mansoni or with the Th1 response-inducing pa

233 The development of Schistosoma mansoni ova-induced granulomas is regulated

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

235 ctural changes that have been documented for Schistosoma mansoni over the past 20 years.

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

237 In infection with Schistosoma mansoni, parasite eggs precipitate an intrah

238 fraction S3) prepared from immature (4-week) Schistosoma mansoni parasites can induce partial, serum-

239 Schistosoma mansoni parasites of both sexes recovered fr

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

241 PCK was identified, and the full recombinant Schistosoma mansoni PEPCK (rSm-PEPCK) of 626 amino acids

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

243 h2-polarizing Ag (soluble egg Ag (SEA)) from Schistosoma mansoni potently stimulate Th2 responses in

244 Here, we characterize two Schistosoma mansoni products, tyrosinase 1 and tyrosinas

245 larvae (cercariae) of the trematode parasite Schistosoma mansoni rapidly penetrate human skin by degr

246 Schistosoma mansoni receptor kinase 1 (SmRK1) is a diver

247 Schistosoma mansoni receptor-regulated Smad1 and SmSmad2

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

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

250 inflammation in infection with the helminth Schistosoma mansoni represents a cellular hypersensitivi

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

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

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

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

255 encoding a second full-length member of the Schistosoma mansoni RXR family (SmRXR-2) was identified.

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

257 cules from the eggs of the helminth parasite Schistosoma mansoni (SEA) suppress LPS-induced activatio

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

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

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

261 in (TCTP) was cloned from the human parasite Schistosoma mansoni (SmTCTP).

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

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

264 bovis purified protein derivative (PPD) and Schistosoma mansoni soluble egg Ags (SEA).

265 This study investigated the effects of Schistosoma mansoni soluble egg antigen (SEA) on angioge

266 onses in vivo in CCR8(-/)- mice in models of Schistosoma mansoni soluble egg antigen (SEA)-induced gr

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

268 velop intestinal inflammation, and a control Schistosoma mansoni-specific Th1 clone did not induce co

269 We previously suggested that the Schistosoma mansoni spliced leader AUG might contribute

270 -term continuously proliferative cultures of Schistosoma mansoni sporocysts capable of generating cer

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

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

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

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

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

276 ant public health problem and infection with Schistosoma mansoni the major cause of liver disease.

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

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

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

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

281 antigen was found to be identical to that of Schistosoma mansoni TPx-1.

282 levels in 177 Ugandans (aged 7-50) in a high Schistosoma mansoni transmission area, both before and 7

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

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

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

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

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

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

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

290 development after the injection of eggs from Schistosoma mansoni was investigated using wild-type (WT

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

292 Using the model helminth Schistosoma mansoni, we have explored the possibility th

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

294 aboons with primary or secondary exposure to Schistosoma mansoni were compared with each other over a

295 Skin-stage schistosomula of Schistosoma mansoni were found to secrete molecules that

296 T) mice infected with the parasitic helminth Schistosoma mansoni, were found to be severely impaired

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

298 Emergence of Schistosoma mansoni with reduced sensitivity to praziqua

299 we challenge one paradigm by targeting adult Schistosoma mansoni worms for immune elimination in an e

300 te the immune response in mice infected with Schistosoma mansoni, yet the specific contributions of I