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

3 ll trafficking in response to challenge with Schistosoma mansoni.

4 anctuary staff, were naturally infected with Schistosoma mansoni.

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

6 llowing infection with the helminth parasite Schistosoma mansoni.

7 aneous infections with the helminth parasite Schistosoma mansoni.

8 Th2 response against the parasitic helminth Schistosoma mansoni.

9 characterized eIF4E from the human parasite Schistosoma mansoni.

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

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

12 igmosomoides polygyrus, Trichuris muris, and Schistosoma mansoni.

13 tissues of mice infected with the trematode Schistosoma mansoni.

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

15 e identified in the Platyhelminth trematode, Schistosoma mansoni.

16 tive against various developmental stages of Schistosoma mansoni.

17 potent activity against pathogenic trematode Schistosoma mansoni.

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

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

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

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

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

23 e fibrosis induced by the parasitic helminth Schistosoma mansoni.

24 sponse development to the parasitic helminth Schistosoma mansoni.

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

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

27 hemokines in experimental mouse models using Schistosoma mansoni.

28 mice to survive infection with the parasite Schistosoma mansoni.

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

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

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

32 against the blood-feeding trematode parasite Schistosoma mansoni.

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

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

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

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

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

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

39 e hosts for the digenetic trematode parasite Schistosoma mansoni.

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

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

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

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

44 Schistosoma mansoni, a causative agent of schistosomiasi

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

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

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

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

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

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

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

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

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

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

55 Schistosoma mansoni, an intravascular parasite, has evol

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

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

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

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

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

61 treatment of schoolchildren coinfected with Schistosoma mansoni and hookworm.

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

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

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

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

66 -21R-/- mice with the Th2-inducing pathogens Schistosoma mansoni and Nippostrongylus brasiliensis and

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

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

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

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

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

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

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

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

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

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

77 The blood flukes Schistosoma mansoni and Schistosoma japonicum inflict im

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

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

80 Schistosoma mansoni (and rarely Schistosoma haematobium)

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

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

83 Schistosoma mansoni- and Mycobacterium tuberculosis-spec

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

101 Schistosoma mansoni cercariae display specific behaviora

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

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

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

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

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

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

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

109 responses have previously been observed with Schistosoma mansoni coinfection.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

129 mycobacterial purified protein derivative or Schistosoma mansoni egg antigens.

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

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

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

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

134 Schistosoma mansoni egg-induced lung pathology requires

135 Schistosoma mansoni egg-induced pulmonary granuloma form

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

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

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

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

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

141 Schistosoma mansoni eggs contain factors that trigger po

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

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

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

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

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

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

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

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

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

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

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

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

154 Th2 cytokine production when challenged with Schistosoma mansoni eggs.

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

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

157 effective TH2 responses when challenged with Schistosoma mansoni eggs.

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

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

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

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

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

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

164 Schistosoma mansoni exposure results in prototypical typ

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

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

167 The recent release of version 3 of the Schistosoma mansoni genome assembly has made a wealth of

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

169 esolution crystal structure of a full-length Schistosoma mansoni hammerhead ribozyme that permits us

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

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

172 The Schistosoma mansoni homologue (SmSmad2) was overexpresse

173 Results: Schistosoma mansoni, hookworm, Strongyloides stercoralis

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

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

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

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

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

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

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

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

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

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

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

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

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

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

188 Praziquantel treatment for Schistosoma mansoni infection enhances Th2 responsivenes

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

190 Intensive MDA reduced Schistosoma mansoni infection intensity: the prevalence

191 Schistosoma mansoni infection is highly endemic in parts

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

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

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

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

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

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

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

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

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

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

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

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

204 Traditionally, human Schistosoma mansoni infections have been detected using

205 Experimental Schistosoma mansoni infections of mice lead to a dynamic

206 In murine Schistosoma mansoni infections, schistosome-specific cro

207 As with Schistosoma mansoni infections, the pathology of urogeni

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

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

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

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

212 Schistosoma mansoni is a parasitic fluke that infects mi

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

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

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

216 Schistosoma mansoni is responsible for the neglected tro

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

218 Schistosoma mansoni is the causative agent of intestinal

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

234 Schistosoma mansoni parasites of both sexes recovered fr

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

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

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

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

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

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

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

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

243 Schistosoma mansoni receptor-regulated Smad1 and SmSmad2

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

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

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

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

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

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

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

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

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

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

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

255 Schistosoma mansoni (Sm) infection has been linked with

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

292 Schistosoma mansoni was associated with lower total chol

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

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

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

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

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

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

299 Emergence of Schistosoma mansoni with reduced sensitivity to praziqua

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