ライフサイエンスコーパス: trophozoite

1 n from the dormant cyst form into the active trophozoite.

2 the nuclei of cysts, but not the vegetative trophozoite.

3 recognition of and response to Acanthamoeba trophozoites.

4 ar algae, and preferentially, Perkinsus spp. trophozoites.

5 ntify the pathogenic behavior of the amoebic trophozoites.

6 ith serially diluted cultured E. histolytica trophozoites.

7 nes, and levels of these target proteases in trophozoites.

8 falcipain-2, the hydrolysis of hemoglobin in trophozoites.

9 e of the main host defenses against invading trophozoites.

10 rafts were then infected with E. histolytica trophozoites.

11 VSPs were detected on the surface of single trophozoites.

12 on of plasminogen activators by Acanthamoeba trophozoites.

13 nt did not affect encystment of Acanthamoeba trophozoites.

14 60-kDa enzyme in extracts of E. histolytica trophozoites.

15 ammatory cells and few Entamoeba histolytica trophozoites.

16 n expressed on the surface of both cysts and trophozoites.

17 ced the number of acidic compartments in the trophozoites.

18 12-kDa protein localized to the cytoplasm of trophozoites.

19 PHIST/CVC-81(95) is most highly expressed in trophozoites.

20 and attachment mechanisms of Giardia lamblia trophozoites.

21 tially in nonencysting and encysting Giardia trophozoites.

22 Trophozoites (10(6)) were injected into the AC of hamste

23 hamoeba cysts/10 microl and 2.3 Acanthamoeba trophozoites/10 microl by both real-time PCR assays.

24 a surface antigen of E. histolytica bound to trophozoites 83.5% +/- 6.7% less than did uncleaved anti

25 mine specifically arrested the maturation of trophozoites, a stage at which the parasite synthesizes

26 Amoebic trophozoites activate the transcription factor NF-kappa

27 re-forming proteins and proteinases, but how trophozoites actually kill host cells has been unclear.

28 The IC(50) of 4a against P. carinii trophozoites after 7 days of continuous drug treatment w

29 ytopathic and cytolytic activities of viable trophozoites against mammalian nucleated cells, as well

30 Against trophozoites, All-in-One, ReNu Multiplus, and Optifree E

31 lower sensitivity to short drug pulses than trophozoites, although we identify a subpopulation of ri

32 ble number approach were used to compare the trophozoite and cysticidal efficacy of four multipurpose

33 s further indicate that FCP is essential for trophozoite and FV maturation and that it traffics to th

34 pypAg-2 expression was localized to both the trophozoite and merozoite membranes.

35 For Pf-RBCs at trophozoite and schizont stages, the presence of cytoadh

36 son, the H3-K9 acetylation increased in late trophozoite and schizont stages, while H4-K16 acetylatio

37 y decreases by approximately 50% at the late trophozoite and schizont stages.

38 g activity is markedly increased at the late trophozoite and schizont stages.

39 ponents of the red cell skeleton at the late trophozoite and schizont stages.

40 ge and reaches its maximal level in the late trophozoite and schizont stages.

41 gene family, to the cell surface of both the trophozoite and the cyst phase of the organism.

42 imals bound to the surface of E. histolytica trophozoites and accelerated amebic lysis via activation

43 efficacies against Acanthamoeba castellanii trophozoites and cysts by using a most probable number (

44 The use of GSP with cultured trophozoites and cysts from corneal scrapings has illust

45 excystment, proliferation, and encystment of trophozoites and cysts of A. castellanii was examined in

46 nly All-in-One proved effective against both trophozoites and cysts over the same time period.

47 ther show that exposure of M. bovis-infected trophozoites and cysts to Balb/c mice leads to pulmonary

48 termining the susceptibility of Acanthamoeba trophozoites and cysts to contact lens care systems has

49 dings indicate that exposure of Acanthamoeba trophozoites and cysts to dexamethasone increases the pa

50 The proliferation of trophozoites and cysts was examined by optical density a

51 GSP stained both trophozoites and cysts, although nonspecific cyst wall a

52 (ii) by determining their ability to detect trophozoites and cysts, and (iii) by testing a battery o

53 bin-hydrolyzing activity is maximum in early trophozoites and declines rapidly at late stages, wherea

54 e the key adherence lectin on E. histolytica trophozoites and decrease their adherence to epithelial

55 Both active trophozoites and dormant cysts of a pathogenic strain of

56 revealed that both kinases were expressed in trophozoites and encysting cells as 44- and 41-kDa polyp

57 ring the parasite growth from rings to early trophozoites and from late trophozoites to schizonts and

58 arasite life cycle (sporozoites, merozoites, trophozoites and gametocytes) by multidimensional protei

59 PN technique, which uses axenically produced trophozoites and mature, double-walled cysts, has the po

60 Here we overexpressed this enzyme in Giardia trophozoites and observed a significantly enhanced susce

61 Growth and maturation of trophozoites and schizonts was markedly inhibited in the

62 limited to ring stage, but also occurred in trophozoites and schizonts.

63 We showed that both Acanthamoeba trophozoites and soluble amoebic products induce an earl

64 ciated with the disappearance of intraocular trophozoites and suggests that cells of the innate immun

65 differentiate various malaria stages (ring, trophozoite, and schizont stage) due to their varied def

66 patic inoculation with Entamoeba histolytica trophozoites, and 12 h after amebic inoculation, reduced

67 e, is secreted in large amounts by encysting trophozoites, and correlates well with O&P.

68 /perinuclear targeting of bodipy-ceramide in trophozoites, and this could be reversed by 3-ketosphing

69 (PyMIF) were used to localize expression in trophozoite- and schizont-stage parasites and demonstrat

70 Trophozoites appear to prepare for switching during ency

71 Entamoeba histolytica trophozoites are covered by lipophosphoglycan-peptidogly

72 When Acanthamoeba castellanii trophozoites are grown in methyl-alpha-D-mannopyranoside

73 phoresis demonstrates that within 24 h after trophozoites are induced to encyst, the level of glucosa

74 tracellular cysteine proteinases from amebic trophozoites are key virulence factors and have a number

75 Raft-like structures in trophozoites are located in the plasma membranes and on

76 The data show that IRBCs with late trophozoites are more resistant to trypsin treatment tha

77 re capable of detecting as few as 100 viable trophozoites as determined by ethidium bromide staining,

78 le the Pf MDH protein level remained high in trophozoites as well as schizonts.

79 Trophozoites attach to enterocytes that mature and die.

80 Trophozoites attached to host cells, in contrast, respon

81 on by host secretions reduces proclivity for trophozoite attachment, while inducing virulence factors

82 wall proteins to the plasma membrane of the trophozoite before laying down the protective cyst wall.

83 nthamoeba keratitis begins when Acanthamoeba trophozoites bind specifically to mannosylated glycoprot

84 washes from orally immunized pigs inhibited trophozoite binding to CHCE cells in vitro by more than

85 The effect of mucosal antibody on trophozoite binding to corneal epithelium and viability

86 the maturation of early trophozoites to late trophozoites but not during the development of rings to

87 oes not affect the viability of Acanthamoeba trophozoites but seems to prevent infection by inhibitin

88 were introduced into GLV-infected G. lamblia trophozoites by electroporation and stablized in the tra

89 ipt was introduced into GLV-infected Giardia trophozoites by electroporation.

90 ynthesis of FBPA was demonstrated in Giardia trophozoites by using an antibody-based fluorescence ass

91 The second hypothesis proposed that the trophozoites can enter the AC; however, the aqueous humo

92 ter comprehension of the mechanisms by which trophozoites can lyse target cells.

93 The first hypothesis proposed that trophozoites cannot penetrate Descemet's membrane and th

94 fection have begun to illuminate how amoebic trophozoites cause intestinal disease and liver abscess,

95 Invasion by Entamoeba histolytica trophozoites causes secretion of proinflammatory cytokin

96 Infection in Muc2(-/-) mice elevated trophozoite colonization in the small intestine and impa

97 E. histolytica trophozoites colonize the colon, where they induce infla

98 ced 4- to 10-fold increases in the number of trophozoites compared with untreated control cultures.

99 gene expression level of 68% of genes under trophozoite conditions.

100 d was used to determine whether Acanthamoeba trophozoites could penetrate this membrane in vitro.

101 A principal trophozoite cysteine protease was purified by affinity c

102 es linked to virulence, are both aberrant in trophozoites deficient in the metallosurface protease Eh

103 at these kinases may play a critical role in trophozoite differentiation into cysts.

104 ring intra-erythrocytic development, malaria trophozoites digest hemoglobin, which leads to parasite

105 A high proportion of ring forms and trophozoites disintegrates within a subset of CC cells,

106 castellanii and reversion of cysts to amoeba trophozoites, dotA and dotB mutants exhibited intracellu

107 stics of helminth eggs, protozoan cysts, and trophozoites, ease of use, and cost.

108 In E. histolytica trophozoites, EhROM1 changed localization to vesicles du

109 monstrated that putrescine induces protozoan trophozoite encystment and adversely affects cyst viabil

110 Exposure of hemocytes to Perkinsus spp. trophozoites enhanced this process further, and their ph

111 form of P. carinii, in that highly purified trophozoites exerted marked inhibition of p34cdc2 activi

112 ending pseudopodia and in phagosomal cups in trophozoites exposed to erythrocytes but did not localiz

113 Trophozoites exposed to Ru(II) compounds die through an

114 Acanthamoeba trophozoites express a mannose binding receptor that fac

115 Transcripts for three trophozoite-expressed genes were lost in AN3661-treated

116 SCID mice were infected with E. histolytica trophozoites expressing an antisense message to ehcp5.

117 by H2O2 in vitro, and infection with Rahman trophozoites expressing higher levels of peroxiredoxin w

118 Moreover, trophozoite extracts of pAP-R2 transfectant displayed lo

119 sient shrinkage of infected cells with young trophozoites followed by continuous volume increase to a

120 reviously showed that falcipain-2 is a major trophozoite food vacuole cysteine protease.

121 Research using the trophozoite form of Entamoeba histolytica has clearly sh

122 ependent kinase activity was mediated by the trophozoite form of P. carinii, in that highly purified

123 sion were identified between the blood stage trophozoite form of the malarial parasite and the sexual

124 With trophozoites, four of four MPDSs and the one-step peroxi

125 and 92 cases with hyperparasitemia (asexual trophozoites, >500,000/mm3).

126 Falcipain-2-knockout trophozoites had markedly diminished cysteine protease a

127 increased deformability of both Pf-free and trophozoite-harboring RBCs.

128 alciparum cysteine protease falcipain-2 is a trophozoite hemoglobinase and potential antimalarial dru

129 de on presence of target images, clusters or trophozoite images (at least 1 of the 3 features), the p

130 Specificity of both target and trophozoite images was 100%.

131 ntiproliferative activity against P. carinii trophozoites in culture at a concentration of 10 microgr

132 Furthermore, culturing of trophozoites in dialyzed medium containing fetal bovine

133 ion of helminth eggs and protozoan cysts and trophozoites in fecal specimens.

134 e we tested the virulence of amoebapore A(-) trophozoites in models of the two major forms of amebic

135 useful in confirming the presence of viable trophozoites in respiratory specimens collected by nonin

136 gest there is frequently a failure to detect trophozoites in routine examination, resulting in an und

137 on of ADP could be obtained in permeabilized trophozoites in the presence of succinate, citrate, alph

138 for the specific detection of E. histolytica trophozoites in unfixed frozen clinical stool samples.

139 inhibits G. lamblia CK and kills G. lamblia trophozoites in vitro at submicromolar IC50 values.

140 rypsin treatment than those containing early trophozoites, indicating that parasite proteins expresse

141 In contrast, trophozoite-infected RBCs exhibited voltage-dependent, n

142 ence phenotype, and E. histolytica HM-1:IMSS trophozoites infecting human intestinal xenografts show

143 Finally, expression of a PH domain in trophozoites inhibited erythrophagocytosis and enhanced

144 inside the infected host cell, we find that trophozoites (intermediate-stage iRBCs) tend to flip due

145 es outside of the host by differentiation of trophozoites into infectious cysts.

146 These data suggest that once trophozoites invade the cornea, MIP-133 production is ne

147 and engulfing red blood cells, E histolytica trophozoites invade the intestinal mucosa, causing amoeb

148 When E. histolytica trophozoites invade the lamina propria of a host colon,

149 testinal epithelial colonization of invasive trophozoites involves a complex interplay in which the u

150 ing, while no signal was obtained from 10(6) trophozoites killed by heat, desiccation, or UV radiatio

151 Moreover, even though Giardia trophozoites lack a morphologically discernible Golgi ap

152 Although Giardia trophozoites lack a morphologically discernible Golgi ap

153 racecal inoculation of Entamoeba histolytica trophozoites led to established infection in 60% of C3H

154 Target images and trophozoite-like images are pathognomonic of AK.

155 rreflective objects (diameter, <30 mum); and trophozoite-like objects (diameter, >30 mum).

156 roteins expressed on the IRBC surface during trophozoite maturation partially mask accessibility of a

157 ect corneal epithelial or stromal cells from trophozoite-mediated cytolysis in vitro.

158 Acanthamoeba trophozoite migration is also voltage-dependent, with in

159 We find that the trophozoite migration response is voltage-dependent, wit

160 In 2-microm channels, trophozoites mimicked "pitting," a normal process in the

161 transition from free swimming to attachment, trophozoites modified their swimming behavior from a rap

162 oxiredoxin in Rahman rendered the transgenic trophozoites more resistant to killing by H2O2 in vitro,

163 ese data suggest an important role of PKA in trophozoite motility during vegetative growth and the ce

164 Acanthamoeba trophozoites move at random in the absence of an EF, but

165 Acanthamoeba trophozoites move directionally in response to an EF in

166 Trophozoite mucosal invasion is triggered only when both

167 Despite strong CvGal1 binding to P. marinus trophozoites, no binding of ABH blood group antibodies w

168 A concentration of 10(4) trophozoites of 3 well-characterized clinical strains of

169 ved macrophages were either coincubated with trophozoites of a clinical isolate of Acanthamoeba (geno

170 Trophozoites of A. castellanii bound avidly to corneal e

171 um from the 2004-2006 keratitis outbreak and trophozoites of Acanthamoeba castellanii were inoculated

172 s shown here by its hybridization to growing trophozoites of all 12 known Acanthamoeba 18S rDNA seque

173 4, as shown here in hybridization tests with trophozoites of all 12 sequence types.

174 In vitro real-time imaging demonstrated that trophozoites of both strains often established evanescen

175 is one of the pathogenicity factors by which trophozoites of E. histolytica exert their remarkable cy

176 row-derived macrophages were cocultured with trophozoites of either the laboratory Neff strain or a c

177 which was subsequently found to display rare trophozoites of Entopolypoides macaci.

178 Analysis of trophozoites of five different species of Acanthamoeba e

179 ucing ability, and MBP expression pattern of trophozoites of four different isolates of Acanthamoeba

180 demonstrated lower detection limits of five trophozoites of G. lamblia.

181 ia swim, we used video microscopy to observe trophozoites of Giardia intestinalis, which were labeled

182 consisting of eggs, larvae, cysts, and a few trophozoites of Giardia intestinalis.

183 and the mitochondrial membrane potential of trophozoites of the malaria parasite Plasmodium berghei

184 Trophozoites of the malaria parasite Plasmodium falcipar

185 site numbers (n = 7) or specimens containing trophozoites only (n = 3); one specimen with a false-neg

186 face of the erythrocyte infected with either trophozoite or early gametocyte parasites.

187 Dexamethasone-treated trophozoites or cysts induced a significant cytopathic e

188 ein on the surfaces of axenic E. histolytica trophozoites or from solubilized amebae.

189 on the development of either rings to early trophozoites or late trophozoites to schizonts and meroz

190 not during the development of rings to early trophozoites or late trophozoites to schizonts and meroz

191 colitis, we demonstrate that E. histolytica trophozoites or their released proteinases, including cy

192 of IL-10; furthermore, challenge with either trophozoites or their soluble metabolites stimulate both

193 E. invadens parasites and in E. histolytica trophozoites overexpressing chitinase under an actin gen

194 surface proteins and by flow cytometry using trophozoites overexpressing epitope-tagged calreticulin.

195 indirect immunofluorescence assay with whole trophozoites (P < 0.01) and Western blot analysis confir

196 otocol was capable of detecting as few as 20 trophozoites per PCR on fecal DNA isolated using a comme

197 A isolated using a commercial method or 1.25 trophozoites per PCR on fecal DNA isolated using a G. la

198 Development proceeds rapidly from the trophozoite phase of nutrient acquisition and growth thr

199 evealed the existence of distinct, nonclonal trophozoite populations with high and low EhMSP-1 surfac

200 Entamoeba histolytica trophozoites produce amoebapores, a family of small amph

201 Besides, all compounds inhibit the trophozoite proliferation in amoebic liver abscess induc

202 Acceleration of trophozoite proliferation was observed when trophozoites

203 In trophozoites, pyruvate-ferredoxin oxidoreductase (PFOR)

204 Finally, trophozoite quorum sensing via the lectin initiates the

205 eding, the healthy oysters ingest P. marinus trophozoites released to the water column by the infecte

206 Most of the SOD activity in P. marinus trophozoites resides in a major component of subunit mol

207 Inside oyster hemocytes, trophozoites resist oxidative killing, proliferate, and

208 Motile trophozoites respond to soluble secreted signals, which

209 Overexpression of EhEBP1 in E. histolytica trophozoites resulted in a 7-fold drop in promoter activ

210 development and that this persists until the trophozoite-schizont boundary.

211 ines, Pbs21 protein was expressed in asexual trophozoites, schizonts, and, when present, in both male

212 subcellular localization of ERK1 and ERK2 in trophozoites showed ERK1 staining mostly in the median b

213 ggest the presence of an H(+) conductance in trophozoites similar to that produced by a mitochondrial

214 les, and was responsible for at least 93% of trophozoite soluble cysteine protease activity.

215 Babesia can also be confused with the early trophozoite stage (ring forms) of Plasmodium parasites.

216 rotease that cleaves hemoglobin at the early trophozoite stage and erythrocyte membrane ankyrin and p

217 tide increases dramatically during the early trophozoite stage and reaches its maximal level in the l

218 ashion, with high levels detected during the trophozoite stage at the peak of parasite membrane bioge

219 The parasite asexual trophozoite stage is susceptible to iron-induced oxidati

220 e as the organelle forms upon entry into the trophozoite stage of development and that this persists

221 rmation and swelling of the IRBCs during the trophozoite stage of P. falciparum that is followed by s

222 es are transcribed simultaneously during the trophozoite stage of the IDC and that only a small subse

223 parum-infected red blood cells (RBCs) in the trophozoite stage were simultaneously loaded with the Ca

224 ript pattern was unique, peaking at mid-late trophozoite stage, but absent in late-stage schizonts.

225 e growth of the parasite specifically at the trophozoite stage, preventing further development to sch

226 ycle, at the highly transcriptionally active trophozoite stage, the genome adopts a more open chromat

227 obin in the acidic food vacuole at the early trophozoite stage, whereas it cleaves specific component

228 organelle forms and persists throughout the trophozoite stage.

229 ages, while H4-K16 acetylation peaked in mid-trophozoite stage.

230 le of the parasite but induced mainly at the trophozoite stage.

231 inhibits parasite differentiation beyond the trophozoite stage.

232 in parasitised cells up to the mature, late trophozoite stage.

233 h Plasmodium falciparum, at the mature, late trophozoite stage.

234 t is significantly elevated during the early trophozoite stage.

235 replicative stage of the asexual cycle, the trophozoite stage.

236 he Pfmc-2tm genes are transcribed during the trophozoite stage; this narrow time frame of transcripti

237 ound distributed on the surface of ring- and trophozoite-stage parasites.

238 Trophozoite stages failed to freely traverse 2- to 4-mic

239 nst HEK293 cells and inhibited both ring and trophozoite stages of the malaria parasite life cycle.

240 core histone gene expression during the late trophozoite stages, consistent with their role in replic

241 f variant histones decreased in mid- or late trophozoite stages.

242 f the parasite life cycle at the ring or the trophozoite stages.

243 CLAG9 at two stages--the early ring and late trophozoite stages.

244 nant var gene occurs in the later (pigmented trophozoite) stages, whereas Northern blot data indicate

245 bition of FBPA gene transcription in Giardia trophozoites suggested that the enzyme is necessary for

246 abscesses consisting of a few E histolytica trophozoites surrounding dead and dying hepatocytes and

247 Recently, E. histolytica trophozoites that are totally deficient in the productio

248 of amebic liver abscess, but E. histolytica trophozoites that do not express amoebapore-A can still

249 The mucus gel layer prevents those trophozoites that escape the hydrolases from reaching th

250 nal morphologic features of the 2 strains of trophozoites that received treatment were similar to tho

251 ally expressed in nonencysting and encysting trophozoites, the giardial ceramide glucosyltransferase

252 ytic enzymes that facilitate the invasion of trophozoites through the basement membrane.

253 ive infection, (b) developmental change from trophozoite to cyst, or (c) invasion and potential death

254 abeling is detected predominantly during the trophozoite to schizont and schizont to ring transitions

255 From the trophozoite to the schizont stage that ensues within 24-

256 treatment on the capacity of A. castellanii trophozoites to adhere to and kill corneal epithelial ce

257 lactose-specific adherence of E. histolytica trophozoites to Chinese hamster ovary cells in vitro (P,

258 Interestingly, adherence of E. histolytica trophozoites to CHO cells was inhibited by MAbs against

259 was upregulated in phagocytic E. histolytica trophozoites to determine whether these genes actually f

260 igated the in vitro response of Acanthamoeba trophozoites to electric fields (EFs).

261 s exclusively during the maturation of early trophozoites to late trophozoites but not during the dev

262 inding receptor that facilitates adhesion of trophozoites to mannosylated proteins on corneal epithel

263 The results suggest that binding of trophozoites to mannosylated proteins on the corneal sur

264 of thioredoxin and enhancing sensitivity of trophozoites to reactive oxygen-mediated killing.

265 om rings to early trophozoites and from late trophozoites to schizonts and merozoites.

266 f either rings to early trophozoites or late trophozoites to schizonts and merozoites.

267 pment of rings to early trophozoites or late trophozoites to schizonts and merozoites.

268 n on corneal epithelial cells and stimulates trophozoites to secrete a mannose-induced 133 kDa protea

269 In addition, the capacity of trophozoites to survive in AH was determined in vitro.

270 The capacity of trophozoites to sustain oxidative phosphorylation was ad

271 x bead treatment did not affect adherence of trophozoites to the corneal epithelium or protect cornea

272 Adherence of EhMSP-1-deficient trophozoites to tissue culture cell monolayers was more

273 Giardia lamblia trophozoites transfected with the transcript of this con

274 vered that, during rapid swimming of Giardia trophozoites, undulations of the caudal region contribut

275 By comparison, host-cell attached trophozoites up-regulated intracellular pathways for ubi

276 revealed that the trailing edge of polarized trophozoites, uroids, are highly enriched in lipid rafts

277 While using this planar swimming motion, the trophozoites used the flagella for propulsion and direct

278 ed transcripts of luciferase gene in Giardia trophozoites via transfection and observed that when the

279 The migration of A. castellanii trophozoites was analyzed and quantified with ImageJ sof

280 amine binding sites on the surface of amoeba trophozoites was confirmed using radiolabeled catecholam

281 nding to corneal epithelium and viability of trophozoites was examined in vitro.

282 d stage parasites, as maturation of rings to trophozoites was markedly stalled.

283 Falcipain-2 was predominantly expressed in trophozoites, was concentrated in food vacuoles, and was

284 of mitochondria of Plasmodium yoelii yoelii trophozoites were assayed in situ after permeabilization

285 ree-dimensional culture system, Acanthamoeba trophozoites were cultured in agar, exposed to an EF, di

286 In all cases, cysts and trophozoites were detected 24 hours after treatment at a

287 Despite induction, E. histolytica trophozoites were found to be resistant to killing by th

288 Acanthamoeba castellanii trophozoites were grown in peptone-yeast extract glucose

289 Giardia trophozoites were persuaded to encyst in vitro by mimick

290 trophozoite proliferation was observed when trophozoites were treated with dexamethasone.

291 However, we found previously that trophozoites which had recovered after completion of the

292 The organism has two life cycle stages, trophozoites, which are responsible for tissue invasion,

293 model, M. bovis would be taken up by amoebal trophozoites, which are the actively feeding, replicatin

294 -expressed genes were lost in AN3661-treated trophozoites, which was not observed in parasites select

295 evels of Pf MDH transcripts were detected in trophozoites while the Pf MDH protein level remained hig

296 domains, as evidenced by reduced staining of trophozoites with CTXB and GM1 antibodies.

297 t of a synchronized culture of P. falciparum trophozoites with gossypol caused induction in expressio

298 the detection of Entamoeba histolytica (Eh) trophozoites with ingested erythrocytes.

299 ur finding that co-culture of E. histolytica trophozoites with mucin-producing T84 cells increased eh

300 inhibitors blocked hemoglobin hydrolysis in trophozoites, with a subsequent block in rupture of eryt