コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 parvum or C. hominis) or trichrome stain (E. histolytica).
2 the initiation of erythrophagocytosis in E. histolytica.
3 mechanism is not very well understood in E. histolytica.
4 ityca) and microarray expression data for E. histolytica.
5 isolated crypts from mice inoculated with E. histolytica.
6 ion during various endocytic processes in E. histolytica.
7 I3-kinase signaling in these processes in E. histolytica.
8 he early stages of phagosome formation in E. histolytica.
9 allei, Clostridium perfringens and Entamoeba histolytica.
10 -specific manner, while ERE2 is unique to E. histolytica.
11 main of C1q were all chemoattractants for E. histolytica.
12 bat disease caused by the parasite Entamoeba histolytica.
13 cteria, the usual source of nutrients for E. histolytica.
14 de transcriptional regulatory patterns in E. histolytica.
15 n V prior to adherence to or ingestion by E. histolytica.
16 rlying erythrocyte phagocytosis by Entamoeba histolytica.
17 elevance of raft-like membrane domains in E. histolytica.
18 iated TGS in the deep-branching eukaryote E. histolytica.
19 polymorphisms on intestinal infection by E. histolytica.
20 erent kinetics of ubiquitin activation in E. histolytica.
21 codon 223 were intracecally infected with E. histolytica.
22 low for a unique polyubiquitin linkage in E. histolytica.
23 nserved mode of E2/RING-E3 interaction in E. histolytica.
26 + ADP), with the exception of the Entamoeba histolytica ACK (EhACK) which uses pyrophosphate (PPi)/i
28 the mechanism of phagocytosis, we used an E. histolytica Affymetrix microarray chip to measure the to
30 We examined rhomboid function in Entamoeba histolytica, an extracellular, parasitic ameba that is s
31 be harnessed for the prevention of Entamoeba histolytica and Cryptosporidium species infection in chi
32 ntly been published for identification of E. histolytica and differentiation from the morphologically
33 re found at syntenic break points between E. histolytica and E. dispar and hence, could work as recom
34 human intestinal IgA antibody response to E. histolytica and E. dispar infection and revealed that AL
36 und a putative transposase-coding gene in E. histolytica and E. dispar related to the mariner transpo
39 Archamoebae, including pathogenic Entamoeba histolytica and free-living Mastigamoeba balamuthi, the
41 dy-state levels in the plasma membrane of E. histolytica and that these levels, unlike those in mamma
42 ll as in the phagolysosomal biogenesis in E. histolytica and thus contributes to the pathogenicity of
44 ptosporidium, Giardia lamblia, and Entamoeba histolytica), and helminths (Ascaris lumbricoides and Tr
45 lamblia, Cryptosporidium spp., and Entamoeba histolytica), and viruses (norovirus GI and GII, adenovi
47 sequence similarity to adhesin in Entamoeba histolytica, and we observed that Alix is secreted, we d
48 sensitive detection for individual Entamoeba histolytica antigen EHI_115350 (limit of detection = 1 p
49 h for the capture and detection of Entamoeba histolytica antigens from disinfected stool, within a sp
52 nce for Golgi apparatus-like functions in E. histolytica as well as for components of glycoprotein fo
53 The lack of a defined Golgi apparatus in E. histolytica as well as in other protists led to the hypo
55 named E. histolytica ILWEQ (EhILWEQ) and E. histolytica BAR (EhBAR), were chosen for localization vi
56 esses following intrahepatic injection of E. histolytica by a combined rate of 68% in two independent
58 is aggregated into caps on the surface of E. histolytica by the N-glycan-specific, anti-retroviral le
59 measure the activity of Dbr1 from Entamoeba histolytica by using a synthetic, dark-quenched bRNA sub
60 determine if calreticulin functions as an E. histolytica C1q receptor during phagocytosis of host cel
63 ay in erythrophagocytosis was observed in E. histolytica cells overexpressing S428A and KDDeltaC prot
65 proteolytic rhomboid (EhROM1) from Entamoeba histolytica cleaves cell surface galactose-binding or N-
66 spectively studied the natural history of E. histolytica colonization and diarrhea among infants in a
69 are caused by Giardia duodenalis, Entamoeba histolytica, Cryptosporidium parvum, and Cryptosporidium
70 cholerae, Yersinia enterocolitica, Entamoeba histolytica, Cryptosporidium spp., and E. coli O157:H7;
71 alnourished at birth had increased Entamoeba histolytica, Cryptosporidium, and ETEC infections and mo
72 ith an increase in phagocytic ability, as E. histolytica cultures exposed to an initial stimulus of p
73 to each specifically detect their cognant E. histolytica cyst antigens was demonstrated in a biologic
75 ves of bovine xanthine oxidase and Entamoeba histolytica cysteine protease 1 allowed active stocks to
77 inal cathelicidins is a novel function of E. histolytica cysteine proteinases in the evasion of the i
78 screte mechanisms of innate resistance to E. histolytica depending on the host background and, in con
79 hment of intestinal infection with Entamoeba histolytica depends on the mouse strain; C57BL/6 mice ar
80 pressive histone mark to be identified in E. histolytica, dimethylation of H3K27 (H3K27Me2), and demo
83 ch as Cryptosporidium, Giardia, or Entamoeba histolytica) disrupt cell functions and cause short- or
87 erstanding the mechanisms by which Entamoeba histolytica drives gut inflammation is critical for the
88 reticulin was localized to the surface of E. histolytica during interaction with both Jurkat lymphocy
90 moebic colitis is the detection of Entamoeba histolytica (Eh) trophozoites with ingested erythrocytes
94 highly repetitive amoeba genomes, Entamoeba histolytica, Entamoeba dispar, and Entamoeba invadens, w
95 e of detecting and discriminating between E. histolytica, Entamoeba dispar, G. lamblia assemblages A
96 school age, for infection by the parasite E. histolytica every other day over 9 years and evaluated t
98 ty of each assay to correctly distinguish E. histolytica from E. dispar was evaluated with DNA extrac
100 own that vaccination with purified Entamoeba histolytica Gal/GalNAc lectin or recombinant subunits ca
101 n A (IgA) antibody response to the Entamoeba histolytica galactose-inhibitable adherence lectin is mo
105 omposition bias and repetitiveness of the E. histolytica genome provide a challenge for short-read ma
106 lication of the protozoan parasite Entamoeba histolytica genome provides new insights into eukaryotic
107 e process has been the publication of the E. histolytica genome, from which has come an explosion in
108 entified a MIF gene homolog in the Entamoeba histolytica genome, raising the question of whether E. h
109 gene transfer of bacterial genes into the E. histolytica genome, the effects of which centre on expan
111 n a variety of parasites including Entamoeba histolytica, Giardia intestinalis, Leishmania spp., Plas
112 ium spp., Cyclospora cayetanensis, Entamoeba histolytica, Giardia lamblia, adenovirus F 40/41, astrov
114 tract include the deadly parasite Entamoeba histolytica;Giardia lamblia, the most common cause of wa
118 arch using the trophozoite form of Entamoeba histolytica has clearly shown us the importance of the i
119 Together, these studies demonstrate that E. histolytica has different vesicles that play a role in p
120 an archetypal family member, from Entamoeba histolytica, has been determined to 1.2 A resolution in
121 phagocytosis-related signaling events in E. histolytica have been characterized, the functions of li
123 d with a reduced virulence phenotype, and E. histolytica HM-1:IMSS trophozoites infecting human intes
128 scribe the crystal structure of an Entamoeba histolytica hybrid IP6K/IP3K, an enzymatic parallel to a
130 nsitivity and specificity compared to the E. histolytica II ELISA of 98.0% (95% confidence interval [
131 ytica microplate assay from Remel and the E. histolytica II enzyme-linked immunosorbent assay (ELISA)
132 creen Entamoeba test (R-Biopharm) and the E. histolytica II test (Techlab), and we found that the E.
133 II test (Techlab), and we found that the E. histolytica II test detects E. histolytica infections mo
134 the five encoded proteins, which we named E. histolytica ILWEQ (EhILWEQ) and E. histolytica BAR (EhBA
138 d lines of the eukaryotic pathogen Entamoeba histolytica in order to develop a picture of genetic div
141 Prior to phagocytosis of host cells, E. histolytica induces apoptotic host cell death, using a m
143 of this subunit were more susceptible to E. histolytica infection as measured by culture results, ce
144 eaks were of higher amplitude following a E. histolytica infection compared to E. dispar (P = 0.01) a
159 ic liver abscesses due to invasive Entamoeba histolytica infections are an important cause of morbidi
160 with E. histolytica; the incidence of new E. histolytica infections in controls (as determined by cul
162 ella, Shigella, Campylobacter, and Entamoeba histolytica infections, and their impact on long-term ef
165 s (ALA) with or without concurrent Entamoeba histolytica intestinal infection or were infection free
178 monstrate that G3-based gene silencing in E. histolytica is mediated by an siRNA pathway, which utili
183 The enteric protozoan parasite Entamoeba histolytica is the cause of potentially fatal amebic col
188 ancient eukaryotic human pathogen, Entamoeba histolytica, is a nucleo-base auxotroph (i.e. lacks the
194 potential for novel metabolic pathways in E. histolytica may allow for the development of new chemoth
195 The discovery of amoebic trogocytosis in E. histolytica may also shed light on an evolutionarily con
197 otic cells, monoclonal antibodies against E. histolytica membrane antigens were screened for inhibiti
200 he commercially available ProSpecT Entamoeba histolytica microplate assay from Remel and the E. histo
202 a genome, raising the question of whether E. histolytica MIF (EhMIF) has proinflammatory activity sim
203 ier family (MCF) complement of the Entamoeba histolytica mitochondrial homolog, also known as a crypt
205 talloprotease leishmanolysin gene, Entamoeba histolytica MSP-1 (EhMSP-1) and EhMSP-2, while the comme
206 lence multiple amebic genes, including an E. histolytica Myb gene, which is upregulated during oxidat
207 n(5)GlcNAc(2), which is the most abundant E. histolytica N-glycan, is aggregated into caps on the sur
209 apio anubis) are natural hosts for Entamoeba histolytica; naturally infected baboons raised in captiv
210 95% CI, 2.02-50.6) more likely to be both E. histolytica negative and serum anti-lectin immunoglobuli
211 homozygous genotypes were found in 55% of E. histolytica-negative children but in only 34% of E. hist
213 lower odds of B hominis (0.52, 0.34-0.78), E histolytica or E dispar (0.61, 0.38-0.99), G intestinali
214 antly lower odds of infection with Entamoeba histolytica or Entamoeba dispar (OR 0.56, 95% CI 0.42-0.
219 ost cell engulfment, or phagocytosis, and E. histolytica phagocytosis alters amebic gene expression i
220 y implicate the SREHP as a participant in E. histolytica phagocytosis and suggest that it may play an
222 psonins on apoptotic cells that stimulate E. histolytica phagocytosis, an effect mediated at least in
223 the collectins are ligands that stimulate E. histolytica phagocytosis, we used a flow cytometry-based
227 tica-negative children but in only 34% of E. histolytica-positive children (overall odds ratio, 2.39;
228 a significantly higher leukocyte count in E. histolytica-positive patients than in negative patients
229 The single-celled human parasite Entamoeba histolytica possesses a dynamic actin cytoskeleton vital
233 red to the ProSpecT microplate assay, the E. histolytica Quik Chek (Quik Chek) assay exhibited 97.0%
234 lyzed the ability of the third-generation E. histolytica Quik Chek assay developed by Techlab to dete
236 stolytica HM-1:IMSS is a virulent strain, E. histolytica Rahman is a nonvirulent strain, and Entamoeb
237 par and 32 genes with lower expression in E. histolytica Rahman than in E. histolytica HM-1:IMSS.
238 :IMSS, the prototype virulent strain, and E. histolytica Rahman, a strain that was reportedly less vi
239 Vietnam, a novel and simple-to-use Entamoeba histolytica rapid antigen test had 97% sensitivity and 1
241 he pattern of polymorphism indicates that E. histolytica reproduces sexually, or has done so in the p
244 overexpression of calreticulin increased E. histolytica's ability to phagocytose apoptotic lymphocyt
246 We previously demonstrated that Entamoeba histolytica secretes a protease capable of dissolving th
248 a, we first defined the phenotypes of two E. histolytica strains, HM-1:IMSS, the prototype virulent s
249 evaluate genetic variability among Entamoeba histolytica strains, we sequenced 9,077 bp from each of
251 es less likely to be infected with Entamoeba histolytica than those carrying the mutant R223 allele.
252 stress-responsive transcription factor in E. histolytica that controls a transcriptional regulatory n
256 identified the protozoan parasite Entamoeba histolytica, the etiological agent of amebiasis, as one
258 e host immune response during invasion of E. histolytica, the protozoan cause of human amebiasis.
259 patients who may be infected with Entamoeba histolytica, the species that causes clinical amebiasis.
260 rdia spp, Cryptosporidium spp, and Entamoeba histolytica, the Tri-Combo parasite screen, was compared
261 , 6.3% of ALA subjects were infected with E. histolytica; the incidence of new E. histolytica infecti
262 says suggested that auranofin targets the E. histolytica thioredoxin reductase, preventing the reduct
264 The ability of the human parasite Entamoeba histolytica to survive reactive oxygen and nitrogen spec
265 e effects(3), and potential resistance of E. histolytica to the drug is an increasing concern(4,5).
266 deep-branching eukaryotic parasite Entamoeba histolytica, transcriptional gene silencing (TGS) of the
267 rase (OST) from Trypanosoma cruzi, Entamoeba histolytica, Trichomonas vaginalis, Cryptococcus neoform
268 o control animals bound to the surface of E. histolytica trophozoites and accelerated amebic lysis vi
269 eases degrade the key adherence lectin on E. histolytica trophozoites and decrease their adherence to
271 obust assay for the specific detection of E. histolytica trophozoites in unfixed frozen clinical stoo
273 lectin protein on the surfaces of axenic E. histolytica trophozoites or from solubilized amebae.
274 is of amebic colitis, we demonstrate that E. histolytica trophozoites or their released proteinases,
277 mouse model of amebic liver abscess, but E. histolytica trophozoites that do not express amoebapore-
278 on of the galactose-specific adherence of E. histolytica trophozoites to Chinese hamster ovary cells
280 expression was upregulated in phagocytic E. histolytica trophozoites to determine whether these gene
282 lated with our finding that co-culture of E. histolytica trophozoites with mucin-producing T84 cells
285 we have cloned and characterized multiple E. histolytica ubiquitination components, spanning ubiquiti
287 ches we have (a) cloned and expressed the E. histolytica UDP-galactose transporter in Saccharomyces c
288 ed that the Q223 allele protected against E. histolytica via STAT3-mediated transcription of genes re
289 EhILWEQ and EhBAR appear to contribute to E. histolytica virulence through their function in phagocyt
294 om South Africans naturally infected with E. histolytica were examined by enzyme-linked immunosorbent
295 pathogenic E. coli, rotavirus, and Entamoeba histolytica were the most frequent probable contributors
296 postchallenge, all Q223 mice had cleared E. histolytica, whereas 39% of 223R mice were infected.
297 e invasion by the intestinal ameba Entamoeba histolytica, which causes amebic dysentery and liver abs
299 ed a new tool for genetic manipulation in E. histolytica with many advantages over currently availabl
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。