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1 e anciently diverged amitochondriate protist Giardia lamblia.
2 alytic subunit from the diplomonad parasite, Giardia lamblia.
3 from the amitochondriate diplomonad protist, Giardia lamblia.
4 fide isomerases from the primitive eukaryote Giardia lamblia.
5 that infects the widespread enteric parasite Giardia lamblia.
6 fecal samples submitted for the detection of Giardia lamblia.
7 e cpn60 homolog from the diplomonad parasite Giardia lamblia.
8 iardiasis is a disease caused by the protist Giardia lamblia.
9 anosine cap (DMG) as observed previously for Giardia lamblia.
10 lagella of the intestinal protozoan parasite Giardia lamblia.
11 -giardin family in the intestinal protozoan, Giardia lamblia.
12 i (STEC), enteroinvasive E. coli (EIEC), and Giardia lamblia.
13 tiation of the intestinal protozoan parasite Giardia lamblia.
14 control in mice infected with the protozoan Giardia lamblia.
15 ripheral vacuoles in the intestinal parasite Giardia lamblia.
16 ba butschlii (8), Blastocystis hominis (19), Giardia lamblia (6), Dientamoeba fragilis (2), yeast (2)
17 sporidium spp., and E. coli O157:H7; 95% for Giardia lamblia; 94% for ETEC and STEC; 93% for Shigella
21 e, but it was no more closely related to the Giardia lamblia acetyl-CoA synthetase than to those of a
22 lospora cayetanensis, Entamoeba histolytica, Giardia lamblia, adenovirus F 40/41, astrovirus, norovir
23 ridium species (the most frequent pathogen), Giardia lamblia, Aeromonas species, Campylobacter specie
24 ine phosphoribosyltransferase (GPRTase) from Giardia lamblia, an enzyme required for guanine salvage
27 rt was obtained by expression of ZK 896.9 in Giardia lamblia, an organism recently characterized as h
29 ound in eubacteria and also in the eukaryote Giardia lamblia and are only distantly related to typica
30 for the rapid and quantitative detection of Giardia lamblia and Cryptosporidium parvum (oo)cysts in
32 assay that detects and distinguishes between Giardia lamblia and Cryptosporidium parvum in aqueous ex
33 assay that detects and distinguishes between Giardia lamblia and Cryptosporidium parvum in human stoo
34 oa endemic to developed countries, including Giardia lamblia and Cryptosporidium spp., using technolo
35 ment of a CT-factor sufficient to inactivate Giardia lamblia and enteric viruses 1 h after treatment.
36 mechanisms responsible for control of acute Giardia lamblia and Giardia muris infections in adult mi
37 microbes, including the pathogenic protozoa Giardia lamblia and Trichomonas vaginalis, and the bacte
38 B and TrichDB house the genome databases for Giardia lamblia and Trichomonas vaginalis, respectively,
39 rts of intervening sequences in the protists Giardia lamblia and Trichomonas vaginalis, which may rep
42 ryptosporidium, Cyclospora cayetanensis, and Giardia lamblia) and 90% or greater for 11/17 targets: a
44 n, findings related to diarrhoea prevalence, Giardia lamblia, and Cryptosporidium parvum were adjuste
46 e E. coli (EIEC), protozoa (Cryptosporidium, Giardia lamblia, and Entamoeba histolytica), and helmint
48 es the sexual transmission of Campylobacter, Giardia lamblia, and Shigella (particularly antimicrobia
50 Cryptosporidium Microplate Assay, Cambridge Giardia lamblia Antigen Microwell ELISA, Meridian Premie
51 e Proteins (VSPs) of the intestinal parasite Giardia lamblia are not cytotoxic, inducing instead VSP
52 Infections with the diarrheagenic pathogen, Giardia lamblia, are commonly treated with the 5-nitroim
54 ed gene expression in the ancient eukaryote, Giardia lamblia, by taking advantage of assays developed
56 hlamydia trachomatis, Neisseria gonorrhoeae, Giardia lamblia, Chilomastix sulcatus, Dientamoeba fragi
57 anism, whereas the human parasitic protozoan Giardia lamblia class II FBPA is a zinc-dependent enzyme
58 ns of modern animals as well as the archezoa Giardia lamblia, confirming the presence of inhibitory p
59 toxigenic Clostridium difficile), parasites (Giardia lamblia, Cryptosporidium spp., and Entamoeba his
61 athogenic E. coli, Campylobacter jejuni, and Giardia lamblia document heterogeneity among enteropatho
63 Here we show that the unicellular pathogen Giardia lamblia encodes an mRNA capping apparatus consis
64 single Tgs1 protein, the primitive eukaryote Giardia lamblia encodes two paralogs, Tgs1 and Tgs2.
66 p comprising the long (>60-kDa) enzymes from Giardia lamblia, Entamoeba histolytica pfk2, the spiroch
67 pathogens, including Cryptosporidium parvum, Giardia lamblia, Entamoeba histolytica, and Cyclospora c
69 immunoassay (EIA) panel for the detection of Giardia lamblia, Entamoeba histolytica/E. dispar, and Cr
70 iga toxin virulence genes, Balantidium coli, Giardia lamblia, Enterocytozoon bieneusi, and Trichuris
76 There was an increase in the prevalence of Giardia lamblia genes, any E. coli virulence gene, and t
80 e corresponding locations in human HGPRT and Giardia lamblia GPRT, respectively, may explain their re
81 In contrast, eradication of the human strain Giardia lamblia GS/M, for which adaptive immunity is les
83 -forming) from the amitochondriate eukaryote Giardia lamblia has been expressed in Escherichia coli.
85 variant-specific surface proteins (VSPs) in Giardia lamblia-host interactions, antigenic variation d
87 ive immunochromatographic assay that detects Giardia lamblia in aqueous extracts of human fecal speci
88 asite (O&P) examination for the detection of Giardia lamblia in preserved stool specimens were determ
89 genomic sequence of the primitive eukaryote Giardia lamblia indicated the presence of an archaeal pr
94 monly considered to be potential sources for Giardia lamblia infections in humans, but the extent of
113 A prominent feature of transcription in Giardia lamblia is the abundant production of sterile an
117 enon, several pathogenic protozoa, including Giardia lamblia, Leishmania species, and Trichomonas vag
119 is crucial to the initiation of infection by Giardia lamblia, little is known about the regulation of
120 d Inc.], Giardia Test [Techlab], and Premier Giardia lamblia [Meridian Diagnostics, Inc.]) and two co
121 ia Antigen Microwell ELISA, Meridian Premier Giardia lamblia, Meridian Premier Cryptosporidium, TechL
124 s in the candidate early-branching eukaryote Giardia lamblia occur in separate pieces, transcribed fr
125 the identification in the protozoan parasite Giardia lamblia of a novel class of small RNAs, which ar
126 poson content of the genome of the protozoan Giardia lamblia, one of the earliest-branching eukaryote
128 formation) is important for the survival of Giardia lamblia outside its human host, the molecular ev
130 ardiavirus (GLV)-luciferase chimeric mRNA in Giardia lamblia requires the presence of the initial 264
131 p70 of Campylobacter lari, Escherichia coli, Giardia lamblia, Salmonella typhimurium, and Listeria mo
132 own of how the primitive protozoan parasite, Giardia lamblia, senses and responds to its changing env
134 evaluated the abilities of three commercial Giardia lamblia-specific enzyme immunoassays (EIAs) (Pro
135 h: stomach (Anisakis), proximal small bowel (Giardia lamblia, Strongyloides stercoralis, Mycobacteriu
137 oa endemic to developed countries, including Giardia lamblia (syn. G. intestinalis/G. duodenalis) and
139 s such as Schizosaccharomyces pombe Tgs1 and Giardia lamblia Tgs2 catalyze methylation of the exocycl
140 und to be less susceptible to infection with Giardia lamblia than were isogenic mice from another fac
141 as been identified in the protozoan pathogen Giardia lamblia that is similar to the core sequence of
143 de the deadly parasite Entamoeba histolytica;Giardia lamblia, the most common cause of waterborne dis
144 double-stranded RNA (dsRNA) virus infecting Giardia lamblia, the most common protozoan pathogen of t
146 tting, ranging from 0.4 (95% CI 0.2-0.6) for Giardia lamblia to 54.1 (95% CI 7.4-393.5) for Vibrio ch
151 ly found that the deeply branching eukaryote Giardia lamblia uses a distinct hexamer (AGURAA) and lac
152 tin-binding proteins, the prevalent parasite Giardia lamblia uses an alternative mechanism for cytoki
153 two human pathogens (Trypanosoma brucei and Giardia lamblia) using a new hybrid vector, pTARBAC1, co
156 ction, we determined the virion structure of Giardia lamblia virus, obtaining new information relatin
158 ine phosphoribosyltransferase (APRTase) from Giardia lamblia was co-crystallized with 9-deazaadenine
159 elicobacter pylori, Salmonella enterica, and Giardia lamblia were detected in sewage, as well as MST
160 a second amitochondriate protozoan parasite, Giardia lamblia, were sequenced, and their phylogenetic
162 highly active form of the enzyme Dicer from Giardia lamblia, which is capable of accurately processi
163 intolerance in a group previously exposed to Giardia lamblia with a control group; secondly, to explo
164 low-cost detection of a foodborne pathogen, Giardia lamblia, with high sensitivity (the detection li
165 osporidium parvum, Cryptosporidium muris and Giardia lamblia, with over 92% certainty was achieved.
166 action of the waterborne protozoan parasite, Giardia lamblia, with polymeric materials was investigat