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1 ) and three partial draft genomes (including Trichomonas vaginalis).
2 (zero for bacterial vaginosis, candida, and Trichomonas vaginalis).
3 drial protist pathogens: Giardia lamblia and Trichomonas vaginalis.
4 , Entamoeba histolytica, Giardia lamblia and Trichomonas vaginalis.
5 t preparation and a culture method to detect Trichomonas vaginalis.
6 Trypanosoma brucei, Leishmania donovani, and Trichomonas vaginalis.
7 in one of the earliest diverging protozoans, Trichomonas vaginalis.
8 is specifically related to a homologue from Trichomonas vaginalis.
9 a, that represented by the parasitic protist Trichomonas vaginalis.
10 ctably transform the human-infective protist Trichomonas vaginalis.
11 ption of protein-coding genes of the protist Trichomonas vaginalis.
12 nscription factor in the protozoan parasite, Trichomonas vaginalis.
13 for Candida spp., Gardnerella vaginalis, and Trichomonas vaginalis.
14 ally transmitted infections (STIs) caused by Trichomonas vaginalis.
15 aginotropic extracellular protozoan parasite Trichomonas vaginalis.
16 Women were also tested for Trichomonas vaginalis.
17 sekeeping genes, to genetically characterize Trichomonas vaginalis.
18 bation of culture media for the detection of Trichomonas vaginalis.
19 terium Anabaena sp. (44%), and the protozoan Trichomonas vaginalis (46%), which targets its POR to an
24 describe the genome sequence of the protist Trichomonas vaginalis, a sexually transmitted human path
25 there was some evidence of association with Trichomonas vaginalis (adjusted OR, 1.56; 95% CI, 1.00-2
26 d Entamoeba histolytica, and the parabasalid Trichomonas vaginalis all belong to Class II of FBAs and
27 ribed in the divergent unicellular eukaryote Trichomonas vaginalis, although genome analyses reveal t
29 7,899 specimens submitted for live clinical Trichomonas vaginalis analyte-specific reagent (ASR) scr
30 o transcription-mediated amplification-based Trichomonas vaginalis analyte-specific-reagent (ASR) tes
31 s specific, since the related human parasite Trichomonas vaginalis and associated purified CPs did no
32 ption-mediated amplification (TMA) assay for Trichomonas vaginalis and BTUB FRET PCR, using self-obta
33 drial carrier family in the hydrogenosome of Trichomonas vaginalis and have shown that this protein,
34 icient in metronidazole-resistant strains of Trichomonas vaginalis and is thought to be necessary for
36 sence of a splicing apparatus in the protist Trichomonas vaginalis and show that RNA motifs found in
37 ent in the amitochondriate parasitic protist Trichomonas vaginalis and some but not all other trichom
39 hlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis) and the E6/E7 mRNA of human papil
40 lastida (Leishmania major), the Parabasalia (Trichomonas vaginalis), and the Microsporidia (Vairimorp
41 hlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis, and bacterial vaginosis testing w
42 the pathogenic protozoa Giardia lamblia and Trichomonas vaginalis, and the bacterial pathogens Helic
43 the slime-mold Dictyostelium, the protozoan Trichomonas vaginalis, and the bacterium Burkholderia ps
46 ing Giardia lamblia, Leishmania species, and Trichomonas vaginalis are persistently infected with dsR
47 omonas vaginalis prevalence using the Aptima Trichomonas vaginalis assay (ATV; Gen-Probe) and the pre
48 ts of a commercial NAA test (GenProbe Aptima Trichomonas vaginalis assay; ATV) for T. vaginalis were
49 clinic for a new complaint were screened for Trichomonas vaginalis by culture and by PCR analysis of
50 on as well as to determine the prevalence of Trichomonas vaginalis by culture in a large and diverse
51 amplification tests (NAATs) for detection of Trichomonas vaginalis by vaginal swabs; NAATs for detect
52 clinic for a new complaint were screened for Trichomonas vaginalis by wet-preparation (wet-prep) micr
53 he three common organisms causing vaginitis: Trichomonas vaginalis, Candida species, and Gardnerella
58 om Trypanosoma cruzi, Entamoeba histolytica, Trichomonas vaginalis, Cryptococcus neoformans, and Sacc
59 thral swabs were obtained at enrollment, for Trichomonas vaginalis culture; semen specimens were also
60 n of macaques with Chlamydia trachomatis and Trichomonas vaginalis decreases the prophylactic efficac
61 determine if secreted cysteine proteases of Trichomonas vaginalis degrade SLPI and render it nonfunc
62 condary test in improving the sensitivity of Trichomonas vaginalis detection in young women over that
64 obe was designed and evaluated for detecting Trichomonas vaginalis DNA in a 5' nuclease (TaqMan) assa
68 odified medium to InPouch for the culture of Trichomonas vaginalis from pooled vaginal secretions.
72 tica, Leishmania spp., Trypanosoma cruzi and Trichomonas vaginalis have genes encoding homologues of
75 ydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis in liquid-based cytology specimens
76 could also detect Mycoplasma genitalium and Trichomonas vaginalis in men and women reporting a histo
79 l SLPI levels have been correlated with both Trichomonas vaginalis infection and poor reproductive he
89 omen in Mombasa, Kenya, to determine whether Trichomonas vaginalis infection was associated with an i
90 = 756 men), we identified 150 men (20%) with Trichomonas vaginalis infection, 358 men (47%) with HIV
91 ns related to the diagnosis and treatment of Trichomonas vaginalis infection, as well as the associat
92 esented regarding conditions associated with Trichomonas vaginalis infection, including human immunod
93 k women, being 30 to 40 years of age, recent Trichomonas vaginalis infection, primary or recurrent ge
94 infection, Chlamydia trachomatis infection, Trichomonas vaginalis infection, vulvovaginal candidiasi
98 eria gonorrhoeae, Mycoplasma genitalium, and Trichomonas vaginalis infections as well as the characte
99 tudy was to evaluate potential mechanisms of Trichomonas vaginalis involvement in human immunodeficie
117 ecreted cysteine protease (CP) fraction from Trichomonas vaginalis is shown here to induce apoptosis
121 es inoculated with Chlamydia trachomatis and Trichomonas vaginalis (n = 9) or medium (controls; n = 7
123 unusual case of extragenital infection with Trichomonas vaginalis of the conjunctiva of a 32-year-ol
124 rican women who used drugs were screened for Trichomonas vaginalis on > or =2 occasions between March
125 230) performed rapid point-of-care tests for Trichomonas vaginalis on self-collected vaginal swabs.
126 ated in patients concomitantly infected with Trichomonas vaginalis or Chlamydia trachomatis in additi
127 Women infected with Neisseria gonorrhoeae, Trichomonas vaginalis, or Chlamydia trachomatis had high
129 ins AP65, AP51, AP33 and AP23 synthesized by Trichomonas vaginalis organisms in high iron play a role
130 culture and evaluated their interaction with Trichomonas vaginalis parasites to complement previous s
132 fungal pathogens, as well as protozoa, e.g., Trichomonas vaginalis, Plasmodium berghei, and sporozoit
135 the genome databases for Giardia lamblia and Trichomonas vaginalis, respectively, and represent the l
137 binding protein from the primitive eukaryote Trichomonas vaginalis reveals how a single protein can o
141 ydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis Sequencing was used to assess macr
146 hydrogenosome-bearing, unicellular eukaryote Trichomonas vaginalis, that contains the active site mot
148 e medically important parasites: the protist Trichomonas vaginalis, the hard tick Ixodes ricinus, and
149 2 (HSV-2), syphilis, chlamydia, gonorrhoea, Trichomonas vaginalis (together defined as 'any STI') an
150 iterature has reported increased accuracy of Trichomonas vaginalis transcription-mediated amplificati
152 omatis (CT), Mycoplasma genitalium (MG), and Trichomonas vaginalis (TV) are sexually transmitted infe
154 n is affected by bacterial vaginosis (BV) or Trichomonas vaginalis (TV) infection has not been adequa
156 Ureaplasma urealyticum biovar 2 (UU-2), and Trichomonas vaginalis (TV) using nucleic acid amplificat
157 sis (BV), vulvovaginal candidiasis (VVC), or Trichomonas vaginalis (TV), were randomly assigned to re
159 s simplex virus 2 infection, genital ulcers, Trichomonas vaginalis, vaginitis or cervicitis, and male
160 ydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis via commercial transcription-media
161 LV was found to be more thermoresistant than Trichomonas vaginalis virus 1, but no specific protein m
164 ransport medium to maintain the viability of Trichomonas vaginalis was determined by comparing transp
165 CR assay, using primers against pfoB gene of Trichomonas vaginalis, was developed and evaluated using
169 equences in the protists Giardia lamblia and Trichomonas vaginalis, which may represent the deepest k
170 tein-encoding genes in the parasitic protist Trichomonas vaginalis, which represents one of the deepe
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