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1 mperature appears to affect the viability of Trichomonas.
2 In men with NGU, 19.9% were infected with trichomonas.
4 nce of RNAs with a distinctive 5' DMG cap in Trichomonas and Giardia lineages that are absent in othe
6 hol-PP-GlcNAc2Man5 (present in Entamoeba and Trichomonas) and dolichol-PP- and N-linked GlcNAc2 (pres
7 Black race, a new sex partner, a history of trichomonas, and the presence of symptoms were associate
13 a indicate that the thioredoxin reductase of Trichomonas differs fundamentally in structure from that
14 enzymes of Plasmodium spp., Trypanosomatida, Trichomonas, Entamoeba and Giardia, with special emphasi
15 s amplified with DNA from Trichomonas tenax, Trichomonas gallinae, Chlamydia trachomatis, Neisseria g
16 ly early branching eukaryotic lineages, like Trichomonas, Galpha is likely to function independently
29 lial clones, recombinant galectins, clinical Trichomonas isolates, and mutant protozoan derivatives t
32 The percent sensitivity versus control for Trichomonas ranged from 100% at time zero with and witho
37 targeted product was amplified with DNA from Trichomonas tenax, Trichomonas gallinae, Chlamydia trach
39 specimen type routinely used for traditional trichomonas testing and the recommended specimen type fo
41 terium Anabaena sp. (44%), and the protozoan Trichomonas vaginalis (46%), which targets its POR to an
42 there was some evidence of association with Trichomonas vaginalis (adjusted OR, 1.56; 95% CI, 1.00-2
43 es inoculated with Chlamydia trachomatis and Trichomonas vaginalis (n = 9) or medium (controls; n = 7
44 2 (HSV-2), syphilis, chlamydia, gonorrhoea, Trichomonas vaginalis (together defined as 'any STI') an
46 omatis (CT), Mycoplasma genitalium (MG), and Trichomonas vaginalis (TV) are sexually transmitted infe
48 n is affected by bacterial vaginosis (BV) or Trichomonas vaginalis (TV) infection has not been adequa
50 Ureaplasma urealyticum biovar 2 (UU-2), and Trichomonas vaginalis (TV) using nucleic acid amplificat
51 sis (BV), vulvovaginal candidiasis (VVC), or Trichomonas vaginalis (TV), were randomly assigned to re
53 d Entamoeba histolytica, and the parabasalid Trichomonas vaginalis all belong to Class II of FBAs and
54 7,899 specimens submitted for live clinical Trichomonas vaginalis analyte-specific reagent (ASR) scr
55 o transcription-mediated amplification-based Trichomonas vaginalis analyte-specific-reagent (ASR) tes
56 s specific, since the related human parasite Trichomonas vaginalis and associated purified CPs did no
57 ption-mediated amplification (TMA) assay for Trichomonas vaginalis and BTUB FRET PCR, using self-obta
58 drial carrier family in the hydrogenosome of Trichomonas vaginalis and have shown that this protein,
59 icient in metronidazole-resistant strains of Trichomonas vaginalis and is thought to be necessary for
61 sence of a splicing apparatus in the protist Trichomonas vaginalis and show that RNA motifs found in
62 ent in the amitochondriate parasitic protist Trichomonas vaginalis and some but not all other trichom
64 ing Giardia lamblia, Leishmania species, and Trichomonas vaginalis are persistently infected with dsR
65 omonas vaginalis prevalence using the Aptima Trichomonas vaginalis assay (ATV; Gen-Probe) and the pre
66 ts of a commercial NAA test (GenProbe Aptima Trichomonas vaginalis assay; ATV) for T. vaginalis were
67 clinic for a new complaint were screened for Trichomonas vaginalis by culture and by PCR analysis of
68 on as well as to determine the prevalence of Trichomonas vaginalis by culture in a large and diverse
69 amplification tests (NAATs) for detection of Trichomonas vaginalis by vaginal swabs; NAATs for detect
70 clinic for a new complaint were screened for Trichomonas vaginalis by wet-preparation (wet-prep) micr
75 thral swabs were obtained at enrollment, for Trichomonas vaginalis culture; semen specimens were also
76 n of macaques with Chlamydia trachomatis and Trichomonas vaginalis decreases the prophylactic efficac
77 determine if secreted cysteine proteases of Trichomonas vaginalis degrade SLPI and render it nonfunc
78 condary test in improving the sensitivity of Trichomonas vaginalis detection in young women over that
80 obe was designed and evaluated for detecting Trichomonas vaginalis DNA in a 5' nuclease (TaqMan) assa
84 odified medium to InPouch for the culture of Trichomonas vaginalis from pooled vaginal secretions.
88 tica, Leishmania spp., Trypanosoma cruzi and Trichomonas vaginalis have genes encoding homologues of
91 ydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis in liquid-based cytology specimens
92 could also detect Mycoplasma genitalium and Trichomonas vaginalis in men and women reporting a histo
95 l SLPI levels have been correlated with both Trichomonas vaginalis infection and poor reproductive he
105 omen in Mombasa, Kenya, to determine whether Trichomonas vaginalis infection was associated with an i
106 = 756 men), we identified 150 men (20%) with Trichomonas vaginalis infection, 358 men (47%) with HIV
107 ns related to the diagnosis and treatment of Trichomonas vaginalis infection, as well as the associat
108 esented regarding conditions associated with Trichomonas vaginalis infection, including human immunod
109 k women, being 30 to 40 years of age, recent Trichomonas vaginalis infection, primary or recurrent ge
110 infection, Chlamydia trachomatis infection, Trichomonas vaginalis infection, vulvovaginal candidiasi
114 eria gonorrhoeae, Mycoplasma genitalium, and Trichomonas vaginalis infections as well as the characte
115 tudy was to evaluate potential mechanisms of Trichomonas vaginalis involvement in human immunodeficie
133 ecreted cysteine protease (CP) fraction from Trichomonas vaginalis is shown here to induce apoptosis
138 unusual case of extragenital infection with Trichomonas vaginalis of the conjunctiva of a 32-year-ol
139 rican women who used drugs were screened for Trichomonas vaginalis on > or =2 occasions between March
140 230) performed rapid point-of-care tests for Trichomonas vaginalis on self-collected vaginal swabs.
141 ated in patients concomitantly infected with Trichomonas vaginalis or Chlamydia trachomatis in additi
142 ins AP65, AP51, AP33 and AP23 synthesized by Trichomonas vaginalis organisms in high iron play a role
143 culture and evaluated their interaction with Trichomonas vaginalis parasites to complement previous s
147 binding protein from the primitive eukaryote Trichomonas vaginalis reveals how a single protein can o
151 ydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis Sequencing was used to assess macr
155 iterature has reported increased accuracy of Trichomonas vaginalis transcription-mediated amplificati
156 ydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis via commercial transcription-media
157 LV was found to be more thermoresistant than Trichomonas vaginalis virus 1, but no specific protein m
160 ransport medium to maintain the viability of Trichomonas vaginalis was determined by comparing transp
163 hlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis) and the E6/E7 mRNA of human papil
164 lastida (Leishmania major), the Parabasalia (Trichomonas vaginalis), and the Microsporidia (Vairimorp
171 describe the genome sequence of the protist Trichomonas vaginalis, a sexually transmitted human path
172 ribed in the divergent unicellular eukaryote Trichomonas vaginalis, although genome analyses reveal t
174 hlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis, and bacterial vaginosis testing w
175 the pathogenic protozoa Giardia lamblia and Trichomonas vaginalis, and the bacterial pathogens Helic
176 the slime-mold Dictyostelium, the protozoan Trichomonas vaginalis, and the bacterium Burkholderia ps
178 he three common organisms causing vaginitis: Trichomonas vaginalis, Candida species, and Gardnerella
179 om Trypanosoma cruzi, Entamoeba histolytica, Trichomonas vaginalis, Cryptococcus neoformans, and Sacc
180 Women infected with Neisseria gonorrhoeae, Trichomonas vaginalis, or Chlamydia trachomatis had high
182 fungal pathogens, as well as protozoa, e.g., Trichomonas vaginalis, Plasmodium berghei, and sporozoit
183 the genome databases for Giardia lamblia and Trichomonas vaginalis, respectively, and represent the l
186 hydrogenosome-bearing, unicellular eukaryote Trichomonas vaginalis, that contains the active site mot
188 e medically important parasites: the protist Trichomonas vaginalis, the hard tick Ixodes ricinus, and
189 s simplex virus 2 infection, genital ulcers, Trichomonas vaginalis, vaginitis or cervicitis, and male
190 CR assay, using primers against pfoB gene of Trichomonas vaginalis, was developed and evaluated using
192 equences in the protists Giardia lamblia and Trichomonas vaginalis, which may represent the deepest k
193 tein-encoding genes in the parasitic protist Trichomonas vaginalis, which represents one of the deepe
214 r gonorrhea, chlamydia, bacterial vaginosis, trichomonas, vulvovaginal candidiasis, pelvic inflammato
215 the major antioxidant defense mechanisms in Trichomonas was confirmed by showing that the parasite r
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