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1 a model for investigating the human pathogen Chlamydia trachomatis.
2 ted with the obligate intracellular bacteria Chlamydia trachomatis.
3 ant role of antibodies in protection against Chlamydia trachomatis.
4 ion with the obligate intracellular bacteria Chlamydia trachomatis.
5 -to-culture, obligate intracellular pathogen Chlamydia trachomatis.
6 re compared to Amplicor for detecting ocular Chlamydia trachomatis.
7 ysis of 52 geographically diverse strains of Chlamydia trachomatis.
8 ellular pathogens Listeria monocytogenes and Chlamydia trachomatis.
9 he obligate intracellular bacterial pathogen Chlamydia trachomatis.
10 uitous in many chlamydial species, including Chlamydia trachomatis.
11 lls for the obligate intracellular bacterium Chlamydia trachomatis.
12 fected with a single cervical inoculation of Chlamydia trachomatis.
13 is often found in the absence of detectable Chlamydia trachomatis.
14 t the major outer membrane protein (MOMP) of Chlamydia trachomatis.
15 xual transmission is probably lower than for Chlamydia trachomatis.
16 is triggered by diverse bacteria, including Chlamydia trachomatis, a frequent intracellular parasite
21 acid amplification tests (NAATs) that detect Chlamydia trachomatis AC2 also detects Neisseria gonorrh
22 ind that C. muridarum and the human pathogen Chlamydia trachomatis activate not only NLRP3 but also A
23 lesion, and changes in sexual behaviors and Chlamydia trachomatis, an infection with similar epidemi
24 is produced by chronic ocular infection with Chlamydia trachomatis, an obligate intracellular bacteri
25 (Versant CT/GC assay, where "CT" represents Chlamydia trachomatis and "GC" represents Neisseria gono
26 RealTime CT/NG assay (where "CT" stands for Chlamydia trachomatis and "NG" stands for Neisseria gono
27 iable analysis were vaccine status, positive Chlamydia trachomatis and >/=4 partners in the preceding
33 itive risk score had point-of-care tests for Chlamydia trachomatis and Neisseria gonorrhoea (nucleic
34 The next-generation amplification test for Chlamydia trachomatis and Neisseria gonorrhoeae (Roche c
35 se of infertility and ectopic pregnancy, and Chlamydia trachomatis and Neisseria gonorrhoeae are reco
38 assay (ATV; Gen-Probe) and the prevalence of Chlamydia trachomatis and Neisseria gonorrhoeae coinfect
39 methods exist for the molecular detection of Chlamydia trachomatis and Neisseria gonorrhoeae in clini
40 ilable molecular assays for the detection of Chlamydia trachomatis and Neisseria gonorrhoeae in recta
42 with detectable T. vaginalis, codetection of Chlamydia trachomatis and Neisseria gonorrhoeae occurred
44 00/8800 systems (Cobas) for the detection of Chlamydia trachomatis and Neisseria gonorrhoeae was esta
45 T) has become the preferred method to detect Chlamydia trachomatis and Neisseria gonorrhoeae, but no
46 ing (NAAT) is the preferred method to detect Chlamydia trachomatis and Neisseria gonorrhoeae, but no
47 isease associations, which parallel those of Chlamydia trachomatis and Neisseria gonorrhoeae, the mec
51 Female pig-tailed macaques inoculated with Chlamydia trachomatis and Trichomonas vaginalis (n = 9)
52 tigated whether coinfection of macaques with Chlamydia trachomatis and Trichomonas vaginalis decrease
53 ification testing for Neisseria gonorrhoeae, Chlamydia trachomatis, and Trichomonas vaginalis were pe
55 he obligate intracellular bacterial parasite Chlamydia trachomatis are the same as its eukaryotic hos
57 rs, how the obligate intracellular bacterium Chlamydia trachomatis arrives at a physiologically simil
58 urethritis (NGU) and cervicitis is aimed at Chlamydia trachomatis, but Mycoplasma genitalium, which
61 r screening adolescents and young adults for Chlamydia trachomatis (C. trachomatis) and Neisseria gon
62 female infertility and genital infection by Chlamydia trachomatis (C. trachomatis) is a major cause.
70 tidoglycan assembles at the pole of dividing Chlamydia trachomatis cells where daughter cell formatio
71 sex or symptoms is used to manage anorectal Chlamydia trachomatis (chlamydia) and Neisseria gonorrho
74 hose who have not been diagnosed with rectal Chlamydia trachomatis (CT) and/or rectal Neisseria gonor
77 cy, and infertility in women with a previous Chlamydia trachomatis (CT) diagnosis compared with women
80 UU) was detected in 25 (17.2%) participants, Chlamydia trachomatis (CT) in 13 (9.0%), Mycoplasma geni
81 he diagnosis and management of uncomplicated Chlamydia trachomatis (CT) infection in adolescents and
84 study was to estimate the probability that a Chlamydia trachomatis (CT) infection will cause an episo
85 screening for Neisseria gonorrhoeae (NG) and Chlamydia trachomatis (CT) infections in all men who hav
89 collected for Neisseria gonorrhoeae (GC) and Chlamydia trachomatis (CT) screening of HIV-1-infected M
90 extragenital Neisseria gonorrhoeae (NG) and Chlamydia trachomatis (CT) so universal extragenital sam
91 odel of HIV, Neisseria gonorrhoeae (NG), and Chlamydia trachomatis (CT) transmission dynamics among M
92 class Ic ribonucleotide reductase (RNR) from Chlamydia trachomatis (Ct) utilizes a Mn/Fe heterobinucl
95 mSIBA) that allows simultaneous detection of Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG),
103 ured derivative of the human genital isolate Chlamydia trachomatis D/UW-3/Cx, strain CTD153, which al
106 her probenecid would have a direct effect on Chlamydia trachomatis development through inhibition of
111 bacter baumannii, Burkholderia pseudomallei, Chlamydia trachomatis, Escherichia coli, Klebsiella pneu
112 oring indicates an absence of infection with Chlamydia trachomatis even if FT persists, may be more c
113 erinary relatives, the oculogenital pathogen Chlamydia trachomatis evolved as a commensal organism of
114 o, the obligate intracellular human pathogen Chlamydia trachomatis exhibits elevated expression of a
116 ancient neglected tropical disease caused by Chlamydia trachomatis for which a vaccine is needed.
118 s for detection of Neisseria gonorrhoeae and Chlamydia trachomatis from pharyngeal and rectal specime
119 ances detection of Neisseria gonorrhoeae and Chlamydia trachomatis from rectal and pharyngeal sources
120 ancy and infertility observed in women after Chlamydia trachomatis genital infection result from asce
122 fy novel transcriptional regulators from the Chlamydia trachomatis genome by predicting proteins with
124 ncluding the obligate intracellular pathogen Chlamydia trachomatis, grow within a membrane-bound bact
126 .09, 0.66), and Neisseria gonorrhoeae and/or Chlamydia trachomatis had 92% lower odds of any adverse
129 tive plasmid of both Chlamydia muridarum and Chlamydia trachomatis has been shown to control virulenc
132 hock proteins of the intracellular bacterium Chlamydia trachomatis have been associated with immune p
133 xiella burnetii, Listeria monocytogenes, and Chlamydia trachomatis have developed bipartite metabolis
136 atural infection induces partial immunity to Chlamydia trachomatis Identification of chlamydial antig
137 ltidomain type III secreted effector used by Chlamydia trachomatis In aggregate, existing data sugges
139 is caused by recurrent ocular infection with Chlamydia trachomatis in childhood, with conjunctival sc
140 he prevalence of trachoma and infection with Chlamydia trachomatis in communities after 3-7 years of
143 nts of the genetically intransigent pathogen Chlamydia trachomatis, in which all mutations have been
147 ned whether TLR variants are associated with Chlamydia trachomatis infection among women with pelvic
148 nces about the true population prevalence of Chlamydia trachomatis infection and disease and the sens
149 A sensing directs IFN-beta expression during Chlamydia trachomatis infection and suggest that effecto
150 ate point-of-care (POC) diagnostic tests for Chlamydia trachomatis infection are urgently needed for
151 obiota in a cohort of 149 women with genital Chlamydia trachomatis infection at baseline who were fol
153 witnessed a disturbing increase in cases of Chlamydia trachomatis infection despite enhanced control
154 served signs of trachomatous inflammation or Chlamydia trachomatis infection diagnosed using PCR.
155 ral discharge to diagnose N. gonorrhoeae and Chlamydia trachomatis infection in certain populations b
156 point of care test for detecting urogenital Chlamydia trachomatis infection in nonpregnant women and
167 ver, when LOS synthesis was inhibited during Chlamydia trachomatis infection, HeLa cells regained sus
168 w-up studies in a murine model of intranasal Chlamydia trachomatis infection, we analogously found th
176 this study, we show that the human pathogen Chlamydia trachomatis infects the murine respiratory and
208 ween genital and ocular clinical isolates of Chlamydia trachomatis is that only the former express a
209 The obligate intracellular human pathogen Chlamydia trachomatis is the etiological agent of blindi
223 a, caused by repeated infections with ocular Chlamydia trachomatis, is targeted for elimination using
224 aused by the obligate intracellular organism Chlamydia trachomatis, is the world's leading cause of p
227 , increased the growth of the human pathogen Chlamydia trachomatis (L2) in wild-type murine fibroblas
228 pecifically bound and repressed promoters of Chlamydia trachomatis late genes, but not early or mid g
233 dered idiopathic when Neisseria gonorrhoeae, Chlamydia trachomatis, Mycoplasma genitalium, Trichomona
234 assessed the intervention effect on incident Chlamydia trachomatis, Neisseria gonorrhoeae, and Mycopl
235 a, and first-void female urine specimens for Chlamydia trachomatis, Neisseria gonorrhoeae, and Tricho
236 sites were tested for M. genitalium and for Chlamydia trachomatis, Neisseria gonorrhoeae, and Tricho
237 s, the prevalences of Mycoplasma genitalium, Chlamydia trachomatis, Neisseria gonorrhoeae, and Tricho
239 e new insights concerning the concurrence of Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma
240 uently drink alcohol and to be infected with Chlamydia trachomatis, Neisseria gonorrhoeae, or herpes
241 d for M. genitalium and other STI organisms (Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomona
242 Specimens were tested for M. genitalium, Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomona
243 ed with those for batches of 24 samples; for Chlamydia trachomatis/Neisseria gonorrhoeae tests, the a
244 rs) was significantly greater than those for Chlamydia trachomatis or N. gonorrhoeae (27.6 and 25.9 y
248 ed on filter paper to test for antibodies to Chlamydia trachomatis pgp3 using a multiplex bead assay.
249 er paper and dried to test for antibodies to Chlamydia trachomatis pgp3 using the Luminex platform.
251 ryngeal and rectal Neisseria gonorrhoeae and Chlamydia trachomatis play important roles in infection
253 A new R2 subclass, R2c, prototyped by the Chlamydia trachomatis protein was recently discovered.
257 he bacterial obligate intracellular pathogen Chlamydia trachomatis replicates within a membrane-bound
259 source, molecular Neisseria gonorrhoeae and Chlamydia trachomatis results, and relative light unit (
260 nd Mn(III)Fe(III) sites in the R2 subunit of Chlamydia trachomatis ribonucleotide reductase using x-r
264 cycle of the obligate intracellular pathogen Chlamydia trachomatis serovar L2 is controlled in part b
265 .) routes with recombinant MOMP (rMOMP) from Chlamydia trachomatis serovars D (UW-3/Cx), E (Bour), or
266 fections caused by Neisseria gonorrhoeae and Chlamydia trachomatis serovars D to K occur at high inci
271 erive the intact structure of the primordial Chlamydia trachomatis T3SS in the presence and absence o
273 id-based genetic transformation protocol for Chlamydia trachomatis that for the first time provides a
275 gnificantly reduces the prevalence of ocular Chlamydia trachomatis, the causative organism of trachom
276 or infertility (TFI) that is attributable to Chlamydia trachomatis, the population excess fraction (P
277 nd include the agent of oculogenital disease Chlamydia trachomatis, the respiratory pathogen C. pneum
278 d mice infected with Chlamydia muridarum and Chlamydia trachomatis to determine if there were differe
279 ating between-strain genomic recombinants of Chlamydia trachomatis to facilitate the organism's evolu
281 address the potential for plasmid-deficient Chlamydia trachomatis to serve as a live attenuated vacc
283 haracterization of a previously undocumented Chlamydia trachomatis transcription factor, designated G
284 cts of control strategies on the dynamics of Chlamydia trachomatis transmission are difficult to quan
285 pants were tested for Neisseria gonorrhoeae, Chlamydia trachomatis, Treponema pallidum (syphilis), he
286 seria gonorrhoeae, Streptococcus agalactiae, Chlamydia trachomatis, Trichomonas vaginalis, and Candid
288 the lifetime was tested for the presence of Chlamydia trachomatis, type-specific human papillomaviru
290 e first, found in the intracellular pathogen Chlamydia trachomatis, uses YhhQ and tRNA guanine transg
291 nd to a common Ag in Chlamydia muridarum and Chlamydia trachomatis Using an adoptive-transfer approac
292 urine samples) for Neisseria gonorrhoeae and Chlamydia trachomatis using nucleic acid amplification t
293 ns with the obligate intracellular bacterium Chlamydia trachomatis, variation in immune activation an
296 n a community with a high prevalence of STI, Chlamydia trachomatis was detected in 8.7% and Neisseria
297 An atypical response regulator, ChxR, from Chlamydia trachomatis, was previously reported to form h
299 llowing repeated conjunctival infection with Chlamydia trachomatis, which causes a chronic inflammato
300 ndida albicans, Streptococcus agalactiae and Chlamydia trachomatis with a single biochip, enabling a