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1 PCR detected, quantified, and differentiated Chlamydophila 23S rRNA gene DNA from vaginal cytobrush s
3 lting from infection of sheep and goats with Chlamydophila abortus is of major economic importance wo
4 enzyme-linked immunosorbent assay with lysed Chlamydophila abortus or Chlamydophila pecorum elementar
5 he obligate intracellular bacterial pathogen Chlamydophila abortus strain S26/3 (formerly the abortio
6 ility of BeWo cells to control the growth of Chlamydophila abortus, in contrast to effects observed i
11 ators upstream of glnPQ in C. pneumoniae and Chlamydophila caviae but not Chlamydia trachomatis, whic
12 nt taxonomic revisions include the return of Chlamydophila caviae to the Chlamydia genus, creation of
13 f the male guinea pig with Chlamydia caviae (Chlamydophila caviae) were characterized both during a p
14 holog of Tarp, although Chlamydia muridarum, Chlamydophila caviae, and Chlamydophila pneumoniae Tarp
27 calves correlated positively (P < 0.01) with Chlamydophila infection in quadratic, but not linear, re
30 Chlamydophila immunoglobulin M antibodies in Chlamydophila PCR-positive calves and dams and in dams t
31 nt assay with lysed Chlamydophila abortus or Chlamydophila pecorum elementary body antigens quantifie
33 he association between the atypical bacteria Chlamydophila pneumoniae and Mycoplasma pneumoniae and a
36 rescence serologic test for the detection of Chlamydophila pneumoniae infection during an outbreak.
38 Since IDO activity is linked to persistent Chlamydophila pneumoniae infection, our results suggest
39 n important role in high-fat diet as well as Chlamydophila pneumoniae infection-mediated acceleration
41 be obese and more likely to be infected with Chlamydophila pneumoniae or Staphylococcus aureus, have
42 be obese and more likely to be infected with Chlamydophila pneumoniae or Staphylococcus aureus, have
43 te and acquired immune responses elicited by Chlamydophila pneumoniae phospholipase D (CpPLD) in the
44 lamydia muridarum, Chlamydophila caviae, and Chlamydophila pneumoniae Tarp lack the large repeat regi
45 ity of culture for Mycoplasma pneumoniae and Chlamydophila pneumoniae to diagnose respiratory tract i
46 Pn1032 homolog from the respiratory pathogen Chlamydophila pneumoniae was heterologously expressed an
47 ncytial virus A and B, Bordetella pertussis, Chlamydophila pneumoniae, and Mycoplasma pneumoniae This
48 ome reports suggest that bacteria, including Chlamydophila pneumoniae, could be involved in the etiol
49 rus A (RSV A), RSV B, Mycoplasma pneumoniae, Chlamydophila pneumoniae, Legionella pneumophila, Legion
51 is study was to use putative TTS proteins of Chlamydophila pneumoniae, whose equivalents in other bac
54 e obligate intracellular pathogen Chlamydia (Chlamydophila) pneumoniae is known to be associated with
55 sma pneumoniae, 5 CFU/ml; and for Chlamydia (Chlamydophila) pneumoniae, 0.01 50% tissue culture infec
60 s from Chlamydia trachomatis, serovar E, and Chlamydophila psittaci, Texas turkey, were also cloned i
61 examined IGHV gene usage and mutations in 67 Chlamydophila psittaci-negative ocular adnexal EMZL.
62 effective initial treatment of patients with Chlamydophila psittaci-positive lymphoma before consider