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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 f the male guinea pig with Chlamydia caviae (Chlamydophila caviae) were characterized both during a p
13 holog of Tarp, although Chlamydia muridarum, Chlamydophila caviae, and Chlamydophila pneumoniae Tarp
25 calves correlated positively (P < 0.01) with Chlamydophila infection in quadratic, but not linear, re
28 Chlamydophila immunoglobulin M antibodies in Chlamydophila PCR-positive calves and dams and in dams t
29 nt assay with lysed Chlamydophila abortus or Chlamydophila pecorum elementary body antigens quantifie
31 he association between the atypical bacteria Chlamydophila pneumoniae and Mycoplasma pneumoniae and a
34 rescence serologic test for the detection of Chlamydophila pneumoniae infection during an outbreak.
36 Since IDO activity is linked to persistent Chlamydophila pneumoniae infection, our results suggest
37 n important role in high-fat diet as well as Chlamydophila pneumoniae infection-mediated acceleration
39 te and acquired immune responses elicited by Chlamydophila pneumoniae phospholipase D (CpPLD) in the
40 lamydia muridarum, Chlamydophila caviae, and Chlamydophila pneumoniae Tarp lack the large repeat regi
41 ity of culture for Mycoplasma pneumoniae and Chlamydophila pneumoniae to diagnose respiratory tract i
42 Pn1032 homolog from the respiratory pathogen Chlamydophila pneumoniae was heterologously expressed an
43 ome reports suggest that bacteria, including Chlamydophila pneumoniae, could be involved in the etiol
44 rus A (RSV A), RSV B, Mycoplasma pneumoniae, Chlamydophila pneumoniae, Legionella pneumophila, Legion
46 is study was to use putative TTS proteins of Chlamydophila pneumoniae, whose equivalents in other bac
49 e obligate intracellular pathogen Chlamydia (Chlamydophila) pneumoniae is known to be associated with
50 sma pneumoniae, 5 CFU/ml; and for Chlamydia (Chlamydophila) pneumoniae, 0.01 50% tissue culture infec
55 s from Chlamydia trachomatis, serovar E, and Chlamydophila psittaci, Texas turkey, were also cloned i
56 examined IGHV gene usage and mutations in 67 Chlamydophila psittaci-negative ocular adnexal EMZL.
57 effective initial treatment of patients with Chlamydophila psittaci-positive lymphoma before consider
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