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1 thway toward the synthesis of menaquinone in Chlamydiaceae.
2 salicylaldehydes, can inhibit the growth of Chlamydiaceae.
3 overall gene content in comparison to other Chlamydiaceae.
4 l bacteria in the order Chlamydiales, family Chlamydiaceae.
6 nted, C.caviae provides a good model for the Chlamydiaceae and a point of comparison against the huma
7 hanism that is central to the biology of the Chlamydiaceae and many other pathogens whose virulence d
8 or circular peptidoglycan-like structures in Chlamydiaceae and penicillin inhibits cytokinesis, a phe
9 hesize tryptophan is not universal among the Chlamydiaceae, but species that have a predicted tryptop
10 a hypothetical protein unique to the family Chlamydiaceae, CT795, elicit strong immune responses in
14 sis that PG is synthesized by members of the Chlamydiaceae family and suggest that D-amino acids, spe
15 ies with a complete genome sequence from the Chlamydiaceae family of obligate intracellular bacterial
16 ned to 1.95 A resolution in complex with the Chlamydiaceae family-specific trisaccharide antigen Kdo(
17 his crucial addition to the set of completed Chlamydiaceae genome sequences is enabling dissection of
20 ndicate that only some members of the family Chlamydiaceae have an arginine-responsive mechanism of g
21 ood from 44 patients were assessed for seven Chlamydiaceae infections by three polymerase chain react
22 with LcrE produced from the three species of Chlamydiaceae; LcrH-2 from C. psittaci reacted with LcrE
23 ch shows that intracellular bacteria such as Chlamydiaceae may also undergo recombination but whether
25 an (PG)-synthesis proteins suggests that the Chlamydiaceae possess the ability to synthesize PG yet b
26 significantly from previously characterized Chlamydiaceae-specific mAbs despite being raised against
28 centration of > or =20 microM; inhibited all Chlamydiaceae tested; and could inhibit the development
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