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1 tively released/secreted by parasites during axenic culture.
2 orly characterized due to few representative axenic cultures.
3 d the replication of Leishmania parasites in axenic cultures.
4 hosts, and four previously unrepresented by axenic cultures.
6 nonessential alternate sigma factor both in axenic culture and for survival in macrophages in vitro.
7 L. amazonensis lacking LIT1 grew normally in axenic culture and had no defects differentiating into i
8 replication reduce B. abortus metabolism in axenic culture and perturb features of mammalian cellula
9 and A. hatchetti (CDC: V573) were adapted to axenic culture and used to produce cysts either with Nef
10 iosynthesis were higher in coculture than in axenic culture, and this was reflected in increased amou
12 complex microbial populations without prior axenic culture, coupled with high-throughput DNA sequenc
14 lected MTB mRNAs were quantified in vitro in axenic culture, in vivo in the lungs of mice, and in lun
15 AB grew comparably to the parental strain in axenic culture, in vivo it exhibited deficiency in react
17 ge to perturbations with DOM derived from an axenic culture of Prochlorococcus, or high-molecular wei
18 actions and polyamine biosynthesis, enhances axenic culture of the AIDS-associated opportunistic fung
21 culi, and E. intestinalis were propagated in axenic cultures of monkey kidney E6 cells, purified with
23 predominantly been performed using the same axenic cultured strain HM-1: IMSS isolated about 50 year
24 ty column of Plasmodium gallinaceum ookinete axenic culture supernatant demonstrated the presence of
27 compounds inhibited B. abortus metabolism in axenic culture, thirteen of which are non-cytotoxic to h
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