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1 tively released/secreted by parasites during axenic culture.
2 ginine that were confirmed experimentally in axenic culture.
3 to culture the pathogens in defined media or axenic cultures.
4 d the replication of Leishmania parasites in axenic cultures.
5 orly characterized due to few representative axenic cultures.
6  hosts, and four previously unrepresented by axenic cultures.
7 V) and phase II (PIIV) vaccines derived from axenic culture 7, 14, and 28 days postvaccination.
8                                           In axenic culture, all strains grew similarly.
9 lts in impaired proliferation of L. major in axenic culture and bone marrow-derived macrophages.
10  nonessential alternate sigma factor both in axenic culture and for survival in macrophages in vitro.
11 L. amazonensis lacking LIT1 grew normally in axenic culture and had no defects differentiating into i
12 sed the genome to profile gene expression in axenic culture and in lichen thalli.
13 on-target whole-cell activity against Mtb in axenic culture and in macrophages with efficacy comparab
14 ated with enhanced antibacterial activity in axenic culture and in primary mouse macrophages.
15  replication reduce B. abortus metabolism in axenic culture and perturb features of mammalian cellula
16         IL-26 directly bound to M. leprae in axenic culture and reduced bacteria viability.
17 and A. hatchetti (CDC: V573) were adapted to axenic culture and used to produce cysts either with Nef
18 d and measured these structures in xenic and axenic cultures and in natural samples.
19 iosynthesis were higher in coculture than in axenic culture, and this was reflected in increased amou
20 ever, the classical microbiology approach of axenic culture cannot provide a complete picture of the
21  serum components in order to multiply under axenic culture conditions.
22  complex microbial populations without prior axenic culture, coupled with high-throughput DNA sequenc
23 r, we can grow and isolate microorganisms in axenic culture in one step.
24 lected MTB mRNAs were quantified in vitro in axenic culture, in vivo in the lungs of mice, and in lun
25 AB grew comparably to the parental strain in axenic culture, in vivo it exhibited deficiency in react
26 Mtb efficiently imports w6 PUFAs via Mce1 in axenic culture, including AA.
27                                   Continuous axenic culture of Pneumocystis carinii has been achieved
28 ge to perturbations with DOM derived from an axenic culture of Prochlorococcus, or high-molecular wei
29 actions and polyamine biosynthesis, enhances axenic culture of the AIDS-associated opportunistic fung
30                 Growth and dechlorination by axenic cultures of Dehalococcoides mccartyi strain 195 w
31  Targeted peptide selection was conducted in axenic cultures of Dhc strains 195, FL2, and BAV1.
32                                           In axenic cultures of Fusarium graminearum, in vitro feedin
33 culi, and E. intestinalis were propagated in axenic cultures of monkey kidney E6 cells, purified with
34  the presence of culture filtrate (CF), from axenic cultures of Mycobacterium tuberculosis (Mtb), to
35                                           In axenic cultures of Prochlorococcus, it was observed that
36 in reasonable and reproducible amounts using axenic cultures of the endophyte.
37 with depleted gut microbiota, either through axenic culture or antibiotic treatment, exhibited signif
38  predominantly been performed using the same axenic cultured strain HM-1: IMSS isolated about 50 year
39 ty column of Plasmodium gallinaceum ookinete axenic culture supernatant demonstrated the presence of
40                                The described axenic culture system will greatly enhance biochemical a
41                                 A cell-free (axenic) culture system was developed, which showed high
42 compounds inhibited B. abortus metabolism in axenic culture, thirteen of which are non-cytotoxic to h
43 c conditions, in experiments with defined or axenic cultures, when high concentrations of PFAS were u