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1 e immune system, the macrophage, can destroy Plasmodia.
2 glutaminase for walling off damaged areas of plasmodia.
3 e mammalian host may be a common property of plasmodia.
4                 These findings indicate that Plasmodia actively interfere with the development of imm
5 parum may have undergone host switching as a Plasmodia adaptation specific for our species.
6  orthologs are present in the genomes of all plasmodia and are mapped between the subtilisin-encoding
7 notated in PlasmoDB, were conserved in other Plasmodia and had no detectable homologs in other specie
8 in the Amoebozoa well known for their motile plasmodia and morphologically complex fruiting bodies.
9 nd CpG-containing DNA derived from bacteria, plasmodia, and mitochondria.
10                                    Damage of plasmodia by brief treatment with 15% ethanol activates
11 ng compounds that acts via the inhibition of Plasmodia CDPK4 enzyme.
12 hibited by the quinoline antimalarial drugs, Plasmodia detoxify heme released during the degradation
13 ntly, 15 of these histone PTMs are novel for Plasmodia (e.g. H3K122ac, H3K27me3, H3K56me3).
14                 These genes are conserved in plasmodia, exhibit expression switching, and encode an i
15      9c was not able to reduce the number of Plasmodia in erythrocytes of mice.
16 hannel induced on erythrocytes infected with plasmodia, including parasites responsible for human mal
17                           Gene expression in Plasmodia integrates post-transcriptional regulation wit
18 ility to acquire protective immunity against Plasmodia is the chief obstacle to malaria control, and
19                   It has been suggested that Plasmodia manipulate their vertebrate hosts to enhance p
20  (39 kDa), in nuclei and nuclear matrix from plasmodia of Physarum polycephalum.
21 fy the migration behavior of P. polycephalum plasmodia on the time scale of days in the absence and p
22                             The emergence of Plasmodia resistant to chemoprophylactic treatment highl
23 er, we show that the FREP1 can directly bind Plasmodia sexual stage gametocytes and ookinetes.
24                                              Plasmodia species cannot synthesize purines de novo, whe
25                                              Plasmodia species, unlike humans, can utilize p-aminoben
26 erine is conjugated principally to LAV1-2, a plasmodia-specific 40-kDa protein with four EF-hand sequ
27 dy demonstrating correlation in a controlled Plasmodia sporozoite challenge study between protection
28             At present, radiation-attenuated plasmodia sporozoites ( gamma -spz) is the only vaccine
29                     As demonstrated in other Plasmodia, such genetic diversity studies can provide in
30                                              Plasmodia, the malaria-causing parasites, have two oblig
31 during starvation-induced differentiation of plasmodia to form spherules, but a 50% reduction in the