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1 is impaired due to infection and subsequent cytopathogenicity.
2 infected cells despite the absence of overt cytopathogenicity.
3 onsidered to account for some of its in vivo cytopathogenicity.
4 ons in nsP2 can also attenuate Sindbis virus cytopathogenicity.
5 plicated in viral assembly, infectivity, and cytopathogenicity.
6 heral blood monocytes, which correlates with cytopathogenicity.
7 s defect in turn corresponded to a defect in cytopathogenicity.
8 apoptosis by L. pneumophila correlates with cytopathogenicity.
9 tween the level of viral RNA replication and cytopathogenicity.
10 BVDV NADL RNA replication and virus-induced cytopathogenicity.
11 mine the potential for this region to affect cytopathogenicity.
12 n Bax, a critical factor for influenza virus cytopathogenicity.
13 trols viral host range, DAF utilization, and cytopathogenicity.
14 uced maturation protects DCs from YF-induced cytopathogenicity.
15 tants that exhibited defective phenotypes of cytopathogenicity and intracellular replication within m
16 lowed the virus to achieve a balance between cytopathogenicity and replication and restored productiv
17 ffect virus replication in vitro but reduces cytopathogenicity and results in attenuation in vivo.
18 flects the complex interplay of direct viral cytopathogenicity and the indirect effects of persistent
19 substitutions for Y2441 also affected viral cytopathogenicity and viability, with Y2441V being cp, Y
20 d using J774A.1 macrophages for reduction in cytopathogenicity based on retention of the cell monolay
22 L. pneumophila-induced nuclear apoptosis and cytopathogenicity during early stages of the infection.
23 us replication or specificity of CV787-based cytopathogenicity for prostate cancer cells (approximate
27 2 mutants with various degrees of defects in cytopathogenicity, intracellular survival, and replicati
29 ve previously shown that the replication and cytopathogenicity of an E1B, 55-kDa gene-attenuated aden
33 of defects in intracellular survival in and cytopathogenicity to macrophages and alveolar epithelial
35 epithelial cells plays an important role in cytopathogenicity to the host cell during early stages o
37 the wild-type strain and the gspA mutant in cytopathogenicity to U937 cells or in their kinetics of
38 sts the presence of a determinant of in vivo cytopathogenicity within HIV-1 Vpr and further indicates
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