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1 cipitated with A32, and (v) localized to the viral factory.
2 oNS and that viral RNA is synthesized within viral factories.
3 cerned transiting away from and back towards viral factories.
4 cytoplasmic inclusion bodies, which we call viral factories.
5 cytoplasmic, nonmembranous structures called viral factories.
6 zed with the viral E3 protein in cytoplasmic viral factories.
7 , type 1 Lang (T1L), which forms filamentous viral factories, altered the distributions of both prote
8 AM-signaling intermediate Syk to cytoplasmic viral factories and this recruitment requires the mu2 IT
9 d localizes to ER-associated inclusions, the viral factories, and along microtubules before it is fin
12 In addition, MVs were shown to move from viral factories at speeds consistent with microtubular t
13 ins A13, A14, D8, and H3 did not localize to viral factories but instead accumulated in the secretory
14 synthesis to assemble morphologically normal viral factories containing functional replicase complexe
15 Although sigma NS colocalized with mu NS in viral factories during infection, it was distributed dif
17 mut2 was normal at viral gene expression and viral factory formation, but it was defective for proteo
18 forms inclusions that resemble the globular viral factories formed in cells infected with reovirus s
19 dsRNA and E3 colocalized within cytoplasmic viral factories in cells infected with a decapping enzym
20 and cellular components are recruited to the viral factories in infected cells and provide further ev
23 ruses contain phase-dense inclusions, called viral factories, in which viral replication and assembly
24 zes with VFs in infected cells and also with viral factory-like structures (VFLs) formed by ectopical
25 the RRM and RGG domains of G3BP1 for maximal viral-factory-like structure (VFL) localization and sigm
27 forms of F10 were stable and concentrated in viral factories, only the wild-type protein complemented
29 in infection, accumulated in the cytoplasmic viral factory regions, and associated primarily with amo
30 ike structures very similar in appearance to viral factories, suggesting that it is involved in formi
31 NA-binding protein essential for forming the viral factories that support replication of the double-s
32 specific chaperone function for Hsc70 within viral factories, the sites of reovirus replication and a
33 d, ER-derived structures that may represent "viral factories." The ER-derived structures required an
34 he core surface proteins may be recruited to viral factories through specific associations with mu NS
35 (IMV) utilizes microtubules to move from the viral factory to the site of intracellular envelopment a
36 forms large inclusion-like structures called viral factories (VFs) in which assembling viral particle
37 t cells, mammalian orthoreovirus (MRV) forms viral factories (VFs), which are sites of viral transcri
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