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1 yte functions by the proteolytic activity of viral proteinase 2A in cases of unexplained dilated card
2 ion and production of proteolytically active viral proteinase 2A in human cardiomyocytes.
3       Mutations that inhibit the activity of viral proteinase 2A were dominant, arguing that inhibiti
4  sensitivity is dramatically enhanced by the viral proteinase 2A, due, most likely, to inhibition of
5 ovirus cardiac pathogenesis is linked to the viral proteinase 2A, we investigated the effect of diffe
6 rsor protein (P1-2A) and wild-type or mutant viral proteinase 3C (plasmids P12X3C or P12X3C-mut, resp
7 that this cleavage event was mediated by the viral proteinases 3C/3CD.
8 rhinovirus infection, AUF1 is cleaved by the viral proteinase 3CD and that AUF1 can interact with the
9                   It has been shown that the viral proteinase 3CD cleaves PCBP2 and contributes to vi
10 hen PCBP2 is cleaved in its linker region by viral proteinase 3CD, translation initiation ceases allo
11  through proteolytic cleavage of AUF1 by the viral proteinase 3CD.
12                                          The viral proteinase 3Cpro was not found to interact with ot
13 omain and to demonstrate that three distinct viral proteinase activities process the MHV replicase po
14 ody disruption correlated with production of viral proteinases and required substantial viral gene pr
15 ction, these deleted viral RNA forms express viral proteinases at levels capable of causing viral pat
16         Late in an adenovirus infection, the viral proteinase (AVP) becomes activated to process viri
17                           One such target of viral proteinase cleavage is AU-rich binding factor 1 (A
18 yproteins are cotranslationally processed by viral proteinases into at least 15 mature proteins, incl
19 to a polyprotein that is cleaved by host and viral proteinases into functional, structural and non-st
20 co- and post-translationally by cellular and viral proteinases into three structural and at least six
21 of polyprotein processing are performed by a viral proteinase located in the N-terminal one-third of
22 argeting the nucleating factor G3BP1 via the viral proteinase NS6(Pro) This work provides new insight
23 t signal peptidase and a novel two-component viral proteinase of the serine proteinase family, NS2B/N
24  In contrast to inhibitors that act upon the viral proteinase, PA-457 appears to block only the final
25     The gene 1 polyproteins are processed by viral proteinases to yield at least 15 mature products,
26  work is the first instance of engineering a viral proteinase with switched cleavage preferences and