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1                Expression of antiviral MxA a karyophilic 75 kd protein induced by IFN in mouse cells
2 The site-specific substitutions that reduced karyophilic activity had no effect on the processing or
3                                          Two karyophilic Agrobacterium virulence (Vir) proteins, VirD
4       This characteristic is due to multiple karyophilic components of the lentiviral vector pre-inte
5 nonical nuclear localization signal, and the karyophilic determinant was mapped to the highly conserv
6                  Wild-type FIV integrase was karyophilic in all cell lines tested and capable of targ
7 cells by allowing for the recruitment of the karyophilic MA into the viral core and preintegration co
8 s are naturally expressed, it is likely that karyophilic MBPs subserve a regulatory function in imple
9                                          The karyophilic properties of the HIV-1 nucleoprotein comple
10                                          The karyophilic properties of two viral proteins, matrix (MA
11              We therefore postulate that the karyophilic property of FIV integrase requires subunit m
12                             To determine its karyophilic property, FIV integrase fused with glutathio
13 clear localization sequence (NLS) within the karyophilic protein by a cytoplasmic receptor such as th
14 roteins--to the host cell nucleus and that a karyophilic protein carrier that can deliver synthetic D
15 e or cotransport to the nucleus with another karyophilic protein.
16 oid receptors, like that of nearly all other karyophilic proteins examined to date, requires ATP, the
17  antibodies did not inhibit import of either karyophilic proteins or snRNPs.
18 assical pathway for the nuclear transport of karyophilic proteins.
19  We assessed whether Mod5p sequences cause a karyophilic reporter to be located in the cytosol.
20                                         This karyophilic sequence includes a high proportion of proli
21                                The potential karyophilic signals within EBNA-LP CR1c and CR2 were als
22  T42A mutation does not block the docking of karyophilic substrates at the nuclear pore.

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