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1 rved from RNAs with a cap and both 5' and 3' TYMV sequences.
2 vivo and directly interacted in vitro with a TYMV RNA translational enhancer, raising the possibility
3  a prototype of polyvalent bionanoparticles, TYMV can be used as scaffold for sensor development with
4 ually the same transformations were shown by TYMV and BMV RNA, and with heating, the RNA from STMV.
5 resent the crystal structure of the complete TYMV TLS to 2.0 A resolution.
6 MV), and that both proteins are required for TYMV-derived small RNA production.
7 sts to show that the 5' 217 nucleotides from TYMV genomic RNA enhance expression relative to a vector
8 n and excitation spectra of the dual-labeled TYMV particle displayed residual virus fluorescence and
9 ssays, in the case of TYMV, the 6318 nt long TYMV RNA was an even better substrate for valylation.
10                        Turnip yellow mosaic (TYMV) and kennedya yellow mosaic virus RNAs had activiti
11 igh activity in these assays, in the case of TYMV, the 6318 nt long TYMV RNA was an even better subst
12 erfered with when anchored to the surface of TYMV.
13 /3'-UTR synergy (i.e., removal of the cap or TYMV 3'-UTR) resulted in a higher proportion of initiati
14                                    Two other TYMV RNA variants of suboptimal infectivities, one that
15 first 43 or 41 codons of the two overlapping TYMV open reading frames (ORFs), ORF-69 and ORF-206, res
16                                          The TYMV TLS.UPD might demonstrate how RNA structural plasti
17                     Directly upstream of the TYMV TLS is an upstream pseudoknot domain (UPD) that has
18                It has been proposed that the TYMV TLS acts as a molecular switch between translation
19 iR-HC-Pro(159) are specifically resistant to TYMV and TuMV, respectively.
20          Our results show that the wild-type TYMV replication proteins are able to amplify genomes wi
21 g the 3' untranslated regions into wild-type TYMV RNA that the high infectivities and replication rat
22 pressors, P69 of turnip yellow mosaic virus (TYMV) and HC-Pro of turnip mosaic virus (TuMV).
23                  Turnip yellow mosaic virus (TYMV) contains a tRNA-like structure (TLS) in its 3' unt
24 ighly infectious turnip yellow mosaic virus (TYMV) genomes with sequence changes in their 3'-terminal
25                  Turnip yellow mosaic virus (TYMV) is an icosahedral plant virus with an average diam
26 at the 3'-UTR of Turnip yellow mosaic virus (TYMV) RNA enhances translation synergistically with a 5'
27 iral response to Turnip yellow mosaic virus (TYMV), and that both proteins are required for TYMV-deri
28 ses (poliovirus, turnip yellow mosaic virus (TYMV), brome mosaic virus (BMV), and satellite tobacco m
29 he 3' end of the turnip yellow mosaic virus (TYMV).

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