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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       Introducing a single-point mutation in TYMV PRO/DUB aimed at improving ubiquitin-binding led to
9 n and excitation spectra of the dual-labeled TYMV particle displayed residual virus fluorescence and
10 ssays, in the case of TYMV, the 6318 nt long TYMV RNA was an even better substrate for valylation.
11                        Turnip yellow mosaic (TYMV) and kennedya yellow mosaic virus RNAs had activiti
12 igh activity in these assays, in the case of TYMV, the 6318 nt long TYMV RNA was an even better subst
13      Here we report the crystal structure of TYMV PRO/DUB in complex with ubiquitin.
14 erfered with when anchored to the surface of TYMV.
15 /3'-UTR synergy (i.e., removal of the cap or TYMV 3'-UTR) resulted in a higher proportion of initiati
16                                    Two other TYMV RNA variants of suboptimal infectivities, one that
17 first 43 or 41 codons of the two overlapping TYMV open reading frames (ORFs), ORF-69 and ORF-206, res
18                                          The TYMV TLS.UPD might demonstrate how RNA structural plasti
19                     Directly upstream of the TYMV TLS is an upstream pseudoknot domain (UPD) that has
20                It has been proposed that the TYMV TLS acts as a molecular switch between translation
21 iR-HC-Pro(159) are specifically resistant to TYMV and TuMV, respectively.
22          Our results show that the wild-type TYMV replication proteins are able to amplify genomes wi
23 g the 3' untranslated regions into wild-type TYMV RNA that the high infectivities and replication rat
24 pressors, P69 of turnip yellow mosaic virus (TYMV) and HC-Pro of turnip mosaic virus (TuMV).
25 h a PRO/DUB from Turnip yellow mosaic virus (TYMV) and of its complex with one of its PRO substrates.
26                  Turnip yellow mosaic virus (TYMV) contains a tRNA-like structure (TLS) in its 3' unt
27 ighly infectious turnip yellow mosaic virus (TYMV) genomes with sequence changes in their 3'-terminal
28                  Turnip yellow mosaic virus (TYMV) is an icosahedral plant virus with an average diam
29 at the 3'-UTR of Turnip yellow mosaic virus (TYMV) RNA enhances translation synergistically with a 5'
30 iral response to Turnip yellow mosaic virus (TYMV), and that both proteins are required for TYMV-deri
31 ses (poliovirus, turnip yellow mosaic virus (TYMV), brome mosaic virus (BMV), and satellite tobacco m
32 he 3' end of the turnip yellow mosaic virus (TYMV).