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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.
7 sts to show that the 5' 217 nucleotides from TYMV genomic RNA enhance expression relative to a vector
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.
12 igh activity in these assays, in the case of TYMV, the 6318 nt long TYMV RNA was an even better subst
15 /3'-UTR synergy (i.e., removal of the cap or TYMV 3'-UTR) resulted in a higher proportion of initiati
17 first 43 or 41 codons of the two overlapping TYMV open reading frames (ORFs), ORF-69 and ORF-206, res
23 g the 3' untranslated regions into wild-type TYMV RNA that the high infectivities and replication rat
25 h a PRO/DUB from Turnip yellow mosaic virus (TYMV) and of its complex with one of its PRO substrates.
27 ighly infectious turnip yellow mosaic virus (TYMV) genomes with sequence changes in their 3'-terminal
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