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1 scovered in satC, a replicon associated with turnip crinkle virus.
2 as we exemplify with the orthologous p38 of turnip crinkle virus.
3 he replicase proteins of the closely related Turnip crinkle virus and distantly related Hepatitis C v
4 vement-defective viruses, Potato virus X and Turnip crinkle virus, and an agroinfiltration assay, we
5 virus, carnation Italian ringspot virus, and turnip crinkle virus-associated RNA; the insect plus-str
8 ritical 3' UTR hairpin in the genomic RNA of turnip crinkle virus did not directly interact with the
9 In contrast, symptom enhancement by satC of Turnip crinkle virus is due to satC interference with vi
10 ior of a subviral RNA (satC) associated with Turnip crinkle virus is required for fitness and that it
11 jected them to infections with CPB-CC-PDS, a turnip crinkle virus mutant capable of inducing silencin
12 liana mutants compromised for recognition of turnip crinkle virus previously identified CRT1, a membe
13 reated plants were resistant to infection by turnip crinkle virus, Pseudomonas syringae pv 'tomato' D
15 ogenetically conserved RSE of the carmovirus Turnip crinkle virus (TCV) adopts an alternative, smalle
16 pots for recombination in the genomic RNA of turnip crinkle virus (TCV) and satellite (sat)-RNA C, a
17 nucleotides (nt) immediately upstream of the Turnip crinkle virus (TCV) coat protein (CP) open readin
19 ancer in the 3' untranslated region (UTR) of Turnip crinkle virus (TCV) contains an internal T-shaped
21 rresponds to the last 283 nucleotides of the turnip crinkle virus (TCV) genome and hence is designate
22 The 3(') untranslated region (3(') UTR) of turnip crinkle virus (TCV) genomic RNA contains a cap-in
24 rees C) that permits rigorous replication of Turnip crinkle virus (TCV) in Arabidopsis, plants contai
32 h in an untranslated satellite RNA (satC) of Turnip crinkle virus (TCV) regulates initiation of minus
33 We report here that the coat protein (CP) of Turnip crinkle virus (TCV) strongly suppresses PTGS.
34 y and tertiary elements within the 3' end of Turnip crinkle virus (TCV) that are required for viral a
35 specifically with the capsid protein (CP) of turnip crinkle virus (TCV) through yeast two-hybrid scre
36 60S subunits, and 80S ribosomes, whereas the Turnip crinkle virus (TCV) TSS binds only to 60S subunit
37 ority of the 3' untranslated region (UTR) of Turnip crinkle virus (TCV) was previously identified as
41 uctures of both native and expanded forms of turnip crinkle virus (TCV), using cryo-electron microsco
43 viously showed that a sat-RNA (sat-RNA C) of turnip crinkle virus (TCV), which normally intensifies s
44 if1-hairpin (M1H), located on (-)-strands of Turnip Crinkle Virus (TCV)-associated satellite RNA C (s
55 n of the hp to the 3' untranslated region of Turnip crinkle virus (TCV-hp) and co-transfection of the
56 e or defective interfering RNAs (DI-RNAs) of Turnip crinkle virus, Tomato bushy stunt virus, Cucumber
57 d colleagues discovered that P38, the VSR of Turnip crinkle virus, uses its glycine/tryptophane (GW)
58 haliana CRT1 (compromised for recognition of Turnip Crinkle Virus) was previously shown to be require