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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
6                    The mutation frequency of Turnip crinkle virus can increase 12-fold without induci
7                                              Turnip crinkle virus contains a T-shaped, ribosome-bindi
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
14         Comparison of the symptoms caused by turnip crinkle virus strain M (TCV-M) and TCV-B infectio
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
18                                              Turnip crinkle virus (TCV) contains a structured 3' regi
19 ancer in the 3' untranslated region (UTR) of Turnip crinkle virus (TCV) contains an internal T-shaped
20                In Arabidopsis, resistance to Turnip Crinkle Virus (TCV) depends on the resistance (R)
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
23                                Resistance to Turnip Crinkle Virus (TCV) in Arabidopsis ecotype Dijon
24 rees C) that permits rigorous replication of Turnip crinkle virus (TCV) in Arabidopsis, plants contai
25                                              Turnip crinkle virus (TCV) inoculation onto TCV-resistan
26                               Inoculation of turnip crinkle virus (TCV) into a (TCV)-resistant line o
27                   The capsid protein (CP) of Turnip crinkle virus (TCV) is a multifunctional protein
28                                              Turnip crinkle virus (TCV) is a small, plus-sense, singl
29                   The 356-nucleotide satC of Turnip crinkle virus (TCV) is unusual in that its 3'-hal
30                               Inoculation of turnip crinkle virus (TCV) on the resistant Arabidopsis
31                               Inoculation of turnip crinkle virus (TCV) on the resistant Arabidopsis
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
38        satC, a satellite RNA associated with Turnip crinkle virus (TCV), enhances the ability of the
39          The 3' ends of RNAs associated with turnip crinkle virus (TCV), including subviral satellite
40                     All RNAs associated with turnip crinkle virus (TCV), including the genomic RNA (4
41 uctures of both native and expanded forms of turnip crinkle virus (TCV), using cryo-electron microsco
42                   Sat-RNA C, associated with turnip crinkle virus (TCV), was previously found to inte
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
45                                            A Turnip crinkle virus (TCV)-based system was devised to d
46 rgeted by some VSRs, such as that encoded by Turnip crinkle virus (TCV).
47 (TSS) similar to the ribosome-binding TSS of Turnip crinkle virus (TCV).
48 the R protein HRT, and thereby resistance to Turnip Crinkle virus (TCV).
49 diG) intensify the symptoms of their helper, turnip crinkle virus (TCV).
50 lation of subviral sat-RNA C associated with turnip crinkle virus (TCV).
51 iably examine the viral RNA encapsidation of turnip crinkle virus (TCV).
52  is produced by the replication machinery of turnip crinkle virus (TCV).
53  similar to the TSS 3'CITE of the carmovirus Turnip crinkle virus (TCV).
54 were screened for antiviral activity towards Turnip crinkle virus (TCV, Tombusviridae).
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