戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 knot (Psi(2)) previously identified in a TCV satellite RNA.
2 ity of a virus to replicate a rolling circle satellite RNA.
3 aphid vectors; and (d) replication of a BYDV satellite RNA.
4 ibution among the recombining TCV-associated satellite RNAs.
5 tests is cucumber mosaic virus (CMV) and its satellite RNAs.
6                However, in this system, some satellite RNAs also intensify viral disease in particula
7 d, but we lack direct evidence that specific satellite RNAs are required for normal organismal functi
8                                              Satellite RNAs are the smallest infectious agents whose
9  risk associated with the use of attenuating satellite RNAs as a form of biocontrol of CMV.
10                                      satC, a satellite RNA associated with Turnip crinkle virus (TCV)
11                                 Unlike other satellite RNAs, both the plus and minus strands proved t
12                           Two subviral RNAs, satellite RNA C (satC) and defective interfering RNA G (
13 nds of Turnip Crinkle Virus (TCV)-associated satellite RNA C (satC), is a replication enhancer and re
14                                              Satellite RNAs can have a dramatic effect on the helper
15 in catalytic motif in tobacco ringspot virus satellite RNA consists of two helix-loop-helix elements
16      Plus strands of several of the most fit satellite RNAs contained insertions of CA-rich sequence
17                                     As such, satellite RNAs could be used as biocontrol agents to red
18 that RNA-binding protein LSM1-mediated major satellite RNA decay plays a central role in the preferen
19                                Here, we show satellite RNAs derived from AAGAG tandem repeats are tra
20 ependent manner, and these DSB-induced alpha-satellite RNAs form into strong speckles in the nucleus.
21 ral families of repetitive sequences, in the satellite RNA from the carrot red leaf luteovirus, in pl
22 wi slicer-deficient mutants, major and minor satellite RNAs from centromeric and pericentromeric sate
23 ammerhead ribozymes previously were found in satellite RNAs from plant viroids and in repetitive DNA
24                                        Plant satellite RNAs generally reduce the level of helper viru
25 ow that MIWI, guided by piRNA, cleaves major satellite RNAs, generating RNA fragments that may form s
26 y plants, or by the transgenic expression of satellite RNA in transformed plants.
27 tion of ATM, and demonstrates a role for the satellite RNA in tumor cell proliferation and movement.
28                                   Support of satellite RNA in whole plants and in protoplasts of zucc
29 t able to support the replication of the WL1 satellite RNA in zucchini squash and that this phenotype
30               Furthermore, Dicer cleaves all satellite RNAs in conjunction with MIWI.
31 less abundant form of tobacco ringspot virus satellite RNA is readily reversible.
32 emonstrate that the inability to support WL1 satellite RNA maps to a single amino acid at residue 978
33        The 110 nt hammerhead ribozyme in the satellite RNA of cereal yellow dwarf virus-RPV (satRPV R
34 erived from a single-stranded 336-nucleotide satellite RNA of CMV were not amplified by either antivi
35                                We passaged a satellite RNA of CMV with its helper virus to determine
36 is delta virus (HDV) is a human pathogen and satellite RNA of the hepatitis B virus.
37                  The hairpin ribozyme in the satellite RNA of Tobacco Ringspot Virus assembles in the
38 ts investigating Cowpea mosaic virus and the satellite RNA of Tobacco ringspot virus.
39 ich MIWI- and Dicer-mediated cleavage of the satellite RNAs prevents the over-expression of satellite
40 cipates in processing intermediates of viral satellite RNA replication in plants.
41  reduction of both strands of major or minor satellite RNAs results in lower frequencies of chromosom
42 on, we discovered numerous putative viroids, satellite RNAs, retrozymes, and ribozy-like viruses.
43 id-like agents with cccRNAs genomes, such as satellite RNAs, ribozyviruses and retrozymes, have been
44 s, retroviroid-like elements, small circular satellite RNAs, ribozyviruses, and retrozymes.
45                                              Satellite RNAs (sat-RNAs) are parasites of viruses that
46                                         Many satellite RNAs (sat-RNAs) can attenuate or intensify the
47  including the genomic RNA (4,054 bases) and satellite RNAs (sat-RNAs) such as sat-RNA D (194 bases),
48 RNA conformational switch in an untranslated satellite RNA (satC) of Turnip crinkle virus (TCV) regul
49 as determined in planta by using a parasitic satellite RNA (satRNA) as a reporter.
50 onomously in the absence of HV, a variant of satellite RNA (satRNA) associated with Cucumber mosaic v
51                                            D satellite RNA (satRNA) is a strain of cucumber mosaic vi
52                           Replication of the satellite RNA (satRNA) of Cucumber Mosaic Virus is depen
53                The subviral agents include a satellite RNA (satRNA) that is devoid of a coding region
54                                            D satellite RNA (satRNA) with its helper virus, namely, cu
55                                              Satellite RNAs (satRNAs), parasites of viruses, depend o
56  serotype RPV (CYDV-RPV), the 322-nucleotide satellite RNA (satRPV RNA) accumulates to high levels in
57 NA virus that can support the replication of satellite RNAs, small molecular parasites of the virus.
58                           We find that alpha-satellite RNA-smFISH foci levels vary across cell lines
59  spindle pole formation, Slug expression and satellite RNA suppression.
60                               One such virus/satellite RNA system already under use in field tests is
61 with its helper virus to determine whether a satellite RNA that attenuates CMV-induced disease on tob
62 tellite RNAs prevents the over-expression of satellite RNAs, thus ensuring proper kinetochore assembl
63 random bases and then subjecting the pool of satellite RNA to functional selection in plants.
64 -situ hybridization (smFISH) to detect alpha-satellite RNA transcripts in intact human cells.
65  and in cells, SUV39H1 associates with alpha-satellite RNA transcripts.
66                                              Satellite RNAs usually lack substantial homology with th
67                                              Satellite RNAs usurp the replication machinery of their
68 re required in the replicative cycles of the satellite RNA viruses from which the hammerhead ribozyme
69 of features with a subset of the small plant satellite RNA viruses, including self-cleaving sequences
70 hammerheads derived from natural viroids and satellite RNAs were constructed with the goal of assessi
71                                        Viral satellite RNAs were my first interest, but I then explor
72 me is a small catalytic motif found in plant satellite RNAs where it catalyzes a reversible self-clea
73 egative strand of the tobacco ringspot virus satellite RNA, where hairpin ribozyme-mediated self-clea
74  defective interfering (DI) RNAs or chimeric satellite RNAs, which are thought to be generated by tem