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1                                              CaMV infection altered the expression of the herbicide t
2                                              CaMV replicates by reverse transcription of a 358 RNA th
3                                              CaMV RT forms a monomeric complex with the hybrid, unlik
4 S enhancer or upstream of a truncated (-209) CaMV 35S promoter, respectively.
5 nsuccessful when a constitutive promoter (2x CaMV 35S) was used in the plasmid construction, but seve
6 ronidase gene terminated with either the 35S CaMV 3' untranslated sequence (UTR) or a cis-acting ribo
7 of the tomato HypSys precursor under the 35S CaMV promoter show that the transgenic plants regulate p
8  most PdfL genes were produced using the 35S CaMV promoter to study their possible in planta function
9 transit peptide under the control of the 35S CaMV promoter.
10 dopsis thaliana under the control of the 35S CaMV promoter.
11               The lethal gene used here is a CaMV 35S-barnase gene with an intron in the coding seque
12 linked uidA gene when placed downstream of a CaMV 35S enhancer or upstream of a truncated (-209) CaMV
13 e SSE or middle region upstream of p109 or a CaMV 35S basal promoter (-64 to +6) were fused to gus.
14 irus (CaMV) 35S promoter-TTS2 transgene or a CaMV 35S-promoter-NAG1 (NAG1 = Nicotiana tabacum Agamous
15  genetic complementation experiments using a CaMV 35S::ZmF3'H1 promoter-gene construct established th
16 ever, our analyses showed that an additional CaMV RT molecule needs to transiently associate with a p
17 tion in the 2-hybrid system between MPI7 and CaMV MP mutants correlated with the infectivity of the m
18  chlorosis and stunting in P6-transgenic and CaMV-infected plants are dependent on interactions betwe
19 us particle acquisition by aphid vectors and CaMV transmission.
20                                      Because CaMV virions accumulate preferentially in P6 IBs, we hyp
21 o inhibits the formation of local lesions by CaMV in Nicotiana edwardsonii leaves.
22  used here act differently than the complete CaMV 35S promoter.
23 ion of a BRL1 cDNA, driven by a constitutive CaMV 35S promoter, recapitulates the bri1-5 suppression
24 MAP65-2 were expressed behind a constitutive CaMV 35S promoter, suggesting a level of post-transcript
25 scripts when transcribed from a constitutive CaMV promoter.
26 lgaris under the control of the constitutive CaMV 35S promoter and Nos terminator via Agrobacterium r
27 ted region (UTR), driven by the constitutive CaMV 35S promoter in Medicago sativa (alfalfa) and Nicot
28  RLK genes under control of the constitutive CaMV 35S promoter or a steroid-inducible Ga14 promoter.
29 ase (OxO) gene regulated by the constitutive CaMV 35S promoter was expressed in a hybrid poplar clone
30 esized that P6 IBs have a role in delivering CaMV virions to the plasmodesmata.
31 f cytoplasmic inclusion bodies formed during CaMV infection.
32 tutive promoters, either the doubly enhanced CaMV 35S promoter or the chimaeric 'Super-Promoter'.
33 rly endosomes, for tubule formation, and for CaMV infection.
34 endent of Box I when fused to a heterologous CaMV 35S minimal promoter and introduced to transgenic r
35 erase activity assays showed that individual CaMV RT molecules are able to perform full polymerase fu
36                  We conclude that infectious CaMV replicons can be used to carry a variety of element
37 owever, in plants inoculated with infectious CaMV DNA rather than virus particles, the onset of syste
38 s found immediately adjacent to the inserted CaMV 35S enhancers, at distances ranging from 380 bp to
39 ly recombinogenic' region of the full-length CaMV RNA that has been shown to promote viral recombinat
40                                     A longer CaMV 35S minimal promoter than was used in the original
41 n of phas 3' MAR or coding sequences lowered CaMV 35S enhancer driven GUS expression from the phas ba
42 ere placed upstream from a -46 to +1 minimal CaMV 35S promoter-luciferase reporter gene and reporter
43 ance pollen-specific expression of a minimal CaMV 35S promoter.
44 d C, each sufficient to activate the minimal CaMV 35S promoter in a pollen-specific manner.
45 (CaMV) 35S promoter required the deletion of CaMV 5' leader and polylinker sequences from the constru
46 on, thereby restricting the establishment of CaMV infection.
47 e details into the structure and function of CaMV RT and describe how the enzyme compares to other re
48  a polypurine tract specifying initiation of CaMV plus strand DNA synthesis was inserted into a 35S e
49  may be involved in cell-to-cell movement of CaMV as an intermediate that is transported through plas
50 n intracellular and cell-to-cell movement of CaMV.
51                              The presence of CaMV and polylinker sequences at the 5' end of the PetE
52 razil nut was placed under the regulation of CaMV 35S promoter and nopaline synthase terminator and i
53 inase complexes as important host targets of CaMV for transcriptional activation of viral genes and c
54                          In plants, the same CaMV sequence has been shown to have an essential role i
55   Altogether, these results demonstrate that CaMV MP traffics in the endocytic pathway and that virus
56                          We report here that CaMV 35S promoter driven overexpression of the Arabidops
57                     Our results suggest that CaMV can perceive aphid vectors, either directly or indi
58                                          The CaMV 35S promoter is the most commonly used promoter for
59                                          The CaMV movement protein (MP) was used in a yeast 2-hybrid
60                                          The CaMV replicon carrying the pds gene fragment produced un
61 modesmata-Localized Protein1 (PDLP1) and the CaMV movement protein (MP).
62 icating an interaction in planta between the CaMV MP and MPI7.
63 FP) from Aequoria victoria was driven by the CaMV 35S promoter (line mGFP3).
64  Expression of a reporter gene driven by the CaMV 35S promoter is markedly reduced in the cdkc;2 and
65 ds for the bar gene expression driven by the CaMV 35S promoter or by the rice actin 1 promoter.
66 lemented by KAT2 or KAT5 cDNAs driven by the CaMV 35S promoter, showing that these enzymes are functi
67  with an artificial intron and driven by the CaMV 35S promoter, transient GUS expression was dramatic
68 A in the antisense orientation driven by the CaMV 35S promoter.
69                    In at least one case, the CaMV 35S enhancers led primarily to an enhancement of th
70 A in transgenic tomato plants containing the CaMV 35S promoter driving the expression of the GAST1 tr
71 detected in nodules of plants containing the CaMV 35S promoter-beta-glucuronidase gene construct, sug
72  (-46 bp) promoter fragment derived from the CaMV 35S gene, no induction by MeJA treatment was detect
73  thought to be sites of translation from the CaMV 35S polycistronic RNA intermediate, the precise rol
74                  Expression of MAX2 from the CaMV 35S promoter complements the max2 mutant, does not
75         In contrast, when expressed from the CaMV 35S promoter in transgenic plants carrying a pOp-GU
76  full-length or truncated petH cDNA from the CaMV 35S promoter in wild-type Arabidopsis.
77 y flowering, because overexpression from the CaMV 35S promoter of the co-3 allele, that has a mutatio
78        Expression of a MYC-146 cDNA from the CaMV 35S promoter was unable to complement the anthocyan
79 HEC genes are ectopically expressed from the CaMV 35S promoter, some of the resulting transgenic plan
80             When LhG4 was expressed from the CaMV 35S promoter, the spatial and quantitative expressi
81 l silencing of transgenes expressed from the CaMV 35S promoter.
82 ecipitation and colocalization assays in the CaMV host Nicotiana benthamiana.
83 ate, the precise role of these bodies in the CaMV infection cycle remains unclear.
84 ese areas with other sequences including the CaMV 35S promoter failed to replace activity.
85 have become incorporated end to end into the CaMV genome.
86                            Intriguingly, the CaMV-induced virus factory inclusions seem to protect ag
87 ow fluorescent proteins under control of the CaMV 35S promoter and several endogenous promoters.
88 -expressing UGT84B1 under the control of the CaMV 35S promoter have been constructed and their phenot
89 expressed CmGA20ox1 under the control of the CaMV 35S promoter in Solanum dulcamara to assess the use
90 d the expression of mfs under control of the CaMV 35S promoter in transformed peppermint plants.
91 haliana under transcriptional control of the CaMV 35S promoter of the APS reductase from Pseudomonas
92 s in transgenic tobacco under control of the CaMV 35S promoter supports the view that they can regula
93 omic sequence, including the TATA box of the CaMV 35S promoter, acted as a recombination hotspot.
94 ssed constitutively under the control of the CaMV 35S promoter, both TaLsi1 and OsLsi1 were expressed
95 orghum F5H (SbF5H), under the control of the CaMV 35S promoter, increased both S-lignin levels and th
96  an AAE14 transgene under the control of the CaMV 35S promoter, led to full complementation of the mu
97 rditis IRES element under the control of the CaMV 35S promoter.
98 imerization domains under the control of the CaMV 35S promoter.
99 at interact with the N-terminal third of the CaMV MP.
100 ng part of the gene under the control of the CaMV promoter, both the transgenic alfalfa and Arabidops
101 exceeded those obtained with pOp/LhG4 or the CaMV 35S promoter but without increased uninduced activi
102 sed to the virion sense promoter (Pv) or the CaMV 35S promoter, to suspension culture cells and immat
103 omoter showed much greater activity than the CaMV 35S promoter.
104 tive ectopic expression, suggesting that the CaMV 35S enhancers used here act differently than the co
105  the yeast genome sequence revealed that the CaMV element had sequence similarity with the R region o
106 threonine dehydratase/deaminase (TD), to the CaMV 35S promoter and transformed these constructs into
107 n-helix motif that specifically binds to the CaMV 35S promoter.
108 nt MAX2, lacking the F-box domain, under the CaMV 35S promoter does not complement max2, and dominant
109 stance genes in transgenic tobacco using the CaMV 35S promoter.
110            Leaves of alfalfa plants with the CaMV 35S promoter-GS1 gene showed high levels of accumul
111 ;4/CYCT1;5 results in complete resistance to CaMV as well as altered leaf and flower growth, trichome
112 ;5 double mutants are extremely resistant to CaMV.
113                  We analyzed the response to CaMV infection of a transgenic oilseed rape line contain
114 ies and ethylene in signaling in response to CaMV infection, but suggest that salicylic acid does not
115 tants, also showed reduced susceptibility to CaMV, whereas in NahG transgenics, virus levels were sim
116               Oilseed rape is susceptible to CaMV, but plants recover from infection.
117 a model in which P6 IBs function to transfer CaMV virions directly to MP at the plasmodesmata.
118                                   Transgenic CaMV 35S::RAN1 plants showed constitutive expression of
119 ted in the least recovery of the transgenic (CaMV 35S promoter) and taxon-specific (zein) target DNA
120 nd vegetative development was examined using CaMV 35STag1-GUS constructs.
121 enhancers from the cauliflower mosaic virus (CaMV) 35S gene has been applied to Arabidopsis plants.
122  consisting of the cauliflower mosaic virus (CaMV) 35S promoter driving a cytosolic isoform of GS (GS
123 the control of the cauliflower mosaic virus (CaMV) 35S promoter exhibited delayed root emergence, red
124    Frequently, the cauliflower mosaic virus (CaMV) 35S promoter is used to drive expression of the he
125 cts containing the cauliflower mosaic virus (CaMV) 35S promoter required the deletion of CaMV 5' lead
126 , two utilized the cauliflower mosaic virus (CaMV) 35S promoter with duplicated enhancer, and four ut
127 tron (AGI) and the Cauliflower Mosaic Virus (CaMV) 35S promoter, respectively, in the presence and ab
128 t express either a cauliflower mosaic virus (CaMV) 35S promoter-TTS2 transgene or a CaMV 35S-promoter
129 sed with a minimal cauliflower mosaic virus (CaMV) 35S promoter.
130 xpressed under the cauliflower mosaic virus (CaMV) 35S promoter.
131 rary driven by the cauliflower mosaic virus (CaMV) 35S promoter.
132 ls compared to the cauliflower mosaic virus (CaMV) 35S promoter.
133 (TAV) protein from Cauliflower mosaic virus (CaMV) can function as a suppressor of nonsense-mediated
134 y the constitutive cauliflower mosaic virus (CaMV) double 35S promoter.
135          Gene I of cauliflower mosaic virus (CaMV) encodes a protein that is required for virus movem
136 enic region of the Cauliflower mosaic virus (CaMV) genome for promoter activity in baker's yeast (Sac
137 haliana PBs during Cauliflower mosaic virus (CaMV) infection.
138                    Cauliflower mosaic virus (CaMV) is a double-stranded DNA (dsDNA) pararetrovirus ca
139 VI product (P6) of Cauliflower mosaic virus (CaMV) is a multifunctional protein known to be a major c
140                    Cauliflower mosaic virus (CaMV) is aphid-transmitted, with the virus being taken u
141  The P6 protein of Cauliflower mosaic virus (CaMV) is responsible for the formation of inclusion bodi
142 Here, we show that cauliflower mosaic virus (CaMV) MP contains three tyrosine-based sorting signals t
143 rds development of cauliflower mosaic virus (CaMV) replicons for propagation of functional elements d
144 ystal structure of cauliflower mosaic virus (CaMV) RT in complex with a duplex made of RNA and DNA st
145 uring infection by Cauliflower mosaic virus (CaMV), a compatible pathogen of Arabidopsis (Arabidopsis
146 ble interaction of cauliflower mosaic virus (CaMV), a double-stranded DNA pararetrovirus, with the mo
147 tom determinant of cauliflower mosaic virus (CaMV), and transgene-mediated expression in Arabidopsis
148 g virus (TVCV) and cauliflower mosaic virus (CaMV).
149  in infection with Cauliflower mosaic virus (CaMV).
150 5S transgenes from cauliflower mosaic virus (CaMV).
151 ation and transcriptional silencing, whereas CaMV RNA remains stable but becomes translationally repr
152                                        While CaMV is normally resilient to RNA silencing, dysfunction
153 becoming infected following inoculation with CaMV was 40% that of wild-type, although in plants that
154 n had previously been shown to interact with CaMV MP, we investigated whether P6 I-LBs might also be
155 olumbia and No-0) that were transformed with CaMV 35S-Tag1-GUS DNA.

 
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