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1 to the heterologous nuclear NIa protein from tobacco etch virus.
2 IYV; a crinivirus), and HC-Pro proteinase of Tobacco etch virus (a potyvirus).
3 iple pathogens: tobacco vein mottling virus, tobacco etch virus, black shank fungus Phytophthora para
4  AtWRI1 driven by seed-specific promoter and Tobacco Etch Virus enhancer.
5 nd competes with structured RNA derived from tobacco etch virus for PAP binding.
6 te that the P1/HC-Pro polyprotein encoded by tobacco etch virus functions as a suppressor of PTGS.
7 for restriction of long-distance movement of tobacco etch virus in Arabidopsis thaliana without causi
8 n the inoculum, high, but not low, levels of tobacco etch virus inoculum resulted in escape of virus
9 ity; and 4) in contrast to cap-dependent and tobacco etch virus internal ribosome entry site interact
10 higher affinity than for either m(7)G cap or tobacco etch virus internal ribosome entry site, suggest
11                                              Tobacco etch virus protease (TEV) is one of the most wid
12                       Using this system, the Tobacco Etch Virus protease (TEV-P), which strongly pref
13 t expression of the highly sequence-specific tobacco etch virus protease (TEVP) is harmless.
14 lease), by employing a circularly permutated tobacco etch virus protease and a blue-light-gated subst
15 sions, we have used a novel method using the tobacco etch virus protease and confirm that Mgm1p is pr
16 taining a double FLAG epitope, followed by a tobacco etch virus protease cleavage site and calmodulin
17            We first show, by introduction of tobacco etch virus protease cleavage site in the middle
18             Engineering NCX1-Met(369) into a tobacco etch virus protease cleavage site revealed that
19 tilizing an N-terminal six-histidine tag and tobacco etch virus protease cleavage site upstream of th
20 nsertion of N-linked glycosylation sites and tobacco etch virus protease cleavage sites provides evid
21  a 390-fold fluorescent signal increase upon tobacco etch virus protease cleavage.
22 ted in mammalian cells was added following a tobacco etch virus protease cut site at the C terminus o
23 Protein translocation assays conducted after tobacco etch virus protease induction revealed a complet
24           By placing a cleavage site for the tobacco etch virus protease prior to the CTD, we have cr
25 ite-specific protein cleavage of YFP-TRF1 by tobacco etch virus protease resolves telomere aggregates
26            By examining the accessibility of tobacco etch virus protease sites and single-cysteine re
27 flicting views, we induced expression of the tobacco etch virus protease to achieve rapid inactivatio
28 domain cleavage of caspase-8 by adapting the tobacco etch virus protease to create a system in which
29                   Spy-C mice express a TEVp (tobacco etch virus protease) cleavage site and a SpyTag
30 sion system based on a light-inducible split tobacco etch virus protease.
31  of the fusion protein at a designed site by tobacco etch virus protease.
32 based on the exogenous enzymatic activity of Tobacco Etch Virus Protease.
33 that is susceptible to inducible cleavage by tobacco etch virus protease.
34 sed from the resin following incubation with tobacco etch virus protease.
35                     Using Protein C Epitope -Tobacco Etch Virus-Protein A Epitope (PTP)-tagged Tb11.0
36      The NH(2)-terminal tag is followed by a tobacco etch virus proteinase cleavage site to ensure th
37 alfa [correction of alfafa] mosaic virus, or tobacco etch virus resulted in necrotic lesions.
38 dsGFP inducer was partially inhibited by the tobacco etch virus silencing suppressor, P1/HC-Pro.
39 he addition of a structured RNA derived from tobacco etch virus suggests that translation initiation
40  eIFiso4F, and a structured RNA derived from tobacco etch virus (TEV RNA).
41                                          The tobacco etch virus (TEV) 5'-leader promotes cap-independ
42                                          The tobacco etch virus (TEV) 6 kDa protein associated with m
43 ence specificity, the 3C-like proteases from tobacco etch virus (TEV) and human rhinovirus are often
44  by which untagged PRMTs can be made using a tobacco etch virus (TEV) cleavage site at the N-terminal
45 nto the CI protein coding region of modified tobacco etch virus (TEV) genomes expressing either beta-
46                             The 5' leader of tobacco etch virus (TEV) genomic RNA directs efficient t
47                             The 5'-leader of tobacco etch virus (TEV) genomic RNA directs the efficie
48  with the use of a viral suppressor of PTGS, tobacco etch virus (TEV) helper component proteinase (HC
49     Restriction of long-distance movement of tobacco etch virus (TEV) in Arabidopsis ecotype Col-0 pl
50 uence specificity, the 3C-type protease from tobacco etch virus (TEV) is frequently used to remove af
51                             This method uses tobacco etch virus (TEV) NIa protease that recognizes a
52 ed an expression cassette that relies on the tobacco etch virus (TEV) nuclear inclusion a (NIa) prote
53 pecificity as the PVY enzyme, but not by the tobacco etch virus (TEV) or the potato virus A (PVA) pro
54 ired for the viral infection in the Capsicum-Tobacco etch virus (TEV) pathosystem.
55 ctivity-based protein profiling (ABPP) and a tobacco etch virus (TEV) protease activation assay, we t
56 ewly generated TAPa tag we have replaced the tobacco etch virus (TEV) protease cleavage site with the
57                                              Tobacco etch virus (TEV) protease is a cysteine protease
58    We constructed mutant hCaRs with a unique tobacco etch virus (TEV) protease recognition site inser
59 ardiac troponin T (hcTnT) and an intervening tobacco etch virus (TEV) protease site that allows purif
60 e revealed the presence of a single putative tobacco etch virus (TEV) protease site within gD, while
61 engineered mammalian cells with an inducible tobacco etch virus (TEV) protease that cleaves TDP-43 co
62                    Our approach uses a split-tobacco etch virus (TEV) protease under small-molecule c
63                       For both myoglobin and tobacco etch virus (TEV) protease, we generated designs
64 f Arabidopsis thaliana for susceptibility to tobacco etch virus (TEV) revealed that each of 10 ecotyp
65                               Two selectable tobacco etch virus (TEV) strains were developed for iden
66 lleles and VPg from two different strains of Tobacco etch virus (TEV) that differentially infected Ca
67  mRNA internal ribosome entry site (IRES) of tobacco etch virus (TEV) to promote translation initiati
68                           The genomic RNA of tobacco etch virus (TEV), a potyvirus that belongs to th
69 ll supported systemic spread of an unrelated tobacco etch virus (TEV), suggesting multiple pathways f
70 DMFE of Vesicular stomatitis virus (VSV) and Tobacco etch virus (TEV), we found that increasing mutat
71                                Surprisingly, tobacco etch virus (TEV)-mediated cleavage of cohesin do
72 latable versions of the coat protein gene of Tobacco etch virus (TEV).
73 fer a highly resistant state to infection by tobacco etch virus (TEV).
74 heless, there was a substantial reduction of tobacco etch virus yield as measured by ELISA assay in t