scholarly article | Q13442814 |
P50 | author | Vitaly Citovsky | Q28112926 |
P2093 | author name string | Shimpei Magori | |
P2860 | cites work | The Ubiquitin-Proteasome System Regulates the Accumulation ofTurnip yellow mosaic virusRNA-Dependent RNA Polymerase during Viral Infection | Q45373236 |
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Transgenic N. glauca plants expressing bacterial virulence gene virF are converted into hosts for nopaline strains of A. tumefaciens | Q59064707 | ||
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Control of Virulence and Pathogenicity Genes of Ralstonia Solanacearum by an Elaborate Sensory Network | Q77149164 | ||
Ubiquitination and degradation of the substrate recognition subunits of SCF ubiquitin-protein ligases | Q77652490 | ||
The Polerovirus F box protein P0 targets ARGONAUTE1 to suppress RNA silencing | Q81297125 | ||
WRKY70 modulates the selection of signaling pathways in plant defense | Q83175538 | ||
The F-box protein CPR1/CPR30 negatively regulates R protein SNC1 accumulation | Q85034002 | ||
Molecular mimicry by an F-box effector of Legionella pneumophila hijacks a conserved polyubiquitination machinery within macrophages and protozoa | Q21131567 | ||
Genome sequence of the plant pathogen Ralstonia solanacearum | Q22122347 | ||
Structure of the Cul1-Rbx1-Skp1-F boxSkp2 SCF ubiquitin ligase complex | Q24294734 | ||
Prophase destruction of Emi1 by the SCF(betaTrCP/Slimb) ubiquitin ligase activates the anaphase promoting complex to allow progression beyond prometaphase | Q24304123 | ||
Structural basis of the Cks1-dependent recognition of p27(Kip1) by the SCF(Skp2) ubiquitin ligase | Q24337721 | ||
New insights into an old story: Agrobacterium-induced tumour formation in plants by plant transformation | Q24614219 | ||
Genetic transformation of HeLa cells by Agrobacterium | Q24616557 | ||
Function and regulation of cullin-RING ubiquitin ligases | Q28131707 | ||
Control of meiotic and mitotic progression by the F box protein beta-Trcp1 in vivo | Q28177348 | ||
RNA silencing in plants | Q28282572 | ||
Induction and suppression of RNA silencing: insights from viral infections | Q28306809 | ||
Involvement of targeted proteolysis in plant genetic transformation by Agrobacterium | Q28492363 | ||
AGROBACTERIUM AND PLANT GENES INVOLVED IN T-DNA TRANSFER AND INTEGRATION | Q28492371 | ||
Pattern of nucleotide substitution at major histocompatibility complex class I loci reveals overdominant selection | Q29616615 | ||
Positive charge is an important feature of the C-terminal transport signal of the VirB/D4-translocated proteins of Agrobacterium. | Q30854480 | ||
Exploitation of eukaryotic ubiquitin signaling pathways by effectors translocated by bacterial type III and type IV secretion systems | Q33270514 | ||
Origin and evolution of GALA-LRR, a new member of the CC-LRR subfamily: from plants to bacteria? | Q33321261 | ||
Clink, a nanovirus-encoded protein, binds both pRB and SKP1. | Q33800789 | ||
Degradation of tobacco mosaic virus movement protein by the 26S proteasome | Q33801592 | ||
Genetic variation: molecular mechanisms and impact on microbial evolution | Q33820587 | ||
Nucleotide substitution at major histocompatibility complex class II loci: evidence for overdominant selection | Q33835136 | ||
Uncoupling of the functions of the Arabidopsis VIP1 protein in transient and stable plant genetic transformation by Agrobacterium | Q33936825 | ||
The transfer of DNA from agrobacterium tumefaciens into plants: a feast of fundamental insights | Q33992852 | ||
The F-box subunit of the SCF E3 complex is encoded by a diverse superfamily of genes in Arabidopsis | Q34039111 | ||
VIP1, an Arabidopsis protein that interacts with Agrobacterium VirE2, is involved in VirE2 nuclear import and Agrobacterium infectivity | Q34079990 | ||
Tome-1, a trigger of mitotic entry, is degraded during G1 via the APC. | Q34188705 | ||
RNA silencing in plants--defense and counterdefense | Q34292165 | ||
F-box-like domain in the polerovirus protein P0 is required for silencing suppressor function | Q34478774 | ||
Partners-in-infection: host proteins involved in the transformation of plant cells by Agrobacterium | Q34540897 | ||
Ralstonia solanacearum requires F-box-like domain-containing type III effectors to promote disease on several host plants | Q34566984 | ||
F-box proteins everywhere. | Q34569323 | ||
Adaptive evolution in two large families of ubiquitin-ligase adapters in nematodes and plants | Q34881890 | ||
Exploitation of Host Polyubiquitination Machinery through Molecular Mimicry by Eukaryotic-Like Bacterial F-Box Effectors | Q35029058 | ||
Stability of plant immune-receptor resistance proteins is controlled by SKP1-CULLIN1-F-box (SCF)-mediated protein degradation | Q35197989 | ||
Conjugative DNA transfer into human cells by the VirB/VirD4 type IV secretion system of the bacterial pathogen Bartonella henselae. | Q35198136 | ||
Ubiquitin-dependent degradation of multiple F-box proteins by an autocatalytic mechanism | Q35596995 | ||
Agrobacterium induces expression of a host F-box protein required for tumorigenicity. | Q36189212 | ||
A case of promiscuity: Agrobacterium's endless hunt for new partners. | Q36313579 | ||
Agrobacterium-mediated genetic transformation of plants: biology and biotechnology. | Q36387276 | ||
Ubiquitination-mediated protein degradation and modification: an emerging theme in plant-microbe interactions. | Q36478232 | ||
Association of the Agrobacterium T-DNA-protein complex with plant nucleosomes. | Q36926915 | ||
Direct and indirect roles of viral suppressors of RNA silencing in pathogenesis. | Q37235294 | ||
Secreted proteins from Ralstonia solanacearum: a hundred tricks to kill a plant. | Q37368646 | ||
The ubiquitin-26S proteasome system at the nexus of plant biology | Q37474364 | ||
Proteasomal degradation in plant-pathogen interactions | Q37511091 | ||
The evolutionary conundrum of pathogen mimicry | Q37608923 | ||
virF, the host-range-determining virulence gene of Agrobacterium tumefaciens, affects T-DNA transfer to Zea mays | Q37627371 | ||
Plant proteins involved in Agrobacterium-mediated genetic transformation | Q37718815 | ||
Agrobacterium tumefaciens-mediated transformation of yeast | Q37722007 | ||
The ubiquitin-proteasome system regulates plant hormone signaling | Q37735375 | ||
The cullin-RING ubiquitin-protein ligases | Q37849305 | ||
Evolution of the major histocompatibility complex: independent origin of nonclassical class I genes in different groups of mammals | Q38213566 | ||
The F-box protein ACRE189/ACIF1 regulates cell death and defense responses activated during pathogen recognition in tobacco and tomato. | Q38292214 | ||
The Legionella pneumophila F-box protein Lpp2082 (AnkB) modulates ubiquitination of the host protein parvin B and promotes intracellular replication. | Q39722305 | ||
Trans-kingdom T-DNA transfer from Agrobacterium tumefaciens to Saccharomyces cerevisiae. | Q40788698 | ||
Agrobacterium-plant cell DNA transport: have virulence proteins, will travel | Q41207472 | ||
Octopine and nopaline strains of Agrobacterium tumefaciens differ in virulence; molecular characterization of the virF locus | Q42629592 | ||
An F-box gene, CPR30, functions as a negative regulator of the defense response in Arabidopsis | Q43291678 | ||
Agrobacterium counteracts host-induced degradation of its effector F-box protein | Q43429716 | ||
Stability in vitro of the 69K movement protein of Turnip yellow mosaic virus is regulated by the ubiquitin-mediated proteasome pathway | Q44238789 | ||
Interaction of the virulence protein VirF of Agrobacterium tumefaciens with plant homologs of the yeast Skp1 protein | Q45269128 | ||
Overexpression of a rice defense-related F-box protein gene OsDRF1 in tobacco improves disease resistance through potentiation of defense gene expression | Q45350609 | ||
P304 | page(s) | 87 | |
P577 | publication date | 2011-11-22 | |
P1433 | published in | Frontiers in Plant Science | Q27723840 |
P1476 | title | Hijacking of the Host SCF Ubiquitin Ligase Machinery by Plant Pathogens | |
P478 | volume | 2 |
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