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Gene Silencing without DNA: RNA-Mediated Cross-Protection between Viruses
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1 of the 51 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1093/emboj/17.22.6739 (notice 2015-10-14).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Genome Amplification and Long-Distance Movement Functions Associated with the Central Domain of Tobacco Etch Potyvirus Helper Component–Proteinase
inferredcites →https://doi.org/10.1006/viro.1998.9457openalex-snapshot
Infection of Tobacco orArabidopsisPlants by CMV Counteracts Systemic Post-transcriptional Silencing of Nonviral (Trans)Genes
inferredcites →https://doi.org/10.1007/bf00039378openalex-snapshot
RNA as a target and an initiator of post-transcriptional gene silencing in trangenic plants
inferredcites →https://doi.org/10.1007/bf02667740openalex-snapshot
Assaying chimeric genes in plants: The GUS gene fusion system
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Cross protection among four viroids
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Multiple small RNA species and the viroid hypothesis for the sunblotch disease of avocado
inferredcites →https://doi.org/10.1016/0042-6822(92)90488-bopenalex-snapshot
Efficient inoculation with CaMV 35 S promoter-driven DNA clones of the tobravirus PEBV
inferredcites →https://doi.org/10.1016/0042-6822(92)90584-copenalex-snapshot
Molecular analysis of a resistance-breaking strain of potato virus X
inferredcites →https://doi.org/10.1016/0167-7799(91)90042-gopenalex-snapshot
Does co-suppression of sense genes in transgenic plants involve antisense RNA?
inferredcites →https://doi.org/10.1016/0378-1119(92)90691-hopenalex-snapshot
Primary structure of the Aequorea victoria green-fluorescent protein
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A Counterdefensive Strategy of Plant Viruses
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Systemic Spread of Sequence-Specific Transgene RNA Degradation in Plants Is Initiated by Localized Introduction of Ectopic Promoterless DNA
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RNA-Mediated RNA Degradation and Chalcone Synthase A Silencing in Petunia
inferredcites →https://doi.org/10.1016/s1360-1385(96)90003-5openalex-snapshot
Gene silencing and virus resistance: a common mechanism
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Plants combat infection by gene silencing
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Improved Green Fluorescent Protein by Molecular Evolution Using DNA Shuffling
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Virus-induced cell death in plants expressing the mammalian 2′,5′ oligoadenylate system
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Transgenic potato expressing a double-stranded RNA-specific ribonuclease is resistant to potato spindle tuber viroid
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Potato virus X as a vector for gene expression in plants
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Homology‐dependent resistance: transgenic virus resistance in plants related to homology‐dependent gene silencing
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Jellyfish green fluorescent protein as a reporter for virus infections
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Requirement of sense transcription for homology‐dependent virus resistance and trans‐inactivation
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Gene silencing from plant DNA carried by a Geminivirus
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Post‐transcriptional silencing of chalcone synthase in petunia using a geminivirus‐based episomal vector
inferredcites →https://doi.org/10.1073/pnas.88.16.7204openalex-snapshot
Systemic expression of a bacterial gene by a tobacco mosaic virus-based vector.
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Cytoplasmic inhibition of carotenoid biosynthesis with virus-derived RNA.
inferredcites →https://doi.org/10.1073/pnas.93.13.6780openalex-snapshot
A mammalian 2-5A system functions as an antiviral pathway in transgenic plants.
inferredcites →https://doi.org/10.1073/pnas.94.6.2122openalex-snapshot
Removal of a cryptic intron and subcellular localization of green fluorescent protein are required to mark transgenic Arabidopsis plants brightly
inferredcites →https://doi.org/10.1073/pnas.95.22.13079openalex-snapshot
A viral suppressor of gene silencing in plants
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Virus resistance and gene silencing in plants can be induced by simultaneous expression of sense and antisense RNA
inferredcites →https://doi.org/10.1093/emboj/16.12.3675openalex-snapshot
Consistent gene silencing in transgenic plants expressing a replicating potato virus X RNA
inferredcites →https://doi.org/10.1093/emboj/17.22.6739openalex-snapshot
Retracted: Viral pathogenicity determinants are suppressors of transgene silencing in Nicotiana benthamiana
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Delayed Resistance to Plum Pox Potyvirus Mediated by a Mutated RNA Replicase Gene: Involvement of a Gene-Silencing Mechanism
inferredcites →https://doi.org/10.1094/phyto-64-102openalex-snapshot
Alfalfa Mosaic Virus Transmission to Seed Through Alfalfa Gametes and Longevity in Alfalfa Seed
inferredcites →https://doi.org/10.1099/0022-1317-70-4-963openalex-snapshot
Infectious RNA Produced by in vitro Transcription of a Full-length Tobacco Rattle Virus RNA-1 cDNA
inferredcites →https://doi.org/10.1099/0022-1317-78-2-465openalex-snapshot
Transmission of tobacco rattle virus isolate PpK20 by its nematode vector requires one of the two non-structural genes in the viral RNA 2.
inferredcites →https://doi.org/10.1099/0022-1317-78-8-2085openalex-snapshot
Replication of in vitro tobravirus recombinants shows that the specificity of template recognition is determined by 5' non-coding but not 3' non-coding sequences.
inferredcites →https://doi.org/10.1105/tpc.10.6.937openalex-snapshot
Initiation and Maintenance of Virus-Induced Gene Silencing
inferredcites →https://doi.org/10.1105/tpc.5.12.1749openalex-snapshot
Induction of a Highly Specific Antiviral State in Transgenic Plants: Implications for Regulation of Gene Expression and Virus Resistance.
inferredcites →https://doi.org/10.1105/tpc.6.10.1441openalex-snapshot
Transgenic plant virus resistance mediated by untranslatable sense RNAs: expression, regulation, and fate of nonessential RNAs.
inferredcites →https://doi.org/10.1105/tpc.8.1.95openalex-snapshot
Genetic and biochemical dissection of transgenic RNA-mediated virus resistance.
inferredcites →https://doi.org/10.1105/tpc.8.10.1833openalex-snapshot
Mechanisms of Pathogen-Derived Resistance to Viruses in Transgenic Plants
inferredcites →https://doi.org/10.1105/tpc.8.2.179openalex-snapshot
Suppression of Virus Accumulation in Transgenic Plants Exhibiting Silencing of Nuclear Genes.
inferredcites →https://doi.org/10.1105/tpc.9.6.859openalex-snapshot
Plant viral synergism: the potyviral genome encodes a broad-range pathogenicity enhancer that transactivates replication of heterologous viruses.
inferredcites →https://doi.org/10.1105/tpc.9.8.1495openalex-snapshot
A Transcriptionally Active State Is Required for Post-Transcriptional Silencing (Cosuppression) of Nitrate Reductase Host Genes and Transgenes.
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STUDIES ON THE PROPERTIES OF SOIL‐BORNE VIRUSES OF THE TOBACCO‐RATTLE TYPE OCCURRING IN SCOTLAND
inferredcites →https://doi.org/10.1111/j.1744-7348.1967.tb04416.xopenalex-snapshot
Seed‐transmission of nematode‐borne viruses
inferredcites →https://doi.org/10.1126/science.276.5318.1558openalex-snapshot
A Similarity Between Viral Defense and Gene Silencing in Plants
inferredcites →https://doi.org/10.1126/science.279.5359.2113openalex-snapshot
Transcriptional and Posttranscriptional Plant Gene Silencing in Response to a Pathogen
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Characterization of Clover Yellow Vein Virus Infecting Pisum Sativum Using its Infectious Clones and Evidence Supporting Viral RNA in Conferring Superinfection Exclusion
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Post-transcriptional gene-silencing: RNAs on the attack or on the defense?
inferred← citeshttps://doi.org/10.1002/1439-7633(20010401)2:4<239::aid-cbic239>3.0.co;2-ropenalex-snapshot
RNA Interference and Small Interfering RNAs
inferred← citeshttps://doi.org/10.1002/9781118025666.ch12openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119312994.apr0193openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119414735.ch2openalex-snapshot
Crop Improvement Using Genome Editing
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VIROIDS AND VIROID DISEASES OF PLANTS
inferred← citeshttps://doi.org/10.1002/ange.200603284openalex-snapshot
Inhibition of siRNA Binding to a p19 Viral Suppressor of RNA Silencing by Cysteine Alkylation
inferred← citeshttps://doi.org/10.1002/anie.200603284openalex-snapshot
Inhibition of siRNA Binding to a p19 Viral Suppressor of RNA Silencing by Cysteine Alkylation
inferred← citeshttps://doi.org/10.1002/btpr.485openalex-snapshot
Transient expression of antibodies in suspension plant cell suspension cultures is enhanced when co‐transformed with the tomato bushy stunt virus p19 viral suppressor of gene silencing
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Processing of virus‐derived cytoplasmic primary‐ microRNAs
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Tobacco Mosaic Virus Replicase-Mediated Cross-Protection: Contributions of RNA and Protein-Derived Mechanisms
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Activation and Suppression of RNA Silencing by Plant Viruses
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Mechanisms Involved in Induced Resistance to Plant Viruses
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RNA Silencing: A Natural Resistance Mechanism in Plants
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Virus Transmission—Getting Out and In
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Plant RNA Silencing in Viral Defence
inferred← citeshttps://doi.org/10.1007/978-1-4615-4199-8_9openalex-snapshot
Are Gene Silencing Mutants Good Tools for Reliable Transgene Expression or Reliable Silencing of Endogenous Genes in Plants?
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Virus-Induced Gene Silencing for Gene Function Studies in Barley
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Screening and Identification of Virus-Encoded RNA Silencing Suppressors
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Endogenous Antiviral Mechanisms of RNA Interference: A Comparative Biology Perspective
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Geminivirus Resistance Strategies
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Novel Technologies for Transgenic Management for Plant Virus Resistance
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Suppressor to Survival: RNAi as a Molecular Weapon in Arms Race Between Virus and Host
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Zucchini Yellow Mosaic Virus
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Key Methods for Synthetic Biology: Genome Engineering and DNA Assembly
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Role of Small RNAs in Virus-Host Interaction
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RNAi-Mediated Protection Against Citrus Tristeza Virus in Transgenic Citrus Plants
inferred← citeshttps://doi.org/10.1007/978-3-642-37765-5_6openalex-snapshot
RNA Interference-Mediated Intrinsic Antiviral Immunity in Plants
inferred← citeshttps://doi.org/10.1007/978-3-7091-6425-9_14openalex-snapshot
Viruses and gene silencing in plants
inferred← citeshttps://doi.org/10.1007/978-94-007-6380-7_6openalex-snapshot
Detection and Identification of Viral Biological Control Agents
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Management of Virus and Viroid Diseases of Crops in the Tropics
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RNA degradation and models for post-transcriptional gene silencing
inferred← citeshttps://doi.org/10.1007/978-94-011-4183-3_12openalex-snapshot
Systemic silencing signal(s)
inferred← citeshttps://doi.org/10.1007/978-94-011-4183-3_13openalex-snapshot
RNA viruses as inducers, suppressors and targets of post-transcriptional gene silencing
inferred← citeshttps://doi.org/10.1007/978-94-011-4183-3_15openalex-snapshot
Transgene silencing in monocots
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Plant DNA Methylation and Gene Expression
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RNA Interference for Plant Disease Management: Updated Methods, Current Applications and Future Directions
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The spread of Tobacco mosaic virus infection: insights into the cellular mechanism of RNA transport
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Characterization of resistance mechanism in transgenic Nicotiana benthamiana containing Turnip crinkle virus coat protein
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Virus-induced silencing of Comt, pAmt and Kas genes results in a reduction of capsaicinoid accumulation in chili pepper fruits
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Recovery from virus infection: plant’s armory in action
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Infection of soybean by cucumber mosaic virus as determined by viral movement protein
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Preferential accumulation of severe variants of Citrus tristeza virus in plants co-inoculated with mild and severe variants
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Inducible viral inoculation system with cultured plant cells facilitates a biochemical approach for virus-induced RNA silencing
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Development and evaluation of a complementation-dependent gene delivery system based on cucumber mosaic virus
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Inhibition of tobacco mosaic virus replication in lateral roots is dependent on an activated meristem-derived signal
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Evaluation of cross-protection with an attenuated isolate of Bean yellow mosaic virus by differential detection of virus isolates using RT-PCR
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Shoot meristem tissue of tobacco inoculated with Cucumber mosaic virus is infected with the virus and subsequently recovers from infection by RNA silencing
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Inverse correlation between mRNA levels in GFP-silenced transgenic Nicotiana benthamiana and resistance to Potato virus X engineered to contain GFP sequence
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Interfamily transfer of Arabidopsis lectin-mediated antiviral gene confers resistance to pepino mosaic virus in tomato
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Genetic resistance for the sustainable control of plant virus diseases: breeding, mechanisms and durability
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Tobacco ringspot virus persists in the shoot apical meristem but not in the root apical meristem of infected tobacco
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The use of attenuated isolates of Pepino mosaic virus for cross-protection
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A geminivirus-induced gene silencing system for gene function validation in cassava
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Post-Transcriptional Gene Silencing of the p23 Silencing Suppressor of Citrus tristeza virus Confers Resistance to the Virus in Transgenic Mexican Lime
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Virus tolerance and recovery from viral induced-symptoms in plants are associated with transcriptome reprograming
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Characterization of Eukaryotic Release Factor 3 (eRF3) Translation Termination Factor in Plants
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Virus-induced gene silencing (VIGS) for elucidation of pathogen defense role of serine/threonine protein kinase in the non-model plant Piper colubrinum Link.
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RNA interference (RNAi) mediated technique for combating plant diseases: Harnessing nanoparticles for effective delivery and enhanced efficacy
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RNA-interference in rice against Rice tungro bacilliform virus results in its decreased accumulation in inoculated rice plants
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VPg of Potato virus A alone does not suppress RNA silencing but affects virulence of a heterologous virus
inferred← citeshttps://doi.org/10.1007/s11262-009-0359-9openalex-snapshot
Transgenic expression of coat protein gene of Rice tungro bacilliform virus in rice reduces the accumulation of viral DNA in inoculated plants
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Inheritance of resistance to Plum pox virus in apricot (Prunus armeniaca L.)
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Strategies and mechanisms of plant virus resistance
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Papaya ringspot virus: from pathogenesis to genetic resistance—a global perspective
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An asymptomatic geminivirus activates autophagy and enhances plant defenses against diverse pathogens
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Structure and Evolution of Viroids
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Virus–Plant Interactions
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Virus–Plant Interactions in Non-Permissive and Permissive Hosts
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Risk Assessment and Biosecurity Considerations in Control of Emergent Plant Viruses
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Overview of host factors and geminivirus proteins involved in virus pathogenesis and resistance
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Papaya ring spot virus: Status of 80 years of global research
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Plant virus disease control by vaccination and transgenic approaches: Current status and perspective
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Enzyme engineering in medicinal plants: Enhancements in the yield of secondary metabolites
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Molecular Biology of Potyviruses
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Antiviral strategies in plants based on RNA silencing
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Stabilized recombinant suppressors of RNA silencing: Functional effects of linking monomers of Carnation Italian Ringspot virus p19
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Cysteine residues of Carnation Italian Ringspot virus p19 suppressor of RNA silencing maintain global structural integrity and stability for siRNA binding
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Herbal genomics as tools for dissecting new metabolic pathways of unexplored medicinal plants and drug discovery
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The Mammalian Response to Virus Infection Is Independent of Small RNA Silencing
inferred← citeshttps://doi.org/10.1016/j.chom.2026.08.005openalex-snapshot
Mobile virus-derived siRNAs drive plant antiviral silencing through reiterated 3–4 cell immunization
inferred← citeshttps://doi.org/10.1016/j.coviro.2017.06.010openalex-snapshot
Prospects for engineering and improvement of cross-protective virus strains
inferred← citeshttps://doi.org/10.1016/j.cropro.2017.02.007openalex-snapshot
Multi-genotype cross-protection against Pepino mosaic virus in tomato
inferred← citeshttps://doi.org/10.1016/j.exger.2004.03.040openalex-snapshot
RNAi: ancient mechanism with a promising future
inferred← citeshttps://doi.org/10.1016/j.ijpara.2025.07.002openalex-snapshot
RNA interference as a tool for functional genomics in parasitic helminths
inferred← citeshttps://doi.org/10.1016/j.jgeb.2011.05.010openalex-snapshot
Differential expression of cytochrome oxidase and ALY-family genes in resistant and susceptible tomato cultivars (Solanum lycopersicum) inoculated with Tomato bushy stunt virus
inferred← citeshttps://doi.org/10.1016/j.jip.2009.06.014openalex-snapshot
The Acute bee paralysis virus–Kashmir bee virus–Israeli acute paralysis virus complex
inferred← citeshttps://doi.org/10.1016/j.jprot.2019.02.002openalex-snapshot
iTRAQ-based analysis of leaf proteome identifies important proteins in secondary metabolite biosynthesis and defence pathways crucial to cross-protection against TMV
inferred← citeshttps://doi.org/10.1016/j.jtbi.2004.10.007openalex-snapshot
GENE impedance: a natural process for control of gene expression and the origin of RNA interference
inferred← citeshttps://doi.org/10.1016/j.jtbi.2010.04.027openalex-snapshot
Asymmetrical over-infection as a process of plant virus emergence
inferred← citeshttps://doi.org/10.1016/j.jtbi.2016.05.018openalex-snapshot
Mathematical model of plant-virus interactions mediated by RNA interference
inferred← citeshttps://doi.org/10.1016/j.jtbi.2017.02.011openalex-snapshot
Exposing the diversity of multiple infection patterns
inferred← citeshttps://doi.org/10.1016/j.jviromet.2004.10.007openalex-snapshot
Construction and properties of a gene-silencing vector based on Poplar mosaic virus (genus Carlavirus)
inferred← citeshttps://doi.org/10.1016/j.jviromet.2014.04.012openalex-snapshot
Reverse transcription loop-mediated isothermal amplification assay for rapid detection of Papaya ringspot virus
inferred← citeshttps://doi.org/10.1016/j.jviromet.2018.03.002openalex-snapshot
Lanai: A small, fast growing tomato variety is an excellent model system for studying geminiviruses
inferred← citeshttps://doi.org/10.1016/j.mrrev.2011.09.001openalex-snapshot
Post-transcriptional gene silencing by RNA interference in non-mammalian vertebrate systems: Where do we stand?
inferred← citeshttps://doi.org/10.1016/j.pbi.2005.01.006openalex-snapshot
RNA silencing and antiviral defense in plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2005.05.012openalex-snapshot
The complex interplay between plant viruses and host RNA-silencing pathways
inferred← citeshttps://doi.org/10.1016/j.phpro.2012.05.029openalex-snapshot
The Feasibility Analysis of PVX and TRV Vectors as the VIGS Tool for Studying the Gene Function
inferred← citeshttps://doi.org/10.1016/j.plantsci.2003.11.018openalex-snapshot
Analysis of RNA-mediated virus resistance by NSs and NSm gene sequences from Tomato spotted wilt virus
inferred← citeshttps://doi.org/10.1016/j.plantsci.2014.04.015openalex-snapshot
Virus resistance in orchids
inferred← citeshttps://doi.org/10.1016/j.plantsci.2014.05.006openalex-snapshot
Molecular biology of viroid–host interactions and disease control strategies
inferred← citeshttps://doi.org/10.1016/j.plantsci.2016.07.015openalex-snapshot
Synergies and antagonisms in virus interactions
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111491openalex-snapshot
Development of tobacco rattle virus-based platform for dual heterologous gene expression and CRISPR/Cas reagent delivery
inferred← citeshttps://doi.org/10.1016/j.pmpp.2003.11.001openalex-snapshot
Effect of substitution of the amino termini of coat proteins of distinct potyvirus species on viral infectivity and host specificity
inferred← citeshttps://doi.org/10.1016/j.virol.2003.08.009openalex-snapshot
Identification and molecular characterization of a naturally occurring RNA virus mutant defective in the initiation of host recovery
inferred← citeshttps://doi.org/10.1016/j.virol.2004.06.046openalex-snapshot
Spatial analysis for exclusive interactions between subgroups I and II of Cucumber mosaic virus in cowpea
inferred← citeshttps://doi.org/10.1016/j.virol.2007.07.033openalex-snapshot
Citrus viroid V: Molecular characterization and synergistic interactions with other members of the genus Apscaviroid
inferred← citeshttps://doi.org/10.1016/j.virol.2007.09.031openalex-snapshot
Double-stranded RNA interferes in a sequence-specific manner with the infection of representative members of the two viroid families
inferred← citeshttps://doi.org/10.1016/j.virol.2013.08.019openalex-snapshot
Preventive and curative effects of Apple latent spherical virus vectors harboring part of the target virus genome against potyvirus and cucumovirus infections
inferred← citeshttps://doi.org/10.1016/j.virol.2014.03.026openalex-snapshot
Temperature-dependent symptom recovery in Nicotiana benthamiana plants infected with tomato ringspot virus is associated with reduced translation of viral RNA2 and requires ARGONAUTE 1
inferred← citeshttps://doi.org/10.1016/j.virol.2014.05.031openalex-snapshot
The capsid protein p38 of turnip crinkle virus is associated with the suppression of cucumber mosaic virus in Arabidopsis thaliana co-infected with cucumber mosaic virus and turnip crinkle virus
inferred← citeshttps://doi.org/10.1016/j.virol.2014.08.031openalex-snapshot
Superinfection exclusion by Citrus tristeza virus does not correlate with the production of viral small RNAs
inferred← citeshttps://doi.org/10.1016/j.virol.2015.01.008openalex-snapshot
Symptom recovery in virus-infected plants: Revisiting the role of RNA silencing mechanisms
inferred← citeshttps://doi.org/10.1016/j.virol.2015.12.008openalex-snapshot
A 5′-proximal region of the Citrus tristeza virus genome encoding two leader proteases is involved in virus superinfection exclusion
inferred← citeshttps://doi.org/10.1016/j.virol.2016.10.001openalex-snapshot
Understanding superinfection exclusion by complex populations of Citrus tristeza virus
inferred← citeshttps://doi.org/10.1016/j.virol.2018.08.016openalex-snapshot
Expression and antiviral function of ARGONAUTE 2 in Nicotiana benthamiana plants infected with two isolates of tomato ringspot virus with varying degrees of virulence
inferred← citeshttps://doi.org/10.1016/j.virol.2024.110032openalex-snapshot
Transcriptome analysis of the synergistic mechanisms between two strains of potato virus Y in Solanum tuberosum L.
inferred← citeshttps://doi.org/10.1016/j.virusres.2004.01.016openalex-snapshot
RNA interference against retroviruses
inferred← citeshttps://doi.org/10.1016/j.virusres.2004.01.017openalex-snapshot
RNA interference, arthropod-borne viruses, and mosquitoes
inferred← citeshttps://doi.org/10.1016/j.virusres.2004.01.019openalex-snapshot
RNA interference as a new biotechnological tool for the control of virus diseases in plants
inferred← citeshttps://doi.org/10.1016/j.virusres.2004.01.021openalex-snapshot
RNA silencing: a conserved antiviral immunity of plants and animals
inferred← citeshttps://doi.org/10.1016/j.virusres.2005.11.004openalex-snapshot
Pepper mild mottle virus pathogenicity determinants and cross protection effect of attenuated mutants in pepper
inferred← citeshttps://doi.org/10.1016/j.virusres.2005.11.012openalex-snapshot
Systemic antiviral silencing in plants
inferred← citeshttps://doi.org/10.1016/j.virusres.2008.11.006openalex-snapshot
Genomic heterogeneity and host recovery of isolates of Malva vein clearing virus
inferred← citeshttps://doi.org/10.1016/j.virusres.2009.04.011openalex-snapshot
Soybean cultivar resistant to Mungbean Yellow Mosaic India Virus infection induces viral RNA degradation earlier than the susceptible cultivar
inferred← citeshttps://doi.org/10.1016/j.virusres.2009.04.018openalex-snapshot
Genetic structure and variability of virus populations in cross-protected grapevines superinfected by Grapevine fanleaf virus
inferred← citeshttps://doi.org/10.1016/j.virusres.2011.06.026openalex-snapshot
Agrobacterium-mediated infection of whole plants by yellow dwarf viruses
inferred← citeshttps://doi.org/10.1016/j.virusres.2015.11.011openalex-snapshot
Mapping and identification of cassava mosaic geminivirus DNA-A and DNA-B genome sequences for efficient siRNA expression and RNAi based virus resistance by transient agro-infiltration studies
inferred← citeshttps://doi.org/10.1016/j.virusres.2016.06.005openalex-snapshot
The interaction between Turnip crinkle virus p38 and Cucumber mosaic virus 2b and its critical domains
inferred← citeshttps://doi.org/10.1016/j.virusres.2018.07.011openalex-snapshot
Simultaneous resistance against the two viruses causing rice tungro disease using RNA interference
inferred← citeshttps://doi.org/10.1016/s0014-5793(04)00184-xopenalex-snapshot
Virus survival of RNA silencing without deploying protein‐mediated suppression in Nicotiana benthamiana
inferred← citeshttps://doi.org/10.1016/s0065-3527(06)66004-1openalex-snapshot
Plant Signal Transduction and Defense Against Viral Pathogens
inferred← citeshttps://doi.org/10.1016/s0074-7696(04)35003-5openalex-snapshot
Macromolecular Transport and Signaling Through Plasmodesmata
inferred← citeshttps://doi.org/10.1016/s0092-8674(00)00095-7openalex-snapshot
A Viral Movement Protein Prevents Spread of the Gene Silencing Signal in Nicotiana benthamiana
inferred← citeshttps://doi.org/10.1016/s0092-8674(00)80863-6openalex-snapshot
Arabidopsis SGS2 and SGS3 Genes Are Required for Posttranscriptional Gene Silencing and Natural Virus Resistance
inferred← citeshttps://doi.org/10.1016/s0092-8674(00)80864-8openalex-snapshot
An RNA-Dependent RNA Polymerase Gene in Arabidopsis Is Required for Posttranscriptional Gene Silencing Mediated by a Transgene but Not by a Virus
inferred← citeshttps://doi.org/10.1016/s0092-8674(01)00547-5openalex-snapshot
ATP Requirements and Small Interfering RNA Structure in the RNA Interference Pathway
inferred← citeshttps://doi.org/10.1016/s0092-8674(04)00218-1openalex-snapshot
RISC Assembly Defects in the Drosophila RNAi Mutant armitage
inferred← citeshttps://doi.org/10.1016/s0167-4781(02)00280-4openalex-snapshot
Antisense-RNA regulation and RNA interference
inferred← citeshttps://doi.org/10.1016/s0168-9452(03)00028-1openalex-snapshot
Analysis of the nucleocapsid protein gene from Tomato spotted wilt virus as target and inducer for posttranscriptional gene silencing
inferred← citeshttps://doi.org/10.1016/s0168-9525(01)02367-8openalex-snapshot
RNA silencing as a plant immune system against viruses
inferred← citeshttps://doi.org/10.1016/s0176-1617(98)80022-9openalex-snapshot
Protein quality and its potential relationship to the cytoskeleton in maize endosperm
inferred← citeshttps://doi.org/10.1016/s0764-4469(01)01369-5openalex-snapshot
Plant viruses and the recent discovery of unforeseen basic cellular processes
inferred← citeshttps://doi.org/10.1016/s0885-5765(03)00040-7openalex-snapshot
Soilborne viruses: advances in virus movement, virus induced gene silencing, and engineered resistance
inferred← citeshttps://doi.org/10.1016/s0958-1669(00)00190-7openalex-snapshot
Viral suppressors of RNA silencing
inferred← citeshttps://doi.org/10.1016/s0958-1669(02)00296-3openalex-snapshot
RNA-mediated virus resistance
inferred← citeshttps://doi.org/10.1016/s0960-9822(01)00226-3openalex-snapshot
RNA-directed transcriptional gene silencing in plants can be inherited independently of the RNA trigger and requires Met1 for maintenance
inferred← citeshttps://doi.org/10.1016/s0960-9822(99)80383-2openalex-snapshot
Gene silencing: RNA makes RNA makes no protein
inferred← citeshttps://doi.org/10.1016/s0965-1748(02)00096-6openalex-snapshot
Developing arbovirus resistance in mosquitoes
inferred← citeshttps://doi.org/10.1016/s0966-842x(02)02387-9openalex-snapshot
Viral suppression of systemic silencing
inferred← citeshttps://doi.org/10.1016/s1046-2023(03)00037-9openalex-snapshot
Virus-induced gene silencing in plants
inferred← citeshttps://doi.org/10.1016/s1360-1385(99)01493-4openalex-snapshot
Virus resistance and gene silencing: killing the messenger
inferred← citeshttps://doi.org/10.1016/s1369-5266(00)00090-xopenalex-snapshot
Insect transmission of plant viruses: a constraint on virus variability
inferred← citeshttps://doi.org/10.1016/s1369-5266(00)00158-8openalex-snapshot
Virus-mediated reprogramming of gene expression in plants
inferred← citeshttps://doi.org/10.1016/s1874-5334(05)80006-1openalex-snapshot
Gene Silencing as a Tool for the Identification of Gene Function in Fungi
inferred← citeshttps://doi.org/10.1017/cbo9780511546402.005openalex-snapshot
Dicer in RNAi: Its roles in vivo and utility in vitro
inferred← citeshttps://doi.org/10.1017/cbo9780511546402.024openalex-snapshot
RNAi and gene silencing phenomena mediated by viral suppressors in plants
inferred← citeshttps://doi.org/10.1017/s0031182021001384openalex-snapshot
Sequential infection ofDaphnia magnaby a gut microsporidium followed by a haemolymph yeast decreases transmission of both parasites
inferred← citeshttps://doi.org/10.1021/acssynbio.5c00153openalex-snapshot
Engineering Encapsidated TRV1 as a Complete VIGS Platform
inferred← citeshttps://doi.org/10.1023/a:1006412318311openalex-snapshot
Transgene silencing in monocots
inferred← citeshttps://doi.org/10.1023/a:1006443731515openalex-snapshot
RNA degradation and models for post-transcriptional gene silencing
inferred← citeshttps://doi.org/10.1023/a:1006456000564openalex-snapshot
RNA viruses as inducers, suppressors and targets of post-transcriptional gene silencing
inferred← citeshttps://doi.org/10.1023/a:1006456603970openalex-snapshot
Expression of a yeast RNase III gene in transgenic tobacco silences host nitrite reductase genes
inferred← citeshttps://doi.org/10.1023/a:1015630516425openalex-snapshot
Virus variation in relation to resistance-breaking in plants
inferred← citeshttps://doi.org/10.1023/a:1015656017326openalex-snapshot
Tobacco Plants Transformed with an Untranslatable Form of the Coat Protein Gene of the Potato Virus Y are Resistant to Viral Infection
inferred← citeshttps://doi.org/10.1023/a:1016000627231openalex-snapshot
Suppression of a key gene involved in chlorophyll biosynthesis by means of virus-inducing gene silencing
inferred← citeshttps://doi.org/10.1023/a:1020122104651openalex-snapshot
Subcellular Location of the Helper Component-Proteinase of Cowpea Aphid-Borne Mosaic Virus
inferred← citeshttps://doi.org/10.1023/a:1020170024713openalex-snapshot
Transgenic Plants Expressing HC-Pro Show Enhanced Virus Sensitivity While Silencing of the Transgene Results in Resistance
inferred← citeshttps://doi.org/10.1023/a:1026346325933openalex-snapshot
RNA Interference. An Approach to Produce Knockout Organisms and Cell Lines
inferred← citeshttps://doi.org/10.1023/b:plan.0000028797.63168.a7openalex-snapshot
Characteristics of RNA Silencing in Plants: Similarities and Differences Across Kingdoms
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