| scholarly article | Q13442814 |
| P2093 | author name string | Jerzy Syller | |
| Anna Grupa | |||
| P2860 | cites work | Interactions in a host plant-virus-vector-parasitoid system: modelling the consequences for virus transmission and disease dynamics | Q45366179 |
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| Pathogen Relatedness Affects the Prevalence of Within‐Host Competition | Q56929317 | ||
| Application of game theory to the interaction between plant viruses during mixed infections | Q57052200 | ||
| Virus Evolution: Insights from an Experimental Approach | Q57052270 | ||
| Multiple infection dynamics has pronounced effects on the fitness of RNA viruses | Q57052362 | ||
| Epidemiological and evolutionary consequences of life-history trade-offs in pathogens | Q57056465 | ||
| Transmission mechanisms shape pathogen effects on host-vector interactions: evidence from plant viruses | Q58103010 | ||
| Different forms of interference between two tobamoviruses in two different hosts | Q58924910 | ||
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| Coat protein interactions involved in tobacco mosaic tobamovirus cross-protection | Q77165144 | ||
| Synergism and negative interference during co-infection of tomato and Nicotiana benthamiana with two bipartite begomoviruses | Q83467998 | ||
| Viral suppressors of RNA silencing | Q83721756 | ||
| Synchronous attack is advantageous: mixed genotype infections lead to higher infection success in trematode parasites | Q84245095 | ||
| Characterization of a viral synergism in the monocot Brachypodium distachyon reveals distinctly altered host molecular processes associated with disease | Q84952552 | ||
| Grapevine Leafroll: A Complex Viral Disease Affecting a High-Value Fruit Crop | Q91280169 | ||
| Co-infection and Disease Severity of Ohio Maize dwarf mosaic virus and Maize chlorotic dwarf virus Strains | Q91292856 | ||
| Gene silencing without DNA. rna-mediated cross-protection between viruses | Q95306310 | ||
| Crop immunity against viruses: outcomes and future challenges | Q21129198 | ||
| Fitness and its role in evolutionary genetics | Q22122004 | ||
| Toward a systems understanding of plant-microbe interactions | Q26865799 | ||
| Silencing and innate immunity in plant defense against viral and non-viral pathogens | Q27010305 | ||
| Viral quasispecies evolution | Q27013917 | ||
| Dual mechanisms of pestiviral superinfection exclusion at entry and RNA replication | Q27469450 | ||
| The Evolution of Viruses in Multi-Host Fitness Landscapes | Q27488856 | ||
| Rates of evolutionary change in viruses: patterns and determinants | Q29616174 | ||
| Illuminating the silence: understanding the structure and function of small RNAs | Q29622905 | ||
| Plant immunity: towards an integrated view of plant-pathogen interactions | Q30004699 | ||
| Competition-colonization trade-off promotes coexistence of low-virulence viral strains | Q30522555 | ||
| Hormone activities and the cell cycle machinery in immunity-triggered growth inhibition | Q30919248 | ||
| Symbiosis versus competition in plant virus evolution | Q33228342 | ||
| Association and host selectivity in multi-host pathogens. | Q33267302 | ||
| Vector-virus mutualism accelerates population increase of an invasive whitefly | Q33271018 | ||
| Preventive and curative effects of Apple latent spherical virus vectors harboring part of the target virus genome against potyvirus and cucumovirus infections. | Q33356617 | ||
| A century of tobamovirus evolution in an Australian population of Nicotiana glauca | Q33391423 | ||
| Coat-protein-mediated resistance to tobacco mosaic virus: discovery mechanisms and exploitation | Q33599714 | ||
| Dynamics of the multiplicity of cellular infection in a plant virus. | Q33700599 | ||
| Virus world as an evolutionary network of viruses and capsidless selfish elements | Q33743494 | ||
| Lifestyles of plant viruses | Q33891614 | ||
| Activation and suppression of RNA silencing by plant viruses | Q34164398 | ||
| Growth-defense tradeoffs in plants: a balancing act to optimize fitness | Q34208987 | ||
| A viral protein mediates superinfection exclusion at the whole-organism level but is not required for exclusion at the cellular level | Q34261965 | ||
| The interaction of plant biotic and abiotic stresses: from genes to the field | Q34265118 | ||
| Strategies for viral cross protection in plants | Q34279790 | ||
| Expanding networks of RNA virus evolution | Q34310578 | ||
| Plant immune responses against viruses: how does a virus cause disease? | Q34346888 | ||
| RNA silencing suppression by plant pathogens: defence, counter-defence and counter-counter-defence | Q34377957 | ||
| Mechanisms of plant resistance to viruses | Q34446982 | ||
| Fitness costs of induced resistance: emerging experimental support for a slippery concept | Q34520459 | ||
| Potato virus Y infection hinders potato defence response and renders plants more vulnerable to Colorado potato beetle attack | Q34541082 | ||
| Human immunodeficiency virus superinfection and recombination: current state of knowledge and potential clinical consequences | Q34577539 | ||
| Model-selection-based approach for calculating cellular multiplicity of infection during virus colonization of multi-cellular hosts | Q34749702 | ||
| Aerial dispersal of pathogens on the global and continental scales and its impact on plant disease | Q34762833 | ||
| Cross talk between signaling pathways in pathogen defense | Q34785534 | ||
| On the biological success of viruses. | Q34786403 | ||
| Dynamics of small RNA profiles of virus and host origin in wheat cultivars synergistically infected by Wheat streak mosaic virus and Triticum mosaic virus: virus infection caused a drastic shift in the endogenous small RNA profile | Q35387694 | ||
| A plant virus evolved by acquiring multiple nonconserved genes to extend its host range | Q35408943 | ||
| Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance | Q35545173 | ||
| Five challenges in evolution and infectious diseases | Q35595374 | ||
| Superinfection exclusion is an active virus-controlled function that requires a specific viral protein | Q35943603 | ||
| The role of viral fitness in HIV pathogenesis | Q36223846 | ||
| Interactions between virus proteins and host cell membranes during the viral life cycle | Q36242115 | ||
| Suppressors of RNA silencing encoded by plant viruses and their role in viral infections | Q36257311 | ||
| Measured, modeled, and causal conceptions of fitness | Q36339740 | ||
| Developing an understanding of cross-protection by Citrus tristeza virus | Q36739425 | ||
| Plant Responses to Simultaneous Biotic and Abiotic Stress: Molecular Mechanisms | Q36833608 | ||
| Disease resistance or growth: the role of plant hormones in balancing immune responses and fitness costs | Q36871832 | ||
| The multilevel and dynamic interplay between plant and pathogen | Q37148107 | ||
| Mild strain cross protection of tristeza: a review of research to protect against decline on sour orange in Florida | Q37150210 | ||
| The evolution of virulence and pathogenicity in plant pathogen populations. | Q37244382 | ||
| Evasion of superinfection exclusion and elimination of primary viral RNA by an adapted strain of hepatitis C virus. | Q37336829 | ||
| A systematic approach to virus-virus interactions. | Q37679389 | ||
| Mechanisms of viral emergence | Q37694793 | ||
| Cross-protection: a century of mystery. | Q37801999 | ||
| Cellular pathways for viral transport through plasmodesmata | Q37815030 | ||
| Silencing signals in plants: a long journey for small RNAs | Q37828648 | ||
| The evolutionary genetics of emerging plant RNA viruses | Q37835829 | ||
| Programmed cell death in the plant immune system | Q37862983 | ||
| Facilitative and antagonistic interactions between plant viruses in mixed infections | Q37897288 | ||
| Recognition events and host-pathogen co-evolution in gene-for-gene resistance to flax rust. | Q37901375 | ||
| How do plant viruses induce disease? Interactions and interference with host components. | Q37928837 | ||
| The role of virus-derived small interfering RNAs in RNA silencing in plants | Q37993480 | ||
| Hormonal modulation of plant immunity | Q38007563 | ||
| Virus population bottlenecks during within-host progression and host-to-host transmission. | Q38037877 | ||
| Viral fitness: definitions, measurement, and current insights | Q38044156 | ||
| Plant innate immunity: an updated insight into defense mechanism. | Q38105459 | ||
| Experimental measures of pathogen competition and relative fitness | Q38114480 | ||
| Small RNAs in plant defense responses during viral and bacterial interactions: similarities and differences | Q38139003 | ||
| Biological and molecular events associated with simultaneous transmission of plant viruses by invertebrate and fungal vectors | Q38171550 | ||
| Abiotic and biotic stress combinations. | Q38203629 | ||
| Dominant resistance against plant viruses | Q38229020 | ||
| Roles of plant hormones in the regulation of host-virus interactions. | Q38249131 | ||
| Extracellular ATP acts as a damage-associated molecular pattern (DAMP) signal in plants | Q38251630 | ||
| Superinfection exclusion in alphabaculovirus infections is concomitant with actin reorganization | Q38326455 | ||
| Symptom recovery in virus-infected plants: Revisiting the role of RNA silencing mechanisms | Q38353992 | ||
| Going mobile: non-cell-autonomous small RNAs shape the genetic landscape of plants | Q38371918 | ||
| Grapevine leafroll disease and associated viruses: a unique pathosystem. | Q38561055 | ||
| The effect of co- and superinfection on the adaptive dynamics of vesicular stomatitis virus | Q40261724 | ||
| Evolutionary potential of an RNA virus | Q40677633 | ||
| The Multiplicity of Cellular Infection Changes Depending on the Route of Cell Infection in a Plant Virus. | Q41106439 | ||
| Movement and nucleocapsid proteins coded by two tospovirus species interact through multiple binding regions in mixed infections. | Q41493402 | ||
| Apple latent spherical virus vector as vaccine for the prevention and treatment of mosaic diseases in pea, broad bean, and eustoma plants by bean yellow mosaic virus. | Q41667993 | ||
| Infection with strains of Citrus tristeza virus does not exclude superinfection by other strains of the virus | Q41821155 | ||
| The role of virulence in in vivo superinfection fitness of the vertebrate RNA virus infectious hematopoietic necrosis virus | Q41973717 | ||
| Different roles for RNA silencing and RNA processing components in virus recovery and virus-induced gene silencing in plants | Q42181779 | ||
| The games plant viruses play | Q42203792 | ||
| Uptake and regulation of resource allocation for optimal plant performance and adaptation to stress. | Q42231321 | ||
| Salicylic acid and jasmonic acid are essential for systemic resistance against tobacco mosaic virus in Nicotiana benthamiana | Q42241928 | ||
| Jasmonic acid negatively regulates resistance to Tobacco mosaic virus in tobacco | Q42266519 | ||
| Hepatitis C virus superinfection of liver grafts: a detailed analysis of early exclusion of non-dominant virus strains. | Q42994218 | ||
| The multiplicity of infection of a plant virus varies during colonization of its eukaryotic host | Q43096934 | ||
| Coinfection and superinfection in RNA virus populations: a selection-mutation model | Q43847253 | ||
| Replication of potato virus X RNA is altered in coinfections with potato virus Y. | Q44042343 | ||
| A coat-independent superinfection exclusion rapidly imposed in Nicotiana benthamiana cells by tobacco mosaic virus is not prevented by depletion of the movement protein. | Q44254515 | ||
| Antagonistic interactions between the SA and JA signaling pathways in Arabidopsis modulate expression of defense genes and gene-for-gene resistance to cucumber mosaic virus | Q44950558 | ||
| P433 | issue | 5 | |
| P921 | main subject | plant virus | Q1495434 |
| P304 | page(s) | 769-782 | |
| P577 | publication date | 2015-12-09 | |
| P1433 | published in | Molecular Plant Pathology | Q11937220 |
| P1476 | title | Antagonistic within-host interactions between plant viruses: molecular basis and impact on viral and host fitness | |
| P478 | volume | 17 |
| Q36273542 | A Framework for the Evaluation of Biosecurity, Commercial, Regulatory, and Scientific Impacts of Plant Viruses and Viroids Identified by NGS Technologies. |
| Q64077506 | Agroinoculation of Grapevine Pinot Gris Virus in tobacco and grapevine provides insights on viral pathogenesis |
| Q89860320 | Differential Accumulation of Innate- and Adaptive-Immune-Response-Derived Transcripts during Antagonism between Papaya Ringspot Virus and Papaya Mosaic Virus |
| Q59132097 | Exploring the Diversity of Mechanisms Associated With Plant Tolerance to Virus Infection |
| Q45332628 | Grapevine-virus-environment interactions: an intriguing puzzle to solve. |
| Q92048518 | Modelling Vector Transmission and Epidemiology of Co-Infecting Plant Viruses |
| Q40525847 | Novel Endorna-like viruses, including three with two open reading frames, challenge the membership criteria and taxonomy of the Endornaviridae |
| Q40139120 | Sequential acquisition of Potato virus Y strains by Myzus persicae favors the transmission of the emerging recombinant strains |
| Q39343415 | The Coat Protein and NIa Protease of Two Potyviridae Family Members Independently Confer Superinfection Exclusion |
| Q46252044 | The alkalophilic fungus Sodiomyces alkalinus hosts beta- and gammapartitiviruses together with a new fusarivirus |
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