| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.1364-3703.2008.00529.X |
| P8608 | Fatcat ID | release_mq67yyxlwjaylhmwivefgw3kbu |
| P932 | PMC publication ID | 6640368 |
| P698 | PubMed publication ID | 19236577 |
| P5875 | ResearchGate publication ID | 24034304 |
| P50 | author | Francisca Blanco-Herrera | Q61113964 |
| Nicolás M Cecchini | Q83308983 | ||
| Mariela Inés Monteoliva | Q83390559 | ||
| P2093 | author name string | María Elena Alvarez | |
| Loreto Holuigue | |||
| P2860 | cites work | The plant immune system | Q28131801 |
| Are innate immune signaling pathways in plants and animals conserved? | Q28273570 | ||
| A J domain virulence effector of Pseudomonas syringae remodels host chloroplasts and suppresses defenses | Q28492431 | ||
| Identification of novel hrp-regulated genes through functional genomic analysis of the Pseudomonas syringae pv. tomato DC3000 genome | Q29346742 | ||
| Host-microbe interactions: shaping the evolution of the plant immune response | Q29617734 | ||
| Identification of new early markers of the hypersensitive response in Arabidopsis thaliana(1). | Q30789465 | ||
| A novel myb oncogene homologue in Arabidopsis thaliana related to hypersensitive cell death | Q30817394 | ||
| Type III secretion system effector proteins: double agents in bacterial disease and plant defense | Q34337243 | ||
| The hypersensitive response; the centenary is upon us but how much do we know? | Q34586065 | ||
| A Pseudomonas syringae type III effector suppresses cell wall-based extracellular defense in susceptible Arabidopsis plants | Q35168706 | ||
| The role and regulation of programmed cell death in plant-pathogen interactions. | Q35649325 | ||
| Influence of Pseudomonas syringae culture conditions on initiation of the hypersensitive response of culture tobacco cells | Q36072158 | ||
| Elicitor-stimulated ion fluxes and O2- from the oxidative burst are essential components in triggering defense gene activation and phytoalexin synthesis in parsley | Q36147979 | ||
| Pathogen virulence factors as molecular probes of basic plant cellular functions | Q36226077 | ||
| Closing the circle on the discovery of genes encoding Hrp regulon members and type III secretion system effectors in the genomes of three model Pseudomonas syringae strains | Q36638315 | ||
| Elicitors, effectors, and R genes: the new paradigm and a lifetime supply of questions | Q36824062 | ||
| Pattern-recognition receptors in plant innate immunity. | Q37060714 | ||
| Two Pseudomonas syringae type III effectors inhibit RIN4-regulated basal defense in Arabidopsis | Q42479313 | ||
| Production of reactive oxygen species in Arabidopsis thaliana cell suspension cultures in response to an elicitor from Fusarium oxysporum: implications for basal resistance | Q42495816 | ||
| Method for the extraction of the volatile compound salicylic acid from tobacco leaf material | Q43920801 | ||
| THE OXIDATIVE BURST IN PLANT DISEASE RESISTANCE. | Q44073104 | ||
| Role of CG and non-CG methylation in immobilization of transposons in Arabidopsis | Q44348859 | ||
| Harpin inactivates mitochondria in Arabidopsis suspension cells | Q44764970 | ||
| Proline accumulation and AtP5CS2 gene activation are induced by plant-pathogen incompatible interactions in Arabidopsis | Q44839462 | ||
| The Hypersensitive Reaction of Tobacco to Pseudomonas syringae pv. pisi: Activation of a Plasmalemma K/H Exchange Mechanism | Q44866393 | ||
| Reactive oxygen intermediates mediate a systemic signal network in the establishment of plant immunity | Q46230697 | ||
| H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response | Q46598823 | ||
| Identification of NPR1-dependent and independent genes early induced by salicylic acid treatment in Arabidopsis. | Q46819603 | ||
| Molecular cloning of a sulfotransferase in Arabidopsis thaliana and regulation during development and in response to infection with pathogenic bacteria | Q48065933 | ||
| Layered basal defenses underlie non-host resistance of Arabidopsis to Pseudomonas syringae pv. phaseolicola. | Q52579853 | ||
| Arabidopsis NHO1 is required for general resistance against Pseudomonas bacteria. | Q54018070 | ||
| Expression profiling of the host response to bacterial infection: the transition from basal to induced defence responses in RPM1-mediated resistance | Q73055783 | ||
| The Active Oxygen Response of Cell Suspensions to Incompatible Bacteria Is Not Sufficient to Cause Hypersensitive Cell Death | Q74776180 | ||
| Plants have a sensitive perception system for the most conserved domain of bacterial flagellin | Q77908621 | ||
| Comparative biochemistry of the oxidative burst produced by rose and french bean cells reveals two distinct mechanisms | Q95432329 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 2 | |
| P921 | main subject | photosynthesis | Q11982 |
| Arabidopsis thaliana | Q158695 | ||
| P304 | page(s) | 305-310 | |
| P577 | publication date | 2009-03-01 | |
| P1433 | published in | Molecular Plant Pathology | Q11937220 |
| P1476 | title | Features of basal and race-specific defences in photosynthetic Arabidopsis thaliana suspension cultured cells | |
| P478 | volume | 10 |
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