scholarly article | Q13442814 |
P50 | author | Benoit Poinssot | Q56056894 |
David Wendehenne | Q43055703 | ||
P2093 | author name string | Felix Mauch | |
Andreas J Meyer | |||
Patrick Frettinger | |||
Laurent Marty | |||
Jan Vitecek | |||
Carole Dubreuil-Maurizi | |||
Lorelise Branciard | |||
P2860 | cites work | Isolation of phytoalexin-deficient mutants of Arabidopsis thaliana and characterization of their interactions with bacterial pathogens | Q24564026 |
Thiol-based regulation of redox-active glutamate-cysteine ligase from Arabidopsis thaliana | Q24564789 | ||
The NADPH-dependent thioredoxin system constitutes a functional backup for cytosolic glutathione reductase in Arabidopsis | Q24651469 | ||
Trp-dependent auxin biosynthesis in Arabidopsis: involvement of cytochrome P450s CYP79B2 and CYP79B3 | Q24682557 | ||
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method | Q25938999 | ||
Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana | Q27860555 | ||
The plant immune system | Q28131801 | ||
Hypersensitive response-related death | Q28200993 | ||
Isochorismate synthase is required to synthesize salicylic acid for plant defence | Q28209340 | ||
A glucosinolate metabolism pathway in living plant cells mediates broad-spectrum antifungal defense | Q28304506 | ||
MAP kinase signalling cascade in Arabidopsis innate immunity. | Q52594626 | ||
PHYTOALEXINS: What Have We Learned After 60 Years? | Q53988491 | ||
Salicylic acid induction-deficient mutants of Arabidopsis express PR-2 and PR-5 and accumulate high levels of camalexin after pathogen inoculation. | Q54082177 | ||
Inducible cell death in plant immunity | Q57748250 | ||
Reactive oxygen species signaling in response to pathogens | Q57748274 | ||
Nitrate efflux is an essential component of the cryptogein signaling pathway leading to defense responses and hypersensitive cell death in tobacco | Q74597716 | ||
Correlation of defense gene induction defects with powdery mildew susceptibility in Arabidopsis enhanced disease susceptibility mutants | Q77767179 | ||
Integrated signaling network involving calcium, nitric oxide, and active oxygen species but not mitogen-activated protein kinases in BcPG1-elicited grapevine defenses | Q83147691 | ||
Glutathione-indole-3-acetonitrile is required for camalexin biosynthesis in Arabidopsis thaliana | Q83216917 | ||
Nitric oxide contributes to cadmium toxicity in Arabidopsis by promoting cadmium accumulation in roots and by up-regulating genes related to iron uptake | Q83236573 | ||
The chloroplast protein RPH1 plays a role in the immune response of Arabidopsis to Phytophthora brassicae | Q83242461 | ||
Cross talk between reactive nitrogen and oxygen species during the hypersensitive disease resistance response | Q83947146 | ||
Reactive oxygen species: metabolism, oxidative stress, and signal transduction | Q29547615 | ||
Reconciling the chemistry and biology of reactive oxygen species | Q29615709 | ||
Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens | Q29616814 | ||
A renaissance of elicitors: perception of microbe-associated molecular patterns and danger signals by pattern-recognition receptors | Q29618149 | ||
The multifunctional enzyme CYP71B15 (PHYTOALEXIN DEFICIENT3) converts cysteine-indole-3-acetonitrile to camalexin in the indole-3-acetonitrile metabolic network of Arabidopsis thaliana | Q30319074 | ||
Molecular basis and structural insight of vascular K(ATP) channel gating by S-glutathionylation. | Q30498793 | ||
In vivo imaging of an elicitor-induced nitric oxide burst in tobacco. | Q30656439 | ||
Evidence for posttranscriptional activation of gamma-glutamylcysteine synthetase during plant stress responses | Q32015284 | ||
The ROOT MERISTEMLESS1/CADMIUM SENSITIVE2 gene defines a glutathione-dependent pathway involved in initiation and maintenance of cell division during postembryonic root development | Q33334246 | ||
Plant homologs of the Plasmodium falciparum chloroquine-resistance transporter, PfCRT, are required for glutathione homeostasis and stress responses | Q33719930 | ||
Arabidopsis gp91phox homologues AtrbohD and AtrbohF are required for accumulation of reactive oxygen intermediates in the plant defense response | Q33898379 | ||
Signal interactions between nitric oxide and reactive oxygen intermediates in the plant hypersensitive disease resistance response | Q33949486 | ||
Photorespiratory metabolism: genes, mutants, energetics, and redox signaling | Q34018398 | ||
Inducers of plant systemic acquired resistance regulate NPR1 function through redox changes | Q34210476 | ||
Nutrient requirements of suspension cultures of soybean root cells | Q34237145 | ||
Control of salicylic acid synthesis and systemic acquired resistance by two members of a plant-specific family of transcription factors | Q34241378 | ||
Significance of inducible defense-related proteins in infected plants. | Q34511918 | ||
Structural basis for the redox control of plant glutamate cysteine ligase. | Q34536831 | ||
Early signaling events induced by elicitors of plant defenses. | Q34569067 | ||
The hypersensitive response; the centenary is upon us but how much do we know? | Q34586065 | ||
Identification of PAD2 as a gamma-glutamylcysteine synthetase highlights the importance of glutathione in disease resistance of Arabidopsis | Q34587091 | ||
Thiol/Disulfide Redox Switches in the Regulation of Heme Binding to Proteins | Q34589250 | ||
Redox-sensitive GFP in Arabidopsis thaliana is a quantitative biosensor for the redox potential of the cellular glutathione redox buffer. | Q34692491 | ||
Real-time imaging of the intracellular glutathione redox potential. | Q34777807 | ||
Confocal imaging of glutathione redox potential in living plant cells. | Q34823352 | ||
The role and regulation of programmed cell death in plant-pathogen interactions. | Q35649325 | ||
THE FUNCTIONS AND REGULATION OF GLUTATHIONE S-TRANSFERASES IN PLANTS. | Q35687249 | ||
NPR1: the spider in the web of induced resistance signaling pathways | Q35825051 | ||
Reactive oxygen gene network of plants. | Q35909671 | ||
Glutathione, photosynthesis and the redox regulation of stress-responsive gene expression | Q36331491 | ||
Biology and biochemistry of glucosinolates | Q36466513 | ||
Calcium in plant defence-signalling pathways | Q36546545 | ||
Metabolic signalling in defence and stress: the central roles of soluble redox couples | Q36642382 | ||
New insights into nitric oxide signaling in plants | Q37010167 | ||
Regulation of the cardiac muscle ryanodine receptor by O(2) tension and S-nitrosoglutathione | Q37085577 | ||
Comparing signaling mechanisms engaged in pattern-triggered and effector-triggered immunity. | Q37752814 | ||
Ascorbate and glutathione: the heart of the redox hub. | Q37825997 | ||
Production of reactive oxygen species by plant NADPH oxidases. | Q39419866 | ||
Mechanisms of nitric-oxide-induced increase of free cytosolic Ca2+ concentration in Nicotiana plumbaginifolia cells | Q40288912 | ||
Use of Arabidopsis for genetic dissection of plant defense responses | Q41689508 | ||
The gene controlling the indole glucosinolate modifier1 quantitative trait locus alters indole glucosinolate structures and aphid resistance in Arabidopsis | Q42025932 | ||
The glutathione-deficient mutant pad2-1 accumulates lower amounts of glucosinolates and is more susceptible to the insect herbivore Spodoptera littoralis | Q42029316 | ||
Arabidopsis GLUTATHIONE REDUCTASE1 plays a crucial role in leaf responses to intracellular hydrogen peroxide and in ensuring appropriate gene expression through both salicylic acid and jasmonic acid signaling pathways. | Q43057979 | ||
Disease resistance of Arabidopsis to Phytophthora brassicae is established by the sequential action of indole glucosinolates and camalexin | Q43129338 | ||
Early signaling through the Arabidopsis pattern recognition receptors FLS2 and EFR involves Ca-associated opening of plasma membrane anion channels. | Q43180395 | ||
Cryptogein-induced anion effluxes: electrophysiological properties and analysis of the mechanisms through which they contribute to the elicitor-triggered cell death. | Q43190178 | ||
Characterization of an Arabidopsis-Phytophthora pathosystem: resistance requires a functional PAD2 gene and is independent of salicylic acid, ethylene and jasmonic acid signalling. | Q43808825 | ||
The plasma membrane oxidase NtrbohD is responsible for AOS production in elicited tobacco cells | Q44066511 | ||
Characterization of the early response of Arabidopsis to Alternaria brassicicola infection using expression profiling. | Q44477444 | ||
Arabidopsis local resistance to Botrytis cinerea involves salicylic acid and camalexin and requires EDS4 and PAD2, but not SID2, EDS5 or PAD4. | Q44505294 | ||
The Arabidopsis NPR1 disease resistance protein is a novel cofactor that confers redox regulation of DNA binding activity to the basic domain/leucine zipper transcription factor TGA1. | Q44571755 | ||
Characterisation of an Arabidopsis-Leptosphaeria maculans pathosystem: resistance partially requires camalexin biosynthesis and is independent of salicylic acid, ethylene and jasmonic acid signalling | Q44693257 | ||
Arabidopsis thaliana glutamate-cysteine ligase: functional properties, kinetic mechanism, and regulation of activity | Q44924238 | ||
Evidence for a direct link between glutathione biosynthesis and stress defense gene expression in Arabidopsis | Q45016725 | ||
Glucosinolate engineering identifies a gamma-glutamyl peptidase. | Q45988823 | ||
The AtrbohD-mediated oxidative burst elicited by oligogalacturonides in Arabidopsis is dispensable for the activation of defense responses effective against Botrytis cinerea | Q46368265 | ||
Kinetics of salicylate-mediated suppression of jasmonate signaling reveal a role for redox modulation | Q46551303 | ||
H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response | Q46598823 | ||
The use of voltage-sensitive dyes to monitor signal-induced changes in membrane potential-ABA triggered membrane depolarization in guard cells | Q46684595 | ||
The redox switch of gamma-glutamylcysteine ligase via a reversible monomer-dimer transition is a mechanism unique to plants | Q46697262 | ||
Characterization of two Arabidopsis thaliana glutathione S-transferases | Q46991205 | ||
The glutathione-deficient, cadmium-sensitive mutant, cad2-1, of Arabidopsis thaliana is deficient in gamma-glutamylcysteine synthetase | Q48009318 | ||
Nitric oxide- and hydrogen peroxide-responsive gene regulation during cell death induction in tobacco | Q48092797 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | glutathione | Q116907 |
P1104 | number of pages | 13 | |
P304 | page(s) | 2000-2012 | |
P577 | publication date | 2011-10-17 | |
P1433 | published in | Plant Physiology | Q3906288 |
P1476 | title | Glutathione deficiency of the Arabidopsis mutant pad2-1 affects oxidative stress-related events, defense gene expression, and the hypersensitive response | |
P478 | volume | 157 |
Q44644030 | A perturbation in glutathione biosynthesis disrupts endoplasmic reticulum morphology and secretory membrane traffic in Arabidopsis thaliana |
Q46256139 | A phi-class glutathione S-transferase gene for Verticillium wilt resistance in Gossypium arboreum identified in a genome-wide association study |
Q64260059 | Application of Data-Independent Acquisition Approach to Study the Proteome Change from Early to Later Phases of Tomato Pathogenesis Responses |
Q38898876 | Arabidopsis HEAT SHOCK TRANSCRIPTION FACTORA1b overexpression enhances water productivity, resistance to drought, and infection |
Q36817352 | Arabidopsis redox status in response to caterpillar herbivory. |
Q41699758 | Association genetics, geography and ecophysiology link stomatal patterning in Populus trichocarpa with carbon gain and disease resistance trade-offs |
Q41918236 | Both the concentration and redox state of glutathione and ascorbate influence the sensitivity of arabidopsis to cadmium. |
Q28543511 | Cadmium-induced hydrogen sulfide synthesis is involved in cadmium tolerance in Medicago sativa by reestablishment of reduced (homo)glutathione and reactive oxygen species homeostases |
Q38370290 | Contribution of glutathione to the control of cellular redox homeostasis under toxic metal and metalloid stress. |
Q47095558 | Effects of Combined Low Glutathione with Mild Oxidative and Low Phosphorus Stress on the Metabolism of Arabidopsis thaliana |
Q36743435 | Expression Patterns of Genes Involved in Ascorbate-Glutathione Cycle in Aphid-Infested Maize (Zea mays L.) Seedlings |
Q39934763 | Functional analysis of Arabidopsis mutants points to novel roles for glutathione in coupling H(2)O(2) to activation of salicylic acid accumulation and signaling. |
Q36915550 | Glutathione and tryptophan metabolism are required for Arabidopsis immunity during the hypersensitive response to hemibiotrophs. |
Q38225319 | Heavy-metal-induced reactive oxygen species: phytotoxicity and physicochemical changes in plants |
Q35230151 | Imposed glutathione-mediated redox switch modulates the tobacco wound-induced protein kinase and salicylic acid-induced protein kinase activation state and impacts on defence against Pseudomonas syringae |
Q38943059 | Increased glutathione contributes to stress tolerance and global translational changes in Arabidopsis. |
Q33734505 | Network Analysis Reveals a Common Host-Pathogen Interaction Pattern in Arabidopsis Immune Responses |
Q42503058 | Nitric oxide production mediates oligogalacturonide-triggered immunity and resistance to Botrytis cinerea in Arabidopsis thaliana. |
Q38165736 | Pectin-modifying enzymes and pectin-derived materials: applications and impacts |
Q51203883 | Post-Translational Regulation of the Dicing Activities of Arabidopsis DICER-LIKE 3 and 4 by Inorganic Phosphate and the Redox State. |
Q36488003 | Pseudomonas syringae enhances herbivory by suppressing the reactive oxygen burst in Arabidopsis |
Q35148365 | Quantitative phosphoproteomics of the ataxia telangiectasia-mutated (ATM) and ataxia telangiectasia-mutated and rad3-related (ATR) dependent DNA damage response in Arabidopsis thaliana |
Q49601521 | Redox and the circadian clock in plant immunity: A balancing act. |
Q51529125 | Redox regulation of free amino acid levels in Arabidopsis thaliana. |
Q42517368 | Regulation of basal and oxidative stress-triggered jasmonic acid-related gene expression by glutathione |
Q37987004 | Role of glutathione in plant signaling under biotic stress |
Q46774654 | S-nitrosylation positively regulates ascorbate peroxidase activity during plant stress responses. |
Q35194086 | Salicylic acid and reactive oxygen species interplay in the transcriptional control of defense genes expression |
Q36295679 | Salicylic acid-related cotton (Gossypium arboreum) ribosomal protein GaRPL18 contributes to resistance to Verticillium dahliae |
Q54979248 | Sulfur partitioning between glutathione and protein synthesis determines plant growth. |
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Q38923724 | The Polyadenylation Factor Subunit CLEAVAGE AND POLYADENYLATION SPECIFICITY FACTOR30: A Key Factor of Programmed Cell Death and a Regulator of Immunity in Arabidopsis. |
Q48962653 | The Ralstonia solanacearum type III effector RipAY targets plant redox regulators to suppress immune responses. |
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Q45783635 | The grapevine flagellin receptor VvFLS2 differentially recognizes flagellin-derived epitopes from the endophytic growth-promoting bacterium Burkholderia phytofirmans and plant pathogenic bacteria. |
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