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Increased glutathione contributes to stress tolerance and global translational changes in Arabidopsis

https://doi.org/10.1111/tpj.12940
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s00299-010-0902-0openalex-snapshot
Arabidopsis root growth dependence on glutathione is linked to auxin transport
inferredcites →https://doi.org/10.1016/0003-2697(80)90139-6openalex-snapshot
Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine
inferredcites →https://doi.org/10.1016/0304-4211(84)90198-6openalex-snapshot
Increased levels of glutathione in a catalase-deficient mutant of barley (Hordeum vulgare L.)
inferredcites →https://doi.org/10.1016/j.tplants.2009.11.009openalex-snapshot
Proline: a multifunctional amino acid
inferredcites →https://doi.org/10.1016/s0021-9258(18)35980-5openalex-snapshot
Potent and specific inhibition of glutathione synthesis by buthionine sulfoximine (S-n-butyl homocysteine sulfoximine).
inferredcites →https://doi.org/10.1016/s0891-5849(01)00480-4openalex-snapshot
Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple
inferredcites →https://doi.org/10.1016/s0968-0004(02)02191-6openalex-snapshot
Nanotransducers in cellular redox signaling: modification of thiols by reactive oxygen and nitrogen species
inferredcites →https://doi.org/10.1016/s1360-1385(00)01601-0openalex-snapshot
Plant glutathione S -transferases: enzymes with multiple functions in sickness and in health
inferredcites →https://doi.org/10.1016/s1360-1385(99)01386-2openalex-snapshot
Selective translation of cytoplasmic mRNAs in plants
inferredcites →https://doi.org/10.1038/6198openalex-snapshot
Plants ectopically expressing the ironbinding protein, ferritin, are tolerant to oxidative damage and pathogens
inferredcites →https://doi.org/10.1038/7036openalex-snapshot
Improving plant drought, salt, and freezing tolerance by gene transfer of a single stress-inducible transcription factor
inferredcites →https://doi.org/10.1038/msb.2011.97openalex-snapshot
Widespread translational control contributes to the regulation of Arabidopsis photomorphogenesis
inferredcites →https://doi.org/10.1038/nmeth.1212openalex-snapshot
Real-time imaging of the intracellular glutathione redox potential
inferredcites →https://doi.org/10.1038/nprot.2008.211openalex-snapshot
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
inferredcites →https://doi.org/10.1038/sj.emboj.7600121openalex-snapshot
The Arabidopsis cytochrome P450 CYP707A encodes ABA 8′‐hydroxylases: key enzymes in ABA catabolism
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01657.xopenalex-snapshot
Transcriptome analysis of sulfur depletion in Arabidopsis thaliana: interlacing of biosynthetic pathways provides response specificity
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01786.xopenalex-snapshot
Molecular characterization of the Arabidopsis 9 ‐cis epoxycarotenoid dioxygenase gene family
inferredcites →https://doi.org/10.1073/pnas.0605639103openalex-snapshot
Dual function of an Arabidopsis transcription factor DREB2A in water-stress-responsive and heat-stress-responsive gene expression
inferredcites →https://doi.org/10.1073/pnas.1108434108openalex-snapshot
The main auxin biosynthesis pathway in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.84.2.439openalex-snapshot
Phytochelatins, a class of heavy-metal-binding peptides from plants, are functionally analogous to metallothioneins
inferredcites →https://doi.org/10.1073/pnas.85.18.6738openalex-snapshot
Glutathione and fungal elicitor regulation of a plant defense gene promoter in electroporated protoplasts
inferredcites →https://doi.org/10.1073/pnas.86.18.6838openalex-snapshot
Phytochelatins, the heavy-metal-binding peptides of plants, are synthesized from glutathione by a specific γ-glutamylcysteine dipeptidyl transpeptidase (phytochelatin synthase)
inferredcites →https://doi.org/10.1093/jexbot/52.363.1991openalex-snapshot
The long‐distance abscisic acid signal in the droughted plant: the fate of the hormone on its way from root to shoot
inferredcites →https://doi.org/10.1093/jexbot/53.366.27openalex-snapshot
Abscisic acid in the xylem: where does it come from, where does it go to?
inferredcites →https://doi.org/10.1093/jexbot/53.372.1283openalex-snapshot
Interactions between biosynthesis, compartmentation and transport in the control of glutathione homeostasis and signalling
inferredcites →https://doi.org/10.1093/mp/ssp008openalex-snapshot
Pyridine Nucleotide Cycling and Control of Intracellular Redox State in Relation to Poly (ADP-Ribose) Polymerase Activity and Nuclear Localization of Glutathione during Exponential Growth of Arabidopsis Cells in Culture
inferredcites →https://doi.org/10.1093/pcp/pch179openalex-snapshot
Induction of PR-1 Accumulation Accompanied by Runaway Cell Death in the lsd1 Mutant of Arabidopsis is Dependent on Glutathione Levels but Independent of the Redox State of Glutathione
inferredcites →https://doi.org/10.1104/pp.008243openalex-snapshot
Control of Demand-Driven Biosynthesis of Glutathione in Green Arabidopsis Suspension Culture Cells
inferredcites →https://doi.org/10.1104/pp.103.033027openalex-snapshot
Intercellular Distribution of Glutathione Synthesis in Maize Leaves and Its Response to Short-Term Chilling
inferredcites →https://doi.org/10.1104/pp.103.037614openalex-snapshot
Arabidopsis CYP707A s Encode (+)-Abscisic Acid 8′-Hydroxylase, a Key Enzyme in the Oxidative Catabolism of Abscisic Acid
inferredcites →https://doi.org/10.1104/pp.103.2.621openalex-snapshot
Oxidative Stimulation of Glutathione Synthesis in Arabidopsis thaliana Suspension Cultures
inferredcites →https://doi.org/10.1104/pp.104.048579openalex-snapshot
Weeds, Worms, and More. Papain's Long-Lost Cousin, Phytochelatin Synthase
inferredcites →https://doi.org/10.1104/pp.106.077701openalex-snapshot
Response of the Leaf Cell Wall to Desiccation in the Resurrection Plant Myrothamnus flabellifolius
inferredcites →https://doi.org/10.1104/pp.106.077982openalex-snapshot
Maturation of Arabidopsis Seeds Is Dependent on Glutathione Biosynthesis within the Embryo
inferredcites →https://doi.org/10.1104/pp.110.153767openalex-snapshot
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
inferredcites →https://doi.org/10.1104/pp.110.167569openalex-snapshot
Ascorbate and Glutathione: The Heart of the Redox Hub
inferredcites →https://doi.org/10.1104/pp.111.181875openalex-snapshot
Drought and Salt Stress Tolerance of an Arabidopsis Glutathione S-Transferase U17 Knockout Mutant Are Attributed to the Combined Effect of Glutathione and Abscisic Acid
inferredcites →https://doi.org/10.1104/pp.111.182667openalex-snapshot
Glutathione Deficiency of the Arabidopsis Mutant pad2-1 Affects Oxidative Stress-Related Events, Defense Gene Expression, and the Hypersensitive Response
inferredcites →https://doi.org/10.1104/pp.111.183210openalex-snapshot
Essential Role of Tissue-Specific Proline Synthesis and Catabolism in Growth and Redox Balance at Low Water Potential
inferredcites →https://doi.org/10.1104/pp.113.1.93openalex-snapshot
Expression and RNA Splicing of the Maize Glutathione S-Transferase Bronze2 Gene Is Regulated by Cadmium and Other Stresses
inferredcites →https://doi.org/10.1104/pp.113.217208openalex-snapshot
Glutamate Receptor-Like Channel3.3 Is Involved in Mediating Glutathione-Triggered Cytosolic Calcium Transients, Transcriptional Changes, and Innate Immunity Responses in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.113.233585openalex-snapshot
Scavenging Iron: A Novel Mechanism of Plant Immunity Activation by Microbial Siderophores
inferredcites →https://doi.org/10.1104/pp.121.4.1169openalex-snapshot
Cadmium Tolerance and Accumulation in Indian Mustard Is Enhanced by Overexpressing γ-Glutamylcysteine Synthetase
inferredcites →https://doi.org/10.1104/pp.124.4.1854openalex-snapshot
Overexpression of the ArabidopsisCBF3Transcriptional Activator Mimics Multiple Biochemical Changes Associated with Cold Acclimation
inferredcites →https://doi.org/10.1104/pp.87.1.206openalex-snapshot
Glutathione Causes a Massive and Selective Induction of Plant Defense Genes
inferredcites →https://doi.org/10.1105/tpc.10.9.1539openalex-snapshot
Glutathione Metabolic Genes Coordinately Respond to Heavy Metals and Jasmonic Acid in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.104.022608openalex-snapshot
Evidence for a Direct Link between Glutathione Biosynthesis and Stress Defense Gene Expression in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.107.050849openalex-snapshot
Inactivation of Thioredoxin Reductases Reveals a Complex Interplay between Thioredoxin and Glutathione Pathways in Arabidopsis Development
inferredcites →https://doi.org/10.1105/tpc.107.055566openalex-snapshot
Arabidopsis WRKY38 and WRKY62 Transcription Factors Interact with Histone Deacetylase 19 in Basal Defense
inferredcites →https://doi.org/10.1105/tpc.109.069757openalex-snapshot
Cotranslational Proteolysis Dominates Glutathione Homeostasis to Support Proper Growth and Development
inferredcites →https://doi.org/10.1105/tpc.109.071225openalex-snapshot
Interplay between the NADP-Linked Thioredoxin and Glutathione Systems in Arabidopsis Auxin Signaling
inferredcites →https://doi.org/10.1105/tpc.11.7.1277openalex-snapshot
Elevated Glutathione Biosynthetic Capacity in the Chloroplasts of Transgenic Tobacco Plants Paradoxically Causes Increased Oxidative Stress
inferredcites →https://doi.org/10.1105/tpc.12.1.97openalex-snapshot
The ROOT MERISTEMLESS1 / CADMIUM SENSITIVE2 Gene Defines a Glutathione-Dependent Pathway Involved in Initiation and Maintenance of Cell Division during Postembryonic Root Development
inferredcites →https://doi.org/10.1105/tpc.7.9.1405openalex-snapshot
Superroot, a recessive mutation in Arabidopsis, confers auxin overproduction.
inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02400.xopenalex-snapshot
Glutathione in plants: an integrated overview
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02269.xopenalex-snapshot
Differential targeting of GSH1 and GSH2 is achieved by multiple transcription initiation: implications for the compartmentation of glutathione biosynthesis in the Brassicaceae
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02938.xopenalex-snapshot
Identification of PAD2 as a γ‐glutamylcysteine synthetase highlights the importance of glutathione in disease resistance of Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03263.xopenalex-snapshot
Conditional oxidative stress responses in the Arabidopsis photorespiratory mutant cat2 demonstrate that redox state is a key modulator of daylength‐dependent gene expression, and define photoperiod as a crucial factor in the regulation of H 2 O 2 ‐induced cell death
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03280.xopenalex-snapshot
Redox‐sensitive GFP in Arabidopsis thaliana is a quantitative biosensor for the redox potential of the cellular glutathione redox buffer
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03389.xopenalex-snapshot
Restricting glutathione biosynthesis to the cytosol is sufficient for normal plant development
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04371.xopenalex-snapshot
Recruitment of glutathione into the nucleus during cell proliferation adjusts whole-cell redox homeostasis in Arabidopsis thaliana and lowers the oxidative defence shield
inferredcites →https://doi.org/10.1111/j.1467-7652.2005.00169.xopenalex-snapshot
Plant cell wall biosynthesis: genetic, biochemical and functional genomics approaches to the identification of key genes
inferredcites →https://doi.org/10.1111/pce.12048openalex-snapshot
Regulation of basal and oxidative stress‐triggered jasmonic acid‐related gene expression by glutathione
inferredcites →https://doi.org/10.1146/annurev.arplant.53.100301.135154openalex-snapshot
P HYTOCHELATINS AND M ETALLOTHIONEINS : Roles in Heavy Metal Detoxification and Homeostasis
inferredcites →https://doi.org/10.1186/1471-2229-11-54openalex-snapshot
Glutathione synthesis is essential for pollen germination in vitro
inferredcites →https://doi.org/10.1199/tab.0058openalex-snapshot
Abscisic Acid Biosynthesis and Response
inferredcites →https://doi.org/10.1199/tab.0140openalex-snapshot
Proline Metabolism and Its Implications for Plant-Environment Interaction

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/etc.4909openalex-snapshot
Phytohormonal Roles in Plant Responses to Heavy Metal Stress: Implications for Using Macrophytes in Phytoremediation of Aquatic Ecosystems
inferred← citeshttps://doi.org/10.1002/jpln.201800692openalex-snapshot
Glutathione foliar fertilisation prevents lime‐induced iron chlorosis in soil grownMedicago scutellata
inferred← citeshttps://doi.org/10.1007/124_2023_73openalex-snapshot
Serine Metabolic Networks in Plants
inferred← citeshttps://doi.org/10.1007/978-3-030-45975-8_7openalex-snapshot
Heavy Metal-Induced Oxidative Stress and Related Cellular Process
inferred← citeshttps://doi.org/10.1007/978-3-030-79229-9_11openalex-snapshot
A Dynamic Crosstalk Between GSH and Salicylic Acid to Mitigate Environmental Stress
inferred← citeshttps://doi.org/10.1007/978-3-319-44081-1_9openalex-snapshot
Glutathione and Related Enzymes in Response to Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-3-319-66682-2_15openalex-snapshot
The Signaling Roles of Glutathione in Plant Disease Resistance
inferred← citeshttps://doi.org/10.1007/978-3-319-66682-2_18openalex-snapshot
Transgenic Plants Over-expressing Glutathione Biosynthetic Genes and Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.1007/978-3-319-66682-2_8openalex-snapshot
Exogenous Glutathione-Mediated Abiotic Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1007/978-981-10-5254-5_12openalex-snapshot
Contribution of Glutathione in Heavy Metal Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1007/978-981-10-9044-8_10openalex-snapshot
The Role of Sulfur in Plant Abiotic Stress Tolerance: Molecular Interactions and Defense Mechanisms
inferred← citeshttps://doi.org/10.1007/978-981-15-2172-0_9openalex-snapshot
Biochemical and Molecular Mechanisms of Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.1007/978-981-16-5059-8_7openalex-snapshot
Role of Phytohormones in Antioxidant Metabolism in Plants under Salinity and Water Stress
inferred← citeshttps://doi.org/10.1007/978-981-19-9794-5_5openalex-snapshot
The Ecology of Reactive Oxygen Species Signalling
inferred← citeshttps://doi.org/10.1007/s00299-026-03990-8openalex-snapshot
Temporal dynamics of sulphur mediated alleviation of lead toxicity in Brassica juncea
inferred← citeshttps://doi.org/10.1007/s00344-017-9691-9openalex-snapshot
Exogenous Glutathione Modulates Salinity Tolerance of Soybean [Glycine max (L.) Merrill] at Reproductive Stage
inferred← citeshttps://doi.org/10.1007/s00344-018-9832-9openalex-snapshot
Role of Exogenous Glutathione in Alleviating Abiotic Stress in Maize (Zea mays L.)
inferred← citeshttps://doi.org/10.1007/s00344-022-10789-wopenalex-snapshot
Long-Term Effects of Cold Atmospheric Plasma-Treated Water on the Antioxidative System of Hordeum vulgare
inferred← citeshttps://doi.org/10.1007/s00344-024-11402-yopenalex-snapshot
Exogenous Glutathione Enhances Salt Tolerance in Kenaf by Mediating Modulation of Oxidative Stress Response and DNA Methylation
inferred← citeshttps://doi.org/10.1007/s00344-024-11476-8openalex-snapshot
Unfolding the Role of Glutathione to Combat Environmental Stresses Through “Omics”-Based Approaches/Studies
inferred← citeshttps://doi.org/10.1007/s00709-017-1127-7openalex-snapshot
Isolation and functional characterization of 3-phosphoglycerate dehydrogenase involved in salt responses in sugar beet
inferred← citeshttps://doi.org/10.1007/s10646-017-1843-yopenalex-snapshot
miR398 and miR395 are involved in response to SO2 stress in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10725-018-0391-7openalex-snapshot
Interactions between plant hormones and thiol-related heavy metal chelators
inferred← citeshttps://doi.org/10.1007/s10811-021-02483-3openalex-snapshot
Quantitative label-free proteomics and biochemical analysis of Phaeodactylum tricornutum cultivation on dairy manure wastewater
inferred← citeshttps://doi.org/10.1007/s11101-021-09786-wopenalex-snapshot
Plant metabolomics in biotic and abiotic stress: a critical overview
inferred← citeshttps://doi.org/10.1007/s11101-023-09862-3openalex-snapshot
The effects of exogenously applied antioxidants on plant growth and resilience
inferred← citeshttps://doi.org/10.1007/s11104-019-04314-4openalex-snapshot
Glutathione supplementation prevents iron deficiency in Medicago scutellata grown in rock sand under different levels of bicarbonate
inferred← citeshttps://doi.org/10.1007/s11240-020-01787-5openalex-snapshot
AAL-toxin induced stress in Arabidopsis thaliana is alleviated through GSH-mediated salicylic acid and ethylene pathways
inferred← citeshttps://doi.org/10.1007/s12298-017-0422-2openalex-snapshot
Glutathione in plants: biosynthesis and physiological role in environmental stress tolerance
inferred← citeshttps://doi.org/10.1007/s12374-016-0057-9openalex-snapshot
Magnificant role of intracellular reactive oxygen species production and its scavenging encompasses downstream processes
inferred← citeshttps://doi.org/10.1007/s12374-020-09265-3openalex-snapshot
Exogenous Glycinebetaine Application Contributes to Abiotic Stress Tolerance in Maize
inferred← citeshttps://doi.org/10.1007/s12892-023-00201-8openalex-snapshot
Evaluation and clustering of rice cultivars tolerance to salt and drought stresses using morpho-physiological and biochemical indices
inferred← citeshttps://doi.org/10.1007/s13237-018-0256-5openalex-snapshot
Transcriptomic changes under stress conditions with special reference to glutathione contents
inferred← citeshttps://doi.org/10.1007/s13237-019-00288-xopenalex-snapshot
Deciphering the involvement of glutathione in phytohormone signaling pathways to mitigate stress in planta
inferred← citeshttps://doi.org/10.1007/s13562-021-00725-6openalex-snapshot
Genome-wide analysis of tomato WIP family genes and their response to salt stress under glutathione treatment
inferred← citeshttps://doi.org/10.1007/s40415-023-00942-4openalex-snapshot
Glutathione and zinc application upregulate the antioxidant system increasing photosynthetic pigments and growth under water stress in maize (Zea mays L.)
inferred← citeshttps://doi.org/10.1007/s40995-020-00917-0openalex-snapshot
Exogenous Glutathione-Mediated Drought Stress Tolerance in Rice (Oryza sativa L.) is Associated with Lower Oxidative Damage and Favorable Ionic Homeostasis
inferred← citeshttps://doi.org/10.1007/s42729-023-01299-zopenalex-snapshot
Glutathione Alleviates Chromium Stress and Promotes Growth of Pisum sativum L. by Improving Nutrient Orchestration, Proline, and Physiochemical Attributes
inferred← citeshttps://doi.org/10.1016/b978-0-12-812689-9.00003-0openalex-snapshot
Environmental Stresses and Metabolomics—Deciphering the Role of Stress Responsive Metabolites
inferred← citeshttps://doi.org/10.1016/bs.abr.2022.02.020openalex-snapshot
Redox metabolism in soybean and its significance in nitrogen-fixing nodules
inferred← citeshttps://doi.org/10.1016/bs.abr.2022.11.004openalex-snapshot
The ascorbate/glutathione cycle
inferred← citeshttps://doi.org/10.1016/j.bcab.2020.101744openalex-snapshot
Impact of glutathione on enhancing sunflower growth and biochemical aspects and yield to alleviate salinity stress
inferred← citeshttps://doi.org/10.1016/j.biochi.2023.12.002openalex-snapshot
Glutathione is required for growth and cadmium tolerance in the amphibian chytrid fungus, Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1016/j.cbd.2025.101671openalex-snapshot
Hydrolyzed Debaryomyces hansenii yeasts as paraprobiotics in fish: Omics-based characterization of Atlantic salmon gut during a natural pathogen outbreak in seawater stage
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.111616openalex-snapshot
Enhanced vacuole compartmentalization of cadmium in root cells contributes to glutathione-induced reduction of cadmium translocation from roots to shoots in pakchoi (Brassica chinensis L.)
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.112682openalex-snapshot
Integrated analysis of miRNA-mRNA regulatory networks of potato (Solanum tuberosum L.) in response to cadmium stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2016.09.009openalex-snapshot
Plant growth-promoting endophyte Sphingomonas sp. LK11 alleviates salinity stress in Solanum pimpinellifolium
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.12.021openalex-snapshot
Overexpression of GmNAC085 enhances drought tolerance in Arabidopsis by regulating glutathione biosynthesis, redox balance and glutathione-dependent detoxification of reactive oxygen species and methylglyoxal
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Friend or foe? Reactive oxygen species production, scavenging and signaling in plant response to environmental stresses
inferred← citeshttps://doi.org/10.1016/j.hpj.2022.09.002openalex-snapshot
Comparison of transcriptome and metabolome analysis revealed differences in cold resistant metabolic pathways in different apple cultivars under low temperature stress
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.145894openalex-snapshot
mdm-miR395 targets MdAPS1(ATP sulfurylase 1) to regulate sulfur homeostasis and anthocyanin accumulation in Malus
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.122312openalex-snapshot
Bna.GSH1 mediate the ABA signal to promote the tolerance of cadmium in Brassica napus L.
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2020.11.011openalex-snapshot
Glutathione improves rice tolerance to submergence: insights into its physiological and biochemical mechanisms
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133954openalex-snapshot
Integrated genome-transcriptome analysis unveiled the mechanism of Debaryomyces hansenii-mediated arsenic stress amelioration in rice
inferred← citeshttps://doi.org/10.1016/j.mcpro.2023.100638openalex-snapshot
Quantitative Time-Course Analysis of Osmotic and Salt Stress in Arabidopsis thaliana Using Short Gradient Multi-CV FAIMSpro BoxCar DIA
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110284openalex-snapshot
PGDH family genes differentially affect Arabidopsis tolerance to salt stress
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112645openalex-snapshot
Exploring the variety-specific roles of glutathione transferases in tomato osmotic stress response
inferred← citeshttps://doi.org/10.1016/j.plaphy.2016.04.020openalex-snapshot
Analysis of salt-induced physiological and proline changes in 46 switchgrass (Panicum virgatum) lines indicates multiple response modes
inferred← citeshttps://doi.org/10.1016/j.plaphy.2017.08.029openalex-snapshot
Plant growth-promoting endophyte Piriformospora indica alleviates salinity stress in Medicago truncatula
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.03.025openalex-snapshot
Elevated nitrogen metabolism and nitric oxide production are involved in Arabidopsis resistance to acid rain
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.11.041openalex-snapshot
Sequenced application of glutathione as an antioxidant with an organic biostimulant improves physiological and metabolic adaptation to salinity in wheat
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.12.021openalex-snapshot
Enhanced alkali tolerance of rhizobia-inoculated alfalfa correlates with altered proteins and metabolic processes as well as decreased oxidative damage
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.107693openalex-snapshot
microRNAomic profiling of maize root reveals multifaceted mechanisms to cope with Cr (VI) stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108390openalex-snapshot
N-acetyl-cysteine mitigates arsenic stress in lettuce: Molecular, biochemical, and physiological perspective
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109366openalex-snapshot
Glutathione mitigates aluminum toxicity in root-apex transition zone of rice through reducing aluminum absorption and maintaining redox balance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109746openalex-snapshot
Seed priming with NaCl boosted the glutathione-ascorbate pool to facilitate photosystem-II function and maintain starch in NaCl-primed chickpea under salt stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111133openalex-snapshot
Transgenic expression of TaGR2-D provides drought and salinity tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111422openalex-snapshot
Rice cold tolerance: Physiological responses, molecular regulatory networks, and improvement strategies
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111836openalex-snapshot
Genotype-dependent sulfur-related metabolic responses under salinity in rice
inferred← citeshttps://doi.org/10.1016/j.sajb.2019.04.014openalex-snapshot
Green spathe of peace lily (Spathiphyllum wallisii): An assimilate source for developing fruit
inferred← citeshttps://doi.org/10.1016/j.sjbs.2018.08.006openalex-snapshot
Identification of physiological and biochemical markers for salt (NaCl) stress in the seedlings of mungbean [Vigna radiata (L.) Wilczek] genotypes
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100486openalex-snapshot
Increase in ascorbate content in leaves of Hordeum vulgare after spraying with cold atmospheric plasma-treated water in combination with waterlogging and re-aeration
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100767openalex-snapshot
Synergistic effects of glutathione and zinc seed priming in alleviating salt stress on maize seed germination, metabolite levels, seedling vigor, and nutrient acquisition
inferred← citeshttps://doi.org/10.1017/s0960258519000047openalex-snapshot
Mechanism of salt-inhibited early seed germination analysed by transcriptomic sequencing
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c00466openalex-snapshot
Quantitative Proteomics Analysis Reveals Proteins Associated with High Melatonin Content in Barley Seeds under NaCl-Induced Salt Stress
inferred← citeshttps://doi.org/10.1021/acs.jproteome.9b00420openalex-snapshot
Comparative Proteomics Unravels the Differences in Salt Stress Response of Own-Rooted and 110R-Grafted Thompson Seedless Grapevines
inferred← citeshttps://doi.org/10.1038/s41598-017-02872-0openalex-snapshot
Functional analysis of the role of hydrogen sulfide in the regulation of dark-induced leaf senescence in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41598-018-19348-4openalex-snapshot
Transcriptomic responses to biotic stresses in Malus x domestica: a meta-analysis study
inferred← citeshttps://doi.org/10.1038/s41598-019-56148-wopenalex-snapshot
PtomtAPX, a mitochondrial ascorbate peroxidase, plays an important role in maintaining the redox balance of Populus tomentosa Carr
inferred← citeshttps://doi.org/10.1038/s41598-022-10835-3openalex-snapshot
Antioxidative and osmoprotecting mechanisms in carrot plants tolerant to soil salinity
inferred← citeshttps://doi.org/10.1038/s41598-022-16440-8openalex-snapshot
Glutathione improves low temperature stress tolerance in pusa sheetal cultivar of Solanum lycopersicum
inferred← citeshttps://doi.org/10.1038/srep36867openalex-snapshot
Transcriptome analysis of Arabidopsis mutants suggests a crosstalk between ABA, ethylene and GSH against combined cold and osmotic stress
inferred← citeshttps://doi.org/10.1042/bcj20180534openalex-snapshot
Gibberellin application ameliorates the adverse impact of short-term flooding onGlycine maxL.
inferred← citeshttps://doi.org/10.1073/pnas.1803841115openalex-snapshot
A stress recovery signaling network for enhanced flooding tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1080/07388551.2019.1597829openalex-snapshot
Manipulation of oxidative stress responses as a strategy to generate stress-tolerant crops. From damage to signaling to tolerance
inferred← citeshttps://doi.org/10.1080/07388551.2019.1709793openalex-snapshot
Sphingomonas : from diversity and genomics to functional role in environmental remediation and plant growth
inferred← citeshttps://doi.org/10.1089/ars.2018.7519openalex-snapshot
Toward an Integrated Understanding of Retrograde Control of Photosynthesis
inferred← citeshttps://doi.org/10.1093/jpe/rtaa063openalex-snapshot
Biochar and alternate partial root-zone irrigation greatly enhance the effectiveness of mulberry in remediating lead-contaminated soils
inferred← citeshttps://doi.org/10.1093/jxb/eraa363openalex-snapshot
The basic helix-loop-helix transcription factor bHLH95 affects fruit ripening and multiple metabolisms in tomato
inferred← citeshttps://doi.org/10.1093/jxb/erab270openalex-snapshot
Photosynthesis and chloroplast redox signaling in the age of global warming: stress tolerance, acclimation, and developmental plasticity
inferred← citeshttps://doi.org/10.1093/jxb/erac442openalex-snapshot
Glutathione and neodiosmin feedback sustain plant immunity
inferred← citeshttps://doi.org/10.1093/jxb/erz119openalex-snapshot
Secondary sulfur metabolism in cellular signalling and oxidative stress responses
inferred← citeshttps://doi.org/10.1093/pcp/pcae020openalex-snapshot
SULTR2;1 Adjusts the Bolting Timing by Transporting Sulfate from Rosette Leaves to the Primary Stem
inferred← citeshttps://doi.org/10.1093/pcp/pcaf150openalex-snapshot
Distinct metabolic signatures associated with drought response, shoot architecture, and flowering time in camelina
inferred← citeshttps://doi.org/10.1093/pcp/pcy194openalex-snapshot
The Mitochondrial Thioredoxin System Contributes to the Metabolic Responses Under Drought Episodes in Arabidopsis
inferred← citeshttps://doi.org/10.1093/treephys/tpag103openalex-snapshot
Optimization of ascorbate and glutathione assays for woody perennial bud tissues: overcoming matrix effects and storage instability
inferred← citeshttps://doi.org/10.1094/mpmi-07-23-0106-ropenalex-snapshot
Enhanced Resistance to Viruses in Nicotiana edwardsonii ‘Columbia’ Is Dependent on Salicylic Acid, Correlates with High Glutathione Levels, and Extends to Plant-Pathogenic Bacteria and Abiotic Stress
inferred← citeshttps://doi.org/10.1101/2023.02.22.529555openalex-snapshot
Quantitative Time-Course Analysis of Osmotic and Salt Stress in Arabidopsis thaliana using Short Gradient Multi-CV FAIMSpro BoxCar DIA
inferred← citeshttps://doi.org/10.1101/2023.05.10.540197openalex-snapshot
Paternal CHH methylation potentiates stress responses against Pseudomonas syringae in Arabidopsis progenies
inferred← citeshttps://doi.org/10.1111/jipb.13799openalex-snapshot
Sulfur metabolism under stress: Oxidized glutathione inhibits methionine biosynthesis by destabilizing the enzyme cystathionine γ‐synthase
inferred← citeshttps://doi.org/10.1111/jipb.70304openalex-snapshot
Mineral nutrients as regulators of plant flowering time: A molecular perspective
inferred← citeshttps://doi.org/10.1111/mpp.13138openalex-snapshot
Glutathione contributes to resistance responses to TMV through a differential modulation of salicylic acid and reactive oxygen species
inferred← citeshttps://doi.org/10.1111/nph.16246openalex-snapshot
Lack of FIBRILLIN6 in Arabidopsis thaliana affects light acclimation and sulfate metabolism
inferred← citeshttps://doi.org/10.1111/pbi.12673openalex-snapshot
The rice Os NAC 6 transcription factor orchestrates multiple molecular mechanisms involving root structural adaptions and nicotianamine biosynthesis for drought tolerance
inferred← citeshttps://doi.org/10.1111/pce.14930openalex-snapshot
CwJAZ4/9 negatively regulates jasmonate‐mediated biosynthesis of terpenoids through interacting with CwMYC2 and confers salt tolerance in Curcuma wenyujin
inferred← citeshttps://doi.org/10.1111/pce.15198openalex-snapshot
Evolutionary Conserved and Divergent Responses to Copper Zinc Superoxide Dismutase Inhibition in Plants
inferred← citeshttps://doi.org/10.1111/ppl.13983openalex-snapshot
Exogenous melatonin mitigates saline‐alkali stress by decreasing DNA oxidative damage and enhancing photosynthetic carbon metabolism in soybean ( Glycine max [L.] Merr.) leaves
inferred← citeshttps://doi.org/10.1111/ppl.70062openalex-snapshot
Biochemical, photosynthetic and metabolomics insights of single and combined effects of salinity, heat, cold and drought in Arabidopsis
inferred← citeshttps://doi.org/10.1111/ppl.70358openalex-snapshot
Alleviating Soybean Salt Stress via Suaeda salsa Intercropping: Roles of Desalinization and Root Interactions
inferred← citeshttps://doi.org/10.1111/tpj.13547openalex-snapshot
Integrated omics analyses of retrograde signaling mutant delineate interrelated stress‐response strata
inferred← citeshttps://doi.org/10.1111/tpj.14632openalex-snapshot
Translational regulation contributes to the elevated CO2 response in two Solanum species
inferred← citeshttps://doi.org/10.1111/tpj.17062openalex-snapshot
Knockdown of β‐conglycinin α′ and α subunits alters seed protein composition and improves salt tolerance in soybean
inferred← citeshttps://doi.org/10.1134/s1021443719060116openalex-snapshot
Overexpression of LmgshF from Listeria monocytogenes in Indica Rice Confers Salt Stress Tolerance
inferred← citeshttps://doi.org/10.1134/s2079059718020077openalex-snapshot
Productivity and Stress-Tolerance of Transgenic Tobacco Plants with a Constitutive Expression of the Rapeseed Glutathione Synthetase Gene BnGSH
inferred← citeshttps://doi.org/10.1186/s12864-021-07368-wopenalex-snapshot
De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.1186/s12864-025-11382-7openalex-snapshot
Mechanisms underlining Kelp (Saccharina japonica) adaptation to relative high seawater temperature
inferred← citeshttps://doi.org/10.1186/s12870-020-02363-xopenalex-snapshot
Internal ammonium excess induces ROS-mediated reactions and causes carbon scarcity in rice
inferred← citeshttps://doi.org/10.1186/s12870-021-02916-8openalex-snapshot
Genome-wide identification of BAM genes in grapevine (Vitis vinifera L.) and ectopic expression of VvBAM1 modulating soluble sugar levels to improve low-temperature tolerance in tomato
inferred← citeshttps://doi.org/10.1186/s12870-023-04126-wopenalex-snapshot
Foliar application of putrescine, salicylic acid, and ascorbic acid mitigates frost stress damage in Vitis vinifera cv. ‘Giziluzum’
inferred← citeshttps://doi.org/10.1186/s12870-023-04507-1openalex-snapshot
Panicle transcriptome of high-yield mutant indica rice reveals physiological mechanisms and novel candidate regulatory genes for yield under reproductive stage drought stress
inferred← citeshttps://doi.org/10.1186/s12870-024-05957-xopenalex-snapshot
Effects of seasonal climates and MIPS1 mutations on soybean germination through multi-omics analysis
inferred← citeshttps://doi.org/10.1186/s12870-025-07993-7openalex-snapshot
Unraveling the role of Cullin3 of E3 ubiquitin ligase in salt stress tolerance via proteomics
inferred← citeshttps://doi.org/10.1371/journal.pone.0217806openalex-snapshot
Microtranscriptome analysis of sugarcane cultivars in response to aluminum stress
inferred← citeshttps://doi.org/10.1371/journal.pone.0220589openalex-snapshot
Low-glutathione mutants are impaired in growth but do not show an increased sensitivity to moderate water deficit
inferred← citeshttps://doi.org/10.1508/cytologia.85.325openalex-snapshot
Analysis on Cytotoxicity and Oxidative Damage of Iron Nano-Composite on Allium cepa L. Root Meristems
inferred← citeshttps://doi.org/10.17816/ecogen15112-19openalex-snapshot
Productivity and stress-tolerance of transgenic tobacco plants with constitutive expression of rapeseed glutathione synthetase gene BnGSH
inferred← citeshttps://doi.org/10.26420/annagriccropsci.2021.1094openalex-snapshot
Stress Effect Induced by Microplastics Coupled with Acid Rain, on Garden Cress, During Short and Long Time: Two Exposures in Comparison
inferred← citeshttps://doi.org/10.31163/2618-964x-2020-3-2-111-117openalex-snapshot
THE INFLUENCE OF ASCORBATE AND GLUTATHIONE ON THE PEA ROOT GROWTH FUNCTION
inferred← citeshttps://doi.org/10.32604/phyton.2025.063086openalex-snapshot
The Role of Glutathione S-Transferase in the Regulation of Plant Growth, and Responses to Environmental Stresses
inferred← citeshttps://doi.org/10.3389/fphys.2022.836810openalex-snapshot
Dietary Inclusion of Hydrolyzed Debaryomyces hansenii Yeasts Modulates Physiological Responses in Plasma and Immune Organs of Atlantic Salmon (Salmo salar) Parr Exposed to Acute Hypoxia Stress
inferred← citeshttps://doi.org/10.3389/fpls.2017.01208openalex-snapshot
Metabolomic Analysis of Alfalfa (Medicago sativa L.) Root-Symbiotic Rhizobia Responses under Alkali Stress
inferred← citeshttps://doi.org/10.3389/fpls.2017.01464openalex-snapshot
Effects of Combined Low Glutathione with Mild Oxidative and Low Phosphorus Stress on the Metabolism of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2018.00800openalex-snapshot
Proteomics and Phosphoproteomics of Heat Stress-Responsive Mechanisms in Spinach
inferred← citeshttps://doi.org/10.3389/fpls.2019.00989openalex-snapshot
Redox Balance-DDR-miRNA Triangle: Relevance in Genome Stability and Stress Responses in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2019.01711openalex-snapshot
Glutathione and Its Biosynthetic Intermediates Alleviate Cesium Stress in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2021.664311openalex-snapshot
Comparative Transcriptomics and Proteomics Analyses of Leaves Reveals a Freezing Stress-Responsive Molecular Network in Winter Rapeseed (Brassica rapa L.)
inferred← citeshttps://doi.org/10.3389/fpls.2021.668029openalex-snapshot
Role of Jasmonates, Calcium, and Glutathione in Plants to Combat Abiotic Stresses Through Precise Signaling Cascade
inferred← citeshttps://doi.org/10.3389/fpls.2022.989048openalex-snapshot
Integrated mRNA and microRNA expression analysis of root response to phosphate deficiency in Medicago sativa
inferred← citeshttps://doi.org/10.3389/fpls.2024.1373801openalex-snapshot
Glutathione-the “master” antioxidant in the regulation of resistant and susceptible host-plant virus-interaction
inferred← citeshttps://doi.org/10.3389/fpls.2026.1725249openalex-snapshot
Interaction with CYP20–3 limits OPDA flux into jasmonate biosynthesis in wounded leaves of arabidopsis grown at eCO2
inferred← citeshttps://doi.org/10.3389/fpls.2026.1857726openalex-snapshot
Comprehensive analysis of physiological characteristic and global transcriptional profiling to unravel the mechanism of wheat yield increase in intercropping
inferred← citeshttps://doi.org/10.3390/agronomy11040764openalex-snapshot
Phenotypic Characterization of Arabidopsis Ascorbate and Glutathione Deficient Mutants under Abiotic Stresses
inferred← citeshttps://doi.org/10.3390/agronomy12051193openalex-snapshot
Effects of Salinity-Stress on Seed Germination and Growth Physiology of Quinclorac-Resistant Echinochloa crus-galli (L.) Beauv
inferred← citeshttps://doi.org/10.3390/agronomy13030806openalex-snapshot
Comparative Analysis of Root Transcriptome of High-NUE Mutant and Wild-Type Barley under Low-Nitrogen Conditions
inferred← citeshttps://doi.org/10.3390/agronomy14092112openalex-snapshot
N-Acetylcysteine Mitigates Oxidative Stress Induced by Transplanting Lettuce Seedlings into a DFT Hydroponic System
inferred← citeshttps://doi.org/10.3390/antiox11020225openalex-snapshot
Reactive Oxygen Species in Plants: From Source to Sink
inferred← citeshttps://doi.org/10.3390/antiox14020140openalex-snapshot
Coenzyme M: An Archaeal Antioxidant as an Agricultural Biostimulant
inferred← citeshttps://doi.org/10.3390/antiox8090384openalex-snapshot
Regulation of Ascorbate-Glutathione Pathway in Mitigating Oxidative Damage in Plants under Abiotic Stress
inferred← citeshttps://doi.org/10.3390/antiox9070604openalex-snapshot
The Apoplast: A Key Player in Plant Survival
inferred← citeshttps://doi.org/10.3390/foods10112771openalex-snapshot
Microscale Thermophoresis Reveals Oxidized Glutathione as High-Affinity Ligand of Mal d 1
inferred← citeshttps://doi.org/10.3390/genes12101620openalex-snapshot
Roles of Glutathione in Mediating Abscisic Acid Signaling and Its Regulation of Seed Dormancy and Drought Tolerance
inferred← citeshttps://doi.org/10.3390/ijms21010078openalex-snapshot
Comparative Proteomic Analysis of Nodulated and Non-Nodulated Casuarina glauca Sieb. ex Spreng. Grown under Salinity Conditions Using Sequential Window Acquisition of All Theoretical Mass Spectra (SWATH-MS)
inferred← citeshttps://doi.org/10.3390/ijms21010180openalex-snapshot
Comparative Transcriptome Analysis of the Molecular Mechanism of the Hairy Roots of Brassica campestris L. in Response to Cadmium Stress
inferred← citeshttps://doi.org/10.3390/ijms21020388openalex-snapshot
Modulation of (Homo)Glutathione Metabolism and H2O2 Accumulation during Soybean Cyst Nematode Infections in Susceptible and Resistant Soybean Cultivars
inferred← citeshttps://doi.org/10.3390/ijms21218164openalex-snapshot
In Vivo Imaging with Genetically Encoded Redox Biosensors
inferred← citeshttps://doi.org/10.3390/ijms21238926openalex-snapshot
Sulfur Homeostasis in Plants
inferred← citeshttps://doi.org/10.3390/ijms23115947openalex-snapshot
Comparative Metabolic Study of Two Contrasting Chinese Cabbage Genotypes under Mild and Severe Drought Stress
inferred← citeshttps://doi.org/10.3390/ijms25105518openalex-snapshot
Differential Transcription Profiling Reveals the MicroRNAs Involved in Alleviating Damage to Photosynthesis under Drought Stress during the Grain Filling Stage in Wheat
inferred← citeshttps://doi.org/10.3390/life12060833openalex-snapshot
Unearthing the Alleviatory Mechanisms of Brassinolide in Cold Stress in Rice
inferred← citeshttps://doi.org/10.3390/plants10050914openalex-snapshot
Sequential Antioxidants Foliar Application Can Alleviate Negative Consequences of Salinity Stress in Vicia faba L.
inferred← citeshttps://doi.org/10.3390/plants11091173openalex-snapshot
Proteomic Investigation of Molecular Mechanisms in Response to PEG-Induced Drought Stress in Soybean Roots
inferred← citeshttps://doi.org/10.3390/plants11152023openalex-snapshot
Antioxidants Application Enhances Regeneration and Conversion of Date Palm (Phoenix dactylifera L.) Somatic Embryos
inferred← citeshttps://doi.org/10.3390/plants12051133openalex-snapshot
Antioxidant Potential of Glutathione and Crosstalk with Phytohormones in Enhancing Abiotic Stress Tolerance in Crop Plants
inferred← citeshttps://doi.org/10.3390/plants12183299openalex-snapshot
Beyond NPK: Mineral Nutrient-Mediated Modulation in Orchestrating Flowering Time
inferred← citeshttps://doi.org/10.3390/plants14091276openalex-snapshot
ABA Enhances Drought Resistance During Rapeseed (Brassica napus L.) Seed Germination Through the Gene Regulatory Network Mediated by ABA Insensitive 5
inferred← citeshttps://doi.org/10.3390/plants15030457openalex-snapshot
Exogenous Glutathione Enhances Salt Tolerance in Patchouli by Promoting the Antioxidant Capacity and Activating the Flavonoid Biosynthesis Pathway
inferred← citeshttps://doi.org/10.3390/plants15182831openalex-snapshot
Multilevel Analysis of Glutathione-Induced Responses in Pepper Seedlings Under Water-Deficit Conditions
inferred← citeshttps://doi.org/10.3390/plants9020259openalex-snapshot
Co-Suppression of NbClpC1 and NbClpC2, Encoding Clp Protease Chaperons, Elicits Significant Changes in the Metabolic Profile of Nicotiana benthamiana
inferred← citeshttps://doi.org/10.3390/plants9091067openalex-snapshot
Subcellular Roles of Glutathione in Mediating Plant Defense during Biotic Stress
inferred← citeshttps://doi.org/10.36632/mejar/2021.10.4.73openalex-snapshot
Antioxidant Glutathione Impacts on Faba Bean Plants Grown Under Drought Stress Conditions
inferred← citeshttps://doi.org/10.48130/frures-0023-0037openalex-snapshot
Comprehensive analysis provides insights into Ziyang xiangcheng (Citrus junos Sieb.) tolerance of alkalinity stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.12096216openalex-snapshot
Additional file 1 of Internal ammonium excess induces ROS-mediated reactions and causes carbon scarcity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.12096222openalex-snapshot
Additional file 2 of Internal ammonium excess induces ROS-mediated reactions and causes carbon scarcity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.12096225openalex-snapshot
Additional file 3 of Internal ammonium excess induces ROS-mediated reactions and causes carbon scarcity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.12096228openalex-snapshot
Additional file 4 of Internal ammonium excess induces ROS-mediated reactions and causes carbon scarcity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.12096234openalex-snapshot
Additional file 5 of Internal ammonium excess induces ROS-mediated reactions and causes carbon scarcity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.12096237openalex-snapshot
Additional file 6 of Internal ammonium excess induces ROS-mediated reactions and causes carbon scarcity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.12096240openalex-snapshot
Additional file 7 of Internal ammonium excess induces ROS-mediated reactions and causes carbon scarcity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662843openalex-snapshot
Additional file 10 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662846openalex-snapshot
Additional file 11 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662849openalex-snapshot
Additional file 12 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662852openalex-snapshot
Additional file 13 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662855openalex-snapshot
Additional file 14 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662858openalex-snapshot
Additional file 15 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662861openalex-snapshot
Additional file 16 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662864openalex-snapshot
Additional file 17 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662867openalex-snapshot
Additional file 18 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662870openalex-snapshot
Additional file 19 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662873openalex-snapshot
Additional file 1 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662876openalex-snapshot
Additional file 2 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662879openalex-snapshot
Additional file 3 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662882openalex-snapshot
Additional file 4 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662885openalex-snapshot
Additional file 5 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662888openalex-snapshot
Additional file 6 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662891openalex-snapshot
Additional file 7 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662894openalex-snapshot
Additional file 8 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13662897openalex-snapshot
Additional file 9 of De novo transcriptome in roots of switchgrass (Panicum virgatum L.) reveals gene expression dynamic and act network under alkaline salt stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.14329372openalex-snapshot
Additional file 10 of Genome-wide identification of BAM genes in grapevine (Vitis vinifera L.) and ectopic expression of VvBAM1 modulating soluble sugar levels to improve low-temperature tolerance in tomato
inferred← citeshttps://doi.org/10.6084/m9.figshare.14329375openalex-snapshot
Additional file 1 of Genome-wide identification of BAM genes in grapevine (Vitis vinifera L.) and ectopic expression of VvBAM1 modulating soluble sugar levels to improve low-temperature tolerance in tomato
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