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Plant DELLAs Restrain Growth and Promote Survival of Adversity by Reducing the Levels of Reactive Oxygen Species
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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/bf02595811openalex-snapshot
Resampling-based multiple testing for microarray data analysis
inferredcites →https://doi.org/10.1016/s0955-0674(98)80147-6openalex-snapshot
Oxygen radicals and signaling
inferredcites →https://doi.org/10.1038/22307openalex-snapshot
‘Green revolution’ genes encode mutant gibberellin response modulators
inferredcites →https://doi.org/10.1038/nature01387openalex-snapshot
Auxin promotes Arabidopsis root growth by modulating gibberellin response
inferredcites →https://doi.org/10.1038/nature01485openalex-snapshot
Reactive oxygen species produced by NADPH oxidase regulate plant cell growth
inferredcites →https://doi.org/10.1038/nature04028openalex-snapshot
GIBBERELLIN INSENSITIVE DWARF1 encodes a soluble receptor for gibberellin
inferredcites →https://doi.org/10.1073/pnas.012452499openalex-snapshot
Arabidopsis gp91 phox homologues AtrbohD and AtrbohF are required for accumulation of reactive oxygen intermediates in the plant defense response
inferredcites →https://doi.org/10.1073/pnas.0610717104openalex-snapshot
The plant stress hormone ethylene controls floral transition via DELLA-dependent regulation of floral meristem-identity genes
inferredcites →https://doi.org/10.1093/emboj/cdg277openalex-snapshot
NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis
inferredcites →https://doi.org/10.1093/nar/gkg071openalex-snapshot
CATMA: a complete Arabidopsis GST database
inferredcites →https://doi.org/10.1093/nar/gkm757openalex-snapshot
CATdb: a public access to Arabidopsis transcriptome data from the URGV-CATMA platform
inferredcites →https://doi.org/10.1101/gad.11.23.3194openalex-snapshot
The Arabidopsis GAI gene defines a signaling pathway that negatively regulates gibberellin responses
inferredcites →https://doi.org/10.1101/gr.2544504openalex-snapshot
Versatile Gene-Specific Sequence Tags forArabidopsisFunctional Genomics: Transcript Profiling and Reverse Genetics Applications
inferredcites →https://doi.org/10.1104/pp.106.079079openalex-snapshot
Control of Plant Development by Reactive Oxygen Species
inferredcites →https://doi.org/10.1104/pp.106.079467openalex-snapshot
Reactive Oxygen Species Signaling in Response to Pathogens
inferredcites →https://doi.org/10.1104/pp.106.082289openalex-snapshot
Gibberellin Mobilizes Distinct DELLA-Dependent Transcriptomes to Regulate Seed Germination and Floral Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.118.2.637openalex-snapshot
Superoxide Dismutase in Arabidopsis: An Eclectic Enzyme Family with Disparate Regulation and Protein Localization
inferredcites →https://doi.org/10.1104/pp.125.4.1591openalex-snapshot
Release of Reactive Oxygen Intermediates (Superoxide Radicals, Hydrogen Peroxide, and Hydroxyl Radicals) and Peroxidase in Germinating Radish Seeds Controlled by Light, Gibberellin, and Abscisic Acid
inferredcites →https://doi.org/10.1104/pp.126.1.156openalex-snapshot
Enzymes That Scavenge Reactive Oxygen Species Are Down-Regulated Prior to Gibberellic Acid-Induced Programmed Cell Death in Barley Aleurone
inferredcites →https://doi.org/10.1104/pp.126.3.1281openalex-snapshot
Superoxide Production by Plant Homologues of the gp91phox NADPH Oxidase. Modulation of Activity by Calcium and by Tobacco Mosaic Virus Infection
inferredcites →https://doi.org/10.1105/tpc.014167openalex-snapshot
The BOTRYTIS SUSCEPTIBLE1 Gene Encodes an R2R3MYB Transcription Factor Protein That Is Required for Biotic and Abiotic Stress Responses in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.104.022236openalex-snapshot
Genome-Wide Analysis of Arabidopsis Pentatricopeptide Repeat Proteins Reveals Their Essential Role in Organelle Biogenesis[W]
inferredcites →https://doi.org/10.1105/tpc.107.051441openalex-snapshot
The DELLA Domain of GA INSENSITIVE Mediates the Interaction with the GA INSENSITIVE DWARF1A Gibberellin Receptor ofArabidopsis
inferredcites →https://doi.org/10.1105/tpc.5.8.887openalex-snapshot
Mutations at the SPINDLY Locus of Arabidopsis Alter Gibberellin Signal Transduction
inferredcites →https://doi.org/10.1105/tpc.8.5.887openalex-snapshot
Chromosomal organization of TOX2, a complex locus controlling host-selective toxin biosynthesis in Cochliobolus carbonum.
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02121.xopenalex-snapshot
The calcium‐dependent protein kinase HvCDPK1 mediates the gibberellic acid response of the barley aleurone through regulation of vacuolar function
inferredcites →https://doi.org/10.1126/science.1081077openalex-snapshot
Accumulation of Phosphorylated Repressor for Gibberellin Signaling in an F-box Mutant
inferredcites →https://doi.org/10.1126/science.1118642openalex-snapshot
Integration of Plant Responses to Environmentally Activated Phytohormonal Signals
inferredcites →https://doi.org/10.1146/annurev.arplant.52.1.67openalex-snapshot
H OW G IBBERELLIN R EGULATES P LANT G ROWTH AND D EVELOPMENT : A Molecular Genetic Analysis of Gibberellin Signaling
inferredcites →https://doi.org/10.1146/annurev.arplant.55.031903.141701openalex-snapshot
REACTIVE OXYGEN SPECIES: Metabolism, Oxidative Stress, and Signal Transduction
inferredcites →https://doi.org/10.1186/1471-2229-5-4openalex-snapshot
Imaging plant cell death: GFP-Nit1 aggregation marks an early step of wound and herbicide induced cell death
inferredcites →https://doi.org/10.1214/lnms/1215091155openalex-snapshot
Normalization for two-color cDNA microarray data
inferredcites →https://doi.org/10.1242/dev.00359openalex-snapshot
Quiescent center formation in maize roots is associated with an auxin-regulated oxidizing environment
inferredcites →https://doi.org/10.1242/dev.00992openalex-snapshot
Gibberellin regulates Arabidopsis floral development via suppression of DELLA protein function
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Transgenic Poplar with the Zygophyllum Xanthoxylon Zinc Finger Protein Transcription Factor Zxzf Gene Shows Improved Drought Resistance by Regulating Hormone Signal
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Crop Radiation Capture and Use Efficiency
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A Biotic or Abiotic Stress?
inferred← citeshttps://doi.org/10.1007/978-94-017-7758-2_2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-017-9484-8_9openalex-snapshot
Integration of Ethylene and Gibberellin Signaling
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Reactive Oxygen Species (ROS): A Way to Stress Survival in Plants
inferred← citeshttps://doi.org/10.1007/978-981-13-2140-5_12openalex-snapshot
Plant Hormones as Mediators of Stress Response in Tea Plants
inferred← citeshttps://doi.org/10.1007/978-981-13-8801-9_3openalex-snapshot
Use of Plant Hormones for the Improvement of Plant Growth and Production Under Salt Stress
inferred← citeshttps://doi.org/10.1007/978-981-13-8922-1_21openalex-snapshot
Integration of Multiple Signaling Cues
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/10.1007/978-981-16-5743-6_11openalex-snapshot
Role of Brassinosteroids and Its Cross Talk with Other Phytohormone in Plant Responses to Heavy Metal Stress
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Drought Stress: Involvement of Plant Hormones in Perception, Signaling, and Response
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Hormonal Response in Plants Influenced by Reactive Oxygen Species
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Ecology and Diversity of Rice Habitats
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SUMO mediated regulation of transcription factors as a mechanism for transducing environmental cues into cellular signaling in plants
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Combined linkage and association mapping of flowering time in Sunflower (Helianthus annuus L.)
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Gibberellins and abscisic acid signal crosstalk: living and developing under unfavorable conditions
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Crosstalk between GA and JA signaling mediates plant growth and defense
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Nitric oxide as a key component in hormone-regulated processes
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Analyzing serial cDNA libraries revealed reactive oxygen species and gibberellins signaling pathways in the salt response of Upland cotton (Gossypium hirsutum L.)
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Overexpression of VaPAT1, a GRAS transcription factor from Vitis amurensis, confers abiotic stress tolerance in Arabidopsis
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A gibberellin-deficient maize mutant exhibits altered plant height, stem strength and drought tolerance
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Arabidopsis retromer subunit AtVPS29 is involved in SLY1-mediated gibberellin signaling
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Gibberellic Acid (GA3) Inhibits ROS Increase in Chloroplasts During Dark-Induced Senescence of Pelargonium Cuttings
inferred← citeshttps://doi.org/10.1007/s00344-016-9656-4openalex-snapshot
DELLAs Contribute to Set the Growth and Mineral Composition of Arabidopsis thaliana Plants Grown Under Conditions of Potassium Deprivation
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Photosynthetic Responses of a Wheat Mutant (Rht-B1c) with Altered DELLA Proteins to Salt Stress
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Signal Function Studies of ROS, Especially RBOH-Dependent ROS, in Plant Growth, Development and Environmental Stress
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Seed Priming with Gibberellin Regulates the Germination of Cotton Seeds Under Low-Temperature Conditions
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Fusarium sp. Strain K-23 Alleviates Salt Stress in Arabidopsis thaliana Through its Root Hair Growth-Promoting Effect
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Plant Signal Cross-Talk during Abiotic Stress
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The six conserved serine/threonine sites of REPRESSOR OF ga1-3 protein are important for its functionality and stability in gibberellin signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00425-026-05168-8openalex-snapshot
DELLA proteins enhance cadmium tolerance by coordinating redox protection and cadmium partitioning in Arabidopsis
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Morphophysiological changes by mepiquat chloride application in Eucalyptus clones
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Phylogenetic and transcriptional analysis of chrysanthemum GRAS transcription factors
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GRAS transcription factors emerging regulator in plants growth, development, and multiple stresses
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Hormonal crosstalk at the plant–microbiome interface governing plant immunity under combined biotic and abiotic stresses
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Role of plant hormones in plant defence responses
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Auxin signaling participates in the adaptative response against oxidative stress and salinity by interacting with redox metabolism in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11105-013-0693-xopenalex-snapshot
The Role of Gibberellin in the CBF1-Mediated Stress-Response Pathway
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Physiological basis of differential zinc and copper tolerance of Verbascum populations from metal-contaminated and uncontaminated areas
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Erratum to: Physiological basis of differential zinc and copper tolerance of Verbascum populations from metal-contaminated and uncontaminated areas
inferred← citeshttps://doi.org/10.1007/s11427-023-2464-2openalex-snapshot
Type-B response regulator OsRR22 forms a transcriptional activation complex with OsSLR1 to modulate OsHKT2;1 expression in rice
inferred← citeshttps://doi.org/10.1007/s11434-009-0629-xopenalex-snapshot
Advances in the regulation and crosstalks of phytohormones
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Somatic and zygotic embryos share common developmental features at the onset of plant embryogenesis
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Effect of localized reduction of gibberellins in different tobacco organs on drought stress tolerance and recovery
inferred← citeshttps://doi.org/10.1007/s11947-016-1712-3openalex-snapshot
Effects of Postharvest Gibberellic Acid Treatment on Chilling Tolerance in Cold-Stored Tomato (Solanum lycopersicum L.) Fruit
inferred← citeshttps://doi.org/10.1007/s12038-014-9471-7openalex-snapshot
Variation in ion leakage parameters of two wheat genotypes with different Rht-B1 alleles in response to drought
inferred← citeshttps://doi.org/10.1007/s12298-023-01385-7openalex-snapshot
Transcriptomic responses to cold stress in Dendrobium huoshanense C.Z. Tang et S.J. Cheng
inferred← citeshttps://doi.org/10.1007/s12374-015-0103-zopenalex-snapshot
Plant hormones in salt stress tolerance
inferred← citeshttps://doi.org/10.1007/s12374-019-0006-5openalex-snapshot
Genome-wide Analysis of Root Hair Preferred RBOH Genes Suggests that Three RBOH Genes are Associated with Auxin-mediated Root Hair Development in Rice
inferred← citeshttps://doi.org/10.1007/s42729-023-01550-7openalex-snapshot
Ultrastructural, Secondary Metabolite, and Antioxidant Modulation in Response to Salt-Affected Habitats Induced Oxidative Stress and Their Accumulation in Malva parviflora L. and Rumex dentatus L.
inferred← citeshttps://doi.org/10.1007/s44378-026-00331-9openalex-snapshot
Plant growth-promoting rhizobacteria as a soil-based strategy to improve nutrient acquisition and drought tolerance in sugarcane
inferred← citeshttps://doi.org/10.1016/b978-0-12-799963-0.00002-2openalex-snapshot
Reactive Oxygen Species and Plant Hormones
inferred← citeshttps://doi.org/10.1016/b978-0-12-800854-6.00020-8openalex-snapshot
DELLA Proteins, a Group of GRAS Transcription Regulators that Mediate Gibberellin Signaling
inferred← citeshttps://doi.org/10.1016/b978-0-12-814864-8.00011-5openalex-snapshot
Damage and Protection of the Photosynthetic Apparatus Under Cadmium Stress
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The Regulatory Signaling of Gibberellin Metabolism and Its Crosstalk With Phytohormones in Response to Plant Abiotic Stresses
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Effect of High-Temperature Stress on the Metabolism of Plant Growth Regulators
inferred← citeshttps://doi.org/10.1016/b978-0-12-818204-8.00019-9openalex-snapshot
Phytohormonal signaling under abiotic stress
inferred← citeshttps://doi.org/10.1016/b978-0-12-818797-5.00002-9openalex-snapshot
Ubiquitin-proteasome system as part of nitric oxide sensing in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-89871-3.00025-2openalex-snapshot
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Abiotic stress and plant response: Adaptive mechanisms of plants against multiple stresses
inferred← citeshttps://doi.org/10.1016/b978-0-323-91225-9.00013-3openalex-snapshot
Silicon-mediated cold stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-91886-2.00010-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-95375-7.00002-1openalex-snapshot
Role of hydrogen peroxide in plant and crosstalk with signaling networks, growth, and development
inferred← citeshttps://doi.org/10.1016/b978-0-443-30244-2.00019-1openalex-snapshot
Gibberellin receptors regulating cell signaling in plants
inferred← citeshttps://doi.org/10.1016/b978-0-443-45576-6.00021-2openalex-snapshot
Brassinosteroids for boosting plant stress tolerance
inferred← citeshttps://doi.org/10.1016/bs.abr.2023.02.001openalex-snapshot
Cross-talk between ROS and phytohormones signaling determines crop sensitivity against ozone
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2016.07.001openalex-snapshot
Molecular Interactions Between Flowering Time and Abiotic Stress Pathways
inferred← citeshttps://doi.org/10.1016/j.arres.2022.100039openalex-snapshot
Reactive Oxygen Species (ROS) and Reactive Nitrogen Species (RNS) in plants– maintenance of structural individuality and functional blend
inferred← citeshttps://doi.org/10.1016/j.baae.2022.01.010openalex-snapshot
Traffic noise induces oxidative stress and phytohormone imbalance in two urban plant species
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2013.10.005openalex-snapshot
Hormonal and metabolic regulation of source–sink relations under salinity and drought: From plant survival to crop yield stability
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2025.108773openalex-snapshot
Plasticity and adaptive architecture of roots for enhanced salinity tolerance in crops
inferred← citeshttps://doi.org/10.1016/j.cap.2013.11.056openalex-snapshot
Plasma induced long-term growth enhancement of Raphanus sativus L. using combinatorial atmospheric air dielectric barrier discharge plasmas
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.126486openalex-snapshot
Hydrogen peroxide as a signalling molecule in plants and its crosstalk with other plant growth regulators under heavy metal stress
inferred← citeshttps://doi.org/10.1016/j.copbio.2010.03.002openalex-snapshot
More from less: plant growth under limited water
inferred← citeshttps://doi.org/10.1016/j.cpb.2025.100508openalex-snapshot
Sodium nitroprusside as a priming agent induces drought stress tolerance in Citrus
inferred← citeshttps://doi.org/10.1016/j.cub.2008.05.036openalex-snapshot
Plant Biology: Do DELLAs Do Defence?
inferred← citeshttps://doi.org/10.1016/j.cub.2009.05.059openalex-snapshot
Gibberellin Signaling Controls Cell Proliferation Rate in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2011.03.013openalex-snapshot
Hormone Signalling Crosstalk in Plant Growth Regulation
inferred← citeshttps://doi.org/10.1016/j.cub.2020.05.015openalex-snapshot
The Mechanosensitive Ion Channel MSL10 Potentiates Responses to Cell Swelling in Arabidopsis Seedlings
inferred← citeshttps://doi.org/10.1016/j.cub.2021.06.010openalex-snapshot
Coordination between growth and stress responses by DELLA in the liverwort Marchantia polymorpha
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.07.011openalex-snapshot
The Cytokinin-Activated Transcription Factor ARR2 Promotes Plant Immunity via TGA3/NPR1-Dependent Salicylic Acid Signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.10.024openalex-snapshot
DELLAs Modulate Jasmonate Signaling via Competitive Binding to JAZs
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.12.004openalex-snapshot
Small Ubiquitin-like Modifier Protein SUMO Enables Plants to Control Growth Independently of the Phytohormone Gibberellin
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2012.05.003openalex-snapshot
Interactions between hormone and redox signalling pathways in the control of growth and cross tolerance to stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2013.11.005openalex-snapshot
Plant hormones and seed germination
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105868openalex-snapshot
Transgenic poplar with the Zygophyllum xanthoxylon zinc finger protein transcription factor ZxZF gene shows improved drought resistance by regulating hormone signal
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2018.01.032openalex-snapshot
Ethylene signaling triggered by low concentrations of ascorbic acid regulates biomass accumulation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.hpj.2025.08.007openalex-snapshot
Multifaceted functions of DELLA proteins in plant ontogeny and the molecular pathways leading to tree dwarfing
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.125824openalex-snapshot
Sl-lncRNA47980, a positive regulator affects tomato resistance to Phytophthora infestans
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.137058openalex-snapshot
TaJUB1 is phosphorylated by TaMPK4 to enhance TaXIP3 transcription and reduce Cd accumulation
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.138686openalex-snapshot
Overexpression of anthocyanin activator LrAN2 improving black goji berry (Lycium ruthenicum) tolerant to cadmium stress
inferred← citeshttps://doi.org/10.1016/j.jplph.2011.06.010openalex-snapshot
Overexpression of GASA5 increases the sensitivity of Arabidopsis to heat stress
inferred← citeshttps://doi.org/10.1016/j.jplph.2011.07.006openalex-snapshot
GsGASA1 mediated root growth inhibition in response to chronic cold stress is marked by the accumulation of DELLAs
inferred← citeshttps://doi.org/10.1016/j.jplph.2014.01.005openalex-snapshot
Programmed cell death in barley aleurone cells is not directly stimulated by reactive oxygen species produced in response to gibberellin
inferred← citeshttps://doi.org/10.1016/j.jplph.2018.04.008openalex-snapshot
KT-HAK-KUP transporters in major terrestrial photosynthetic organisms: A twenty years tale
inferred← citeshttps://doi.org/10.1016/j.jplph.2019.01.009openalex-snapshot
Root phenotypes of dwarf and “overgrowth” SLN1 barley mutants, and implications for hypoxic stress tolerance
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154608openalex-snapshot
ARABIDOPSIS NITRATE REGULATED 1 negatively regulates the tolerance of salt stress by controlling ion homeostasis and GA metabolism
inferred← citeshttps://doi.org/10.1016/j.molp.2015.09.011openalex-snapshot
A Pivotal Role of DELLAs in Regulating Multiple Hormone Signals
inferred← citeshttps://doi.org/10.1016/j.molp.2016.01.014openalex-snapshot
DELLA Proteins Promote Anthocyanin Biosynthesis via Sequestering MYBL2 and JAZ Suppressors of the MYB/bHLH/WD40 Complex in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.molp.2025.03.015openalex-snapshot
Reprogrammable design of DELLA as a strategy to mitigate alkaline–heat stress for sustainable agriculture
inferred← citeshttps://doi.org/10.1016/j.molp.2026.03.008openalex-snapshot
Green Revolution-associated DELLA accumulation enhances salt tolerance in cereals by disrupting INDETERMINATE SPIKELET1 biomolecular condensates
inferred← citeshttps://doi.org/10.1016/j.pbi.2008.09.004openalex-snapshot
Shedding light on gibberellic acid signalling
inferred← citeshttps://doi.org/10.1016/j.pbi.2012.07.005openalex-snapshot
Tuning growth to the environmental demands
inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.09.002openalex-snapshot
The metabolomics of oxidative stress
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.01.002openalex-snapshot
Overexpression of FTL1/DDF1, an AP2 transcription factor, enhances tolerance to cold, drought, and heat stresses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.10.011openalex-snapshot
Near-isogenic wheat lines carrying altered function alleles of the Rht-1 genes exhibit differential responses to potassium deprivation
inferred← citeshttps://doi.org/10.1016/j.plantsci.2014.10.002openalex-snapshot
To grow or not to grow: A stressful decision for plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.03.023openalex-snapshot
The R2R3-type MYB gene OsMYB91 has a function in coordinating plant growth and salt stress tolerance in rice
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110672openalex-snapshot
Overexpression of SlMBP22 in Tomato Affects Plant Growth and Enhances Tolerance to Drought Stress
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110804openalex-snapshot
Stress-responsive tomato gene SlGRAS4 function in drought stress and abscisic acid signaling
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112242openalex-snapshot
Overexpression of two DELLA subfamily genes MiSLR1 and MiSLR2 from mango promotes early flowering and enhances abiotic stress tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2009.11.005openalex-snapshot
Redox regulation of root apical meristem organization: Connecting root development to its environment
inferred← citeshttps://doi.org/10.1016/j.plaphy.2014.04.008openalex-snapshot
NADPH-dependent thioredoxin reductase A (NTRA) confers elevated tolerance to oxidative stress and drought
inferred← citeshttps://doi.org/10.1016/j.plaphy.2014.04.019openalex-snapshot
Plant hormones in defense response of Brassica napus to Sclerotinia sclerotiorum – Reassessing the role of salicylic acid in the interaction with a necrotroph
inferred← citeshttps://doi.org/10.1016/j.plaphy.2015.12.001openalex-snapshot
Microarray-based gene expression analysis of strong seed dormancy in rice cv. N22 and less dormant mutant derivatives
inferred← citeshttps://doi.org/10.1016/j.plaphy.2017.02.015openalex-snapshot
The wheat mutant DELLA-encoding gene (Rht-B1c) affects plant photosynthetic responses to cadmium stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2017.12.022openalex-snapshot
Identification and functional analysis of cassava DELLA proteins in plant disease resistance against cassava bacterial blight
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.12.004openalex-snapshot
Light contributes to salt resistance through GAI protein regulation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108229openalex-snapshot
COI1 dependent jasmonic acid signalling positively modulates ROS scavenging system in transgenic hairy root culture of tomato
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108259openalex-snapshot
The molecular paradigm of reactive oxygen species (ROS) and reactive nitrogen species (RNS) with different phytohormone signaling pathways during drought stress in plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108424openalex-snapshot
Gibberellic acid signaling promotes resistance to saline-alkaline stress by increasing the uptake of ammonium in rice
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109541openalex-snapshot
How to survive mild winters: Cold acclimation, deacclimation, and reacclimation in winter wheat and barley
inferred← citeshttps://doi.org/10.1016/j.sajb.2010.04.014openalex-snapshot
Alleviation of dormancy by reactive oxygen species in Bidens pilosa L. seeds
inferred← citeshttps://doi.org/10.1016/j.scienta.2014.05.020openalex-snapshot
Why calcium deficiency is not the cause of blossom-end rot in tomato and pepper fruit – a reappraisal
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111693openalex-snapshot
Gibberellins regulate root growth by antagonizing the jasmonate pathway in tomato plants in response to potassium deficiency
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113193openalex-snapshot
Exogenous application of gibberellic acid reduces antioxidant capacity of leaves, resulting in increased Tipburn damages in Lisianthus cultivars
inferred← citeshttps://doi.org/10.1016/j.scienta.2026.114966openalex-snapshot
Multiomics dissection of the gibberellin-mediated runner inhibition in a tufted wild strawberry (Fragaria nilgerrensis)
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.170626openalex-snapshot
Strigolactones alleviate the toxicity of polystyrene nanoplastics (PS-NPs) in maize (Zea mays L.)
inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.06.005openalex-snapshot
No hormone to rule them all: Interactions of plant hormones during the responses of plants to pathogens
inferred← citeshttps://doi.org/10.1016/j.semcdb.2020.04.009openalex-snapshot
Origin and evolution of gibberellin signaling and metabolism in plants
inferred← citeshttps://doi.org/10.1016/j.tplants.2011.03.007openalex-snapshot
ROS signaling: the new wave?
inferred← citeshttps://doi.org/10.1016/j.tplants.2013.10.001openalex-snapshot
Gibberellins and DELLAs: central nodes in growth regulatory networks
inferred← citeshttps://doi.org/10.1016/j.tplants.2015.06.008openalex-snapshot
Tuning plant signaling and growth to survive salt
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.04.002openalex-snapshot
The BAP Module: A Multisignal Integrator Orchestrating Growth
inferred← citeshttps://doi.org/10.1016/j.tplants.2022.08.002openalex-snapshot
Signaling events for photomorphogenic root development
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101972openalex-snapshot
Cytokinin-activated DIRIGENT13 promotes lignan synthesis to regulate root growth and abiotic stress tolerance by modulating ROS homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.ymeth.2016.07.009openalex-snapshot
In vivo ROS and redox potential fluorescent detection in plants: Present approaches and future perspectives
inferred← citeshttps://doi.org/10.1016/s0065-2296(10)52001-9openalex-snapshot
Chapter 1 Oxidation of Proteins in Plants—Mechanisms and Consequences
inferred← citeshttps://doi.org/10.1016/s0065-2296(10)54002-3openalex-snapshot
Molecular Mechanisms of Sex Determination in Monoecious and Dioecious Plants
inferred← citeshttps://doi.org/10.1016/s0070-2153(10)91002-8openalex-snapshot
Light-Regulated Plant Growth and Development
inferred← citeshttps://doi.org/10.1016/s1937-6448(08)01403-2openalex-snapshot
Chapter 3: Programmed Cell Death in Plants
inferred← citeshttps://doi.org/10.1016/s2095-3119(15)61214-xopenalex-snapshot
Combining QTL mapping and expression profile analysis to identify candidate genes of cold tolerance from Dongxiang common wild rice (Oryza rufipogon Griff.)
inferred← citeshttps://doi.org/10.1016/s2095-3119(15)61275-8openalex-snapshot
Cloning and characterization of CaGID1s and CaGAI in Capsicum annuum L.
inferred← citeshttps://doi.org/10.1016/s2095-3119(16)61608-8openalex-snapshot
Effects of salt stress on rice growth, development characteristics, and the regulating ways: A review
inferred← citeshttps://doi.org/10.1021/acs.est.0c08493openalex-snapshot
Identifying the Phytotoxicity and Defense Mechanisms Associated with Graphene-Based Nanomaterials by Integrating Multiomics and Regular Analysis
inferred← citeshttps://doi.org/10.1021/acs.jafc.6c04159openalex-snapshot
The E3 Ubiquitin-Protein Ligase ZmBOIR3 Is a Key Regulator of Low-Temperature Tolerance in Maize Seedlings
inferred← citeshttps://doi.org/10.1038/cr.2011.118openalex-snapshot
Plant ubiquitin-proteasome pathway and its role in gibberellin signaling
inferred← citeshttps://doi.org/10.1038/emboj.2012.273openalex-snapshot
ROS‐mediated vascular homeostatic control of root‐to‐shoot soil Na delivery in Arabidopsis
inferred← citeshttps://doi.org/10.1038/hortres.2014.43openalex-snapshot
Elucidating the molecular responses of apple rootstock resistant to ARD pathogens: challenges and opportunities for development of genomics-assisted breeding tools
inferred← citeshttps://doi.org/10.1038/hortres.2014.45openalex-snapshot
Genomic variants of genes associated with three horticultural traits in apple revealed by genome re-sequencing
inferred← citeshttps://doi.org/10.1038/ncb2546openalex-snapshot
Brassinosteroid, gibberellin and phytochrome impinge on a common transcription module in Arabidopsis
inferred← citeshttps://doi.org/10.1038/ncomms9041openalex-snapshot
A novel thiol-reductase activity of Arabidopsis YUC6 confers drought tolerance independently of auxin biosynthesis
inferred← citeshttps://doi.org/10.1038/nplants.2016.13openalex-snapshot
Arabidopsis NAC transcription factor JUB1 regulates GA/BR metabolism and signalling
inferred← citeshttps://doi.org/10.1038/s41467-025-60733-1openalex-snapshot
Growth arrest is a DNA damage protection strategy in Arabidopsis
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