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RBOH-mediated ROS production facilitates lateral root emergence in Arabidopsis

https://doi.org/10.1242/dev.136465
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What this work says

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

inferredcites →https://doi.org/10.1007/978-1-62703-221-6_9openalex-snapshot
Inducible System for Lateral Roots in Arabidopsis thaliana and Maize
inferredcites →https://doi.org/10.1007/s00344-011-9235-7openalex-snapshot
Ca2+ and CaM are Involved in NO- and H2O2-Induced Adventitious Root Development in Marigold
inferredcites →https://doi.org/10.1007/s00425-004-1394-3openalex-snapshot
Xylem parenchyma cells deliver the H2O2 necessary for lignification in differentiating xylem vessels
inferredcites →https://doi.org/10.1007/s11103-013-0168-3openalex-snapshot
Interaction between HY1 and H2O2 in auxin-induced lateral root formation in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2013.02.045openalex-snapshot
A Mechanism for Localized Lignin Deposition in the Endodermis
inferredcites →https://doi.org/10.1016/j.plantsci.2013.03.017openalex-snapshot
The mitochondrial glutathione peroxidase GPX3 is essential for H2O2 homeostasis and root and shoot development in rice
inferredcites →https://doi.org/10.1016/j.tiv.2013.01.016openalex-snapshot
Dichloro-dihydro-fluorescein diacetate (DCFH-DA) assay: A quantitative method for oxidative stress assessment of nanoparticle-treated cells
inferredcites →https://doi.org/10.1016/j.tplants.2006.07.003openalex-snapshot
A novel role for abscisic acid emerges from underground
inferredcites →https://doi.org/10.1016/j.tplants.2013.04.006openalex-snapshot
Lateral root development in Arabidopsis: fifty shades of auxin
inferredcites →https://doi.org/10.1016/s0092-8674(03)00924-3openalex-snapshot
Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
inferredcites →https://doi.org/10.1038/emboj.2012.303openalex-snapshot
Auxin reflux between the endodermis and pericycle promotes lateral root initiation
inferredcites →https://doi.org/10.1038/msb.2013.43openalex-snapshot
Sequential induction of auxin efflux and influx carriers regulates lateral root emergence
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/nature04198openalex-snapshot
A RhoGDP dissociation inhibitor spatially regulates growth in root hair cells
inferredcites →https://doi.org/10.1038/ncb1754openalex-snapshot
The auxin influx carrier LAX3 promotes lateral root emergence
inferredcites →https://doi.org/10.1038/ncb2573openalex-snapshot
Auxin regulates aquaporin function to facilitate lateral root emergence
inferredcites →https://doi.org/10.1038/nchembio.1044openalex-snapshot
A role for the root cap in root branching revealed by the non-auxin probe naxillin
inferredcites →https://doi.org/10.1046/j.0960-7412.2001.01201.xopenalex-snapshot
Lateral root formation is blocked by a gain‐of‐function mutation in the SOLITARY‐ROOT/IAA14 gene of Arabidopsis
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.0708586104openalex-snapshot
Oscillations in extracellular pH and reactive oxygen species modulate tip growth of Arabidopsis root hairs
inferredcites →https://doi.org/10.1073/pnas.1210807110openalex-snapshot
Lateral root morphogenesis is dependent on the mechanical properties of the overlaying tissues
inferredcites →https://doi.org/10.1073/pnas.1210835110openalex-snapshot
Floral organ abscission peptide IDA and its HAE/HSL2 receptors control cell separation during lateral root emergence
inferredcites →https://doi.org/10.1073/pnas.1308412110openalex-snapshot
Dirigent domain-containing protein is part of the machinery required for formation of the lignin-based Casparian strip in the root
inferredcites →https://doi.org/10.1073/pnas.1333899100openalex-snapshot
Reactive oxygen species and ethylene play a positive role in lateral root base nodulation of a semiaquatic legume
inferredcites →https://doi.org/10.1073/pnas.1403016111openalex-snapshot
Periodic root branching in Arabidopsis requires synthesis of an uncharacterized carotenoid derivative
inferredcites →https://doi.org/10.1093/aob/mcj604openalex-snapshot
Lateral Root Initiation in Arabidopsis: Developmental Window, Spatial Patterning, Density and Predictability
inferredcites →https://doi.org/10.1093/aob/mct181openalex-snapshot
Auxin increases the hydrogen peroxide (H2O2) concentration in tomato (Solanum lycopersicum) root tips while inhibiting root growth
inferredcites →https://doi.org/10.1093/bioinformatics/btg405openalex-snapshot
affy—analysis of Affymetrix GeneChip data at the probe level
inferredcites →https://doi.org/10.1093/bioinformatics/bti270openalex-snapshot
Use of within-array replicate spots for assessing differential expression in microarray experiments
inferredcites →https://doi.org/10.1093/dnares/6.1.13openalex-snapshot
A Novel Subtilisin-like Protease Gene from Arabidopsis thaliana is Expressed at Sites of Lateral Root Emergence
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/jxb/erm222openalex-snapshot
Expression of polygalacturonases and evidence to support their role during cell separation processes in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/ers040openalex-snapshot
Live imaging of intra- and extracellular pH in plants using pHusion, a novel genetically encoded biosensor
inferredcites →https://doi.org/10.1093/jxb/ert172openalex-snapshot
Auxin induces redox regulation of ascorbate peroxidase 1 activity by S-nitrosylation/denitrosylation balance resulting in changes of root growth pattern in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/eru056openalex-snapshot
Cell wall properties play an important role in the emergence of lateral root primordia from the parent root
inferredcites →https://doi.org/10.1093/nar/29.9.e45openalex-snapshot
A new mathematical model for relative quantification in real-time RT-PCR
inferredcites →https://doi.org/10.1093/pcp/pce176openalex-snapshot
Involvement of Superoxide Generation in Salicylic Acid-Induced Stomatal Closure in Vicia faba
inferredcites →https://doi.org/10.1093/pcp/pci145openalex-snapshot
Reactive Oxygen Species and Root Hairs in Arabidopsis Root Response to Nitrogen, Phosphorus and Potassium Deficiency
inferredcites →https://doi.org/10.1098/rstb.2011.0232openalex-snapshot
Multiple AUX/IAA–ARF modules regulate lateral root formation: the role of Arabidopsis SHY2/IAA3-mediated auxin signalling
inferredcites →https://doi.org/10.1104/pp.105.068254openalex-snapshot
The Zinc-Finger Protein Zat12 Plays a Central Role in Reactive Oxygen and Abiotic Stress Signaling in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.078089openalex-snapshot
Production of Reactive Oxygen Species by Plant NADPH Oxidases
inferredcites →https://doi.org/10.1104/pp.110.154567openalex-snapshot
Ethylene Signaling Regulates Accumulation of the FLS2 Receptor and Is Required for the Oxidative Burst Contributing to Plant Immunity
inferredcites →https://doi.org/10.1104/pp.111.192740openalex-snapshot
Reactive Oxygen Species Are Involved in Gibberellin/Abscisic Acid Signaling in Barley Aleurone Cells
inferredcites →https://doi.org/10.1104/pp.112.206029openalex-snapshot
Transcriptional and Functional Classification of the GOLVEN/ROOT GROWTH FACTOR/CLE-Like Signaling Peptides Reveals Their Role in Lateral Root and Hair Formation
inferredcites →https://doi.org/10.1104/pp.114.238873openalex-snapshot
The Emerging Role of Reactive Oxygen Species Signaling during Lateral Root Development
inferredcites →https://doi.org/10.1104/pp.126.3.1055openalex-snapshot
Role of Auxin-Induced Reactive Oxygen Species in Root Gravitropism
inferredcites →https://doi.org/10.1105/tpc.004960openalex-snapshot
Auxin-Mediated Cell Cycle Activation during Early Lateral Root Initiation
inferredcites →https://doi.org/10.1105/tpc.010354openalex-snapshot
AUX1 Promotes Lateral Root Formation by Facilitating Indole-3-Acetic Acid Distribution between Sink and Source Tissues in the Arabidopsis Seedling
inferredcites →https://doi.org/10.1105/tpc.014613openalex-snapshot
Dissection of Arabidopsis Bax Inhibitor-1 Suppressing Bax–, Hydrogen Peroxide–, and Salicylic Acid–Induced Cell Death
inferredcites →https://doi.org/10.1105/tpc.104.024737openalex-snapshot
Structure-Function Analysis of the Presumptive Arabidopsis Auxin Permease AUX1[W]
inferredcites →https://doi.org/10.1105/tpc.105.035493openalex-snapshot
Cell Cycle Progression in the Pericycle Is Not Sufficient for SOLITARY ROOT/IAA14-Mediated Lateral Root Initiation inArabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.106.047761openalex-snapshot
ARF7 and ARF19 Regulate Lateral Root Formation via Direct Activation of LBD/ASL Genes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.097766openalex-snapshot
AUX/LAX Genes Encode a Family of Auxin Influx Transporters That Perform Distinct Functions during Arabidopsis Development
inferredcites →https://doi.org/10.1105/tpc.112.107227openalex-snapshot
Endodermal ABA Signaling Promotes Lateral Root Quiescence during Salt Stress in Arabidopsis Seedlings
inferredcites →https://doi.org/10.1105/tpc.113.113985openalex-snapshot
A Membrane-Bound NAC Transcription Factor, ANAC017, Mediates Mitochondrial Retrograde Signaling in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.114868openalex-snapshot
A Kinetic Analysis of the Auxin Transcriptome Reveals Cell Wall Remodeling Proteins That Modulate Lateral Root Development in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.3.465openalex-snapshot
A Gain-of-Function Mutation in IAA28 Suppresses Lateral Root Development
inferredcites →https://doi.org/10.1105/tpc.13.4.843openalex-snapshot
Auxin Transport Promotes Arabidopsis Lateral Root Initiation
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.03005.xopenalex-snapshot
The NADPH‐oxidase AtrbohB plays a role in Arabidopsis seed after‐ripening
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03996.xopenalex-snapshot
Lateral root initiation: one step at a time
inferredcites →https://doi.org/10.1126/science.1245871openalex-snapshot
A Spatial Accommodation by Neighboring Cells Is Required for Organ Initiation in Arabidopsis
inferredcites →https://doi.org/10.1242/dev.00926openalex-snapshot
Partial loss-of-function alleles reveal a role forGNOMin auxin transport-related, post-embryonic development ofArabidopsis
inferredcites →https://doi.org/10.1242/dev.02753openalex-snapshot
Auxin-dependent regulation of lateral root positioning in the basal meristem of Arabidopsis
inferredcites →https://doi.org/10.1242/dev.118.2.575openalex-snapshot
The role of the monopteros gene in organising the basal body region of the Arabidopsis embryo
inferredcites →https://doi.org/10.1242/dev.124.1.33openalex-snapshot
Organization and cell differentiation in lateral roots of Arabidopsis thaliana
inferredcites →https://doi.org/10.1242/dev.125.15.2925openalex-snapshot
Localized changes in apoplastic and cytoplasmic pH are associated with root hair development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1242/dev.126.4.711openalex-snapshot
Control of auxin-regulated root development by the Arabidopsis thaliana SHY2/IAA3 gene
inferredcites →https://doi.org/10.1242/dev.136283openalex-snapshot
Lateral root emergence in Arabidopsis is dependent on transcription factor LBD29 regulating auxin influx carrier LAX3
inferredcites →https://doi.org/10.1371/journal.pbio.1001719openalex-snapshot
ANXUR Receptor-Like Kinases Coordinate Cell Wall Integrity with Growth at the Pollen Tube Tip Via NADPH Oxidases
inferredcites →https://doi.org/10.1590/s1415-47572012000600016openalex-snapshot
Plant responses to stresses: role of ascorbate peroxidase in the antioxidant protection
inferredcites →https://doi.org/10.21769/bioprotoc.263openalex-snapshot
Detection of Hydrogen Peroxide by DAB Staining in Arabidopsis Leaves
inferredcites →https://doi.org/10.3389/fpls.2012.00225openalex-snapshot
AUX/LAX family of auxin influx carriers—an overview
inferredcites →https://doi.org/10.3389/fpls.2012.00292openalex-snapshot
ROS-talk – how the apoplast, the chloroplast, and the nucleus get the message through
inferredcites →https://doi.org/10.4161/psb.25052openalex-snapshot
Hydrogen peroxide is involved in cGMP modulating the lateral root development ofArabidopsis thaliana

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4822288openalex-extracted
Real-Time Live Imaging of Cytosolic Reactive Oxygen Species and Ca2+ of Marchantia Polymorpha Gemmalings Reveal Immediate Initial Responses of Plant Cells Triggered by Nonthermal Plasma Irradiation
inferred← citeshttps://doi.org/10.1002/9780470015902.a0029515openalex-snapshot
Lateral Root Formation
inferred← citeshttps://doi.org/10.1007/978-3-030-11129-8_8openalex-snapshot
Nitric Oxide and Hydrogen Peroxide in Root Organogenesis
inferred← citeshttps://doi.org/10.1007/978-3-030-17597-9_2openalex-snapshot
NADPH Oxidases Have Key Roles in Mutulistic Associations with Rhizobia or with Mycorrhizal Fungi in Root Legumes
inferred← citeshttps://doi.org/10.1007/978-3-030-54478-2_5openalex-snapshot
Serotonin Control of Root Growth via ROS and Hormone Signaling
inferred← citeshttps://doi.org/10.1007/978-3-319-74057-7_2openalex-snapshot
The Role of Ascorbate in Plant Growth and Development
inferred← citeshttps://doi.org/10.1007/978-981-13-8625-1_23openalex-snapshot
Abiotic Stress Tolerance in Plants by Priming and Pretreatments with Ascorbic Acid
inferred← citeshttps://doi.org/10.1007/s00299-019-02372-7openalex-snapshot
Hydrogen peroxide is involved in methane-induced tomato lateral root formation
inferred← citeshttps://doi.org/10.1007/s00299-020-02630-zopenalex-snapshot
Impact of green synthesized WcAgNPs on in-vitro plant regeneration and withanolides production by inducing key biosynthetic genes in Withania coagulans
inferred← citeshttps://doi.org/10.1007/s00299-023-03120-8openalex-snapshot
Arabidopsis PDE1 confers phosphate-deficiency tolerance in primary root growth
inferred← citeshttps://doi.org/10.1007/s00344-022-10614-4openalex-snapshot
Reduced Soybean Water Stress Tolerance by miR393a-Mediated Repression of GmTIR1 and Abscisic Acid Accumulation
inferred← citeshttps://doi.org/10.1007/s00344-023-11046-4openalex-snapshot
Endogenous Serotonin Accumulation Coincides with Reorganization of Auxin Efflux Protein (PIN1) and Actin (ACT8) Accompanying Primary Root Growth Inhibition in NaCl-Stress-Induced Etiolated Sunflower (Helianthus annuus; cv. KBSH 44) Seedlings
inferred← citeshttps://doi.org/10.1007/s00709-020-01508-xopenalex-snapshot
Transcriptional analysis reveals sodium nitroprusside affects alfalfa in response to PEG-induced osmotic stress at germination stage
inferred← citeshttps://doi.org/10.1007/s00709-022-01819-1openalex-snapshot
Brachypodium BdCHS is a homolog of Arabidopsis AtCHS involved in the synthesis of flavonoids and lateral root development
inferred← citeshttps://doi.org/10.1007/s00709-023-01847-5openalex-snapshot
Reactive oxygen species and NADPH oxidase-encoding genes underly the plant growth and developmental responses to Trichoderma
inferred← citeshttps://doi.org/10.1007/s00709-024-01959-6openalex-snapshot
Hydrogen peroxide modulates the expression of the target of rapamycin (TOR) and cell division in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10265-026-01744-xopenalex-snapshot
Regulatory responses to phosphorus deficiency in pecan (Carya illinoinensis): transcriptomic and microscopic approaches
inferred← citeshttps://doi.org/10.1007/s10725-017-0292-1openalex-snapshot
AtRBOH I confers submergence tolerance and is involved in auxin-mediated signaling pathways under hypoxic stress
inferred← citeshttps://doi.org/10.1007/s10886-021-01337-zopenalex-snapshot
Survival of Plants During Short-Term BOA-OH Exposure: ROS Related Gene Expression and Detoxification Reactions Are Accompanied With Fast Membrane Lipid Repair in Root Tips
inferred← citeshttps://doi.org/10.1007/s11103-018-00817-3openalex-snapshot
l-Cysteine desulfhydrase-dependent hydrogen sulfide is required for methane-induced lateral root formation
inferred← citeshttps://doi.org/10.1007/s11103-025-01630-5openalex-snapshot
Control of heat and oxidative stress adaptation by the DJ-1 paralogs in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11104-018-3859-3openalex-snapshot
Comparative transcriptome combined with metabolomic and physiological analyses revealed ROS-mediated redox signaling affecting rice growth and cellular iron homeostasis under varying pH conditions
inferred← citeshttps://doi.org/10.1007/s11104-023-06326-7openalex-snapshot
The phytohormones underlying the plant lateral root development in fluctuated soil environments
inferred← citeshttps://doi.org/10.1007/s12042-021-09286-3openalex-snapshot
Genome-wide Identification, Classification, Evolutionary Expansion and Expression of Rboh Family Genes in Pepper (Capsicum annuum L.)
inferred← citeshttps://doi.org/10.1007/s40502-026-01006-xopenalex-snapshot
Comparative evolutionary analysis reveals diversification of the RBOH gene family in cultivated and wild rice
inferred← citeshttps://doi.org/10.1007/s40626-020-00187-6openalex-snapshot
Abscisic acid-nitric oxide and auxin interaction modulates salt stress response in tomato roots
inferred← citeshttps://doi.org/10.1007/s44154-022-00061-2openalex-snapshot
Multiple forms of vitamin B6 regulate salt tolerance by balancing ROS and abscisic acid levels in maize root
inferred← citeshttps://doi.org/10.1007/s44154-024-00162-0openalex-snapshot
Physiological and molecular bases of the nickel toxicity responses in tomato
inferred← citeshttps://doi.org/10.1016/b978-0-323-85790-1.00010-5openalex-snapshot
EF-hand domain-containing proteins: diversity and role in plants
inferred← citeshttps://doi.org/10.1016/bs.abr.2022.08.024openalex-snapshot
ROS metabolism and ripening of fleshy fruits
inferred← citeshttps://doi.org/10.1016/j.cej.2020.126905openalex-snapshot
Nanomaterial-mediated sustainable hydrogen supply induces lateral root formation via nitrate reductase-dependent nitric oxide
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114030openalex-snapshot
Trichoderma-secreted anthranilic acid promotes lateral root development via auxin signaling and RBOHF-induced endodermal cell wall remodeling
inferred← citeshttps://doi.org/10.1016/j.cub.2021.06.055openalex-snapshot
Periodic root branching is influenced by light through an HY1-HY5-auxin pathway
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2019.04.015openalex-snapshot
Mycorrhizal and non-mycorrhizal Medicago truncatula roots exhibit differentially regulated NADPH oxidase and antioxidant response under Pb stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104279openalex-snapshot
Respiratory burst oxidases and apoplastic peroxidases facilitate ammonium syndrome development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104544openalex-snapshot
NITRIC OXIDE ASSOCIATED PROTEIN1 (AtNOA1) is necessary for copper-induced lateral root elongation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2025.106187openalex-snapshot
Microcystis aeruginosa exudate alters root development by impacting plant hormone accumulation and auxin signal transduction
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2019.09.011openalex-snapshot
Melatonin facilitates lateral root development by coordinating PAO-derived hydrogen peroxide and Rboh-derived superoxide radical
inferred← citeshttps://doi.org/10.1016/j.gde.2017.03.010openalex-snapshot
Spatiotemporal mechanisms of root branching
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101978openalex-snapshot
Highlighting reactive oxygen species as multitaskers in root development
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2018.08.035openalex-snapshot
New adventitious root formation and primary root biomass accumulation are regulated by nitric oxide and reactive oxygen species in rice seedlings under arsenate stress
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2022.129020openalex-snapshot
Thiourea mediated ROS-metabolites reprogramming restores root system architecture under arsenic stress in rice
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154242openalex-snapshot
AtHD2D is involved in regulating lateral root development and participates in abiotic stress response in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.molp.2019.03.015openalex-snapshot
The Systems Biology of Lateral Root Formation: Connecting the Dots
inferred← citeshttps://doi.org/10.1016/j.molp.2020.06.002openalex-snapshot
A Kinase–Phosphatase–Transcription Factor Module Regulates Adventitious Root Emergence in Arabidopsis Root–Hypocotyl Junctions
inferred← citeshttps://doi.org/10.1016/j.molp.2023.09.007openalex-snapshot
Rice roots avoid asymmetric heavy metal and salinity stress via an RBOH-ROS-auxin signaling cascade
inferred← citeshttps://doi.org/10.1016/j.nantod.2023.102045openalex-snapshot
Functionalized carbon nano-enabled plant ROS signal engineering for growth / defense balance
inferred← citeshttps://doi.org/10.1016/j.niox.2019.01.013openalex-snapshot
The era of nitric oxide in plant biology: Twenty years tying up loose ends
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.09.005openalex-snapshot
Breakout — lateral root emergence in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.pbi.2018.06.002openalex-snapshot
Getting physical: invasive growth events during plant development
inferred← citeshttps://doi.org/10.1016/j.pbi.2022.102293openalex-snapshot
Reactive oxygen species function as signaling molecules in controlling plant development and hormonal responses
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.12.029openalex-snapshot
Methane-induced lateral root formation requires the participation of nitric oxide signaling
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108032openalex-snapshot
ROS interplay between plant growth and stress biology: Challenges and future perspectives
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108272openalex-snapshot
Unraveling lipid peroxidation-mediated regulation of redox homeostasis for sustaining plant health
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108273openalex-snapshot
The hidden harmony: Exploring ROS-phytohormone nexus for shaping plant root architecture in response to environmental cues
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108429openalex-snapshot
Lateral root primordium: Formation, influencing factors and regulation
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108682openalex-snapshot
Sub1 QTL confers submergence tolerance in rice through nitro-oxidative regulation and phytohormonal signaling
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108698openalex-snapshot
MYB4, a member of R2R3-subfamily of MYB transcription factor functions as a repressor of key genes involved in flavonoid biosynthesis and repair of UV-B induced DNA double strand breaks in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109172openalex-snapshot
Real-time live imaging of cytosolic hydrogen peroxide and Ca2+ of Marchantia polymorpha gemmalings reveal immediate initial responses of plant cells triggered by nonthermal plasma irradiation
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109855openalex-snapshot
The functional conservation of SSR1 homologs in plants
inferred← citeshttps://doi.org/10.1016/j.plgene.2019.100182openalex-snapshot
Antioxidant enzymes regulation in plants in reference to reactive oxygen species (ROS) and reactive nitrogen species (RNS)
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.06.015openalex-snapshot
Lateral Root Formation in Arabidopsis: A Well-Ordered LRexit
inferred← citeshttps://doi.org/10.1016/j.tplants.2023.03.003openalex-snapshot
Sound perception in plants: from ecological significance to molecular understanding
inferred← citeshttps://doi.org/10.1016/j.tplants.2024.09.018openalex-snapshot
Multiple layers of regulators emerge in the network controlling lateral root organogenesis
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100306openalex-snapshot
Transcriptional landscapes of de novo root regeneration from detached Arabidopsis leaves revealed by time-lapse and single-cell RNA sequencing analyses
inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100771openalex-snapshot
OsEIL1 and OsEIL2, two master regulators of rice ethylene signaling, promote the expression of ROS scavenging genes to facilitate coleoptile elongation and seedling emergence from soil
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.9b00028openalex-snapshot
RBOH-Dependent ROS Synthesis and ROS Scavenging by Plant Specialized Metabolites To Modulate Plant Development and Stress Responses
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c02146openalex-snapshot
Interaction between TaNOX7 and TaCDPK13 Contributes to Plant Fertility and Drought Tolerance by Regulating ROS Production
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c01605openalex-snapshot
Cross-Talk between Hydrogen Peroxide and Nitric Oxide during Plant Development and Responses to Stress
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c07741openalex-snapshot
Root Hair Development and Adaptation to Abiotic Stress
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c08019openalex-snapshot
Pseudomonas chlororaphis subsp. aurantiaca Stimulates Lateral Root Development by Integrating Auxin and Reactive Oxygen Species Signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41438-021-00674-0openalex-snapshot
Production of reactive oxygen species by PuRBOHF is critical for stone cell development in pear fruit
inferred← citeshttps://doi.org/10.1038/s41467-022-28833-4openalex-snapshot
Apoplastic class III peroxidases PRX62 and PRX69 promote Arabidopsis root hair growth at low temperature
inferred← citeshttps://doi.org/10.1038/s41477-025-02028-3openalex-snapshot
Wounding induces multilayered barrier formation in mature leaves via phytohormone signalling and ATML1-mediated epidermal specification
inferred← citeshttps://doi.org/10.1038/s41598-020-60163-7openalex-snapshot
Laterals take it better – Emerging and young lateral roots survive lethal salinity longer than the primary root in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41598-024-53104-1openalex-snapshot
Growth control of Marchantia polymorpha gemmae using nonthermal plasma irradiation
inferred← citeshttps://doi.org/10.1071/fp20093openalex-snapshot
Transcriptome analysis provides insights into the molecular bases in response to different nitrogen forms-induced oxidative stress in tea plant roots (Camellia sinensis)
inferred← citeshttps://doi.org/10.1073/pnas.1701536114openalex-snapshot
Molecular link between auxin and ROS-mediated polar growth
inferred← citeshttps://doi.org/10.1073/pnas.1714410114openalex-snapshot
PLETHORA transcription factors orchestrate de novo organ patterning during Arabidopsis lateral root outgrowth
inferred← citeshttps://doi.org/10.1073/pnas.2406373122openalex-snapshot
Abscisic acid signaling gates salt-induced responses of plant roots
inferred← citeshttps://doi.org/10.1073/pnas.2529740123openalex-snapshot
Nanoscale regulation of ROS signaling at the plasma membrane tunes the plant response to osmotic stress
inferred← citeshttps://doi.org/10.1074/jbc.ra120.014543openalex-snapshot
Flavonols modulate lateral root emergence by scavenging reactive oxygen species in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1080/09168451.2020.1808444openalex-snapshot
A single seed treatment mediated through reactive oxygen species increases germination, growth performance, and abiotic stress tolerance inArabidopsisand rice
inferred← citeshttps://doi.org/10.1080/15592324.2019.1657343openalex-snapshot
NADPH oxidases, essential players of hormone signalings in plant development and response to stresses
inferred← citeshttps://doi.org/10.1080/15592324.2019.1703503openalex-snapshot
Stimulation of adventitious root formation by the oligosaccharin OSRG at the transcriptome level
inferred← citeshttps://doi.org/10.1080/19420889.2018.1467188openalex-snapshot
RbohA coordinates lateral root emergence in common bean
inferred← citeshttps://doi.org/10.1088/1755-1315/421/6/062014openalex-snapshot
The use of biogenic nanoparticles of ferrihydrite in the propagation of horticultural crops by cutting
inferred← citeshttps://doi.org/10.1093/aob/mcx207openalex-snapshot
Hydrogen peroxide acts downstream of melatonin to induce lateral root formation
inferred← citeshttps://doi.org/10.1093/hr/uhac267openalex-snapshot
Theanine, a tea-plant-specific non-proteinogenic amino acid, is involved in the regulation of lateral root development in response to nitrogen status
inferred← citeshttps://doi.org/10.1093/jxb/eraa160openalex-snapshot
The isoleucic acid triad: distinct impacts on plant defense, root growth, and formation of reactive oxygen species
inferred← citeshttps://doi.org/10.1093/jxb/eraa195openalex-snapshot
A glutathione-dependent control of the indole butyric acid pathway supports Arabidopsis root system adaptation to phosphate deprivation
inferred← citeshttps://doi.org/10.1093/jxb/erab501openalex-snapshot
The transcription factor WRKY75 regulates the development of adventitious roots, lateral buds and callus by modulating hydrogen peroxide content in poplar
inferred← citeshttps://doi.org/10.1093/jxb/erac115openalex-snapshot
PHB3 regulates lateral root primordia formation via NO-mediated degradation of AUXIN/INDOLE-3-ACETIC ACID proteins
inferred← citeshttps://doi.org/10.1093/jxb/erac346openalex-snapshot
Non-volatile signals and redox mechanisms are required for the responses of Arabidopsis roots toPseudomonas oryzihabitans
inferred← citeshttps://doi.org/10.1093/jxb/erae090openalex-snapshot
Superoxide signalling and antioxidant processing in the plant nucleus
inferred← citeshttps://doi.org/10.1093/jxb/erae201openalex-snapshot
Stem cell quiescence and dormancy in plant meristems
inferred← citeshttps://doi.org/10.1093/jxb/erae415openalex-snapshot
The MADS-box gene XAANTAL1 participates in Arabidopsis thaliana primary root growth and columella stem cell patterns in response to ROS, via direct regulation of PEROXIDASE 28 and RETINOBLASTOMA-RELATED genes
inferred← citeshttps://doi.org/10.1093/jxb/erx223openalex-snapshot
Lateral root formation and the multiple roles of auxin
inferred← citeshttps://doi.org/10.1093/jxb/erx290openalex-snapshot
Peroxisomal CuAOζ and its product H2O2 regulate the distribution of auxin and IBA-dependent lateral root development in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pcac012openalex-snapshot
Exposure to Low UV-B Dose Induces DNA Double-Strand Breaks Mediated Onset of Endoreduplication in Vigna radiata (L.) R. Wilczek Seedlings
inferred← citeshttps://doi.org/10.1093/pcp/pcac138openalex-snapshot
Auxin Crosstalk with Reactive Oxygen and Nitrogen Species in Plant Development and Abiotic Stress
inferred← citeshttps://doi.org/10.1093/pcp/pcy107openalex-snapshot
Evidence for the Involvement of Auxin, Ethylene and ROS Signaling During Primary Root Inhibition of Arabidopsis by the Allelochemical Benzoic Acid
inferred← citeshttps://doi.org/10.1093/pcp/pcz001openalex-snapshot
Root Adaptation to H2O2-Induced Oxidative Stress by ARF-GEF BEN1- and Cytoskeleton-Mediated PIN2 Trafficking
inferred← citeshttps://doi.org/10.1093/plcell/koad019openalex-snapshot
Salt stress-induced chloroplastic hydrogen peroxide stimulates pdTPI sulfenylation and methylglyoxal accumulation
inferred← citeshttps://doi.org/10.1093/plphys/kiaa032openalex-snapshot
Characterization ofCYCLOPHILLIN38shows that a photosynthesis-derived systemic signal controls lateral root emergence
inferred← citeshttps://doi.org/10.1093/plphys/kiaa077openalex-snapshot
Oxygen and reactive oxygen species-dependent regulation of plant growth and development
inferred← citeshttps://doi.org/10.1093/plphys/kiad207openalex-snapshot
Multi-copper oxidases SKU5 and SKS1 coordinate cell wall formation using apoplastic redox-based reactions in roots
inferred← citeshttps://doi.org/10.1093/plphys/kiad366openalex-snapshot
Transcription factor RcNAC091 enhances rose drought tolerance through the abscisic acid–dependent pathway
inferred← citeshttps://doi.org/10.1093/plphys/kiaf036openalex-snapshot
ELONGATED HYPOCOTYL 5 promotes root growth by maintaining redox homeostasis and repressing oxidative stress response
inferred← citeshttps://doi.org/10.1101/116517openalex-snapshot
The molecular link between auxin and ROS-Mediated polar root hair growth
inferred← citeshttps://doi.org/10.1101/2020.02.04.932376openalex-snapshot
Class III peroxidases PRX01, PRX44, and PRX73 potentially target extensins during root hair growth in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2020.03.24.005363openalex-snapshot
FSD1: a plastidial, nuclear and cytoplasmic enzyme relocalizing to the plasma membrane under salinity
inferred← citeshttps://doi.org/10.1101/2021.07.19.452882openalex-snapshot
Auxin and pectin remodeling interplay during rootlet emergence in white lupin
inferred← citeshttps://doi.org/10.1101/2021.08.20.456256openalex-snapshot
Apoplastic class III peroxidases PRX62 and PRX69 regulate ROS-homeostasis and cell wall associated extensins linked to root hair growth at low-temperature in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2021.12.23.474045openalex-snapshot
Reactive oxygen species signalling is involved in alkamide-induced alterations in root development
inferred← citeshttps://doi.org/10.1101/2024.01.31.578125openalex-snapshot
Receptor kinase LecRK-I.9 regulates cell wall remodelling and signalling during lateral root formation in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2024.06.25.600713openalex-snapshot
Cytokinin-inducible DIRIGENT13 involved in lignan synthesis and ROS accumulation promotes root growth and abiotic stress tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2024.09.02.607870openalex-snapshot
Mature leaves produce a multi-layered wound periderm by integrating phytohormone signaling with ATML1-mediated epidermal specification
inferred← citeshttps://doi.org/10.1101/2025.01.07.631646openalex-snapshot
Calcium-triggered apoplastic ROS bursts balance gravity and mechanical signals to navigate soil
inferred← citeshttps://doi.org/10.1104/pp.17.01010openalex-snapshot
Abscisic Acid-Induced Reactive Oxygen Species Are Modulated by Flavonols to Control Stomata Aperture
inferred← citeshttps://doi.org/10.1111/jipb.13020openalex-snapshot
Salicylic acid promotes quiescent center cell division through ROS accumulation and down‐regulation of PLT1, PLT2, and WOX5
inferred← citeshttps://doi.org/10.1111/jipb.13844openalex-snapshot
Cell wall dynamic changes and signaling during plant lateral root development
inferred← citeshttps://doi.org/10.1111/nph.14304openalex-snapshot
Control of Arabidopsis lateral root primordium boundaries by MYB 36
inferred← citeshttps://doi.org/10.1111/nph.15488openalex-snapshot
Hydrogen peroxide metabolism and functions in plants
inferred← citeshttps://doi.org/10.1111/nph.15917openalex-snapshot
A novel CO 2 ‐responsive systemic signaling pathway controlling plant mycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1111/nph.20367openalex-snapshot
Membrane nanodomains to shape plant cellular functions and signaling
inferred← citeshttps://doi.org/10.1111/nph.70279openalex-snapshot
Endodermal lignification coordinates with root calcium levels to govern lateral root emergence
inferred← citeshttps://doi.org/10.1111/nph.70349openalex-snapshot
ARABIDOPSIS HOMOLOG OF TRITHORAX1 impacts lateral root development by epigenetic regulation of targets involved in root system architecture
inferred← citeshttps://doi.org/10.1111/pbi.14504openalex-snapshot
Mitochondrial AOX1a and an H2O2 feed‐forward signalling loop regulate flooding tolerance in rice
inferred← citeshttps://doi.org/10.1111/pce.13894openalex-snapshot
In vivo light‐sheet microscopy resolves localisation patterns of FSD1 , a superoxide dismutase with function in root development and osmoprotection
inferred← citeshttps://doi.org/10.1111/pce.14504openalex-snapshot
Integration of reactive oxygen species and nutrient signalling to shape root system architecture
inferred← citeshttps://doi.org/10.1111/pce.14531openalex-snapshot
H 2 O 2 , NO, and H 2 S networks during root development and signalling under physiological and challenging environments: Beneficial or toxic?
inferred← citeshttps://doi.org/10.1111/pce.70827openalex-snapshot
Reactive Oxygen Species and Phytohormone Signalling: Redox Modifications Shaping Plant Growth and Stress Acclimation
inferred← citeshttps://doi.org/10.1111/ppl.12839openalex-snapshot
Nitrate affects transcriptional regulation of UPBEAT1 and ROS localisation in roots of Zea mays L.
inferred← citeshttps://doi.org/10.1111/ppl.13050openalex-snapshot
NO and ROS implications in the organization of root system architecture
inferred← citeshttps://doi.org/10.1111/ppl.14047openalex-snapshot
IRR1 contributes to de novo root regeneration from Arabidopsis thaliana leaf explants
inferred← citeshttps://doi.org/10.1111/ppl.14200openalex-snapshot
A cotton APS REDUCTASE represses root hair elongation via sulfur assimilation and hydrogen peroxide‐mediated cell wall damage
inferred← citeshttps://doi.org/10.1111/ppl.70315openalex-snapshot
Crosstalk Between Auxin Signalling and Growth Regulating Factor 5: Implications for Chloroplast Division and Leaf Development
inferred← citeshttps://doi.org/10.1111/tpj.14212openalex-snapshot
Comparative analysis of the reactive oxygen species‐producing enzymatic activity of Arabidopsis NADPH oxidases
inferred← citeshttps://doi.org/10.1111/tpj.14456openalex-snapshot
Reactive oxygen species and reactive carbonyl species constitute a feed‐forward loop in auxin signaling for lateral root formation
inferred← citeshttps://doi.org/10.1111/tpj.14891openalex-snapshot
The fungal NADPH oxidase is an essential element for the molecular dialog between Trichoderma and Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.15361openalex-snapshot
A mechanism coordinating root elongation, endodermal differentiation, redox homeostasis and stress response
inferred← citeshttps://doi.org/10.1111/tpj.15561openalex-snapshot
Oxidative stress response and programmed cell death guided by NAC013 modulate pithiness in radish taproots
inferred← citeshttps://doi.org/10.1111/tpj.15993openalex-snapshot
Auxin triggers pectin modification during rootlet emergence in white lupin
inferred← citeshttps://doi.org/10.1111/tpj.15996openalex-snapshot
The Arabidopsis transcription factor TCP9 modulates root architectural plasticity, reactive oxygen species‐mediated processes, and tolerance to cyst nematode infections
inferred← citeshttps://doi.org/10.1111/tpj.16981openalex-snapshot
AT ‐hook motif nuclear localized transcription factors function redundantly in promoting root growth through modulation of redox homeostasis
inferred← citeshttps://doi.org/10.1126/science.abc6107openalex-snapshot
Pollen PCP-B peptides unlock a stigma peptide–receptor kinase gating mechanism for pollination
inferred← citeshttps://doi.org/10.1126/science.adu1470openalex-snapshot
Redox-regulated Aux/IAA multimerization modulates auxin responses
inferred← citeshttps://doi.org/10.1126/science.adu8197openalex-snapshot
Calcium-triggered apoplastic ROS bursts balance gravity and mechanical signals for soil navigation
inferred← citeshttps://doi.org/10.1134/s0006350918040036openalex-snapshot
The Influence of Nanoparticles of Biogenic Ferrihydrite on the Rooting of Lignified Cuttings of the Ledebour Willow
inferred← citeshttps://doi.org/10.1134/s1021443725603696openalex-snapshot
Networking of Plastoquinone Pool and Reactive Oxygen Species in Higher Plant Signaling
inferred← citeshttps://doi.org/10.11606/d.11.2018.tde-03052018-161612openalex-snapshot
Ácido salicílico e mancozebe na cultura de feijão: parâmetros fisiológicos e componentes de produção
inferred← citeshttps://doi.org/10.1163/22238980-20191115openalex-snapshot
The contribution of cell wall remodeling and signaling to lateral organs formation
inferred← citeshttps://doi.org/10.1186/s12284-019-0364-0openalex-snapshot
OsFPFL4 is Involved in the Root and Flower Development by Affecting Auxin Levels and ROS Accumulation in Rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1186/s12864-019-6162-7openalex-snapshot
Transcriptome analysis of the differential effect of the NADPH oxidase gene RbohB in Phaseolus vulgaris roots following Rhizobium tropici and Rhizophagus irregularis inoculation
inferred← citeshttps://doi.org/10.1186/s12864-021-08283-wopenalex-snapshot
De novo and comparative transcriptomic analysis explain morphological differences in Panax notoginseng taproots
inferred← citeshttps://doi.org/10.1186/s12864-025-11303-8openalex-snapshot
Identification of VcRBOH genes in blueberry and functional characterization of VcRBOHF in plant defense
inferred← citeshttps://doi.org/10.1186/s12870-017-1110-7openalex-snapshot
Hydrogen peroxide is involved in hydrogen sulfide-induced lateral root formation in tomato seedlings
inferred← citeshttps://doi.org/10.1186/s12870-021-03060-zopenalex-snapshot
An NADPH oxidase regulates carbon metabolism and the cell cycle during root nodule symbiosis in common bean (Phaseolus vulgaris)
inferred← citeshttps://doi.org/10.1186/s12870-022-03524-wopenalex-snapshot
Wound-induced signals regulate root organogenesis in Arabidopsis explants
inferred← citeshttps://doi.org/10.1186/s12870-022-03977-zopenalex-snapshot
Bradyrhizobium japonicum IRAT FA3 promotes salt tolerance through jasmonic acid priming in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1186/s12870-023-04571-7openalex-snapshot
Systematic analysis of the Rboh gene family in seven gramineous plants and its roles in response to arbuscular mycorrhizal fungi in maize
inferred← citeshttps://doi.org/10.1186/s12951-021-01222-7openalex-snapshot
Quaternary ammonium iminofullerenes improve root growth of oxidative-stress maize through ASA-GSH cycle modulating redox homeostasis of roots and ROS-mediated root-hair elongation
inferred← citeshttps://doi.org/10.1186/s40538-025-00764-4openalex-snapshot
Humic acids modify root architecture in Arabidopsis through H+-ATPase-dependent target of rapamycin activation in concert with Ca2+ and ROS signaling
inferred← citeshttps://doi.org/10.1201/9781003204091openalex-snapshot
Redox Regulation of Differentiation and De-Differentiation
inferred← citeshttps://doi.org/10.1242/dev.164376openalex-snapshot
Reactive oxygen species in plant development
inferred← citeshttps://doi.org/10.1242/dev.185819openalex-snapshot
Flavonols regulate root hair development by modulating accumulation of reactive oxygen species in the root epidermis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007144openalex-snapshot
Brassinosteroids regulate root growth by controlling reactive oxygen species homeostasis and dual effect on ethylene synthesis in Arabidopsis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007662openalex-snapshot
Rice transcription factor OsMADS25 modulates root growth and confers salinity tolerance via the ABA–mediated regulatory pathway and ROS scavenging
inferred← citeshttps://doi.org/10.1371/journal.pone.0188923openalex-snapshot
Development of a GAL4-VP16/UAS trans-activation system for tissue specific expression in Medicago truncatula
inferred← citeshttps://doi.org/10.1371/journal.pone.0239705openalex-snapshot
Genome-wide identification and characterization of Respiratory Burst Oxidase Homolog genes in six Rosaceae species and an analysis of their effects on adventitious rooting in apple
inferred← citeshttps://doi.org/10.1515/hsz-2020-0291openalex-snapshot
Shifting paradigms and novel players in Cys-based redox regulation and ROS signaling in plants - and where to go next
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2791713/v1openalex-snapshot
The role of hydrogen peroxide in tomato axillary shoot growth
inferred← citeshttps://doi.org/10.21203/rs.3.rs-667372/v1openalex-snapshot
Survival of Plants During Short-Term Boa-Oh Exposure: Ros Related Gene Expression and Detoxification Reactions are Accompaniedwithfast Membrane Lipid Repair in Root Tips
inferred← citeshttps://doi.org/10.21203/rs.3.rs-667372/v2openalex-snapshot
Survival of Plants During Short-Term Boa-Oh Exposure: Ros Related Gene Expression and Detoxification Reactions are Accompanied with Fast Membrane Lipid Repair in Root Tips
inferred← citeshttps://doi.org/10.2139/ssrn.4879949openalex-snapshot
Genome-Wide Identification of Blueberry Vcrboh Genes and Functional Analysis in Plant Denfense
inferred← citeshttps://doi.org/10.22541/au.159819295.56193824openalex-snapshot
Regulation of root architecture by Pseudomonas oryzihabitans is mediated by strigolactones and redox processes.
inferred← citeshttps://doi.org/10.3117/plantroot.17.36openalex-snapshot
Strontium-induced mineral imbalance, cell death, and reactive oxygen species generation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fcell.2018.00002openalex-snapshot
A Salutary Role of Reactive Oxygen Species in Intercellular Tunnel-Mediated Communication
inferred← citeshttps://doi.org/10.3389/fpls.2017.01445openalex-snapshot
Hydrogen Peroxide Is Involved in β-Cyclodextrin-hemin Complex-Induced Lateral Root Formation in Tomato Seedlings
inferred← citeshttps://doi.org/10.3389/fpls.2017.02003openalex-snapshot
Respiratory Burst Oxidase Homolog Gene A Is Crucial for Rhizobium Infection and Nodule Maturation and Function in Common Bean
inferred← citeshttps://doi.org/10.3389/fpls.2019.00206openalex-snapshot
Lateral Root Primordium Morphogenesis in Angiosperms
inferred← citeshttps://doi.org/10.3389/fpls.2019.01306openalex-snapshot
Developmental Roles of AUX1/LAX Auxin Influx Carriers in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2020.569687openalex-snapshot
Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation
inferred← citeshttps://doi.org/10.3389/fpls.2021.660274openalex-snapshot
Reactive Oxygen Species Link Gene Regulatory Networks During Arabidopsis Root Development
inferred← citeshttps://doi.org/10.3389/fpls.2021.720867openalex-snapshot
Lipid Peroxide-Derived Reactive Carbonyl Species as Mediators of Oxidative Stress and Signaling
inferred← citeshttps://doi.org/10.3389/fpls.2021.817101openalex-snapshot
Generating Novel Male Sterile Tomatoes by Editing Respiratory Burst Oxidase Homolog Genes
inferred← citeshttps://doi.org/10.3389/fpls.2023.1326080openalex-snapshot
Genome-wide analysis of respiratory burst oxidase homolog (Rboh) genes in Aquilaria species and insight into ROS-mediated metabolites biosynthesis and resin deposition
inferred← citeshttps://doi.org/10.3389/fpls.2024.1348295openalex-snapshot
Ambient temperature regulates root circumnutation in rice through the ethylene pathway: transcriptome analysis reveals key genes involved
inferred← citeshttps://doi.org/10.3390/agriculture8110179openalex-snapshot
Phylogeny and Expression of NADPH Oxidases during Symbiotic Nodule Formation
inferred← citeshttps://doi.org/10.3390/agronomy15040784openalex-snapshot
Thymol Stimulates Lateral Root Formation via Regulating Endogenous Reactive Oxygen Species
inferred← citeshttps://doi.org/10.3390/antiox10091494openalex-snapshot
Peroxisomal PEX7 Receptor Affects Cadmium-Induced ROS and Auxin Homeostasis in Arabidopsis Root System
inferred← citeshttps://doi.org/10.3390/antiox11112106openalex-snapshot
Review of the Mechanisms by Which Transcription Factors and Exogenous Substances Regulate ROS Metabolism under Abiotic Stress
inferred← citeshttps://doi.org/10.3390/antiox12071451openalex-snapshot
24-Epibrassinolide Facilitates Adventitious Root Formation by Coordinating Cell-Wall Polyamine Oxidase- and Plasma Membrane Respiratory Burst Oxidase Homologue-Derived Reactive Oxygen Species in Capsicum annuum L.
inferred← citeshttps://doi.org/10.3390/antiox9030235openalex-snapshot
Some Physiological and Biochemical Mechanisms during Seed-to-Seedling Transition in Tomato as Influenced by Garlic Allelochemicals
inferred← citeshttps://doi.org/10.3390/biology13121033openalex-snapshot
ROS, an Important Plant Growth Regulator in Root Growth and Development: Functional Genes and Mechanism
inferred← citeshttps://doi.org/10.3390/biom11010077openalex-snapshot
Jasmonates, Ethylene and Brassinosteroids Control Adventitious and Lateral Rooting as Stress Avoidance Responses to Heavy Metals and Metalloids
inferred← citeshttps://doi.org/10.3390/genes14091665openalex-snapshot
Genome-Wide Identification and Expression Analysis of Respiratory Burst Oxidase Homolog (RBOH) Gene Family in Eggplant (Solanum melongena L.) under Abiotic and Biotic Stress
inferred← citeshttps://doi.org/10.3390/horticulturae9010121openalex-snapshot
Hormone–Flavonoid Patterns in Two Genotypes of Campanula portenschlagiana with Distinct Adventitious Rooting Competence
inferred← citeshttps://doi.org/10.3390/ijms20081863openalex-snapshot
Deep Transcriptome Analysis Reveals Reactive Oxygen Species (ROS) Network Evolution, Response to Abiotic Stress, and Regulation of Fiber Development in Cotton
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