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Shoot phytochrome B modulates reactive oxygen species homeostasis in roots via abscisic acid signaling in Arabidopsis
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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/s10265-008-0201-9openalex-snapshot
Activation of abscisic acid biosynthesis in the leaves of Arabidopsis thaliana in response to water deficit
inferredcites →https://doi.org/10.1016/j.cell.2010.10.020openalex-snapshot
Transcriptional Regulation of ROS Controls Transition from Proliferation to Differentiation in the Root
inferredcites →https://doi.org/10.1016/j.pbi.2015.10.012openalex-snapshot
Control of root growth and development by reactive oxygen species
inferredcites →https://doi.org/10.1038/cr.2008.271openalex-snapshot
Heterotrimeric G-protein is involved in phytochrome A-mediated cell death of Arabidopsis hypocotyls
inferredcites →https://doi.org/10.1038/ncomms9669openalex-snapshot
S-nitrosylation triggers ABI5 degradation to promote seed germination and seedling growth
inferredcites →https://doi.org/10.1073/pnas.081594298openalex-snapshot
A postgermination developmental arrest checkpoint is mediated by abscisic acid and requires the ABI5 transcription factor in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1105892108openalex-snapshot
Lotus japonicus nodulation is photomorphogenetically controlled by sensing the red/far red (R/FR) ratio through jasmonic acid (JA) signaling
inferredcites →https://doi.org/10.1080/15592324.2018.1473684openalex-snapshot
Abscisic acid-mediated phytochrome B signaling promotes primary root growth in Arabidopsis
inferredcites →https://doi.org/10.1080/19420889.2016.1261769openalex-snapshot
Underground roots monitor aboveground environment by sensing stem-piped light
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/eri206openalex-snapshot
A mutational analysis of the ABA1 gene of Arabidopsis thaliana highlights the involvement of ABA in vegetative development
inferredcites →https://doi.org/10.1093/jxb/erq171openalex-snapshot
Production and diffusion of chloroplastic H2O2 and its implication to signalling
inferredcites →https://doi.org/10.1098/rstb.2011.0234openalex-snapshot
Root system architecture: insights from Arabidopsis and cereal crops
inferredcites →https://doi.org/10.1104/pp.107.109413openalex-snapshot
Salt Modulates Gravity Signaling Pathway to Regulate Growth Direction of Primary Roots in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.184689openalex-snapshot
Root-Localized Phytochrome Chromophore Synthesis Is Required for Photoregulation of Root Elongation and Impacts Root Sensitivity to Jasmonic Acid in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.114.255455openalex-snapshot
SOS2-LIKE PROTEIN KINASE5, an SNF1-RELATED PROTEIN KINASE3-Type Protein Kinase, Is Important for Abscisic Acid Responses in Arabidopsis through Phosphorylation of ABSCISIC ACID-INSENSITIVE5
inferredcites →https://doi.org/10.1104/pp.16.00342openalex-snapshot
New Constitutively Active Phytochromes Exhibit Light-Independent Signaling Activity
inferredcites →https://doi.org/10.1105/tpc.108.058859openalex-snapshot
SOMNUS, a CCCH-Type Zinc Finger Protein inArabidopsis, Negatively Regulates Light-Dependent Seed Germination Downstream of PIL5
inferredcites →https://doi.org/10.1105/tpc.108.061143openalex-snapshot
Eleven Golden Rules of Quantitative RT-PCR
inferredcites →https://doi.org/10.1105/tpc.113.119974openalex-snapshot
ABD1 Is anArabidopsisDCAF Substrate Receptor for CUL4-DDB1–Based E3 Ligases That Acts as a Negative Regulator of Abscisic Acid Signaling
inferredcites →https://doi.org/10.1105/tpc.12.7.1117openalex-snapshot
Regulation of Abscisic Acid Signaling by the Ethylene Response Pathway in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03059.xopenalex-snapshot
Phytochrome coordinates Arabidopsis shoot and root development
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04579.xopenalex-snapshot
Quantitative transcriptomic analysis of abscisic acid‐induced and reactive oxygen species‐dependent expression changes and proteomic profiling in Arabidopsis suspension cells
inferredcites →https://doi.org/10.1111/nph.13079openalex-snapshot
The A rabidopsis thaliana RNA ‐binding protein FCA regulates thermotolerance by modulating the detoxification of reactive oxygen species
inferredcites →https://doi.org/10.1111/pce.12669openalex-snapshot
Shoot‐derived abscisic acid promotes root growth
inferredcites →https://doi.org/10.1126/scisignal.aaf6530openalex-snapshot
Stem-piped light activates phytochrome B to trigger light responses in Arabidopsis thaliana roots
inferredcites →https://doi.org/10.1186/1746-4811-9-14openalex-snapshot
An efficient flat-surface collar-free grafting method for Arabidopsis thaliana seedlings
inferredcites →https://doi.org/10.1186/s12864-019-5933-5openalex-snapshot
Uncovering the molecular signature underlying the light intensity-dependent root development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1186/s13007-016-0130-xopenalex-snapshot
High-throughput quantification of more than 100 primary- and secondary-metabolites, and phytohormones by a single solid-phase extraction based sample preparation with analysis by UHPLC–HESI–MS/MS
inferredcites →https://doi.org/10.3389/fpls.2014.00718openalex-snapshot
Light as stress factor to plant roots – case of root halotropism
inferredcites →https://doi.org/10.3389/fpls.2015.00292openalex-snapshot
LSD1 and HY5 antagonistically regulate red light induced-programmed cell death in Arabidopsis
inferredcites →https://doi.org/10.3389/fpls.2015.00775openalex-snapshot
How and why do root apices sense light under the soil surface?
inferredcites →https://doi.org/10.3389/fpls.2015.01162openalex-snapshot
UV-B Induced Generation of Reactive Oxygen Species Promotes Formation of BFA-Induced Compartments in Cells of Arabidopsis Root Apices
inferredcites →https://doi.org/10.3389/fpls.2017.01493openalex-snapshot
The Biphasic Root Growth Response to Abscisic Acid in Arabidopsis Involves Interaction with Ethylene and Auxin Signalling Pathways
inferredcites →https://doi.org/10.3390/ijms19092812openalex-snapshot
Hydrogen Peroxide: Its Role in Plant Biology and Crosstalk with Signalling Networks
inferredcites →https://doi.org/10.3390/ijms19124062openalex-snapshot
The Arabidopsis Ca2+-Dependent Protein Kinase CPK12 Is Involved in Plant Response to Salt Stress
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.4753281openalex-extracted
Physiological and Biochemical Mechanisms of High Oxidative Homeostasis in Root Tubers Of Tetrastigma Hemsleyanum Induced by Blue Light
inferred← citeshttps://doi.org/10.1002/pld3.70079openalex-snapshot
Phytochrome E Plays a Role in the Suppression of Germination in Far‐Red Light in Tomato
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/10.1007/978-3-030-73678-1_1openalex-snapshot
Hydrogen Sulfide on the Crossroad of Regulation, Protection, Interaction and Signaling in Plant Systems Under Different Environmental Conditions
inferred← citeshttps://doi.org/10.1007/s00299-023-02999-7openalex-snapshot
Integration of light and ABA signaling pathways to combat drought stress in plants
inferred← citeshttps://doi.org/10.1007/s12298-023-01364-yopenalex-snapshot
Light signaling as cellular integrator of multiple environmental cues in plants
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/b978-0-443-21727-2.00005-8openalex-snapshot
Control and coordination between light spectrum and plant metabolism
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105146openalex-snapshot
Rice glutamate receptor-like channel OsGLR3.4 modulates the root tropism growth towards amino acids via plasma membrane depolarization and ROS generation
inferred← citeshttps://doi.org/10.1016/j.fgb.2019.04.014openalex-snapshot
Hydrogen sulfide, a novel small molecule signalling agent, participates in the regulation of ganoderic acids biosynthesis induced by heat stress in Ganoderma lucidum
inferred← citeshttps://doi.org/10.1016/j.jgg.2026.07.010openalex-snapshot
Regulation of root-to-shoot ratio in plant resource allocation by external and internal cues
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108824openalex-snapshot
The influence of prolonged but low intensity blue light on the physiological properties of root tubers and the accumulation of flavonoids in Tetrastigma hemsleyanum Diels et Gilg
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.2020.100078openalex-snapshot
Local HY5 Activity Mediates Hypocotyl Growth and Shoot-to-Root Communication
inferred← citeshttps://doi.org/10.1080/15592324.2018.1473684openalex-snapshot
Abscisic acid-mediated phytochrome B signaling promotes primary root growth in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erae192openalex-snapshot
Interplay of light and abscisic acid signaling to modulate plant development
inferred← citeshttps://doi.org/10.1093/jxb/erae217openalex-snapshot
Lights, location, action: shade avoidance signalling over spatial scales
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/kiag050openalex-snapshot
Light regulation of seed-to-seedling transition under dynamic environment
inferred← citeshttps://doi.org/10.1093/treephys/tpaa162openalex-snapshot
The apple columnar gene candidate MdCoL and the AP2/ERF factor MdDREB2 positively regulate ABA biosynthesis by activating the expression of MdNCED6/9
inferred← citeshttps://doi.org/10.1101/2022.07.24.501316openalex-snapshot
A survey of transcriptomic datasets identifies ABA-responsive factors as regulators of photomorphogenesis in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2023.11.15.567161openalex-snapshot
The polyamines spermine and spermidine inhibit or induce programmed cell death in Arabidopsis thaliana in vitro and in vivo in a dose dependent manner
inferred← citeshttps://doi.org/10.1104/pp.20.01084openalex-snapshot
Phytochrome B Is Required for Systemic Stomatal Responses and Reactive Oxygen Species Signaling during Light Stress
inferred← citeshttps://doi.org/10.1111/febs.17165openalex-snapshot
Spermine and spermidine inhibit or induce programmed cell death in Arabidopsis thaliana in vitro and in vivo in a dose‐dependent manner
inferred← citeshttps://doi.org/10.1111/mpp.70356openalex-snapshot
Genome‐Wide Screening and Functional Verification of the Tobacco SGR Family Identify Transcription‐Factor‐Like NtSGRL as a Negative Regulator of Tomato Yellow Leaf Curl Virus Resistance
inferred← citeshttps://doi.org/10.1111/nph.18348openalex-snapshot
Abscisic acid‐controlled redox proteome of Arabidopsis and its regulation by heterotrimeric Gβ protein
inferred← citeshttps://doi.org/10.1111/nph.18626openalex-snapshot
Phytochrome B regulates reactive oxygen signaling during abiotic and biotic stress in plants
inferred← citeshttps://doi.org/10.1111/pce.15532openalex-snapshot
Red Light Induces Powdery Mildew Resistance by Activating the Expression of CmLOX10 in Oriental Melon
inferred← citeshttps://doi.org/10.1111/pce.70350openalex-snapshot
Molecular Mechanisms of Light Signalling in Root Architecture: From Photoreception to Developmental Regulation
inferred← citeshttps://doi.org/10.1111/ppl.13722openalex-snapshot
Root growth direction in simulated microgravity is modulated by a light avoidance mechanism mediated by flavonols
inferred← citeshttps://doi.org/10.1111/tpj.14151openalex-snapshot
MEDIATOR 18 modulates viability of root initial cells
inferred← citeshttps://doi.org/10.1111/tpj.14613openalex-snapshot
The cloning and characterization of hypersensitive to salt stress mutant, affected in quinolinate synthase, highlights the involvement of NAD in stress‐induced accumulation of ABA and proline
inferred← citeshttps://doi.org/10.1186/s12864-019-5933-5openalex-snapshot
Uncovering the molecular signature underlying the light intensity-dependent root development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1186/s12864-020-07098-5openalex-snapshot
Gene expression profiling reveals the effects of light on adventitious root formation in lotus seedlings (Nelumbo nucifera Gaertn.)
inferred← citeshttps://doi.org/10.1186/s12870-024-05242-xopenalex-snapshot
A comprehensive assessment of photosynthetic acclimation to shade in C4 grass (Cynodon dactylon (L.) Pers.)
inferred← citeshttps://doi.org/10.17660/actahortic.2025.1423.6openalex-snapshot
The role of phytochromes in the adaptation of tomato plants to light with different ratios of red and far-red light
inferred← citeshttps://doi.org/10.22541/au.164432278.81807192/v1openalex-snapshot
Cell division zones are maintained by the photoassimilate--auxin--brassinosteroid--polar auxin transport signal relay in Arabidopsis root tips
inferred← citeshttps://doi.org/10.31163/2618-964x-2019-2-4-582-587openalex-snapshot
INFLUENCE OF ABSCISIC ACID ON PEROXIDE PRODUCTION DURING SEED GERMINATION AND ROOT BRANCHING OF BARLEY PLANTS
inferred← citeshttps://doi.org/10.3389/fpls.2021.659712openalex-snapshot
A Multifaceted Action of Phytochrome B in Plant Environmental Adaptation
inferred← citeshttps://doi.org/10.3389/fpls.2021.808960openalex-snapshot
Basic Protein Modules Combining Abscisic Acid and Light Signaling in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2022.846294openalex-snapshot
Phytochrome B Positively Regulates Red Light-Mediated ER Stress Response in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2022.883363openalex-snapshot
Cytoplasmic Linker Protein-Associating Protein at the Nexus of Hormone Signaling, Microtubule Organization, and the Transition From Division to Differentiation in Primary Roots
inferred← citeshttps://doi.org/10.3390/antiox11071311openalex-snapshot
Light Intensity- and Spectrum-Dependent Redox Regulation of Plant Metabolism
inferred← citeshttps://doi.org/10.3390/antiox13010099openalex-snapshot
Application of Multi-Omics Technologies to the Study of Phytochromes in Plants
inferred← citeshttps://doi.org/10.3390/ijms19092812openalex-snapshot
Hydrogen Peroxide: Its Role in Plant Biology and Crosstalk with Signalling Networks
inferred← citeshttps://doi.org/10.3390/ijms19124062openalex-snapshot
The Arabidopsis Ca2+-Dependent Protein Kinase CPK12 Is Involved in Plant Response to Salt Stress
inferred← citeshttps://doi.org/10.3390/ijms232214134openalex-snapshot
Phytochromes and Their Role in Diurnal Variations of ROS Metabolism and Plant Proteome
inferred← citeshttps://doi.org/10.3390/ijms24098323openalex-snapshot
Light-Dependent Regulatory Interactions between the Redox System and miRNAs and Their Biochemical and Physiological Effects in Plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.26737308openalex-snapshot
Additional file 1 of A comprehensive assessment of photosynthetic acclimation to shade in C4 grass (Cynodon dactylon (L.) Pers.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26737311openalex-snapshot
Additional file 2 of A comprehensive assessment of photosynthetic acclimation to shade in C4 grass (Cynodon dactylon (L.) Pers.)
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