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The ARF7 and ARF19 Transcription Factors Positively Regulate PHOSPHATE STARVATION RESPONSE1 in Arabidopsis Roots
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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/bf00023610openalex-snapshot
Identification of protein-binding DNA sequences in an auxin-regulated gene of soybean
inferredcites →https://doi.org/10.1007/s11103-009-9589-4openalex-snapshot
Involvement of auxin signaling mediated by IAA14 and ARF7/19 in membrane lipid remodeling during phosphate starvation
inferredcites →https://doi.org/10.1007/s11103-014-0249-yopenalex-snapshot
A Brassica napus PHT1 phosphate transporter, BnPht1;4, promotes phosphate uptake and affects roots architecture of transgenic Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2009.03.001openalex-snapshot
Auxin: A Trigger for Change in Plant Development
inferredcites →https://doi.org/10.1038/ncomms4617openalex-snapshot
Structural basis for oligomerization of auxin transcriptional regulators
inferredcites →https://doi.org/10.1038/nprot.2008.66openalex-snapshot
An efficient chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in Arabidopsis plants
inferredcites →https://doi.org/10.1046/j.1365-3040.2003.01030.xopenalex-snapshot
Temporal responses of Arabidopsis root architecture to phosphate starvation: evidence for the involvement of auxin signalling
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00562.xopenalex-snapshot
A type 5 acid phosphatase gene from Arabidopsis thaliana is induced by phosphate starvation and by some other types of phosphate mobilising/oxidative stress conditions
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00695.xopenalex-snapshot
Phosphorus acquisition and use: critical adaptations by plants for securing a nonrenewable resource
inferredcites →https://doi.org/10.1071/s96047openalex-snapshot
Soil phosphorus: its measurement, and its uptake by plants
inferredcites →https://doi.org/10.1073/pnas.0505266102openalex-snapshot
A genome-wide transcriptional analysis using Arabidopsis thaliana Affymetrix gene chips determined plant responses to phosphate deprivation
inferredcites →https://doi.org/10.1073/pnas.1400074111openalex-snapshot
Molecular basis for AUXIN RESPONSE FACTOR protein interaction and the control of auxin response repression
inferredcites →https://doi.org/10.1073/pnas.92.8.3483openalex-snapshot
Two auxin-responsive domains interact positively to induce expression of the early indoleacetic acid-inducible gene PS-IAA4/5.
inferredcites →https://doi.org/10.1073/pnas.96.26.15336openalex-snapshot
Psr1, a nuclear localized protein that regulates phosphorus metabolism in Chlamydomonas
inferredcites →https://doi.org/10.1093/aob/mct080openalex-snapshot
A phosphate starvation response regulator Ta-PHR1 is involved in phosphate signalling and increases grain yield in wheat
inferredcites →https://doi.org/10.1093/mp/ssn081openalex-snapshot
Phosphate Starvation Responses and Gibberellic Acid Biosynthesis are Regulated by the MYB62 Transcription Factor in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.204401openalex-snapshot
A conserved MYB transcription factor involved in phosphate starvation signaling both in vascular plants and in unicellular algae
inferredcites →https://doi.org/10.1104/pp.010934openalex-snapshot
Phosphate Availability Alters Architecture and Causes Changes in Hormone Sensitivity in the Arabidopsis Root System
inferredcites →https://doi.org/10.1104/pp.103.021022openalex-snapshot
Phosphate Starvation Triggers Distinct Alterations of Genome Expression in Arabidopsis Roots and Leaves
inferredcites →https://doi.org/10.1104/pp.105.060061openalex-snapshot
A Role for Auxin Redistribution in the Responses of the Root System Architecture to Phosphate Starvation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.079707openalex-snapshot
PHO2, MicroRNA399, and PHR1 Define a Phosphate-Signaling Pathway in Plants
inferredcites →https://doi.org/10.1104/pp.106.092130openalex-snapshot
Differential Effects of Sucrose and Auxin on Localized Phosphate Deficiency-Induced Modulation of Different Traits of Root System Architecture in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.093971openalex-snapshot
WRKY75 Transcription Factor Is a Modulator of Phosphate Acquisition and Root Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.111443openalex-snapshot
OsPHR2 Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
inferredcites →https://doi.org/10.1104/pp.126.2.875openalex-snapshot
Phosphate Availability Regulates Root System Architecture in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.15.01336openalex-snapshot
Arabidopsis PHL2 and PHR1 Act Redundantly as the Key Components of the Central Regulatory System Controlling Transcriptional Responses to Phosphate Starvation
inferredcites →https://doi.org/10.1105/tpc.104.028316openalex-snapshot
Functional Genomic Analysis of the AUXIN RESPONSE FACTOR Gene Family Members in Arabidopsis thaliana : Unique and Overlapping Functions of ARF7 and ARF19
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.108.058719openalex-snapshot
Phosphate Availability Alters Lateral Root Development inArabidopsisby Modulating Auxin Sensitivity via a Mechanism Involving the TIR1 Auxin Receptor
inferredcites →https://doi.org/10.1105/tpc.114.133744openalex-snapshot
SCF TIR1/AFB -Based Auxin Perception: Mechanism and Role in Plant Growth and Development
inferredcites →https://doi.org/10.1105/tpc.9.1.49openalex-snapshot
Rapid induction by wounding and bacterial infection of an S gene family receptor-like kinase gene in Brassica oleracea.
inferredcites →https://doi.org/10.1111/j.1365-3040.2007.01734.xopenalex-snapshot
Increased expression of the MYB‐related transcription factor, PHR1, leads to enhanced phosphate uptake in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-3040.2008.01883.xopenalex-snapshot
Essential role of MYB transcription factor: PvPHR1 and microRNA: PvmiR399 in phosphorus‐deficiency signalling in common bean roots
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02161.xopenalex-snapshot
Phosphate transport in Arabidopsis : Pht1;1 and Pht1;4 play a major role in phosphate acquisition from both low‐ and high‐phosphate environments
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02432.xopenalex-snapshot
NPH4/ARF7 and ARF19 promote leaf expansion and auxin‐induced lateral root formation
inferredcites →https://doi.org/10.1126/science.1123841openalex-snapshot
TOPLESS Regulates Apical Embryonic Fate in Arabidopsis
inferredcites →https://doi.org/10.1126/science.1151461openalex-snapshot
TOPLESS Mediates Auxin-Dependent Transcriptional Repression During Arabidopsis Embryogenesis
inferredcites →https://doi.org/10.1126/science.276.5320.1865openalex-snapshot
ARF1, a Transcription Factor That Binds to Auxin Response Elements
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.665openalex-snapshot
PHOSPHATE ACQUISITION
inferredcites →https://doi.org/10.1242/dev.032177openalex-snapshot
DORNROSCHEN is a direct target of the auxin response factor MONOPTEROS in the Arabidopsis embryo
inferredcites →https://doi.org/10.1242/dev.152132openalex-snapshot
Non-canonical WOX11 -mediated root branching contributes to plasticity in Arabidopsis root system architecture
inferredcites →https://doi.org/10.1371/journal.pgen.1001102openalex-snapshot
A Central Regulatory System Largely Controls Transcriptional Activation and Repression Responses to Phosphate Starvation in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0044005openalex-snapshot
Brassica napus PHR1 Gene Encoding a MYB-Like Protein Functions in Response to Phosphate Starvation
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.4837258openalex-extracted
Genome-Wide Characterization and Expression of the Myb-Cc Gene Family in Salvia Miltiorrhiza Andsmmyb-Cc7-Mediated Response to Phosphate Starvation in Arabidopsis
inferred← citeshttps://doi.org/10.1002/pld3.504openalex-snapshot
Light and jasmonic acid coordinately regulate the phosphate responses under shade and phosphate starvation conditions in Arabidopsis
inferred← citeshttps://doi.org/10.1007/978-3-030-84985-6_2openalex-snapshot
Root Architectural Plasticity in Changing Nutrient Availability
inferred← citeshttps://doi.org/10.1007/978-3-031-05427-3_6openalex-snapshot
Integrative Approach of the Root Architecture by Interaction Between Auxin and Nutrients
inferred← citeshttps://doi.org/10.1007/s00299-021-02721-5openalex-snapshot
Expression dynamics indicate the role of Jasmonic acid biosynthesis pathway in regulating macronutrient (N, P and K+) deficiency tolerance in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s00299-024-03146-6openalex-snapshot
ABA functions in low phosphate-induced anthocyanin accumulation through the transcription factor ABI5 in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-025-03461-6openalex-snapshot
Genome-wide identification of the SmPHR gene family in Salvia miltiorrhiza and SmPHR7-mediated response to phosphate starvation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00344-020-10237-7openalex-snapshot
Co-regulation of Auxin and Cytokinin in Anthocyanin Accumulation During Natural Development of Purple Wheat Grains
inferred← citeshttps://doi.org/10.1007/s00344-023-11011-1openalex-snapshot
Flavonoids Mediate the Modulation of Phosphate Uptake and Phosphate-Starvation Signaling in Tobacco
inferred← citeshttps://doi.org/10.1007/s00344-023-11106-9openalex-snapshot
The Transcriptional MEDIATOR Complex: Linking Root Development, Hormonal Responses, and Nutrient Stress
inferred← citeshttps://doi.org/10.1007/s00344-025-11907-0openalex-snapshot
Carbon-Phosphorus Nexus in Plants: Unraveling the Intricate Relationship in Plant Physiology and Crop Production
inferred← citeshttps://doi.org/10.1007/s00425-025-04731-zopenalex-snapshot
The IAA7-ARF7-ARF19 auxin signaling module plays diverse roles in Arabidopsis growth and development
inferred← citeshttps://doi.org/10.1007/s00425-026-05034-7openalex-snapshot
Transcription factors in phosphorus utilization: enhancing crop productivity and stress resilience
inferred← citeshttps://doi.org/10.1007/s00709-021-01724-zopenalex-snapshot
Micrococcus luteus LS570 promotes root branching in Arabidopsis via decreasing apical dominance of the primary root and an enhanced auxin response
inferred← citeshttps://doi.org/10.1007/s10265-019-01100-2openalex-snapshot
A gene regulatory network for root hair development
inferred← citeshttps://doi.org/10.1007/s10265-024-01545-0openalex-snapshot
Recent advances in research on phosphate starvation signaling in plants
inferred← citeshttps://doi.org/10.1007/s10725-023-00994-2openalex-snapshot
TaEF1A is involved in low phosphorus stress responses and affects root development
inferred← citeshttps://doi.org/10.1007/s11032-023-01399-9openalex-snapshot
Integrating genome-wide association studies with selective sweep reveals genetic loci associated with tolerance to low phosphate availability in Brassica napus
inferred← citeshttps://doi.org/10.1007/s11103-021-01224-xopenalex-snapshot
Early sensing of phosphate deprivation triggers the formation of extra root cap cell layers via SOMBRERO through a process antagonized by auxin signaling
inferred← citeshttps://doi.org/10.1007/s11103-024-01470-9openalex-snapshot
Maize auxin response factor ZmARF1 confers multiple abiotic stresses resistances in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11104-023-05976-xopenalex-snapshot
Emerging roles of inositol pyrophosphates in signaling plant phosphorus status and phytohormone signaling
inferred← citeshttps://doi.org/10.1007/s11240-024-02901-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11627-025-10623-4openalex-snapshot
Genome-wide identification of the ARF gene family and its expression in somatic embryogenesis of Canna generalis L.H. Bailey
inferred← citeshttps://doi.org/10.1007/s11738-022-03413-7openalex-snapshot
Root system responses to phosphate nutrition involve plasma membrane H+-ATPases in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s12298-024-01479-wopenalex-snapshot
Opportunity for genome engineering to enhance phosphate homeostasis in crops
inferred← citeshttps://doi.org/10.1007/s44154-022-00039-0openalex-snapshot
Plant phosphate nutrition: sensing the stress
inferred← citeshttps://doi.org/10.1007/s44372-026-00734-6openalex-snapshot
Novel insights into phosphate starvation response in plants from mycorrhiza perspective
inferred← citeshttps://doi.org/10.1016/b978-0-12-819334-1.00011-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-18675-2.00001-8openalex-snapshot
Molecular basis of plant nutrient use efficiency - concepts and challenges for its improvement
inferred← citeshttps://doi.org/10.1016/b978-0-443-30188-9.00022-6openalex-snapshot
Debaryomyces hansenii and its role on mineral nutrition of dicot plants
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.08.088openalex-snapshot
The bHLH transcription factor gene AtUPB1 regulates growth by mediating cell cycle progression in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111913openalex-snapshot
Control of lateral root initiation by DA3 in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.01.002openalex-snapshot
Tackling Plant Phosphate Starvation by the Roots
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104162openalex-snapshot
Phosphate starvation responses in crop roots: from well-known players to novel candidates
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.11.298openalex-snapshot
Characterization and evolutionary analysis of phosphate starvation response genes in wheat and other major gramineous plants
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.142291openalex-snapshot
Identification and characterization of auxin response factor (ARF) gene family in five Bambusoideae species reveals the role of PedARF 23 in regulating lignin synthesis through auxin signaling
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.134719openalex-snapshot
NtARF11 positively regulates cadmium tolerance in tobacco by inhibiting expression of the nitrate transporter NtNRT1.1
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154815openalex-snapshot
Phytohormonal orchestration of plant phosphate starvation responses
inferred← citeshttps://doi.org/10.1016/j.micres.2024.127602openalex-snapshot
Bacterial indole-3-acetic acid: A key regulator for plant growth, plant-microbe interactions, and agricultural adaptive resilience
inferred← citeshttps://doi.org/10.1016/j.molp.2021.12.004openalex-snapshot
Nutrient–hormone relations: Driving root plasticity in plants
inferred← citeshttps://doi.org/10.1016/j.molp.2021.12.005openalex-snapshot
Plant adaptation to low phosphorus availability: Core signaling, crosstalks, and applied implications
inferred← citeshttps://doi.org/10.1016/j.ncrops.2024.100064openalex-snapshot
Molecular mechanisms underlying plant responses to low phosphate stress and potential applications in crop improvement
inferred← citeshttps://doi.org/10.1016/j.pbi.2021.102117openalex-snapshot
Integration of nutrient and water availabilities via auxin into the root developmental program
inferred← citeshttps://doi.org/10.1016/j.pbi.2023.102386openalex-snapshot
Understanding signaling pathways governing the polar development of root hairs in low-temperature, nutrient-deficient environments
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112103openalex-snapshot
PbARF19-mediated auxin signaling regulates lignification in pear fruit stone cells
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112855openalex-snapshot
Unearthing the secrets of drought-driven root system architecture: Nutrient acquisition and rhizosphere microbe interplay
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.112986openalex-snapshot
MeJA regulates plant root growth, development and phosphorus uptake to adapt to low phosphorus stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.05.035openalex-snapshot
Wheat heat shock factor TaHsfA2d contributes to plant responses to phosphate deficiency
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.01.029openalex-snapshot
Molecular mechanism of phosphorous signaling inducing anthocyanin accumulation in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110308openalex-snapshot
TaHAK1 promotes salt tolerance via synergistic modulation of K+/Na+ ion homeostasis and auxin signaling in rice
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111103openalex-snapshot
SlIAA9 mutation enhances tomato seed resilience to heat stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111113openalex-snapshot
Plastid glucose-6-phosphate dehydrogenase 3 is involved in root system reshaping under low phosphorus stress through regulating auxin and cytokinin signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.03.010openalex-snapshot
The potential application of genome editing by using CRISPR/Cas9, and its engineered and ortholog variants for studying the transcription factors involved in the maintenance of phosphate homeostasis in model plants
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101263openalex-snapshot
Phosphorus availability alleviates chilling injury through modulation of phosphorus metabolism and cold-responsive gene expression in cucumber (Cucumis sativus L.) fruit
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.2025.101350openalex-snapshot
Enhanced auxin signaling promotes root-hair growth at moderately low temperature in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c06031openalex-snapshot
Novel Camellia sinensis O-Methyltransferase Regulated by CsMADSL1 Specifically Methylates EGCG in Cultivar “GZMe4”
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/s41598-025-97266-yopenalex-snapshot
A systematic review to identify target genes that modulate root system architecture in response to abiotic stress
inferred← citeshttps://doi.org/10.1042/bcj20230163openalex-snapshot
Dynamic interactions between SPX proteins, the ubiquitination machinery, and signalling molecules for stress adaptation at a whole-plant level
inferred← citeshttps://doi.org/10.1071/fp19107openalex-snapshot
Hydrogen-rich water promotes elongation of hypocotyls and roots in plants through mediating the level of endogenous gibberellin and auxin
inferred← citeshttps://doi.org/10.1093/aob/mcag034openalex-snapshot
ZmPHR1 coordinates root–rhizosphere processes and phosphorus allocation to enhance phosphorus efficiency and yield in maize
inferred← citeshttps://doi.org/10.1093/jxb/eraa048openalex-snapshot
Hormonal regulation of root hair growth and responses to the environment in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/eraa259openalex-snapshot
PLATZ2 negatively regulates salt tolerance in Arabidopsis seedlings by directly suppressing the expression of the CBL4/SOS3 and CBL10/SCaBP8 genes
inferred← citeshttps://doi.org/10.1093/jxb/erad035openalex-snapshot
Getting to the roots of N, P, and K uptake
inferred← citeshttps://doi.org/10.1093/jxb/erad259openalex-snapshot
To bind or not to bind: how AUXIN RESPONSE FACTORs select their target genes
inferred← citeshttps://doi.org/10.1093/jxb/erag002openalex-snapshot
Phosphate starvation response 1 (PHR1): a versatile master regulator shaping plant resilience beyond phosphate deprivation
inferred← citeshttps://doi.org/10.1093/jxb/erz148openalex-snapshot
Perception, transduction, and integration of nitrogen and phosphorus nutritional signals in the transcriptional regulatory network in plants
inferred← citeshttps://doi.org/10.1093/plcell/koad057openalex-snapshot
PHOSPHATE STARVATION RESPONSE1 (PHR1) interacts with JASMONATE ZIM-DOMAIN (JAZ) and MYC2 to modulate phosphate deficiency-induced jasmonate signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiab441openalex-snapshot
Diverse phosphate and auxin transport loci distinguish phosphate tolerant from sensitive Arabidopsis accessions
inferred← citeshttps://doi.org/10.1093/plphys/kiac497openalex-snapshot
The auxin response factor TaARF15-A1 negatively regulates senescence in common wheat (Triticum aestivumL.)
inferred← citeshttps://doi.org/10.1093/plphys/kiae478openalex-snapshot
The soybean NUCLEAR FACTOR-Y C4 and α-EXPANSIN 7 module influences phosphorus uptake by regulating root morphology
inferred← citeshttps://doi.org/10.1093/plphys/kiae495openalex-snapshot
Developmental responses of roots to limited phosphate availability: Research progress and application in cereals
inferred← citeshttps://doi.org/10.1093/plphys/kiag457openalex-snapshot
Loss of the phosphate sensor CsSPX2 impairs lateral root initiation and development in cucumber
inferred← citeshttps://doi.org/10.1093/treephys/tpad138openalex-snapshot
Low phosphorus impact on Moso bamboo (Phyllostachys edulis) root morphological polymorphism and expression pattern of the related genes
inferred← citeshttps://doi.org/10.1101/2020.01.17.909945openalex-snapshot
Gene expression in isolated cowpea (Vigna unguiculata L. Walp) cells from meiosis to seed initiation
inferred← citeshttps://doi.org/10.1101/2023.08.15.553439openalex-snapshot
The Auxin Response Factor ARF27 is required for maize root morphogenesis
inferred← citeshttps://doi.org/10.1101/830612openalex-snapshot
GmPTF1 Modifies Root Architecture Responses to Phosphate Starvation in Soybean
inferred← citeshttps://doi.org/10.1101/cshperspect.a039941openalex-snapshot
Auxin-Regulated Lateral Root Organogenesis
inferred← citeshttps://doi.org/10.1101/cshperspect.a040030openalex-snapshot
Auxin–Environment Integration in Growth Responses to Forage for Resources
inferred← citeshttps://doi.org/10.1104/pp.20.00378openalex-snapshot
ZmCCD10a Encodes a Distinct Type of Carotenoid Cleavage Dioxygenase and Enhances Plant Tolerance to Low Phosphate
inferred← citeshttps://doi.org/10.1111/1462-2920.14952openalex-snapshot
The auxin‐inducible phosphate transporter AsPT5 mediates phosphate transport and is indispensable for arbuscule formation in Chinese milk vetch at moderately high phosphate supply
inferred← citeshttps://doi.org/10.1111/jipb.13496openalex-snapshot
NIGT1 represses plant growth and mitigates phosphate starvation signaling to balance the growth response tradeoff in rice
inferred← citeshttps://doi.org/10.1111/jipb.70090openalex-snapshot
Collapsed auxin transport by iron inhibits primary root growth under low phosphate stress
inferred← citeshttps://doi.org/10.1111/nph.18499openalex-snapshot
Nitrogen‐inducible GLK1 modulates phosphate starvation response via the PHR1 ‐dependent pathway
inferred← citeshttps://doi.org/10.1111/nph.18933openalex-snapshot
The good, the bad, and the phosphate: regulation of beneficial and detrimental plant–microbe interactions by the plant phosphate status
inferred← citeshttps://doi.org/10.1111/nph.20174openalex-snapshot
Crystal structure and function of a phosphate starvation responsive protein phosphatase, GmHAD1 ‐2 regulating soybean root development and flavonoid metabolism
inferred← citeshttps://doi.org/10.1111/pce.14451openalex-snapshot
Impacts of iron on phosphate starvation‐induced root hair growth in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.14457openalex-snapshot
Molecular mechanisms and genetic improvement of low‐phosphorus tolerance in rice
inferred← citeshttps://doi.org/10.1111/pce.14494openalex-snapshot
Roles of auxin response factors in rice development and stress responses
inferred← citeshttps://doi.org/10.1111/pce.14790openalex-snapshot
PHR1 involved in the regulation of low phosphate‐induced leaf senescence by modulating phosphorus homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.15378openalex-snapshot
FvPHR1 Improves the Quality of Woodland Strawberry Fruit by Up‐Regulating the Expression of FvPHT1;7 and FvSWEET9
inferred← citeshttps://doi.org/10.1111/pce.70083openalex-snapshot
Phosphoenolpyruvic Carboxylase Gene GmPPC6 Negatively Regulates Root System Development Under Low Phosphorus Stress in Soybean
inferred← citeshttps://doi.org/10.1111/pce.70680openalex-snapshot
Lateral Root Development: Molecular Mechanisms and Adaptive Regulation
inferred← citeshttps://doi.org/10.1111/pce.70963openalex-snapshot
RAP2.3 Is Required for MYB51 and SIGMA3 Expression During the Response of Arabidopsis thaliana to Multifactorial Stress Combination
inferred← citeshttps://doi.org/10.1111/ppl.70307openalex-snapshot
Auxin Biosynthesis Is Required for Phosphorus Deficiency‐Induced Root Architecture Remodelling in Rice
inferred← citeshttps://doi.org/10.1111/ppl.70563openalex-snapshot
Auxin/ ROS ‐Mediated Coordination of Lateral Root and Root Hair Development in Wheat ( Triticum aestivum L.) Under Low‐Temperature Stress
inferred← citeshttps://doi.org/10.1111/tpj.14717openalex-snapshot
Overexpression of MsGH3.5 inhibits shoot and root development through the auxin and cytokinin pathways in apple plants
inferred← citeshttps://doi.org/10.1111/tpj.15307openalex-snapshot
GmPTF1 modifies root architecture responses to phosphate starvation primarily through regulating GmEXPB2 expression in soybean
inferred← citeshttps://doi.org/10.1111/tpj.15778openalex-snapshot
Sorting Nexin1 negatively modulates phosphate uptake by facilitating Phosphate Transporter1;1 degradation in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.15791openalex-snapshot
Abscisic acid facilitates phosphate acquisition through the transcription factor ABA INSENSITIVE5 in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.70284openalex-snapshot
14‐3‐3 proteins GRF6 and GRF8 negatively regulate phosphate acquisition by interacting with and inhibiting PHR1 in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.70744openalex-snapshot
Arabidopsis ADF8 and ADF11 contribute to root hair growth to respond to hormone and environmental signals
inferred← citeshttps://doi.org/10.1111/tpj.71068openalex-snapshot
The PHR1 – RSL2 module regulates root hair elongation induced by phosphate deficiency
inferred← citeshttps://doi.org/10.1126/sciadv.adx4417openalex-snapshot
Salicylic acid and ROS signaling modulate hypocotyl elongation in darkness via NPR1 and EX1
inferred← citeshttps://doi.org/10.1126/sciadv.aea2275openalex-snapshot
A plant NLR receptor activates auxin signaling through Aux/IAAs-ARF19 and YUC8-TIR1/AFBs to promote callose-mediated antiviral defense
inferred← citeshttps://doi.org/10.1139/cjps-2019-0173openalex-snapshot
Strategic timing and rate of phosphorus fertilization improves phosphorus-use efficiency in two contrasting cultivars of subirrigated greenhouse-grown chrysanthemum
inferred← citeshttps://doi.org/10.1146/annurev-arplant-050718-100423openalex-snapshot
Molecular and Environmental Regulation of Root Development
inferred← citeshttps://doi.org/10.1186/s12870-025-06366-4openalex-snapshot
Genome-wide identification and functional analysis of the ARF gene family in tetraploid potato reveal its potential role in anthocyanin biosynthesis
inferred← citeshttps://doi.org/10.1186/s12870-025-07423-8openalex-snapshot
Genome-wide identification and expression analysis of the GARP superfamily in response to abiotic stresses in alfalfa (Medicago sativa L.)
inferred← citeshttps://doi.org/10.12688/f1000research.140649.1openalex-snapshot
Tapping into the plasticity of plant architecture for increased stress resilience
inferred← citeshttps://doi.org/10.1360/ssv-2023-0048openalex-snapshot
Molecular regulation network of phosphorus starvation signaling and genetic improvement of phosphorus efficiency in plants
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011135openalex-snapshot
ZmARF1 positively regulates low phosphorus stress tolerance via modulating lateral root development in maize
inferred← citeshttps://doi.org/10.15302/j-fase-2019278openalex-snapshot
Genetic study and molecular breeding for high phosphorus use efficiency in maize
inferred← citeshttps://doi.org/10.2139/ssrn.5239872openalex-snapshot
Tahak1 Promotes Salt Tolerance Via Synergistic Modulation of Auxin Signaling
inferred← citeshttps://doi.org/10.3389/fpls.2020.01239openalex-snapshot
A Gain-of-Function Mutant of IAA15 Inhibits Lateral Root Development by Transcriptional Repression of LBD Genes in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2021.641087openalex-snapshot
Association Analysis Revealed That TaPYL4 Genes Are Linked to Plant Growth Related Traits in Multiple Environment
inferred← citeshttps://doi.org/10.3389/fpls.2021.643585openalex-snapshot
Influence of Ethylene Signaling in the Crosstalk Between Fe, S, and P Deficiency Responses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2021.700651openalex-snapshot
Transcription Factor GmWRKY46 Enhanced Phosphate Starvation Tolerance and Root Development in Transgenic Plants
inferred← citeshttps://doi.org/10.3389/fpls.2022.862171openalex-snapshot
The Root Hair Development of Pectin Polygalacturonase PGX2 Activation Tagging Line in Response to Phosphate Deficiency
inferred← citeshttps://doi.org/10.3389/fpls.2022.880423openalex-snapshot
WHIRLIES Are Multifunctional DNA-Binding Proteins With Impact on Plant Development and Stress Resistance
inferred← citeshttps://doi.org/10.3389/fpls.2024.1274610openalex-snapshot
SUMOylation of OsPSTOL1 is essential for regulating phosphate starvation responses in rice and Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2024.1364086openalex-snapshot
Genome mining of WOX-ARF gene linkage in Machilus pauhoi underpinned cambial activity associated with IAA induction
inferred← citeshttps://doi.org/10.3389/fpls.2024.1398818openalex-snapshot
Enigmatic role of auxin response factors in plant growth and stress tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2025.1527547openalex-snapshot
From genes to traits: maximizing phosphorus utilization efficiency in crop plants
inferred← citeshttps://doi.org/10.3390/agronomy15051186openalex-snapshot
Transcriptomic Analysis for Key Periods of Radicle Development in Contrasting Soybean Varieties HN75 and HN76
inferred← citeshttps://doi.org/10.3390/genes10121018openalex-snapshot
Plant PHR Transcription Factors: Put on A Map
inferred← citeshttps://doi.org/10.3390/iecps2020-08729openalex-snapshot
Phosphate Starvation Triggers Transcriptional Changes in the Biosynthesis and Signaling Pathways of Phytohormones in Marchantia polymorpha
inferred← citeshttps://doi.org/10.3390/ijms19103146openalex-snapshot
Phytohormones Regulate the Development of Arbuscular Mycorrhizal Symbiosis
inferred← citeshttps://doi.org/10.3390/ijms20092237openalex-snapshot
High External K+ Concentrations Impair Pi Nutrition, Induce the Phosphate Starvation Response, and Reduce Arsenic Toxicity in Arabidopsis Plants
inferred← citeshttps://doi.org/10.3390/ijms21175955openalex-snapshot
The Plasticity of Root Systems in Response to External Phosphate
inferred← citeshttps://doi.org/10.3390/ijms21186817openalex-snapshot
Genome-Wide Analysis Reveals Dynamic Epigenomic Differences in Soybean Response to Low-Phosphorus Stress
inferred← citeshttps://doi.org/10.3390/ijms21218354openalex-snapshot
Transcriptional and Morpho-Physiological Responses of Marchantia polymorpha upon Phosphate Starvation
inferred← citeshttps://doi.org/10.3390/ijms21249437openalex-snapshot
Protein Levels of Several Arabidopsis Auxin Response Factors Are Regulated by Multiple Factors and ABA Promotes ARF6 Protein Ubiquitination
inferred← citeshttps://doi.org/10.3390/ijms22094904openalex-snapshot
Ethylene and Nitric Oxide Involvement in the Regulation of Fe and P Deficiency Responses in Dicotyledonous Plants
inferred← citeshttps://doi.org/10.3390/ijms22179311openalex-snapshot
Genetic Dissection of Phosphorus Use Efficiency in a Maize Association Population under Two P Levels in the Field
inferred← citeshttps://doi.org/10.3390/ijms23041933openalex-snapshot
Auxin/Cytokinin Antagonistic Control of the Shoot/Root Growth Ratio and Its Relevance for Adaptation to Drought and Nutrient Deficiency Stresses
inferred← citeshttps://doi.org/10.3390/ijms23105309openalex-snapshot
Genome-Wide Identification of Auxin Response Factors in Peanut (Arachis hypogaea L.) and Functional Analysis in Root Morphology
inferred← citeshttps://doi.org/10.3390/ijms231911477openalex-snapshot
Root-Related Genes in Crops and Their Application under Drought Stress Resistance—A Review
inferred← citeshttps://doi.org/10.3390/ijms232012495openalex-snapshot
Molecular Mechanisms of Diverse Auxin Responses during Plant Growth and Development
inferred← citeshttps://doi.org/10.3390/ijms241713445openalex-snapshot
Study on the Interactions of Cyclins with CDKs Involved in Auxin Signal during Leaf Development by WGCNA in Populus alba
inferred← citeshttps://doi.org/10.3390/ijms241914840openalex-snapshot
Integrated Analysis of Metabolome and Transcriptome Reveals Insights for Low Phosphorus Tolerance in Wheat Seedling
inferred← citeshttps://doi.org/10.3390/ijms26052373openalex-snapshot
The Aldehyde Dehydrogenase Superfamily in Brassica napus L.: Genome-Wide Identification and Expression Analysis Under Low-Temperature Conditions
inferred← citeshttps://doi.org/10.3390/ijms26094087openalex-snapshot
A Comprehensive Analysis on the Regulatory Network Underlying Callus Induction and Adventitious Organogenesis Process in Stem of Populus Alba L.
inferred← citeshttps://doi.org/10.3390/plants11172251openalex-snapshot
Transcriptional Memory in Taraxacum mongolicum in Response to Long-Term Different Grazing Intensities
inferred← citeshttps://doi.org/10.3390/plants12152765openalex-snapshot
A Review: Systemic Signaling in the Regulation of Plant Responses to Low N, P and Fe
inferred← citeshttps://doi.org/10.3390/plants12203617openalex-snapshot
Phloem-Mobile MYB44 Negatively Regulates Expression of PHOSPHATE TRANSPORTER 1 in Arabidopsis Roots
inferred← citeshttps://doi.org/10.3390/plants13213102openalex-snapshot
Overexpression of Cassava MeSTP7 Promotes Arabidopsis Seedling Development
inferred← citeshttps://doi.org/10.7554/elife.95891openalex-snapshot
Root-specific theanine metabolism and regulation at the single-cell level in tea plants (Camellia sinensis)
inferred← citeshttps://doi.org/10.7717/peerj.17341openalex-snapshot
Genome-wide identification and characterization of SPXdomain-containing genes family in eggplant
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