On the public citation graph

PHOSPHATE STARVATION RESPONSE1 (PHR1) interacts with JASMONATE ZIM-DOMAIN (JAZ) and MYC2 to modulate phosphate deficiency-induced jasmonate signaling in Arabidopsis

https://doi.org/10.1093/plcell/koad057
0 signed · 289 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1007/s00425-021-03657-6openalex-snapshot
OsJAZ11 regulates phosphate starvation responses in rice
inferredcites →https://doi.org/10.1007/s00425-022-03952-wopenalex-snapshot
PHR1 positively regulates phosphate starvation-induced anthocyanin accumulation through direct upregulation of genes F3’H and LDOX in Arabidopsis
inferredcites →https://doi.org/10.1007/s11103-015-0289-yopenalex-snapshot
Genetic manipulation of a high-affinity PHR1 target cis-element to improve phosphorous uptake in Oryza sativa L.
inferredcites →https://doi.org/10.1016/j.cell.2019.03.006openalex-snapshot
A Jasmonate Signaling Network Activates Root Stem Cells and Promotes Regeneration
inferredcites →https://doi.org/10.1016/j.copbio.2017.07.005openalex-snapshot
Insights into plant phosphate sensing and signaling
inferredcites →https://doi.org/10.1016/j.cub.2008.03.060openalex-snapshot
DELLAs Control Plant Immune Responses by Modulating the Balance of Jasmonic Acid and Salicylic Acid Signaling
inferredcites →https://doi.org/10.1016/j.cub.2013.04.072openalex-snapshot
Anthocyanins Double the Shelf Life of Tomatoes by Delaying Overripening and Reducing Susceptibility to Gray Mold
inferredcites →https://doi.org/10.1016/j.devcel.2010.10.024openalex-snapshot
DELLAs Modulate Jasmonate Signaling via Competitive Binding to JAZs
inferredcites →https://doi.org/10.1016/j.devcel.2015.02.007openalex-snapshot
Iron-Dependent Callose Deposition Adjusts Root Meristem Maintenance to Phosphate Availability
inferredcites →https://doi.org/10.1016/j.devcel.2019.01.002openalex-snapshot
Tackling Plant Phosphate Starvation by the Roots
inferredcites →https://doi.org/10.1016/j.envexpbot.2018.02.006openalex-snapshot
When are foliar anthocyanins useful to plants? Re-evaluation of the photoprotection hypothesis using Arabidopsis thaliana mutants that differ in anthocyanin accumulation
inferredcites →https://doi.org/10.1016/j.molp.2016.11.001openalex-snapshot
An Arabidopsis ABC Transporter Mediates Phosphate Deficiency-Induced Remodeling of Root Architecture by Modulating Iron Homeostasis in Roots
inferredcites →https://doi.org/10.1016/j.molp.2017.08.007openalex-snapshot
The bHLH Transcription Factors MYC2, MYC3, and MYC4 Are Required for Jasmonate-Mediated Inhibition of Flowering in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molp.2021.05.020openalex-snapshot
Arsenite provides a selective signal that coordinates arsenate uptake and detoxification through the regulation of PHR1 stability in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molp.2021.09.011openalex-snapshot
A reciprocal inhibitory module for Pi and iron signaling
inferredcites →https://doi.org/10.1016/j.molp.2021.12.004openalex-snapshot
Nutrient–hormone relations: Driving root plasticity in plants
inferredcites →https://doi.org/10.1016/j.molp.2021.12.005openalex-snapshot
Plant adaptation to low phosphorus availability: Core signaling, crosstalks, and applied implications
inferredcites →https://doi.org/10.1016/j.molp.2022.08.011openalex-snapshot
Jasmonate perception: Ligand–receptor interaction, regulation, and evolution
inferredcites →https://doi.org/10.1016/j.molp.2022.09.017openalex-snapshot
Regulation of floral senescence in Arabidopsis by coordinated action of CONSTANS and jasmonate signaling
inferredcites →https://doi.org/10.1016/j.pbi.2008.05.004openalex-snapshot
Jasmonate signaling: a conserved mechanism of hormone sensing
inferredcites →https://doi.org/10.1016/j.pbi.2009.07.013openalex-snapshot
The jasmonate pathway: the ligand, the receptor and the core signalling module
inferredcites →https://doi.org/10.1016/j.pbi.2013.03.002openalex-snapshot
Improvement of phosphorus efficiency in rice on the basis of understanding phosphate signaling and homeostasis
inferredcites →https://doi.org/10.1016/j.pbi.2014.07.005openalex-snapshot
Jasmonate signaling and crosstalk with gibberellin and ethylene
inferredcites →https://doi.org/10.1016/j.pbi.2016.07.005openalex-snapshot
Redundancy and specificity in jasmonate signalling
inferredcites →https://doi.org/10.1016/j.pbi.2017.05.007openalex-snapshot
Novel signals in the regulation of Pi starvation responses in plants: facts and promises
inferredcites →https://doi.org/10.1016/j.pbi.2018.02.009openalex-snapshot
Resolution of growth–defense conflict: mechanistic insights from jasmonate signaling
inferredcites →https://doi.org/10.1016/j.pbi.2020.06.006openalex-snapshot
Mediator subunit MED25: at the nexus of jasmonate signaling
inferredcites →https://doi.org/10.1016/j.plaphy.2017.11.010openalex-snapshot
Transcriptional responses to phosphate starvation in Brachypodium distachyon roots
inferredcites →https://doi.org/10.1016/j.semcdb.2017.06.013openalex-snapshot
Molecular mechanisms of phosphate transport and signaling in higher plants
inferredcites →https://doi.org/10.1016/j.tplants.2011.05.006openalex-snapshot
Root developmental adaptation to phosphate starvation: better safe than sorry
inferredcites →https://doi.org/10.1016/j.xplc.2021.100231openalex-snapshot
Metabolism, signaling, and transport of jasmonates
inferredcites →https://doi.org/10.1038/nature05960openalex-snapshot
JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling
inferredcites →https://doi.org/10.1038/nature06006openalex-snapshot
The JAZ family of repressors is the missing link in jasmonate signalling
inferredcites →https://doi.org/10.1038/nature09430openalex-snapshot
Jasmonate perception by inositol-phosphate-potentiated COI1–JAZ co-receptor
inferredcites →https://doi.org/10.1038/nature21417openalex-snapshot
Root microbiota drive direct integration of phosphate stress and immunity
inferredcites →https://doi.org/10.1038/ncomms12570openalex-snapshot
Rewiring of jasmonate and phytochrome B signalling uncouples plant growth-defense tradeoffs
inferredcites →https://doi.org/10.1038/ncomms13925openalex-snapshot
Jasmonate response decay and defense metabolite accumulation contributes to age-regulated dynamics of plant insect resistance
inferredcites →https://doi.org/10.1038/nprot.2007.199openalex-snapshot
Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis
inferredcites →https://doi.org/10.1038/nprot.2008.38openalex-snapshot
Chromatin immunoprecipitation (ChIP) coupled to detection by quantitative real-time PCR to study transcription factor binding to DNA in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/s41467-020-20681-4openalex-snapshot
Inositol pyrophosphates promote the interaction of SPX domains with the coiled-coil motif of PHR transcription factors to regulate plant phosphate homeostasis
inferredcites →https://doi.org/10.1038/s41477-019-0384-1openalex-snapshot
Nitrate–NRT1.1B–SPX4 cascade integrates nitrogen and phosphorus signalling networks in plants
inferredcites →https://doi.org/10.1038/s41477-019-0441-9openalex-snapshot
MED25 connects enhancer–promoter looping and MYC2-dependent activation of jasmonate signalling
inferredcites →https://doi.org/10.1038/s41477-020-0605-7openalex-snapshot
Integrated multi-omics framework of the plant response to jasmonic acid
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.6050673.xopenalex-snapshot
The Arabidopsis ribonuclease gene RNS1 is tightly controlled in response to phosphate limitation
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00893.xopenalex-snapshot
Influence of cytokinins on the expression of phosphate starvation responsive genes in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01356.xopenalex-snapshot
Expression analysis suggests novel roles for members of the Pht1 family of phosphate transporters in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0500778102openalex-snapshot
The Arabidopsis SUMO E3 ligase SIZ1 controls phosphate deficiency responses
inferredcites →https://doi.org/10.1073/pnas.0708139104openalex-snapshot
Regulation of tradeoffs between plant defenses against pathogens with different lifestyles
inferredcites →https://doi.org/10.1073/pnas.1103959108openalex-snapshot
Derepression of ethylene-stabilized transcription factors (EIN3/EIL1) mediates jasmonate and ethylene signaling synergy in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1404654111openalex-snapshot
SPX1 is a phosphate-dependent inhibitor of PHOSPHATE STARVATION RESPONSE 1 in Arabidopsis
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/10.1080/15592324.2015.1045174openalex-snapshot
Strigolactone signaling in root development and phosphate starvation
inferredcites →https://doi.org/10.1093/aob/mcq015openalex-snapshot
Regulation of phosphate starvation responses in higher plants
inferredcites →https://doi.org/10.1093/aob/mct067openalex-snapshot
Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany
inferredcites →https://doi.org/10.1093/jxb/erac441openalex-snapshot
Jasmonate-regulated root growth inhibition and root hair elongation
inferredcites →https://doi.org/10.1093/jxb/erq408openalex-snapshot
Characterization of JAZ-interacting bHLH transcription factors that regulate jasmonate responses in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erw478openalex-snapshot
Jasmonate signaling and manipulation by pathogens and insects
inferredcites →https://doi.org/10.1093/jxb/erw495openalex-snapshot
Jasmonate action in plant growth and development
inferredcites →https://doi.org/10.1093/jxb/erx004openalex-snapshot
Jasmonate regulates leaf senescence and tolerance to cold stress: crosstalk with other phytohormones
inferredcites →https://doi.org/10.1093/jxb/erz174openalex-snapshot
Jasmonate action in plant defense against insects
inferredcites →https://doi.org/10.1093/mp/sss128openalex-snapshot
MYC2: The Master in Action
inferredcites →https://doi.org/10.1093/pcp/pcv197openalex-snapshot
Modulation of the Phosphate-Deficient Responses by MicroRNA156 and its Targeted SQUAMOSA PROMOTER BINDING PROTEIN-LIKE 3 in Arabidopsis
inferredcites →https://doi.org/10.1093/plcell/koab168openalex-snapshot
The Arabidopsis circadian clock protein PRR5 interacts with and stimulates ABI5 to modulate abscisic acid signaling during seed germination
inferredcites →https://doi.org/10.1093/plcell/koac331openalex-snapshot
CO interacts with JAZ repressors and bHLH subgroup IIId factors to negatively regulate jasmonate signaling in Arabidopsis seedlings
inferredcites →https://doi.org/10.1093/plcell/koac362openalex-snapshot
Auxin contributes to jasmonate-mediated regulation of abscisic acid signaling during seed germination 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/10.1101/gad.297704openalex-snapshot
Conserved MYC transcription factors play a key role in jasmonate signaling both in tomato and Arabidopsis
inferredcites →https://doi.org/10.1104/pp.010820openalex-snapshot
Signal Transduction in Maize and Arabidopsis Mesophyll Protoplasts
inferredcites →https://doi.org/10.1104/pp.105.060517openalex-snapshot
Interaction between Phosphate-Starvation, Sugar, and Cytokinin Signaling in Arabidopsis and the Roles of Cytokinin Receptors CRE1/AHK4 and AHK3
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.107.103788openalex-snapshot
Phosphate Starvation Root Architecture and Anthocyanin Accumulation Responses Are Modulated by the Gibberellin-DELLA Signaling Pathway in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.115691openalex-snapshot
Regulation and Function of Arabidopsis JASMONATE ZIM -Domain Genes in Response to Wounding and Herbivory
inferredcites →https://doi.org/10.1104/pp.108.119321openalex-snapshot
Induction of the Arabidopsis PHO1;H10 Gene by 12-Oxo-Phytodienoic Acid But Not Jasmonic Acid via a CORONATINE INSENSITIVE1-Dependent Pathway
inferredcites →https://doi.org/10.1104/pp.112.202358openalex-snapshot
Strigolactones Are Involved in Root Response to Low Phosphate Conditions in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.113.220129openalex-snapshot
Basic Helix-Loop-Helix Transcription Factors JASMONATE-ASSOCIATED MYC2-LIKE1 (JAM1), JAM2, and JAM3 Are Negative Regulators of Jasmonate Responses in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.113.235077openalex-snapshot
Arabidopsis WRKY45 Transcription Factor Activates PHOSPHATE TRANSPORTER1;1 Expression in Response to Phosphate Starvation
inferredcites →https://doi.org/10.1104/pp.15.00736openalex-snapshot
Integrative Comparison of the Role of the PHOSPHATE RESPONSE1 Subfamily in Phosphate Signaling and Homeostasis in Rice
inferredcites →https://doi.org/10.1104/pp.15.00975openalex-snapshot
The EXS Domain of PHO1 Participates in the Response of Shoots to Phosphate Deficiency via a Root-to-Shoot Signal
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/10.1104/pp.16.00278openalex-snapshot
Phosphate Deficiency Induces the Jasmonate Pathway and Enhances Resistance to Insect Herbivory
inferredcites →https://doi.org/10.1104/pp.17.00444openalex-snapshot
Jasmonate Negatively Regulates Stomatal Development in Arabidopsis Cotyledons
inferredcites →https://doi.org/10.1104/pp.17.01713openalex-snapshot
The ARF7 and ARF19 Transcription Factors Positively Regulate PHOSPHATE STARVATION RESPONSE1 in Arabidopsis Roots
inferredcites →https://doi.org/10.1104/pp.18.00594openalex-snapshot
SPX4 Acts on PHR1-Dependent and -Independent Regulation of Shoot Phosphorus Status in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.000745openalex-snapshot
Identification and Characterization of the Arabidopsis PHO1 Gene Involved in Phosphate Loading to the Xylem
inferredcites →https://doi.org/10.1105/tpc.003368openalex-snapshot
The SCF COI1 Ubiquitin-Ligase Complexes Are Required for Jasmonate Response in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.009159openalex-snapshot
NPR1 Modulates Cross-Talk between Salicylate- and Jasmonate-Dependent Defense Pathways through a Novel Function in the Cytosol
inferredcites →https://doi.org/10.1105/tpc.017772openalex-snapshot
The ASK1 and ASK2 Genes Are Essential for Arabidopsis Early Development
inferredcites →https://doi.org/10.1105/tpc.022319openalex-snapshot
JASMONATE-INSENSITIVE1 Encodes a MYC Transcription Factor Essential to Discriminate between Different Jasmonate-Regulated Defense Responses in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.105.036640openalex-snapshot
PHOSPHATE TRANSPORTER TRAFFIC FACILITATOR1 Is a Plant-Specific SEC12-Related Protein That Enables the Endoplasmic Reticulum Exit of a High-Affinity Phosphate Transporter in Arabidopsis [W]
inferredcites →https://doi.org/10.1105/tpc.106.048017openalex-snapshot
MYC2 Differentially Modulates Diverse Jasmonate-Dependent Functions in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.055566openalex-snapshot
Arabidopsis WRKY38 and WRKY62 Transcription Factors Interact with Histone Deacetylase 19 in Basal Defense
inferredcites →https://doi.org/10.1105/tpc.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.108.064303openalex-snapshot
Arabidopsis ASA1 Is Important for Jasmonate-Mediated Regulation of Auxin Biosynthesis and Transport during Lateral Root Formation
inferredcites →https://doi.org/10.1105/tpc.109.065730openalex-snapshot
The Arabidopsis CORONATINE INSENSITIVE1 Protein Is a Jasmonate Receptor
inferredcites →https://doi.org/10.1105/tpc.110.080788openalex-snapshot
The Arabidopsis bHLH Transcription Factors MYC3 and MYC4 Are Targets of JAZ Repressors and Act Additively with MYC2 in the Activation of Jasmonate Responses
inferredcites →https://doi.org/10.1105/tpc.110.081067openalex-snapshot
Arabidopsis thaliana High-Affinity Phosphate Transporters Exhibit Multiple Levels of Posttranslational Regulation
inferredcites →https://doi.org/10.1105/tpc.111.083089openalex-snapshot
The Jasmonate-ZIM Domain Proteins Interact with the R2R3-MYB Transcription Factors MYB21 and MYB24 to Affect Jasmonate-Regulated Stamen Development in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.083261openalex-snapshot
The Jasmonate-ZIM-Domain Proteins Interact with the WD-Repeat/bHLH/MYB Complexes to Regulate Jasmonate-Mediated Anthocyanin Accumulation and Trichome Initiation inArabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.111.089870openalex-snapshot
The Basic Helix-Loop-Helix Transcription Factor MYC2 Directly Represses PLETHORA Expression during Jasmonate-Mediated Modulation of the Root Stem Cell Niche in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.098277openalex-snapshot
The Arabidopsis Mediator Subunit MED25 Differentially Regulates Jasmonate and Abscisic Acid Signaling through Interacting with the MYC2 and ABI5 Transcription Factors
inferredcites →https://doi.org/10.1105/tpc.112.105486openalex-snapshot
The Arabidopsis F-Box Protein CORONATINE INSENSITIVE1 Is Stabilized by SCFCOI1 and Degraded via the 26S Proteasome Pathway
inferredcites →https://doi.org/10.1105/tpc.113.111112openalex-snapshot
A bHLH-Type Transcription Factor, ABA-INDUCIBLE BHLH-TYPE TRANSCRIPTION FACTOR/JA-ASSOCIATED MYC2-LIKE1, Acts as a Repressor to Negatively Regulate Jasmonate Signaling in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.112631openalex-snapshot
Jasmonate Regulates the INDUCER OF CBF EXPRESSION–C-REPEAT BINDING FACTOR/DRE BINDING FACTOR1 Cascade and Freezing Tolerance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.115139openalex-snapshot
Arabidopsis Basic Helix-Loop-Helix Transcription Factors MYC2, MYC3, and MYC4 Regulate Glucosinolate Biosynthesis, Insect Performance, and Feeding Behavior
inferredcites →https://doi.org/10.1105/tpc.113.116012openalex-snapshot
NITROGEN LIMITATION ADAPTATION, a Target of MicroRNA827, Mediates Degradation of Plasma Membrane–Localized Phosphate Transporters to Maintain Phosphate Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.117838openalex-snapshot
Arabidopsis WRKY57 Functions as a Node of Convergence for Jasmonic Acid– and Auxin-Mediated Signaling in Jasmonic Acid–Induced Leaf Senescence
inferredcites →https://doi.org/10.1105/tpc.113.121731openalex-snapshot
Arabidopsis DELLA and JAZ Proteins Bind the WD-Repeat/bHLH/MYB Complex to Modulate Gibberellin and Jasmonate Signaling Synergy
inferredcites →https://doi.org/10.1105/tpc.114.123208openalex-snapshot
SPX4 Negatively Regulates Phosphate Signaling and Homeostasis through Its Interaction with PHR2 in Rice
inferredcites →https://doi.org/10.1105/tpc.15.00116openalex-snapshot
Regulation of Jasmonate-Mediated Stamen Development and Seed Production by a bHLH-MYB Complex in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.15.00220openalex-snapshot
FILAMENTOUS FLOWER Is a Direct Target of JAZ3 and Modulates Responses to Jasmonate
inferredcites →https://doi.org/10.1105/tpc.15.00619openalex-snapshot
Transcriptional Mechanism of Jasmonate Receptor COI1-Mediated Delay of Flowering Time in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.17.00268openalex-snapshot
Light and Ethylene Coordinately Regulate the Phosphate Starvation Response through Transcriptional Regulation of PHOSPHATE STARVATION RESPONSE1
inferredcites →https://doi.org/10.1105/tpc.18.00405openalex-snapshot
MYC2 Regulates the Termination of Jasmonate Signaling via an Autoregulatory Negative Feedback Loop
inferredcites →https://doi.org/10.1105/tpc.18.00656openalex-snapshot
Identification of Molecular Integrators Shows that Nitrogen Actively Controls the Phosphate Starvation Response in Plants
inferredcites →https://doi.org/10.1105/tpc.19.00115openalex-snapshot
LEUNIG_HOMOLOG Mediates MYC2-Dependent Transcriptional Activation in Cooperation with the Coactivators HAC1 and MED25
inferredcites →https://doi.org/10.1105/tpc.19.00583openalex-snapshot
Mediator Subunit MED25 Couples Alternative Splicing of JAZ Genes with Fine-Tuning of Jasmonate Signaling
inferredcites →https://doi.org/10.1105/tpc.19.00617openalex-snapshot
Arabidopsis JAZ Proteins Interact with and Suppress RHD6 Transcription Factor to Regulate Jasmonate-Stimulated Root Hair Development
inferredcites →https://doi.org/10.1105/tpc.19.00838openalex-snapshot
Molecular Mechanism Underlying the Synergetic Effect of Jasmonate on Abscisic Acid Signaling during Seed Germination in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01608.xopenalex-snapshot
Genome‐wide reprogramming of metabolism and regulatory networks of Arabidopsis in response to phosphorus
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.1365-313x.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.2005.02394.xopenalex-snapshot
Point mutations in Arabidopsis Cullin1 reveal its essential role in jasmonate response
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03108.xopenalex-snapshot
Members of the PHO1 gene family show limited functional redundancy in phosphate transfer to the shoot, and are regulated by phosphate deficiency via distinct pathways
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03460.xopenalex-snapshot
Characterization of a sub‐family of Arabidopsis genes with the SPX domain reveals their diverse functions in plant tolerance to phosphorus starvation
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04375.xopenalex-snapshot
Dissection of local and systemic transcriptional responses to phosphate starvation in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05004.xopenalex-snapshot
Functional expression of PHO1 to the Golgi and trans‐Golgi network and its role in export of inorganic phosphate
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04190.xopenalex-snapshot
Opportunities for improving phosphorus‐use efficiency in crop plants
inferredcites →https://doi.org/10.1111/j.1744-7909.2008.00709.xopenalex-snapshot
Signaling Components Involved in Plant Responses to Phosphate Starvation
inferredcites →https://doi.org/10.1111/jipb.12163openalex-snapshot
Molecular mechanisms underlying phosphate sensing, signaling, and adaptation in plants
inferredcites →https://doi.org/10.1111/jipb.12840openalex-snapshot
Determination of sex by jasmonate
inferredcites →https://doi.org/10.1111/jipb.13248openalex-snapshot
The jasmonate‐induced bHLH gene SlJIG functions in terpene biosynthesis and resistance to insects and fungus
inferredcites →https://doi.org/10.1111/jipb.13319openalex-snapshot
A molecular framework for signaling crosstalk between jasmonate and ethylene in anthocyanin biosynthesis, trichome development, and defenses against insect herbivores in Arabidopsis
inferredcites →https://doi.org/10.1111/nph.15757openalex-snapshot
JAZ proteins modulate seed germination through interaction with ABI 5 in bread wheat and Arabidopsis
inferredcites →https://doi.org/10.1111/nph.16102openalex-snapshot
Nitrogen–phosphorus interplay: old story with molecular tale
inferredcites →https://doi.org/10.1111/nph.16272openalex-snapshot
Anthocyanin Fruit encodes an R2R3‐MYB transcription factor, SlAN2‐like, activating the transcription of SlMYBATV to fine‐tune anthocyanin content in tomato fruit
inferredcites →https://doi.org/10.1111/nph.17139openalex-snapshot
SPX4 interacts with both PHR1 and PAP1 to regulate critical steps in phosphorus‐status‐dependent anthocyanin biosynthesis
inferredcites →https://doi.org/10.1111/pce.14078openalex-snapshot
OsPHR2 modulates phosphate starvation‐induced OsMYC2 signalling and resistance to Xanthomonas oryzae pv. oryzae
inferredcites →https://doi.org/10.1111/tpj.14637openalex-snapshot
Nitrate‐inducible NIGT1 proteins modulate phosphate uptake and starvation signalling via transcriptional regulation of SPX genes
inferredcites →https://doi.org/10.1126/science.1173771openalex-snapshot
Hormone (Dis)harmony Moulds Plant Health and Disease
inferredcites →https://doi.org/10.1126/science.280.5366.1091openalex-snapshot
COI1 : An Arabidopsis Gene Required for Jasmonate-Regulated Defense and Fertility
inferredcites →https://doi.org/10.1126/science.aad9858openalex-snapshot
Control of eukaryotic phosphate homeostasis by inositol polyphosphate sensor domains
inferredcites →https://doi.org/10.1146/annurev-arplant-042817-040047openalex-snapshot
Modularity in Jasmonate Signaling for Multistress Resilience
inferredcites →https://doi.org/10.1146/annurev-arplant-050213-035949openalex-snapshot
Phosphate Nutrition: Improving Low-Phosphate Tolerance in Crops
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.665openalex-snapshot
PHOSPHATE ACQUISITION
inferredcites →https://doi.org/10.1186/1471-2229-13-26openalex-snapshot
Common bean (Phaseolus vulgarisL.) PvTIFY orchestrates global changes in transcript profile response to jasmonate and phosphorus deficiency
inferredcites →https://doi.org/10.1186/1746-4811-1-13openalex-snapshot
Transient expression vectors for functional genomics, quantification of promoter activity and RNA silencing in plants
inferredcites →https://doi.org/10.1371/journal.pgen.1000440openalex-snapshot
Gibberellin Acts through Jasmonate to Control the Expression of MYB21, MYB24, and MYB57 to Promote Stamen Filament Growth in Arabidopsis
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.pgen.1002021openalex-snapshot
Genetic Regulation by NLA and MicroRNA827 for Maintaining Nitrate-Dependent Phosphate Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pgen.1003422openalex-snapshot
Phosphorylation-Coupled Proteolysis of the Transcription Factor MYC2 Is Important for Jasmonate-Signaled Plant Immunity
inferredcites →https://doi.org/10.1371/journal.pgen.1003653openalex-snapshot
The bHLH Subgroup IIId Factors Negatively Regulate Jasmonate-Mediated Plant Defense and Development
inferredcites →https://doi.org/10.1371/journal.pone.0086182openalex-snapshot
bHLH003, bHLH013 and bHLH017 Are New Targets of JAZ Repressors Negatively Regulating JA Responses
inferredcites →https://doi.org/10.15252/embj.2021109102openalex-snapshot
Plant immunity suppression via PHR1‐RALF‐FERONIA shapes the root microbiome to alleviate phosphate starvation
inferredcites →https://doi.org/10.3389/fpls.2011.00083openalex-snapshot
Phosphate import in plants: focus on the PHT1 transporters
inferredcites →https://doi.org/10.3389/fpls.2021.628328openalex-snapshot
Isoleucine Enhances Plant Resistance Against Botrytis cinerea via Jasmonate Signaling Pathway
inferredcites →https://doi.org/10.3390/cells11071167openalex-snapshot
Identification, Structural, and Expression Analyses of SPX Genes in Giant Duckweed (Spirodela polyrhiza) Reveals Its Role in Response to Low Phosphorus and Nitrogen Stresses
inferredcites →https://doi.org/10.3390/genes10121018openalex-snapshot
Plant PHR Transcription Factors: Put on A Map
inferredcites →https://doi.org/10.4161/psb.6.3.14160openalex-snapshot
Global expression pattern comparison betweenlow phosphorus insensitive 4and WT Arabidopsis reveals an important role of reactive oxygen species and jasmonic acid in the root tip 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.4847325openalex-extracted
Soybean Phr1-Regulated Low Phosphorus-Responsive Gmralf22 Increases Uptake of Phosphate Via Stimulating Gmpts Expression
inferred← citeshttps://doi.org/10.1007/s00122-024-04697-8openalex-snapshot
Advances in functional studies of plant MYC transcription factors
inferred← citeshttps://doi.org/10.1007/s00299-025-03661-0openalex-snapshot
The apple phosphate starvation response transcription factor MdPHR1 positively regulates zinc and cadmium tolerance
inferred← citeshttps://doi.org/10.1007/s00344-024-11364-1openalex-snapshot
Cellular Transport and Multifaceted Roles of Jasmonates in Nutrient Deficiency Response in Plants
inferred← citeshttps://doi.org/10.1007/s00344-025-11831-3openalex-snapshot
The Physiological and Transcriptional Responses of Arabidopsis thaliana to an Innovative Controlled-Release Phosphorus–Chitosan Fertilizer: The Identification of a Gene Signature for Diagnostic and Prognostic Analyses of Plant Nutritional Status
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/s10265-024-01545-0openalex-snapshot
Recent advances in research on phosphate starvation signaling in plants
inferred← citeshttps://doi.org/10.1007/s10265-024-01546-zopenalex-snapshot
Modulation of plant immunity and biotic interactions under phosphate deficiency
inferred← citeshttps://doi.org/10.1007/s11032-024-01508-2openalex-snapshot
Functional analysis of ZmPHR1 and ZmPHR2 under low-phosphate stress in maize
inferred← citeshttps://doi.org/10.1007/s11104-023-06355-2openalex-snapshot
Jasmonic acid participating in the systemic regulation of phosphate starvation response in Brassica napus
inferred← citeshttps://doi.org/10.1007/s11427-025-3157-8openalex-snapshot
Holistic overview of regulatory networks governing seed dormancy and germination in plants
inferred← citeshttps://doi.org/10.1007/s40502-026-01020-zopenalex-snapshot
Multifaceted roles of phosphate starvation response (PHRs) transcription factors: beyond phosphate acquisition and homeostasis
inferred← citeshttps://doi.org/10.1007/s40626-024-00311-wopenalex-snapshot
Eucalypt seedlings lack a clear phosphate starvation response under low phosphorus availability
inferred← citeshttps://doi.org/10.1007/s42729-026-03386-3openalex-snapshot
Deciphering Phosphorus Deficiency Tolerance in Rice: Genetic, Molecular, and Omics Perspectives
inferred← citeshttps://doi.org/10.1007/s42994-025-00244-1openalex-snapshot
Robustness in jasmonate signaling: mechanisms of concerted regulation and implications for crop improvement
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/j.biotechadv.2025.108686openalex-snapshot
Understanding low-phosphate stress responses in plants: Opportunities for genome editing to improve phosphorous use efficiency (PUE)
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.113825openalex-snapshot
Jasmonate signaling pathway confers salt tolerance through a NUCLEAR FACTOR-Y trimeric transcription factor complex in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.115222openalex-snapshot
ERF114/115/109 are essential for jasmonate-repressed non-canonical JAZ8 activity in JA signaling
inferred← citeshttps://doi.org/10.1016/j.cj.2024.11.001openalex-snapshot
JAZ proteins: Key regulators of plant growth and stress response
inferred← citeshttps://doi.org/10.1016/j.cpb.2025.100505openalex-snapshot
Integrative multi-omics analysis of rice grown continuously under P-starvation stress unravels Pup1-mediated regulatory complex for resilience to phosphorus deficiency
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105646openalex-snapshot
Physiological and transcriptomic regulation of Populus simonii fine roots exposed to a heterogeneous phosphorus environment in soil
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2026.106353openalex-snapshot
Phosphate availability switches nitrate-driven phosphorus acquisition strategies in poplar: Arbuscular mycorrhizal symbiosis reshapes emergency foraging and homeostatic maintenance
inferred← citeshttps://doi.org/10.1016/j.gene.2026.150362openalex-snapshot
ZmMYC7 negatively regulates salt tolerance in maize through ZmMAPK3-mediated phosphorylation-dependent proteasomal degradation
inferred← citeshttps://doi.org/10.1016/j.hpj.2025.06.022openalex-snapshot
Uncovering the interaction between PatJAZs and PatSWC4 to control the expression of the PatPTS gene and the biosynthesis of patchouli alcohol
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.136822openalex-snapshot
Comprehensive characterization of gibberellin oxidase gene family in Brassica napus reveals BnGA2ox15 involved in hormone signaling and response to drought stress
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144539openalex-snapshot
Optimizing plant phosphate uptake: Advances in the core regulatory mechanisms of phosphate starvation response proteins and their macromolecular partners: A review
inferred← citeshttps://doi.org/10.1016/j.jare.2025.11.014openalex-snapshot
Unraveling competitive protein interactions: A critical step toward improved production and therapeutics
inferred← citeshttps://doi.org/10.1016/j.jfutfo.2025.12.029openalex-snapshot
Molecular mechanisms underlying ClO₂-mediated disease resistance and delayed ripening in postharvest apricot fruit
inferred← citeshttps://doi.org/10.1016/j.jgg.2024.09.018openalex-snapshot
Phosphorus acquisition, translocation, and redistribution in maize
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.135703openalex-snapshot
The MYC2 and MYB43 transcription factors cooperate to repress HMA2 and HMA4 expression, altering cadmium tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.136968openalex-snapshot
Transcription-metabolism analysis of various signal transduction pathways in Brassica chinensis L. exposed to PLA-MPs
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.2024.128030openalex-snapshot
Root metabolites regulated by FERONIA promote phosphorus-solubilizing rhizobacteria enrichment induced by Arabidopsis thaliana coping with phosphorus deficiency
inferred← citeshttps://doi.org/10.1016/j.molp.2024.03.014openalex-snapshot
Phosphorus lights up the trade-off between growth and immunity
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.plantsci.2023.111816openalex-snapshot
Review: Losing JAZ4 for growth and defense
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112211openalex-snapshot
Soybean PHR1-regulated low phosphorus-responsive GmRALF22 promotes phosphate uptake by stimulating the expression of GmPTs
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112685openalex-snapshot
Review: Adaptation of plants to phosphorus scarcity: From nutritional crosstalk to organellar function
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112928openalex-snapshot
Low pH attenuates anthocyanin accumulation via the STOP1-MYB75 module in Arabidopsis
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.plantsci.2026.113387openalex-snapshot
The circadian clock proteins PRR modulate root hair development via the RHD6/RSL module in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphe.2025.100138openalex-snapshot
Rapid acquisition of ionomic and morphological data from plant seeds through fast X-ray fluorescence microscopy and computer vision
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109642openalex-snapshot
Genome-wide analysis of PHT gene family and their role in LP and salt stress in sweet potato
inferred← citeshttps://doi.org/10.1016/j.pld.2024.05.003openalex-snapshot
Transcription factor ABF3 modulates salinity stress-enhanced jasmonate signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2024.112796openalex-snapshot
Pichia galeiformis-secreted protein PgSLP increases citrus fruit disease resistance by activating amino acid metabolism
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2026.114326openalex-snapshot
A PpTIFY5A/10A-PpTGA2.1-L complex delaying fruit senescence via salicylic acid antagonized ethylene and jasmonic acid in sand pear
inferred← citeshttps://doi.org/10.1016/j.scib.2026.05.049openalex-snapshot
GhZAT10 integrates jasmonic acid and ethylene pathways to synergistically regulate the GhKUP3aD-mediated high-affinity K+ uptake in Gossypium hirsutum
inferred← citeshttps://doi.org/10.1016/j.stress.2025.101069openalex-snapshot
Tissue-specific phosphorus stress adaptation in Brassica rapa: WGCNA reveals root hormonal triad and leaf lipid remodeling as key tolerance mechanisms
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101537openalex-snapshot
Heterologous expression of soybean GmIAA9 enhances the tolerance of tobacco to low phosphorus stress
inferred← citeshttps://doi.org/10.1016/j.tplants.2025.07.010openalex-snapshot
Phosphorus acquisition and pathogen defense: synergies versus trade-offs
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c06383openalex-snapshot
Sesquiterpenoids in Agarwood: Biosynthesis, Microbial Induction, and Pharmacological Activities
inferred← citeshttps://doi.org/10.1038/s41477-024-01682-3openalex-snapshot
iJAZ-based approach to engineer lepidopteran pest resistance in multiple crop species
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/10.1079/9781836990598.0013openalex-snapshot
Strigolactones in Nutrient-use Efficiency Regulation in Crop Plants
inferred← citeshttps://doi.org/10.1080/01904167.2025.2558890openalex-snapshot
Changes in root morphology and rhizosphere metabolites in field-grown maize with different sources of phosphorus supply
inferred← citeshttps://doi.org/10.1080/07352689.2026.2663753openalex-snapshot
Decoding the Plant Nutrient Continuum: Regulatory Logic from Deficiency to Sufficiency and Toxicity
inferred← citeshttps://doi.org/10.1080/29932297.2026.2698303openalex-snapshot
Phosphate starvation responses in Arabidopsis provide a scaffold to interrogate plant carnivory in Triphyophyllum and allied genera
inferred← citeshttps://doi.org/10.1093/hr/uhae178openalex-snapshot
CsPHRs-CsJAZ3 incorporates phosphate signaling and jasmonate pathway to regulate catechin biosynthesis in Camellia sinensis
inferred← citeshttps://doi.org/10.1093/hr/uhae228openalex-snapshot
The transcription factor MYC2 positively regulates terpene trilactone biosynthesis through activating GbGGPPS expression in Ginkgo biloba
inferred← citeshttps://doi.org/10.1093/jxb/erad326openalex-snapshot
Phosphate starvation: response mechanisms and solutions
inferred← citeshttps://doi.org/10.1093/jxb/erae005openalex-snapshot
TARGET OF MONOPTEROS: key transcription factors orchestrating plant development and environmental response
inferred← citeshttps://doi.org/10.1093/jxb/erae222openalex-snapshot
PHOSPHATE1-mediated phosphate translocation from roots to shoots regulates floral transition in plants
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/erag259openalex-snapshot
The link between phosphate starvation-triggered anthocyanin biosynthesis and jasmonate-driven regulation in tomato
inferred← citeshttps://doi.org/10.1093/plcell/koad071openalex-snapshot
Coordinating phosphorus and jasmonate signaling: PHR1 partners with transcriptional regulators
inferred← citeshttps://doi.org/10.1093/plcell/koae096openalex-snapshot
INDUCER OF CBF EXPRESSION 1 promotes cold-enhanced immunity by directly activating salicylic acid signaling
inferred← citeshttps://doi.org/10.1093/plcell/koae294openalex-snapshot
Jasmonate induces translation of the Arabidopsis transfer RNA-binding protein YUELAO1, which activates MYC2 in jasmonate signaling
inferred← citeshttps://doi.org/10.1093/plcell/koaf178openalex-snapshot
Jasmonate signaling coordinates with the SOD7–KLU pathway to regulate seed size in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/plphys/kiad370openalex-snapshot
CONSTANS interacts with and antagonizes ABF transcription factors during salt stress under long-day conditions
inferred← citeshttps://doi.org/10.1093/plphys/kiaf015openalex-snapshot
UBIQUITIN-CONJUGATING ENZYME34 mediates pyrophosphatase AVP1 turnover and regulates abiotic stress responses in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiaf390openalex-snapshot
Function and regulatory mechanism of HvSPX4 in maintaining phosphate homeostasis in barley
inferred← citeshttps://doi.org/10.1093/plphys/kiaf630openalex-snapshot
Bidirectional crosstalk between plant hormone signaling and metabolism
inferred← citeshttps://doi.org/10.1093/plphys/kiag063openalex-snapshot
The BBX6-2–NF-YC4–JAZ1 complex mediates SOC1 activation to control jasmonate-responsive flowering time in Brassica juncea
inferred← citeshttps://doi.org/10.1093/plphys/kiag199openalex-snapshot
OsPHR2 and OsMYC2 coordinate phosphate starvation-induced sakuranetin biosynthesis for enhanced rice blast resistance
inferred← citeshttps://doi.org/10.1093/plphys/kiag321openalex-snapshot
Jasmonates promote myrosin idioblast cell development via MYC2-mediated activation of the FAMA-bHLH090 pathway in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiag394openalex-snapshot
Arabidopsis MYC2–ARF16–ABI5 complex functions as a transcriptional switch to regulate jasmonate, auxin, and abscisic acid signaling synergy
inferred← citeshttps://doi.org/10.1093/plphys/kiag399openalex-snapshot
The cotton 1R-MYB transcription factor GhMYS1 promotes fiber cell elongation by inhibiting secondary cell wall synthesis
inferred← citeshttps://doi.org/10.1093/treephys/tpaf028openalex-snapshot
The MYB transcription factor PtoPHL3 positively regulates poplar resistance to canker disease caused by Dothiorella gregaria
inferred← citeshttps://doi.org/10.1101/2023.11.14.566975openalex-snapshot
Plant pathogenic fungi hijack phosphate starvation signaling with conserved enzymatic effectors
inferred← citeshttps://doi.org/10.1101/2024.05.29.596424openalex-snapshot
Soybean PHR1-regulated low phosphorus-responsive GmRALF22 increases uptake of phosphate via stimulating GmPT s expression
inferred← citeshttps://doi.org/10.1111/1755-0998.70013openalex-snapshot
Pan‐Genome of Jasminum sambac Reveals the Genetic Diversity of Different Petal Morphology and Aroma‐Related Genes
inferred← citeshttps://doi.org/10.1111/jipb.13732openalex-snapshot
A pair of nuclear factor Y transcription factors act as positive regulators in jasmonate signaling and disease resistance in Arabidopsis
inferred← citeshttps://doi.org/10.1111/jipb.13827openalex-snapshot
The interaction of nutrient uptake with biotic and abiotic stresses in plants
inferred← citeshttps://doi.org/10.1111/jipb.13941openalex-snapshot
Jasmonate activates a SlJAZ2/3‐SlMYC3‐like module regulating K+ uptake in tomato response to low K+ stress
inferred← citeshttps://doi.org/10.1111/jipb.70147openalex-snapshot
Jasmonic acid activates the ZmZIM13–ZmbHLH99 module to regulate ZmNLP3.2 to mediate nitrate uptake in maize
inferred← citeshttps://doi.org/10.1111/jipb.70268openalex-snapshot
Arabidopsis inositol polyphosphate kinase activities regulate COP9 deneddylation functions in phosphate homeostasis
inferred← citeshttps://doi.org/10.1111/jipb.70278openalex-snapshot
SlMED25‐SlPHR3‐SlSPX2 module fine‐tunes SlPHR3‐mediated transcriptional activation of phosphate starvation response in tomato
inferred← citeshttps://doi.org/10.1111/nph.20152openalex-snapshot
Phosphate promotes Arabidopsis root skewing and circumnutation through reorganisation of the microtubule cytoskeleton
inferred← citeshttps://doi.org/10.1111/nph.70446openalex-snapshot
To immunity and beyond: the central role of jasmonate signalling in beneficial root–microbe–environment interactions
inferred← citeshttps://doi.org/10.1111/nph.71235openalex-snapshot
The MYC2 ‐ MYB113 module governs JA signaling to regulate anthocyanin accumulation and secondary wall thickening under high light in Populus
inferred← citeshttps://doi.org/10.1111/pbi.70496openalex-snapshot
PPSR1 Protein Functions as an Important Regulator to Enhance Plant Growth Performance Under N, P, and K Deficient Stress Conditions
inferred← citeshttps://doi.org/10.1111/pbr.70047openalex-snapshot
QTL Mapping of Several Seed Quality Traits in the DH Population NPZ06 × NPZ09 ( Brassica napus L.) for Marker‐Assisted Selection
inferred← citeshttps://doi.org/10.1111/pce.14920openalex-snapshot
A bamboo bHLH transcription factor PeRHL4 has dual functions in enhancing drought and phosphorus starvation tolerance
inferred← citeshttps://doi.org/10.1111/pce.15593openalex-snapshot
Inducer of CBF Expression1 (ICE1) Interacts With WRKY46 to Modulate Salicylic Acid‐Induced Leaf Senescence in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.70262openalex-snapshot
From Soil to Cell: Systemic Signalling and Regulatory Networks in Zea mays Under Phosphorus Deprivation
inferred← citeshttps://doi.org/10.1111/ppl.14197openalex-snapshot
SlPHL1 positively modulates acid phosphatase in response to phosphate starvation by directly activating the genes SlPAP10b and SlPAP15 in tomato
inferred← citeshttps://doi.org/10.1111/ppl.70101openalex-snapshot
GAI1 underlines the antagonism between gibberellin and jasmonic acid in modulating disease resistance
inferred← citeshttps://doi.org/10.1111/ppl.70143openalex-snapshot
LvWRKY75 enhances the transcription of LvMYB5 and promotes anthocyanin biosynthesis in lily petals during the blooming phase
inferred← citeshttps://doi.org/10.1111/ppl.70777openalex-snapshot
Exogenous Quercetin Enhances Soybean Salt Tolerance via Multimodal Mechanisms
inferred← citeshttps://doi.org/10.1111/tpj.16800openalex-snapshot
Phosphate deficiency increases plant susceptibility to Botrytis cinerea infection by inducing the abscisic acid pathway
inferred← citeshttps://doi.org/10.1111/tpj.17098openalex-snapshot
Balancing act: The dynamic relationship between nutrient availability and plant defence
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.70315openalex-snapshot
Enhancing inositol pyrophosphate accumulation in plants alters growth, phosphate homeostasis, and insect herbivory
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/10.1134/s1021443725608249openalex-snapshot
Root Architecture Dynamics and Signal Transduction Mechanisms Regulating Mineral Nutrient Acquisition in Plants
inferred← citeshttps://doi.org/10.1186/s12864-023-09911-3openalex-snapshot
Basic helix-loop-helix (bHLH) gene family in rye (Secale cereale L.): genome-wide identification, phylogeny, evolutionary expansion and expression analyses
inferred← citeshttps://doi.org/10.1186/s12870-024-05654-9openalex-snapshot
A systematic regulatory network related to bulbil formation in Lilium lancifolium based on metabolome and transcriptome analyses
inferred← citeshttps://doi.org/10.1186/s12870-025-06315-1openalex-snapshot
Genome-wide identification and analysis of phosphate utilization related genes (PURs) reveal their roles involved in low phosphate responses in Brassica napus L.
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/s12870-025-07995-5openalex-snapshot
Candidate genes and molecular mechanisms regulating tiller development in wild Kentucky bluegrass
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.pone.0314396openalex-snapshot
Transcriptomic and biochemical insights into key gene networks driving bulbil development of Pinellia ternata (Thunb.) Breit
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7860168/v1openalex-snapshot
Genome-wide Identification of JAZ Family and Functional Analysis of GmJAZ6 in Response to Phosphorus Deficiency in Soybean
inferred← citeshttps://doi.org/10.2139/ssrn.5807639openalex-snapshot
Transcriptome analysis and functional validation of JAZ subfamily genes of Sesuvium portulacastrum under salinity and cadmium stresses
inferred← citeshttps://doi.org/10.3389/fpls.2024.1379562openalex-snapshot
Comparative functional analyses of PHR1, PHL1, and PHL4 transcription factors in regulating Arabidopsis responses to phosphate starvation
inferred← citeshttps://doi.org/10.3389/fpls.2025.1658530openalex-snapshot
Salt stress enhances bioactive compound accumulation in Glycyrrhiza inflata: integrated transcriptomics and physiological analysis reveals germplasm-specific adaptation mechanisms
inferred← citeshttps://doi.org/10.3389/fpls.2026.1846817openalex-snapshot
Transcriptome analysis and physiological indicators reveal the role of physiological integration in heterogeneous cadmium and phenanthrene stress in Zoysia japonica
inferred← citeshttps://doi.org/10.3390/biology14050490openalex-snapshot
The Impact of Nitrogen and Phosphorus Interaction on Growth, Nutrient Absorption, and Signal Regulation in Woody Plants
inferred← citeshttps://doi.org/10.3390/ijms25116149openalex-snapshot
Endogenous Hormone Levels and Transcriptomic Analysis Reveal the Mechanisms of Bulbil Initiation in Pinellia ternata
inferred← citeshttps://doi.org/10.3390/ijms25158022openalex-snapshot
Arabidopsis thaliana MYC2 and MYC3 Are Involved in Ethylene-Regulated Hypocotyl Growth as Negative Regulators
inferred← citeshttps://doi.org/10.3390/ijms252212030openalex-snapshot
Epigenetic Regulation of Anthocyanin Biosynthesis in Betula pendula ‘Purple Rain’
inferred← citeshttps://doi.org/10.3390/ijms26072958openalex-snapshot
Decoding PHR-Orchestrated Stress Adaptation: A Genome-Wide Integrative Analysis of Transcriptional Regulation Under Abiotic Stress in Eucalyptus grandis
inferred← citeshttps://doi.org/10.3390/ijms26104684openalex-snapshot
Genome-Wide Analysis and Expression Profiling of the JAZ Gene Family in Response to Abiotic Stress in Alfalfa
inferred← citeshttps://doi.org/10.3390/ijms27052101openalex-snapshot
Transcriptome Analysis and Functional Validation of JAZ Subfamily Genes of Sesuvium portulacastrum Under Salt and Cadmium Stresses
inferred← citeshttps://doi.org/10.3390/ijms27156824openalex-snapshot
Coordinated MBW, GIS, and RSL Regulatory Networks in Plant Epidermal Patterning Under Environmental Cues
inferred← citeshttps://doi.org/10.3390/plants13020273openalex-snapshot
Nitrogen Deficiency Enhances Eggplant Defense against Western Flower Thrips via the Induction of the Jasmonate Pathway
inferred← citeshttps://doi.org/10.3390/plants13131873openalex-snapshot
Beneficial Effects of Phosphite in Arabidopsis thaliana Mediated by Activation of ABA, SA, and JA Biosynthesis and Signaling Pathways
inferred← citeshttps://doi.org/10.3390/plants14193037openalex-snapshot
Concentration-Dependent N-P Interactions Cause Organ-Specific Responses and Nutrient Allocation in Poplar Seedlings
inferred← citeshttps://doi.org/10.3390/plants15101543openalex-snapshot
Genome-Wide Identification of the JAZ Gene Family in Garlic (Allium sativum L.) and the Functional Role of AsJAZ17 in Salt Tolerance
inferred← citeshttps://doi.org/10.48130/seedbio-0026-0008openalex-snapshot
The NtMYC2-NtABI5 module regulates abscisic acid mediated seed germination in tobacco
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.