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Sensing and Signaling of Phosphate Starvation: From Local to Long Distance
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00299-012-1328-7openalex-snapshot
Overexpression of GbWRKY1 positively regulates the Pi starvation response by alteration of auxin sensitivity in Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-006-0408-8openalex-snapshot
Phosphate starvation responses are mediated by sugar signaling in Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-006-0410-1openalex-snapshot
Phosphorus deficiency in red clover promotes exudation of orobanchol, the signal for mycorrhizal symbionts and germination stimulant for root parasites
inferredcites →https://doi.org/10.1007/s00425-010-1310-yopenalex-snapshot
Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-011-1568-8openalex-snapshot
How do nitrogen and phosphorus deficiencies affect strigolactone production and exudation?
inferredcites →https://doi.org/10.1016/j.cell.2009.07.004openalex-snapshot
CHL1 Functions as a Nitrate Sensor in Plants
inferredcites →https://doi.org/10.1016/j.devcel.2013.10.004openalex-snapshot
Side-Chain Modification of Cytokinins Controls Shoot Growth in Arabidopsis
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.2017.05.009openalex-snapshot
Phosphate Starvation-Dependent Iron Mobilization Induces CLE14 Expression to Trigger Root Meristem Differentiation through CLV2/PEPR2 Signaling
inferredcites →https://doi.org/10.1016/j.molcel.2018.02.009openalex-snapshot
Metal Sensing by the IRT1 Transporter-Receptor Orchestrates Its Own Degradation and Plant Metal Nutrition
inferredcites →https://doi.org/10.1016/j.pbi.2017.06.007openalex-snapshot
MicroRNA-mediated signaling and regulation of nutrient transport and utilization
inferredcites →https://doi.org/10.1016/j.tplants.2014.06.004openalex-snapshot
MicroRNA-mediated surveillance of phosphate transporters on the move
inferredcites →https://doi.org/10.1038/nature07272openalex-snapshot
Inhibition of shoot branching by new terpenoid plant hormones
inferredcites →https://doi.org/10.1038/ncomms11095openalex-snapshot
Identification of plant vacuolar transporters mediating phosphate storage
inferredcites →https://doi.org/10.1038/ncomms15300openalex-snapshot
Low phosphate activates STOP1-ALMT1 to rapidly inhibit root cell elongation
inferredcites →https://doi.org/10.1038/ng.529openalex-snapshot
A basic helix-loop-helix transcription factor controls cell growth and size in root hairs
inferredcites →https://doi.org/10.1038/ng2041openalex-snapshot
Root tip contact with low-phosphate media reprograms plant root architecture
inferredcites →https://doi.org/10.1038/ng2079openalex-snapshot
Target mimicry provides a new mechanism for regulation of microRNA activity
inferredcites →https://doi.org/10.1038/nplants.2015.25openalex-snapshot
Endogenous Arabidopsis messenger RNAs transported to distant tissues
inferredcites →https://doi.org/10.1038/nplants.2016.33openalex-snapshot
Vascular-mediated signalling involved in early phosphate stress response in plants
inferredcites →https://doi.org/10.1038/s41467-018-03851-3openalex-snapshot
A mechanistic framework for auxin dependent Arabidopsis root hair elongation to low external phosphate
inferredcites →https://doi.org/10.1046/j.1365-3040.1999.00405.xopenalex-snapshot
Ethylene: a regulator of root architectural responses to soil phosphorus availability
inferredcites →https://doi.org/10.1046/j.1365-3040.2001.00695.xopenalex-snapshot
Regulation of root hair density by phosphorus availability in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-3040.2003.00957.xopenalex-snapshot
Shoot P status regulates cluster‐root growth and citrate exudation in Lupinus albus grown with a divided root system
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/10.1073/pnas.0603522103openalex-snapshot
Roles of Arabidopsis ATP/ADP isopentenyltransferases and tRNA isopentenyltransferases in cytokinin biosynthesis
inferredcites →https://doi.org/10.1073/pnas.0805619105openalex-snapshot
Cytokinins are central regulators of cambial activity
inferredcites →https://doi.org/10.1073/pnas.0901778106openalex-snapshot
ER-resident proteins PDR2 and LPR1 mediate the developmental response of root meristems to phosphate availability
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.1404680111openalex-snapshot
Rice SPX1 and SPX2 inhibit phosphate starvation responses through interacting with PHR2 in a phosphate-dependent manner
inferredcites →https://doi.org/10.1073/pnas.1514598112openalex-snapshot
A vacuolar phosphate transporter essential for phosphate homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1701952114openalex-snapshot
Malate-dependent Fe accumulation is a critical checkpoint in the root developmental response to low phosphate
inferredcites →https://doi.org/10.1093/jxb/erq335openalex-snapshot
The regulation of arbuscular mycorrhizal symbiosis by phosphate in pea involves early and systemic signalling events
inferredcites →https://doi.org/10.1093/jxb/ers131openalex-snapshot
HPS4/SABRE regulates plant responses to phosphate starvation through antagonistic interaction with ethylene signalling
inferredcites →https://doi.org/10.1093/jxb/ert431openalex-snapshot
Long-distance call from phosphate: systemic regulation of phosphate starvation responses
inferredcites →https://doi.org/10.1093/jxb/erv025openalex-snapshot
Differentiating phosphate-dependent and phosphate-independent systemic phosphate-starvation response networks in Arabidopsis thaliana through the application of phosphite
inferredcites →https://doi.org/10.1093/jxb/erx317openalex-snapshot
OsPht1;8, a phosphate transporter, is involved in auxin and phosphate starvation response in rice
inferredcites →https://doi.org/10.1093/mp/ssq008openalex-snapshot
Systemic Signaling and Local Sensing of Phosphate in Common Bean: Cross-Talk between Photosynthate and MicroRNA399
inferredcites →https://doi.org/10.1093/pcp/pcq170openalex-snapshot
Complex Regulation of Two Target Genes Encoding SPX-MFS Proteins by Rice miR827 in Response to Phosphate Starvation
inferredcites →https://doi.org/10.1093/pcp/pcy051openalex-snapshot
Phosphite-Mediated Suppression of Anthocyanin Accumulation Regulated by Mitochondrial ATP Synthesis and Sugars 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.256603openalex-snapshot
MAX4 and RMS1 are orthologous dioxygenase-like genes that regulate shoot branching in Arabidopsis and pea
inferredcites →https://doi.org/10.1104/pp.010835openalex-snapshot
Phosphite, an Analog of Phosphate, Suppresses the Coordinated Expression of Genes under Phosphate Starvation
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.101.2.339openalex-snapshot
Metabolic Adaptations of Plant Respiration to Nutritional Phosphate Deprivation
inferredcites →https://doi.org/10.1104/pp.103.037945openalex-snapshot
Structure and Expression Profile of the Arabidopsis PHO1 Gene Family Indicates a Broad Role in Inorganic Phosphate Homeostasis
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.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.105.073825openalex-snapshot
Characterization of low phosphorus insensitive Mutants Reveals a Crosstalk between Low Phosphorus-Induced Determinate Root Development and the Activation of Genes Involved in the Adaptation of Arabidopsis to Phosphorus Deficiency
inferredcites →https://doi.org/10.1104/pp.106.078063openalex-snapshot
pho2, a Phosphate Overaccumulator, Is Caused by a Nonsense Mutation in a MicroRNA399 Target Gene
inferredcites →https://doi.org/10.1104/pp.107.1.207openalex-snapshot
Characterization of a Phosphate-Accumulator Mutant of Arabidopsis thaliana
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.108.116269openalex-snapshot
Regulatory Network of MicroRNA399 and PHO2 by Systemic Signaling
inferredcites →https://doi.org/10.1104/pp.109.139139openalex-snapshot
Identification of Nutrient-Responsive Arabidopsis and Rapeseed MicroRNAs by Comprehensive Real-Time Polymerase Chain Reaction Profiling and Small RNA Sequencing
inferredcites →https://doi.org/10.1104/pp.109.147280openalex-snapshot
Uncovering Small RNA-Mediated Responses to Phosphate Deficiency in Arabidopsis by Deep Sequencing
inferredcites →https://doi.org/10.1104/pp.110.164640openalex-snapshot
Strigolactones Are Transported through the Xylem and Play a Key Role in Shoot Architectural Response to Phosphate Deficiency in Nonarbuscular Mycorrhizal Host Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.175257openalex-snapshot
Vacuolar Ca2+/H+ Transport Activity Is Required for Systemic Phosphate Homeostasis Involving Shoot-to-Root Signaling in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.114.238410openalex-snapshot
Expression of Sucrose Transporter cDNAs Specifically in Companion Cells Enhances Phloem Loading and Long-Distance Transport of Sucrose but Leads to an Inhibition of Growth and the Perception of a Phosphate Limitation
inferredcites →https://doi.org/10.1104/pp.114.244376openalex-snapshot
The S-Domain Receptor Kinase Arabidopsis Receptor Kinase2 and the U Box/Armadillo Repeat-Containing E3 Ubiquitin Ligase9 Module Mediates Lateral Root Development under Phosphate Starvation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.114.252338openalex-snapshot
Reducing the Genetic Redundancy of Arabidopsis PHOSPHATE TRANSPORTER1 Transporters to Study Phosphate Uptake and Signaling
inferredcites →https://doi.org/10.1104/pp.115.3.1251openalex-snapshot
The rms1 Mutant of Pea Has Elevated Indole-3-Acetic Acid Levels and Reduced Root-Sap Zeatin Riboside Content but Increased Branching Controlled by Graft-Transmissible Signal(s)
inferredcites →https://doi.org/10.1104/pp.126.1.203openalex-snapshot
Long-Distance Signaling and the Control of Branching in therms1 Mutant of Pea
inferredcites →https://doi.org/10.1104/pp.97.3.1087openalex-snapshot
Mutant of Arabidopsis Deficient in Xylem Loading of Phosphate
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.105.038943openalex-snapshot
Regulation of Phosphate Homeostasis by MicroRNA 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.112.096636openalex-snapshot
PHO2-Dependent Degradation of PHO1 Modulates Phosphate Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.115998openalex-snapshot
Identification of Downstream Components of Ubiquitin-Conjugating Enzyme PHOSPHATE2 by Quantitative Membrane Proteomics in Arabidopsis Roots
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.15.00956openalex-snapshot
Transcript Abundance Explains mRNA Mobility Data in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.15.01056openalex-snapshot
tRNA-Related Sequences Trigger Systemic mRNA Transport in Plants
inferredcites →https://doi.org/10.1111/j.1365-3040.1996.tb00386.xopenalex-snapshot
Stimulation of root hair elongation in Arabidopsis thaliana by low phosphorus availability
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01568.xopenalex-snapshot
Cytokinin represses phosphate‐starvation response through increasing of intracellular phosphate level
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02289.xopenalex-snapshot
Signaling of phosphorus deficiency‐induced gene expression in white lupin requires sugar and phloem transport
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02778.xopenalex-snapshot
Membrane lipid alteration during phosphate starvation is regulated by phosphate signaling and auxin/cytokinin cross‐talk
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03368.xopenalex-snapshot
Identification and characterization of small RNAs from the phloem of Brassica napus
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.1365-3180.2011.00847.xopenalex-snapshot
Quantification of the relationship between strigolactones and Striga hermonthica infection in rice under varying levels of nitrogen and phosphorus
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03555.xopenalex-snapshot
Ethylene signalling is involved in regulation of phosphate starvation‐induced gene expression and production of acid phosphatases and anthocyanin in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.04002.xopenalex-snapshot
The emerging importance of the SPX domain‐containing proteins in phosphate homeostasis
inferredcites →https://doi.org/10.1111/nph.12499openalex-snapshot
Auxin response factor (Os ARF 12), a novel regulator for phosphate homeostasis in rice (Oryza sativa)
inferredcites →https://doi.org/10.1111/nph.13405openalex-snapshot
Distinct sensitivities to phosphate deprivation suggest that RGF peptides play disparate roles in Arabidopsis thaliana root development
inferredcites →https://doi.org/10.1111/nph.13591openalex-snapshot
A chemical genetic strategy identify the PHOSTIN , a synthetic molecule that triggers phosphate starvation responses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/nph.14938openalex-snapshot
Evolution of micro RNA 827 targeting in the plant kingdom
inferredcites →https://doi.org/10.1111/pce.12001openalex-snapshot
OsARF16, a transcription factor, is required for auxin and phosphate starvation response in rice ( Oryza sativa L.)
inferredcites →https://doi.org/10.1111/plb.12568openalex-snapshot
Long‐distance movement of phosphate starvation‐responsive microRNAs in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.13974openalex-snapshot
Arabidopsis inositol phosphate kinases IPK 1 and ITPK 1 constitute a metabolic pathway in maintaining phosphate homeostasis
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-042110-103849openalex-snapshot
Signaling Network in Sensing Phosphate Availability in Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.665openalex-snapshot
PHOSPHATE ACQUISITION
inferredcites →https://doi.org/10.1242/dev.120006openalex-snapshot
Strigolactone biosynthesis and signaling in plant development
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.1006194openalex-snapshot
The Molecular Mechanism of Ethylene-Mediated Root Hair Development Induced by 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.4766567openalex-extracted
Egphl7, Egphr1 and Egphr2 Bind to P1bs and a Unique Motif, Agatwc, for Phosphate Starvation Transcriptional Regulation in Oil Palm
inferred← citeshttps://doi.org/10.1002/pld3.416openalex-snapshot
Thepho1;2a′‐m1.1allele ofPhosphate1conditions misregulation of the phosphorus starvation response in maize ( Zea maysssp.mays L.)
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/s00425-019-03313-0openalex-snapshot
Expression analysis and functional characterization of two PHT1 family phosphate transporters in ryegrass
inferred← citeshttps://doi.org/10.1007/s11033-022-07354-9openalex-snapshot
Phosphorus homeostasis: acquisition, sensing, and long-distance signaling in plants
inferred← citeshttps://doi.org/10.1007/s11103-024-01496-zopenalex-snapshot
Silencing Osa-miR827 via CRISPR/Cas9 protects rice against the blast fungus Magnaporthe oryzae
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/s11104-025-07807-7openalex-snapshot
Plant STOP1 family: a helmsman in the soil multiple stress adaptation
inferred← citeshttps://doi.org/10.1007/s11816-026-01086-zopenalex-snapshot
Characterization of TaSPX1-7B in regulating phosphate homeostasis and low phosphate responses in wheat
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/s13562-021-00715-8openalex-snapshot
Phosphorus starvation response dynamics and management in plants for sustainable agriculture
inferred← citeshttps://doi.org/10.1007/s42729-026-03346-xopenalex-snapshot
Nitrogen and Phosphorus Deficiency Coordinate Stomatal Closure and Disrupt Leaf Thermoregulation and Stress Metabolism in Rice Seedlings
inferred← citeshttps://doi.org/10.1016/b978-0-443-16082-0.00020-5openalex-snapshot
Soil properties influencing nutrient signaling in plant soil systems
inferred← citeshttps://doi.org/10.1016/j.agee.2026.110276openalex-snapshot
Optimizing phosphorus input and straw return enhances soil health: Insights into microbial functional gene indicators in Solanum lycopersicum
inferred← citeshttps://doi.org/10.1016/j.cej.2025.168707openalex-snapshot
Heterogeneous catalytic system enhances water purification and phosphorus recovery potential in constructed wetlands
inferred← citeshttps://doi.org/10.1016/j.cj.2021.03.020openalex-snapshot
TaMADS2-3D, a MADS transcription factor gene, regulates phosphate starvation responses in plants
inferred← citeshttps://doi.org/10.1016/j.cj.2026.06.003openalex-snapshot
The microRNA399-PHOSPHATE2 module acts as a dual regulator of root architecture and systemic signaling under phosphate starvation in rice
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.2025.144611openalex-snapshot
Open stomata 1 and phosphate starvation response 1 regulate tomato root system architecture during heterogeneous phosphate availability
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.117065openalex-snapshot
The key physiological and molecular responses of Neolamarckia cadamba to phosphorus deficiency stress by hydroponics
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153363openalex-snapshot
Epigenetic regulation of nitrogen and phosphorus responses in plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.05.018openalex-snapshot
Intracellular phosphate homeostasis – A short way from metabolism to signaling
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.plaphy.2021.11.022openalex-snapshot
The effect of silicon supply on photosynthesis and carbohydrate metabolism in two wheat (Triticum aestivum L.) cultivars contrasting in response to phosphorus nutrition
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.11.039openalex-snapshot
Integrative analysis of the metabolome and transcriptome reveal the phosphate deficiency response pathways of alfalfa
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.03.019openalex-snapshot
ATL8, a RING E3 ligase, modulates root growth and phosphate homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108313openalex-snapshot
Can nutrients act as signals under abiotic stress?
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110965openalex-snapshot
SlSTOP1–SlFRDL1–mediated citrate exudation modulates apoplastic iron–redox homeostasis to promote primary root elongation under phosphate deficiency in tomato
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111229openalex-snapshot
Spatially distinct regulation of strigolactone exudation by phosphate and phytohormones in rice
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111810openalex-snapshot
Genotype-dependent phosphorus acquisition responses of two soybean genotypes under combined low phosphorus and salt stress: evidence from root traits, exudates and rhizosphere microbiome
inferred← citeshttps://doi.org/10.1016/j.plgene.2026.100589openalex-snapshot
EgPHL7, EgPHR1 and EgPHR2 bind to the P1BS and a unique motif, AGATACT for transcriptional regulation of phosphate-starvation inducible genes in oil palm
inferred← citeshttps://doi.org/10.1016/j.rhisph.2022.100549openalex-snapshot
Root traits distinguish phosphorus acquisition of two wheat cultivars growing in phosphorus-deficient acid soil
inferred← citeshttps://doi.org/10.1017/qpb.2025.1openalex-snapshot
Mobilization and recycling of intracellular phosphorus in response to availability
inferred← citeshttps://doi.org/10.1038/s41598-021-88419-wopenalex-snapshot
NH787 EMS mutant of rice variety Nagina22 exhibits higher phosphate use efficiency
inferred← citeshttps://doi.org/10.1038/s41598-023-31154-1openalex-snapshot
Comparative transcriptome analysis reveals the phosphate starvation alleviation mechanism of phosphate accumulating Pseudomonas putida in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/s41598-024-61767-zopenalex-snapshot
Comparative transcriptomic and physiological analyses unravel wheat source root adaptation to phosphorous deficiency
inferred← citeshttps://doi.org/10.1038/s41598-026-43829-6openalex-snapshot
Genome-wide identification of phosphate transporter gene family in Trichoderma harzianum and expression in response to biotic and abiotic stress
inferred← citeshttps://doi.org/10.1042/bsr20193329openalex-snapshot
The interplay of phloem-mobile signals in plant development and stress response
inferred← citeshttps://doi.org/10.1071/fp19250openalex-snapshot
Barley plants carrying the altered function Sln1d allele display modified responses to low phosphorus supply: implications for phosphorus utilisation efficiency
inferred← citeshttps://doi.org/10.1079/cabireviews202217048openalex-snapshot
Gene editing to improve drought tolerance
inferred← citeshttps://doi.org/10.1080/00103624.2026.2682382openalex-snapshot
Legacy Phosphorus in Agricultural Soils: Accessibility, Mobilization, Diagnostics, and Management Implications—a Review
inferred← citeshttps://doi.org/10.1080/01140671.2022.2127797openalex-snapshot
Effect of selenium supplementation on mycorrhizal onion ( Allium cepa L.) plants
inferred← citeshttps://doi.org/10.1093/aob/mcaf091openalex-snapshot
A novel P indicator to evaluate bread wheat ( Triticum aestivum ) genotypes to identify tolerance to phosphorus deficiency based on two distinct root phenotyping platforms
inferred← citeshttps://doi.org/10.1093/jxb/eraa482openalex-snapshot
Recent insights into the metabolic adaptations of phosphorus-deprived plants
inferred← citeshttps://doi.org/10.1093/jxb/erac177openalex-snapshot
Local and systemic responses conferring acclimation of Brassica napus roots to low phosphorus conditions
inferred← citeshttps://doi.org/10.1093/jxb/erac192openalex-snapshot
Monogalactosyl diacylglycerol synthase 3 affects phosphate utilization and acquisition in rice
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/erz028openalex-snapshot
Integration of nutrient, energy, light, and hormone signalling via TOR in plants
inferred← citeshttps://doi.org/10.1093/jxb/erz349openalex-snapshot
Phosphate acquisition efficiency in wheat is related to root:shoot ratio, strigolactone levels, and PHO2 regulation
inferred← citeshttps://doi.org/10.1093/pcp/pcaa168openalex-snapshot
The Impact of Phosphorus on Plant Immunity
inferred← citeshttps://doi.org/10.1093/pcp/pcab096openalex-snapshot
Editorial Feature: Meet the PCP Editor—Tzyy-Jen Chiou
inferred← citeshttps://doi.org/10.1093/pcp/pcad015openalex-snapshot
Autophagy-Mediated Phosphate Homeostasis in Arabidopsis Involves Modulation of Phosphate Transporters
inferred← citeshttps://doi.org/10.1093/pcp/pcaf117openalex-snapshot
Interplant signal transduction between dodder ( Cuscuta ) and their hosts
inferred← citeshttps://doi.org/10.1093/pcp/pcy151openalex-snapshot
International Symposium on Long-Distance Signaling in Plants
inferred← citeshttps://doi.org/10.1093/plcell/koad326openalex-snapshot
Milestones in understanding transport, sensing, and signaling of the plant nutrient phosphorus
inferred← citeshttps://doi.org/10.1093/plcell/koaf197openalex-snapshot
Deciphering the tomato phosphate starvation response: Functional and transcriptional roles of SlPHR3 and SlPHR4
inferred← citeshttps://doi.org/10.1093/plphys/kiae453openalex-snapshot
A lipid synthase maintains metabolic flux for jasmonate synthesis to regulate root growth and phosphate homeostasis
inferred← citeshttps://doi.org/10.1093/plphys/kiae582openalex-snapshot
Using native and synthetic genes to disrupt inositol pyrophosphates and phosphate accumulation in plants
inferred← citeshttps://doi.org/10.1093/plphys/kiag167openalex-snapshot
Don’t make me blush: msSPX4/MsPHL11-MsWRKY91 regulates anthocyanin synthesis in Malus spectabilis under low phosphorus stress
inferred← citeshttps://doi.org/10.1093/plphys/kiag549openalex-snapshot
Strigolactone effects on Sorghum bicolor ecophysiology and symbioses
inferred← citeshttps://doi.org/10.1094/mpmi-08-20-0233-ropenalex-snapshot
A Network of Phosphate Starvation and Immune-Related Signaling and Metabolic Pathways Controls the Interaction between Arabidopsis thaliana and the Beneficial Fungus Colletotrichum tofieldiae
inferred← citeshttps://doi.org/10.1101/2021.12.09.471910openalex-snapshot
NITROGEN LIMITATION ADAPTATION functions as a negative regulator of Arabidopsis immunity
inferred← citeshttps://doi.org/10.1101/2022.05.02.489396openalex-snapshot
Translational approach to increase phosphate accumulation in two plant species through perturbance of inositol pyrophosphates
inferred← citeshttps://doi.org/10.1101/2022.09.21.508943openalex-snapshot
The Phosphate Deprivation Response is Mediated by an Interaction between Brassinosteroid Signaling and Zinc in Tomato
inferred← citeshttps://doi.org/10.1101/2023.11.29.569173openalex-snapshot
Lack of Purple Acid Phosphatase SlPAP26b compromises the phosphorus starvation response in tomato independent of SlPHR1 and SlPHL1
inferred← citeshttps://doi.org/10.1104/pp.18.01469openalex-snapshot
Phosphate Starvation Alters Abiotic-Stress-Induced Cytosolic Free Calcium Increases in Roots
inferred← citeshttps://doi.org/10.1104/pp.20.01008openalex-snapshot
Spatial Profiles of Phosphate in Roots Indicate Developmental Control of Uptake, Recycling, and Sequestration
inferred← citeshttps://doi.org/10.1111/jipb.13053openalex-snapshot
Potassium and phosphorus transport and signaling in plants
inferred← citeshttps://doi.org/10.1111/jipb.13560openalex-snapshot
Non‐specific phospholipase C4 hydrolyzes phosphosphingolipids and phosphoglycerolipids and promotes rapeseed growth and yield
inferred← citeshttps://doi.org/10.1111/nph.18593openalex-snapshot
Cooperative interactions between nitrogen fixation and phosphorus nutrition in legumes
inferred← citeshttps://doi.org/10.1111/nph.19007openalex-snapshot
Phosphate deprivation‐induced changes in tomato are mediated by an interaction between brassinosteroid signaling and zinc
inferred← citeshttps://doi.org/10.1111/nph.19155openalex-snapshot
Argonaute7 ( AGO7 ) optimizes arbuscular mycorrhizal fungal associations and enhances competitive growth inNicotiana attenuata
inferred← citeshttps://doi.org/10.1111/nph.19182openalex-snapshot
Dose‐dependent long‐distance movement of microRNA399 duplex regulates phosphate homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.20266openalex-snapshot
MicroRNA399s and strigolactones mediate systemic phosphate signaling between dodder‐connected host plants and control association of host plants with rhizosphere microbes
inferred← citeshttps://doi.org/10.1111/nph.71090openalex-snapshot
The PtoTCP19 – PtoOBE2 complex orchestrates phosphate deficiency tolerance and biomass production in Populus
inferred← citeshttps://doi.org/10.1111/pce.13935openalex-snapshot
Phosphate or nitrate imbalance induces stronger molecular responses than combined nutrient deprivation in roots and leaves of chickpea plants
inferred← citeshttps://doi.org/10.1111/pce.14504openalex-snapshot
Integration of reactive oxygen species and nutrient signalling to shape root system architecture
inferred← citeshttps://doi.org/10.1111/pce.15405openalex-snapshot
PagSND1‐B1 Regulates Wood Formation by Influencing Phosphorus Absorption and Distribution in Poplar
inferred← citeshttps://doi.org/10.1111/pce.15421openalex-snapshot
The Crucial Roles of Phloem Companion Cells in Response to Phosphorus Deficiency
inferred← citeshttps://doi.org/10.1111/ppl.13539openalex-snapshot
Phosphate availability regulates flavonoid accumulation associated with photosynthetic carbon partitioning in Cyclocarya paliurus
inferred← citeshttps://doi.org/10.1111/ppl.70115openalex-snapshot
Mutation of Ugp1 Leads to Impaired Sucrose Synthesis, Retarded Growth and Altered Phosphate Accumulation
inferred← citeshttps://doi.org/10.1111/tpj.14607openalex-snapshot
PEATmoss (Physcomitrella Expression Atlas Tool): a unified gene expression atlas for the model plant Physcomitrella patens
inferred← citeshttps://doi.org/10.1111/tpj.14998openalex-snapshot
Two ADP‐glucose pyrophosphorylase subunits, OsAGPL1 and OsAGPS1, modulate phosphorus homeostasis in rice
inferred← citeshttps://doi.org/10.1111/tpj.15011openalex-snapshot
Cytokinin biosynthesis and transport for systemic nitrogen signaling
inferred← citeshttps://doi.org/10.1111/tpj.15630openalex-snapshot
A systems‐biology approach identifies co‐expression modules in response to low phosphate supply in maize lines of different breeding history
inferred← citeshttps://doi.org/10.1111/tpj.16140openalex-snapshot
Transcriptome analysis of the phosphate starvation response sheds light on strigolactone biosynthesis in rice
inferred← citeshttps://doi.org/10.1111/tpj.16511openalex-snapshot
Recent advances in unraveling the mystery of combined nutrient stress in plants
inferred← citeshttps://doi.org/10.1111/tpj.16598openalex-snapshot
OsbZIP1 regulates phosphorus uptake and nitrogen utilization, contributing to improved yield
inferred← citeshttps://doi.org/10.1111/tpj.17134openalex-snapshot
Defense‐related callose synthase PMR4 promotes root hair callose deposition and adaptation to phosphate deficiency in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/tpj.70070openalex-snapshot
MdPHR2 and MdARF6‐4 synergistically regulate arbuscular mycorrhizal symbiosis and the transcription of MdPHT1;13 , enhancing phosphorus uptake in apple rootstocks
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/10.1126/sciadv.adw7727openalex-snapshot
Limited phosphate resources are efficiently allocated to each organ by the PHR1-EIN3/EIL1 module to coordinate their establishment
inferred← citeshttps://doi.org/10.1126/science.aba0196openalex-snapshot
A plant’s diet, surviving in a variable nutrient environment
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-010521-015047openalex-snapshot
Dynamic Nutrient Signaling Networks in Plants
inferred← citeshttps://doi.org/10.1186/s12863-021-00962-7openalex-snapshot
Comparative transcriptome analysis reveals novel insights into transcriptional responses to phosphorus starvation in oil palm (Elaeis guineensis) root
inferred← citeshttps://doi.org/10.1186/s12870-020-02578-yopenalex-snapshot
Scion genotypes exert long distance control over rootstock transcriptome responses to low phosphate in grafted grapevine
inferred← citeshttps://doi.org/10.1186/s40659-026-00683-0openalex-snapshot
Phosphorus and cold stress: physiological and biochemical assessment in two grape (Vitis vinifera L.) cultivars
inferred← citeshttps://doi.org/10.1270/jsbbs.20102openalex-snapshot
Modulation of plant root traits by nitrogen and phosphate: transporters, long-distance signaling proteins and peptides, and potential artificial traps
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/10.18174/550352openalex-snapshot
Nieuwe balansen in Het Nieuwe Telen: hormonen en ecologie
inferred← citeshttps://doi.org/10.20944/preprints202306.0686.v1openalex-snapshot
Molecular Regulation for Maintenance of Plant Phosphate Homeostasis in Crop Plants as Basis for Precision Genome Engineering
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1905790/v1openalex-snapshot
Selection of reference genes for qPCR analysis and variations in the expression of Phosphate (Pi) responsive genes in Brassica rapa
inferred← citeshttps://doi.org/10.21273/jashs05433-24openalex-snapshot
Differential Expression of Phosphate Starvation-responsive Genes among Sweetpotato Cultivars during Establishment and Onset of Storage Root Formation
inferred← citeshttps://doi.org/10.21608/ejoh.2019.16154.1113openalex-snapshot
Can Hydroxyapatite and Boron Oxide Nano-fertilizers Substitute Calcium Superphosphate and Boric Acid for Broccoli (Brassica oleracea var. italica) Grown on A Heavy Clay Soil?
inferred← citeshttps://doi.org/10.31274/td-20240329-64openalex-snapshot
Analysis of the effect of autophagy on lipid content and the impact of vps45-3 point mutation on plant growth in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.32604/phyton.2022.017633openalex-snapshot
EoPHR2, a Phosphate Starvation Response Transcription Factor, is Involved in Improving Low-Phosphorus Stress Resistance in Eremochloa ophiuroides
inferred← citeshttps://doi.org/10.3389/fpls.2020.565339openalex-snapshot
Root Adaptation via Common Genetic Factors Conditioning Tolerance to Multiple Stresses for Crops Cultivated on Acidic Tropical Soils
inferred← citeshttps://doi.org/10.3389/fpls.2023.1094157openalex-snapshot
Improving phosphorus acquisition efficiency through modification of root growth responses to phosphate starvation in legumes
inferred← citeshttps://doi.org/10.3389/fsufs.2024.1432599openalex-snapshot
Phytase-producing rhizobacteria enhance barley growth and phosphate nutrition
inferred← citeshttps://doi.org/10.3390/agriculture11080747openalex-snapshot
Crosstalk between Nutrient Signalling Pathways and Immune Responses in Rice
inferred← citeshttps://doi.org/10.3390/agronomy13071665openalex-snapshot
Transcriptome Analysis of Vicia villosa in Response to Low Phosphorus Stress at Seedling Stage
inferred← citeshttps://doi.org/10.3390/agronomy16030388openalex-snapshot
Enhancing Cereal Crop Tolerance to Low-Phosphorus Conditions Through Fertilisation Strategies: The Role of Silicon in Mitigating Phosphate Deficiency
inferred← citeshttps://doi.org/10.3390/cells12030441openalex-snapshot
Deciphering Interactions between Phosphorus Status and Toxic Metal Exposure in Plants and Rhizospheres to Improve Crops Reared on Acid Soil
inferred← citeshttps://doi.org/10.3390/crops4030029openalex-snapshot
Phosphate Turnover in Various Parts of Nodulated Soybean (Glycine max (L.) Merr.) Plants and the Relation to the Xylem Transport
inferred← citeshttps://doi.org/10.3390/genes11030241openalex-snapshot
Transcriptomic Analysis Reveals the Molecular Adaptation of Three Major Secondary Metabolic Pathways to Multiple Macronutrient Starvation in Tea (Camellia sinensis)
inferred← citeshttps://doi.org/10.3390/ijms21218259openalex-snapshot
Target of Rapamycin in Control of Autophagy: Puppet Master and Signal Integrator
inferred← citeshttps://doi.org/10.3390/ijms24032437openalex-snapshot
Mutation of OsLPR3 Enhances Tolerance to Phosphate Starvation in Rice
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/ijms25147692openalex-snapshot
Transcriptomics Provide Insights into Early Responses to Sucrose Signaling in Lupinus albus, a Model Plant for Adaptations to Phosphorus and Iron Deficiency
inferred← citeshttps://doi.org/10.3390/ijms27177963openalex-snapshot
Darkness Attenuates the Early Transcriptional Response to Phosphate Deficiency in Soybean Roots
inferred← citeshttps://doi.org/10.3390/metabo11090601openalex-snapshot
A Role for Inositol Pyrophosphates in the Metabolic Adaptations to Low Phosphate in Arabidopsis
inferred← citeshttps://doi.org/10.3390/plants12102062openalex-snapshot
Molecular Responses of Red Ripe Tomato Fruit to Copper Deficiency Stress
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/plants13223144openalex-snapshot
Plants Under Stress: Exploring Physiological and Molecular Responses to Nitrogen and Phosphorus Deficiency
inferred← citeshttps://doi.org/10.3390/plants14243869openalex-snapshot
Glucose-6-Phosphate 1-Epimerase Responds to Phosphate Starvation by Regulating Carbohydrate Homeostasis in Rice and Arabidopsis
inferred← citeshttps://doi.org/10.3390/plants15020253openalex-snapshot
Effects of Exogenous Phosphorus and Hydrogen Peroxide on Wheat Root Architecture
inferred← citeshttps://doi.org/10.3390/plants9010115openalex-snapshot
Can Inositol Pyrophosphates Inform Strategies for Developing Low Phytate Crops?
inferred← citeshttps://doi.org/10.3410/f.738775517.793583087openalex-snapshot
Faculty Opinions recommendation of Spatial profiles of phosphate in roots indicate developmental control of uptake, recycling, and sequestration.
inferred← citeshttps://doi.org/10.6084/m9.figshare.13725230openalex-snapshot
Additional file 1 of Comparative transcriptome analysis reveals novel insights into transcriptional responses to phosphorus starvation in oil palm (Elaeis guineensis) root
inferred← citeshttps://doi.org/10.6084/m9.figshare.13725233openalex-snapshot
Additional file 2 of Comparative transcriptome analysis reveals novel insights into transcriptional responses to phosphorus starvation in oil palm (Elaeis guineensis) root
inferred← citeshttps://doi.org/10.70675/736b1d6fz82d8z405bzb340zbcaa21303873openalex-snapshot
Physiological and molecular characterization of the mitigation of nitrogen deficiency stress by the arbuscular mycorrhizal fungus Rhizophagus irregularis associated with Maize (Zea mays L.)
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