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Tackling Plant Phosphate Starvation by the Roots
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-3-319-55729-8openalex-snapshot
Legume Nitrogen Fixation in Soils with Low Phosphorus Availability
inferredcites →https://doi.org/10.1007/978-3-319-55729-8_13openalex-snapshot
White Lupin: A Model System for Understanding Plant Adaptation to Low Phosphorus Availability
inferredcites →https://doi.org/10.1007/s00299-012-1381-2openalex-snapshot
Arabidopsis Brassinosteroid-overproducing gulliver3-D/dwarf4-D mutants exhibit altered responses to Jasmonic acid and pathogen
inferredcites →https://doi.org/10.1007/s00374-016-1112-xopenalex-snapshot
Microbial immobilisation of phosphorus in soils exposed to drying-rewetting and freeze-thawing cycles
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/s004250000271openalex-snapshot
Conditional identification of phosphate-starvation-response mutants in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s11103-009-9589-4openalex-snapshot
Involvement of auxin signaling mediated by IAA14 and ARF7/19 in membrane lipid remodeling during phosphate starvation
inferredcites →https://doi.org/10.1007/s11103-012-9917-yopenalex-snapshot
A gain-of-function mutation in IAA16 confers reduced responses to auxin and abscisic acid and impedes plant growth and fertility
inferredcites →https://doi.org/10.1007/s11104-011-0907-7openalex-snapshot
The chemical nature of P accumulation in agricultural soils—implications for fertiliser management and design: an Australian perspective
inferredcites →https://doi.org/10.1007/s11104-012-1540-9openalex-snapshot
PP2A mediates lateral root development under NaCl-induced osmotic stress throughout auxin redistribution in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.cell.2016.02.028openalex-snapshot
Root Endophyte Colletotrichum tofieldiae Confers Plant Fitness Benefits that Are Phosphate Status Dependent
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.cropro.2011.08.025openalex-snapshot
Phosphite applications induce molecular modifications in potato tuber periderm and cortex that enhance resistance to pathogens
inferredcites →https://doi.org/10.1016/j.cub.2007.02.047openalex-snapshot
Cytokinins Determine Arabidopsis Root-Meristem Size by Controlling Cell Differentiation
inferredcites →https://doi.org/10.1016/j.cub.2009.06.023openalex-snapshot
Gibberellin Signaling in the Endodermis Controls Arabidopsis Root Meristem Size
inferredcites →https://doi.org/10.1016/j.cub.2010.05.035openalex-snapshot
The Rate of Cell Differentiation Controls the Arabidopsis Root Meristem Growth Phase
inferredcites →https://doi.org/10.1016/j.cub.2010.09.007openalex-snapshot
A Novel Aux/IAA28 Signaling Cascade Activates GATA23-Dependent Specification of Lateral Root Founder Cell Identity
inferredcites →https://doi.org/10.1016/j.cub.2013.08.008openalex-snapshot
Cytokinin Induces Cell Division in the Quiescent Center of the Arabidopsis Root Apical Meristem
inferredcites →https://doi.org/10.1016/j.cub.2014.04.002openalex-snapshot
Cytokinin Controls Polarity of PIN1-Dependent Auxin Transport during Lateral Root Organogenesis
inferredcites →https://doi.org/10.1016/j.cub.2015.03.046openalex-snapshot
Root Cap-Derived Auxin Pre-patterns the Longitudinal Axis of the Arabidopsis Root
inferredcites →https://doi.org/10.1016/j.devcel.2008.05.008openalex-snapshot
Key Divisions in the Early Arabidopsis Embryo Require POL and PLL1 Phosphatases to Establish the Root Stem Cell Organizer and Vascular Axis
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.2011.10.006openalex-snapshot
Callose Biosynthesis Regulates Symplastic Trafficking during Root Development
inferredcites →https://doi.org/10.1016/j.devcel.2013.06.025openalex-snapshot
Spatial Coordination between Stem Cell Activity and Cell Differentiation in the Root Meristem
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.2016.09.031openalex-snapshot
Establishment of Expression in the SHORTROOT-SCARECROW Transcriptional Cascade through Opposing Activities of Both Activators and Repressors
inferredcites →https://doi.org/10.1016/j.devcel.2017.03.019openalex-snapshot
PHR1 Balances between Nutrition and Immunity in Plants
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.devcel.2018.06.002openalex-snapshot
Interdependent Nutrient Availability and Steroid Hormone Signals Facilitate Root Growth Plasticity
inferredcites →https://doi.org/10.1016/j.gloenvcha.2008.10.009openalex-snapshot
The story of phosphorus: Global food security and food for thought
inferredcites →https://doi.org/10.1016/j.jplph.2012.05.002openalex-snapshot
The jasmonate receptor COI1 plays a role in jasmonate-induced lateral root formation and lateral root positioning in Arabidopsis thaliana
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.pbi.2017.04.016openalex-snapshot
Phosphate scouting by root tips
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.tibs.2016.10.008openalex-snapshot
Eukaryotic Phosphate Homeostasis: The Inositol Pyrophosphate Perspective
inferredcites →https://doi.org/10.1016/j.ydbio.2003.12.037openalex-snapshot
The ENHANCER OF TRY AND CPC1 gene acts redundantly with TRIPTYCHON and CAPRICE in trichome and root hair cell patterning in Arabidopsis
inferredcites →https://doi.org/10.1016/s0092-8674(00)80300-1openalex-snapshot
Activation of the Ethylene Gas Response Pathway in Arabidopsis by the Nuclear Protein ETHYLENE-INSENSITIVE3 and Related Proteins
inferredcites →https://doi.org/10.1016/s0092-8674(00)80865-xopenalex-snapshot
The SHORT-ROOT Gene Controls Radial Patterning of the Arabidopsis Root through Radial Signaling
inferredcites →https://doi.org/10.1016/s0092-8674(00)81858-9openalex-snapshot
The Arabidopsis NPR1 Gene That Controls Systemic Acquired Resistance Encodes a Novel Protein Containing Ankyrin Repeats
inferredcites →https://doi.org/10.1016/s0092-8674(03)00924-3openalex-snapshot
Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
inferredcites →https://doi.org/10.1016/s0092-8674(03)00968-1openalex-snapshot
EIN3-Dependent Regulation of Plant Ethylene Hormone Signaling by Two Arabidopsis F Box Proteins
inferredcites →https://doi.org/10.1016/s0092-8674(03)00969-3openalex-snapshot
Plant Responses to Ethylene Gas Are Mediated by SCFEBF1/EBF2-Dependent Proteolysis of EIN3 Transcription Factor
inferredcites →https://doi.org/10.1023/a:1004380832118openalex-snapshot
Root excretion of carboxylic acids and protons in phosphorus-deficient plants
inferredcites →https://doi.org/10.1038/embor.2009.103openalex-snapshot
Expression of the Arabidopsis jasmonate signalling repressor JAZ1/TIFY10A is stimulated by auxin
inferredcites →https://doi.org/10.1038/nature01387openalex-snapshot
Auxin promotes Arabidopsis root growth by modulating gibberellin response
inferredcites →https://doi.org/10.1038/nature01485openalex-snapshot
Reactive oxygen species produced by NADPH oxidase regulate plant cell growth
inferredcites →https://doi.org/10.1038/nature03184openalex-snapshot
The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots
inferredcites →https://doi.org/10.1038/nature03608openalex-snapshot
Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1038/nature05703openalex-snapshot
Conserved factors regulate signalling in Arabidopsis thaliana shoot and root stem cell organizers
inferredcites →https://doi.org/10.1038/nature05731openalex-snapshot
Mechanism of auxin perception by the TIR1 ubiquitin ligase
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/nature06943openalex-snapshot
Cytokinin and auxin interaction in root stem-cell specification during early embryogenesis
inferredcites →https://doi.org/10.1038/nature08843openalex-snapshot
Control of Arabidopsis apical–basal embryo polarity by antagonistic transcription factors
inferredcites →https://doi.org/10.1038/nature10873openalex-snapshot
A petunia ABC protein controls strigolactone-dependent symbiotic signalling and branching
inferredcites →https://doi.org/10.1038/nature21417openalex-snapshot
Root microbiota drive direct integration of phosphate stress and immunity
inferredcites →https://doi.org/10.1038/ncb2893openalex-snapshot
A secreted peptide acts on BIN2-mediated phosphorylation of ARFs to potentiate auxin response during lateral root development
inferredcites →https://doi.org/10.1038/nchembio.1044openalex-snapshot
A role for the root cap in root branching revealed by the non-auxin probe naxillin
inferredcites →https://doi.org/10.1038/ncomms15300openalex-snapshot
Low phosphate activates STOP1-ALMT1 to rapidly inhibit root cell elongation
inferredcites →https://doi.org/10.1038/ncomms6833openalex-snapshot
Arabidopsis ERF109 mediates cross-talk between jasmonic acid and auxin biosynthesis during lateral root formation
inferredcites →https://doi.org/10.1038/ncomms9717openalex-snapshot
Cytokinin response factors regulate PIN-FORMED auxin transporters
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/nplants.2015.138openalex-snapshot
Intensity of a pulse of RSL4 transcription factor synthesis determines Arabidopsis root hair cell size
inferredcites →https://doi.org/10.1038/s41467-018-03850-4openalex-snapshot
Rice auxin influx carrier OsAUX1 facilitates root hair elongation in response to low external phosphate
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/10.1038/srep24778openalex-snapshot
AtOPR3 specifically inhibits primary root growth in Arabidopsis under phosphate deficiency
inferredcites →https://doi.org/10.1038/srep26820openalex-snapshot
Discriminative gene co-expression network analysis uncovers novel modules involved in the formation of phosphate deficiency-induced root hairs in Arabidopsis
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.1365-313x.1996.10030403.xopenalex-snapshot
Mutations in the AXR3 gene of Arabidopsis result in altered auxin response including ectopic expression from the SAUR‐AC1 promoter
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01191.xopenalex-snapshot
Constitutive expression of ETHYLENE‐RESPONSE‐FACTOR1 in Arabidopsis confers resistance to several necrotrophic fungi
inferredcites →https://doi.org/10.1046/j.1469-8137.2000.00776.xopenalex-snapshot
Extraradical hyphae of the mycorrhizal fungus Glomus intraradices can hydrolyse organic phosphate
inferredcites →https://doi.org/10.1073/pnas.0401698101openalex-snapshot
Arabidopsis EIN3-binding F-box 1 and 2 form ubiquitin-protein ligases that repress ethylene action and promote growth by directing EIN3 degradation
inferredcites →https://doi.org/10.1073/pnas.0438070100openalex-snapshot
Five components of the ethylene-response pathway identified in a screen for weak ethylene-insensitive mutants in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0600863103openalex-snapshot
Phospholipase DZ2 plays an important role in extraplastidic galactolipid biosynthesis and phosphate recycling in Arabidopsis roots
inferredcites →https://doi.org/10.1073/pnas.0608136104openalex-snapshot
A Medicago truncatula phosphate transporter indispensable for the arbuscular mycorrhizal symbiosis
inferredcites →https://doi.org/10.1073/pnas.0712307105openalex-snapshot
Auxin acts as a local morphogenetic trigger to specify lateral root founder cells
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.1002828107openalex-snapshot
Arabidopsis resistance protein SNC1 activates immune responses through association with a transcriptional corepressor
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.1201616109openalex-snapshot
Plant hormone jasmonate prioritizes defense over growth by interfering with gibberellin signaling cascade
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.1407371111openalex-snapshot
A plausible mechanism, based upon SHORT-ROOT movement, for regulating the number of cortex cell layers in roots
inferredcites →https://doi.org/10.1073/pnas.1522301112openalex-snapshot
Methylome analysis reveals an important role for epigenetic changes in the regulation of the Arabidopsis response to phosphate starvation
inferredcites →https://doi.org/10.1073/pnas.1701536114openalex-snapshot
Molecular link between auxin and ROS-mediated polar growth
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/10.1073/pnas.1710455114openalex-snapshot
Root-associated fungal microbiota of nonmycorrhizal Arabis alpina and its contribution to plant phosphorus nutrition
inferredcites →https://doi.org/10.1073/pnas.202474599openalex-snapshot
Rice phosphate transporters include an evolutionarily divergent gene specifically activated in arbuscular mycorrhizal symbiosis
inferredcites →https://doi.org/10.1073/pnas.89.15.6837openalex-snapshot
Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana mutant.
inferredcites →https://doi.org/10.1074/jbc.m113.482281openalex-snapshot
Arabidopsis Ferritin 1 (AtFer1) Gene Regulation by the Phosphate Starvation Response 1 (AtPHR1) Transcription Factor Reveals a Direct Molecular Link between Iron and Phosphate Homeostasis
inferredcites →https://doi.org/10.1093/jexbot/50.333.487openalex-snapshot
Maize root system growth and development as influenced by phosphorus deficiency
inferredcites →https://doi.org/10.1093/jxb/err143openalex-snapshot
Loss of ACS7 confers abiotic stress tolerance by modulating ABA sensitivity and accumulation in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/eru029openalex-snapshot
Strigolactones are involved in phosphate- and nitrate-deficiency-induced root development and auxin transport in rice
inferredcites →https://doi.org/10.1093/jxb/eru529openalex-snapshot
Underground tuning: quantitative regulation of root growth
inferredcites →https://doi.org/10.1093/jxb/erv252openalex-snapshot
Cytokinin as a positional cue regulating lateral root spacing inArabidopsis
inferredcites →https://doi.org/10.1093/jxb/erv515openalex-snapshot
OsWRKY74, a WRKY transcription factor, modulates tolerance to phosphate starvation in rice
inferredcites →https://doi.org/10.1093/jxb/erw400openalex-snapshot
Multiple phytohormones promote root hair elongation by regulating a similar set of genes in the root epidermis in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erx223openalex-snapshot
Lateral root formation and the multiple roles of auxin
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/jxb/erx454openalex-snapshot
Buffered delivery of phosphate to Arabidopsis alters responses to low phosphate
inferredcites →https://doi.org/10.1093/molbev/msw263openalex-snapshot
Two-Step Functional Innovation of the Stem-Cell Factors WUS/WOX5 during Plant Evolution
inferredcites →https://doi.org/10.1093/mp/ssp023openalex-snapshot
Expression of PIN Genes in Rice ( Oryza sativa L.): Tissue Specificity and Regulation by Hormones
inferredcites →https://doi.org/10.1093/mp/ssp086openalex-snapshot
Ubiquitin-Specific Protease 14 (UBP14) Is Involved in Root Responses to Phosphate Deficiency in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pci095openalex-snapshot
The Arabidopsis Gene CAD1 Controls Programmed Cell Death in the Plant Immune System and Encodes a Protein Containing a MACPF Domain
inferredcites →https://doi.org/10.1093/pcp/pci183openalex-snapshot
A PIN1 Family Gene, OsPIN1, involved in Auxin-dependent Adventitious Root Emergence and Tillering in Rice
inferredcites →https://doi.org/10.1093/pcp/pcq004openalex-snapshot
The Function of LPR1 is Controlled by an Element in the Promoter and is Independent of SUMO E3 Ligase SIZ1 in Response to Low Pi Stress in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcs072openalex-snapshot
The Arabidopsis gene HYPERSENSITIVE TO PHOSPHATE STARVATION 3 encodes ETHYLENE OVERPRODUCTION 1
inferredcites →https://doi.org/10.1093/pcp/pcu048openalex-snapshot
Syntaxin of Plant Proteins SYP123 and SYP132 Mediate Root Hair Tip Growth in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcv016openalex-snapshot
Mathematical Modeling and Experimental Validation of the Spatial Distribution of Boron in the Root of Arabidopsis thaliana Identify High Boron Accumulation in the Tip and Predict a Distinct Root Tip Uptake Function
inferredcites →https://doi.org/10.1094/mpmi-06-11-0165openalex-snapshot
Ethylene-Responsive Element-Binding Factor 5, ERF5, Is Involved in Chitin-Induced Innate Immunity Response
inferredcites →https://doi.org/10.1101/gad.11.23.3194openalex-snapshot
The Arabidopsis GAI gene defines a signaling pathway that negatively regulates gibberellin responses
inferredcites →https://doi.org/10.1101/gad.12.2.198openalex-snapshot
The TIR1 protein of Arabidopsis functions in auxin response and is related to human SKP2 and yeast Grr1p
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/10.1101/gad.314096.118openalex-snapshot
Root stem cell niche organizer specification by molecular convergence of PLETHORA and SCARECROW transcription factor modules
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.102.017814openalex-snapshot
A Role for the GCC-Box in Jasmonate-Mediated Activation of the PDF1.2 Gene of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.036897openalex-snapshot
Brassinosteroids Interact with Auxin to Promote Lateral Root Development in Arabidopsis
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.105.068544openalex-snapshot
Repressor- and Activator-Type Ethylene Response Factors Functioning in Jasmonate Signaling and Disease Resistance Identified via a Genome-Wide Screen of Arabidopsis Transcription Factor Gene Expression
inferredcites →https://doi.org/10.1104/pp.105.070995openalex-snapshot
Double Knockouts of Phospholipases Dζ1 and Dζ2 in Arabidopsis Affect Root Elongation during Phosphate-Limited Growth But Do Not Affect Root Hair Patterning
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.106.080119openalex-snapshot
ZmPIN1aandZmPIN1bEncode Two Novel Putative Candidates for Polar Auxin Transport and Plant Architecture Determination of Maize
inferredcites →https://doi.org/10.1104/pp.106.093971openalex-snapshot
WRKY75 Transcription Factor Is a Modulator of Phosphate Acquisition and Root Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.101691openalex-snapshot
Phosphate Homeostasis and Root Development in Arabidopsis Are Synchronized by the Zinc Finger Transcription Factor ZAT6
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.107.106302openalex-snapshot
Ethylene Is One of the Key Elements for Cell Death and Defense Response Control in the Arabidopsis Lesion Mimic Mutant vad1
inferredcites →https://doi.org/10.1104/pp.107.113829openalex-snapshot
MYB72 Is Required in Early Signaling Steps of Rhizobacteria-Induced Systemic Resistance in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.124529openalex-snapshot
BAH1/NLA, a RING-Type Ubiquitin E3 Ligase, Regulates the Accumulation of Salicylic Acid and Immune Responses toPseudomonas syringaeDC3000
inferredcites →https://doi.org/10.1104/pp.109.140202openalex-snapshot
A Leaky Mutation in DWARF4 Reveals an Antagonistic Role of Brassinosteroid in the Inhibition of Root Growth by Jasmonate in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.140905openalex-snapshot
cis-Element- and Transcriptome-Based Screening of Root Hair-Specific Genes and Their Functional Characterization in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.145532openalex-snapshot
Histone H2A.Z Regulates the Expression of Several Classes of Phosphate Starvation Response Genes But Not as a Transcriptional Activator
inferredcites →https://doi.org/10.1104/pp.109.151803openalex-snapshot
Identification of MicroRNAs Involved in Pathogen-Associated Molecular Pattern-Triggered Plant Innate Immunity
inferredcites →https://doi.org/10.1104/pp.110.156505openalex-snapshot
Differential Auxin-Transporting Activities of PIN-FORMED Proteins in Arabidopsis Root Hair Cells
inferredcites →https://doi.org/10.1104/pp.110.163717openalex-snapshot
Functional Interconnection of MYC2 and SPA1 in the Photomorphogenic Seedling Development of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.165191openalex-snapshot
SIZ1 Regulation of Phosphate Starvation-Induced Root Architecture Remodeling Involves the Control of Auxin Accumulation
inferredcites →https://doi.org/10.1104/pp.111.175414openalex-snapshot
Root Phenes for Enhanced Soil Exploration and Phosphorus Acquisition: Tools for Future Crops
inferredcites →https://doi.org/10.1104/pp.112.194217openalex-snapshot
OsMYB2P-1 , an R2R3 MYB Transcription Factor, Is Involved in the Regulation of Phosphate-Starvation Responses and Root Architecture in Rice
inferredcites →https://doi.org/10.1104/pp.127.4.1773openalex-snapshot
Role of Root Hairs and Lateral Roots in Silicon Uptake by Rice
inferredcites →https://doi.org/10.1104/pp.17.01188openalex-snapshot
Deubiquitinating Enzyme OTU5 Contributes to DNA Methylation Patterns and Is Critical for Phosphate Nutrition Signals
inferredcites →https://doi.org/10.1104/pp.17.01525openalex-snapshot
The Deubiquitinase OTU5 Regulates Root Responses to Phosphate Starvation
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/10.1105/tpc.004861openalex-snapshot
A Phosphate Transporter from Medicago truncatula Involved in the Acquisition of Phosphate Released by Arbuscular Mycorrhizal Fungi
inferredcites →https://doi.org/10.1105/tpc.006437openalex-snapshot
Regulation of Root Hair Initiation and Expansin Gene Expression in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.007468openalex-snapshot
ETHYLENE RESPONSE FACTOR1 Integrates Signals from Ethylene and Jasmonate Pathways in Plant Defense[W]
inferredcites →https://doi.org/10.1105/tpc.012211openalex-snapshot
Salicylic Acid and NPR1 Induce the Recruitment of trans- Activating TGA Factors to a Defense Gene Promoter in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.014928openalex-snapshot
Cytokinin-Deficient Transgenic Arabidopsis Plants Show Multiple Developmental Alterations Indicating Opposite Functions of Cytokinins in the Regulation of Shoot and Root Meristem Activity
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.10.9.1571openalex-snapshot
A Novel Signaling Pathway Controlling Induced Systemic Resistance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.104.028316openalex-snapshot
Functional Genomic Analysis of the AUXIN RESPONSE FACTOR Gene Family Members in Arabidopsis thaliana : Unique and Overlapping Functions of ARF7 and ARF19
inferredcites →https://doi.org/10.1105/tpc.105.031716openalex-snapshot
MicroRNA-Directed Regulation of Arabidopsis AUXIN RESPONSE FACTOR17 Is Essential for Proper Development and Modulates Expression of Early Auxin Response Genes
inferredcites →https://doi.org/10.1105/tpc.105.035972openalex-snapshot
PINOID Positively Regulates Auxin Efflux inArabidopsisRoot Hair Cells and Tobacco Cells
inferredcites →https://doi.org/10.1105/tpc.106.041426openalex-snapshot
Arabidopsis PLD ζ 2 Regulates Vesicle Trafficking and Is Required for Auxin Response
inferredcites →https://doi.org/10.1105/tpc.106.047415openalex-snapshot
Genetic Characterization and Functional Analysis of the GID1 Gibberellin Receptors in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.052100openalex-snapshot
Ethylene Upregulates Auxin Biosynthesis in Arabidopsis Seedlings to Enhance Inhibition of Root Cell Elongation
inferredcites →https://doi.org/10.1105/tpc.107.052126openalex-snapshot
Ethylene Regulates Root Growth through Effects on Auxin Biosynthesis and Transport-Dependent Auxin Distribution
inferredcites →https://doi.org/10.1105/tpc.107.053009openalex-snapshot
Auxin Synthesized by the YUCCA Flavin Monooxygenases Is Essential for Embryogenesis and Leaf Formation 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.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.108.064980openalex-snapshot
The WRKY6 Transcription Factor Modulates PHOSPHATE1 Expression in Response to Low Pi Stress in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.068676openalex-snapshot
Functional Analyses of LONELY GUY Cytokinin-Activating Enzymes Reveal the Importance of the Direct Activation Pathway in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.072553openalex-snapshot
miR390, Arabidopsis TAS3 tasiRNAs, and Their AUXIN RESPONSE FACTOR Targets Define an Autoregulatory Network Quantitatively Regulating Lateral Root Growth
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.112.097881openalex-snapshot
Arabidopsis Annexin1 Mediates the Radical-Activated Plasma Membrane Ca 2+ - and K + -Permeable Conductance in Root Cells
inferredcites →https://doi.org/10.1105/tpc.112.100222openalex-snapshot
Failure of the Tomato Trans-Acting Short Interfering RNA Program to Regulate AUXIN RESPONSE FACTOR3 and ARF4 Underlies the Wiry Leaf Syndrome
inferredcites →https://doi.org/10.1105/tpc.112.101428openalex-snapshot
The Arabidopsis DELLA RGA - LIKE3 Is a Direct Target of MYC2 and Modulates Jasmonate Signaling Responses
inferredcites →https://doi.org/10.1105/tpc.113.114868openalex-snapshot
A Kinetic Analysis of the Auxin Transcriptome Reveals Cell Wall Remodeling Proteins That Modulate Lateral Root Development in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.116582openalex-snapshot
Phosphatidylinositol 4,5-Bisphosphate Influences PIN Polarization by Controlling Clathrin-Mediated Membrane Trafficking inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.120311openalex-snapshot
NITROGEN LIMITATION ADAPTATION Recruits PHOSPHATE2 to Target the Phosphate Transporter PT2 for Degradation during the Regulation of Arabidopsis Phosphate Homeostasis
inferredcites →https://doi.org/10.1105/tpc.114.132993openalex-snapshot
Inference of the Arabidopsis Lateral Root Gene Regulatory Network Suggests a Bifurcation Mechanism That Defines Primordia Flanking and Central Zones
inferredcites →https://doi.org/10.1105/tpc.16.00656openalex-snapshot
The PLETHORA Gene Regulatory Network Guides Growth and Cell Differentiation in Arabidopsis Roots
inferredcites →https://doi.org/10.1105/tpc.6.11.1583openalex-snapshot
Characterization of an Arabidopsis Mutant That Is Nonresponsive to Inducers of Systemic Acquired Resistance.
inferredcites →https://doi.org/10.1105/tpc.6.5.751openalex-snapshot
Arabidopsis Mutants Selected for Resistance to the Phytotoxin Coronatine Are Male Sterile, Insensitive to Methyl Jasmonate, and Resistant to a Bacterial Pathogen.
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01405.xopenalex-snapshot
Identification of QTL controlling root growth response to phosphate starvation in Arabidopsis thaliana
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.1365-313x.2004.02005.xopenalex-snapshot
Arabidopsis pdr2 reveals a phosphate‐sensitive checkpoint in root development
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.2008.03629.xopenalex-snapshot
A role for inositol hexakisphosphate in the maintenance of basal resistance to plant pathogens
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04591.xopenalex-snapshot
The microRNA miR393 re‐directs secondary metabolite biosynthesis away from camalexin and towards glucosinolates
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04668.xopenalex-snapshot
Type‐A response regulators are required for proper root apical meristem function through post‐transcriptional regulation of PIN auxin efflux carriers
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.04965.xopenalex-snapshot
The Arabidopsis RING‐type E3 ligase XBAT32 mediates the proteasomal degradation of the ethylene biosynthetic enzyme, 1‐aminocyclopropane‐1‐carboxylate synthase 7
inferredcites →https://doi.org/10.1111/j.1469-8137.1992.tb00096.xopenalex-snapshot
Biosynthesis and root exudation of citric and malic acids in phosphate‐starved rape plants
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02406.xopenalex-snapshot
Tomato strigolactones are derived from carotenoids and their biosynthesis is promoted by phosphate starvation
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.03067.xopenalex-snapshot
Distinct relationships between GLABRA2 and single‐repeat R3 MYB transcription factors in the regulation of trichome and root hair patterning 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/j.1744-7909.2012.01124.xopenalex-snapshot
Somatic Embryogenesis Receptor Kinases Control Root Development Mainly via Brassinosteroid‐Independent Actions in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/nph.12092openalex-snapshot
Root gravitropism and root hair development constitute coupled developmental responses regulated by auxin homeostasis in the Arabidopsis root apex
inferredcites →https://doi.org/10.1111/nph.12194openalex-snapshot
ALFIN ‐ LIKE 6 is involved in root hair elongation during phosphate deficiency in Arabidopsis
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.13838openalex-snapshot
Carbon and phosphorus exchange may enable cooperation between an arbuscular mycorrhizal fungus and a phosphate‐solubilizing bacterium
inferredcites →https://doi.org/10.1111/nph.14095openalex-snapshot
ROOT HAIR DEFECTIVE SIX ‐ LIKE 4 ( RSL 4) promotes root hair elongation by transcriptionally regulating the expression of genes required for cell growth
inferredcites →https://doi.org/10.1111/nph.14403openalex-snapshot
Phosphorus acquisition efficiency in arbuscular mycorrhizal maize is correlated with the abundance of root‐external hyphae and the accumulation of transcripts encoding PHT1 phosphate transporters
inferredcites →https://doi.org/10.1111/nph.14847openalex-snapshot
Changes in the allocation of endogenous strigolactone improve plant biomass production on phosphate‐poor soils
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/pce.12378openalex-snapshot
Identification of primary and secondary metabolites with phosphorus status‐dependent abundance in A rabidopsis, and of the transcription factor PHR 1 as a major regulator of metabolic changes during phosphorus limitation
inferredcites →https://doi.org/10.1111/tpj.12741openalex-snapshot
Phosphatidylinositol phosphate 5‐kinase genes respond to phosphate deficiency for root hair elongation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.13097openalex-snapshot
The cytokinin response factors modulate root and shoot growth and promote leaf senescence in Arabidopsis
inferredcites →https://doi.org/10.1126/science.1083695openalex-snapshot
Modulation of Phospholipid Signaling by GLABRA2 in Root-Hair Pattern Formation
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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RootHairML: A Simple Machine-Learning Tool for Quantifying Root Hairs
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Root Architectural Plasticity in Changing Nutrient Availability
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Arabidopsis PDE1 confers phosphate-deficiency tolerance in primary root growth
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A transcriptomic perspective of P trade in mycorrhizal grapevine
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Modulation of plant immunity and biotic interactions under phosphate deficiency
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Changes in root architecture and endogenous hormone levels in alfalfa under phosphorus stress
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Ectomycorrhizal fungi and hyphosphere bacteria form a relay team to unlock chelated organic phosphorus for Pinus massoniana
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Pup1 QTL-Mediated Tissue-Specific Differential Expression of Transcription Factors Help Mitigate Deleterious Effects of Phosphorus-Starvation in Rice (Oryza sativa L.)
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Root system responses to phosphate nutrition involve plasma membrane H+-ATPases in Arabidopsis thaliana
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Functional characterization and comparative analysis of AtMYB42 and AtMYB85 promoters to gain insights into transcriptional regulation during development and hormonal induction
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Genome-wide identification, phylogeny, and differential expression of wheat phosphate transporters under drought and salinity stress conditions
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Novel insights into phosphate starvation response in plants from mycorrhiza perspective
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Molecular genetics of arbuscular mycorrhizal symbiosis
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Regulation of plants nutrient deficiency responses by phytohormones
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Mineral nutrients and root architecture
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Digitalized pencil trace modified electrodes for real time evaluation of salicylic acid in detached Arabidopsis thaliana leaves during regeneration
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Rhizosphere effect and water constraint jointly determined the roles of microorganism in soil phosphorus cycling in arid desert regions
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Heterogeneous catalytic system enhances water purification and phosphorus recovery potential in constructed wetlands
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Symbiotic regulation: How plants seek salvation in starvation
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Bacterial-type ferroxidase tunes iron-dependent phosphate sensing during Arabidopsis root development
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A spatially concerted epidermal auxin signaling framework steers the root hair foraging response under low nitrogen
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.113685openalex-snapshot
Distribution of phenanthrene in the ospho2 reveals the involvement of phosphate on phenanthrene translocation and accumulation in rice
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Regulation of soil microorganisms and phosphorus cycling genes on soil phosphorus availability in desert steppe under warming and phosphorus input
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Phosphate starvation responses in crop roots: from well-known players to novel candidates
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Characterization of COMT1-mediated low phosphorus resistance mechanism by metabolomics in tomato plants
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Genome-wide expression analysis reveals contrasting regulation of phosphate starvation response (PSR) in root and shoot of Arabidopsis and its association with biotic stress
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
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Optimized fertilizer recommendation method for nitrate residue control in a wheat–maize double cropping system in dryland farming
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The plant microbiota: From theoretical advances to applications
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Optimizing plant phosphate uptake: Advances in the core regulatory mechanisms of phosphate starvation response proteins and their macromolecular partners: A review
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The molecular mechanism of plasma membrane H+-ATPases in plant responses to abiotic stress
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Knockdown of OsSAE1a affects the growth and development and phosphate homeostasis in rice
inferred← citeshttps://doi.org/10.1016/j.molp.2021.06.002openalex-snapshot
Long-distance blue light signalling regulates phosphate deficiency-induced primary root growth inhibition
inferred← citeshttps://doi.org/10.1016/j.molp.2021.12.004openalex-snapshot
Nutrient–hormone relations: Driving root plasticity in plants
inferred← citeshttps://doi.org/10.1016/j.molp.2021.12.005openalex-snapshot
Plant adaptation to low phosphorus availability: Core signaling, crosstalks, and applied implications
inferred← citeshttps://doi.org/10.1016/j.pbi.2021.102117openalex-snapshot
Integration of nutrient and water availabilities via auxin into the root developmental program
inferred← citeshttps://doi.org/10.1016/j.pbi.2023.102386openalex-snapshot
Understanding signaling pathways governing the polar development of root hairs in low-temperature, nutrient-deficient environments
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.111060openalex-snapshot
PERK13 modulates phosphate deficiency-induced root hair elongation in Arabidopsis
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Karrikin increases tomato cold tolerance via strigolactone and the abscisic acid signaling network
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112779openalex-snapshot
Understanding the mechanistic insight and relevance of root hair-driven rhizobia for developing climate-smart crops
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Molecular basis of plasma membrane H+-ATPase function and potential application in the agricultural production
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.12.001openalex-snapshot
Differential efficacy of water lily cultivars in phytoremediation of eutrophic water contaminated with phosphorus and nitrogen
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.2022.08.017openalex-snapshot
Genome-wide identification of apple PPI genes and a functional analysis of the response of MxPPI1 to Fe deficiency stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111185openalex-snapshot
SgPAP10b-mediated phospholipid degradation under acidic soil conditions: a mechanism for high phosphorus utilization efficiency in the green manure crop Stylosanthes guianensis
inferred← citeshttps://doi.org/10.1016/j.saa.2026.128292openalex-snapshot
Quantitative analysis of nitrogen and phosphorus in dairy cow slurry based on near-infrared spectroscopy combined with deep learning and characteristic selection algorithm
inferred← citeshttps://doi.org/10.1016/j.sciaf.2022.e01320openalex-snapshot
Comparative effects of nitrogen, phosphorus and potassium on Radopholus similis infection in East African highland banana plants as influenced by rhizosphere biota
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101308openalex-snapshot
Parental dominance of the cleopatra mandarin parent in the citrandarin allotetraploid hybrid shapes root-mediated salt tolerance
inferred← citeshttps://doi.org/10.1016/j.tim.2021.08.002openalex-snapshot
The phosphate language of fungi
inferred← citeshttps://doi.org/10.1016/j.tplants.2020.03.002openalex-snapshot
Root-Apex Proton Fluxes at the Centre of Soil-Stress Acclimation
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101695openalex-snapshot
The Medicago SPX1/3-PHR2 network relays phosphate signaling to orchestrate root nodulation-dependent nitrogen acquisition by controlling flavonoid biosynthesis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.4c00687openalex-snapshot
Synthetic Biology of Plants and Microbes for Agriculture, Environment, and Future Applications
inferred← citeshttps://doi.org/10.1038/s41467-023-43911-xopenalex-snapshot
A CYBDOM protein impacts iron homeostasis and primary root growth under phosphate deficiency in Arabidopsis
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/s43247-026-03472-5openalex-snapshot
Phosphorus cycling dynamics in stratified low-phosphorus lakes
inferred← citeshttps://doi.org/10.1042/bcj20180615openalex-snapshot
Interactions between plants and soil shaping the root microbiome under abiotic stress
inferred← citeshttps://doi.org/10.1079/9781836990598.0014openalex-snapshot
Reprogramming of Salt Stress under the Influence of Strigolactones
inferred← citeshttps://doi.org/10.1080/01904167.2024.2377815openalex-snapshot
Nutrient transporters as plant strategy to adapt to nutrient fluctuations in the soil
inferred← citeshttps://doi.org/10.1080/01904167.2026.2714211openalex-snapshot
Delayed P application enhances root development and growth of tomato in a soil with low P content
inferred← citeshttps://doi.org/10.1093/jxb/erac023openalex-snapshot
Jasmonic acid is involved in root cell wall phosphorus remobilization through the nitric oxide dependent pathway in rice
inferred← citeshttps://doi.org/10.1093/jxb/erac346openalex-snapshot
Non-volatile signals and redox mechanisms are required for the responses of Arabidopsis roots toPseudomonas oryzihabitans
inferred← citeshttps://doi.org/10.1093/jxb/erad419openalex-snapshot
New molecular components that regulate the transcriptional hub in root hairs: coupling environmental signals with endogenous hormones to coordinate growth
inferred← citeshttps://doi.org/10.1093/jxb/erad504openalex-snapshot
A cucumber protein, Phloem Phosphate Stress-Repressed 1, rapidly degrades in response to a phosphate stress condition
inferred← citeshttps://doi.org/10.1093/jxb/erae041openalex-snapshot
The centrality of redox regulation and sensing of reactive oxygen species in abiotic and biotic stress acclimatization
inferred← citeshttps://doi.org/10.1093/jxb/erae483openalex-snapshot
Ethylene modulates wheat response to phosphate deficiency
inferred← citeshttps://doi.org/10.1093/jxb/eraf204openalex-snapshot
Phosphorus deficiency and root growth: the role of TOR signaling in adaptive responses
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/pcp/pcad015openalex-snapshot
Autophagy-Mediated Phosphate Homeostasis in Arabidopsis Involves Modulation of Phosphate Transporters
inferred← citeshttps://doi.org/10.1093/pcp/pcad052openalex-snapshot
OsIPK2, a Rice Inositol Polyphosphate Kinase Gene, Is Involved in Phosphate Homeostasis and Root Development
inferred← citeshttps://doi.org/10.1093/plcell/koad057openalex-snapshot
PHOSPHATE STARVATION RESPONSE1 (PHR1) interacts with JASMONATE ZIM-DOMAIN (JAZ) and MYC2 to modulate phosphate deficiency-induced jasmonate signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plcell/koad268openalex-snapshot
The transcription factor MYB110 regulates plant height, lodging resistance, and grain yield in rice
inferred← citeshttps://doi.org/10.1093/plphys/kiab145openalex-snapshot
Lateral root formation and nutrients: nitrogen in the spotlight
inferred← citeshttps://doi.org/10.1093/plphys/kiac595openalex-snapshot
Endoplasmic reticulum calnexins participate in the primary root growth response to phosphate deficiency
inferred← citeshttps://doi.org/10.1093/plphys/kiad607openalex-snapshot
Chloroplast phosphate transporter CrPHT4-7 regulates phosphate homeostasis and photosynthesis in Chlamydomonas
inferred← citeshttps://doi.org/10.1093/plphys/kiae346openalex-snapshot
Filling the gaps on root hair development under salt stress and phosphate starvation using current evidence coupled with a meta-analysis approach
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/treephys/tpaf118openalex-snapshot
The transcription factor GRF1 enhances tolerance to Pi starvation through improving root development in poplar
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/10.1098/rstb.2023.0355openalex-snapshot
Evolution of phosphate scouting in the terrestrial biosphere
inferred← citeshttps://doi.org/10.1101/2021.03.19.436157openalex-snapshot
Bacterial-type plant ferroxidases tune local phosphate sensing in root development
inferred← citeshttps://doi.org/10.1101/2023.09.08.556869openalex-snapshot
The chloroplastic phosphate transporter CrPHT4-7 supports phosphate homeostasis and photosynthesis in Chlamydomonas
inferred← citeshttps://doi.org/10.1101/2024.05.22.595400openalex-snapshot
Nitrogen starvation response in hornworts and liverworts provides little evidence for complex priming to the cyanobiont
inferred← citeshttps://doi.org/10.1101/cshperspect.a039941openalex-snapshot
Auxin-Regulated Lateral Root Organogenesis
inferred← citeshttps://doi.org/10.1101/cshperspect.a040030openalex-snapshot
Auxin–Environment Integration in Growth Responses to Forage for Resources
inferred← citeshttps://doi.org/10.1111/jipb.13090openalex-snapshot
Root developmental responses to phosphorus nutrition
inferred← citeshttps://doi.org/10.1111/jipb.13345openalex-snapshot
The chromatin remodeler BRAHMA recruits HISTONE DEACETYLASE6 to regulate root growth inhibition in response to phosphate starvation in Arabidopsis
inferred← citeshttps://doi.org/10.1111/jipb.70090openalex-snapshot
Collapsed auxin transport by iron inhibits primary root growth under low phosphate stress
inferred← citeshttps://doi.org/10.1111/nph.20152openalex-snapshot
Phosphate promotes Arabidopsis root skewing and circumnutation through reorganisation of the microtubule cytoskeleton
inferred← citeshttps://doi.org/10.1111/nph.20174openalex-snapshot
Crystal structure and function of a phosphate starvation responsive protein phosphatase, GmHAD1 ‐2 regulating soybean root development and flavonoid metabolism
inferred← citeshttps://doi.org/10.1111/pbi.13833openalex-snapshot
Two high hierarchical regulators, PuMYB40 and PuWRKY75, control the low phosphorus driven adventitious root formation in Populus ussuriensis
inferred← citeshttps://doi.org/10.1111/pbi.14565openalex-snapshot
Ethylene increases the NaHCO3 stress tolerance of grapevines partially via the VvERF1B ‐ VvMYC2 ‐ VvPMA10 pathway
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/pce.14078openalex-snapshot
OsPHR2 modulates phosphate starvation‐induced OsMYC2 signalling and resistance to Xanthomonas oryzae pv. oryzae
inferred← citeshttps://doi.org/10.1111/pce.14316openalex-snapshot
A novel calmodulin‐interacting Domain of Unknown Function 506 protein represses root hair elongation in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.14451openalex-snapshot
Impacts of iron on phosphate starvation‐induced root hair growth in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.14504openalex-snapshot
Integration of reactive oxygen species and nutrient signalling to shape root system architecture
inferred← citeshttps://doi.org/10.1111/pce.14553openalex-snapshot
Compartmentalisation: A strategy for optimising symbiosis and tradeoff management
inferred← citeshttps://doi.org/10.1111/ppl.14396openalex-snapshot
Natural variation in root traits identifies significant SNPs and candidate genes for phosphate deficiency tolerance in Zea mays L.
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.70315openalex-snapshot
Enhancing inositol pyrophosphate accumulation in plants alters growth, phosphate homeostasis, and insect herbivory
inferred← citeshttps://doi.org/10.1126/sciadv.adz6873openalex-snapshot
Hooked hairs: A cellular key adaptation aiding seedling survival in nutrient-limited and drought conditions
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-arplant-050718-100423openalex-snapshot
Molecular and Environmental Regulation of Root Development
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/s12870-023-04039-8openalex-snapshot
The auxin signaling pathway contributes to phosphorus-mediated zinc homeostasis in maize
inferred← citeshttps://doi.org/10.1186/s12870-025-07677-2openalex-snapshot
The role of sucrose in phosphate starvation response: transcriptomic and physiological insights in Arabidopsis Thaliana
inferred← citeshttps://doi.org/10.1186/s12870-026-09379-9openalex-snapshot
Co-expression analysis identifies organ-specific gene regulatory networks responsive to phosphate limitation in hemp (Cannabis sativa L.)
inferred← citeshttps://doi.org/10.1242/dev.181446openalex-snapshot
The dynamic nature and regulation of the root clock
inferred← citeshttps://doi.org/10.1371/journal.pone.0223217openalex-snapshot
Analysis of gene co-expression networks of phosphate starvation and aluminium toxicity responses in Populus spp.
inferred← citeshttps://doi.org/10.1590/1519-6984.261797openalex-snapshot
Expression analysis of phosphate induced genes in contrasting maize genotypes for phosphorus use efficiency
inferred← citeshttps://doi.org/10.21273/hortsci15358-20openalex-snapshot
Variation in Phosphorus Availability, Root Architecture Attributes, and Onset of Storage Root Formation among Sweetpotato Cultivars
inferred← citeshttps://doi.org/10.22541/au.161711007.76017850/v1openalex-snapshot
OsPHR2 modulates phosphate starvation-induced jasmonic acid response and resistance to Xanthomonas oryzae pv. oryzae
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1083270openalex-snapshot
Plant-growth promotion by proteobacterial strains depends on the availability of phosphorus and iron in Arabidopsis thaliana plants
inferred← citeshttps://doi.org/10.3389/fpls.2021.643585openalex-snapshot
Influence of Ethylene Signaling in the Crosstalk Between Fe, S, and P Deficiency Responses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2021.719436openalex-snapshot
Responses of Root Endophytes to Phosphorus Availability in Peach Rootstocks With Contrasting Phosphorus-Use Efficiencies
inferred← citeshttps://doi.org/10.3389/fpls.2022.914648openalex-snapshot
Involvement of PtPHR1 in phosphates starvation-induced alkaloid biosynthesis in Pinellia ternata (Thunb.) Breit
inferred← citeshttps://doi.org/10.3389/fpls.2022.932926openalex-snapshot
Integration of small RNA, degradome, and transcriptome sequencing data illustrates the mechanism of low phosphorus adaptation in Camellia oleifera
inferred← citeshttps://doi.org/10.3389/fpls.2022.947558openalex-snapshot
Non-target molecular network and putative genes of flavonoid biosynthesis in Erythrina velutina Willd., a Brazilian semiarid native woody plant
inferred← citeshttps://doi.org/10.3389/fpls.2023.1018984openalex-snapshot
Role of autophagy-related proteins ATG8f and ATG8h in the maintenance of autophagic activity in Arabidopsis roots under phosphate starvation
inferred← citeshttps://doi.org/10.3389/fpls.2023.1122285openalex-snapshot
Distinct metabolite classes in root exudates are indicative for field- or hydroponically-grown cover crops
inferred← citeshttps://doi.org/10.3389/fpls.2024.1274610openalex-snapshot
SUMOylation of OsPSTOL1 is essential for regulating phosphate starvation responses in rice and Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2024.1343073openalex-snapshot
Nitrate and ammonium, the yin and yang of nitrogen uptake: a time-course transcriptomic study in rice
inferred← citeshttps://doi.org/10.3389/fpls.2024.1542150openalex-snapshot
Editorial: Advanced approaches identifying novel nutrient-use-enhancing biostimulants
inferred← citeshttps://doi.org/10.3389/fsufs.2022.706072openalex-snapshot
Soil Microbes Determine Outcomes of Pathogenic Interactions Between Radopholus similis and Fusarium oxysporum V5w2 in Tissue Culture Banana Rhizospheres Starved of Nitrogen, Phosphorus, and Potassium
inferred← citeshttps://doi.org/10.3390/agriculture16181966openalex-snapshot
Polyaspartic Acid-Urea Enriches Nitrate in Topsoil and Optimizes Root Architecture to Improve Nitrogen Use Efficiency in Rice
inferred← citeshttps://doi.org/10.3390/f16081265openalex-snapshot
Effects of Different Phosphorus Addition Levels on Physiological and Growth Traits of Pinus massoniana (Masson Pine) Seedlings
inferred← citeshttps://doi.org/10.3390/genes10121018openalex-snapshot
Plant PHR Transcription Factors: Put on A Map
inferred← citeshttps://doi.org/10.3390/genes16040438openalex-snapshot
Overexpression of FLZ12 Suppresses Root Hair Development and Enhances Iron-Deficiency Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms22094904openalex-snapshot
Ethylene and Nitric Oxide Involvement in the Regulation of Fe and P Deficiency Responses in Dicotyledonous Plants
inferred← citeshttps://doi.org/10.3390/ijms23041933openalex-snapshot
Auxin/Cytokinin Antagonistic Control of the Shoot/Root Growth Ratio and Its Relevance for Adaptation to Drought and Nutrient Deficiency Stresses
inferred← citeshttps://doi.org/10.3390/ijms23042273openalex-snapshot
The Ubiquitin E3 Ligase PRU2 Modulates Phosphate Uptake in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms23095241openalex-snapshot
One AP2/ERF Transcription Factor Positively Regulates Pi Uptake and Drought Tolerance in Poplar
inferred← citeshttps://doi.org/10.3390/ijms241512431openalex-snapshot
Multi-Omics Analysis Reveals Mechanisms of Strong Phosphorus Adaptation in Tea Plant Roots
inferred← citeshttps://doi.org/10.3390/ijms25179491openalex-snapshot
Phosphatases: Decoding the Role of Mycorrhizal Fungi in Plant Disease Resistance
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/metabo11090601openalex-snapshot
A Role for Inositol Pyrophosphates in the Metabolic Adaptations to Low Phosphate in Arabidopsis
inferred← citeshttps://doi.org/10.3390/plants11060752openalex-snapshot
Metabolite Profiles Provide Insights into Underlying Mechanism in Bupleurum (Apiaceae) in Response to Three Levels of Phosphorus Fertilization
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/plants12213760openalex-snapshot
Isolation and Characterization of Erianthus arundinaceus Phosphate Transporter 1 (PHT1) Gene Promoter and 5′ Deletion Analysis of Transcriptional Regulation Regions under Phosphate Stress in Transgenic Tobacco
inferred← citeshttps://doi.org/10.3724/sp.j.1249.2023.04415openalex-snapshot
Function of miR399a in tomato in responding to phosphorus starvation
inferred← citeshttps://doi.org/10.4081/ija.2023.2181openalex-snapshot
Systemic adaptation of rice plants under low phosphate conditions and interaction with endophytic bacteria
inferred← citeshttps://doi.org/10.6084/m9.figshare.22600901openalex-snapshot
Additional file 1 of The auxin signaling pathway contributes to phosphorus-mediated zinc homeostasis in maize
inferred← citeshttps://doi.org/10.64898/2026.02.12.705259openalex-snapshot
CANE1-mediated autophagosome size regulation fine-tunes phosphate starvation tolerance in Arabidopsis thaliana
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