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Root tip contact with low-phosphate media reprograms plant root architecture
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-94-010-0566-1_6openalex-snapshot
The nutritional control of root development
inferredcites →https://doi.org/10.1007/s00018-004-5076-xopenalex-snapshot
Function and molecular evolution of multicopper blue proteins
inferredcites →https://doi.org/10.1007/s00122-001-0825-9openalex-snapshot
Bay-0 × Shahdara recombinant inbred line population: a powerful tool for the genetic dissection of complex traits in Arabidopsis
inferredcites →https://doi.org/10.1007/s11103-004-0501-yopenalex-snapshot
Rapid one-step protein purification from plant material using the eight-amino acid StrepII epitope
inferredcites →https://doi.org/10.1007/s11103-004-1965-5openalex-snapshot
Transcriptional regulation and functional properties of Arabidopsis Pht1;4, a high affinity transporter contributing greatly to phosphate uptake in phosphate deprived plants
inferredcites →https://doi.org/10.1007/s11103-004-3380-3openalex-snapshot
Root cap specific expression of an endo-?-1,4--glucanase (cellulase): a new marker to study root development in Arabidopsis
inferredcites →https://doi.org/10.1016/0162-0134(84)85008-4openalex-snapshot
Inhibition of ceruloplasmin and other copper oxidases by thiomolybdate
inferredcites →https://doi.org/10.1016/j.biochi.2006.04.018openalex-snapshot
Genome-wide transcriptome profiling of the early cadmium response of Arabidopsis roots and shoots
inferredcites →https://doi.org/10.1016/j.tplants.2004.09.003openalex-snapshot
Short on phosphate: plant surveillance and countermeasures
inferredcites →https://doi.org/10.1016/j.tplants.2006.06.002openalex-snapshot
Auxin transport: a field in flux
inferredcites →https://doi.org/10.1016/s1369-5266(03)00035-9openalex-snapshot
The role of nutrient availability in regulating root architecture
inferredcites →https://doi.org/10.1021/cr950046oopenalex-snapshot
Multicopper Oxidases and Oxygenases
inferredcites →https://doi.org/10.1023/a:1010329902165openalex-snapshot
The nutritional control of root development
inferredcites →https://doi.org/10.1023/a:1013324727040openalex-snapshot
Topsoil foraging – an architectural adaptation of plants to low phosphorus availability
inferredcites →https://doi.org/10.1023/a:1013351617532openalex-snapshot
Bioavailability of soil inorganic P in the rhizosphere as affected by root-induced chemical changes: a review
inferredcites →https://doi.org/10.1042/bj0770066openalex-snapshot
The effects of some ions and chelating agents on the oxidase activity of caeruloplasmin
inferredcites →https://doi.org/10.1046/j.1365-3040.2003.01100.xopenalex-snapshot
Effects of phosphate availability on the root system architecture: large‐scale analysis of the natural variation between Arabidopsis accessions
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.96.22.12941openalex-snapshot
Genetic ablation of root cap cells in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m200827200openalex-snapshot
Molecular and Biochemical Characterization of a Highly Stable Bacterial Laccase That Occurs as a Structural Component of the Bacillus subtilis Endospore Coat
inferredcites →https://doi.org/10.1074/jbc.m301251200openalex-snapshot
Crystal Structure of a Bacterial Endospore Coat Component
inferredcites →https://doi.org/10.1093/pcp/pci011openalex-snapshot
Phosphate Starvation Induces a Determinate Developmental Program in the Roots of Arabidopsis thaliana
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.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.126.2.875openalex-snapshot
Phosphate Availability Regulates Root System Architecture in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01306.xopenalex-snapshot
Intrinsic and environmental response pathways that regulate root system architecture
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/10.1126/science.1086391openalex-snapshot
Genome-Wide Insertional Mutagenesis of Arabidopsis thaliana
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.665openalex-snapshot
PHOSPHATE ACQUISITION
inferredcites →https://doi.org/10.1534/genetics.104.033654openalex-snapshot
Transmissible and Nontransmissible Mutations Induced by Irradiating Arabidopsis thaliana Pollen With γ-Rays and Carbon IonsThis article is dedicated to Toshiya Takano, who passed away in December 2003.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The Growth and Physiological Response of Gleditsia Sinensis Lam. Seedlings with Different Phosphorus Efficiencies to Low Phosphorus Stress
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Plant Behavioural Ecology
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Plant Responses to Phosphorus Availability
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Sensing, signaLling, and CONTROL of phosphate starvation in plants: molecular players and applications
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Sensing, Signalling, and Control of Phosphate Starvation in Plants: Molecular Players and Applications
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Interplay Between Root Structure and Function in Enhancing Efficiency of Nitrogen and Phosphorus Acquisition
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The Brachypodium distachyon Root System: A Tractable Model to Investigate Grass Roots
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Natural Variation in Arabidopsis thaliana
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Automated High-Throughput Root Phenotyping of Arabidopsis thaliana Under Nutrient Deficiency Conditions
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Identification of Chemical Inducers of the Phosphate-Starvation Signaling Pathway in A. thaliana Using Chemical Genetics
inferred← citeshttps://doi.org/10.1007/978-3-030-01743-9_9openalex-snapshot
Phosphate Homeostasis: Links with Seed Quality and Stress Tolerance in Chickpea
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Plant Nutritional Deficiency and Its Impact on Crop Production
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Root Apex Cognition: From Neuronal Molecules to Root-Fungal Networks
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Integrative Approach of the Root Architecture by Interaction Between Auxin and Nutrients
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Efficient Mineral Nutrition: Genetic Improvement of Phosphate Uptake and Use Efficiency in Crops
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Phosphate Signaling in Plants: Biochemical and Molecular Approach
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The Influence of Phosphate Deficiency on Legume Symbiotic N2 Fixation
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Plant Cognition and Behavior: From Environmental Awareness to Synaptic Circuits Navigating Root Apices
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Arbuscular Mycorrhizal Fungi and Their Responses to Nutrient Enrichment
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Plants and Animals: Convergent Evolution in Action?
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Roots: The Acquisition of Water and Nutrients from the Heterogeneous Soil Environment
inferred← citeshttps://doi.org/10.1007/978-3-642-10613-2_8openalex-snapshot
Phosphorus: Plant Strategies to Cope with its Scarcity
inferred← citeshttps://doi.org/10.1007/978-3-642-13431-9_10openalex-snapshot
Plant Plasma Membrane and Phosphate Deprivation
inferred← citeshttps://doi.org/10.1007/978-3-642-14369-4_7openalex-snapshot
Sensing and Signaling of PO 4 3−
inferred← citeshttps://doi.org/10.1007/978-3-642-15271-9_10openalex-snapshot
Phosphorus Nutrition: Rhizosphere Processes, Plant Response and Adaptations
inferred← citeshttps://doi.org/10.1007/978-3-642-23524-5_6openalex-snapshot
Multitude of Long-Distance Signal Molecules Acting Via Phloem
inferred← citeshttps://doi.org/10.1007/978-3-642-42011-5_9openalex-snapshot
Phospholipases in Plant Response to Nitrogen and Phosphorus Availability
inferred← citeshttps://doi.org/10.1007/978-81-322-1542-4_16openalex-snapshot
Salicylic Acid Signaling
inferred← citeshttps://doi.org/10.1007/978-981-10-4115-0_5openalex-snapshot
Arbuscular Mycorrhizal Fungi and Adaption of P Stress in Plants
inferred← citeshttps://doi.org/10.1007/978-981-13-8922-1_3openalex-snapshot
Nutrient Perception and Signaling in Plants
inferred← citeshttps://doi.org/10.1007/978-981-16-1350-0_26openalex-snapshot
Biomolecular Painstaking Utilization and Assimilation of Phosphorus Under Indigent Stage in Agricultural Crops
inferred← citeshttps://doi.org/10.1007/s00018-012-1090-6openalex-snapshot
Transcriptional regulation of phosphate acquisition by higher plants
inferred← citeshttps://doi.org/10.1007/s00018-012-1094-2openalex-snapshot
SUMO, a heavyweight player in plant abiotic stress responses
inferred← citeshttps://doi.org/10.1007/s00122-008-0838-8openalex-snapshot
Genetic analysis of root elongation induced by phosphorus deficiency in rice (Oryza sativa L.): fine QTL mapping and multivariate analysis of related traits
inferred← citeshttps://doi.org/10.1007/s00122-010-1301-1openalex-snapshot
Quantitative trait loci for root morphology in response to low phosphorus stress in Brassica napus
inferred← citeshttps://doi.org/10.1007/s00122-010-1456-9openalex-snapshot
Yield quantitative trait loci from wild tomato are predominately expressed by the shoot
inferred← citeshttps://doi.org/10.1007/s00122-020-03719-5openalex-snapshot
Multiple origins of Indian dwarf wheat by mutations targeting the TREE domain of a GSK3-like kinase for drought tolerance, phosphate uptake, and grain quality
inferred← citeshttps://doi.org/10.1007/s00122-022-04095-yopenalex-snapshot
Prospects of genetics and breeding for low-phosphate tolerance: an integrated approach from soil to cell
inferred← citeshttps://doi.org/10.1007/s00122-022-04173-1openalex-snapshot
An allelic variant in the ACS7 gene promotes primary root growth in watermelon
inferred← citeshttps://doi.org/10.1007/s00299-017-2127-yopenalex-snapshot
Quantitative trait loci from identification to exploitation for crop improvement
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Expression dynamics indicate the role of Jasmonic acid biosynthesis pathway in regulating macronutrient (N, P and K+) deficiency tolerance in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s00299-023-03120-8openalex-snapshot
Arabidopsis PDE1 confers phosphate-deficiency tolerance in primary root growth
inferred← citeshttps://doi.org/10.1007/s00425-007-0677-xopenalex-snapshot
Expression analyses of three members of the AtPHO1 family reveal differential interactions between signaling pathways involved in phosphate deficiency and the responses to auxin, cytokinin, and abscisic acid
inferred← citeshttps://doi.org/10.1007/s00425-008-0754-9openalex-snapshot
PRD, an Arabidopsis AINTEGUMENTA-like gene, is involved in root architectural changes in response to phosphate starvation
inferred← citeshttps://doi.org/10.1007/s00425-019-03212-4openalex-snapshot
Mitogen-activated protein kinase 6 integrates phosphate and iron responses for indeterminate root growth in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00425-019-03317-wopenalex-snapshot
Heterologous expression of an acid phosphatase gene and phosphate limitation leads to substantial production of chicoric acid in Echinacea purpurea transgenic hairy roots
inferred← citeshttps://doi.org/10.1007/s00425-022-03922-2openalex-snapshot
A tale of two players: the role of phosphate in iron and zinc homeostatic interactions
inferred← citeshttps://doi.org/10.1007/s00425-023-04307-9openalex-snapshot
Phosphorus absorption kinetics and exudation strategies of roots developed by three lupin species to tackle P deficiency
inferred← citeshttps://doi.org/10.1007/s00425-024-04596-8openalex-snapshot
An intron-split microRNA mediates cleavage of the mRNA encoded by low phosphate root in Solanaceae
inferred← citeshttps://doi.org/10.1007/s00425-026-05034-7openalex-snapshot
Transcription factors in phosphorus utilization: enhancing crop productivity and stress resilience
inferred← citeshttps://doi.org/10.1007/s00709-015-0845-yopenalex-snapshot
NPKS uptake, sensing, and signaling and miRNAs in plant nutrient stress
inferred← citeshttps://doi.org/10.1007/s00709-021-01700-7openalex-snapshot
Impact of phosphorous-deficit conditions on morpho-physiological traits and phosphorous metabolism in chickpea genotypes
inferred← citeshttps://doi.org/10.1007/s10265-024-01545-0openalex-snapshot
Recent advances in research on phosphate starvation signaling in plants
inferred← citeshttps://doi.org/10.1007/s10534-021-00299-9openalex-snapshot
Changes induced by lead in root system architecture of Arabidopsis seedlings are mediated by PDR2-LPR1/2 phosphate dependent way
inferred← citeshttps://doi.org/10.1007/s10535-013-0327-zopenalex-snapshot
The involvement of auxin in root architecture plasticity in Arabidopsis induced by heterogeneous phosphorus availability
inferred← citeshttps://doi.org/10.1007/s10535-017-0713-zopenalex-snapshot
Response of Arabidopsis thaliana root growth to phosphorus and its relation to media chemical composition
inferred← citeshttps://doi.org/10.1007/s10681-019-2512-4openalex-snapshot
Identification of QTLs for relative root traits associated with phosphorus efficiency in two culture systems in Brassica napus
inferred← citeshttps://doi.org/10.1007/s10725-024-01201-6openalex-snapshot
Phosphate and zinc interaction in soil and plants: a reciprocal cross-talk
inferred← citeshttps://doi.org/10.1007/s11032-019-1059-3openalex-snapshot
Molecular control and genetic improvement of phosphorus use efficiency in rice
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/s11103-008-9380-yopenalex-snapshot
Plant hormones and nutrient signaling
inferred← citeshttps://doi.org/10.1007/s11103-010-9639-yopenalex-snapshot
The two Arabidopsis RPS6 genes, encoding for cytoplasmic ribosomal proteins S6, are functionally equivalent
inferred← citeshttps://doi.org/10.1007/s11103-014-0249-yopenalex-snapshot
A Brassica napus PHT1 phosphate transporter, BnPht1;4, promotes phosphate uptake and affects roots architecture of transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11103-014-0254-1openalex-snapshot
OsCYCP1;1, a PHO80 homologous protein, negatively regulates phosphate starvation signaling in the roots of rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s11103-021-01224-xopenalex-snapshot
Early sensing of phosphate deprivation triggers the formation of extra root cap cell layers via SOMBRERO through a process antagonized by auxin signaling
inferred← citeshttps://doi.org/10.1007/s11104-009-9929-9openalex-snapshot
Plant root growth, architecture and function
inferred← citeshttps://doi.org/10.1007/s11104-010-0516-xopenalex-snapshot
Detection of QTL for phosphorus efficiency at vegetative stage in Brassica napus
inferred← citeshttps://doi.org/10.1007/s11104-011-1026-1openalex-snapshot
Rare earth elements lanthanum and gadolinium induce phosphate-deficiency responses in Arabidopsis thaliana seedlings
inferred← citeshttps://doi.org/10.1007/s11104-013-1645-9openalex-snapshot
Nitrogen acquisition by roots: physiological and developmental mechanisms ensuring plant adaptation to a fluctuating resource
inferred← citeshttps://doi.org/10.1007/s11104-013-1722-0openalex-snapshot
Aluminum induces low phosphate adaptive responses and modulates primary and lateral root growth by differentially affecting auxin signaling in Arabidopsis seedlings
inferred← citeshttps://doi.org/10.1007/s11104-015-2598-yopenalex-snapshot
Root morphology and cluster root formation by seabuckthorn (Hippophaë rhamnoides L.) in response to nitrogen, phosphorus and iron deficiency
inferred← citeshttps://doi.org/10.1007/s11104-015-2775-zopenalex-snapshot
Development of root system architecture of Arabidopsis thaliana in response to colonization by Martelella endophytica YC6887 depends on auxin signaling
inferred← citeshttps://doi.org/10.1007/s11104-023-06266-2openalex-snapshot
Role of soil abiotic processes on phosphorus availability and plant responses with a focus on strigolactones in tomato plants
inferred← citeshttps://doi.org/10.1007/s11104-024-07178-5openalex-snapshot
Root architectural plasticity optimizes nutrient acquisition in switchgrass under variable phosphorus forms
inferred← citeshttps://doi.org/10.1007/s11105-021-01323-5openalex-snapshot
Genetic Control of the Root System Traits in Oilseed Rape Under Contrasting Phosphate Supply Conditions by Genome-wide Association Study
inferred← citeshttps://doi.org/10.1007/s11105-024-01512-yopenalex-snapshot
Pup1 QTL-Mediated Tissue-Specific Differential Expression of Transcription Factors Help Mitigate Deleterious Effects of Phosphorus-Starvation in Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s11738-011-0776-yopenalex-snapshot
Acid phosphatases and growth of barley (Hordeum vulgare L.) cultivars under diverse phosphorus nutrition
inferred← citeshttps://doi.org/10.1007/s11738-011-0918-2openalex-snapshot
Differential responses of oat cultivars to phosphate deprivation: plant growth and acid phosphatase activities
inferred← citeshttps://doi.org/10.1007/s11816-021-00737-7openalex-snapshot
Regulation of OsLPR1 gene on the formation of rice root iron plaque under low phosphorus
inferred← citeshttps://doi.org/10.1007/s12010-021-03662-1openalex-snapshot
Morphological, Biochemical, and Proteomic Studies Revealed Impact of Fe and P Crosstalk on Root Development in Phaseolus vulgaris L
inferred← citeshttps://doi.org/10.1007/s12033-016-9919-0openalex-snapshot
Emerging Trends in Epigenetic Regulation of Nutrient Deficiency Response in Plants
inferred← citeshttps://doi.org/10.1007/s12038-018-9843-5openalex-snapshot
AtMBD4: A methylated DNA binding protein negatively regulates a subset of phosphate starvation genes
inferred← citeshttps://doi.org/10.1007/s12229-025-09320-zopenalex-snapshot
Plant Tropism: Cue Detection and Control Over Growth Direction – The Many Ways for Plants to Explore and Exploit the Environment
inferred← citeshttps://doi.org/10.1007/s12298-020-00800-7openalex-snapshot
Mapping QTLs for 15 morpho-metric traits in Arabidopsis thaliana using Col-0 × Don-0 population
inferred← citeshttps://doi.org/10.1007/s12374-026-09526-7openalex-snapshot
An Auxin Signaling Repressor IAA12 Enhances Phosphate Deficiency-Induced Inhibition of Primary Root Growth Through Blue Light Signaling in Arabidopsis
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/s40502-018-0415-3openalex-snapshot
Efficient root systems for enhancing tolerance of crops to water and phosphorus limitation
inferred← citeshttps://doi.org/10.1007/s40626-024-00311-wopenalex-snapshot
Eucalypt seedlings lack a clear phosphate starvation response under low phosphorus availability
inferred← citeshttps://doi.org/10.1007/s42729-022-00970-1openalex-snapshot
The Endophytic Fungus Phomopsis liquidambaris Promotes Phosphorus Uptake by Arachis hypogaea L. by Regulating Host Auxin, Gibberellins, and Cytokinins Signaling Pathways
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Phosphorus Use Kinetics of Citrus Grafts Versus Rootstocks Alone: Morphological, Physiological, and Biochemical Responses
inferred← citeshttps://doi.org/10.1007/s42729-025-02649-9openalex-snapshot
Effect of Local Application of Potassium on Cesium Uptake in Rice
inferred← citeshttps://doi.org/10.1007/s44154-022-00039-0openalex-snapshot
Plant phosphate nutrition: sensing the stress
inferred← citeshttps://doi.org/10.1016/b978-0-12-380868-4.00002-8openalex-snapshot
Root System Architecture
inferred← citeshttps://doi.org/10.1016/b978-0-12-381466-1.00024-9openalex-snapshot
Growth control of root architecture
inferred← citeshttps://doi.org/10.1016/b978-0-12-811308-0.00007-7openalex-snapshot
The role of root morphology and architecture in phosphorus acquisition: physiological, genetic, and molecular basis
inferred← citeshttps://doi.org/10.1016/b978-0-12-818204-8.00007-2openalex-snapshot
Regulation of low phosphate stress in plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-819773-8.00010-1openalex-snapshot
Genetic and environmental regulation of root growth and development
inferred← citeshttps://doi.org/10.1016/b978-0-443-18927-2.00009-1openalex-snapshot
Plant growth coordination during stress conditions: Role of phytohormones
inferred← citeshttps://doi.org/10.1016/b978-0-443-44712-9.00021-9openalex-snapshot
Mineral nutrients and root architecture
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Enhancing phosphorus-solubilizing microorganism potential for alleviating plant phosphorus limitation through amino acid co-application
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.05.016openalex-snapshot
The zinc homeostasis network of land plants
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2009.02.006openalex-snapshot
Molecular mechanisms in response to phosphate starvation in rice
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2015.03.011openalex-snapshot
Physiological and molecular alterations in plants exposed to high [CO2] under phosphorus stress
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2025.108686openalex-snapshot
Understanding low-phosphate stress responses in plants: Opportunities for genome editing to improve phosphorous use efficiency (PUE)
inferred← citeshttps://doi.org/10.1016/j.cell.2026.07.048openalex-snapshot
Mutually beneficial interactions between bacteria and Arabidopsis promote phosphorus nutrition and growth
inferred← citeshttps://doi.org/10.1016/j.cj.2016.10.001openalex-snapshot
Drought-responsive genes expressed predominantly in root tissues are enriched with homotypic cis -regulatory clusters in promoters of major cereal crops
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.cj.2026.06.017openalex-snapshot
Activation of GmGCS1 by GmPHR1 modulates root architecture and phosphorus acquisition in soybean
inferred← citeshttps://doi.org/10.1016/j.coisb.2017.07.008openalex-snapshot
System-level understanding of plant mineral nutrition in the big data era
inferred← citeshttps://doi.org/10.1016/j.crvi.2010.01.011openalex-snapshot
The root cap at the forefront
inferred← citeshttps://doi.org/10.1016/j.cub.2022.04.005openalex-snapshot
Bacterial-type ferroxidase tunes iron-dependent phosphate sensing during Arabidopsis root development
inferred← citeshttps://doi.org/10.1016/j.cub.2023.07.045openalex-snapshot
Immature leaves are the dominant volatile-sensing organs of maize
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.02.007openalex-snapshot
Iron-Dependent Callose Deposition Adjusts Root Meristem Maintenance to Phosphate Availability
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.06.002openalex-snapshot
Interdependent Nutrient Availability and Steroid Hormone Signals Facilitate Root Growth Plasticity
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.01.002openalex-snapshot
Tackling Plant Phosphate Starvation by the Roots
inferred← citeshttps://doi.org/10.1016/j.ecolmodel.2021.109649openalex-snapshot
Simulating root distribution of plant individual with a three-dimensional model
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2009.09.001openalex-snapshot
Use of phosphate to avoid uranium toxicity in Arabidopsis thaliana leads to alterations of morphological and physiological responses regulated by phosphate availability
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.10.004openalex-snapshot
Uncovering the physiological and cellular effects of uranium on the root system of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104212openalex-snapshot
The role of different root orders in nutrient uptake
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104753openalex-snapshot
Molecular analysis indicates the involvement of Jasmonic acid biosynthesis pathway in low-potassium (K+) stress response and development in chickpea (Cicer arietinum)
inferred← citeshttps://doi.org/10.1016/j.fcr.2010.03.001openalex-snapshot
Strategies for improving phosphorus acquisition efficiency of crop plants
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104029openalex-snapshot
Primary nutrient sensors in plants
inferred← citeshttps://doi.org/10.1016/j.jgg.2024.09.008openalex-snapshot
Epigenetic control of plant abiotic stress responses
inferred← citeshttps://doi.org/10.1016/j.jgg.2024.09.018openalex-snapshot
Phosphorus acquisition, translocation, and redistribution in maize
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.135165openalex-snapshot
Co-mutation of OsLPR1/3/4/5 provides a promising strategy to minimize Cd contamination in rice grains
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2026.141117openalex-snapshot
Localized nitrate uptake by NRT1.8 antagonizes root meristem growth inhibition upon cadmium stress
inferred← citeshttps://doi.org/10.1016/j.jia.2023.05.002openalex-snapshot
Genome-wide and candidate gene association studies identify BnPAP17 as conferring the utilization of organic phosphorus in oilseed rape
inferred← citeshttps://doi.org/10.1016/j.jplph.2012.04.011openalex-snapshot
Ammonium enhances resistance to salinity stress in citrus plants
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154257openalex-snapshot
Physiological and molecular mechanisms of plant-root responses to iron toxicity
inferred← citeshttps://doi.org/10.1016/j.mee.2014.01.017openalex-snapshot
Growth assay of individual pollen tubes arrayed by microchannel device
inferred← citeshttps://doi.org/10.1016/j.molp.2014.11.014openalex-snapshot
Iron- and Ferritin-Dependent Reactive Oxygen Species Distribution: Impact on Arabidopsis Root System Architecture
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.molp.2019.08.001openalex-snapshot
Blue Light-Triggered Chemical Reactions Underlie Phosphate Deficiency-Induced Inhibition of Root Elongation of Arabidopsis Seedlings Grown in Petri Dishes
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.2021.06.024openalex-snapshot
A transcription factor STOP1-centered pathway coordinates ammonium and phosphate acquisition in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.molp.2021.11.011openalex-snapshot
“Je t'aime moi non plus": A love-hate relationship between iron and phosphate
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.molp.2022.11.003openalex-snapshot
The ferroxidases LPR1 and LPR2 control iron translocation in the xylem of Arabidopsis plants
inferred← citeshttps://doi.org/10.1016/j.ncrops.2024.100030openalex-snapshot
Crop designs: The ideal root architecture for future crop breeding
inferred← citeshttps://doi.org/10.1016/j.pbi.2007.10.003openalex-snapshot
Root branching responses to phosphate and nitrate
inferred← citeshttps://doi.org/10.1016/j.pbi.2008.05.006openalex-snapshot
Phosphate starvation signaling: a threesome controls systemic Pi homeostasis
inferred← citeshttps://doi.org/10.1016/j.pbi.2009.04.015openalex-snapshot
Root uptake regulation: a central process for NPS homeostasis in plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2011.03.024openalex-snapshot
What does Arabidopsis natural variation teach us (and does not teach us) about adaptation in plants?
inferred← citeshttps://doi.org/10.1016/j.pbi.2011.04.007openalex-snapshot
Phosphate sensing in root development
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.04.016openalex-snapshot
Phosphate scouting by root tips
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.05.007openalex-snapshot
Novel signals in the regulation of Pi starvation responses in plants: facts and promises
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.06.008openalex-snapshot
Food for thought: how nutrients regulate root system architecture
inferred← citeshttps://doi.org/10.1016/j.pbi.2020.07.002openalex-snapshot
Nitrogen and Phosphorus interactions in plants: from agronomic to physiological and molecular insights
inferred← citeshttps://doi.org/10.1016/j.plantsci.2007.10.007openalex-snapshot
Inner voices meet outer signals: The plasticity of rhizodermic cells
inferred← citeshttps://doi.org/10.1016/j.plantsci.2008.09.007openalex-snapshot
Phosphate signaling in Arabidopsis and Oryza sativa
inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.06.020openalex-snapshot
miRNA778 and SUVH6 are involved in phosphate homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2016.07.009openalex-snapshot
miRNA alterations are important mechanism in maize adaptations to low-phosphate environments
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.11.019openalex-snapshot
CONSTITUTIVE TRIPLE RESPONSE1 and PIN2 act in a coordinate manner to support the indeterminate root growth and meristem cell proliferating activity in Arabidopsis seedlings
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.02.011openalex-snapshot
Auxin and GA signaling play important roles in the maize response to phosphate deficiency
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110474openalex-snapshot
Review: Emerging roles of brassinosteroid in nutrient foraging
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110526openalex-snapshot
Phosphate regulates malate/citrate-mediated iron uptake and transport in apple
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112024openalex-snapshot
Review: Nutrient-nutrient interactions governing underground plant adaptation strategies in a heterogeneous environment
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112685openalex-snapshot
Review: Adaptation of plants to phosphorus scarcity: From nutritional crosstalk to organellar function
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112855openalex-snapshot
Unearthing the secrets of drought-driven root system architecture: Nutrient acquisition and rhizosphere microbe interplay
inferred← citeshttps://doi.org/10.1016/j.plaphy.2009.06.009openalex-snapshot
Natural variation in Arabidopsis adaptation to growth at low nitrogen conditions
inferred← citeshttps://doi.org/10.1016/j.plaphy.2013.12.009openalex-snapshot
Arabidopsis thaliana mutant lpsi reveals impairment in the root responses to local phosphate availability
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.12.037openalex-snapshot
OsPDR2 mediates the regulation on the development response and maintenance of Pi homeostasis in rice
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.02.003openalex-snapshot
The overexpression of LOW PHOSPHATE ROOT 1 (LPR1) negatively regulates Arabidopsis growth in response to Cadmium (Cd) stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108386openalex-snapshot
Unlocking dynamic root phenotypes for simultaneous enhancement of water and phosphorus uptake
inferred← citeshttps://doi.org/10.1016/j.plgene.2021.100321openalex-snapshot
Transcriptome analysis revealed cellular pathways associated with abiotic stress tolerance and disease resistance induced by Pseudomonas aeruginosa in banana plants
inferred← citeshttps://doi.org/10.1016/j.scienta.2026.114874openalex-snapshot
PoSPX1 enhances phosphorus deficiency tolerance by improving root growth in tree peony (Paeonia ostii ‘Fengdan’) with dual medicinal and ornamental value
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.174719openalex-snapshot
The impact of alternative recycled and synthetic phosphorus sources on plant growth and responses, soil interactions and sustainable agriculture - lettuce (Lactuca sativa) as a case model
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.06.013openalex-snapshot
Molecular mechanisms of phosphate transport and signaling in higher plants
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.10.003openalex-snapshot
Regulation and functional diversification of root hairs
inferred← citeshttps://doi.org/10.1016/j.sjbs.2021.05.066openalex-snapshot
Phosphorus tolerance levels of different chickpea genotypes
inferred← citeshttps://doi.org/10.1016/j.still.2018.02.009openalex-snapshot
Polymer coated novel controlled release rock phosphate formulations for improving phosphorus use efficiency by wheat in an Inceptisol
inferred← citeshttps://doi.org/10.1016/j.tplants.2007.11.008openalex-snapshot
Identifying the molecular basis of QTLs: eQTLs add a new dimension
inferred← citeshttps://doi.org/10.1016/j.tplants.2010.08.009openalex-snapshot
The roots of a new green revolution
inferred← citeshttps://doi.org/10.1016/j.tplants.2011.05.006openalex-snapshot
Root developmental adaptation to phosphate starvation: better safe than sorry
inferred← citeshttps://doi.org/10.1016/j.tplants.2014.01.007openalex-snapshot
Shaping a root system: regulating lateral versus primary root growth
inferred← citeshttps://doi.org/10.1016/j.tplants.2018.04.006openalex-snapshot
Adaptation to Phosphate Scarcity: Tips from Arabidopsis Roots
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.03.008openalex-snapshot
Getting to the Root of Plant Mineral Nutrition: Combinatorial Nutrient Stresses Reveal Emergent Properties
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.05.002openalex-snapshot
Regulation of Ubiquitination Is Central to the Phosphate Starvation Response
inferred← citeshttps://doi.org/10.1016/j.tplants.2023.03.007openalex-snapshot
Beyond iron-storage pool: functions of plant apoplastic iron during stress
inferred← citeshttps://doi.org/10.1016/j.tree.2020.12.009openalex-snapshot
Predictability of Biotic Stress Structures Plant Defence Evolution
inferred← citeshttps://doi.org/10.1021/acs.est.0c04384openalex-snapshot
High-Affinity Sulfate Transporter Sultr1;2 Is a Major Transporter for Cr(VI) Uptake in Plants
inferred← citeshttps://doi.org/10.1038/ncomms15300openalex-snapshot
Low phosphate activates STOP1-ALMT1 to rapidly inhibit root cell elongation
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