On the public citation graph
Identification and Characterization of the Arabidopsis PHO1 Gene Involved in Phosphate Loading to the Xylem
0 signed · 586 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/jmbi.2000.4315openalex-snapshot
Predicting transmembrane protein topology with a hidden markov model: application to complete genomes11Edited by F. Cohen
inferredcites →https://doi.org/10.1007/bf00014672openalex-snapshot
The small, versatilepPZP family ofAgrobacterium binary vectors for plant transformation
inferredcites →https://doi.org/10.1007/bf00386944openalex-snapshot
The tertiary endodermis in barley roots: Fine structure in relation to radial transport of ions and water
inferredcites →https://doi.org/10.1007/bf03262926openalex-snapshot
Versatile Vectors for Expressing Genes in Plants
inferredcites →https://doi.org/10.1007/s004250000271openalex-snapshot
Conditional identification of phosphate-starvation-response mutants in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s004250000450openalex-snapshot
pho3 : a phosphorus-deficient mutant of Arabidopsis thaliana (L.) Heynh.
inferredcites →https://doi.org/10.1007/s004250050318openalex-snapshot
Uptake and translocation of phosphate by pho2 mutant and wild-type seedlings of Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s004250050394openalex-snapshot
Functional analysis and cell-specific expression of a phosphate transporter from tomato
inferredcites →https://doi.org/10.1016/0076-6879(66)08014-5openalex-snapshot
[10] Assay of inorganic phosphate, total phosphate and phosphatases
inferredcites →https://doi.org/10.1016/s0092-8674(00)81606-2openalex-snapshot
Identification and Disruption of a Plant Shaker-like Outward Channel Involved in K+ Release into the Xylem Sap
inferredcites →https://doi.org/10.1016/s0304-4157(99)00010-6openalex-snapshot
Phosphate permeases of Saccharomyces cerevisiae: structure, function and regulation
inferredcites →https://doi.org/10.1016/s1369-5266(00)00062-5openalex-snapshot
Phosphate transport and signaling
inferredcites →https://doi.org/10.1016/s1369-5266(00)80063-1openalex-snapshot
Phosphate transport and signaling
inferredcites →https://doi.org/10.1034/j.1399-3054.1992.860211.xopenalex-snapshot
Adaptation of potassium translocation into the shoot of maize (Zea mays) to shoot demand: Evidence for xylem loading as a regulating step
inferredcites →https://doi.org/10.1034/j.1399-3054.1996.970323.xopenalex-snapshot
Functions of passage cells in the endodermis and exodermis of roots
inferredcites →https://doi.org/10.1038/325321a0openalex-snapshot
The βγ subunits of GTP-binding proteins activate the muscarinic K+ channel in heart
inferredcites →https://doi.org/10.1038/352729a0openalex-snapshot
Cell-surface receptor for ecotropic murine retroviruses is a basic amino-acid transporter
inferredcites →https://doi.org/10.1038/6005openalex-snapshot
Receptors for polytropic and xenotropic mouse leukaemia viruses encoded by a single gene at Rmc1
inferredcites →https://doi.org/10.1038/ki.1996.135openalex-snapshot
Identification and characterization of a widely expressed phosphate transporter/retrovirus receptor family
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.09020195.xopenalex-snapshot
Tissue‐specific expression of Arabidopsis AKT1 gene is consistent with a role in K + nutrition
inferredcites →https://doi.org/10.1046/j.1365-313x.1997.11010083.xopenalex-snapshot
The cloning of two Arabidopsis genes belonging to a phosphate transporter family
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00086.xopenalex-snapshot
Cytogenetics for the model system Arabidopsis thaliana
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.93.19.10519openalex-snapshot
Phosphate transporters from the higher plant Arabidopsis thaliana.
inferredcites →https://doi.org/10.1073/pnas.94.13.7098openalex-snapshot
Overexpression of an Arabidopsis thaliana high-affinity phosphate transporter gene in tobacco cultured cells enhances cell growth under phosphate-limited conditions
inferredcites →https://doi.org/10.1073/pnas.96.10.5868openalex-snapshot
Transcriptional regulation of plant phosphate transporters
inferredcites →https://doi.org/10.1073/pnas.96.3.927openalex-snapshot
Cloning and characterization of a cell surface receptor for xenotropic and polytropic murine leukemia viruses
inferredcites →https://doi.org/10.1073/pnas.96.4.1385openalex-snapshot
A human cell-surface receptor for xenotropic and polytropic murine leukemia viruses: Possible role in G protein-coupled signal transduction
inferredcites →https://doi.org/10.1073/pnas.96.5.2129openalex-snapshot
The RD114/simian type D retrovirus receptor is a neutral amino acid transporter
inferredcites →https://doi.org/10.1073/pnas.97.3.1107openalex-snapshot
Pho86p, an endoplasmic reticulum (ER) resident protein in Saccharomyces cerevisiae , is required for ER exit of the high-affinity phosphate transporter Pho84p
inferredcites →https://doi.org/10.1074/jbc.270.43.25435openalex-snapshot
Truncated Forms of a Novel Yeast Protein Suppress the Lethality of a G Protein α Subunit Deficiency by Interacting with the β Subunit
inferredcites →https://doi.org/10.1080/00380768.1997.10414730openalex-snapshot
Isolation and characterization of a cDNA from Catharanthus roseus which is highly homologous with phosphate transporter
inferredcites →https://doi.org/10.1093/dnares/5.5.261openalex-snapshot
Phosphate Transporter Gene Family of Arabidopsis thaliana
inferredcites →https://doi.org/10.1094/mpmi.1998.11.1.14openalex-snapshot
Cloning and Characterization of Two Phosphate Transporters from Medicago truncatula Roots: Regulation in Response to Phosphate and to Colonization by Arbuscular Mycorrhizal (AM) Fungi
inferredcites →https://doi.org/10.1098/rstb.1993.0086openalex-snapshot
Roots and the delivery of solutes to the xylem
inferredcites →https://doi.org/10.1104/pp.106.4.1241openalex-snapshot
Genes Galore: A Summary of Methods for Accessing Results from Large-Scale Partial Sequencing of Anonymous Arabidopsis cDNA Clones
inferredcites →https://doi.org/10.1104/pp.107.1.207openalex-snapshot
Characterization of a Phosphate-Accumulator Mutant of Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.116.1.91openalex-snapshot
Tomato Phosphate Transporter Genes Are Differentially Regulated in Plant Tissues by Phosphorus1
inferredcites →https://doi.org/10.1104/pp.97.3.1087openalex-snapshot
Mutant of Arabidopsis Deficient in Xylem Loading of Phosphate
inferredcites →https://doi.org/10.1105/tpc.11.11.2153openalex-snapshot
Pht2;1 Encodes a Low-Affinity Phosphate Transporter from Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.9.3.381openalex-snapshot
Two cDNAs from potato are able to complement a phosphate uptake-deficient yeast mutant: identification of phosphate transporters from higher plants.
inferredcites →https://doi.org/10.1111/j.1399-3054.1962.tb08052.xopenalex-snapshot
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
inferredcites →https://doi.org/10.1111/j.1399-3054.1981.tb04518.xopenalex-snapshot
Release of ions to the xylem in roots
inferredcites →https://doi.org/10.1111/j.1399-3054.1982.tb00264.xopenalex-snapshot
Mild phosphorus stress in barley and a related low‐phosphorus‐adapted barleygrass: Phosphorus fractions and phosphate absorption in relation to growth
inferredcites →https://doi.org/10.1126/science.270.5235.480openalex-snapshot
Physical Map and Organization of Arabidopsis thaliana Chromosome 4
inferredcites →https://doi.org/10.1128/mmbr.62.1.1-34.1998openalex-snapshot
Major Facilitator Superfamily
inferredcites →https://doi.org/10.1146/annurev.arplant.36.1.77openalex-snapshot
Factors Affecting Mineral Nutrient Acquisition by Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.665openalex-snapshot
PHOSPHATE ACQUISITION
inferredcites →https://doi.org/10.1146/annurev.bi.61.070192.005313openalex-snapshot
PHEROMONE RESPONSE IN YEAST
inferredcites →https://doi.org/10.1146/annurev.pp.36.060185.000453openalex-snapshot
Factors Affecting Mineral Nutrient Acquisition by Plants
inferredcites →https://doi.org/10.1242/dev.121.10.3303openalex-snapshot
Formation of lateral root meristems is a two-stage process
inferredcites →https://doi.org/10.2307/3870489openalex-snapshot
Two cDNAs from Potato Are Able to Complement a Phosphate Uptake-Deficient Yeast Mutant: Identification of Phosphate Transporters from Higher Plants
inferredcites →https://doi.org/10.2307/3871016openalex-snapshot
Pht2;1 Encodes a Low-Affinity Phosphate Transporter from Arabidopsis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4846400openalex-extracted
MYB68 Regulates Suberin Patterning and Radially Distinct Endodermal Differentiation
inferred← citeshttps://doi.org/10.1002/9781118951446.ch12openalex-snapshot
Phosphorus metabolism and transport in arbuscular mycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1002/9781118958841.ch2openalex-snapshot
Sensing, signaLling, and CONTROL of phosphate starvation in plants: molecular players and applications
inferred← citeshttps://doi.org/10.1002/9781119279723.ch4openalex-snapshot
Nitrogen and Phosphorus Use Efficiencies in Wheat: Physiology, Phenotyping, Genetics, and Breeding
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0381openalex-snapshot
From the Ionome to the Genome: Identifying the Gene Networks that Control the Mineral Content Of Plants
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0517openalex-snapshot
Sensing, Signalling, and Control of Phosphate Starvation in Plants: Molecular Players and Applications
inferred← citeshttps://doi.org/10.1002/9783527632930.ch26openalex-snapshot
Transcription Factors: Improving Abiotic Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1002/9783527675265.ch37openalex-snapshot
Phosphorus Starvation Response in Plants and Opportunities for Crop Improvement
inferred← citeshttps://doi.org/10.1002/jsfa.10367openalex-snapshot
Positron‐emitting tracer imaging of fluoride transport and distribution in tea plant
inferred← citeshttps://doi.org/10.1002/pld3.250openalex-snapshot
A single‐population GWAS identified AtMATE expression level polymorphism caused by promoter variants is associated with variation in aluminum tolerance in a local Arabidopsis population
inferred← citeshttps://doi.org/10.1002/pld3.416openalex-snapshot
Thepho1;2a′‐m1.1allele ofPhosphate1conditions misregulation of the phosphorus starvation response in maize ( Zea maysssp.mays L.)
inferred← citeshttps://doi.org/10.1007/978-1-4020-5843-1_14openalex-snapshot
Loading of Ions into the Xylem of the Root
inferred← citeshttps://doi.org/10.1007/978-1-4020-8435-5_11openalex-snapshot
Potential and limitations to improving crops for enhanced phosphorus utilization
inferred← citeshttps://doi.org/10.1007/978-1-4939-7136-7_3openalex-snapshot
The Role of Long Noncoding RNAs in Plant Stress Tolerance
inferred← citeshttps://doi.org/10.1007/978-3-030-27165-7_12openalex-snapshot
Plant Nutritional Deficiency and Its Impact on Crop Production
inferred← citeshttps://doi.org/10.1007/978-3-030-96925-7_15openalex-snapshot
Genome Editing for Nutrient Use Efficiency in Crops
inferred← citeshttps://doi.org/10.1007/978-3-031-15568-0_16openalex-snapshot
Genetic and Molecular Factors Modulating Phosphorus Use Efficiency in Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-10635-9_4openalex-snapshot
Efficient Mineral Nutrition: Genetic Improvement of Phosphate Uptake and Use Efficiency in Crops
inferred← citeshttps://doi.org/10.1007/978-3-642-02167-1_5openalex-snapshot
Adaptation to a Changing Environment: The Regulatory Role of Small RNAs
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/10.1007/978-3-642-14369-4_7openalex-snapshot
Sensing and Signaling of PO 4 3−
inferred← citeshttps://doi.org/10.1007/978-3-642-36470-9_7openalex-snapshot
Systemic Signaling in the Maintenance of Phosphate Homeostasis
inferred← citeshttps://doi.org/10.1007/978-94-007-4500-1_8openalex-snapshot
Bioavailability of Soil P for Plant Nutrition
inferred← citeshttps://doi.org/10.1007/978-94-010-0243-1_6openalex-snapshot
Phosphate transport in plants
inferred← citeshttps://doi.org/10.1007/978-981-13-9349-5_17openalex-snapshot
Arbuscular Mycorrhizal Fungi in Alleviation of Cold Stress in Plants
inferred← citeshttps://doi.org/10.1007/978-981-15-9380-2_5openalex-snapshot
Plant Roots and Mineral Nutrition: An Overview of Molecular Basis of Uptake and Regulation, and Strategies to Improve Nutrient Use Efficiency (NUE)
inferred← citeshttps://doi.org/10.1007/bf03036122openalex-snapshot
Long-distance transporters of inorganic nutrients in plants
inferred← citeshttps://doi.org/10.1007/s00122-002-1177-9openalex-snapshot
The genetics of phytate and phosphate accumulation in seeds and leaves of Arabidopsis thaliana, using natural variation
inferred← citeshttps://doi.org/10.1007/s00122-018-3108-4openalex-snapshot
Genome-wide association study dissects yield components associated with low-phosphorus stress tolerance in maize
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/s00122-024-04667-0openalex-snapshot
Exploring the phosphorus–starch content balance mechanisms in maize grains using GWAS population and transcriptome data
inferred← citeshttps://doi.org/10.1007/s00424-018-2231-zopenalex-snapshot
Physiological regulation of phosphate by vitamin D, parathyroid hormone (PTH) and phosphate (Pi)
inferred← citeshttps://doi.org/10.1007/s00425-002-0921-3openalex-snapshot
Molecular mechanisms of phosphate transport in plants
inferred← citeshttps://doi.org/10.1007/s00425-007-0603-2openalex-snapshot
Molecular cloning and characterization of phosphorus starvation responsive genes in common bean (Phaseolus vulgaris L.)
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/s10142-025-01542-zopenalex-snapshot
Molecular signatures that translate across omics layers and crops under high aluminium and low phosphorus stress facilitate the identification of reliable molecular targets for genotyping in lentil
inferred← citeshttps://doi.org/10.1007/s10265-005-0257-8openalex-snapshot
Organic substances in xylem sap delivered to above-ground organs by the roots
inferred← citeshttps://doi.org/10.1007/s10295-005-0255-9openalex-snapshot
Strategies for the engineered phytoremediation of toxic element pollution: mercury and arsenic
inferred← citeshttps://doi.org/10.1007/s10528-023-10375-zopenalex-snapshot
Comprehensive Evolution and Expression anaLysis of PHOSPHATE 1 Gene Family in Allotetraploid Brassica napus and Its Diploid Ancestors
inferred← citeshttps://doi.org/10.1007/s10681-011-0428-8openalex-snapshot
Development of gene-based markers from functional Arabidopsis thaliana genes involved in phosphorus homeostasis and mapping in Brassica napus
inferred← citeshttps://doi.org/10.1007/s10725-011-9575-0openalex-snapshot
Identification and expression analysis of genes induced by phosphate starvation in leaves and roots of Brassica napus
inferred← citeshttps://doi.org/10.1007/s10725-018-0426-0openalex-snapshot
The involvement of long non-coding RNAs in the formation of high temperature-induced grain chalkiness in rice
inferred← citeshttps://doi.org/10.1007/s11032-025-01596-8openalex-snapshot
Genetic dissection for phosphorus uptake and utilization efficiency at seedling stage in wheat (Triticum aestivum L.)
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/s11033-022-07679-5openalex-snapshot
Narrowing down molecular targets for improving phosphorus-use efficiency in maize (Zea mays L.)
inferred← citeshttps://doi.org/10.1007/s11101-023-09868-xopenalex-snapshot
Phytic acid: a reservoir of phosphorus in seeds plays a dynamic role in plant and animal metabolism
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/s11103-019-00896-wopenalex-snapshot
Common and specific responses to iron and phosphorus deficiencies in roots of apple tree (Malus × domestica)
inferred← citeshttps://doi.org/10.1007/s11103-025-01635-0openalex-snapshot
Physiological and transcriptomic analysis reveal the response mechanisms to nutrient deficiencies in aquatic plant Spirodela polyrhiza
inferred← citeshttps://doi.org/10.1007/s11104-011-0913-9openalex-snapshot
Characterization of phosphorus starvation-induced gene BnSPX3 in Brassica napus
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/s11104-022-05337-0openalex-snapshot
Tomato plant responses induced by sparingly available inorganic and organic phosphorus forms are modulated by strigolactones
inferred← citeshttps://doi.org/10.1007/s11104-022-05484-4openalex-snapshot
Aluminum-activated Malate Transporter 12 is involved in restricting root-to-shoot Cl− transport in Arabidopsis under Cl−-salt stress
inferred← citeshttps://doi.org/10.1007/s11104-022-05564-5openalex-snapshot
The promotion of legume nodulation in plant-soil-microbe systems under phosphorus-limited conditions
inferred← citeshttps://doi.org/10.1007/s11104-023-05976-xopenalex-snapshot
Emerging roles of inositol pyrophosphates in signaling plant phosphorus status and phytohormone signaling
inferred← citeshttps://doi.org/10.1007/s11515-011-1050-9openalex-snapshot
Molecular mechanisms regulating Pi-signaling and Pi homeostasis under OsPHR2, a central Pi-signaling regulator, in rice
inferred← citeshttps://doi.org/10.1007/s11738-011-0832-7openalex-snapshot
Transcriptome response to phosphorus starvation in rice
inferred← citeshttps://doi.org/10.1007/s11738-014-1687-5openalex-snapshot
Transcriptome responses to phosphate deficiency in Poncirus trifoliata (L.) Raf
inferred← citeshttps://doi.org/10.1007/s11738-020-03167-0openalex-snapshot
Transcriptome analysis of low phosphate stress response in the roots of masson pine (Pinus massoniana) seedlings
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/s12042-025-09410-7openalex-snapshot
Phosphorus Uptake in Eucalypt Plants Under Split Root System
inferred← citeshttps://doi.org/10.1007/s12374-016-0117-1openalex-snapshot
Physiological and biochemical characterization of sheepgrass (Leymus chinensis) reveals insights into photosynthetic apparatus coping with low-phosphate stress conditions
inferred← citeshttps://doi.org/10.1007/s12374-018-0198-0openalex-snapshot
Transgenic Rice Overexperessing a Tomato Mitochondrial Phosphate Transporter, SlMPT3;1, Promotes Phosphate Uptake and Increases Grain Yield
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/s40626-024-00311-wopenalex-snapshot
Eucalypt seedlings lack a clear phosphate starvation response under low phosphorus availability
inferred← citeshttps://doi.org/10.1007/s42729-021-00418-yopenalex-snapshot
An Overview of the Morphological, Genetic and Metabolic Mechanisms Regulating Phosphorus Efficiency Via Root Traits in Soybean
inferred← citeshttps://doi.org/10.1007/s44154-026-00307-3openalex-snapshot
The SPX protein family in plants: from phosphate sensors to multifunctional signaling hubs
inferred← citeshttps://doi.org/10.1016/b978-0-12-811308-0.00015-6openalex-snapshot
Genetic improvements of traits for enhancing NPK acquisition and utilization efficiency in plants
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/b978-0-12-822916-3.00009-3openalex-snapshot
Biotechnological tools for manipulating nutrient homeostasis in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-85665-2.00017-0openalex-snapshot
Mechanism of temperature stress acclimation and the role of transporters in plants
inferred← citeshttps://doi.org/10.1016/b978-044451018-1/50057-9openalex-snapshot
Molecular Physiology of the Mineral Nutrition of the Potato
inferred← citeshttps://doi.org/10.1016/j.ab.2004.04.040openalex-snapshot
Genetic mutant screening by direct metabolite analysis
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2008.04.004openalex-snapshot
The role of microRNAs and other endogenous small RNAs in plant stress responses
inferred← citeshttps://doi.org/10.1016/j.bbrc.2010.07.022openalex-snapshot
RANKL–RANK signaling regulates expression of xenotropic and polytropic virus receptor (XPR1) in osteoclasts
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.2025.108686openalex-snapshot
Understanding low-phosphate stress responses in plants: Opportunities for genome editing to improve phosphorous use efficiency (PUE)
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115794openalex-snapshot
MYB68 regulates radial endodermal differentiation and suberin patterning
inferred← citeshttps://doi.org/10.1016/j.copbio.2017.08.012openalex-snapshot
Control of plant phosphate homeostasis by inositol pyrophosphates and the SPX domain
inferred← citeshttps://doi.org/10.1016/j.cub.2017.08.026openalex-snapshot
PHO1 Exports Phosphate from the Chalazal Seed Coat to the Embryo in Developing Arabidopsis Seeds
inferred← citeshttps://doi.org/10.1016/j.cub.2017.08.050openalex-snapshot
Plant Biology: Unravelling the Transient Physiological Role for PHO1 in the Seed
inferred← citeshttps://doi.org/10.1016/j.cub.2021.11.063openalex-snapshot
Direct inhibition of phosphate transport by immune signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2014.05.011openalex-snapshot
The dynamic regulation of microRNAs circuits in plant adaptation to abiotic stresses: A survey on molecular, physiological and methodological aspects
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2014.05.013openalex-snapshot
Molecular mechanisms of phosphate and zinc signalling crosstalk in plants: Phosphate and zinc loading into root xylem in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.04.013openalex-snapshot
Phosphorus assimilation of Chinese fir from two provenances during acclimation to changing phosphorus availability
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104386openalex-snapshot
ANAC044 is associated with P reutilization in P deficient Arabidopsis thaliana root cell wall in an ethylene dependent manner
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104597openalex-snapshot
Identification and expression analysis of phosphate transporter genes and metabolites in response to phosphate stress in Capsicum annuum
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105241openalex-snapshot
WRKY transcription factors regulate phosphate uptake in plants
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.febslet.2004.09.023openalex-snapshot
Overexpression of AtHMA4 enhances root‐to‐shoot translocation of zinc and cadmium and plant metal tolerance
inferred← citeshttps://doi.org/10.1016/j.febslet.2012.01.036openalex-snapshot
Phosphate homeostasis in the yeast Saccharomyces cerevisiae, the key role of the SPX domain‐containing proteins
inferred← citeshttps://doi.org/10.1016/j.febslet.2013.12.013openalex-snapshot
Expression of the mammalian Xenotropic Polytropic Virus Receptor 1 (XPR1) in tobacco leaves leads to phosphate export
inferred← citeshttps://doi.org/10.1016/j.genrep.2021.101351openalex-snapshot
Comparative in silico analysis of phosphate transporter gene family, PHT, in Camelina sativa gemome
inferred← citeshttps://doi.org/10.1016/j.gpb.2015.02.003openalex-snapshot
Long Non-Coding RNAs and their Biological Roles in Plants
inferred← citeshttps://doi.org/10.1016/j.hpj.2025.06.008openalex-snapshot
CoWRKY53 positively modulates low phosphate tolerance through facilitation of CoPHO1;H3 in Camellia oleifera
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2019.08.105openalex-snapshot
Genome-wide identification, characterization, and expression profiling of SPX gene family in wheat
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2021.08.037openalex-snapshot
Identification, structure analysis, and transcript profiling of phosphate transporters under Pi deficiency in duckweeds
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144539openalex-snapshot
Optimizing plant phosphate uptake: Advances in the core regulatory mechanisms of phosphate starvation response proteins and their macromolecular partners: A review
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.117065openalex-snapshot
The key physiological and molecular responses of Neolamarckia cadamba to phosphorus deficiency stress by hydroponics
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.123385openalex-snapshot
Phosphate availability shapes source–sink dynamics and nitrogen balance in dual-purpose hemp (Cannabis sativa L.): Insights from physiological and transcriptomic analyses
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2017.10.012openalex-snapshot
Identification and characterization of phosphate transporter genes in potato
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.jplph.2020.153266openalex-snapshot
A novel role of the calcium sensor CBL1 in response to phosphate deficiency in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153363openalex-snapshot
Epigenetic regulation of nitrogen and phosphorus responses in plants
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154317openalex-snapshot
Comprehensive evaluation of phosphate deficiency tolerance in common vetch germplasms and the adaption mechanism to phosphate deficiency
inferred← citeshttps://doi.org/10.1016/j.molcel.2025.08.003openalex-snapshot
KIDINS220 and InsP8 safeguard the stepwise regulation of phosphate exporter XPR1
inferred← citeshttps://doi.org/10.1016/j.molp.2015.01.005openalex-snapshot
Arabidopsis NIP3;1 Plays an Important Role in Arsenic Uptake and Root-to-Shoot Translocation under Arsenite Stress Conditions
inferred← citeshttps://doi.org/10.1016/j.molp.2016.08.011openalex-snapshot
Arbuscular Mycorrhizal Symbiosis Requires a Phosphate Transceptor in the Gigaspora margarita Fungal Symbiont
inferred← citeshttps://doi.org/10.1016/j.molp.2017.10.001openalex-snapshot
A Critical Role of AMT2;1 in Root-To-Shoot Translocation of Ammonium in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.molp.2019.04.003openalex-snapshot
Two RING-Finger Ubiquitin E3 Ligases Regulate the Degradation of SPX4, An Internal Phosphate Sensor, for Phosphate Homeostasis and Signaling in Rice
inferred← citeshttps://doi.org/10.1016/j.molp.2019.08.002openalex-snapshot
Inositol Pyrophosphate InsP8 Acts as an Intracellular Phosphate Signal in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.molp.2021.01.015openalex-snapshot
Loss of two families of SPX domain-containing proteins required for vacuolar polyphosphate accumulation coincides with the transition to phosphate storage in green plants
inferred← citeshttps://doi.org/10.1016/j.molp.2021.05.020openalex-snapshot
Arsenite provides a selective signal that coordinates arsenate uptake and detoxification through the regulation of PHR1 stability in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.molp.2021.06.008openalex-snapshot
Unloading phosphate for starch synthesis in cereal grains
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.2006.03.015openalex-snapshot
Put the metal to the petal: metal uptake and transport throughout plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2013.03.002openalex-snapshot
Improvement of phosphorus efficiency in rice on the basis of understanding phosphate signaling and homeostasis
inferred← citeshttps://doi.org/10.1016/j.pbi.2014.12.001openalex-snapshot
Cellular interactions during tracheary elements formation and function
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.08.004openalex-snapshot
Suberization — the second life of an endodermal cell
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.2019.05.010openalex-snapshot
Polarized transport across root epithelia
inferred← citeshttps://doi.org/10.1016/j.plantsci.2008.06.007openalex-snapshot
Identification of temporally and spatially phosphate-starvation responsive genes in Glycine max
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.2014.10.001openalex-snapshot
Phosphate transporter OsPht1;8 in rice plays an important role in phosphorus redistribution from source to sink organs and allocation between embryo and endosperm of seeds
inferred← citeshttps://doi.org/10.1016/j.plantsci.2016.04.010openalex-snapshot
Soybean SPX1 is an important component of the response to phosphate deficiency for phosphorus homeostasis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.03.013openalex-snapshot
Functions and regulation of phosphate starvation-induced secreted acid phosphatases in higher plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.04.026openalex-snapshot
Physiological and transcriptomic data highlight common features between iron and phosphorus acquisition mechanisms in white lupin roots
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.05.018openalex-snapshot
Intracellular phosphate homeostasis – A short way from metabolism to signaling
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112702openalex-snapshot
Mineral nutrient acquisition under stress: Sensing, signaling, and transportation
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113069openalex-snapshot
Overexpression of PbWRKY66 negatively regulate phosphate uptake and root-to-shoot distribution in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2006.06.016openalex-snapshot
Arabidopsis thaliana wild type, pho1, and pho2 mutant plants show different responses to exogenous cytokinins
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.06.038openalex-snapshot
Genome-wide identification and characterization of phosphate transporter gene family members in tea plants (Camellia sinensis L. O. kuntze) under different selenite levels
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.11.022openalex-snapshot
The effect of silicon supply on photosynthesis and carbohydrate metabolism in two wheat (Triticum aestivum L.) cultivars contrasting in response to phosphorus nutrition
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.04.029openalex-snapshot
Phytic acid contributes to the phosphate-zinc signaling crosstalk in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.09.024openalex-snapshot
Dissection of the response mechanism of alfalfa under phosphite stress based on metabolomic and transcriptomic data
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108165openalex-snapshot
Long non-coding RNA-mediated epigenetic response for abiotic stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108215openalex-snapshot
Phosphate deficiency responsive TaSPX3 is involved in the regulation of shoot phosphorus in Arabidopsis plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109279openalex-snapshot
Pseudomonas putida triggers phosphorus bioavailability and P-transporters under different phosphate regimes to enhance maize growth
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109417openalex-snapshot
Response of ZmPHO1 family members to low phosphorus stress and association of natural variation in ZmPHO1;2a reveal the role of low phosphorus tolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109994openalex-snapshot
Transport channels enabling uptake, translocation and detoxification of arsenic in plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110386openalex-snapshot
Overexpression of MdTGA1 enhances the adaptability to nitrogen and phosphorus deficiency in apple (Malus domestica Borkh.)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110827openalex-snapshot
The Tartary buckwheat WRKY transcription factor FtWRKY28 positively regulates low phosphate stress tolerance in transgenic Arabidopsis plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111135openalex-snapshot
The slow-type anion channel PcSLAH3 from the xerophyte Pugionium cornutum is involved in Cl− transport and Cl−/Na+ homeostasis under saline condition
inferred← citeshttps://doi.org/10.1016/j.rhisph.2025.101142openalex-snapshot
Inoculation with a rhizobacteria synthetic community enhances sugarcane stress resilience through targeted modulation of plant-microbe interactions
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111767openalex-snapshot
Genome-wide identification and characterization of SPX domain-containing proteins and their responses to phosphorus and/or nitrogen deficiency in apple (Malus domestica Borkh.)
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.151099openalex-snapshot
Heavy metal transporters: Functional mechanisms, regulation, and application in phytoremediation
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.stress.2025.100761openalex-snapshot
Small open reading frames (sORFs): Driving big improvements in plant development and quality
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101220openalex-snapshot
HvPHR1 as a key gene in maintaining phosphate homeostasis in barley
inferred← citeshttps://doi.org/10.1016/j.tibs.2016.10.008openalex-snapshot
Eukaryotic Phosphate Homeostasis: The Inositol Pyrophosphate Perspective
inferred← citeshttps://doi.org/10.1016/j.tibs.2026.05.012openalex-snapshot
A unified mechanism of phosphate export across eukaryotes through EXS domain-containing proteins
inferred← citeshttps://doi.org/10.1016/j.tplants.2004.09.003openalex-snapshot
Short on phosphate: plant surveillance and countermeasures
inferred← citeshttps://doi.org/10.1016/j.tplants.2014.06.004openalex-snapshot
MicroRNA-mediated surveillance of phosphate transporters on the move
inferred← citeshttps://doi.org/10.1016/j.tplants.2025.05.010openalex-snapshot
Nutrient cues control flowering time in plants
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100302openalex-snapshot
scCloudMine: A cloud-based app for visualization, comparison, and exploration of single-cell transcriptomic data
inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100636openalex-snapshot
ABI5–FLZ13 module transcriptionally represses growth-related genes to delay seed germination in response to ABA
inferred← citeshttps://doi.org/10.1016/j.ygeno.2022.110363openalex-snapshot
Systems biology-based analysis indicates that PHO1;H10 positively modulates high light-induced anthocyanin biosynthesis in Arabidopsis leaves
inferred← citeshttps://doi.org/10.1016/s0065-2296(05)43005-0openalex-snapshot
Nutrient Sensing and Signalling in Plants: Potassium and Phosphorus
inferred← citeshttps://doi.org/10.1016/s0958-1669(02)00364-6openalex-snapshot
Phytochemicals in plants: genomics-assisted plant improvement for nutritional and health benefits
inferred← citeshttps://doi.org/10.1016/s2095-3119(16)61433-8openalex-snapshot
Expression and functional analysis of FaPH01;H9 gene of strawberry ( Fragariaxananassa )
inferred← citeshttps://doi.org/10.1017/qpb.2025.1openalex-snapshot
Mobilization and recycling of intracellular phosphorus in response to availability
inferred← citeshttps://doi.org/10.1017/wsc.2018.58openalex-snapshot
Phosphate Status Affects Phosphate Transporter Expression and Glyphosate Uptake and Transport in Grand Eucalyptus (Eucalyptus grandis)
inferred← citeshttps://doi.org/10.1021/acs.jafc.7b01687openalex-snapshot
Improvement in Fruit Quality by Overexpressing miR399a in Woodland Strawberry
inferred← citeshttps://doi.org/10.1021/acssynbio.3c00070openalex-snapshot
A Hitchhiker’s Guide to Supplying Enzymatic Reducing Power into Synthetic Cells
inferred← citeshttps://doi.org/10.1023/a:1022376332180openalex-snapshot
Phosphate transport in plants
inferred← citeshttps://doi.org/10.1038/d41586-018-02861-xopenalex-snapshot
A cellular passage to the root interior
inferred← citeshttps://doi.org/10.1038/nature25976openalex-snapshot
Diffusible repression of cytokinin signalling produces endodermal symmetry and passage cells
inferred← citeshttps://doi.org/10.1038/s41421-026-00883-8openalex-snapshot
Structural insights into the gating mechanism of the fission yeast phosphate exporter SpXpr1
inferred← citeshttps://doi.org/10.1038/s41422-025-01081-zopenalex-snapshot
Structural basis of phosphate export by human XPR1
inferred← citeshttps://doi.org/10.1038/s41467-025-58200-yopenalex-snapshot
Synergistic activation of the human phosphate exporter XPR1 by KIDINS220 and inositol pyrophosphate
inferred← citeshttps://doi.org/10.1038/s41467-025-59331-yopenalex-snapshot
N 6-methyladenosine modifications stabilize phosphate starvation response–related mRNAs in plant adaptation to nutrient-deficient stress
inferred← citeshttps://doi.org/10.1038/s41477-022-01231-wopenalex-snapshot
SHORT-ROOT stabilizes PHOSPHATE1 to regulate phosphate allocation in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41477-023-01612-9openalex-snapshot
Visualizing plant intracellular inorganic orthophosphate distribution
inferred← citeshttps://doi.org/10.1038/s41477-024-01895-6openalex-snapshot
Structural mechanism underlying PHO1;H1-mediated phosphate transport in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41586-024-07852-9openalex-snapshot
Human XPR1 structures reveal phosphate export mechanism
inferred← citeshttps://doi.org/10.1038/s41598-023-41339-3openalex-snapshot
Phosphorus deficiency induces sexual reproduction in the dinoflagellate Prorocentrum cordatum
inferred← citeshttps://doi.org/10.1038/srep29850openalex-snapshot
Knock out of the PHOSPHATE 2 Gene TaPHO2-A1 Improves Phosphorus Uptake and Grain Yield under Low Phosphorus Conditions in Common Wheat
inferred← citeshttps://doi.org/10.1039/c4mt00182fopenalex-snapshot
Modulation of Zn/Cd P1B2-ATPase activities in Arabidopsis impacts differently on Zn and Cd contents in shoots and seeds
inferred← citeshttps://doi.org/10.1042/bcj20230156openalex-snapshot
Calcium signalling components underlying NPK homeostasis: potential avenues for exploration
inferred← citeshttps://doi.org/10.1042/bcj20230163openalex-snapshot
Dynamic interactions between SPX proteins, the ubiquitination machinery, and signalling molecules for stress adaptation at a whole-plant level
inferred← citeshttps://doi.org/10.1042/bst20160026openalex-snapshot
Pi sensing and signalling: from prokaryotic to eukaryotic cells
inferred← citeshttps://doi.org/10.1071/cp07125openalex-snapshot
Plant mechanisms to optimise access to soil phosphorus
inferred← citeshttps://doi.org/10.1071/cp13135openalex-snapshot
Genetic approaches to enhancing phosphorus-use efficiency (PUE) in crops: challenges and directions
inferred← citeshttps://doi.org/10.1071/fp08283openalex-snapshot
Reduction of root flavonoid level and its potential involvement in lateral root emergence in Arabidopsis thaliana grown under low phosphate supply
inferred← citeshttps://doi.org/10.1071/fp15106openalex-snapshot
Impact of arbuscular mycorrhizal fungi (AMF) on cucumber growth and phosphorus uptake under cold stress
inferred← citeshttps://doi.org/10.1071/fp16003openalex-snapshot
Molecular cloning and functional characterisation of the tomato E3 ubiquitin ligase SlBAH1 gene
inferred← citeshttps://doi.org/10.1071/fp16435openalex-snapshot
Insights into the functional relationship between cytokinin-induced root system phenotypes and nitrate uptake in Brassica napus
inferred← citeshttps://doi.org/10.1073/pnas.1305883110openalex-snapshot
Integration of responses within and across Arabidopsis natural accessions uncovers loci controlling root systems architecture
inferred← citeshttps://doi.org/10.1073/pnas.1404654111openalex-snapshot
SPX1 is a phosphate-dependent inhibitor of PHOSPHATE STARVATION RESPONSE 1 in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.1514598112openalex-snapshot
A vacuolar phosphate transporter essential for phosphate homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1080/00380768.2025.2612625openalex-snapshot
Oxidized glutathione improves phosphorus acquisition efficiency in plants
showing the first 200 of 531 · page through all 531
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.