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OsPHR2 Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1460-2075.1984.tb02031.xopenalex-snapshot
Tissue‐specific and light‐regulated expression of a pea nuclear gene encoding the small subunit of ribulose‐1,5‐bisphosphate carboxylase.
inferredcites →https://doi.org/10.1007/s00425-004-1305-7openalex-snapshot
Transcripts of MYB-like genes respond to phosphorous and nitrogen deprivation in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2005.10.016openalex-snapshot
A miRNA Involved in Phosphate-Starvation Response in Arabidopsis
inferredcites →https://doi.org/10.1038/ng2079openalex-snapshot
Target mimicry provides a new mechanism for regulation of microRNA activity
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01251.xopenalex-snapshot
Nitrate and phosphate availability and distribution have different effects on root system architecture of Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01860.xopenalex-snapshot
Distribution and characterization of over 1000 T‐DNA tags in rice genome
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00748.xopenalex-snapshot
Expression of the OsPI1 gene, cloned from rice roots using cDNA microarray, rapidly responds to phosphorus status
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00865.xopenalex-snapshot
Long‐term increase in nitrogen supply alters above‐ and below‐ground ectomycorrhizal communities and increases the dominance of Russula spp. in a temperate oak savanna
inferredcites →https://doi.org/10.1073/pnas.0500778102openalex-snapshot
The Arabidopsis SUMO E3 ligase SIZ1 controls phosphate deficiency responses
inferredcites →https://doi.org/10.1073/pnas.0505266102openalex-snapshot
A genome-wide transcriptional analysis using Arabidopsis thaliana Affymetrix gene chips determined plant responses to phosphate deprivation
inferredcites →https://doi.org/10.1073/pnas.082696499openalex-snapshot
Arabidopsis disrupted in SQD2 encoding sulfolipid synthase is impaired in phosphate-limited growth
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.95.4.1950openalex-snapshot
Phosphate availability affects the thylakoid lipid composition and the expression of SQD1 , a gene required for sulfolipid biosynthesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/erh009openalex-snapshot
The transcriptional control of plant responses to phosphate limitation
inferredcites →https://doi.org/10.1093/nar/25.24.4876openalex-snapshot
The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools
inferredcites →https://doi.org/10.1093/nar/8.19.4321openalex-snapshot
Rapid isolation of high molecular weight plant DNA
inferredcites →https://doi.org/10.1093/pcp/pch056openalex-snapshot
Low Phosphorus Tolerance Mechanisms: Phosphorus Recycling and Photosynthate Partitioning in the Tropical Forage Grass, Brachiaria Hybrid Cultivar Mulato Compared with Rice
inferredcites →https://doi.org/10.1097/00010694-194501000-00006openalex-snapshot
DETERMINATION OF TOTAL, ORGANIC, AND AVAILABLE FORMS OF PHOSPHORUS IN SOILS
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/10.1104/pp.103.020941openalex-snapshot
Changes in Gene Expression in Arabidopsis Shoots during Phosphate Starvation and the Potential for Developing Smart Plants
inferredcites →https://doi.org/10.1104/pp.103.021022openalex-snapshot
Phosphate Starvation Triggers Distinct Alterations of Genome Expression in Arabidopsis Roots and Leaves
inferredcites →https://doi.org/10.1104/pp.103.029306openalex-snapshot
How Do Plants Achieve Tolerance to Phosphorus Deficiency? Small Causes with Big Effects
inferredcites →https://doi.org/10.1104/pp.105.063115openalex-snapshot
OsPTF1, a Novel Transcription Factor Involved in Tolerance to Phosphate Starvation in Rice
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.106.078063openalex-snapshot
pho2, a Phosphate Overaccumulator, Is Caused by a Nonsense Mutation in a MicroRNA399 Target Gene
inferredcites →https://doi.org/10.1104/pp.106.079707openalex-snapshot
PHO2, MicroRNA399, and PHR1 Define a Phosphate-Signaling Pathway in Plants
inferredcites →https://doi.org/10.1104/pp.126.2.875openalex-snapshot
Phosphate Availability Regulates Root System Architecture in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.038943openalex-snapshot
Regulation of Phosphate Homeostasis by MicroRNA in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-3040.1996.tb00386.xopenalex-snapshot
Stimulation of root hair elongation in Arabidopsis thaliana by low phosphorus availability
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01272.xopenalex-snapshot
Regulation of the expression of OsIPS1 and OsIPS2 in rice via systemic and local Pi signalling and hormones
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01568.xopenalex-snapshot
Cytokinin represses phosphate‐starvation response through increasing of intracellular phosphate level
inferredcites →https://doi.org/10.1111/j.1365-3040.2007.01734.xopenalex-snapshot
Increased expression of the MYB‐related transcription factor, PHR1, leads to enhanced phosphate uptake in Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1068037openalex-snapshot
A Draft Sequence of the Rice Genome ( Oryza sativa L. ssp. indica )
inferredcites →https://doi.org/10.1126/science.1068275openalex-snapshot
A Draft Sequence of the Rice Genome ( Oryza sativa L. ssp. japonica )
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.665openalex-snapshot
PHOSPHATE ACQUISITION
inferredcites →https://doi.org/10.1146/annurev.arplant.58.032806.103750openalex-snapshot
Nutrient Sensing and Signaling: NPKS
inferredcites →https://doi.org/10.1199/tab.0024openalex-snapshot
Phosphate Transport and Homeostasis in 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.4766567openalex-extracted
Egphl7, Egphr1 and Egphr2 Bind to P1bs and a Unique Motif, Agatwc, for Phosphate Starvation Transcriptional Regulation in Oil Palm
inferred← citeshttps://doi.org/10.2139/ssrn.4782305openalex-extracted
Tamyb-Cc5 Gene Specifically Expressed in Root Improve Tolerance of Phosphorus Deficiency and Drought Stress in Wheat
inferred← citeshttps://doi.org/10.2139/ssrn.4837258openalex-extracted
Genome-Wide Characterization and Expression of the Myb-Cc Gene Family in Salvia Miltiorrhiza Andsmmyb-Cc7-Mediated Response to Phosphate Starvation in Arabidopsis
inferred← citeshttps://doi.org/10.1002/1873-3468.13902openalex-snapshot
MYB‐like transcription factor NoPSR1 is crucial for membrane lipid remodeling under phosphate starvation in the oleaginous microalga Nannochloropsis oceanica
inferred← citeshttps://doi.org/10.1002/1873-3468.70236openalex-snapshot
The expanding landscape of inositol phosphate signaling network in land plants
inferred← citeshttps://doi.org/10.1002/9781118728482.ch5openalex-snapshot
Molecular Breeding for Phosphorus‐efficient Rice
inferred← citeshttps://doi.org/10.1002/9781118958841.ch10openalex-snapshot
The Role of Intracellular and Secreted Purple Acid Phosphatases in Plant Phosphorus Scavenging and Recycling
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/10.1002/9781118958841.ch6openalex-snapshot
Molecular Components that Drive Phosphorus‐Remobilisation During Leaf Senescence
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.apr0517openalex-snapshot
Sensing, Signalling, and Control of Phosphate Starvation in Plants: Molecular Players and Applications
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0521openalex-snapshot
Molecular Components that Drive Phosphorus‐Remobilisation during Leaf Senescence
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0525openalex-snapshot
The Role of Intracellular and Secreted Purple Acid Phosphatases in Plant Phosphorus Scavenging and Recycling
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/advs.202502911openalex-snapshot
PHR‐Mediated Pi Starvation Response Mobile Messenger RNAs Represent Noncoding Transcripts in Recipient Tissues
inferred← citeshttps://doi.org/10.1002/pld3.272openalex-snapshot
A curated list of genes that affect the plant ionome
inferred← citeshttps://doi.org/10.1002/pld3.393openalex-snapshot
Sorghum root epigenetic landscape during limiting phosphorus conditions
inferred← citeshttps://doi.org/10.1007/978-1-0716-4799-8_16openalex-snapshot
Hydroponic Cultivation Systems to Study Nutrient-Dependent Changes in Inositol Polyphosphate Metabolism in Plants
inferred← citeshttps://doi.org/10.1007/978-1-4614-7903-1_14openalex-snapshot
Nitrogen and Phosphorus Uptake and Utilization
inferred← citeshttps://doi.org/10.1007/978-1-4614-7903-1_24openalex-snapshot
Transformation and Transgenic Breeding
inferred← citeshttps://doi.org/10.1007/978-1-4614-9466-9_3openalex-snapshot
Role of Arbuscular Mycorrhizal Fungi in Alleviation of Acidity Stress on Plant Growth
inferred← citeshttps://doi.org/10.1007/978-1-62703-194-3_17openalex-snapshot
Analysis of Rice Root Hair Morphology Using Cryo-Scanning Electron Microscopy
inferred← citeshttps://doi.org/10.1007/978-3-030-19103-0_6openalex-snapshot
System Biology of Metal Tolerance in Plants: An Integrated View of Genomics, Transcriptomics, Metabolomics, and Phenomics
inferred← citeshttps://doi.org/10.1007/978-3-030-19103-0_7openalex-snapshot
Crosstalk Between Plant miRNA and Heavy Metal Toxicity
inferred← citeshttps://doi.org/10.1007/978-3-030-20732-8_2openalex-snapshot
Molecular Mechanism and Signaling Response of Heavy Metal Stress Tolerance in Plants
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/10.1007/978-3-030-84985-6_2openalex-snapshot
Root Architectural Plasticity in Changing Nutrient Availability
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/10.1007/978-3-319-42183-4_4openalex-snapshot
Phosphate Signaling in Plants: Biochemical and Molecular Approach
inferred← citeshttps://doi.org/10.1007/978-3-319-45105-3_11openalex-snapshot
Setaria viridis: A Model for Understanding Panicoid Grass Root Systems
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/10.1007/978-81-322-2662-8_6openalex-snapshot
Enhancing Nutrient Starvation Tolerance in Rice
inferred← citeshttps://doi.org/10.1007/978-94-017-7612-7_6openalex-snapshot
Assessing the Plant Phosphorus Status
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/10.1007/978-981-10-9044-8_22openalex-snapshot
Molecular Approaches to Nutrient Uptake and Cellular Homeostasis in Plants Under Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-981-15-0025-1_4openalex-snapshot
Sugar Beet: A Sustainable Crop for Saline Environment
inferred← citeshttps://doi.org/10.1007/978-981-15-4120-9_18openalex-snapshot
Genetic Engineering to Enhance Rice Survival in Nutrient-Deficient Soil
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/10.1007/978-981-16-2339-4_20openalex-snapshot
miRNA-Mediated Regulation of Biotic and Abiotic Stress Responses in Plants
inferred← citeshttps://doi.org/10.1007/978-981-16-7751-9_9openalex-snapshot
Comparative Transcriptome and MicroRNAs Analyses Between Low- and High-Cd Accumulating Cultivars of Water Spinach
inferred← citeshttps://doi.org/10.1007/978-981-33-6068-6_11openalex-snapshot
Mechanisms of Arsenic Transport, Accumulation, and Distribution in Rice
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/s00122-019-03527-6openalex-snapshot
Improvement of nutrient use efficiency in rice: current toolbox and future perspectives
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/s00203-026-05236-3openalex-snapshot
Pseudomonas atacamensis SJA1 enhances root development and phosphorus accumulation in rice under organic fertilization
inferred← citeshttps://doi.org/10.1007/s00299-014-1588-5openalex-snapshot
GmPAP4, a novel purple acid phosphatase gene isolated from soybean (Glycine max), enhanced extracellular phytate utilization in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-017-2153-9openalex-snapshot
Overexpression of the nitrate transporter, OsNRT2.3b, improves rice phosphorus uptake and translocation
inferred← citeshttps://doi.org/10.1007/s00299-018-2262-0openalex-snapshot
Genome-wide identification and comparative analysis of phosphate starvation-responsive transcription factors in maize and three other gramineous plants
inferred← citeshttps://doi.org/10.1007/s00299-022-02902-wopenalex-snapshot
An Agrobacterium-mediated transient expression method contributes to functional analysis of a transcription factor and potential application of gene editing in Chenopodium quinoa
inferred← citeshttps://doi.org/10.1007/s00299-025-03461-6openalex-snapshot
Genome-wide identification of the SmPHR gene family in Salvia miltiorrhiza and SmPHR7-mediated response to phosphate starvation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00344-020-10161-wopenalex-snapshot
Mechanism of Low Phosphorus Inducing the Main Root Lengthening of Rice
inferred← citeshttps://doi.org/10.1007/s00344-023-11011-1openalex-snapshot
Flavonoids Mediate the Modulation of Phosphate Uptake and Phosphate-Starvation Signaling in Tobacco
inferred← citeshttps://doi.org/10.1007/s00344-025-12013-xopenalex-snapshot
Overexpression of MdMATE3 Promotes Citric Acid Secretion and Therefore Facilitates Phosphorus Uptake in Apple Plant
inferred← citeshttps://doi.org/10.1007/s00425-020-03503-1openalex-snapshot
Expression of PHT1 family transporter genes contributes for low phosphate stress tolerance in foxtail millet (Setaria italica) genotypes
inferred← citeshttps://doi.org/10.1007/s00425-021-03657-6openalex-snapshot
OsJAZ11 regulates phosphate starvation responses in rice
inferred← citeshttps://doi.org/10.1007/s00425-024-04400-7openalex-snapshot
Transcription factor OsSHR2 regulates rice architecture and yield per plant in response to nitrogen
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/s00572-025-01200-zopenalex-snapshot
A transcriptomic perspective of P trade in mycorrhizal grapevine
inferred← citeshttps://doi.org/10.1007/s00709-021-01702-5openalex-snapshot
Transgenic expression of rice OsPHR2 increases phosphorus uptake and yield in wheat
inferred← citeshttps://doi.org/10.1007/s10142-016-0538-4openalex-snapshot
Genome-wide analysis of miRNAs and Tasi-RNAs in Zea mays in response to phosphate deficiency
inferred← citeshttps://doi.org/10.1007/s10265-014-0628-0openalex-snapshot
Oxygen deficit alleviates phosphate overaccumulation toxicity in OsPHR2 overexpression plants
inferred← citeshttps://doi.org/10.1007/s10265-017-0964-yopenalex-snapshot
The physiological and metabolic changes in sugar beet seedlings under different levels of salt stress
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/s10311-018-0741-8openalex-snapshot
Toxicity and detoxification of heavy metals during plant growth and metabolism
inferred← citeshttps://doi.org/10.1007/s10535-016-0672-9openalex-snapshot
Characterization of the high-affinity phosphate transporter PHT1;4 gene promoter of Arabidopsis thaliana in transgenic wheat
inferred← citeshttps://doi.org/10.1007/s10709-018-0042-yopenalex-snapshot
Genome-wide analysis of the MYB-CC gene family of maize
inferred← citeshttps://doi.org/10.1007/s10725-017-0326-8openalex-snapshot
Genetic dissection of QTL against phosphate deficiency in the hybrid rice ‘Xieyou9308’
inferred← citeshttps://doi.org/10.1007/s10725-020-00688-zopenalex-snapshot
Characterization of two cis-acting elements, P1BS and W-box, in the regulation of OsPT6 responsive to phosphors deficiency
inferred← citeshttps://doi.org/10.1007/s10725-023-01020-1openalex-snapshot
The miRNAs regulated by SPX-PHR signaling module under phosphorus starvation in rice
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/s11032-022-01301-zopenalex-snapshot
Functional study and elite haplotype identification of soybean phosphate starvation response transcription factors GmPHR14 and GmPHR32
inferred← citeshttps://doi.org/10.1007/s11032-023-01399-9openalex-snapshot
Integrating genome-wide association studies with selective sweep reveals genetic loci associated with tolerance to low phosphate availability in Brassica napus
inferred← citeshttps://doi.org/10.1007/s11032-024-01508-2openalex-snapshot
Functional analysis of ZmPHR1 and ZmPHR2 under low-phosphate stress in maize
inferred← citeshttps://doi.org/10.1007/s11033-011-1399-5openalex-snapshot
Molecular cloning and characterization of OsUPS, a U-box containing E3 ligase gene that respond to phosphate starvation in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1007/s11033-012-2183-xopenalex-snapshot
Identification of genes differentially expressed in the roots of rubber tree (Hevea brasiliensis Muell. Arg.) in response to phosphorus deficiency
inferred← citeshttps://doi.org/10.1007/s11033-020-05337-2openalex-snapshot
In silico characterization, and expression analysis of rice golden 2-like (OsGLK) members in response to low phosphorous
inferred← citeshttps://doi.org/10.1007/s11033-021-06835-7openalex-snapshot
Response of root development and nutrient uptake of two chinese cultivars of hybrid rice to nitrogen and phosphorus fertilization in Sichuan Province, China
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/s11103-008-9380-yopenalex-snapshot
Plant hormones and nutrient signaling
inferred← citeshttps://doi.org/10.1007/s11103-013-0106-4openalex-snapshot
Diversity in the complexity of phosphate starvation transcriptomes among rice cultivars based on RNA-Seq profiles
inferred← citeshttps://doi.org/10.1007/s11103-014-0186-9openalex-snapshot
Are rice (Oryza sativa L.) phosphate transporters regulated similarly by phosphate and arsenate? A comprehensive study
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/s11103-015-0289-yopenalex-snapshot
Genetic manipulation of a high-affinity PHR1 target cis-element to improve phosphorous uptake in Oryza sativa L.
inferred← citeshttps://doi.org/10.1007/s11103-016-0564-6openalex-snapshot
Phosphate starvation induced OsPHR4 mediates Pi-signaling and homeostasis in rice
inferred← citeshttps://doi.org/10.1007/s11103-019-00932-9openalex-snapshot
Identification of transcription factors that bind to the 5′-UTR of the barley PHO2 gene
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/s11104-009-0219-3openalex-snapshot
Transgenic tomato overexpressing ath-miR399d has enhanced phosphorus accumulation through increased acid phosphatase and proton secretion as well as phosphate transporters
inferred← citeshttps://doi.org/10.1007/s11104-010-0711-9openalex-snapshot
Real-time RT-PCR profiling of transcription factors including 34 MYBs and signaling components in white lupin reveals their P status dependent and organ-specific expression
inferred← citeshttps://doi.org/10.1007/s11104-019-04130-wopenalex-snapshot
Paecilomyces variotii extracts (ZNC) enhance plant immunity and promote plant growth
inferred← citeshttps://doi.org/10.1007/s11104-022-05444-yopenalex-snapshot
Evolution of phosphate metabolism in Tibetan wild barley to adapt to aluminum stress
inferred← citeshttps://doi.org/10.1007/s11104-022-05692-yopenalex-snapshot
Linking root morphology and anatomy with transporters for mineral element uptake in plants
inferred← citeshttps://doi.org/10.1007/s11105-012-0534-3openalex-snapshot
Overexpression of a Maize Transcription Factor ZmPHR1 Improves Shoot Inorganic Phosphate Content and Growth of Arabidopsis under Low-Phosphate Conditions
inferred← citeshttps://doi.org/10.1007/s11105-012-0537-0openalex-snapshot
Characterization of a Novel NBS-LRR Gene Involved in Bacterial Blight Resistance in Rice
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/s11240-019-01716-1openalex-snapshot
SmMYB98b positive regulation to tanshinones in Salvia miltiorrhiza Bunge hairy roots
inferred← citeshttps://doi.org/10.1007/s11356-017-8593-5openalex-snapshot
miRNA-based heavy metal homeostasis and plant growth
inferred← citeshttps://doi.org/10.1007/s11427-020-1683-xopenalex-snapshot
Plant abiotic stress response and nutrient use efficiency
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/s11703-009-0001-6openalex-snapshot
Transcriptional responses and regulations to deficient phosphorus in plants
inferred← citeshttps://doi.org/10.1007/s11738-021-03282-6openalex-snapshot
Genome-wide molecular characterization of Phosphate Transporter 1 and Phosphate Starvation Response gene families in Elaeis guineensis Jacq. and their transcriptional response under different levels of phosphate starvation
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/s12041-014-0424-6openalex-snapshot
Phosphate acquisition efficiency and phosphate starvation tolerance locus (PSTOL1) in rice
inferred← citeshttps://doi.org/10.1007/s12041-015-0532-yopenalex-snapshot
Transcriptome analysis reveals dynamic changes in the gene expression of tobacco seedlings under low potassium stress
inferred← citeshttps://doi.org/10.1007/s12298-022-01155-xopenalex-snapshot
Fine-tuning the transcriptional regulatory model of adaptation response to phosphate stress in maize (Zea mays L.)
inferred← citeshttps://doi.org/10.1007/s12298-023-01368-8openalex-snapshot
Overexpressing Ugp1 promotes phosphate uptake and accumulation in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1007/s12374-013-0213-4openalex-snapshot
The role of rice microRNAs in abiotic stress responses
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/s12374-016-0535-0openalex-snapshot
Overexpression of rice phosphate transporter gene OsPT2 enhances nitrogen fixation and ammonium assimilation in transgenic soybean under phosphorus deficiency
inferred← citeshttps://doi.org/10.1007/s13237-016-0159-2openalex-snapshot
Transcription factors involved in acid stress responses in plants
inferred← citeshttps://doi.org/10.1007/s40502-026-01020-zopenalex-snapshot
Multifaceted roles of phosphate starvation response (PHRs) transcription factors: beyond phosphate acquisition and homeostasis
inferred← citeshttps://doi.org/10.1007/s42729-026-03386-3openalex-snapshot
Deciphering Phosphorus Deficiency Tolerance in Rice: Genetic, Molecular, and Omics Perspectives
inferred← citeshttps://doi.org/10.1007/s44154-022-00039-0openalex-snapshot
Plant phosphate nutrition: sensing the stress
inferred← citeshttps://doi.org/10.1007/s44154-024-00181-xopenalex-snapshot
MicroRNAs as potent regulators in nitrogen and phosphorus signaling transduction and their applications
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/b978-0-12-811308-0.00001-6openalex-snapshot
Molecular and genetic basis of plant macronutrient use efficiency: concepts, opportunities, and challenges
inferred← citeshttps://doi.org/10.1016/b978-0-12-811308-0.00018-1openalex-snapshot
Transgenic approaches for improving phosphorus use 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/b978-0-12-819334-1.00011-3openalex-snapshot
Transcription factors and their roles in phosphorus stress tolerance in crop plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-91734-6.00019-3openalex-snapshot
Molecular genetics of arbuscular mycorrhizal symbiosis
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.cej.2025.170407openalex-snapshot
Novel phosphate zinc controlled release nano-composite (P Zn CRnC) escalates early growth and development in rice under P and Zn deficiency
inferred← citeshttps://doi.org/10.1016/j.cell.2016.02.028openalex-snapshot
Root Endophyte Colletotrichum tofieldiae Confers Plant Fitness Benefits that Are Phosphate Status Dependent
inferred← citeshttps://doi.org/10.1016/j.cell.2021.09.030openalex-snapshot
A phosphate starvation response-centered network regulates mycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1016/j.cj.2020.05.005openalex-snapshot
Vacuolar phosphate transporters account for variation in phosphate accumulation in Astragalus sinicus cultivars
inferred← citeshttps://doi.org/10.1016/j.cj.2021.03.020openalex-snapshot
TaMADS2-3D, a MADS transcription factor gene, regulates phosphate starvation responses in plants
inferred← citeshttps://doi.org/10.1016/j.cj.2023.06.003openalex-snapshot
Phosphorylation regulation of nitrogen, phosphorus, and potassium uptake systems in plants
inferred← citeshttps://doi.org/10.1016/j.cj.2026.06.003openalex-snapshot
The microRNA399-PHOSPHATE2 module acts as a dual regulator of root architecture and systemic signaling under phosphate starvation in rice
inferred← citeshttps://doi.org/10.1016/j.cj.2026.08.004openalex-snapshot
Phosphate starvation signaling restricts leaf angle in rice by PHR2-mediated repression of brassinosteroid biosynthesis
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2015.05.006openalex-snapshot
Construction of regulatory networks mediated by small RNAs responsive to abiotic stresses in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1016/j.copbio.2012.03.002openalex-snapshot
Bioengineering and management for efficient phosphorus utilization in crops and pastures
inferred← citeshttps://doi.org/10.1016/j.copbio.2024.103180openalex-snapshot
Bioengineering and management for efficient and sustainable utilization of phosphorus in crops
inferred← citeshttps://doi.org/10.1016/j.cpb.2024.100332openalex-snapshot
Enhancement of rice traits for the maintenance of the phosphorus balance between rice plants and the soil
inferred← citeshttps://doi.org/10.1016/j.cub.2021.11.059openalex-snapshot
Symbiotic regulation: How plants seek salvation in starvation
inferred← citeshttps://doi.org/10.1016/j.ecoleng.2017.11.001openalex-snapshot
The linkage between vegetation and soil nutrients and their variation under different grazing intensities in an alpine meadow on the eastern Qinghai-Tibetan Plateau
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.2014.06.014openalex-snapshot
MYB transcription factors, active players in abiotic stress signaling
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104162openalex-snapshot
Phosphate starvation responses in crop roots: from well-known players to novel candidates
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105241openalex-snapshot
WRKY transcription factors regulate phosphate uptake in plants
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105875openalex-snapshot
Phosphorus (P) and Zinc (Zn) nutrition constraints: A perspective of linking soil application with plant regulations
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2026.106353openalex-snapshot
Phosphate availability switches nitrate-driven phosphorus acquisition strategies in poplar: Arbuscular mycorrhizal symbiosis reshapes emergency foraging and homeostatic maintenance
inferred← citeshttps://doi.org/10.1016/j.envpol.2021.116778openalex-snapshot
High level of zinc triggers phosphorus starvation by inhibiting root-to-shoot translocation and preferential distribution of phosphorus in rice plants
inferred← citeshttps://doi.org/10.1016/j.envres.2023.116261openalex-snapshot
The ppk-expressing transgenic rice floating bed improves P removal in slightly polluted water
inferred← citeshttps://doi.org/10.1016/j.fcr.2014.04.013openalex-snapshot
Root genetic research, an opportunity and challenge to rice improvement
inferred← citeshttps://doi.org/10.1016/j.fcr.2020.107715openalex-snapshot
The improved phosphorus utilization and reduced phosphorus consumption of ppk-expressing transgenic rice
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.11.298openalex-snapshot
Characterization and evolutionary analysis of phosphate starvation response genes in wheat and other major gramineous plants
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.139315openalex-snapshot
Transcription factor CaPHR3 enhances phosphate starvation tolerance by up-regulating the expression of the CaPHT1;4 phosphate transporter gene in pepper
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144611openalex-snapshot
Open stomata 1 and phosphate starvation response 1 regulate tomato root system architecture during heterogeneous phosphate availability
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.116730openalex-snapshot
Regulatory network mediated by CmMKK5–CmMPK13 cascade response to phosphorus starvation in chrysanthemum
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.jare.2022.05.007openalex-snapshot
Tissue-specific enhancement of OsRNS1 with root-preferred expression is required for the increase of crop yield
inferred← citeshttps://doi.org/10.1016/j.jclepro.2022.130924openalex-snapshot
Revealing the underlying molecular basis of phosphorus recycling in the green manure crop Astragalus sinicus
inferred← citeshttps://doi.org/10.1016/j.jes.2022.08.017openalex-snapshot
Ionome profiling and arsenic speciation provide evidence of arsenite detoxification in rice by phosphate and arsenite-oxidizing bacteria
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.jgg.2026.07.010openalex-snapshot
Regulation of root-to-shoot ratio in plant resource allocation by external and internal cues
inferred← citeshttps://doi.org/10.1016/j.jplph.2013.07.010openalex-snapshot
Fine characterization of OsPHO2 knockout mutants reveals its key role in Pi utilization in rice
inferred← citeshttps://doi.org/10.1016/j.jplph.2019.02.007openalex-snapshot
Gibberellins play dual roles in response to phosphate starvation of tomato seedlings, negatively in shoots but positively in roots
inferred← citeshttps://doi.org/10.1016/j.jplph.2019.153003openalex-snapshot
Hydrogen peroxide alleviates P starvation in rice by facilitating P remobilization from the root cell wall
inferred← citeshttps://doi.org/10.1016/j.jplph.2022.153713openalex-snapshot
Combined metabolomic and transcriptomic analysis evidences the interaction between sugars and phosphate in rice
inferred← citeshttps://doi.org/10.1016/j.jplph.2022.153771openalex-snapshot
Growth status and physiological changes of sugar beet seedlings in response to acidic pH environments
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154382openalex-snapshot
PHR1 negatively regulates nitrate reductase activity by directly inhibiting the transcription of NIA1 in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154582openalex-snapshot
Revealing the role of the plasma membrane H+-ATPase in plant adaptation to phosphorus deficiency in rice under various nitrogen sources and rhizosphere pH
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154815openalex-snapshot
Phytohormonal orchestration of plant phosphate starvation responses
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154874openalex-snapshot
Programmable plant nutrition through synthetic transportome engineering
inferred← citeshttps://doi.org/10.1016/j.jprot.2013.08.015openalex-snapshot
Proteomics identifies ubiquitin–proteasome targets and new roles for chromatin-remodeling in the Arabidopsis response to phosphate starvation
inferred← citeshttps://doi.org/10.1016/j.molp.2014.10.013openalex-snapshot
Genome-Wide Identification and Functional Analysis of Genes Expressed Ubiquitously in Rice
inferred← citeshttps://doi.org/10.1016/j.molp.2015.12.012openalex-snapshot
Complex Regulation of Plant Phosphate Transporters and the Gap between Molecular Mechanisms and Practical Application: What Is Missing?
inferred← citeshttps://doi.org/10.1016/j.molp.2017.07.012openalex-snapshot
Nutrient Exchange and Regulation in Arbuscular Mycorrhizal Symbiosis
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.2020.12.005openalex-snapshot
Modulation of nitrate-induced phosphate response by the MYB transcription factor RLI1/HINGE1 in the nucleus
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.2021.09.011openalex-snapshot
A reciprocal inhibitory module for Pi and iron signaling
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.2023.07.013openalex-snapshot
Spotlight: Antisense regulation of miRNA action during phosphate starvation
inferred← citeshttps://doi.org/10.1016/j.molp.2023.09.012openalex-snapshot
Sailing in complex nutrient signaling networks: Where I am, where to go, and how to go?
inferred← citeshttps://doi.org/10.1016/j.molp.2023.09.022openalex-snapshot
Low phosphorus promotes NSP1–NSP2 heterodimerization to enhance strigolactone biosynthesis and regulate shoot and root architecture in rice
inferred← citeshttps://doi.org/10.1016/j.molp.2023.12.003openalex-snapshot
The OsBZR1–OsSPX1/2 module fine-tunes the growth–immunity trade-off in adaptation to phosphate availability in rice
inferred← citeshttps://doi.org/10.1016/j.molp.2026.01.014openalex-snapshot
Presymbiotic activation of karrikin signaling creates a permissive state for arbuscular mycorrhizal symbiosis by derepressing the NSP1–NSP2–SLR1 transcriptional complex in rice
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.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.2017.06.007openalex-snapshot
MicroRNA-mediated signaling and regulation of nutrient transport and utilization
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.2015.06.020openalex-snapshot
miRNA778 and SUVH6 are involved in phosphate homeostasis in Arabidopsis
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.2018.12.025openalex-snapshot
The FvPHR1 transcription factor control phosphate homeostasis by transcriptionally regulating miR399a in woodland strawberry
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111540openalex-snapshot
Root epidermis-specific expression of a phosphate transporter TaPT2 enhances the growth of transgenic Arabidopsis under Pi-replete and Pi-depleted conditions
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