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Low Phosphorus Tolerance Mechanisms: Phosphorus Recycling and Photosynthate Partitioning in the Tropical Forage Grass, Brachiaria Hybrid Cultivar Mulato Compared with Rice
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Aluminum stress stimulates the accumulation of organic acids in root apices of Brachiaria species
inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot
A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
inferredcites →https://doi.org/10.1007/978-94-009-2103-0openalex-snapshot
Progress in Plant Cellular and Molecular Biology
inferredcites →https://doi.org/10.1007/978-94-009-2103-0_51openalex-snapshot
Intracellular Pi-Compartmentation during Phosphate Starvation-Triggered Induction of an Extracellular Ribonuclease in Tomato Cell Culture
inferredcites →https://doi.org/10.1007/978-94-011-1880-4_13openalex-snapshot
Secretion of acid phosphatase by the roots of crop plants under phosphorus-deficient conditions and some properties of the enzyme secreted by lupin Roots
inferredcites →https://doi.org/10.1007/s004250050268openalex-snapshot
Compensation of decreased triose phosphate/phosphate translocator activity by accelerated starch turnover and glucose transport in transgenic tobacco
inferredcites →https://doi.org/10.1007/s004250050273openalex-snapshot
Extracellular administration of phosphate-sequestering metabolites induces ribonucleases in cultured tomato cells
inferredcites →https://doi.org/10.1016/s0378-4290(98)00106-3openalex-snapshot
Differences in tolerance to infertile acid soil stress among germplasm accessions and genetic recombinants of the tropical forage grass genus, Brachiaria
inferredcites →https://doi.org/10.1023/a:1004341415878openalex-snapshot
Distribution and chemical speciation of aluminum in the Al accumulator plant, Melastoma malabathricum L.
inferredcites →https://doi.org/10.1023/a:1004356007312openalex-snapshot
Organic acids in the rhizosphere – a critical review
inferredcites →https://doi.org/10.1023/a:1013329430212openalex-snapshot
Induction of maize acid phosphatase activities under phosphorus starvation
inferredcites →https://doi.org/10.1034/j.1399-3054.1994.900414.xopenalex-snapshot
Carbohydrate accumulation and utilization in soybean plants in response to altered phosphorus nutrition
inferredcites →https://doi.org/10.1046/j.1365-3040.1998.00289.xopenalex-snapshot
Influence of phosphate starvation on phosphohydrolases during development of tomato seedlings
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.6050673.xopenalex-snapshot
The Arabidopsis ribonuclease gene RNS1 is tightly controlled in response to phosphate limitation
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00695.xopenalex-snapshot
Phosphorus acquisition and use: critical adaptations by plants for securing a nonrenewable resource
inferredcites →https://doi.org/10.1080/00380768.1995.10419608openalex-snapshot
Purification and properties of acid phosphatase secreted from lupin roots under phosphorus-deficiency conditions
inferredcites →https://doi.org/10.1080/00380768.1998.10414489openalex-snapshot
Effects of nitrogen source and aluminum on growth of tropical tree seedlings adapted to low pH soils
inferredcites →https://doi.org/10.1080/01904169509365052openalex-snapshot
Adaptive attributes of tropical forage species to acid soils I. Differences in plant growth, nutrient acquisition and nutrient utilization among C4grasses and C3legumes
inferredcites →https://doi.org/10.1093/jexbot/52.358.1083openalex-snapshot
Low sink demand limits photosynthesis under Pi deficiency
inferredcites →https://doi.org/10.1093/jxb/42.8.1003openalex-snapshot
Stomatal and Mesophyll Limitations of Photosynthesis in Phosphate Deficient Sunflower, Maize and Wheat Plants
inferredcites →https://doi.org/10.1093/jxb/47.4.497openalex-snapshot
Phosphorus responses of C 3 and C 4 species
inferredcites →https://doi.org/10.1093/jxb/48.7.1461openalex-snapshot
The role of Pirecycling processes during photosynthesis in phosphate-deficient bean plants
inferredcites →https://doi.org/10.1104/pp.101.2.339openalex-snapshot
Metabolic Adaptations of Plant Respiration to Nutritional Phosphate Deprivation
inferredcites →https://doi.org/10.1104/pp.107.4.1313openalex-snapshot
Leaf Phosphate Status, Photosynthesis, and Carbon Partitioning in Sugar Beet (IV. Changes with Time Following Increased Supply of Phosphate to Low-Phosphate Plants)
inferredcites →https://doi.org/10.1104/pp.125.3.1473openalex-snapshot
The High Level of Aluminum Resistance in Signalgrass Is Not Associated with Known Mechanisms of External Aluminum Detoxification in Root Apices
inferredcites →https://doi.org/10.1104/pp.125.4.1901openalex-snapshot
Induction of a Major Leaf Acid Phosphatase Does Not Confer Adaptation to Low Phosphorus Availability in Common Bean
inferredcites →https://doi.org/10.1104/pp.90.2.734openalex-snapshot
Purification and Characterization of a Phosphoenolpyruvate Phosphatase from Brassica nigra Suspension Cells
inferredcites →https://doi.org/10.1104/pp.90.3.820openalex-snapshot
Leaf Phosphate Status, Photosynthesis and Carbon Partitioning in Sugar Beet
inferredcites →https://doi.org/10.1104/pp.92.4.970openalex-snapshot
Induction of an Extracellular Ribonuclease in Cultured Tomato Cells upon Phosphate Starvation
inferredcites →https://doi.org/10.1104/pp.98.4.1472openalex-snapshot
Phosphate-Regulated Induction of Intracellular Ribonucleases in Cultured Tomato ( Lycopersicon esculentum ) Cells
inferredcites →https://doi.org/10.1111/j.1399-3054.1994.tb02539.xopenalex-snapshot
The role of acid phosphatases in plant phosphorus metabolism
inferredcites →https://doi.org/10.1146/annurev.pp.29.060178.001205openalex-snapshot
Biochemistry and Function of Vacuoles
inferredcites →https://doi.org/10.1146/annurev.pp.45.060194.002225openalex-snapshot
The Ribonucleases of Higher Plants
inferredcites →https://doi.org/10.1201/9780824746728.ch4openalex-snapshot
Plant Adaptation to Phosphorus-Limited Tropical Soils
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Egphl7, Egphr1 and Egphr2 Bind to P1bs and a Unique Motif, Agatwc, for Phosphate Starvation Transcriptional Regulation in Oil Palm
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Interactions between Nitrogen and Phosphorus metabolism
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Interactions between Nitrogen and Phosphorus Metabolism
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A simple high‐throughput protocol for the extraction and quantification of inorganic phosphate in rice leaves
inferred← citeshttps://doi.org/10.1002/csc2.20613openalex-snapshot
Variation of forage quality traits in Tunisian populations of Brachypodium hybridum in response to phosphorus deficiency
inferred← citeshttps://doi.org/10.1002/csc2.21102openalex-snapshot
Straw mulching combined with phosphorus fertilization increased photosynthesis rate and grain yield of wheat due to reduced stomatal and mesophyll limitations
inferred← citeshttps://doi.org/10.1002/pmic.200600960openalex-snapshot
Proteomic analysis of roots growth and metabolic changes under phosphorus deficit in maize ( Zea mays L.) plants
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Proteomics of phosphate use and deprivation in plants
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Proteomics Approach for Identification of Nutrient Deficiency Related Proteins in Crop Plants
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Savannas. II. The Environmental FactorsWater,Mineral Nutrients and Fire
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Roles of Organic Acid Metabolism in Plant Tolerance to Phosphorus-Deficiency
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Phosphorus Deficiency in Plants: Responses, Adaptive Mechanisms, and Signaling
inferred← citeshttps://doi.org/10.1007/978-981-33-4654-3_1openalex-snapshot
Basic Information About Tropical Peatland Ecosystems
inferred← citeshttps://doi.org/10.1007/s00122-018-3257-5openalex-snapshot
ZmAPRG, an uncharacterized gene, enhances acid phosphatase activity and Pi concentration in maize leaf during phosphate starvation
inferred← citeshttps://doi.org/10.1007/s00374-024-01833-wopenalex-snapshot
Assessment of phosphorus use and availability by contrasting crop plants in a tropical soil
inferred← citeshttps://doi.org/10.1007/s00425-010-1311-xopenalex-snapshot
Comparative proteome analysis of metabolic changes by low phosphorus stress in two Brassica napus genotypes
inferred← citeshttps://doi.org/10.1007/s00425-011-1568-8openalex-snapshot
How do nitrogen and phosphorus deficiencies affect strigolactone production and exudation?
inferred← citeshttps://doi.org/10.1007/s00425-013-1943-8openalex-snapshot
Nitrogen and phosphorus fertilization negatively affects strigolactone production and exudation in sorghum
inferred← citeshttps://doi.org/10.1007/s00425-014-2208-xopenalex-snapshot
Shoot-derived signals other than auxin are involved in systemic regulation of strigolactone production in roots
inferred← citeshttps://doi.org/10.1007/s10681-013-1058-0openalex-snapshot
Identification of QTL for acid phosphatase activity in root and rhizosphere soil of maize under low phosphorus stress
inferred← citeshttps://doi.org/10.1007/s10967-020-07383-3openalex-snapshot
Radiochemical evidence validates the involvement of root released organic acid and phytosiderphore in regulating the uptake of phosphorus and certain metal micronutrients in wheat under phosphorus and iron deficiency
inferred← citeshttps://doi.org/10.1007/s11032-013-9895-zopenalex-snapshot
Fine mapping of quantitative trait loci for acid phosphatase activity in maize leaf under low phosphorus stress
inferred← citeshttps://doi.org/10.1007/s11104-004-5026-2openalex-snapshot
Evaluation of phosphorus starvation inducible genes relating to efficient phosphorus utilization in rice
inferred← citeshttps://doi.org/10.1007/s11104-008-9595-3openalex-snapshot
Phosphatase and phytase activities in nodules of common bean genotypes at different levels of phosphorus supply
inferred← citeshttps://doi.org/10.1007/s11104-009-0093-zopenalex-snapshot
A comparative study on plant growth and root plasticity responses of two Brachiaria forage grasses grown in nutrient solution at low and high phosphorus supply
inferred← citeshttps://doi.org/10.1007/s11104-019-04020-1openalex-snapshot
Differences in the relationship between metabolomic and ionomic traits of Quercus variabilis growing at contrasting geologic-phosphorus sites in subtropics
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/s11105-012-0534-3openalex-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/s11105-024-01512-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/s11427-010-4008-2openalex-snapshot
Analysis of the contribution of acid phosphatase to P efficiency in Brassica napus under low phosphorus conditions
inferred← citeshttps://doi.org/10.1007/s11434-007-0277-yopenalex-snapshot
Involvement of a cytoplasmic glyceraldehyde-3-phosphate dehydrogenase GapC-2 in low-phosphate-induced anthocyanin accumulation in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s12374-009-9050-xopenalex-snapshot
Root Proliferation, Proton Efflux, and Acid Phosphatase Activity in Common Bean (Phaseolus vulgaris) Under Phosphorus Shortage
inferred← citeshttps://doi.org/10.1016/j.catena.2016.12.024openalex-snapshot
Slope aspect affects the non-structural carbohydrates and C:N:P stoichiometry of Artemisia sacrorum on the Loess Plateau in China
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2013.06.038openalex-snapshot
Mitigation of peroxidative stress for barley exposed to cadmium in the presence of water-extractable organic matter from compost-like materials
inferred← citeshttps://doi.org/10.1016/j.cj.2021.11.010openalex-snapshot
Agronomic and physiological traits associated with genetic improvement of phosphorus use efficiency of wheat grown in a purple lithomorphic soil
inferred← citeshttps://doi.org/10.1016/j.cpb.2025.100505openalex-snapshot
Integrative multi-omics analysis of rice grown continuously under P-starvation stress unravels Pup1-mediated regulatory complex for resilience to phosphorus deficiency
inferred← citeshttps://doi.org/10.1016/j.ecolind.2015.11.017openalex-snapshot
Leaf non-structural carbohydrates regulated by plant functional groups and climate: Evidences from a tropical to cold-temperate forest transect
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105646openalex-snapshot
Physiological and transcriptomic regulation of Populus simonii fine roots exposed to a heterogeneous phosphorus environment in soil
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.flora.2023.152362openalex-snapshot
Proteaceae species show different strategies for phosphorus acquisition and utilisation in P poor soils in the Mediterranean-type Fynbos ecosystem
inferred← citeshttps://doi.org/10.1016/j.indcrop.2021.114095openalex-snapshot
Effects of low phosphorus stress on the main active ingredients and antioxidant activities of Dendrobium officinale
inferred← citeshttps://doi.org/10.1016/j.jplph.2010.09.017openalex-snapshot
Root release and metabolism of organic acids in tea plants in response to phosphorus supply
inferred← citeshttps://doi.org/10.1016/j.jplph.2011.09.002openalex-snapshot
Transcriptome profiling characterizes phosphate deficiency effects on carbohydrate metabolism in rice leaves
inferred← citeshttps://doi.org/10.1016/j.jplph.2019.153051openalex-snapshot
Photosynthetic metabolism during phosphate limitation in a legume from the Mediterranean-type Fynbos ecosystem
inferred← citeshttps://doi.org/10.1016/j.jplph.2022.153838openalex-snapshot
Watermelon responds to organic fertilizer by enhancing root-associated acid phosphatase activity to improve organic phosphorus utilization
inferred← citeshttps://doi.org/10.1016/j.plantsci.2007.02.020openalex-snapshot
Metabolic alterations proposed by proteome in rice roots grown under low P and high Al concentration under low pH
inferred← citeshttps://doi.org/10.1016/j.plaphy.2014.02.024openalex-snapshot
Overexpression of OsMYB4P, an R2R3-type MYB transcriptional activator, increases phosphate acquisition in rice
inferred← citeshttps://doi.org/10.1016/j.plaphy.2014.03.029openalex-snapshot
Identification of nutrient deficiency in maize and tomato plants by in vivo chlorophyll a fluorescence measurements
inferred← citeshttps://doi.org/10.1016/j.plaphy.2016.10.017openalex-snapshot
Comparative transcript profiling of maize inbreds in response to long-term phosphorus deficiency stress
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.2023.108006openalex-snapshot
Polyphosphate promotes oxidation resistance of ppk-expressing transgenic rice in low phosphorus culture
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110230openalex-snapshot
A novel glycerophosphodiester phosphodiesterase 13 is involved in the phosphate starvation-induced phospholipid degradation in rice
inferred← citeshttps://doi.org/10.1016/j.plares.2026.100008openalex-snapshot
Straw returning improves rice yield by enhancing phosphorus availability and promoting root development in coastal saline-alkali soils
inferred← citeshttps://doi.org/10.1016/j.rhisph.2022.100486openalex-snapshot
Soil pH influences the organic acid metabolism and exudation in cluster roots of Protea species from the Mediterranean-type fynbos ecosystem, Western Cape, South Africa
inferred← citeshttps://doi.org/10.1016/j.rsci.2023.03.007openalex-snapshot
Polyphosphate Accelerates Transformation of Nonstructural Carbohydrates to Improve Growth of ppk-Expressing Transgenic Rice in Phosphorus Deficiency Culture
inferred← citeshttps://doi.org/10.1016/j.rsci.2023.04.007openalex-snapshot
Phosphorus Starvation Tolerance in Rice Through Combined Physiological, Biochemical, and Proteome Analyses
inferred← citeshttps://doi.org/10.1016/j.sajb.2025.07.030openalex-snapshot
Seasonality alters nitrogen and phosphorus metabolism of Aspalathus linearis (Burm.f.) R.Dahlgren
inferred← citeshttps://doi.org/10.1016/j.scienta.2014.07.037openalex-snapshot
Overexpression of the rice phosphate transporter gene OsPT6 enhances tolerance to low phosphorus stress in vegetable soybean
inferred← citeshttps://doi.org/10.1016/j.still.2024.106228openalex-snapshot
Legacy soil phosphorus bioavailability in tropical and temperate soils: Implications for sustainable crop production
inferred← citeshttps://doi.org/10.1017/s0021859619000133openalex-snapshot
Time to move beef cattle to a new paddock: forage quality and grazing behaviour
inferred← citeshttps://doi.org/10.1038/s41598-020-73398-1openalex-snapshot
Exudation of organic acid anions by tropical grasses in response to low phosphorus availability
inferred← citeshttps://doi.org/10.1071/fp15262openalex-snapshot
Variable P supply affects N metabolism in a legume tree, Virgilia divaricata, from nutrient-poor Mediterranean-type ecosystems
inferred← citeshttps://doi.org/10.1080/00380768.2019.1666301openalex-snapshot
Research on ways to improve crop productivity through the regulation of rhizosphere environments
inferred← citeshttps://doi.org/10.1080/01904167.2013.780613openalex-snapshot
METABOLITE PROFILING OF SHOOT EXTRACTS, ROOT EXTRACTS, AND ROOT EXUDATES OF RICE PLANT UNDER PHOSPHORUS DEFICIENCY
inferred← citeshttps://doi.org/10.1080/01904167.2013.867979openalex-snapshot
METABOLIC CHANGE, TILLERING AND ROOT SYSTEM OFBRACHIARIA BRIZANTHAIN RESPONSE TO PHOSPHORUS AND ZINC NUTRITION
inferred← citeshttps://doi.org/10.1080/01904167.2014.939758openalex-snapshot
Photosynthesis and Leaf Area ofBrachiaria brizanthain Response to Phosphorus and Zinc Nutrition
inferred← citeshttps://doi.org/10.1080/01904167.2015.1061543openalex-snapshot
Inoculation with Phosphate Solubilizing Mesorhizobium Strains Improves the Performance of Chickpea (Cicer ariteniumL.) Under Phosphorus Deficiency
inferred← citeshttps://doi.org/10.1080/01904167.2015.1109117openalex-snapshot
Non-labile phosphorus acquisition byBrachiaria
inferred← citeshttps://doi.org/10.1080/01904167.2019.1567774openalex-snapshot
Partitioning of above and below ground costs during phosphate stress in Medicago truncatula
inferred← citeshttps://doi.org/10.1093/jxb/eraa211openalex-snapshot
The ferroxidase LPR5 functions in the maintenance of phosphate homeostasis and is required for normal growth and development of rice
inferred← citeshttps://doi.org/10.1093/jxb/erae068openalex-snapshot
The ZmNF-YC1–ZmAPRG pathway modulates low phosphorus tolerance in maize
inferred← citeshttps://doi.org/10.1093/jxb/erj158openalex-snapshot
Transcriptomic analysis indicates putative metabolic changes caused by manipulation of phosphorus availability in rice leaves
inferred← citeshttps://doi.org/10.1093/jxb/erq183openalex-snapshot
Nitrogen to phosphorus ratio of plant biomass versus soil solution in a tropical pioneer tree, Ficus insipida
inferred← citeshttps://doi.org/10.1093/jxb/erq335openalex-snapshot
The regulation of arbuscular mycorrhizal symbiosis by phosphate in pea involves early and systemic signalling events
inferred← citeshttps://doi.org/10.1093/pcp/pcn044openalex-snapshot
Metabolite Profiling Reveals Distinct Changes in Carbon and Nitrogen Metabolism in Phosphate-Deficient Barley Plants (Hordeum vulgare L.)
inferred← citeshttps://doi.org/10.1093/pcp/pcv162openalex-snapshot
OsSIZ1, a SUMO E3 Ligase Gene, is Involved in the Regulation of the Responses to Phosphate and Nitrogen in Rice
inferred← citeshttps://doi.org/10.1093/treephys/tpr064openalex-snapshot
How does P affect photosynthesis and metabolite profiles of Eucalyptus globulus?
inferred← citeshttps://doi.org/10.1094/pdis-10-24-2202-reopenalex-snapshot
The Power of Daldinia eschscholtzii MFLUCC 20-0215 Fungal Endophytes Native to Nibung Palm ( Oncosperma sp.) in Stimulating Plant Growth
inferred← citeshttps://doi.org/10.1104/pp.107.111443openalex-snapshot
OsPHR2 Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
inferred← citeshttps://doi.org/10.1104/pp.110.170209openalex-snapshot
LEAF TIP NECROSIS1 Plays a Pivotal Role in the Regulation of Multiple Phosphate Starvation Responses in Rice
inferred← citeshttps://doi.org/10.1105/tpc.18.00051openalex-snapshot
Alternative Splicing Plays a Critical Role in Maintaining Mineral Nutrient Homeostasis in Rice ( Oryza sativa )
inferred← citeshttps://doi.org/10.1111/aab.12694openalex-snapshot
Differential responses of three Urochloa species to low phosphorus availability
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2005.01002.xopenalex-snapshot
Nutrient limitation and enzyme activities during litter decomposition of nine wetland species in relation to litter N : P ratios
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2008.01478.xopenalex-snapshot
N : P ratios influence litter decomposition and colonization by fungi and bacteria in microcosms
inferred← citeshttps://doi.org/10.1111/j.1365-2486.2008.01618.xopenalex-snapshot
Accentuation of phosphorus limitation in Geranium dissectum by nitrogen: an ecological genomics study
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2006.01568.xopenalex-snapshot
Cytokinin represses phosphate‐starvation response through increasing of intracellular phosphate level
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2004.01192.xopenalex-snapshot
N : P ratios in terrestrial plants: variation and functional significance
inferred← citeshttps://doi.org/10.1111/j.1747-0765.2005.tb00058.xopenalex-snapshot
The Function of a Maize-Derived Phosphoenolpyruvate Carboxylase (PEPC) in Phosphorus-Deficient Transgenic Rice
inferred← citeshttps://doi.org/10.1111/j.1747-0765.2008.00329.xopenalex-snapshot
Overexpression of theLASAP2gene for secretory acid phosphatase in white lupin improves the phosphorus uptake and growth of tobacco plants
inferred← citeshttps://doi.org/10.1111/nph.20266openalex-snapshot
MicroRNA399s and strigolactones mediate systemic phosphate signaling between dodder‐connected host plants and control association of host plants with rhizosphere microbes
inferred← citeshttps://doi.org/10.1111/pbi.12394openalex-snapshot
Suppression of glucan, water dikinase in the endosperm alters wheat grain properties, germination and coleoptile growth
inferred← citeshttps://doi.org/10.1111/pce.12170openalex-snapshot
Functional properties and expression quantitative trait loci for phosphate transporter GmPT1 in soybean
inferred← citeshttps://doi.org/10.1111/pce.12224openalex-snapshot
Phosphate transporters OsPHT1 ;9 and OsPHT1 ;10 are involved in phosphate uptake in rice
inferred← citeshttps://doi.org/10.1111/ppl.70082openalex-snapshot
Unravelling OsPHT2 ;1 function in Chloroplast Phosphorus Homeostasis and Photosynthetic Efficiency under Low Phosphorus Stress in Rice
inferred← citeshttps://doi.org/10.1111/ppl.70551openalex-snapshot
Integrated Proteomic and Physiological Profiling of Phosphate Stress Response in Potato ( Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.1111/tpj.17014openalex-snapshot
Arabidopsis hydathodes are sites of auxin accumulation and nutrient scavenging
inferred← citeshttps://doi.org/10.1155/2015/405970openalex-snapshot
Response of Sugarcane in a Red Ultisol to Phosphorus Rates, Phosphorus Sources, and Filter Cake
inferred← citeshttps://doi.org/10.11606/d.11.2011.tde-11022011-091924openalex-snapshot
Respostas fisiológicas, metabólicas, estruturais e produtivas do capim-marandu às disponibilidades de fósforo e zinco
inferred← citeshttps://doi.org/10.11606/d.11.2018.tde-15052018-102745openalex-snapshot
Desempenho de biofertilizante fosfatado na nutrição de plantas de milho
inferred← citeshttps://doi.org/10.11606/d.11.2020.tde-05052020-145936openalex-snapshot
Ciclagem de fósforo pela braquiária consorciada com o cafeeiro
inferred← citeshttps://doi.org/10.11606/t.11.2014.tde-17042014-085602openalex-snapshot
Eficiência de uso de fósforo por cultivares de café e adaptação morfológica do sistema radicular sob deficiência do nutriente.
inferred← citeshttps://doi.org/10.11606/t.74.2014.tde-31032015-085538openalex-snapshot
Manejo do horário da colheita do capim-marandu sob corte ou pastejo
inferred← citeshttps://doi.org/10.1186/1471-2229-9-43openalex-snapshot
CO2assimilation, ribulose-1,5-bisphosphate carboxylase/oxygenase, carbohydrates and photosynthetic electron transport probed by the JIP-test, of tea leaves in response to phosphorus supply
inferred← citeshttps://doi.org/10.1186/s12870-023-04521-3openalex-snapshot
Nanosilica enhances morphogenic and chemical parameters of Megathyrsus maximus grass under conditions of phosphorus deficiency and excess stress in different soils
inferred← citeshttps://doi.org/10.1186/s13007-017-0227-xopenalex-snapshot
A dual isotopic approach using radioactive phosphorus and the isotopic composition of oxygen associated to phosphorus to understand plant reaction to a change in P nutrition
inferred← citeshttps://doi.org/10.1201/b16675-49openalex-snapshot
Advances in Improving Adaptation of Common Bean and Brachiaria Forage Grasses to Abiotic Stresses in the Tropics
inferred← citeshttps://doi.org/10.1371/journal.pone.0129520openalex-snapshot
Metabolite Profiling of Low-P Tolerant and Low-P Sensitive Maize Genotypes under Phosphorus Starvation and Restoration Conditions
inferred← citeshttps://doi.org/10.1590/18069657rbcs20150128openalex-snapshot
Brachiaria as a Cover Crop to Improve Phosphorus Use Efficiency in a No-till Oxisol
inferred← citeshttps://doi.org/10.1590/18069657rbcs20170245openalex-snapshot
Rhizophagus Clarus and Phosphorus in Crotalaria juncea: Growth, Glomalin Content and Acid Phosphatase Activity in a Copper-Contaminated Soil
inferred← citeshttps://doi.org/10.1590/s0100-06832008000200025openalex-snapshot
Frações de fósforo em solo adubado com fosfatos em diferentes modos de aplicação e cultivado com milho
inferred← citeshttps://doi.org/10.1590/s0100-06832008000500011openalex-snapshot
Atividade de fosfatases em gramíneas forrageiras em resposta à disponibilidade de fósforo no solo e à altura de corte das plantas
inferred← citeshttps://doi.org/10.1590/s0100-06832012000200018openalex-snapshot
Eficiência de absorção e utilização de fósforo em porta-enxertos cítricos
inferred← citeshttps://doi.org/10.17138/tgft(5)103-116openalex-snapshot
Temporal differences in plant growth and root exudation of two Brachiaria grasses in response to low phosphorus supply
inferred← citeshttps://doi.org/10.17221/348/2020-pseopenalex-snapshot
Genotype difference in the physiological characteristics of phosphorus acquisition by wheat seedlings in alkaline soils
inferred← citeshttps://doi.org/10.18539/cast.v14i4.1949openalex-snapshot
Advances in developing screening methods and improving aluminum resistance in common bean and Brachiaria
inferred← citeshttps://doi.org/10.20710/dojo.83.2_173openalex-snapshot
リン酸資源の枯渇に対応したリン栄養研究 : 1. 講座のねらい
inferred← citeshttps://doi.org/10.20710/dojo.83.6_703openalex-snapshot
リン酸資源の枯渇に対応したリン栄養研究 : 5. 植物体内におけるリン酸利用効率
inferred← citeshttps://doi.org/10.2134/agronj2017.08.0451openalex-snapshot
Soil Phosphorus Bioavailability and Soybean Grain Yield Impaired by Ruzigrass
inferred← citeshttps://doi.org/10.22541/au.164864228.85785532/v1openalex-snapshot
Broad adaptive genetic differentiation in forage quality traits but similar phenotypic plasticity in Tunisian populations of Brachypodium hybridum in response to phosphorus deficiency
inferred← citeshttps://doi.org/10.24198/dharmakarya.v11i2.35850openalex-snapshot
PENGENALAN PEMANFAATAN RUMPUT MULATO DAN TEKNOLOGI PENGAWETANNYA SEBAGAI UPAYA PENINGKATAN PRODUKTIVITAS TERNAK RUMINANSIA
inferred← citeshttps://doi.org/10.3389/fpls.2013.00426openalex-snapshot
High phosphate reduces host ability to develop arbuscular mycorrhizal symbiosis without affecting root calcium spiking responses to the fungus
inferred← citeshttps://doi.org/10.3389/fpls.2019.00995openalex-snapshot
Genotypic Variation in the Root and Shoot Metabolite Profiles of Wheat (Triticum aestivum L.) Indicate Sustained, Preferential Carbon Allocation as a Potential Mechanism in Phosphorus Efficiency
inferred← citeshttps://doi.org/10.3389/fpls.2020.00438openalex-snapshot
Do Phosphate and Cytokinin Interact to Regulate Strigolactone Biosynthesis or Act Independently?
inferred← citeshttps://doi.org/10.3389/fpls.2020.607878openalex-snapshot
Ca14-3-3 Interacts With CaWRKY58 to Positively Modulate Pepper Response to Low-Phosphorus Starvation
inferred← citeshttps://doi.org/10.3389/fpls.2022.943788openalex-snapshot
Genome-Wide Analysis of DoSPX Genes and the Function of DoSPX4 in Low Phosphorus Response in Dendrobium officinale
inferred← citeshttps://doi.org/10.3389/fpls.2022.989827openalex-snapshot
Low phosphorus induces differential metabolic responses in eucalyptus species improving nutrient use efficiency
inferred← citeshttps://doi.org/10.3390/agronomy12071613openalex-snapshot
Effects of Nitrogen and Phosphorus Addition on Agronomic Characters, Photosynthetic Performance and Anatomical Structure of Alfalfa in Northern Xinjiang, China
inferred← citeshttps://doi.org/10.3390/cimb43020081openalex-snapshot
Combined Transcriptome and Proteome Analysis of Maize (Zea mays L.) Reveals A Complementary Profile in Response to Phosphate Deficiency
inferred← citeshttps://doi.org/10.3390/grasses3030013openalex-snapshot
Dynamics of Mulatto Grass Regrowth Depending on Rotational Cattle Grazing Management
inferred← citeshttps://doi.org/10.3390/ijms19010241openalex-snapshot
Improvement of Verticillium Wilt Resistance by Applying Arbuscular Mycorrhizal Fungi to a Cotton Variety with High Symbiotic Efficiency under Field Conditions
inferred← citeshttps://doi.org/10.3390/jof8070690openalex-snapshot
Comparative Genomics of Three Aspergillus Strains Reveals Insights into Endophytic Lifestyle and Endophyte-Induced Plant Growth Promotion
inferred← citeshttps://doi.org/10.3390/metabo11040217openalex-snapshot
The Dynamic Responses of Oil Palm Leaf and Root Metabolome to Phosphorus Deficiency
inferred← citeshttps://doi.org/10.3390/molecules23051132openalex-snapshot
Salvia castanea Hairy Roots are More Tolerant to Phosphate Deficiency than Salvia miltiorrhiza Hairy Roots Based on the Secondary Metabolism and Antioxidant Defenses
inferred← citeshttps://doi.org/10.3390/plants12122326openalex-snapshot
The Splicing Factor OsSCL26 Regulates Phosphorus Homeostasis in Rice
inferred← citeshttps://doi.org/10.3390/plants15162444openalex-snapshot
Genome-Wide Identification of the Maize TALE Gene Family and Their Expression Analysis Under Low-Phosphorus Response in Maize (Zea mays L.)
inferred← citeshttps://doi.org/10.3839/jksabc.2011.102openalex-snapshot
A Comparative Proteomics Survey of Proteins Responsive to Phosphorous Starvation in Roots of Hydroponically-grown Rice Seedlings
inferred← citeshttps://doi.org/10.4236/ajps.2014.54059openalex-snapshot
Overexpression of OsMAPK2 Enhances Low Phosphate Tolerance in Rice and Arabidopsis thaliana
inferred← citeshttps://doi.org/10.5772/30334openalex-snapshot
Physiological and Biochemical Mechanisms of Plant Adaptation to Low-Fertility Acid Soils of the Tropics: The Case of Brachiariagrasses
inferred← citeshttps://doi.org/10.70675/fad735c1za992z40dcza0e7z13d4b660b6e3openalex-snapshot
Modélisation mécaniste des interactions rhizosphériques déterminant la facilitation d’acquisition du phosphore en association céréale-légumineuse
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