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Phosphorus Stress in Common Bean: Root Transcript and Metabolic Responses

https://doi.org/10.1104/pp.107.096958

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/anbo.2000.1133openalex-snapshot

Proteoid Root Development of Phosphorus Deficient Lupin is Mimicked by Auxin and Phosphonate

inferredcites →https://doi.org/10.1007/978-1-59745-244-1_2openalex-snapshot

Nonsupervised Construction and Application of Mass Spectral and Retention Time Index Libraries From Time-of-Flight Gas Chromatography-Mass Spectrometry Metabolite Profiles

inferredcites →https://doi.org/10.1007/978-94-010-0566-1_11openalex-snapshot

Sulphur and phosphorus transport systems in plants

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A sucrose-synthase gene of Vicia faba L.: Expression pattern in developing seeds in relation to starch synthesis and metabolic regulation

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A simple and efficient method for isolating RNA from pine trees

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Transcripts of MYB-like genes respond to phosphorous and nitrogen deprivation in Arabidopsis

inferredcites →https://doi.org/10.1007/s00425-006-0408-8openalex-snapshot

Phosphate starvation responses are mediated by sugar signaling in Arabidopsis

inferredcites →https://doi.org/10.1007/s11104-004-2005-6openalex-snapshot

Phosphate Acquisition

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/10.1016/j.febslet.2005.01.029openalex-snapshot

GC–MS libraries for the rapid identification of metabolites in complex biological samples

inferredcites →https://doi.org/10.1016/s0021-9258(18)66180-0openalex-snapshot

A MICROCOLORIMETRIC METHOD FOR THE DETERMINATION OF INORGANIC PHOSPHORUS

inferredcites →https://doi.org/10.1016/s0031-9422(02)00703-3openalex-snapshot

Construction and application of a mass spectral and retention time index database generated from plant GC/EI-TOF-MS metabolite profiles

inferredcites →https://doi.org/10.1016/s0098-8472(02)00009-6openalex-snapshot

Exudation of organic acids in common bean as related to mobilization of aluminum- and iron-bound phosphates

inferredcites →https://doi.org/10.1016/s0176-1617(11)81192-2openalex-snapshot

The Spectral Determination of Chlorophylls a and b, as well as Total Carotenoids, Using Various Solvents with Spectrophotometers of Different Resolution

inferredcites →https://doi.org/10.1016/s0378-4290(03)00037-6openalex-snapshot

Addressing edaphic constraints to bean production: the Bean/Cowpea CRSP project in perspective

inferredcites →https://doi.org/10.1016/s1369-5266(03)00035-9openalex-snapshot

The role of nutrient availability in regulating root architecture

inferredcites →https://doi.org/10.1017/s0014479700007638openalex-snapshot

Plant Husbandry and Management Techniques for Growing Grain Legumes Under Simulated Tropical Conditions in Controlled Environments

inferredcites →https://doi.org/10.1017/s0014479700007705openalex-snapshot

A Simple Unit for Extracting Leaf Protein in Bulk

inferredcites →https://doi.org/10.1023/a:1004380832118openalex-snapshot

Root excretion of carboxylic acids and protons in phosphorus-deficient plants

inferredcites →https://doi.org/10.1023/a:1006873932486openalex-snapshot

The influence of phosphate deficiency on photosynthesis, respiration and adenine nucleotide pool in bean leaves

inferredcites →https://doi.org/10.1023/a:1010381919003openalex-snapshot

Effect of phosphorus availability on basal root shallowness in common bean

inferredcites →https://doi.org/10.1023/a:1010390120820openalex-snapshot

Sulphur and phosphorus transport systems in plants

inferredcites →https://doi.org/10.1023/a:1013324727040openalex-snapshot

Topsoil foraging – an architectural adaptation of plants to low phosphorus availability

inferredcites →https://doi.org/10.1023/a:1014987710937openalex-snapshot

The importance of root gravitropism for inter-root competition and phosphorus acquisition efficiency: results from a geometric simulation model

inferredcites →https://doi.org/10.1023/a:1024146710611openalex-snapshot

Beans (Phaseolus spp.) – model food legumes

inferredcites →https://doi.org/10.1034/j.1399-3054.1994.910305.xopenalex-snapshot

The effect of phosphate deficiency on carbohydrate metabolism in bean roots

inferredcites →https://doi.org/10.1046/j.0960-7412.2001.00233.xopenalex-snapshot

Prior exposure to lipopolysaccharide potentiates expression of plant defenses in response to bacteria

inferredcites →https://doi.org/10.1046/j.1365-3040.2003.01030.xopenalex-snapshot

Temporal responses of Arabidopsis root architecture to phosphate starvation: evidence for the involvement of auxin signalling

inferredcites →https://doi.org/10.1046/j.1365-3040.2003.01074.xopenalex-snapshot

Transcriptomic analysis of metabolic changes by phosphorus stress in rice plant roots

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/10.1071/fp06101openalex-snapshot

Identification of candidate phosphorus stress induced genes in Phaseolus vulgaris through clustering analysis across several plant species

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.96.9.5322openalex-snapshot

Regulatory interaction of PRL1 WD protein with Arabidopsis SNF1-like protein kinases

inferredcites →https://doi.org/10.1078/0176-1617-00541openalex-snapshot

Oxidative stress during phosphate deficiency in roots of bean plants (Phaseolus vulgaris L.)

inferredcites →https://doi.org/10.1093/bioinformatics/bth270openalex-snapshot

Metabolite fingerprinting: detecting biological features by independent component analysis

inferredcites →https://doi.org/10.1093/bioinformatics/bti236openalex-snapshot

GMD@CSB.DB: the Golm Metabolome Database

inferredcites →https://doi.org/10.1093/bioinformatics/bti634openalex-snapshot

Non-linear PCA: a missing data approach

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/erj158openalex-snapshot

Transcriptomic analysis indicates putative metabolic changes caused by manipulation of phosphorus availability in rice leaves

inferredcites →https://doi.org/10.1093/nar/25.17.3389openalex-snapshot

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

inferredcites →https://doi.org/10.1093/nar/29.1.159openalex-snapshot

The TIGR Gene Indices: analysis of gene transcript sequences in highly sampled eukaryotic species

inferredcites →https://doi.org/10.1093/nar/gkh063openalex-snapshot

The KEGG resource for deciphering the genome

inferredcites →https://doi.org/10.1093/nar/gkh131openalex-snapshot

UniProt: the Universal Protein knowledgebase

inferredcites →https://doi.org/10.1093/pcp/pci011openalex-snapshot

Phosphate Starvation Induces a Determinate Developmental Program in the Roots of Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/pcp/pci145openalex-snapshot

Reactive Oxygen Species and Root Hairs in Arabidopsis Root Response to Nitrogen, Phosphorus and Potassium Deficiency

inferredcites →https://doi.org/10.1094/mpmi-19-0330openalex-snapshot

Insights into Symbiotic Nitrogen Fixation in Medicago truncatula

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.008854openalex-snapshot

Rapid Induction of Regulatory and Transporter Genes in Response to Phosphorus, Potassium, and Iron Deficiencies in Tomato Roots. Evidence for Cross Talk and Root/Rhizosphere-Mediated Signals

inferredcites →https://doi.org/10.1104/pp.012161openalex-snapshot

Regulation of Root Elongation under Phosphorus Stress Involves Changes in Ethylene Responsiveness

inferredcites →https://doi.org/10.1104/pp.102.016881openalex-snapshot

Nylon Filter Arrays Reveal Differential Gene Expression in Proteoid Roots of White Lupin in Response to Phosphorus Deficiency

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.104.046482openalex-snapshot

The Potassium-Dependent Transcriptome of Arabidopsis Reveals a Prominent Role of Jasmonic Acid in Nutrient Signaling

inferredcites →https://doi.org/10.1104/pp.104.054957openalex-snapshot

Lotus japonicus Metabolic Profiling. Development of Gas Chromatography-Mass Spectrometry Resources for the Study of Plant-Microbe Interactions

inferredcites →https://doi.org/10.1104/pp.104.054999openalex-snapshot

Sequencing and Analysis of Common Bean ESTs. Building a Foundation for Functional Genomics

inferredcites →https://doi.org/10.1104/pp.105.060061openalex-snapshot

A Role for Auxin Redistribution in the Responses of the Root System Architecture to Phosphate Starvation in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.105.063115openalex-snapshot

OsPTF1, a Novel Transcription Factor Involved in Tolerance to Phosphate Starvation in Rice

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.106.082073openalex-snapshot

Large Expression Differences in Genes for Iron and Zinc Homeostasis, Stress Response, and Lignin Biosynthesis Distinguish Roots of Arabidopsis thaliana and the Related Metal Hyperaccumulator Thlaspi caerulescens

inferredcites →https://doi.org/10.1104/pp.106.087965openalex-snapshot

Heterologous Expression and Molecular and Cellular Characterization of CaPUB1 Encoding a Hot Pepper U-Box E3 Ubiquitin Ligase Homolog

inferredcites →https://doi.org/10.1104/pp.106.090167openalex-snapshot

Genome-Wide Analysis of the Arabidopsis Leaf Transcriptome Reveals Interaction of Phosphate and Sugar Metabolism

inferredcites →https://doi.org/10.1104/pp.106.093971openalex-snapshot

WRKY75 Transcription Factor Is a Modulator of Phosphate Acquisition and Root Development in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.107.1.7openalex-snapshot

The Shikimate Pathway as an Entry to Aromatic Secondary Metabolism

inferredcites →https://doi.org/10.1104/pp.109.1.7openalex-snapshot

Root Architecture and Plant Productivity

inferredcites →https://doi.org/10.1104/pp.112.1.19openalex-snapshot

Root Carbon Dioxide Fixation by Phosphorus-Deficient Lupinus albus (Contribution to Organic Acid Exudation by Proteoid Roots)

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.010410openalex-snapshot

Expression Profile Matrix of Arabidopsis Transcription Factor Genes Suggests Their Putative Functions in Response to Environmental Stresses[W]

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.1365-3040.2006.01608.xopenalex-snapshot

Genome‐wide reprogramming of metabolism and regulatory networks of Arabidopsis in response to phosphorus

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02051.xopenalex-snapshot

Real‐time RT‐PCR profiling of over 1400 Arabidopsis transcription factors: unprecedented sensitivity reveals novel root‐ and shoot‐specific genes

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02150.xopenalex-snapshot

Global changes in transcription orchestrate metabolic differentiation during symbiotic nitrogen fixation in Lotus japonicus

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02289.xopenalex-snapshot

Signaling of phosphorus deficiency‐induced gene expression in white lupin requires sugar and phloem transport

inferredcites →https://doi.org/10.1111/j.1399-3054.2004.00373.xopenalex-snapshot

Organic acid exudation induced by phosphorus deficiency and/or aluminium toxicity in two contrasting soybean genotypes

inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.665openalex-snapshot

PHOSPHATE ACQUISITION

inferredcites →https://doi.org/10.1199/tab.0085openalex-snapshot

Transcriptional Regulation: a Genomic Overview

inferredcites →https://doi.org/10.1378/chest.93.2.446aopenalex-snapshot

Effect of Phosphates?

inferredcites →https://doi.org/10.1385/1-59259-192-2:365openalex-snapshot

Primer3 on the WWW for General Users and for Biologist Programmers

inferredcites →https://doi.org/10.2135/cropsci2005.0226openalex-snapshot

Quantitative Trait Loci for Root Architecture Traits Correlated with Phosphorus Acquisition in Common Bean

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.4793846openalex-extracted

The Growth and Physiological Response of Gleditsia Sinensis Lam. Seedlings with Different Phosphorus Efficiencies to Low Phosphorus Stress

inferred← citeshttps://doi.org/10.1002/9780470015902.a0020105.pub2openalex-snapshot

Metabolite Profiling in Plants

inferred← citeshttps://doi.org/10.1002/9780470960707.ch12openalex-snapshot

Phosphorus as a Critical Macronutrient

inferred← citeshttps://doi.org/10.1002/9781118517994.ch10openalex-snapshot

Breeding Approaches to Increasing Nutrient‐Use Efficiency

inferred← citeshttps://doi.org/10.1002/9781118789971.ch4openalex-snapshot

Alternative pathways and phosphate and nitrogen nutrition

inferred← citeshttps://doi.org/10.1002/9781118917091.ch13openalex-snapshot

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inferred← citeshttps://doi.org/10.1002/9781118958841.ch3openalex-snapshot

‘Omics’ Approaches Towards Understanding Plant Phosphorus Acquisition and Use

inferred← citeshttps://doi.org/10.1002/9781118958841.ch8openalex-snapshot

Metabolomics of plant phosphorus‐starvation response

inferred← citeshttps://doi.org/10.1002/9781119312994.apr0518openalex-snapshot

‘Omics’ Approaches Towards Understanding Plant Phosphorus Acquisition and Use

inferred← citeshttps://doi.org/10.1002/9781119312994.apr0523openalex-snapshot

Metabolomics of Plant Phosphorus‐Starvation Response

inferred← citeshttps://doi.org/10.1002/9781119312994.apr0627openalex-snapshot

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inferred← citeshttps://doi.org/10.1002/pmic.200800292openalex-snapshot

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inferred← citeshttps://doi.org/10.1002/tpg2.20098openalex-snapshot

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Genome-wide identification of phosphate-deficiency-responsive genes in soybean roots by high-throughput sequencing

inferred← citeshttps://doi.org/10.1007/s11104-018-3701-yopenalex-snapshot

Effects of Bacillus amyloliquefaciens and different phosphorus sources on Maize plants as revealed by NMR and GC-MS based metabolomics

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/s11104-023-05939-2openalex-snapshot

Plantation rhizosphere soil microbes promote soil‒plant phosphorus feedback on the Tibetan Plateau

inferred← citeshttps://doi.org/10.1007/s11105-019-01188-9openalex-snapshot

Expression of the Legume-Specific Nod Factor Receptor Proteins Alters Developmental and Immune Responses in Rice

inferred← citeshttps://doi.org/10.1007/s11306-008-0152-0openalex-snapshot

Environmental metabolomics: a critical review and future perspectives

inferred← citeshttps://doi.org/10.1007/s11738-010-0612-9openalex-snapshot

MAX4 gene is involved in the regulation of low inorganic phosphate stress responses in Arabidopsis thaliana

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/s11738-021-03280-8openalex-snapshot

Variation in P-acquisition ability and acid phosphatase activity at the early vegetative stage of lentil and their validation on P-deficiency field

inferred← citeshttps://doi.org/10.1007/s11816-016-0422-7openalex-snapshot

Rhizobium etli bacteroids engineered for Vitreoscilla hemoglobin expression alleviate oxidative stress in common bean nodules that reprogramme global gene expression

inferred← citeshttps://doi.org/10.1007/s11816-021-00737-7openalex-snapshot

Regulation of OsLPR1 gene on the formation of rice root iron plaque under low phosphorus

inferred← citeshttps://doi.org/10.1007/s12298-023-01319-3openalex-snapshot

Metabolic footprints in phosphate-starved plants

inferred← citeshttps://doi.org/10.1007/s12892-019-0277-0openalex-snapshot

Effects of Nitrogen, Phosphorus and Potassium Fertilizers on Growth Characteristics of Two Species of Bellflower (Platycodon grandiflorum)

inferred← citeshttps://doi.org/10.1007/s13199-022-00882-9openalex-snapshot

Nitrogen fixation capacity and metabolite responses to phosphorus in soybean nodules

inferred← citeshttps://doi.org/10.1007/s40502-022-00650-3openalex-snapshot

Regulatory role of organic acids and phytochelators in influencing the rhizospheric availability of phosphorus and iron and their uptake by plants

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/10.1016/b978-0-12-802922-0.00007-8openalex-snapshot

Exploration and Utilization of Aluminum-Tolerant Barley Germplasm

inferred← citeshttps://doi.org/10.1016/b978-0-12-812689-9.00024-8openalex-snapshot

Plant Physiological Responses to Nutrient Solution

inferred← citeshttps://doi.org/10.1016/b978-0-12-814872-3.00003-5openalex-snapshot

Metabolomics Studies of Stress in Plants

inferred← citeshttps://doi.org/10.1016/b978-0-12-818204-8.00025-4openalex-snapshot

Abiotic-stress tolerance in plants-system biology approach

inferred← citeshttps://doi.org/10.1016/b978-0-443-27424-4.00012-4openalex-snapshot

Transcription factors and their role in multiple abiotic stress tolerance in plants

inferred← citeshttps://doi.org/10.1016/b978-0-443-36457-0.00013-4openalex-snapshot

Introduction to systems biology in crop improvement

inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00690-0openalex-snapshot

1-Aminocyclopropane-1-Carboxylate Synthase, an Enzyme of Ethylene Biosynthesis

inferred← citeshttps://doi.org/10.1016/j.apsoil.2013.12.011openalex-snapshot

Compatibility of Rhizobium inoculant and water hyacinth compost formulations in Rosecoco bean and consequences on Aphis fabae and Colletotrichum lindemuthianum infestations

inferred← citeshttps://doi.org/10.1016/j.bbrc.2025.152426openalex-snapshot

Overexpression of the GsPPC4 gene from Gleditsia sinensis enhances low phosphate tolerance in tobacco by promoting organic acid secretion

inferred← citeshttps://doi.org/10.1016/j.bcab.2012.01.004openalex-snapshot

Progeny of tobacco mosaic virus-infected Nicotiana tabacum plants exhibit trans-generational changes in metabolic profiles

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.chemosphere.2021.130318openalex-snapshot

Sufficient nitrogen promoted high phosphorus tolerance and phosphorus-accumulating capability of Polygonum hydropiper in relation to changes of phytohormones and phenols

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.ecoenv.2020.111211openalex-snapshot

A novel spectral analysis method for distinguishing heavy metal stress of maize due to copper and lead: RDA and EMD-PSD

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.2020.104187openalex-snapshot

Characterization of COMT1-mediated low phosphorus resistance mechanism by metabolomics in tomato plants

inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105120openalex-snapshot

Breeding and genomics approaches for improving phosphorus-use efficiency in grain legumes

inferred← citeshttps://doi.org/10.1016/j.envpol.2021.118331openalex-snapshot

Phosphorus enrichment affects trait network topologies and the growth of submerged macrophytes

inferred← citeshttps://doi.org/10.1016/j.gene.2011.06.026openalex-snapshot

Identification of a MYB3R gene involved in drought, salt and cold stress in wheat (Triticum aestivum L.)

inferred← citeshttps://doi.org/10.1016/j.jclepro.2015.05.002openalex-snapshot

Towards the current need to enhance legume productivity and soil sustainability worldwide: a book review

inferred← citeshttps://doi.org/10.1016/j.jia.2026.07.035openalex-snapshot

Study on the root structure and nutrition efficiency traits of wheat cultivar Zhengmai 1860

inferred← citeshttps://doi.org/10.1016/j.jplph.2012.03.013openalex-snapshot

Is genotypic variation of H+ efflux under P deficiency linked with nodulated-root respiration of N2 – Fixing common-bean (Phaseolus vulgaris L.)?

inferred← citeshttps://doi.org/10.1016/j.jplph.2019.153053openalex-snapshot

Glutamate dehydrogenase is essential in the acclimation of Virgilia divaricata, a legume indigenous to the nutrient-poor Mediterranean-type ecosystems of the Cape Fynbos

inferred← citeshttps://doi.org/10.1016/j.micres.2025.128159openalex-snapshot

The Rhizobium etli response regulator CenR is essential for both: Free-life and the rhizobial nitrogen-fixing symbiosis

inferred← citeshttps://doi.org/10.1016/j.pbi.2009.04.014openalex-snapshot

Effects of N, P, K and S on metabolism: new knowledge gained from multi-level analysis

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.2012.01.009openalex-snapshot

Changes in expression of soluble inorganic pyrophosphatases of Phaseolus vulgaris under phosphate starvation

inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.09.027openalex-snapshot

Metabolomic profiling from leaves and roots of tomato ( Solanum lycopersicum L.) plants grown under nitrogen, phosphorus or potassium-deficient condition

inferred← citeshttps://doi.org/10.1016/j.plantsci.2016.07.009openalex-snapshot

miRNA alterations are important mechanism in maize adaptations to low-phosphate environments

inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110260openalex-snapshot

Impact of high or low levels of phosphorus and high sodium in soils on productivity and stress tolerance of Arundo donax plants

inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111618openalex-snapshot

Transcription factor OsNAC016 negatively regulates phosphate-starvation response in rice

inferred← citeshttps://doi.org/10.1016/j.plaphy.2011.02.017openalex-snapshot

Suppression subtractive hybridization reveals differential gene expression in sunflower grown in high P

inferred← citeshttps://doi.org/10.1016/j.plaphy.2014.08.007openalex-snapshot

Phosphoproteome and proteome analyses reveal low-phosphate mediated plasticity of root developmental and metabolic regulation in maize (Zea mays L.)

inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.03.028openalex-snapshot

Effect of phosphate nutrition on growth, physiology and phosphate transporter expression of cucumber seedlings

inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.04.033openalex-snapshot

Integration of metabolome and transcriptome analyses highlights soybean roots responding to phosphorus deficiency by modulating phosphorylated metabolite processes

inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.05.043openalex-snapshot

Comparative transcriptomic and metabolomic analyses reveal the protective effects of silicon against low phosphorus stress in tomato plants

inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.08.040openalex-snapshot

Transcriptome and metabolome analyses revealed the response mechanism of apple to different phosphorus stresses

inferred← citeshttps://doi.org/10.1016/j.scienta.2019.05.061openalex-snapshot

Phosphorus and iron in soil play dominating roles in regulating bioactive compounds of Glechoma longituba (Nakai) Kupr

inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112238openalex-snapshot

Effects of exogenous selenium application for enhancing salinity stress tolerance in dry bean

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.136599openalex-snapshot

Simulating long-term carbon nitrogen and phosphorus biogeochemical cycling in agricultural environments

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.174719openalex-snapshot

The impact of alternative recycled and synthetic phosphorus sources on plant growth and responses, soil interactions and sustainable agriculture - lettuce (Lactuca sativa) as a case model

inferred← citeshttps://doi.org/10.1016/j.sjbs.2019.11.018openalex-snapshot

Legume genomics and transcriptomics: From classic breeding to modern technologies

inferred← citeshttps://doi.org/10.1016/j.tplants.2018.10.004openalex-snapshot

How Does Evolution in Phosphorus-Impoverished Landscapes Impact Plant Nitrogen and Sulfur Assimilation?

inferred← citeshttps://doi.org/10.1016/s2095-3119(14)60775-9openalex-snapshot

GmPHR1, a Novel Homolog of the AtPHR1 Transcription Factor, Plays a Role in Plant Tolerance to Phosphate Starvation

inferred← citeshttps://doi.org/10.1021/acs.est.7b05836openalex-snapshot

Phosphorus Stress-Induced Changes in Plant Root Exudation Could Potentially Facilitate Uranium Mobilization from Stable Mineral Forms

inferred← citeshttps://doi.org/10.1021/jf201430kopenalex-snapshot

Metabolomic Analysis of Ranunculus spp. as Potential Agents Involved in the Etiology of Equine Grass Sickness

inferred← citeshttps://doi.org/10.1038/s41598-024-82071-wopenalex-snapshot

Screening and identification of evaluation indicators of low phosphorus tolerant germplasm in Gleditsia sinensis Lam.

inferred← citeshttps://doi.org/10.1042/bj20082397openalex-snapshot

In vivo regulatory phosphorylation of the phosphoenolpyruvate carboxylase AtPPC1 in phosphate-starved Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1042/bsr20160148openalex-snapshot

Phosphate availability regulates ethylene biosynthesis gene expression and protein accumulation in white clover (Trifolium repens L.) roots

inferred← citeshttps://doi.org/10.1071/bt13264openalex-snapshot

Low-phosphorus conditions affect the nitrogen nutrition and associated carbon costs of two legume tree species from a Mediterranean-type ecosystem

inferred← citeshttps://doi.org/10.1071/bt14216openalex-snapshot

The role of phosphorus deficiency in nodule microbial composition, and carbon and nitrogen nutrition of a native legume tree in the Cape fynbos ecosystem

inferred← citeshttps://doi.org/10.1071/bt18016openalex-snapshot

Variable soil phosphorus effects on nitrogen nutrition, abundance and associated carbon costs of a savanna legume, Vachellia sieberiana grown in soils from varying altitudes

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/10.1071/fp17209openalex-snapshot

Linking root traits to superior phosphorus uptake and utilisation efficiency in three Fabales in the Core Cape Subregion, South Africa

inferred← citeshttps://doi.org/10.1074/mcp.m112.020461openalex-snapshot

Complementary Proteome and Transcriptome Profiling in Phosphate-deficient Arabidopsis Roots Reveals Multiple Levels of Gene Regulation

inferred← citeshttps://doi.org/10.1080/00103624.2022.2071928openalex-snapshot

Potential of Legumes Species Submitted to Phosphate Fertilization Levels: Morphological, Productive and Chemical Characteristics

inferred← citeshttps://doi.org/10.1080/00380768.2014.945390openalex-snapshot

Metabolite profiling of soybean root exudates under phosphorus deficiency

inferred← citeshttps://doi.org/10.1080/00380768.2019.1709543openalex-snapshot

Agronomic traits at the seedling stage, yield, and fiber quality in two cotton ( Gossypium hirsutum L.) cultivars in response to phosphorus deficiency

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/10.1080/01904167.2013.867981openalex-snapshot

PHOSPHORUS USE EFFICIENCY FOR SYMBIOTIC NITROGEN FIXATION VARIES AMONG COMMON BEAN RECOMBINANT INBRED LINES UNDER P DEFICIENCY

inferred← citeshttps://doi.org/10.1080/01904167.2022.2064302openalex-snapshot

Genotypic variability for tolerance to low soil phosphorus availability in faba bean ( Vicia faba L.)

inferred← citeshttps://doi.org/10.1080/01904167.2022.2092509openalex-snapshot

Pinto bean yield and phosphorus uptake as affected by the application of composted chicken manure and anaerobically digested dairy manure

inferred← citeshttps://doi.org/10.1080/02571862.2022.2142972openalex-snapshot

Genotypic variability in nutrient uptake and use efficiency in chickpea grown under low phosphorus availability in a Mediterranean climate

inferred← citeshttps://doi.org/10.1080/03650340.2017.1373764openalex-snapshot

Traits-related QTLs and genes and their potential applications in rice improvement under low phosphorus condition

inferred← citeshttps://doi.org/10.1080/07352689.2014.898445openalex-snapshot

Achievements and Challenges in Legume Breeding for Pest and Disease Resistance

inferred← citeshttps://doi.org/10.1080/13102818.2021.1920462openalex-snapshot

Common bean as a potential crop for future food security: an overview of past, current and future contributions in genomics, transcriptomics, transgenics and proteomics

inferred← citeshttps://doi.org/10.1080/15226510903051732openalex-snapshot

Interaction of Arsenic and Phosphate on Their Uptake and Accumulation in Chinese Brake Fern

inferred← citeshttps://doi.org/10.1093/aob/mcq015openalex-snapshot

Regulation of phosphate starvation responses in higher plants

inferred← citeshttps://doi.org/10.1093/aob/mcq234openalex-snapshot

Early response mechanisms of perennial ryegrass (Lolium perenne) to phosphorus deficiency

inferred← citeshttps://doi.org/10.1093/aob/mcu072openalex-snapshot

Legume genomics: understanding biology through DNA and RNA sequencing

inferred← citeshttps://doi.org/10.1093/aobpla/pls028openalex-snapshot

Approaches towards nitrogen- and phosphorus-efficient rice

inferred← citeshttps://doi.org/10.1093/aobpla/plt013openalex-snapshot

Ethylene and the responses of plants to phosphate deficiency

inferred← citeshttps://doi.org/10.1093/jxb/erab559openalex-snapshot

Metabolite shift in Medicago truncatula occurs in phosphorus deprivation

inferred← citeshttps://doi.org/10.1093/jxb/erae434openalex-snapshot

Comparative transcriptomics pinpoints conserved and specific transcriptional responses to phosphorus limitation

inferred← citeshttps://doi.org/10.1093/jxb/ern115openalex-snapshot

Transcript profiling of Zea mays roots reveals gene responses to phosphate deficiency at the plant- and species-specific levels

inferred← citeshttps://doi.org/10.1093/jxb/ern130openalex-snapshot

Sugar signalling mediates cluster root formation and phosphorus starvation-induced gene expression in white lupin

inferred← citeshttps://doi.org/10.1093/jxb/erq203openalex-snapshot

Ethylene and nitric oxide involvement in the up-regulation of key genes related to iron acquisition and homeostasis in Arabidopsis

inferred← citeshttps://doi.org/10.1093/jxb/erv539openalex-snapshot

Non-targeted profiling of semi-polar metabolites in Arabidopsis root exudates uncovers a role for coumarin secretion and lignification during the local response to phosphate limitation

inferred← citeshttps://doi.org/10.1093/jxb/ery176openalex-snapshot

Transcriptome and metabolome analyses provide insights into root and root-released organic anion responses to phosphorus deficiency in oat

inferred← citeshttps://doi.org/10.1093/jxb/erz074openalex-snapshot

Editing of the OsACS locus alters phosphate deficiency-induced adaptive responses in rice seedlings

inferred← citeshttps://doi.org/10.1093/mp/ssn081openalex-snapshot

Phosphate Starvation Responses and Gibberellic Acid Biosynthesis are Regulated by the MYB62 Transcription Factor in Arabidopsis

inferred← citeshttps://doi.org/10.1093/pcp/pcab016openalex-snapshot

The Phosphate Starvation Response System: Its Role in the Regulation of Plant–Microbe Interactions

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/pcr186openalex-snapshot

Ethylene's Role in Phosphate Starvation Signaling: More than Just a Root Growth Regulator

inferred← citeshttps://doi.org/10.1093/plphys/kiaa115openalex-snapshot

Phosphorus deprivation affects composition and spatial distribution of membrane lipids in legume nodules

inferred← citeshttps://doi.org/10.1093/treephys/tpr064openalex-snapshot

How does P affect photosynthesis and metabolite profiles of Eucalyptus globulus?

inferred← citeshttps://doi.org/10.1093/treephys/tpz074openalex-snapshot

Metabolic and physiological analyses reveal that Populus cathayana males adopt an energy-saving strategy to cope with phosphorus deficiency

inferred← citeshttps://doi.org/10.1098/rsos.170770openalex-snapshot

Genotype-specific relationships among phosphorus use, growth and abundance in Daphnia pulicaria

inferred← citeshttps://doi.org/10.1101/2024.05.22.595400openalex-snapshot

Nitrogen starvation response in hornworts and liverworts provides little evidence for complex priming to the cyanobiont

inferred← citeshttps://doi.org/10.1101/2024.07.02.601706openalex-snapshot

Comparative Transcriptomics of Arabidopsis , Medicago , Brachypodium and Setaria species during Phosphorus limitation

inferred← citeshttps://doi.org/10.1104/pp.107.097386openalex-snapshot

Genomic and Genetic Control of Phosphate Stress in Legumes

inferred← citeshttps://doi.org/10.1104/pp.109.141481openalex-snapshot

Integrated Metabolite and Transcript Profiling Identify a Biosynthetic Mechanism for Hispidol in Medicago truncatula Cell Cultures

inferred← citeshttps://doi.org/10.1104/pp.109.143842openalex-snapshot

Global Changes in the Transcript and Metabolic Profiles during Symbiotic Nitrogen Fixation in Phosphorus-Stressed Common Bean Plants

inferred← citeshttps://doi.org/10.1104/pp.109.144105openalex-snapshot

Legume Transcription Factor Genes: What Makes Legumes So Special?

inferred← citeshttps://doi.org/10.1104/pp.109.145144openalex-snapshot

Abnormal Physiological and Molecular Mutant Phenotypes Link Chloroplast Polynucleotide Phosphorylase to the Phosphorus Deprivation Response in Arabidopsis

inferred← citeshttps://doi.org/10.1104/pp.109.147918openalex-snapshot

Biochemical and Molecular Characterization of PvPAP3, a Novel Purple Acid Phosphatase Isolated from Common Bean Enhancing Extracellular ATP Utilization

inferred← citeshttps://doi.org/10.1104/pp.110.161067openalex-snapshot

Quantitative Trait Loci, Epigenetics, Sugars, and MicroRNAs: Quaternaries in Phosphate Acquisition and Use

inferred← citeshttps://doi.org/10.1104/pp.111.174987openalex-snapshot

Phosphate Deprivation in Maize: Genetics and Genomics

inferred← citeshttps://doi.org/10.1104/pp.112.209254openalex-snapshot

An RNA-Seq Transcriptome Analysis of Orthophosphate-Deficient White Lupin Reveals Novel Insights into Phosphorus Acclimation in Plants

inferred← citeshttps://doi.org/10.1104/pp.114.255547openalex-snapshot

The Micro-RNA172c-APETALA2-1 Node as a Key Regulator of the Common Bean-Rhizobium etli Nitrogen Fixation Symbiosis

inferred← citeshttps://doi.org/10.1104/pp.15.00708openalex-snapshot

Ethylene and the Regulation of Physiological and Morphological Responses to Nutrient Deficiencies

inferred← citeshttps://doi.org/10.1104/pp.15.01336openalex-snapshot

Arabidopsis PHL2 and PHR1 Act Redundantly as the Key Components of the Central Regulatory System Controlling Transcriptional Responses to Phosphate Starvation

inferred← citeshttps://doi.org/10.1111/febs.14846openalex-snapshot

Structural basis for the Target DNA recognition and binding by the MYB domain of phosphate starvation response 1

inferred← citeshttps://doi.org/10.1111/j.1365-3040.2008.01883.xopenalex-snapshot

Essential role of MYB transcription factor: PvPHR1 and microRNA: PvmiR399 in phosphorus‐deficiency signalling in common bean roots

inferred← citeshttps://doi.org/10.1111/j.1365-3040.2010.02184.xopenalex-snapshot

Biochemical and molecular characterization of AtPAP12 and AtPAP26: the predominant purple acid phosphatase isozymes secreted by phosphate‐starved Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1111/j.1365-313x.2008.03561.xopenalex-snapshot

Comparative proteome analyses of phosphorus responses in maize (Zea mays L.) roots of wild‐type and a low‐P‐tolerant mutant reveal root characteristics associated with phosphorus efficiency

inferred← citeshttps://doi.org/10.1111/j.1365-313x.2010.04385.xopenalex-snapshot

Phosphate systemically inhibits development of arbuscular mycorrhiza in Petunia hybrida and represses genes involved in mycorrhizal functioning

inferred← citeshttps://doi.org/10.1111/j.1399-3054.2007.01005.xopenalex-snapshot

Characterization of a type A response regulator in the common bean (Phaseolus vulgaris) in response to phosphate starvation

inferred← citeshttps://doi.org/10.1111/j.1399-3054.2007.01025.xopenalex-snapshot

Metabolomics for plant stress response

inferred← citeshttps://doi.org/10.1111/j.1399-3054.2010.01356.xopenalex-snapshot

Dissecting the plant transcriptome and the regulatory responses to phosphate deprivation

inferred← citeshttps://doi.org/10.1111/j.1399-3054.2011.01512.xopenalex-snapshot

Characterization of upregulated genes associated with high phosphorus accumulation in cucumber

inferred← citeshttps://doi.org/10.1111/j.1469-8137.2010.03291.xopenalex-snapshot

Does abscisic acid affect strigolactone biosynthesis?

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