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A genome-wide transcriptional analysis using Arabidopsis thaliana Affymetrix gene chips determined plant responses to phosphate deprivation

https://doi.org/10.1073/pnas.0505266102
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What this work says

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

inferredcites →https://doi.org/10.1007/s004250000345openalex-snapshot
Fumaric acid: an overlooked form of fixed carbon in Arabidopsis and other plant species
inferredcites →https://doi.org/10.1007/s11103-004-1965-5openalex-snapshot
Transcriptional regulation and functional properties of Arabidopsis Pht1;4, a high affinity transporter contributing greatly to phosphate uptake in phosphate deprived plants
inferredcites →https://doi.org/10.1007/s11104-004-2005-6openalex-snapshot
Phosphate Acquisition
inferredcites →https://doi.org/10.1016/j.tplants.2004.08.009openalex-snapshot
Reactive oxygen gene network of plants
inferredcites →https://doi.org/10.1016/s0014-5793(03)00477-0openalex-snapshot
Transient increase of phosphatidylcholine in plant cells in response to phosphate deprivation
inferredcites →https://doi.org/10.1016/s0021-9258(18)64849-5openalex-snapshot
A SIMPLE METHOD FOR THE ISOLATION AND PURIFICATION OF TOTAL LIPIDES FROM ANIMAL TISSUES
inferredcites →https://doi.org/10.1042/0264-6021:3590575openalex-snapshot
Structure and differential expression of the four members of the Arabidopsis thaliana ferritin gene family
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.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.1365-313x.1999.00538.xopenalex-snapshot
Dimerization and DNA binding of auxin response factors
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01356.xopenalex-snapshot
Expression analysis suggests novel roles for members of the Pht1 family of phosphate transporters in Arabidopsis
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.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/10.1074/jbc.r400032200openalex-snapshot
Three Enzyme Systems for Galactoglycerolipid Biosynthesis Are Coordinately Regulated in Plants
inferredcites →https://doi.org/10.1083/jcb.200407022openalex-snapshot
Phosphate deprivation induces transfer of DGDG galactolipid from chloroplast to mitochondria
inferredcites →https://doi.org/10.1093/aob/mch156openalex-snapshot
Genetic Responses to Phosphorus Deficiency
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.010934openalex-snapshot
Phosphate Availability Alters Architecture and Causes Changes in Hormone Sensitivity in the Arabidopsis Root System
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.020007openalex-snapshot
Regulated Expression of Arabidopsis Phosphate Transporters
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.103.021253openalex-snapshot
Microarray Analysis of the Nitrate Response in Arabidopsis Roots and Shoots Reveals over 1,000 Rapidly Responding Genes and New Linkages to Glucose, Trehalose-6-Phosphate, Iron, and Sulfate Metabolism
inferredcites →https://doi.org/10.1104/pp.103.032235openalex-snapshot
Microarray Analyses of Gene Expression during Adventitious Root Development in Pinus contorta
inferredcites →https://doi.org/10.1104/pp.103.037945openalex-snapshot
Structure and Expression Profile of the Arabidopsis PHO1 Gene Family Indicates a Broad Role in Inorganic Phosphate Homeostasis
inferredcites →https://doi.org/10.1104/pp.125.2.728openalex-snapshot
LEPS2, a Phosphorus Starvation-Induced Novel Acid Phosphatase from Tomato
inferredcites →https://doi.org/10.1104/pp.125.2.912openalex-snapshot
Origin of the Cytoplasmic pH Changes during Anaerobic Stress in Higher Plant Cells. Carbon-13 and Phosphorous-31 Nuclear Magnetic Resonance Studies
inferredcites →https://doi.org/10.1104/pp.126.2.524openalex-snapshot
Flavonoids Act as Negative Regulators of Auxin Transport in Vivo in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.47.5.649openalex-snapshot
An Analysis of Phytochrome-mediated Anthocyanin Synthesis
inferredcites →https://doi.org/10.1105/tpc.13.1.113openalex-snapshot
Microarray Analysis of Diurnal and Circadian-Regulated Genes in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02061.xopenalex-snapshot
Development and evaluation of an Arabidopsis whole genome Affymetrix probe array
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.arplant.50.1.665openalex-snapshot
PHOSPHATE ACQUISITION
inferredcites →https://doi.org/10.2307/2419652openalex-snapshot
Plant Life Histories: Ecology, Phylogeny and Evolution.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Proteomic analysis of alterations in the secretome of Arabidopsis thaliana suspension cells subjected to nutritional phosphate deficiency
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Chemical Genetics in Dissecting Membrane Glycerolipid Functions
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Phosphate Signaling in Plants: Biochemical and Molecular Approach
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Phosphorus: Plant Strategies to Cope with its Scarcity
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Plant Plasma Membrane and Phosphate Deprivation
inferred← citeshttps://doi.org/10.1007/978-3-642-14369-4_7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-15271-9_10openalex-snapshot
Phosphorus Nutrition: Rhizosphere Processes, Plant Response and Adaptations
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Molecular Approaches to the Study of Biological Phosphorus Cycling
inferred← citeshttps://doi.org/10.1007/978-3-642-30967-0_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-37045-8_3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-42011-5_9openalex-snapshot
Phospholipases in Plant Response to Nitrogen and Phosphorus Availability
inferred← citeshttps://doi.org/10.1007/978-81-322-2334-4_3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-90-481-2863-1_16openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00018-012-1090-6openalex-snapshot
Transcriptional regulation of phosphate acquisition by higher plants
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Promotion of Zinc Tolerance, Acquisition and Translocation of Phosphorus in Mimosa pudica L. Mediated by Arbuscular Mycorrhizal Fungi
inferred← citeshttps://doi.org/10.1007/s00299-012-1328-7openalex-snapshot
Overexpression of GbWRKY1 positively regulates the Pi starvation response by alteration of auxin sensitivity in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-013-1391-8openalex-snapshot
Phosphorus starvation induces post-transcriptional CHS gene silencing in Petunia corolla
inferred← citeshttps://doi.org/10.1007/s00299-016-1984-0openalex-snapshot
Rice and chickpea GDPDs are preferentially influenced by low phosphate and CaGDPD1 encodes an active glycerophosphodiester phosphodiesterase enzyme
inferred← citeshttps://doi.org/10.1007/s00299-016-2007-xopenalex-snapshot
Phosphate starvation promoted the accumulation of phenolic acids by inducing the key enzyme genes in Salvia miltiorrhiza hairy roots
inferred← citeshttps://doi.org/10.1007/s00299-023-03120-8openalex-snapshot
Arabidopsis PDE1 confers phosphate-deficiency tolerance in primary root growth
inferred← citeshttps://doi.org/10.1007/s00344-021-10495-zopenalex-snapshot
Nutrient Reabsorption Mechanism Adapted to Low Phosphorus in Wild and Cultivated Soybean Varieties
inferred← citeshttps://doi.org/10.1007/s00344-022-10781-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00344-023-11002-2openalex-snapshot
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Post-anthesis Roots Metabolic Activities Relate Low Phosphorus (P)-Tolerance in Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s00344-025-11831-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-007-0569-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-007-0603-2openalex-snapshot
Molecular cloning and characterization of phosphorus starvation responsive genes in common bean (Phaseolus vulgaris L.)
inferred← citeshttps://doi.org/10.1007/s00425-007-0677-xopenalex-snapshot
Expression analyses of three members of the AtPHO1 family reveal differential interactions between signaling pathways involved in phosphate deficiency and the responses to auxin, cytokinin, and abscisic acid
inferred← citeshttps://doi.org/10.1007/s00425-008-0736-yopenalex-snapshot
Biochemical and molecular analysis of LePS2;1: a phosphate starvation induced protein phosphatase gene from tomato
inferred← citeshttps://doi.org/10.1007/s00425-008-0754-9openalex-snapshot
PRD, an Arabidopsis AINTEGUMENTA-like gene, is involved in root architectural changes in response to phosphate starvation
inferred← citeshttps://doi.org/10.1007/s00425-008-0809-yopenalex-snapshot
Development of tobacco callus cultures over expressing Arabidopsis PAP1/MYB75 transcription factor and characterization of anthocyanin biosynthesis
inferred← citeshttps://doi.org/10.1007/s00425-010-1142-9openalex-snapshot
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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
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inferred← citeshttps://doi.org/10.1007/s00425-012-1645-7openalex-snapshot
Transcriptional response of Medicago truncatula sulphate transporters to arbuscular mycorrhizal symbiosis with and without sulphur stress
inferred← citeshttps://doi.org/10.1007/s00425-019-03201-7openalex-snapshot
Two-factor ANOVA of SSH and RNA-seq analysis reveal development-associated Pi-starvation genes in oilseed rape
inferred← citeshttps://doi.org/10.1007/s00425-022-03897-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00425-022-03922-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00438-018-1496-4openalex-snapshot
Tissue-specific transcriptomic profiling of Plantago major provides insights for the involvement of vasculature in phosphate deficiency responses
inferred← citeshttps://doi.org/10.1007/s00572-010-0352-0openalex-snapshot
Arbuscular mycorrhizal symbiosis elicits proteome responses opposite of P-starvation in SO4 grapevine rootstock upon root colonisation with two Glomus species
inferred← citeshttps://doi.org/10.1007/s00606-021-01764-1openalex-snapshot
Genetic variation and differentiation of Quercus variabilis populations at phosphate and non-phosphate rock sites in southwestern China
inferred← citeshttps://doi.org/10.1007/s00709-015-0845-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00709-016-0986-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00709-018-1304-3openalex-snapshot
Lanthanum nitrate improves phosphorus-use efficiency and tolerance to phosphorus-deficiency stress in Vigna angularis seedlings
inferred← citeshttps://doi.org/10.1007/s00709-026-02186-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10142-024-01301-6openalex-snapshot
Genetics and metabolic responses of Artemisia annua L to the lake of phosphorus under the sparingly soluble phosphorus fertilizer: evidence from transcriptomics analysis
inferred← citeshttps://doi.org/10.1007/s10265-016-0851-yopenalex-snapshot
Immunolocalization of cell wall polymers in grapevine (Vitis vinifera) internodes under nitrogen, phosphorus or sulfur deficiency
inferred← citeshttps://doi.org/10.1007/s10265-024-01533-4openalex-snapshot
Reviewing impacts of biotic and abiotic stresses on the regulation of phosphate homeostasis in plants
inferred← citeshttps://doi.org/10.1007/s10528-023-10375-zopenalex-snapshot
Comprehensive Evolution and Expression anaLysis of PHOSPHATE 1 Gene Family in Allotetraploid Brassica napus and Its Diploid Ancestors
inferred← citeshttps://doi.org/10.1007/s10681-011-0428-8openalex-snapshot
Development of gene-based markers from functional Arabidopsis thaliana genes involved in phosphorus homeostasis and mapping in Brassica napus
inferred← citeshttps://doi.org/10.1007/s10725-011-9575-0openalex-snapshot
Identification and expression analysis of genes induced by phosphate starvation in leaves and roots of Brassica napus
inferred← citeshttps://doi.org/10.1007/s10725-024-01201-6openalex-snapshot
Phosphate and zinc interaction in soil and plants: a reciprocal cross-talk
inferred← citeshttps://doi.org/10.1007/s10886-009-9735-0openalex-snapshot
Direct and Indirect Effects of Invasive Plants on Soil Chemistry and Ecosystem Function
inferred← citeshttps://doi.org/10.1007/s11032-020-01156-2openalex-snapshot
Genetic variation associated with the shoot biomass of upland cotton seedlings under contrasting phosphate supplies
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/s11033-013-2636-xopenalex-snapshot
Transcriptional responses of maize seedling root to phosphorus starvation
inferred← citeshttps://doi.org/10.1007/s11103-007-9215-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11103-008-9380-yopenalex-snapshot
Plant hormones and nutrient signaling
inferred← citeshttps://doi.org/10.1007/s11103-008-9401-xopenalex-snapshot
Molecular cloning and characterization of phosphate (Pi) responsive genes in Gulf ryegrass (Lolium multiflorum L.): a Pi hyperaccumulator
inferred← citeshttps://doi.org/10.1007/s11103-009-9580-0openalex-snapshot
Gene expression profiles in rice roots under low phosphorus stress
inferred← citeshttps://doi.org/10.1007/s11103-010-9671-yopenalex-snapshot
Proteomic alterations of Brassica napus root in response to boron deficiency
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/s11103-014-0249-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/s11103-016-0564-6openalex-snapshot
Phosphate starvation induced OsPHR4 mediates Pi-signaling and homeostasis in rice
inferred← citeshttps://doi.org/10.1007/s11104-009-0002-5openalex-snapshot
White Lupin (Lupinus albus) response to phosphorus stress: evidence for complex regulation of LaSAP1
inferred← citeshttps://doi.org/10.1007/s11104-009-0071-5openalex-snapshot
Regulating the phosphorus nutrition of plants: molecular biology meeting agronomic needs
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/s11104-010-0373-7openalex-snapshot
Identification of genes induced in proteoid roots of white lupin under nitrogen and phosphorus deprivation, with functional characterization of a formamidase
inferred← citeshttps://doi.org/10.1007/s11104-011-0913-9openalex-snapshot
Characterization of phosphorus starvation-induced gene BnSPX3 in Brassica napus
inferred← citeshttps://doi.org/10.1007/s11104-011-1060-zopenalex-snapshot
Transcriptional response of Pseudomonas aeruginosa to a phosphate-deficient Lolium perenne rhizosphere
inferred← citeshttps://doi.org/10.1007/s11104-011-1107-1openalex-snapshot
Contribution of phosphorus (32P) absorption and remobilization for citrus growth
inferred← citeshttps://doi.org/10.1007/s11104-015-2657-4openalex-snapshot
Genome-wide identification of phosphate-deficiency-responsive genes in soybean roots by high-throughput sequencing
inferred← citeshttps://doi.org/10.1007/s11104-018-3787-2openalex-snapshot
The effect of pH on morphological and physiological root traits of Lupinus angustifolius treated with struvite as a recycled phosphorus source
inferred← citeshttps://doi.org/10.1007/s11104-019-03972-8openalex-snapshot
Root-released organic anions in response to low phosphorus availability: recent progress, challenges and future perspectives
inferred← citeshttps://doi.org/10.1007/s11104-019-04296-3openalex-snapshot
Effects of different inhibitors such as malonic acid, Na3PO4 and HgCl2 on uptake of different forms of antimony in rice plant
inferred← citeshttps://doi.org/10.1007/s11104-021-04849-5openalex-snapshot
No evidence of regulation in root-mediated iron reduction in two Strategy I cluster-rooted Banksia species (Proteaceae)
inferred← citeshttps://doi.org/10.1007/s11104-023-06088-2openalex-snapshot
GABA responds to low phosphorus stress by interfering with endogenous auxin levels in apple
inferred← citeshttps://doi.org/10.1007/s11104-024-06710-xopenalex-snapshot
Attenuated down-regulation of PHOSPHATE TRANSPORTER1 genes as a mechanism for phosphorus sensitivity in phosphorus-efficient Hakea prostrata (Proteaceae)
inferred← citeshttps://doi.org/10.1007/s11105-012-0485-8openalex-snapshot
Comparative Analysis of Differentially Expressed Genes in Rice Under Nitrogen and Phosphorus Starvation Stress Conditions
inferred← citeshttps://doi.org/10.1007/s11105-019-01170-5openalex-snapshot
Over-Expression of Masson Pine PmPT1 Gene in Transgenic Tobacco Confers Tolerance Enhancement to Pi Deficiency by Ameliorating P Level and the Antioxidants
inferred← citeshttps://doi.org/10.1007/s11120-007-9195-8openalex-snapshot
Chloroplast envelope membranes: a dynamic interface between plastids and the cytosol
inferred← citeshttps://doi.org/10.1007/s11157-016-9390-1openalex-snapshot
Mechanism of Zinc absorption in plants: uptake, transport, translocation and accumulation
inferred← citeshttps://doi.org/10.1007/s11368-015-1342-9openalex-snapshot
Effects of phosphate on trace element accumulation in rice (Oryza sativa L.): a 5-year phosphate application study
inferred← citeshttps://doi.org/10.1007/s11427-009-0137-xopenalex-snapshot
The expression profile of genes in rice roots under low phosphorus stress
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/s11434-010-0012-yopenalex-snapshot
Transcriptomic analysis of rice responses to low phosphorus stress
inferred← citeshttps://doi.org/10.1007/s11703-010-1040-8openalex-snapshot
The molecular characterization and function of miRNAs on mediation of target gene silencing in plants
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/s11738-011-0832-7openalex-snapshot
Transcriptome response to phosphorus starvation in rice
inferred← citeshttps://doi.org/10.1007/s11738-011-0889-3openalex-snapshot
Physiological and transcriptional analysis of the effects of formaldehyde exposure on Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11738-012-0937-7openalex-snapshot
Erratum to: Physiological and transcriptional analysis of the effects of formaldehyde exposure on Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11738-014-1499-7openalex-snapshot
Cloning and functional analysis of two flavanone-3-hydroxylase genes from Reaumuria trigyna
inferred← citeshttps://doi.org/10.1007/s11738-014-1687-5openalex-snapshot
Transcriptome responses to phosphate deficiency in Poncirus trifoliata (L.) Raf
inferred← citeshttps://doi.org/10.1007/s11738-015-1952-2openalex-snapshot
Plant and microbe genomics and beyond: potential for developing a novel molecular plant nutrition approach
inferred← citeshttps://doi.org/10.1007/s11738-015-2055-9openalex-snapshot
Phosphate deprivation decreases cadmium (Cd) uptake but enhances sensitivity to Cd by increasing iron (Fe) uptake and inhibiting phytochelatins synthesis in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1007/s11816-013-0308-xopenalex-snapshot
Identification of AtWRKY75 as a transcriptional regulator in the defense response to Pcc through the screening of Arabidopsis activation-tagged lines
inferred← citeshttps://doi.org/10.1007/s11816-018-0490-yopenalex-snapshot
A systemic view of phosphate starvation-responsive genes in rice roots to enhance phosphate use efficiency in rice
inferred← citeshttps://doi.org/10.1007/s12038-012-9242-2openalex-snapshot
Transcriptome response to nitrogen starvation 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/s12284-009-9032-0openalex-snapshot
Stress Response Versus Stress Tolerance: A Transcriptome Analysis of Two Rice Lines Contrasting in Tolerance to Phosphorus Deficiency
inferred← citeshttps://doi.org/10.1007/s12298-020-00902-2openalex-snapshot
A genome-wide association study reveals the quantitative trait locus and candidate genes that regulate phosphate efficiency in a Vietnamese rice collection
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/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/s40626-020-00183-wopenalex-snapshot
Transcriptome and ionome analysis of nitrogen, phosphorus and potassium interactions in sorghum seedlings
inferred← citeshttps://doi.org/10.1007/s42729-020-00216-yopenalex-snapshot
Characterizing Lentil Germplasm for Zinc Biofortification and High Grain Output
inferred← citeshttps://doi.org/10.1007/s42729-021-00418-yopenalex-snapshot
An Overview of the Morphological, Genetic and Metabolic Mechanisms Regulating Phosphorus Efficiency Via Root Traits in Soybean
inferred← citeshttps://doi.org/10.1007/s42729-023-01524-9openalex-snapshot
Organo-mineral Fertilizer Containing Struvite from Liquid Digestate for Cucurbita pepo L. Seedling Production
inferred← citeshttps://doi.org/10.1007/s42729-026-03213-9openalex-snapshot
Transcriptomic Analysis Reveals a Tripartite Adaptive Strategy for Phosphorus-Iron Homeostasis in Pepper Seedling Roots
inferred← citeshttps://doi.org/10.1007/s44154-022-00035-4openalex-snapshot
High transcriptome plasticity drives phosphate starvation responses in tomato
inferred← citeshttps://doi.org/10.1016/b978-0-12-811308-0.00003-xopenalex-snapshot
Macronutrient sensing and signaling in plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-814217-2.00024-xopenalex-snapshot
Gene chips for food quality evaluation
inferred← citeshttps://doi.org/10.1016/b978-0-12-821430-5.00006-7openalex-snapshot
Phosphorus and sulfur uptake, assimilation, and deprivation responses
inferred← citeshttps://doi.org/10.1016/b978-0-323-90943-3.00005-5openalex-snapshot
Physiological and molecular strategies of plant adaptationin phosphorus-deficient soils
inferred← citeshttps://doi.org/10.1016/b978-0-323-95989-6.00008-5openalex-snapshot
Current understanding of genomics, transcriptomics, proteomics, and metabolomics of crop plants under low nutrient stress
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.bbagrm.2008.04.004openalex-snapshot
The role of microRNAs and other endogenous small RNAs in plant stress responses
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2016.10.012openalex-snapshot
The multifaceted roles of NUCLEAR FACTOR-Y in Arabidopsis thaliana development and stress responses
inferred← citeshttps://doi.org/10.1016/j.bbalip.2020.158763openalex-snapshot
Phosphate starvation causes different stress responses in the lipid metabolism of tomato leaves and roots
inferred← citeshttps://doi.org/10.1016/j.bbapap.2011.10.003openalex-snapshot
Arabidopsis thaliana PECP1 — Enzymatic characterization and structural organization of the first plant phosphoethanolamine/phosphocholine phosphatase
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.06.015openalex-snapshot
Arabidopsis RING E3 ubiquitin ligase AtATL80 is negatively involved in phosphate mobilization and cold stress response in sufficient phosphate growth conditions
inferred← citeshttps://doi.org/10.1016/j.biochi.2006.04.018openalex-snapshot
Genome-wide transcriptome profiling of the early cadmium response of Arabidopsis roots and shoots
inferred← citeshttps://doi.org/10.1016/j.biochi.2006.05.007openalex-snapshot
Phosphate deficiency promotes modification of iron distribution in Arabidopsis plants
inferred← citeshttps://doi.org/10.1016/j.biochi.2011.03.012openalex-snapshot
Role of phosphatidic acid in plant galactolipid synthesis
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.ceca.2014.02.011openalex-snapshot
Whole genome transcriptome analysis of rice seedling reveals alterations in Ca2+ ion signaling and homeostasis in response to Ca2+ deficiency
inferred← citeshttps://doi.org/10.1016/j.ceca.2015.04.003openalex-snapshot
Plant phospholipase C family: Regulation and functional role in lipid signaling
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2011.01.062openalex-snapshot
A transgenic approach to enhance phosphorus use efficiency in crops as part of a comprehensive strategy for sustainable agriculture
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2014.01.030openalex-snapshot
Role of phosphate fertilizers in heavy metal uptake and detoxification of toxic metals
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2017.09.033openalex-snapshot
Ecophysiological responses to excess iron in lowland and upland rice cultivars
inferred← citeshttps://doi.org/10.1016/j.coisb.2017.07.008openalex-snapshot
System-level understanding of plant mineral nutrition in the big data era
inferred← citeshttps://doi.org/10.1016/j.copbio.2017.08.012openalex-snapshot
Control of plant phosphate homeostasis by inositol pyrophosphates and the SPX domain
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2017.09.043openalex-snapshot
Phosphate alleviates arsenate toxicity by altering expression of phosphate transporters in the tolerant barley genotypes
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2013.05.001openalex-snapshot
Estimation of flavonoid and centelloside accumulation in leaves of Centella asiatica L. Urban by multiparametric fluorescence measurements
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2014.05.013openalex-snapshot
Molecular mechanisms of phosphate and zinc signalling crosstalk in plants: Phosphate and zinc loading into root xylem in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2014.06.014openalex-snapshot
MYB transcription factors, active players in abiotic stress signaling
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104386openalex-snapshot
ANAC044 is associated with P reutilization in P deficient Arabidopsis thaliana root cell wall in an ethylene dependent manner
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104483openalex-snapshot
Genome-wide expression analysis reveals contrasting regulation of phosphate starvation response (PSR) in root and shoot of Arabidopsis and its association with biotic stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104631openalex-snapshot
Split-root, grafting and girdling as experimental tools to study root-to shoot-to root signaling
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105599openalex-snapshot
Recent progress of molecular mechanisms of DNA methylation in plant response to abiotic stress
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.envexpbot.2024.105726openalex-snapshot
Integrated transcriptome and proteome analysis of near-isogenic line provides insights on regulatory function of Pup1 QTL in rice under phosphorus-starvation stress
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.envpol.2017.05.066openalex-snapshot
Zinc oxide nanoparticle exposure triggers different gene expression patterns in maize shoots and roots
inferred← citeshttps://doi.org/10.1016/j.fcr.2010.08.005openalex-snapshot
Localized application of phosphorus and ammonium improves growth of maize seedlings by stimulating root proliferation and rhizosphere acidification
inferred← citeshttps://doi.org/10.1016/j.fct.2008.05.025openalex-snapshot
Safety assessment considerations for food and feed derived from plants with genetic modifications that modulate endogenous gene expression and pathways
inferred← citeshttps://doi.org/10.1016/j.febslet.2008.01.039openalex-snapshot
Phosphate availability affects the tonoplast localization of PLDζ2, an Arabidopsis thaliana phospholipase D
inferred← citeshttps://doi.org/10.1016/j.gep.2013.08.001openalex-snapshot
Expression pattern and subcellular localization of Arabidopsis purple acid phosphatase AtPAP9
inferred← citeshttps://doi.org/10.1016/j.hal.2021.102078openalex-snapshot
Growth and ionomic responses of a freshwater cyanobacterium to supplies of nitrogen and iron
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