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Repression of Nitrogen Starvation Responses by Members of the Arabidopsis GARP-Type Transcription Factor NIGT1/HRS1 Subfamily
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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A Rapid, Simple Spectrophotometric Method for Simultaneous Detection of Nitrate and Nitrite
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Photosynthesis and ribulose-1,5-bisphosphate carboxylase/oxygenase in rice leaves from emergence through senescence. Quantitative analysis by carboxylation/oxygenation and regeneration of ribulose 1,5-bisphosphate
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Immobilization and mineralization of tracer nitrogen in forest raw humus
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Root Nitrogen Acquisition and Assimilation
inferredcites →https://doi.org/10.1007/s11104-013-1645-9openalex-snapshot
Nitrogen acquisition by roots: physiological and developmental mechanisms ensuring plant adaptation to a fluctuating resource
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The calcium sensor CBL7 modulates plant responses to low nitrate in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2009.07.004openalex-snapshot
CHL1 Functions as a Nitrate Sensor in Plants
inferredcites →https://doi.org/10.1016/j.cell.2016.04.038openalex-snapshot
Cistrome and Epicistrome Features Shape the Regulatory DNA Landscape
inferredcites →https://doi.org/10.1016/j.febslet.2007.03.034openalex-snapshot
Molecular mechanisms of ammonium transport and accumulation in plants
inferredcites →https://doi.org/10.1016/j.jplph.2011.10.011openalex-snapshot
Reciprocal regulation between AtNRT2.1 and AtAMT1.1 expression and the kinetics of NH4+ and NO3− influxes
inferredcites →https://doi.org/10.1016/j.pbi.2014.06.004openalex-snapshot
Nitrogen signalling pathways shaping root system architecture: an update
inferredcites →https://doi.org/10.1016/j.pbi.2017.05.007openalex-snapshot
Novel signals in the regulation of Pi starvation responses in plants: facts and promises
inferredcites →https://doi.org/10.1016/j.pbi.2017.07.006openalex-snapshot
The world according to GARP transcription factors
inferredcites →https://doi.org/10.1016/j.tplants.2004.10.008openalex-snapshot
Can less yield more? Is reducing nutrient input into the environment compatible with maintaining crop production?
inferredcites →https://doi.org/10.1016/j.tplants.2006.10.007openalex-snapshot
How do plants respond to nutrient shortage by biomass allocation?
inferredcites →https://doi.org/10.1016/j.tplants.2011.03.012openalex-snapshot
The biochemistry of nitrogen mobilization: purine ring catabolism
inferredcites →https://doi.org/10.1016/s0005-2728(89)80347-0openalex-snapshot
Determination of accurate extinction coefficients and simultaneous equations for assaying chlorophylls a and b extracted with four different solvents: verification of the concentration of chlorophyll standards by atomic absorption spectroscopy
inferredcites →https://doi.org/10.1016/s0014-5793(01)02096-8openalex-snapshot
An Arabidopsis T‐DNA mutant affected in Nrt2 genes is impaired in nitrate uptake
inferredcites →https://doi.org/10.1016/s1369-5266(98)80108-8openalex-snapshot
Regulation of cytosolic enzymes in primary metabolism by reversible protein phosphorylation
inferredcites →https://doi.org/10.1023/a:1024899808018openalex-snapshot
Regulation of the nitrate transporter gene AtNRT2.1 in Arabidopsis thaliana: responses to nitrate, amino acids and developmental stage
inferredcites →https://doi.org/10.1038/nature22077openalex-snapshot
Discovery of nitrate–CPK–NLP signalling in central nutrient–growth networks
inferredcites →https://doi.org/10.1038/ncomms13179openalex-snapshot
NIN-like protein 8 is a master regulator of nitrate-promoted seed germination in Arabidopsis
inferredcites →https://doi.org/10.1038/ncomms2621openalex-snapshot
Arabidopsis NIN-like transcription factors have a central role in nitrate signalling
inferredcites →https://doi.org/10.1038/ncomms2650openalex-snapshot
Nuclear retention of the transcription factor NLP7 orchestrates the early response to nitrate in plants
inferredcites →https://doi.org/10.1038/ncomms7274openalex-snapshot
AtNIGT1/HRS1 integrates nitrate and phosphate signals at the Arabidopsis root tip
inferredcites →https://doi.org/10.1042/bc20040516openalex-snapshot
Starvation‐induced expression of autophagy‐related genes in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00868.xopenalex-snapshot
An estrogen receptor‐based transactivator XVE mediates highly inducible gene expression in transgenic plants
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01016.xopenalex-snapshot
Differential regulation of the NO 3 – and NH 4 + transporter genes AtNrt2.1 and AtAmt1.1 in Arabidopsis : relation with long‐distance and local controls by N status of the plant
inferredcites →https://doi.org/10.1073/pnas.1017863108openalex-snapshot
HIGH NITROGEN INSENSITIVE 9 (HNI9)-mediated systemic repression of root NO 3 − uptake is associated with changes in histone methylation
inferredcites →https://doi.org/10.1073/pnas.1205156109openalex-snapshot
Transcriptional repressor PRR5 directly regulates clock-output pathways
inferredcites →https://doi.org/10.1073/pnas.1316278111openalex-snapshot
DNA-binding specificities of plant transcription factors and their potential to define target genes
inferredcites →https://doi.org/10.1073/pnas.1319953111openalex-snapshot
CLE-CLAVATA1 peptide-receptor signaling module regulates the expansion of plant root systems in a nitrogen-dependent manner
inferredcites →https://doi.org/10.1073/pnas.1404654111openalex-snapshot
SPX1 is a phosphate-dependent inhibitor of PHOSPHATE STARVATION RESPONSE 1 in Arabidopsis
inferredcites →https://doi.org/10.1093/aob/mcq028openalex-snapshot
Nitrogen uptake, assimilation and remobilization in plants: challenges for sustainable and productive agriculture
inferredcites →https://doi.org/10.1093/bioinformatics/btg405openalex-snapshot
affy—analysis of Affymetrix GeneChip data at the probe level
inferredcites →https://doi.org/10.1093/biomet/34.1-2.28openalex-snapshot
THE GENERALIZATION OF ‘STUDENT'S’ PROBLEM WHEN SEVERAL DIFFERENT POPULATION VARLANCES ARE INVOLVED
inferredcites →https://doi.org/10.1093/jxb/erab114openalex-snapshot
GARP transcription factors repress Arabidopsis nitrogen starvation response via ROS-dependent and -independent pathways
inferredcites →https://doi.org/10.1093/jxb/erm089openalex-snapshot
Protein dynamics and proteolysis in plant vacuoles
inferredcites →https://doi.org/10.1093/jxb/eru001openalex-snapshot
Nitrate transport and signalling in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/eru039openalex-snapshot
Autophagy, plant senescence, and nutrient recycling
inferredcites →https://doi.org/10.1093/pcp/pcg036openalex-snapshot
Regulation of NRT1 and NRT2 Gene Families of Arabidopsis thaliana: Responses to Nitrate Provision
inferredcites →https://doi.org/10.1093/pcp/pcq161openalex-snapshot
Efficient Yeast One-/Two-Hybrid Screening Using a Library Composed Only of Transcription Factors in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcr113openalex-snapshot
Identification of Reference Genes for RT–qPCR Expression Analysis in Arabidopsis and Tomato Seeds
inferredcites →https://doi.org/10.1093/pcp/pct007openalex-snapshot
A Nitrate-Inducible GARP Family Gene Encodes an Auto-Repressible Transcriptional Repressor in Rice
inferredcites →https://doi.org/10.1093/pcp/pcv184openalex-snapshot
Asparagine Metabolic Pathways in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcw052openalex-snapshot
Plant Nitrogen Acquisition Under Low Availability: Regulation of Uptake and Root Architecture
inferredcites →https://doi.org/10.1093/pcp/pcw063openalex-snapshot
Arabidopsis MYB-Related HHO2 Exerts a Regulatory Influence on a Subset of Root Traits and Genes Governing Phosphate Homeostasis
inferredcites →https://doi.org/10.1104/pp.106.093237openalex-snapshot
Nitrogen-Dependent Posttranscriptional Regulation of the Ammonium Transporter AtAMT1;1
inferredcites →https://doi.org/10.1104/pp.111.188532openalex-snapshot
Regulation of High-Affinity Nitrate Uptake in Roots of Arabidopsis Depends Predominantly on Posttranscriptional Control of the NRT2.1/NAR2.1 Transport System
inferredcites →https://doi.org/10.1104/pp.127.1.262openalex-snapshot
Major Alterations of the Regulation of Root NO3 − Uptake Are Associated with the Mutation of Nrt2.1 and Nrt2.2 Genes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.007120openalex-snapshot
AtDUR3 Encodes a New Type of High-Affinity Urea/H+ Symporter in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.104.027078openalex-snapshot
The Vegetative Vacuole Proteome of Arabidopsis thaliana Reveals Predicted and Unexpected Proteins[W]
inferredcites →https://doi.org/10.1105/tpc.107.052134openalex-snapshot
The Organization of High-Affinity Ammonium Uptake in Arabidopsis Roots Depends on the Spatial Arrangement and Biochemical Properties of AMT1-Type Transporters
inferredcites →https://doi.org/10.1105/tpc.109.067041openalex-snapshot
Members of the LBD Family of Transcription Factors Repress Anthocyanin Synthesis and Affect Additional Nitrogen Responses in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.072892openalex-snapshot
PSEUDO-RESPONSE REGULATORS 9, 7, and 5 Are Transcriptional Repressors in the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1105/tpc.11.5.865openalex-snapshot
CHL1 Is a Dual-Affinity Nitrate Transporter of Arabidopsis Involved in Multiple Phases of Nitrate Uptake
inferredcites →https://doi.org/10.1105/tpc.111.092221openalex-snapshot
The Arabidopsis Nitrate Transporter NRT2.4 Plays a Double Role in Roots and Shoots of Nitrogen-Starved Plants
inferredcites →https://doi.org/10.1105/tpc.112.096636openalex-snapshot
PHO2-Dependent Degradation of PHO1 Modulates Phosphate Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.115998openalex-snapshot
Identification of Downstream Components of Ubiquitin-Conjugating Enzyme PHOSPHATE2 by Quantitative Membrane Proteomics in Arabidopsis Roots
inferredcites →https://doi.org/10.1105/tpc.12.3.393openalex-snapshot
Arabidopsis Ethylene-Responsive Element Binding Factors Act as Transcriptional Activators or Repressors of GCC Box–Mediated Gene Expression
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Additive contribution of AMT1;1 and AMT1;3 to high‐affinity ammonium uptake across the plasma membrane of nitrogen‐deficient Arabidopsis roots
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03223.xopenalex-snapshot
AtDUR3 represents the major transporter for high‐affinity urea transport across the plasma membrane of nitrogen‐deficient Arabidopsis roots
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03695.xopenalex-snapshot
The nodule inception‐like protein 7 modulates nitrate sensing and metabolism in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1438-8677.2008.00097.xopenalex-snapshot
Leaf nitrogen remobilisation for plant development and grain filling
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03647.xopenalex-snapshot
Involvement of miR169 in the nitrogen‐starvation responses in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04094.xopenalex-snapshot
Nitrate transport capacity of the Arabidopsis thaliana NRT2 family members and their interactions with AtNAR2.1
inferredcites →https://doi.org/10.1111/j.1744-7909.2009.00819.xopenalex-snapshot
Overexpressing HRS1 Confers Hypersensitivity to Low Phosphate‐Elicited Inhibition of Primary Root Growth in Arabidopsis thaliana
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Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
inferredcites →https://doi.org/10.1111/tpj.12448openalex-snapshot
Auxin biosynthetic gene TAR 2 is involved in low nitrogen‐mediated reprogramming of root architecture in A rabidopsis
inferredcites →https://doi.org/10.1111/tpj.12626openalex-snapshot
The Arabidopsis nitrate transporter NRT 2.5 plays a role in nitrate acquisition and remobilization in nitrogen‐starved plants
inferredcites →https://doi.org/10.1111/tpj.13272openalex-snapshot
Early nitrogen‐deprivation responses in Arabidopsis roots reveal distinct differences on transcriptome and (phospho‐) proteome levels between nitrate and ammonium nutrition
inferredcites →https://doi.org/10.1126/science.1141319openalex-snapshot
Genome-Wide Mapping of in Vivo Protein-DNA Interactions
inferredcites →https://doi.org/10.1186/gb-2011-12-8-r83openalex-snapshot
Cistrome: an integrative platform for transcriptional regulation studies
inferredcites →https://doi.org/10.1199/tab.0011openalex-snapshot
Molecular and Developmental Biology of Inorganic Nitrogen Nutrition
inferredcites →https://doi.org/10.2307/1939320openalex-snapshot
The Scale of Nutrient Heterogeneity Around Individual Plants and Its Quantification with Geostatistics
inferredcites →https://doi.org/10.2307/2340521openalex-snapshot
On the Interpretation of χ 2 from Contingency Tables, and the Calculation of P
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Glutaredoxin AtGRXS8 represses transcriptional and developmental responses to nitrate in Arabidopsis thaliana roots
inferred← citeshttps://doi.org/10.1007/978-981-19-3800-9_7openalex-snapshot
CDPKs Based Signalling Network: Protecting the Wheat from Heat
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Expression dynamics indicate the role of Jasmonic acid biosynthesis pathway in regulating macronutrient (N, P and K+) deficiency tolerance in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s00299-026-03826-5openalex-snapshot
The rice cysteine protease OsEP3A promotes seedling growth and seed development and contains a nitrogen-starvation-responsive sequence
inferred← citeshttps://doi.org/10.1007/s00344-022-10746-7openalex-snapshot
Comparative Genomic Analysis of GARP Transcription Factor Family in Legumes and Identification of Stress-Responsive Candidate Genes
inferred← citeshttps://doi.org/10.1007/s00344-023-11002-2openalex-snapshot
The Research Progress and Prospects of the NIGT1.2 Gene in Plants
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The Physiological and Transcriptional Responses of Arabidopsis thaliana to an Innovative Controlled-Release Phosphorus–Chitosan Fertilizer: The Identification of a Gene Signature for Diagnostic and Prognostic Analyses of Plant Nutritional Status
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inferred← citeshttps://doi.org/10.1007/s11104-022-05655-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1017/s1479262126100574openalex-snapshot
Divergent nitrogen regulation of dhurrin biosynthesis in Sorghum macrospermum , a crop wild relative of Sorghum
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c05100openalex-snapshot
Strigolactones Regulate Secondary Metabolism and Nitrogen/Phosphate Signaling in Tea Plants via Transcriptional Reprogramming and Hormonal Interactions
inferred← citeshttps://doi.org/10.1038/s41467-018-03832-6openalex-snapshot
A NIGT1-centred transcriptional cascade regulates nitrate signalling and incorporates phosphorus starvation signals in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41467-021-25893-wopenalex-snapshot
Evolutionarily informed machine learning enhances the power of predictive gene-to-phenotype relationships
inferred← citeshttps://doi.org/10.1038/s41467-022-31802-6openalex-snapshot
Trypsin is a coordinate regulator of N and P nutrients in marine phytoplankton
inferred← citeshttps://doi.org/10.1038/s41467-023-40867-wopenalex-snapshot
A fungal sesquiterpene biosynthesis gene cluster critical for mutualist-pathogen transition in Colletotrichum tofieldiae
inferred← citeshttps://doi.org/10.1038/s41467-024-52339-wopenalex-snapshot
HASTY-mediated miRNA dynamics modulate nitrogen starvation-induced leaf senescence in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41467-024-53325-yopenalex-snapshot
Inorganic nitrogen inhibits symbiotic nitrogen fixation through blocking NRAMP2-mediated iron delivery in soybean nodules
inferred← citeshttps://doi.org/10.1038/s41467-025-58519-6openalex-snapshot
Autophagy is induced during plant grafting to promote wound healing
inferred← citeshttps://doi.org/10.1038/s41477-019-0384-1openalex-snapshot
Nitrate–NRT1.1B–SPX4 cascade integrates nitrogen and phosphorus signalling networks in plants
inferred← citeshttps://doi.org/10.1038/s41477-019-0403-2openalex-snapshot
When nitrate and phosphate sensors meet
inferred← citeshttps://doi.org/10.1038/s41477-025-02052-3openalex-snapshot
Trans-organ analysis of gene co-expression networks reveals a mobile long-distance regulator that balances shoot and root development in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41598-021-04758-8openalex-snapshot
New insights into the role of chrysanthemum calcineurin B–like interacting protein kinase CmCIPK23 in nitrate signaling in Arabidopsis roots
inferred← citeshttps://doi.org/10.1038/s42003-023-05601-8openalex-snapshot
Organ-specific characteristics govern the relationship between histone code dynamics and transcriptional reprogramming during nitrogen response in tomato
inferred← citeshttps://doi.org/10.1038/s44318-024-00107-3openalex-snapshot
The Arabidopsis SGN3/GSO1 receptor kinase integrates soil nitrogen status into shoot development
inferred← citeshttps://doi.org/10.1073/pnas.2022942118openalex-snapshot
Low nitrogen conditions accelerate flowering by modulating the phosphorylation state of FLOWERING BHLH 4 in Arabidopsis
inferred← citeshttps://doi.org/10.1080/00380768.2018.1537643openalex-snapshot
Shoot nitrate underlies a perception of nitrogen satiety to trigger local and systemic signaling cascades in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1080/00380768.2020.1717905openalex-snapshot
Genome-wide responses to shoot nitrate satiety are attenuated by external ammonium in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1080/00380768.2021.1908094openalex-snapshot
A cellophane-supported Arabidopsis culture for seamless transfer between different media is useful for studying various nitrogen responses
inferred← citeshttps://doi.org/10.1080/00380768.2024.2410313openalex-snapshot
Time-course analysis of the transcriptome of Arabidopsis thaliana leaves under high-concentration ammonium sulfate treatment
inferred← citeshttps://doi.org/10.1080/15592324.2026.2684389openalex-snapshot
Active ROP2 triggers leaf senescence and orchestrates the growth-senescence trade-off under nitrogen starvation
inferred← citeshttps://doi.org/10.1093/bioinformatics/btae415openalex-snapshot
Optimizing data integration improves gene regulatory network inference in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/hr/uhae242openalex-snapshot
CsSPX3-CsPHL7-CsGS1/CsTS1 module mediated Pi-regulated negatively theanine biosynthesis in tea ( Camellia sinensis )
inferred← citeshttps://doi.org/10.1093/jxb/eraa309openalex-snapshot
Improving nitrogen use efficiency: from cells to plant systems
inferred← citeshttps://doi.org/10.1093/jxb/eraa361openalex-snapshot
NRT1.1-centered nitrate signaling in plants
inferred← citeshttps://doi.org/10.1093/jxb/erab103openalex-snapshot
Cis-regulation of the amino acid transporter genes ZmAAP2 and ZmLHT1 by ZmPHR1 transcription factors in maize ear under phosphate limitation
inferred← citeshttps://doi.org/10.1093/jxb/erab114openalex-snapshot
GARP transcription factors repress Arabidopsis nitrogen starvation response via ROS-dependent and -independent pathways
inferred← citeshttps://doi.org/10.1093/jxb/erab131openalex-snapshot
Adjusting plant nutrient acquisition to fluctuating availability: transcriptional co-regulation of the nitrate and phosphate deprivation responses in roots
inferred← citeshttps://doi.org/10.1093/jxb/erab246openalex-snapshot
Nitrate-responsive NIN-like protein transcription factors perform unique and redundant roles in Arabidopsis
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/erac229openalex-snapshot
RWP-RK domain-containing transcription factors in the Viridiplantae: biology and phylogenetic relationships
inferred← citeshttps://doi.org/10.1093/jxb/erad149openalex-snapshot
Characterization of the signalling pathways involved in the repression of root nitrate uptake by nitrate in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/jxb/erae440openalex-snapshot
Down-regulation of the rice HRS1 HOMOLOG3 transcriptional repressor gene due to N deficiency directly co-activates ammonium and phosphate transporter genes
inferred← citeshttps://doi.org/10.1093/jxb/eraf202openalex-snapshot
A DUF630 and 632 domains-containing protein, ZmNRL1, acts as a positive regulator of nitrogen stress response in maize
inferred← citeshttps://doi.org/10.1093/jxb/erz148openalex-snapshot
Perception, transduction, and integration of nitrogen and phosphorus nutritional signals in the transcriptional regulatory network in plants
inferred← citeshttps://doi.org/10.1093/jxb/erz230openalex-snapshot
Ammonium and nitrate regulate NH4+ uptake activity of Arabidopsis ammonium transporter AtAMT1;3 via phosphorylation at multiple C-terminal sites
inferred← citeshttps://doi.org/10.1093/pcp/pcab010openalex-snapshot
Environmental Control of Phosphorus Acquisition: A Piece of the Molecular Framework Underlying Nutritional Homeostasis
inferred← citeshttps://doi.org/10.1093/pcp/pcag052openalex-snapshot
Cytokinin receptor AHK3 influences leaf size by modulating trans -zeatin-type cytokinin levels in xylem
inferred← citeshttps://doi.org/10.1093/pcp/pcz048openalex-snapshot
Genome-Wide Analysis of Long Intergenic Noncoding RNAs Responding to Low-Nutrient Conditions in Arabidopsis thaliana: Possible Involvement of Trans-Acting siRNA3 in Response to Low Nitrogen
inferred← citeshttps://doi.org/10.1093/plcell/koad025openalex-snapshot
The Arabidopsis transcription factor NLP2 regulates early nitrate responses and integrates nitrate assimilation with energy and carbon skeleton supply
inferred← citeshttps://doi.org/10.1093/plcell/koag201openalex-snapshot
HHO5 orchestrates dose-dependent feedback regulation of organic versus inorganic nitrogen signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiab047openalex-snapshot
Genome-wide analysis in response to nitrogen and carbon identifies regulators for root AtNRT2 transporters
inferred← citeshttps://doi.org/10.1093/plphys/kiad197openalex-snapshot
The trans -zeatin-type side-chain modification of cytokinins controls rice growth
inferred← citeshttps://doi.org/10.1093/plphys/kiad438openalex-snapshot
CHLORIDE CHANNEL-b mediates vacuolar nitrate efflux to improve low nitrogen adaptation in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiad458openalex-snapshot
Transcription factor module NLP–NIGT1 fine-tunes NITRATE TRANSPORTER2.1 expression
inferred← citeshttps://doi.org/10.1093/plphys/kiad504openalex-snapshot
The rice NUCLEAR FACTOR-YA5 and MICRORNA169a module promotes nitrogen utilization during nitrogen deficiency
inferred← citeshttps://doi.org/10.1093/plphys/kiae277openalex-snapshot
Transcription factor ZmEREB97 regulates nitrate uptake in maize (Zea mays) roots
inferred← citeshttps://doi.org/10.1093/plphys/kiae489openalex-snapshot
Phosphorylation of the transcription factor SlBIML1 by SlBIN2 kinases delays flowering in tomato
inferred← citeshttps://doi.org/10.1093/plphys/kiae628openalex-snapshot
The cytokinin efflux transporter ABCC4 participates in Arabidopsis root system development
inferred← citeshttps://doi.org/10.1093/plphys/kiaf180openalex-snapshot
The N6-methyladenosine reader ECT1 regulates seed germination via gibberellic acid- and phytochrome B-mediated signaling
inferred← citeshttps://doi.org/10.1101/2020.02.14.949453openalex-snapshot
Autophagy is induced during plant grafting for wound healing
inferred← citeshttps://doi.org/10.1101/2020.12.22.424016openalex-snapshot
A WD40 repeat-like protein pathway connects F-BOX STRESS INDUCED (FBS) proteins to the NIGT1.1 transcriptional repressor in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2022.03.14.484309openalex-snapshot
Nitrogen and phosphorus deficiencies alter primary and secondary metabolites of soybean roots
inferred← citeshttps://doi.org/10.1101/2022.04.15.488190openalex-snapshot
Stepwise origin and evolution of a transcriptional activator and repressor system integrating nutrient signaling in plants
inferred← citeshttps://doi.org/10.1101/2022.10.07.511332openalex-snapshot
Signaling pathways involved in the repression of root nitrate uptake by nitrate in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2023.04.19.537470openalex-snapshot
Root Barrier Surveillance Mechanisms Convey Soil Nitrogen Status to Shoots
inferred← citeshttps://doi.org/10.1101/2024.05.14.594121openalex-snapshot
Arabidopsis ABCC4 encodes a cytokinin efflux transporter and is involved in root system development
inferred← citeshttps://doi.org/10.1101/2025.04.10.648086openalex-snapshot
Establishment, maintenance and consequences of inter-individual transcriptional variability for a gene involved in nitrate nutrition in plants
inferred← citeshttps://doi.org/10.1101/2025.07.31.667803openalex-snapshot
HHO5: A key orchestrator of dose-dependent nitrogen signaling pathways in Arabidopsis
inferred← citeshttps://doi.org/10.1101/551069openalex-snapshot
Transcriptional dynamics of bread wheat in response to nitrate and phosphate supply reveal functional divergence of genetic factors involved in nitrate and phosphate signaling
inferred← citeshttps://doi.org/10.1105/tpc.18.00656openalex-snapshot
Identification of Molecular Integrators Shows that Nitrogen Actively Controls the Phosphate Starvation Response in Plants
inferred← citeshttps://doi.org/10.1105/tpc.19.00748openalex-snapshot
Nitrate in 2020: Thirty Years from Transport to Signaling Networks
inferred← citeshttps://doi.org/10.1105/tpc.20.00361openalex-snapshot
The Transcription Factor NIGT1.2 Modulates Both Phosphate Uptake and Nitrate Influx during Phosphate Starvation in Arabidopsis and Maize
inferred← citeshttps://doi.org/10.1111/jipb.13053openalex-snapshot
Potassium and phosphorus transport and signaling in plants
inferred← citeshttps://doi.org/10.1111/jipb.13057openalex-snapshot
Abscisic acid signaling negatively regulates nitrate uptake via phosphorylation of NRT1.1 by SnRK2s in Arabidopsis
inferred← citeshttps://doi.org/10.1111/jipb.13073openalex-snapshot
Functional assembly of root‐associated microbial consortia improves nutrient efficiency and yield in soybean
inferred← citeshttps://doi.org/10.1111/jipb.13496openalex-snapshot
NIGT1 represses plant growth and mitigates phosphate starvation signaling to balance the growth response tradeoff in rice
inferred← citeshttps://doi.org/10.1111/jipb.70304openalex-snapshot
Mineral nutrients as regulators of plant flowering time: A molecular perspective
inferred← citeshttps://doi.org/10.1111/jipb.70367openalex-snapshot
Networks in plant nitrate foraging: From model plants to crop improvement
inferred← citeshttps://doi.org/10.1111/nph.16102openalex-snapshot
Nitrogen–phosphorus interplay: old story with molecular tale
inferred← citeshttps://doi.org/10.1111/nph.16627openalex-snapshot
Gene regulatory network and its constituent transcription factors that control nitrogen‐deficiency responses in rice
inferred← citeshttps://doi.org/10.1111/nph.18499openalex-snapshot
Nitrogen‐inducible GLK1 modulates phosphate starvation response via the PHR1 ‐dependent pathway
inferred← citeshttps://doi.org/10.1111/nph.18788openalex-snapshot
A gene regulatory network in Arabidopsis roots reveals features and regulators of the plant response to elevated CO2
inferred← citeshttps://doi.org/10.1111/nph.19579openalex-snapshot
TaLBD41 interacts with TaNAC2 to regulate nitrogen uptake and metabolism in response to nitrate availability
inferred← citeshttps://doi.org/10.1111/nph.19695openalex-snapshot
Dof1.7 and NIGT1 transcription factors mediate multilayered transcriptional regulation for different expression patterns of NITRATE TRANSPORTER2 genes under nitrogen deficiency stress
inferred← citeshttps://doi.org/10.1111/nph.20236openalex-snapshot
CPK 28‐mediated phosphorylation enhances nitrate transport activity of NRT 2.1 during nitrogen deprivation
inferred← citeshttps://doi.org/10.1111/nph.70115openalex-snapshot
Symbiotic nitrogen fixation suppresses root nitrate uptake in Medicago truncatula under nitrate limitation
inferred← citeshttps://doi.org/10.1111/nph.70609openalex-snapshot
Reciprocal regulation of nitrate and jasmonate signaling by JASMONATE ZIM DOMAIN PROTEIN 1 coordinates plant growth and defense
inferred← citeshttps://doi.org/10.1111/pbi.14167openalex-snapshot
CRISPR/Cas9‐mediated elimination of OsHHO3, a transcriptional repressor of three AMMONIUM TRANSPORTER1 genes, improves nitrogen use efficiency in rice
inferred← citeshttps://doi.org/10.1111/pce.14212openalex-snapshot
Strigolactones: New players in the nitrogen–phosphorus signalling interplay
inferred← citeshttps://doi.org/10.1111/pce.70371openalex-snapshot
ZmPT7 Regulates Nitrate Utilization in Maize by Interacting With ZmNRT2.2
inferred← citeshttps://doi.org/10.1111/pce.70624openalex-snapshot
CsSPX‐PHR/PHL‐PHT1 and CsmiR399a‐PHO2‐PHT1/PHO1 Modules Orchestrate Pi Use Efficiency and Aluminium Tolerance in Tea Plants
inferred← citeshttps://doi.org/10.1111/ppl.14118openalex-snapshot
Single‐cell transcriptome analyses reveal cellular and molecular responses to low nitrogen in burley tobacco leaves
inferred← citeshttps://doi.org/10.1111/ppl.14486openalex-snapshot
Nitrate transporters and mechanisms of nitrate signal transduction in Arabidopsis and rice
inferred← citeshttps://doi.org/10.1111/ppl.70542openalex-snapshot
Shoot Nitrate Status Regulates Arabidopsis Shoot Growth and Systemic Transcriptional Responses via Shoot Adenosine Phosphate‐Isopentenyltransferase 3
inferred← citeshttps://doi.org/10.1111/tpj.14637openalex-snapshot
Nitrate‐inducible NIGT1 proteins modulate phosphate uptake and starvation signalling via transcriptional regulation of SPX genes
inferred← citeshttps://doi.org/10.1111/tpj.14667openalex-snapshot
Distinct non‐coding RNAs confer root‐dependent sense transgene‐induced post‐transcriptional gene silencing and nitrogen‐dependent post‐transcriptional regulation to AtAMT1;1 transcripts in Arabidopsis roots
inferred← citeshttps://doi.org/10.1111/tpj.14998openalex-snapshot
Two ADP‐glucose pyrophosphorylase subunits, OsAGPL1 and OsAGPS1, modulate phosphorus homeostasis in rice
inferred← citeshttps://doi.org/10.1111/tpj.15011openalex-snapshot
Cytokinin biosynthesis and transport for systemic nitrogen signaling
inferred← citeshttps://doi.org/10.1111/tpj.15796openalex-snapshot
A collection of inducible transcription factor‐glucocorticoid receptor fusion lines for functional analyses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/tpj.16369openalex-snapshot
NIGT1 .4 maintains primary root elongation in response to salt stress through induction of ERF1 in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.16511openalex-snapshot
Recent advances in unraveling the mystery of combined nutrient stress in plants
inferred← citeshttps://doi.org/10.1111/tpj.16976openalex-snapshot
At the crossroads: strigolactones mediate changes in cytokinin synthesis and signalling in response to nitrogen limitation
inferred← citeshttps://doi.org/10.1111/tpj.17198openalex-snapshot
A novel transcription factor CsSNACA2 plays a pivotal role within nitrogen assimilation in tea plants
inferred← citeshttps://doi.org/10.1111/tpj.70831openalex-snapshot
Identification of symbiotic nitrogen fixation‐modulating factors in alfalfa and mechanism elucidation of MsHHO3
inferred← citeshttps://doi.org/10.1126/sciadv.adq0187openalex-snapshot
Cold-induced degradation of core clock proteins implements temperature compensation in the Arabidopsis circadian clock
inferred← citeshttps://doi.org/10.1146/annurev-arplant-070121-015752openalex-snapshot
Improving Crop Nitrogen Use Efficiency Toward Sustainable Green Revolution
inferred← citeshttps://doi.org/10.1146/annurev-arplant-083123-053039openalex-snapshot
Nitrate Sensing and Signaling in Plants: Comparative Insights and Nutritional Interactions
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-010521-015047openalex-snapshot
Dynamic Nutrient Signaling Networks in Plants
inferred← citeshttps://doi.org/10.11606/d.64.2021.tde-04092023-134221openalex-snapshot
Characterization of natural genetic variation in tomato (Solanum lycopersicum) for root ammonium uptake
inferred← citeshttps://doi.org/10.1186/s12864-025-12135-2openalex-snapshot
Proteomics analysis of nitrogen stress on the influence of carbon and nitrogen metabolism of flue-cured tobacco
inferred← citeshttps://doi.org/10.1186/s12870-019-1692-3openalex-snapshot
The role of protein-protein interactions mediated by the PB1 domain of NLP transcription factors in nitrate-inducible gene expression
inferred← citeshttps://doi.org/10.1186/s12870-022-03696-5openalex-snapshot
Identification and expression analysis of GARP superfamily genes in response to nitrogen and phosphorus stress in Spirodela polyrhiza
inferred← citeshttps://doi.org/10.1186/s12870-025-06638-zopenalex-snapshot
Synergistic effect of grassland plants and beneficial rhizosphere bacteria helps plants cope with overgrazing stress
inferred← citeshttps://doi.org/10.1186/s12870-025-07423-8openalex-snapshot
Genome-wide identification and expression analysis of the GARP superfamily in response to abiotic stresses in alfalfa (Medicago sativa L.)
inferred← citeshttps://doi.org/10.1186/s12870-026-09056-xopenalex-snapshot
Functional characterization of PpGS2 promoter in response to hormonal and environmental signals in Kentucky bluegrass
inferred← citeshttps://doi.org/10.1186/s12870-026-09242-xopenalex-snapshot
Genome-wide analyses of NPF and NRT2 reveal a potential role for a key gene, CqNRT2.2, in the quinoa response to nitrate
inferred← citeshttps://doi.org/10.1186/s42397-025-00219-zopenalex-snapshot
Insights from model plants to improve cotton’s use of nitrogen and phosphorus
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009197openalex-snapshot
NIGT1 family proteins exhibit dual mode DNA recognition to regulate nutrient response-associated genes in Arabidopsis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011984openalex-snapshot
Establishment and maintenance of NRT2.1 inter-individual variability in plants
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1384808/v1openalex-snapshot
Identification and Expression Analysis of GARP Superfamily Genes in Response to Nitrogen and Phosphorus Stress in Spirodela Polyrhiza
inferred← citeshttps://doi.org/10.32615/bp.2019.093openalex-snapshot
Comparative analysis of nitrogen metabolism-related genes in two inbred maize lines with different low-nitrogen tolerance
inferred← citeshttps://doi.org/10.3389/fgene.2024.1469704openalex-snapshot
Genome-wide identification and expression analysis of phosphate-sensing SPX proteins in oats
inferred← citeshttps://doi.org/10.3389/fpls.2020.00187openalex-snapshot
Adaptation of Foxtail Millet (Setaria italica L.) to Abiotic Stresses: A Special Perspective of Responses to Nitrogen and Phosphate Limitations
inferred← citeshttps://doi.org/10.3389/fpls.2020.574246openalex-snapshot
Novel Aspects of Nitrate Regulation in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2021.665583openalex-snapshot
Interaction Between Macro‐ and Micro-Nutrients in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2022.1005077openalex-snapshot
Histone methyltransferases SDG33 and SDG34 regulate organ-specific nitrogen responses in tomato
inferred← citeshttps://doi.org/10.3389/fpls.2022.1013304openalex-snapshot
Molecular basis of nitrogen starvation-induced leaf senescence
inferred← citeshttps://doi.org/10.3389/fpls.2022.1052659openalex-snapshot
Identification of GOLDEN2-like transcription factor genes in soybeans and their role in regulating plant development and metal ion stresses
inferred← citeshttps://doi.org/10.3389/fpls.2022.908129openalex-snapshot
Effects of Strigolactone on Torreya grandis Gene Expression and Soil Microbial Community Structure Under Simulated Nitrogen Deposition
inferred← citeshttps://doi.org/10.3389/fpls.2022.932767openalex-snapshot
The apple GARP family gene MdHHO3 regulates the nitrate response and leaf senescence
inferred← citeshttps://doi.org/10.3389/fpls.2022.947072openalex-snapshot
Genome-Wide Identification and Characterization of GARP Transcription Factor Gene Family Members Reveal Their Diverse Functions in Tea Plant (Camellia sinensis)
inferred← citeshttps://doi.org/10.3389/fpls.2023.1121073openalex-snapshot
Nitrogen use efficiency—a key to enhance crop productivity under a changing climate
inferred← citeshttps://doi.org/10.3389/fpls.2023.1164441openalex-snapshot
Integrated transcriptomic analysis identifies coordinated responses to nitrogen and phosphate deficiency in rice
inferred← citeshttps://doi.org/10.3389/fpls.2025.1591808openalex-snapshot
Rice transcription factors OsNIGT2/3 regulate nitrogen acquisition by repressing OsNRTs and OsAMTs under high-nitrogen conditions
inferred← citeshttps://doi.org/10.3389/fpls.2026.1965737openalex-snapshot
NRT1.1 as central signaling hub orchestrating plant growth and stress trade-offs
inferred← citeshttps://doi.org/10.3390/agronomy13020604openalex-snapshot
Comprehensive Evaluation of Low Nitrogen Tolerance in Oat (Avena sativa L.) Seedlings
inferred← citeshttps://doi.org/10.3390/antiox15030359openalex-snapshot
Advances in Synthetic Strategies for Microalgal Carotenoid Enhancement and Emerging Applications
inferred← citeshttps://doi.org/10.3390/genes16030322openalex-snapshot
Genome-Wide Identification and Comprehensive Analysis of the GARP Transcription Factor Superfamily in Populus deltoides
inferred← citeshttps://doi.org/10.3390/ijms19082450openalex-snapshot
Cytokinin at the Crossroads of Abiotic Stress Signalling Pathways
inferred← citeshttps://doi.org/10.3390/ijms20225587openalex-snapshot
Transgenerational Response to Nitrogen Deprivation in Arabidopsis thaliana
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