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A transcription factor hierarchy defines an environmental stress response network

https://doi.org/10.1126/science.aag1550
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471142727.mb2129s109openalex-snapshot
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inferredcites →https://doi.org/10.1002/0471250953.bi1107s32openalex-snapshot
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inferredcites →https://doi.org/10.1002/cppb.20014openalex-snapshot
Profiling of Transcription Factor Binding Events by Chromatin Immunoprecipitation Sequencing (ChIP‐seq)
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inferredcites →https://doi.org/10.1016/j.bbrc.2012.12.039openalex-snapshot
Phosphorylation of the zinc finger transcriptional regulator ZAT6 by MPK6 regulates Arabidopsis seed germination under salt and osmotic stress
inferredcites →https://doi.org/10.1016/j.cell.2014.08.009openalex-snapshot
Determination and Inference of Eukaryotic Transcription Factor Sequence Specificity
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.devcel.2014.04.004openalex-snapshot
A Mesoscale Abscisic Acid Hormone Interactome Reveals a Dynamic Signaling Landscape in Arabidopsis
inferredcites →https://doi.org/10.1016/j.febslet.2006.11.002openalex-snapshot
Gain‐ and loss‐of‐function mutations in Zat10 enhance the tolerance of plants to abiotic stress
inferredcites →https://doi.org/10.1016/j.fob.2013.07.006openalex-snapshot
ATAF1 transcription factor directly regulates abscisic acid biosynthetic gene NCED3 in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.jplph.2011.02.006openalex-snapshot
Ectopic expression of different cytokinin-regulated transcription factor genes of Arabidopsis thaliana alters plant growth and development
inferredcites →https://doi.org/10.1016/j.molcel.2014.07.005openalex-snapshot
Histone-Fold Domain Protein NF-Y Promotes Chromatin Accessibility for Cell Type-Specific Master Transcription Factors
inferredcites →https://doi.org/10.1016/j.plantsci.2012.01.013openalex-snapshot
Functional roles of the protein phosphatase 2C, AtAIP1, in abscisic acid signaling and sugar tolerance in Arabidopsis
inferredcites →https://doi.org/10.1016/j.tplants.2007.08.003openalex-snapshot
The true story of the HD-Zip family
inferredcites →https://doi.org/10.1023/a:1006423324025openalex-snapshot
DNA-binding and dimerization preferences of Arabidopsis homeodomain-leucine zipper transcription factors in vitro
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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
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inferredcites →https://doi.org/10.1038/nature08599openalex-snapshot
In vitro reconstitution of an abscisic acid signalling pathway
inferredcites →https://doi.org/10.1038/nature11245openalex-snapshot
Architecture of the human regulatory network derived from ENCODE data
inferredcites →https://doi.org/10.1038/nature14123openalex-snapshot
Agrochemical control of plant water use using engineered abscisic acid receptors
inferredcites →https://doi.org/10.1038/nature15518openalex-snapshot
DNA-dependent formation of transcription factor pairs alters their binding specificity
inferredcites →https://doi.org/10.1038/nature18912openalex-snapshot
DNA-dependent formation of transcription factor pairs alters their binding specificity
inferredcites →https://doi.org/10.1038/nmeth819openalex-snapshot
A guide to choosing fluorescent proteins
inferredcites →https://doi.org/10.1042/bj20091234openalex-snapshot
The Arabidopsis thaliana NAC transcription factor family: structure–function relationships and determinants of ANAC019 stress signalling
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.2003.01708.xopenalex-snapshot
Interaction between two cis ‐acting elements, ABRE and DRE, in ABA‐dependent expression of Arabidopsis rd29A gene in response to dehydration and high‐salinity stresses
inferredcites →https://doi.org/10.1073/pnas.0505667103openalex-snapshot
Abscisic acid-dependent multisite phosphorylation regulates the activity of a transcription activator AREB1
inferredcites →https://doi.org/10.1073/pnas.0508637103openalex-snapshot
Genomic analysis of the hierarchical structure of regulatory networks
inferredcites →https://doi.org/10.1073/pnas.0709453104openalex-snapshot
Delayed leaf senescence induces extreme drought tolerance in a flowering plant
inferredcites →https://doi.org/10.1073/pnas.0904863106openalex-snapshot
ChIP-Seq of transcription factors predicts absolute and differential gene expression in embryonic stem cells
inferredcites →https://doi.org/10.1073/pnas.0911965107openalex-snapshot
Molecular cloning of Sdr4 , a regulator involved in seed dormancy and domestication of rice
inferredcites →https://doi.org/10.1073/pnas.1012232108openalex-snapshot
SCARECROW-LIKE 3 promotes gibberellin signaling by antagonizing master growth repressor DELLA in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1112871109openalex-snapshot
Characterization of MADS-domain transcription factor complexes in Arabidopsis flower development
inferredcites →https://doi.org/10.1073/pnas.1308974110openalex-snapshot
Quantitative phosphoproteomics identifies SnRK2 protein kinase substrates and reveals the effectors of abscisic acid action
inferredcites →https://doi.org/10.1089/cmb.2015.0010openalex-snapshot
cDREM: Inferring Dynamic Combinatorial Gene Regulation
inferredcites →https://doi.org/10.1093/bioinformatics/8.3.275openalex-snapshot
The rapid generation of mutation data matrices from protein sequences
inferredcites →https://doi.org/10.1093/bioinformatics/btm563openalex-snapshot
Defining clusters from a hierarchical cluster tree: the Dynamic Tree Cut package for R
inferredcites →https://doi.org/10.1093/bioinformatics/btp616openalex-snapshot
edgeR : a Bioconductor package for differential expression analysis of digital gene expression data
inferredcites →https://doi.org/10.1093/bioinformatics/btr064openalex-snapshot
FIMO: scanning for occurrences of a given motif
inferredcites →https://doi.org/10.1093/bioinformatics/bts251openalex-snapshot
DAVID-WS: a stateful web service to facilitate gene/protein list analysis
inferredcites →https://doi.org/10.1093/bioinformatics/bts529openalex-snapshot
Genome-wide in silico prediction of gene expression
inferredcites →https://doi.org/10.1093/bioinformatics/btt487openalex-snapshot
RDAVIDWebService: a versatile R interface to DAVID
inferredcites →https://doi.org/10.1093/bioinformatics/btu638openalex-snapshot
HTSeq—a Python framework to work with high-throughput sequencing data
inferredcites →https://doi.org/10.1093/emboj/cdf316openalex-snapshot
Homeodomain protein ATHB6 is a target of the protein phosphatase ABI1 and regulates hormone responses in Arabidopsis
inferredcites →https://doi.org/10.1093/molbev/mst197openalex-snapshot
MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/nar/gkr1090openalex-snapshot
The Arabidopsis Information Resource (TAIR): improved gene annotation and new tools
inferredcites →https://doi.org/10.1093/nar/gkt979openalex-snapshot
Ensembl Genomes 2013: scaling up access to genome-wide data
inferredcites →https://doi.org/10.1093/nar/gku1179openalex-snapshot
Gene Ontology Consortium: going forward
inferredcites →https://doi.org/10.1093/nar/gku365openalex-snapshot
deepTools: a flexible platform for exploring deep-sequencing data
inferredcites →https://doi.org/10.1093/nar/gkv416openalex-snapshot
The MEME Suite
inferredcites →https://doi.org/10.1093/pcp/pcr026openalex-snapshot
Age-Dependent Action of an ABA-Inducible Receptor Kinase, RPK1, as a Positive Regulator of Senescence in Arabidopsis Leaves
inferredcites →https://doi.org/10.1101/gr.118992.110openalex-snapshot
Prioritizing candidate disease genes by network-based boosting of genome-wide association data
inferredcites →https://doi.org/10.1101/gr.136184.111openalex-snapshot
ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia
inferredcites →https://doi.org/10.1104/pp.104.046599openalex-snapshot
Arabidopsis Cys2/His2-Type Zinc-Finger Proteins Function as Transcription Repressors under Drought, Cold, and High-Salinity Stress Conditions
inferredcites →https://doi.org/10.1104/pp.106.079475openalex-snapshot
CYP707A1 and CYP707A2, Which Encode Abscisic Acid 8′-Hydroxylases, Are Indispensable for Proper Control of Seed Dormancy and Germination in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.110981openalex-snapshot
Overexpression of AtMYB44 Enhances Stomatal Closure to Confer Abiotic Stress Tolerance in Transgenic Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.151704openalex-snapshot
Genome-Wide Analysis of Ethylene-Responsive Element Binding Factor-Associated Amphiphilic Repression Motif-Containing Transcriptional Regulators in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.154617openalex-snapshot
DREB2C Interacts with ABF2, a bZIP Protein Regulating Abscisic Acid-Responsive Gene Expression, and Its Overexpression Affects Abscisic Acid Sensitivity
inferredcites →https://doi.org/10.1104/pp.111.186999openalex-snapshot
The TOPLESS Interactome: A Framework for Gene Repression in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.010362openalex-snapshot
Arabidopsis Basic Leucine Zipper Proteins That Mediate Stress-Responsive Abscisic Acid Signaling
inferredcites →https://doi.org/10.1105/tpc.10.8.1391openalex-snapshot
Two Transcription Factors, DREB1 and DREB2, with an EREBP/AP2 DNA Binding Domain Separate Two Cellular Signal Transduction Pathways in Drought- and Low-Temperature-Responsive Gene Expression, Respectively, in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.104.022699openalex-snapshot
Isolation and Functional Analysis of Arabidopsis Stress-Inducible NAC Transcription Factors That Bind to a Drought-Responsivecis-Element in theearly responsive to dehydration stress 1Promoter[W]
inferredcites →https://doi.org/10.1105/tpc.106.047688openalex-snapshot
Analysis of Transcription Factor HY5 Genomic Binding Sites Revealed Its Hierarchical Role in Light Regulation of Development
inferredcites →https://doi.org/10.1105/tpc.8.5.847openalex-snapshot
Transcription factor veracity: is GBF3 responsible for ABA-regulated expression of Arabidopsis Adh?
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02171.xopenalex-snapshot
A dehydration‐induced NAC protein, RD26, is involved in a novel ABA‐dependent stress‐signaling pathway
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03981.xopenalex-snapshot
EXPRESSION OF CONCERN: Modulation of drought resistance by the abscisic acid receptor PYL5 through inhibition of clade A PP2Cs
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04092.xopenalex-snapshot
AREB1, AREB2, and ABF3 are master transcription factors that cooperatively regulate ABRE-dependent ABA signaling involved in drought stress tolerance and require ABA for full activation
inferredcites →https://doi.org/10.1111/j.1467-9868.2005.00503.xopenalex-snapshot
Regularization and Variable Selection Via the Elastic Net
inferredcites →https://doi.org/10.1111/nph.12607openalex-snapshot
b HLH 122 is important for drought and osmotic stress resistance in A rabidopsis and in the repression of ABA catabolism
inferredcites →https://doi.org/10.1111/pce.12228openalex-snapshot
Functional characterization of A rabidopsis HsfA6a as a heat‐shock transcription factor under high salinity and dehydration conditions
inferredcites →https://doi.org/10.1111/tpj.12259openalex-snapshot
ABA and the ubiquitin E3 ligase KEEP ON GOING affect proteolysis of the A rabidopsis thaliana transcription factors ABF 1 and ABF 3
inferredcites →https://doi.org/10.1126/science.1172408openalex-snapshot
Regulators of PP2C Phosphatase Activity Function as Abscisic Acid Sensors
inferredcites →https://doi.org/10.1126/science.1173041openalex-snapshot
Abscisic Acid Inhibits Type 2C Protein Phosphatases via the PYR/PYL Family of START Proteins
inferredcites →https://doi.org/10.1126/science.1196914openalex-snapshot
Integrative Analysis of the Caenorhabditis elegans Genome by the modENCODE Project
inferredcites →https://doi.org/10.1126/science.1198374openalex-snapshot
Identification of Functional Elements and Regulatory Circuits by Drosophila modENCODE
inferredcites →https://doi.org/10.1126/science.1250322openalex-snapshot
A Chloroplast Retrograde Signal Regulates Nuclear Alternative Splicing
inferredcites →https://doi.org/10.1126/science.aad1171openalex-snapshot
Transcriptional control of tissue formation throughout root development
inferredcites →https://doi.org/10.1126/scisignal.2003760openalex-snapshot
bHLH Transcription Factors That Facilitate K + Uptake During Stomatal Opening Are Repressed by Abscisic Acid Through Phosphorylation
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112122openalex-snapshot
Abscisic Acid: Emergence of a Core Signaling Network
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105444openalex-snapshot
TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES
inferredcites →https://doi.org/10.1186/1471-2105-11-237openalex-snapshot
ChIPpeakAnno: a Bioconductor package to annotate ChIP-seq and ChIP-chip data
inferredcites →https://doi.org/10.1186/1752-0509-6-104openalex-snapshot
DREM 2.0: Improved reconstruction of dynamic regulatory networks from time-series expression data
inferredcites →https://doi.org/10.1186/gb-2013-14-4-r36openalex-snapshot
TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
inferredcites →https://doi.org/10.1186/s13007-015-0087-1openalex-snapshot
Improved DNase-seq protocol facilitates high resolution mapping of DNase I hypersensitive sites in roots in Arabidopsis thaliana
inferredcites →https://doi.org/10.12688/f1000research.6354.1openalex-snapshot
AGRIS: providing access to agricultural research data exploiting open data on the web
inferredcites →https://doi.org/10.1371/journal.pcbi.0030061openalex-snapshot
DNA Familial Binding Profiles Made Easy: Comparison of Various Motif Alignment and Clustering Strategies
inferredcites →https://doi.org/10.1371/journal.pone.0059481openalex-snapshot
NUCLEAR FACTOR Y Transcription Factors Have Both Opposing and Additive Roles in ABA-Mediated Seed Germination
inferredcites →https://doi.org/10.18637/jss.v028.i05openalex-snapshot
Building Predictive Models in R Using the caret Package
inferredcites →https://doi.org/10.18637/jss.v033.i01openalex-snapshot
Regularization Paths for Generalized Linear Models via Coordinate Descent
inferredcites →https://doi.org/10.4161/psb.4.1.7331openalex-snapshot
The GA-signaling repressor RGL3 represses testa rupture in response to changes in GA and ABA levels
inferredcites →https://doi.org/10.5483/bmbrep.2007.40.6.1083openalex-snapshot
AtHAP3b Plays a Crucial Role in the Regulation of Flowering Time in Arabidopsis during Osmotic Stress

What points at this work

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

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Unveiling the secrets of abiotic stress tolerance in plants through molecular and hormonal insights
inferred← citeshttps://doi.org/10.1007/s13562-026-01115-6openalex-snapshot
Biochemical defence of plants: redox molecules and their role in the alleviation of heavy metal stress
inferred← citeshttps://doi.org/10.1007/s40626-018-0128-zopenalex-snapshot
Development and cell death domain-containing asparagine-rich protein (DCD/NRP): an essential protein in plant development and stress responses
inferred← citeshttps://doi.org/10.1016/b978-0-12-817819-5.00009-7openalex-snapshot
Networks of transcription factors
inferred← citeshttps://doi.org/10.1016/j.bbagen.2026.130924openalex-snapshot
Application of surface plasmon resonance to elucidate the cooperative DNA binding mechanisms of NFATc1 and c-Jun
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2019.194447openalex-snapshot
Inference of plant gene regulatory networks using data-driven methods: A practical overview
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.04.048openalex-snapshot
H2A.Z-containing nucleosomes are evicted to activate AtMYB44 transcription in response to salt stress
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.03.006openalex-snapshot
AtMYB44 suppresses transcription of the late embryogenesis abundant protein gene AtLEA4-5
inferred← citeshttps://doi.org/10.1016/j.biortech.2026.135573openalex-snapshot
Multi-omics framework reveals molecular determinants of small peptide trileucine enhancing ethanol stress tolerance in industrial yeast
inferred← citeshttps://doi.org/10.1016/j.biosystems.2021.104486openalex-snapshot
Metacode: One code to rule them all
inferred← citeshttps://doi.org/10.1016/j.cell.2021.12.006openalex-snapshot
The Chinese pine genome and methylome unveil key features of conifer evolution
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.107717openalex-snapshot
Functional Divergence of the Arabidopsis Florigen-Interacting bZIP Transcription Factors FD and FDP
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112163openalex-snapshot
JMJ28 guides sequence-specific targeting of ATX1/2-containing COMPASS-like complex in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115770openalex-snapshot
HIPP26L-NF-YC9-SRMT module regulates drought response in poplar
inferred← citeshttps://doi.org/10.1016/j.cels.2021.04.010openalex-snapshot
Single-cell co-expression analysis reveals that transcriptional modules are shared across cell types in the brain
inferred← citeshttps://doi.org/10.1016/j.cels.2023.05.002openalex-snapshot
The trans-regulatory landscape of gene networks in plants
inferred← citeshttps://doi.org/10.1016/j.coisb.2020.07.005openalex-snapshot
Analysis of time-series regulatory networks
inferred← citeshttps://doi.org/10.1016/j.coviro.2020.02.002openalex-snapshot
Interplay between ABA signaling and RNA silencing in plant viral resistance
inferred← citeshttps://doi.org/10.1016/j.cpb.2026.100641openalex-snapshot
Directed SiGaResNet: A supervised graph neural network framework for inferring stability-aware ABA-responsive gene regulatory networks via transcriptomic meta-analysis
inferred← citeshttps://doi.org/10.1016/j.cpb.2026.100664openalex-snapshot
An autoencoder-based framework for uncovering tomato transcriptional strategies in response to stress
inferred← citeshttps://doi.org/10.1016/j.cub.2019.03.042openalex-snapshot
Soil Salinity Limits Plant Shade Avoidance
inferred← citeshttps://doi.org/10.1016/j.cub.2021.04.057openalex-snapshot
Abscisic acid signaling activates distinct VND transcription factors to promote xylem differentiation in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2023.08.073openalex-snapshot
The Polycomb repressive complex 2 deposits H3K27me3 and represses transposable elements in a broad range of eukaryotes
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.10.012openalex-snapshot
Thriving under Stress: How Plants Balance Growth and the Stress Response
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2018.12.084openalex-snapshot
New insight into the molecular basis of cadmium stress responses of wild paper mulberry plant by transcriptome analysis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104555openalex-snapshot
Genome-wide investigation on transcriptional responses to drought stress in wild and cultivated rice
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104945openalex-snapshot
N6-methyladenosine methylation analysis reveals transcriptome-wide expression response to salt stress in rice roots
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105453openalex-snapshot
ThDIV2, an R-R-type MYB transcription factor of Tamarix hispida, negatively regulates cadmium stress by modulating ROS homeostasis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105868openalex-snapshot
Transgenic poplar with the Zygophyllum xanthoxylon zinc finger protein transcription factor ZxZF gene shows improved drought resistance by regulating hormone signal
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2025.106293openalex-snapshot
Altitude markedly influenced moss functional traits and trait associations at the community level in the eastern Pamir Plateau
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2026.106455openalex-snapshot
Loss of OsMBTB3 function enhances drought tolerance and alters ABA responsiveness and ubiquitination in rice
inferred← citeshttps://doi.org/10.1016/j.fsi.2025.110680openalex-snapshot
GATA transcription factors in bivalves: Genomic diversity, evolutionary conservation, and roles in environmental adaptation
inferred← citeshttps://doi.org/10.1016/j.gene.2018.09.018openalex-snapshot
Effect of water-deficit on tassel development in maize
inferred← citeshttps://doi.org/10.1016/j.gpb.2020.02.004openalex-snapshot
Structural and Functional Analyses of Hub MicroRNAs in An Integrated Gene Regulatory Network of Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.hpj.2022.06.009openalex-snapshot
Drought-induced proline is mainly synthesized in leaves and transported to roots in watermelon under water deficit
inferred← citeshttps://doi.org/10.1016/j.ibmb.2024.104217openalex-snapshot
Annotation of transcription factors, chromatin-associated factors, and basal transcription machinery in the pea aphid, Acyrthosiphon pisum, and development of the ATFdb database, a resource for studies of transcriptional regulation
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.10.195openalex-snapshot
Identification and molecular evolution of the La and LARP genes in 16 plant species: A focus on the Gossypium hirsutum
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.116441openalex-snapshot
Male and female poplars exhibited sex-specific differences in metabolic and transcriptional responses to two levels of water deficit
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.120455openalex-snapshot
Mechanisms of pathogenic microorganisms, root antioxidant systems, and secondary metabolites of Codonopsis pilosula (Franch.) Nannf. in response to continuous cropping obstacles
inferred← citeshttps://doi.org/10.1016/j.ins.2020.04.016openalex-snapshot
Hierarchical clustering supported by reciprocal nearest neighbors
inferred← citeshttps://doi.org/10.1016/j.isci.2019.07.045openalex-snapshot
The Nutrient Response Transcriptional Regulome of Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.isci.2021.102965openalex-snapshot
Mitigating tradeoffs in plant breeding
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110081openalex-snapshot
Heat-stress-induced ROS in maize silks cause late pollen tube growth arrest and sterility
inferred← citeshttps://doi.org/10.1016/j.jap.2026.100027openalex-snapshot
Aquatic plant responses to microplastic and metal pollution: Stress mechanisms and remediation approaches
inferred← citeshttps://doi.org/10.1016/j.jare.2024.11.002openalex-snapshot
A molecular perspective on the role of FERONIA in root growth, nutrient uptake, stress sensing and microbiome assembly
inferred← citeshttps://doi.org/10.1016/j.jenvman.2025.124408openalex-snapshot
From benefit to burden: Assessing the full range of health impacts in urban green spaces using a threshold model
inferred← citeshttps://doi.org/10.1016/j.jgg.2024.04.005openalex-snapshot
Genetic variations in ZmEREB179 are associated with waterlogging tolerance in maize
inferred← citeshttps://doi.org/10.1016/j.jgg.2025.01.008openalex-snapshot
Uncovering the chromatin-mediated transcriptional regulatory network governing cold stress responses in fish immune cells
inferred← citeshttps://doi.org/10.1016/j.jgg.2025.08.008openalex-snapshot
The interplay between phosphorus nutrition and abiotic stresses in plants
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133528openalex-snapshot
The C2H2 family protein ZAT17 engages in the cadmium stress response by interacting with PRL1 in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jplph.2023.154060openalex-snapshot
A novel ABA-induced transcript factor from Millettia pinnata, MpAITR1, enhances salt and drought tolerance through ABA signaling in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2025.118507openalex-snapshot
Unveiling cellular resilience: Exploring cellular stress-regulating proteins in mediterranean Mussel (Mytilus galloprovincialis) larvae exposed to heat stress and metal contamination
inferred← citeshttps://doi.org/10.1016/j.molp.2017.12.013openalex-snapshot
Abscisic Acid Signaling Inhibits Brassinosteroid Signaling through Dampening the Dephosphorylation of BIN2 by ABI1 and ABI2
inferred← citeshttps://doi.org/10.1016/j.molp.2019.01.002openalex-snapshot
Arabidopsis ABF3 and ABF4 Transcription Factors Act with the NF-YC Complex to Regulate SOC1 Expression and Mediate Drought-Accelerated Flowering
inferred← citeshttps://doi.org/10.1016/j.molp.2019.02.002openalex-snapshot
The A-B-A of Floral Transition: The to Do List for Perfect Escape
inferred← citeshttps://doi.org/10.1016/j.molp.2022.02.007openalex-snapshot
The lncRNA MARS modulates the epigenetic reprogramming of the marneral cluster in response to ABA
inferred← citeshttps://doi.org/10.1016/j.molp.2022.10.016openalex-snapshot
MINI-EX: Integrative inference of single-cell gene regulatory networks in plants
inferred← citeshttps://doi.org/10.1016/j.molp.2022.12.018openalex-snapshot
Wheat-RegNet: An encyclopedia of common wheat hierarchical regulatory networks
inferred← citeshttps://doi.org/10.1016/j.patcog.2022.109230openalex-snapshot
Scalable clustering by aggregating representatives in hierarchical groups
inferred← citeshttps://doi.org/10.1016/j.pbi.2018.05.001openalex-snapshot
The Arabidopsis bZIP transcription factor family — an update
inferred← citeshttps://doi.org/10.1016/j.pbi.2018.05.015openalex-snapshot
NUCLEAR FACTOR-Y: still complex after all these years?
inferred← citeshttps://doi.org/10.1016/j.pbi.2021.102057openalex-snapshot
Network biology to uncover functional and structural properties of the plant immune system
inferred← citeshttps://doi.org/10.1016/j.pbi.2026.102955openalex-snapshot
Predicting transcriptional regulators in plants in the era of artificial intelligence
inferred← citeshttps://doi.org/10.1016/j.physa.2019.122772openalex-snapshot
Structural controllability of dynamic transcriptional regulatory networks for Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110273openalex-snapshot
Heat stress transcription factor OsSPL7 plays a critical role in reactive oxygen species balance and stress responses in rice
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110689openalex-snapshot
The BTB-TAZ protein MdBT2 negatively regulates the drought stress response by interacting with the transcription factor MdNAC143 in apple
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111304openalex-snapshot
The protein phosphatase 2C clade A TaPP2CA interact with calcium-dependent protein kinases, TaCDPK5/TaCDPK9-1, that phosphorylate TabZIP60 transcription factor from wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112235openalex-snapshot
Characterization and functions of Myeloblastosis (MYB) transcription factors in cucurbit crops
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112658openalex-snapshot
Genome-wide identification of histone acetyltransferase members and functional dissection of histone acetylation-mediated desiccation tolerance in Syntrichia caninervis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.04.002openalex-snapshot
PpHB22, a member of HD-Zip proteins, activates PpDAM1 to regulate bud dormancy transition in ‘Suli’ pear (Pyrus pyrifolia White Pear Group)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.06.012openalex-snapshot
Chromatin remodeling for the transcription of type 2C protein phosphatase genes in response to salt stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.11.032openalex-snapshot
ZmSNAC13, a maize NAC transcription factor conferring enhanced resistance to multiple abiotic stresses in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108265openalex-snapshot
Nitraria sibirica adapts to long-term soil water deficit by reducing photosynthesis, stimulating antioxidant systems, and accumulating osmoregulators
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108663openalex-snapshot
The PbbHLH62/PbVHA-B1 module confers salt tolerance through modulating intracellular Na+/K+ homeostasis and reactive oxygen species removal in pear
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109568openalex-snapshot
Deciphering crucial salt-responsive genes in Brassica napus via statistical modeling and network analysis on dynamic transcriptomic data
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109729openalex-snapshot
FtbHLH1, a transcription factor that interacts with FtATG8a, enhances the drought stress response in Tartary buckwheat
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109735openalex-snapshot
The salt and ABA inducible transcription factor gene, SlAITR3, negatively regulates tomato salt tolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110995openalex-snapshot
Crosstalk between physiological and genetic mechanisms during maintenance of acquired thermotolerance in tomato
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2025.114079openalex-snapshot
CmCIGR1 antagonizes CmICE1-mediated activation of CmPP2CA1, thereby promoting ABA-dependent postharvest ripening in melons
inferred← citeshttps://doi.org/10.1016/j.redox.2025.103934openalex-snapshot
Functional S-persulfidation exploration reveals a novel regulatory mechanism of HNF1α
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109655openalex-snapshot
Physiological, biochemical and transcriptional responses of Passiflora edulis Sims f. edulis under progressive drought stress
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113531openalex-snapshot
Polyamine oxidase induces flower formation by promoting spermidine and ABA accumulation in cherry (Cerasus pseudocerasus Lindl.)
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.152322openalex-snapshot
Identification of StAP2/ERF genes of potato (Solanum tuberosum) and their multiple functions in detoxification and accumulation of cadmium in yest: Implication for Genetic-based phytoremediation
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.03.010openalex-snapshot
The potential application of genome editing by using CRISPR/Cas9, and its engineered and ortholog variants for studying the transcription factors involved in the maintenance of phosphate homeostasis in model plants
inferred← citeshttps://doi.org/10.1016/j.stress.2022.100058openalex-snapshot
Improving drought tolerance: Can comparative transcriptomics support strategic rice breeding?
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100740openalex-snapshot
Strigolactones affect the stomatal and transcriptomic memory of repeated drought stress in tomato
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100890openalex-snapshot
Transcription factor ZmGBF1 enhances heat stress tolerance in maize by directly increasing expression of ZmCXE2 involved in GA pathway
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101341openalex-snapshot
DUF538-domain proteins SVB and SVB2 act as positive regulators of ABA and salt stress responses in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.tplants.2017.12.006openalex-snapshot
Combinatorial Transcriptional Control of Plant Specialized Metabolism
inferred← citeshttps://doi.org/10.1016/j.tplants.2021.07.009openalex-snapshot
Proline metabolism as regulatory hub
inferred← citeshttps://doi.org/10.1016/j.virusres.2023.199061openalex-snapshot
Identifying Transcription Factors Associated with Fusarium Graminearum Virus 2 Accumulation in Fusarium Graminearum by Phenome-Based Investigation
inferred← citeshttps://doi.org/10.1016/j.xinn.2020.100017openalex-snapshot
Mechanisms of Plant Responses and Adaptation to Soil Salinity
inferred← citeshttps://doi.org/10.1016/j.xplc.2020.100099openalex-snapshot
Abscisic Acid Connects Phytohormone Signaling with RNA Metabolic Pathways and Promotes an Antiviral Response that Is Evaded by a Self-Controlled RNA Virus
inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100684openalex-snapshot
Orthogroup and phylotranscriptomic analyses identify transcription factors involved in the plant cold response: A case study of Arabidopsis BBX29
inferred← citeshttps://doi.org/10.1016/j.xplc.2024.101137openalex-snapshot
Pan-genome analyses of 11 Fraxinus species provide insights into salt adaptation in ash trees
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101924openalex-snapshot
Rewiring the unfolded protein response for plant growth recovery after stress
inferred← citeshttps://doi.org/10.1016/j.yhbeh.2020.104756openalex-snapshot
Functional genomics of parental care of insects
inferred← citeshttps://doi.org/10.1016/s2095-3119(18)62127-6openalex-snapshot
Kiwifruit (Actinidia chinensis) R1R2R3-MYB transcription factor AcMYB3R enhances drought and salinity tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c07163openalex-snapshot
Multi-Omics Analysis Provides Crucial Insights into the Drought Adaptation of Glycyrrhiza uralensis Fisch
inferred← citeshttps://doi.org/10.1021/acschembio.5c01011openalex-snapshot
Li-BrU-seq: A Low-Input and Simplified Metabolic Labeling Method for Nascent RNA Sequencing
inferred← citeshttps://doi.org/10.1038/ncomms14573openalex-snapshot
RD26 mediates crosstalk between drought and brassinosteroid signalling pathways
inferred← citeshttps://doi.org/10.1038/s41467-018-07044-wopenalex-snapshot
Baleen whale cortisol levels reveal a physiological response to 20th century whaling
inferred← citeshttps://doi.org/10.1038/s41467-019-09522-1openalex-snapshot
Network Walking charts transcriptional dynamics of nitrogen signaling by integrating validated and predicted genome-wide interactions
inferred← citeshttps://doi.org/10.1038/s41467-020-14979-6openalex-snapshot
Transient genome-wide interactions of the master transcription factor NLP7 initiate a rapid nitrogen-response cascade
inferred← citeshttps://doi.org/10.1038/s41467-020-18782-1openalex-snapshot
TERMINAL FLOWER 1-FD complex target genes and competition with FLOWERING LOCUS T
inferred← citeshttps://doi.org/10.1038/s41467-020-19977-2openalex-snapshot
Role of Raf-like kinases in SnRK2 activation and osmotic stress response in plants
inferred← citeshttps://doi.org/10.1038/s41467-022-30770-1openalex-snapshot
ChIP-Hub provides an integrative platform for exploring plant regulome
inferred← citeshttps://doi.org/10.1038/s41467-022-35438-4openalex-snapshot
Limited conservation in cross-species comparison of GLK transcription factor binding suggested wide-spread cistrome divergence
inferred← citeshttps://doi.org/10.1038/s41467-023-38096-2openalex-snapshot
Double DAP-seq uncovered synergistic DNA binding of interacting bZIP transcription factors
inferred← citeshttps://doi.org/10.1038/s41467-023-40773-1openalex-snapshot
Phosphate starvation response precedes abscisic acid response under progressive mild drought in plants
inferred← citeshttps://doi.org/10.1038/s41467-025-59329-6openalex-snapshot
Unveiling the regulatory role of GRP7 in ABA signal-mediated mRNA translation efficiency regulation
inferred← citeshttps://doi.org/10.1038/s41467-025-59571-yopenalex-snapshot
The immune NIK1/RPL10/LIMYB signaling module regulates photosynthesis and translation under biotic and abiotic stresses.
inferred← citeshttps://doi.org/10.1038/s41467-026-75947-0openalex-snapshot
Positional grammar of transcription factor binding partitions developmental and stress-response regulation in plants
inferred← citeshttps://doi.org/10.1038/s41477-020-0605-7openalex-snapshot
Integrated multi-omics framework of the plant response to jasmonic acid
inferred← citeshttps://doi.org/10.1038/s41477-021-00894-1openalex-snapshot
Integrative inference of transcriptional networks in Arabidopsis yields novel ROS signalling regulators
inferred← citeshttps://doi.org/10.1038/s41477-021-00929-7openalex-snapshot
Evolutionarily conserved hierarchical gene regulatory networks for plant salt stress response
inferred← citeshttps://doi.org/10.1038/s41477-022-01139-5openalex-snapshot
Divergence in the ABA gene regulatory network underlies differential growth control
inferred← citeshttps://doi.org/10.1038/s41477-022-01150-wopenalex-snapshot
Transcriptional competition shapes proteotoxic ER stress resolution
inferred← citeshttps://doi.org/10.1038/s41576-019-0105-7openalex-snapshot
Old cogs, new tricks: the evolution of gene expression in a chromatin context
inferred← citeshttps://doi.org/10.1038/s41576-024-00710-4openalex-snapshot
Dynamics of ER stress-induced gene regulation in plants
inferred← citeshttps://doi.org/10.1038/s41580-022-00479-6openalex-snapshot
Plant hormone regulation of abiotic stress responses
inferred← citeshttps://doi.org/10.1038/s41586-024-07424-xopenalex-snapshot
The temperature sensor TWA1 is required for thermotolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41587-025-02727-4openalex-snapshot
Unlocking gene regulatory networks for crop resilience and sustainable agriculture
inferred← citeshttps://doi.org/10.1038/s41588-021-00882-3openalex-snapshot
PHYTOCHROME-INTERACTING FACTORs trigger environmentally responsive chromatin dynamics in plants
inferred← citeshttps://doi.org/10.1038/s41598-020-80695-2openalex-snapshot
AITRL, an evolutionarily conserved plant specific transcription repressor regulates ABA response in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41598-024-58161-0openalex-snapshot
Expression of the Arabidopsis redox-related LEA protein, SAG21 is regulated by ERF, NAC and WRKY transcription factors
inferred← citeshttps://doi.org/10.1038/s41598-026-37856-6openalex-snapshot
Identification and analysis of the MYB transcription factors against seawater tolerance in daylily (Hemerocallis fulva L.)
inferred← citeshttps://doi.org/10.1038/s42003-018-0091-xopenalex-snapshot
The HTPmod Shiny application enables modeling and visualization of large-scale biological data
inferred← citeshttps://doi.org/10.1038/s42003-020-0866-8openalex-snapshot
An abscisic acid-responsive protein interaction network for sucrose non-fermenting related kinase1 in abiotic stress response
inferred← citeshttps://doi.org/10.1038/s44454-025-00016-yopenalex-snapshot
Molecular clustering enhances perfluorocarboxylic acid bioaccumulation in lactuca sativa by disrupting the tricarboxylic acid cycle
inferred← citeshttps://doi.org/10.1039/d5en00174aopenalex-snapshot
Nanoparticle-mediated mitigation of salt stress-induced oxidative damage in plants: insights into signaling, gene expression, and antioxidant mechanisms
inferred← citeshttps://doi.org/10.1042/bcj20160633openalex-snapshot
Cross-talk of Brassinosteroid signaling in controlling growth and stress responses
inferred← citeshttps://doi.org/10.1073/pnas.1613199114openalex-snapshot
Abscisic acid signaling is controlled by a BRANCHED1/HD-ZIP I cascade in Arabidopsis axillary buds
inferred← citeshttps://doi.org/10.1073/pnas.1702613114openalex-snapshot
Pathogen exploitation of an abscisic acid- and jasmonate-inducible MAPK phosphatase and its interception by Arabidopsis immunity
inferred← citeshttps://doi.org/10.1073/pnas.1804971115openalex-snapshot
Transcripts from downstream alternative transcription start sites evade uORF-mediated inhibition of gene expression in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.2001928117openalex-snapshot
Intertwined signatures of desiccation and drought tolerance in grasses
inferred← citeshttps://doi.org/10.1073/pnas.2310670120openalex-snapshot
Distinct guard cell–specific remodeling of chromatin accessibility during abscisic acid– and CO 2 -dependent stomatal regulation
inferred← citeshttps://doi.org/10.1073/pnas.2316825121openalex-snapshot
The interplay between the circadian clock and abiotic stress responses mediated by ABF3 and CCA1/LHY
inferred← citeshttps://doi.org/10.1073/pnas.2509904122openalex-snapshot
Antagonistic regulation of nitrogen and drought signaling mediated by NIN-like protein 7 transcription factor in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1073/pnas.2602105123openalex-snapshot
Convergent innovation of (crypto)vivipary via asymmetric dismantling of seed desiccation and dormancy machinery
inferred← citeshttps://doi.org/10.1080/01140671.2024.2409775openalex-snapshot
Breeding 4.0 vis‐à‐vis application of artificial intelligence (AI) in crop improvement: an overview
inferred← citeshttps://doi.org/10.1080/15592324.2018.1525998openalex-snapshot
Protein kinase CK2α subunits constitutively activate ABA signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1080/15592324.2020.1744293openalex-snapshot
Cell wall/vacuolar inhibitor of fructosidase 1 regulates ABA response and salt tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1080/17429145.2020.1778110openalex-snapshot
AIW1 and AIW2, two ABA-induced WD40 repeat-containing transcription repressors function redundantly to regulate ABA and salt responses in Arabidopsis
inferred← citeshttps://doi.org/10.1080/21645698.2020.1790287openalex-snapshot
SlEAD1, an EAR motif-containing ABA down-regulated novel transcription repressor regulates ABA response in tomato
inferred← citeshttps://doi.org/10.1086/706780openalex-snapshot
Gene Type and Mutation Position Influence Responses in Root Traits across Nutrient Environments
inferred← citeshttps://doi.org/10.1089/dna.2020.6245openalex-snapshot
Genome-Wide Identification of Key Candidate microRNAs and Target Genes Associated with Peanut Drought Tolerance
inferred← citeshttps://doi.org/10.1093/bib/bbaf421openalex-snapshot
Cell type heterogeneity in gene co-expression networks: implications for toxicological research
inferred← citeshttps://doi.org/10.1093/gigascience/giy080openalex-snapshot
A workflow for simplified analysis of ATAC-cap-seq data in R
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