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Wheat Transcription Factor TaAREB3 Participates in Drought and Freezing Tolerances in Arabidopsis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/0-387-25856-6_9openalex-snapshot
Salt Stress Signaling and Mechanisms of Plant Salt Tolerance
inferredcites →https://doi.org/10.1007/bf00039526openalex-snapshot
Characterization and differential expression of dhn/lea/rab-like genes during cold acclimation and drought stress in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf00277130openalex-snapshot
Characterization of the expression of a desiccation-responsive rd29 gene of Arabidopsis thaliana and analysis of its promoter in transgenic plants
inferredcites →https://doi.org/10.1007/s00299-013-1418-1openalex-snapshot
ABA signaling in stress-response and seed development
inferredcites →https://doi.org/10.1007/s10142-014-0394-zopenalex-snapshot
ABI-like transcription factor gene TaABL1 from wheat improves multiple abiotic stress tolerances in transgenic plants
inferredcites →https://doi.org/10.1007/s10265-011-0412-3openalex-snapshot
ABA-mediated transcriptional regulation in response to osmotic stress in plants
inferredcites →https://doi.org/10.1007/s11033-010-0664-3openalex-snapshot
Abscisic acid response element binding factor 1 is required for establishment of Arabidopsis seedlings during winter
inferredcites →https://doi.org/10.1007/s11103-008-9298-4openalex-snapshot
A bZIP transcription factor, OsABI5, is involved in rice fertility and stress tolerance
inferredcites →https://doi.org/10.1007/s11103-008-9354-0openalex-snapshot
The wheat PKABA1-interacting factor TaABF1 mediates both abscisic acid-suppressed and abscisic acid-induced gene expression in bombarded aleurone cells
inferredcites →https://doi.org/10.1016/j.bbamem.2010.05.015openalex-snapshot
Interaction of two intrinsically disordered plant stress proteins (COR15A and COR15B) with lipid membranes in the dry state
inferredcites →https://doi.org/10.1016/j.eja.2007.01.001openalex-snapshot
The freezing characteristics of wheat at ear emergence
inferredcites →https://doi.org/10.1016/j.tplants.2010.06.005openalex-snapshot
MYB transcription factors in Arabidopsis
inferredcites →https://doi.org/10.1016/s0092-8674(02)01133-9openalex-snapshot
ROS1, a Repressor of Transcriptional Gene Silencing in Arabidopsis, Encodes a DNA Glycosylase/Lyase
inferredcites →https://doi.org/10.1016/s0981-9428(98)80093-4openalex-snapshot
The genetic and molecular dissection of abscisic acid biosynthesis and signal transduction in Arabidopsis
inferredcites →https://doi.org/10.1016/s1357-2725(97)00085-xopenalex-snapshot
Transcription factors: An overview
inferredcites →https://doi.org/10.1016/s1360-1385(01)02223-3openalex-snapshot
bZIP transcription factors in Arabidopsis
inferredcites →https://doi.org/10.1016/s1369-5266(00)00067-4openalex-snapshot
Molecular responses to dehydration and low temperature: differences and cross-talk between two stress signaling pathways
inferredcites →https://doi.org/10.1016/s1369-5266(00)80068-0openalex-snapshot
Molecular responses to dehydration and low temperature: differences and cross-talk between two stress signaling pathways
inferredcites →https://doi.org/10.1017/s0960258513000081openalex-snapshot
Functional analysis of TaABF1 during abscisic acid and gibberellin signalling in aleurone cells of cereal grains
inferredcites →https://doi.org/10.1023/a:1006058700720openalex-snapshot
Regulation of abscisic acid-induced transcription
inferredcites →https://doi.org/10.1038/nature11997openalex-snapshot
Draft genome of the wheat A-genome progenitor Triticum urartu
inferredcites →https://doi.org/10.1038/nature12028openalex-snapshot
Aegilops tauschii draft genome sequence reveals a gene repertoire for wheat adaptation
inferredcites →https://doi.org/10.1038/nprot.2008.66openalex-snapshot
An efficient chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in Arabidopsis plants
inferredcites →https://doi.org/10.1046/j.1365-313x.1995.07050751.xopenalex-snapshot
Correlation between the induction of a gene for Δ1‐pyrroline‐5‐carboxylate synthetase and the accumulation of proline in Arabidopsis thaliana under osmotic stress
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.081594298openalex-snapshot
A postgermination developmental arrest checkpoint is mediated by abscisic acid and requires the ABI5 transcription factor in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1118651109openalex-snapshot
Structural basis for basal activity and autoactivation of abscisic acid (ABA) signaling SnRK2 kinases
inferredcites →https://doi.org/10.1073/pnas.190309197openalex-snapshot
Arabidopsis basic leucine zipper transcription factors involved in an abscisic acid-dependent signal transduction pathway under drought and high-salinity conditions
inferredcites →https://doi.org/10.1073/pnas.85.19.7089openalex-snapshot
An evolutionarily conserved protein binding sequence upstream of a plant light-regulated gene.
inferredcites →https://doi.org/10.1073/pnas.87.4.1406openalex-snapshot
Nuclear proteins bind conserved elements in the abscisic acid-responsive promoter of a rice rab gene.
inferredcites →https://doi.org/10.1073/pnas.93.23.13404openalex-snapshot
Constitutive expression of the cold-regulated Arabidopsis thaliana COR15a gene affects both chloroplast and protoplast freezing tolerance
inferredcites →https://doi.org/10.1073/pnas.95.24.14570openalex-snapshot
Mode of action of the COR15a gene on the freezing tolerance of Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/jbc.275.3.1723openalex-snapshot
ABFs, a Family of ABA-responsive Element Binding Factors
inferredcites →https://doi.org/10.1093/emboj/21.11.2692openalex-snapshot
LOS2, a genetic locus required for cold‐responsive gene transcription encodes a bi‐functional enolase
inferredcites →https://doi.org/10.1093/jxb/err462openalex-snapshot
TaNAC2, a NAC-type wheat transcription factor conferring enhanced multiple abiotic stress tolerances in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.001354openalex-snapshot
The Abscisic Acid-Responsive Kinase PKABA1 Interacts with a Seed-Specific Abscisic Acid Response Element-Binding Factor, TaABF, and Phosphorylates TaABF Peptide Sequences
inferredcites →https://doi.org/10.1104/pp.003566openalex-snapshot
Arabidopsis ABI5 Subfamily Members Have Distinct DNA-Binding and Transcriptional Activities
inferredcites →https://doi.org/10.1104/pp.005793openalex-snapshot
Regulation and Role of the ArabidopsisAbscisic Acid-Insensitive 5Gene in Abscisic Acid, Sugar, and Stress Response
inferredcites →https://doi.org/10.1104/pp.100.2.733openalex-snapshot
Effects of Water-Deficit Stress on Photosynthesis, Its Components and Component Limitations, and on Water Use Efficiency in Wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.1104/pp.106.094581openalex-snapshot
Arabidopsis Cor15am Is a Chloroplast Stromal Protein That Has Cryoprotective Activity and Forms Oligomers
inferredcites →https://doi.org/10.1105/tpc.000869openalex-snapshot
The Homologous ABI5 and EEL Transcription Factors Function Antagonistically to Fine-Tune Gene Expression during Late Embryogenesis
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.105.035659openalex-snapshot
AREB1 Is a Transcription Activator of Novel ABRE-Dependent ABA Signaling That Enhances Drought Stress Tolerance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.110.074369openalex-snapshot
Rice MADS3 Regulates ROS Homeostasis during Late Anther Development
inferredcites →https://doi.org/10.1105/tpc.112.098640openalex-snapshot
Ethylene Signaling Negatively Regulates Freezing Tolerance by Repressing Expression of CBF and Type-A ARR Genes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.6.2.251openalex-snapshot
A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature, or high-salt stress.
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02192.xopenalex-snapshot
ABF2, an ABRE‐binding bZIP factor, is an essential component of glucose signaling and its overexpression affects multiple stress tolerance
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02583.xopenalex-snapshot
Abscisic acid‐activated SNRK2 protein kinases function in the gene‐regulation pathway of ABA signal transduction by phosphorylating ABA response element‐binding factors
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.1365-313x.2010.04280.xopenalex-snapshot
ABA overly-sensitive 5 (ABO5), encoding a pentatricopeptide repeat protein required for cis-splicing of mitochondrial nad2 intron 3, is involved in the abscisic acid response in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1399-3054.2008.01107.xopenalex-snapshot
Positive role of a wheat HvABI5 ortholog in abiotic stress response of seedlings
inferredcites →https://doi.org/10.1111/j.1399-3054.2012.01635.xopenalex-snapshot
Pivotal role of the AREB/ABF‐SnRK2 pathway in ABRE‐mediated transcription in response to osmotic stress in plants
inferredcites →https://doi.org/10.1111/j.1753-4887.1981.tb06752.xopenalex-snapshot
Proceedings of the National Academy of Sciences of the United States of America
inferredcites →https://doi.org/10.1111/ppl.12261openalex-snapshot
A novel wheat bZIP transcription factor, TabZIP60 , confers multiple abiotic stress tolerances in transgenic Arabidopsis
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.2145628openalex-snapshot
A Plant Leucine Zipper Protein That Recognizes an Abscisic Acid Response Element
inferredcites →https://doi.org/10.1126/science.250.4981.612-aopenalex-snapshot
A Plant Leucine Zipper Protein That Recognizes an Abscisic Acid Response Element
inferredcites →https://doi.org/10.1146/annurev.arplant.53.091401.143329openalex-snapshot
S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS
inferredcites →https://doi.org/10.1186/1471-2164-9-118openalex-snapshot
LEA (Late Embryogenesis Abundant) proteins and their encoding genes in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0002944openalex-snapshot
The Role of bZIP Transcription Factors in Green Plant Evolution: Adaptive Features Emerging from Four Founder Genes
inferredcites →https://doi.org/10.1371/journal.pone.0084359openalex-snapshot
Novel NAC Transcription Factor TaNAC67 Confers Enhanced Multi-Abiotic Stress Tolerances in Arabidopsis
inferredcites →https://doi.org/10.2307/3869643openalex-snapshot
A Novel cis-Acting Element in an Arabidopsis Gene Is Involved in Responsiveness to Drought, Low-Temperature, or High-Salt Stress
inferredcites →https://doi.org/10.3389/fpls.2015.00025openalex-snapshot
The regulatory network of ThbZIP1 in response to abscisic acid treatment
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4814706openalex-extracted
Analysis of the Function of the Anoectochilus Roxburghii Hd-Zip19 in Flower Development and Drought Responses
inferred← citeshttps://doi.org/10.2139/ssrn.4822669openalex-extracted
Analysis of the Function of the Anoectochilus Roxburghii Hd-Zip19 in Flower Development and Drought Responses
inferred← citeshttps://doi.org/10.1002/9781119463665.ch9openalex-snapshot
Abscisic Acid in Abiotic Stress‐responsive Gene Expression
inferred← citeshttps://doi.org/10.1002/ece3.5894openalex-snapshot
Association between blooming time and climatic adaptation in Prunus mume
inferred← citeshttps://doi.org/10.1007/978-3-031-24181-9_9openalex-snapshot
Microbial Mitigation of Abiotic Stress in Crops
inferred← citeshttps://doi.org/10.1007/978-3-319-90650-8_7openalex-snapshot
Transgenic Plants for Improved Salinity and Drought Tolerance
inferred← citeshttps://doi.org/10.1007/978-981-10-2854-0_4openalex-snapshot
Microbial Ecology at Rhizosphere: Bioengineering and Future Prospective
inferred← citeshttps://doi.org/10.1007/978-981-13-6883-7_1openalex-snapshot
Abiotic Stresses-Induced Physiological Alteration in Wheat
inferred← citeshttps://doi.org/10.1007/978-981-15-2172-0_4openalex-snapshot
Molecular Mechanism of Plant Adaptation and Tolerance to Cold Stress
inferred← citeshttps://doi.org/10.1007/978-981-95-5183-5_4openalex-snapshot
Transcriptomic Reprogramming in Plants: Insights into Gene Expression Modulation and Stress Adaptation
inferred← citeshttps://doi.org/10.1007/s00122-016-2794-zopenalex-snapshot
Transcription factors involved in drought tolerance and their possible role in developing drought tolerant cultivars with emphasis on wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.1007/s00122-024-04810-xopenalex-snapshot
Unlocking ABA’s role in rice cold tolerance: insights from Zhonghua 11 and Kasalath
inferred← citeshttps://doi.org/10.1007/s00299-025-03520-yopenalex-snapshot
Enhanced drought and salt stress tolerance in Arabidopsis via ectopic expression of the PvMLP19 gene
inferred← citeshttps://doi.org/10.1007/s10265-016-0857-5openalex-snapshot
A R2R3-MYB transcription factor gene in common wheat (namely TaMYBsm1) involved in enhancement of drought tolerance in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11032-017-0758-xopenalex-snapshot
Guard-cell-specific expression of Arabidopsis ABF4 improves drought tolerance of tomato and tobacco
inferred← citeshttps://doi.org/10.1007/s11103-018-0713-1openalex-snapshot
The wheat TabZIP2 transcription factor is activated by the nutrient starvation-responsive SnRK3/CIPK protein kinase
inferred← citeshttps://doi.org/10.1007/s11756-022-01028-4openalex-snapshot
Physio-biochemical assessment and CBF genes expression analysis in wheat under dehydration condition
inferred← citeshttps://doi.org/10.1007/s13258-021-01115-xopenalex-snapshot
Identification of a 193 bp promoter region of TaNRX1-D gene from common wheat that contributes to osmotic or ABA stress inducibility in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1007/s42535-024-00901-8openalex-snapshot
Harnessing phytohormone dynamics to fortify crop resilience against drought: a comprehensive review
inferred← citeshttps://doi.org/10.1007/s44154-022-00048-zopenalex-snapshot
Regulatory network established by transcription factors transmits drought stress signals in plant
inferred← citeshttps://doi.org/10.1007/s44372-026-00723-9openalex-snapshot
Drought stress induces morphophysiological adaptations and upregulates group A bZIP transcription factors in Triticum aestivum cultivar Excalibur
inferred← citeshttps://doi.org/10.1016/b978-0-12-819334-1.00009-5openalex-snapshot
The role of key transcription factors for cold tolerance in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-98332-7.00013-5openalex-snapshot
Role of abscisic acid in regulating plant's physiological and molecular aspects under abiotic stress
inferred← citeshttps://doi.org/10.1016/b978-0-443-26614-0.00019-9openalex-snapshot
Genome engineering in wheat against drought stress
inferred← citeshttps://doi.org/10.1016/j.cj.2016.10.001openalex-snapshot
Drought-responsive genes expressed predominantly in root tissues are enriched with homotypic cis -regulatory clusters in promoters of major cereal crops
inferred← citeshttps://doi.org/10.1016/j.cj.2021.09.011openalex-snapshot
Straw mulch-based no-tillage improves tillering capability of dryland wheat by reducing asymmetric competition between main stem and tillers
inferred← citeshttps://doi.org/10.1016/j.cj.2024.02.010openalex-snapshot
Wheat kinase TaSnRK2.4 forms a functional module with phosphatase TaPP2C01 and transcription factor TaABF2 to regulate drought response
inferred← citeshttps://doi.org/10.1016/j.cpb.2022.100239openalex-snapshot
Genomic and proteomic responses to drought stress and biotechnological interventions for enhanced drought tolerance in plants
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105190openalex-snapshot
Low temperature stress-induced perception and molecular signaling pathways in plants
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.122561openalex-snapshot
Cotton GhABF3-GhAO1 module regulates the cold tolerance via influencing the ascorbic acid metabolism and flavonoid biosynthesis
inferred← citeshttps://doi.org/10.1016/j.jare.2026.03.018openalex-snapshot
TaWAK5 perceives OGs to activate drought responses in wheat
inferred← citeshttps://doi.org/10.1016/j.jplph.2019.153004openalex-snapshot
TaEXPB7-B, a β-expansin gene involved in low-temperature stress and abscisic acid responses, promotes growth and cold resistance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.lwt.2024.117308openalex-snapshot
Regulatory role of AdABI5 transcription factor in enhancing aroma biosynthesis in cold-stored kiwifruit
inferred← citeshttps://doi.org/10.1016/j.molp.2023.09.001openalex-snapshot
Wheat adaptation to environmental stresses under climate change: Molecular basis and genetic improvement
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.plaphy.2018.01.008openalex-snapshot
Overexpression of a wheat (Triticum aestivum L.) bZIP transcription factor gene, TabZIP6, decreased the freezing tolerance of transgenic Arabidopsis seedlings by down-regulating the expression of CBFs
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.01.015openalex-snapshot
Gracilaria dura extract confers drought tolerance in wheat by modulating abscisic acid homeostasis
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2017.07.004openalex-snapshot
Unravelling the role of abscisic acid in chilling tolerance of zucchini during postharvest cold storage
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113336openalex-snapshot
Cytosolic invertase SlCIN8 promotes sugar and ABA accumulation to improve cold tolerance in tomato
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100298openalex-snapshot
Revisiting the molecular mechanisms and adaptive strategies associated with drought stress tolerance in common wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.1038/s41438-018-0054-xopenalex-snapshot
VlbZIP30 of grapevine functions in dehydration tolerance via the abscisic acid core signaling pathway
inferred← citeshttps://doi.org/10.1038/s41598-018-37859-yopenalex-snapshot
Identification of wheat stress-responding genes and TaPR-1-1 function by screening a cDNA yeast library prepared following abiotic stress
inferred← citeshttps://doi.org/10.1038/s41598-019-40659-7openalex-snapshot
Genome-wide Analysis of bZIP Transcription Factors in wheat and Functional Characterization of a TabZIP under Abiotic Stress
inferred← citeshttps://doi.org/10.1071/cp17387openalex-snapshot
Breeding for increased drought tolerance in wheat: a review
inferred← citeshttps://doi.org/10.1080/07352689.2020.1778924openalex-snapshot
Impact of “Omics” in Improving Drought Tolerance in Wheat
inferred← citeshttps://doi.org/10.1080/07388551.2025.2475127openalex-snapshot
AREB/ABF/ABI5 transcription factors in plant defense: regulatory cascades and functional diversity
inferred← citeshttps://doi.org/10.1080/15592324.2019.1685728openalex-snapshot
Overexpression of the Arabidopsis and winter squash superoxide dismutase genes enhances chilling tolerance via ABA-sensitive transcriptional regulation in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1093/hr/uhac105openalex-snapshot
DgbZIP3 interacts with DgbZIP2 to increase the expression of DgPOD for cold stress tolerance in chrysanthemum
inferred← citeshttps://doi.org/10.1093/jxb/eraa271openalex-snapshot
RING finger ubiquitin E3 ligase gene TaSDIR1-4A contributes to determination of grain size in common wheat
inferred← citeshttps://doi.org/10.1101/231811openalex-snapshot
VlbZIP30 of grapevine functions in drought tolerance via the abscisic acid core signaling pathway
inferred← citeshttps://doi.org/10.1111/jipb.13504openalex-snapshot
DIW1 encoding a clade I PP2C phosphatase negatively regulates drought tolerance by de‐phosphorylating TaSnRK1.1 in wheat
inferred← citeshttps://doi.org/10.1111/pbi.13989openalex-snapshot
PRpnp , a novel dual activity PNP family protein improves plant vigour and confers multiple stress tolerance in Citrus aurantifolia
inferred← citeshttps://doi.org/10.1111/ppl.13328openalex-snapshot
Crosstalk between phytohormones and secondary metabolites in the drought stress tolerance of crop plants: A review
inferred← citeshttps://doi.org/10.1111/tpj.15975openalex-snapshot
TaFDL2‐1A confers drought stress tolerance by promoting ABA biosynthesis, ABA responses, and ROS scavenging in transgenic wheat
inferred← citeshttps://doi.org/10.1134/s1022795418010039openalex-snapshot
Perspectives of Use of Transcription Factors for Improving Resistance of Wheat Productive Varieties to Abiotic Stresses by Transgenic Technologies
inferred← citeshttps://doi.org/10.1186/s12864-019-6092-4openalex-snapshot
Comprehensive analysis of bZIP transcription factors uncovers their roles during dimorphic floret differentiation and stress response in Cleistogenes songorica
inferred← citeshttps://doi.org/10.1186/s12870-024-05007-6openalex-snapshot
Gene expression analysis of drought tolerance and cuticular wax biosynthesis in diploid and tetraploid induced wallflowers
inferred← citeshttps://doi.org/10.1186/s12870-025-06543-5openalex-snapshot
Integrative physiological and transcriptomic analysis provides insights on the molecular basis of ABA-enhanced drought tolerance in pear (Pyrus betulaefolia)
inferred← citeshttps://doi.org/10.1186/s41065-018-0064-6openalex-snapshot
Characterization of TaDREB1 in wheat genotypes with different seed germination under osmotic stress
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1985628/v1openalex-snapshot
Transcriptional Regulation of Cold Stress Tolerance in Plants. Present Status and Future Prospects
inferred← citeshttps://doi.org/10.22541/au.158567055.59568640openalex-snapshot
Regulation mechanisms of bZIP transcription factors in plant grown on drought, salt and cold soils
inferred← citeshttps://doi.org/10.32615/bp.2020.164openalex-snapshot
Overexpression of the Panax ginseng MYB4 gene enhances stress tolerance in transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2016.01029openalex-snapshot
Transcription Factors and Plants Response to Drought Stress: Current Understanding and Future Directions
inferred← citeshttps://doi.org/10.3389/fpls.2017.00710openalex-snapshot
A Novel Wheat C-bZIP Gene, TabZIP14-B, Participates in Salt and Freezing Tolerance in Transgenic Plants
inferred← citeshttps://doi.org/10.3389/fpls.2019.00630openalex-snapshot
Sweetpotato bZIP Transcription Factor IbABF4 Confers Tolerance to Multiple Abiotic Stresses
inferred← citeshttps://doi.org/10.3389/fpls.2020.01258openalex-snapshot
Regulation Mechanisms of Plant Basic Leucine Zippers to Various Abiotic Stresses
inferred← citeshttps://doi.org/10.3389/fpls.2021.641087openalex-snapshot
Association Analysis Revealed That TaPYL4 Genes Are Linked to Plant Growth Related Traits in Multiple Environment
inferred← citeshttps://doi.org/10.3389/fpls.2022.850216openalex-snapshot
Fine-Tuning Cold Stress Response Through Regulated Cellular Abundance and Mechanistic Actions of Transcription Factors
inferred← citeshttps://doi.org/10.3389/fpls.2026.1813434openalex-snapshot
Molecular and morphological signatures of drought and salinity stress in Olea europaea
inferred← citeshttps://doi.org/10.3390/biology13110856openalex-snapshot
Genetic Adaptations of Soybean to Cold Stress Reveal Key Insights Through Transcriptomic Analysis
inferred← citeshttps://doi.org/10.3390/biom14091177openalex-snapshot
Identification of the Novel Small Compound Stress Response Regulators 1 and 2 That Affect Plant Abiotic Stress Signaling
inferred← citeshttps://doi.org/10.3390/cells10081996openalex-snapshot
Updates on the Role of ABSCISIC ACID INSENSITIVE 5 (ABI5) and ABSCISIC ACID-RESPONSIVE ELEMENT BINDING FACTORs (ABFs) in ABA Signaling in Different Developmental Stages in Plants
inferred← citeshttps://doi.org/10.3390/genes8120402openalex-snapshot
SlbZIP38, a Tomato bZIP Family Gene Downregulated by Abscisic Acid, Is a Negative Regulator of Drought and Salt Stress Tolerance
inferred← citeshttps://doi.org/10.3390/ijms20020311openalex-snapshot
Genome-Wide Identification and Characterization of the AREB/ABF/ABI5 Subfamily Members from Solanum tuberosum
inferred← citeshttps://doi.org/10.3390/ijms21031123openalex-snapshot
Tartary Buckwheat Transcription Factor FtbZIP5, Regulated by FtSnRK2.6, Can Improve Salt/Drought Resistance in Transgenic Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms22126378openalex-snapshot
One Hundred Candidate Genes and Their Roles in Drought and Salt Tolerance in Wheat
inferred← citeshttps://doi.org/10.3390/ijms221910265openalex-snapshot
Exploitation of Drought Tolerance-Related Genes for Crop Improvement
inferred← citeshttps://doi.org/10.3390/ijms222413658openalex-snapshot
Molecular Characterization of U-box E3 Ubiquitin Ligases (TaPUB2 and TaPUB3) Involved in the Positive Regulation of Drought Stress Response in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms23136907openalex-snapshot
Identification of Candidate Genes Regulating Drought Tolerance in Pearl Millet
inferred← citeshttps://doi.org/10.3390/ijms231911573openalex-snapshot
Genome-Wide Identification and Salt Stress Response Analysis of the bZIP Transcription Factor Family in Sugar Beet
inferred← citeshttps://doi.org/10.3390/ijms25073783openalex-snapshot
Genome-Wide Identification and Expression Profiling of the ABF Transcription Factor Family in Wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.3390/ijms26010253openalex-snapshot
Protein-Based Mechanism of Wheat Growth Under Salt Stress in Seeds Irradiated with Millimeter Waves
inferred← citeshttps://doi.org/10.3390/ijms26178309openalex-snapshot
Green Synthesized Titanium Oxide Nanoparticles Promote Salt Tolerance in Soybean
inferred← citeshttps://doi.org/10.3390/ijms27062759openalex-snapshot
Genome-Wide Association Study (GWAS) for Freezing and De-Acclimation Tolerance in Polish Winter Barley
inferred← citeshttps://doi.org/10.3390/ijms27156838openalex-snapshot
Modulatory Effects of Pre- and Post-Drought Root Application of Melatonin on the Antioxidant Defense in Young Wheat Plants
inferred← citeshttps://doi.org/10.3390/plants12132465openalex-snapshot
Duplicate Genes Contribute to Variability in Abiotic Stress Resistance in Allopolyploid Wheat
inferred← citeshttps://doi.org/10.3390/plants13060774openalex-snapshot
Identification and Characterization of the AREB/ABF Gene Family in Three Orchid Species and Functional Analysis of DcaABI5 in Arabidopsis
inferred← citeshttps://doi.org/10.3390/plants13223113openalex-snapshot
Stress-Inducible Expression of HvABF2 Transcription Factor Improves Water Deficit Tolerance in Transgenic Barley Plants
inferred← citeshttps://doi.org/10.48130/frures-0025-0039openalex-snapshot
Regulatory function of plant basic region/leucine zipper transcription factors in stress, metabolism, and developmental processes
inferred← citeshttps://doi.org/10.5513/jcea01/21.3.2760openalex-snapshot
A method for estimating nitrogen supply index in crop plants: case study on wheat
inferred← citeshttps://doi.org/10.5958/0974-4479.2021.00016.2openalex-snapshot
Understanding Transcription Factors in Plant Response to Drought Stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.26711885openalex-snapshot
Additional file 1 of Gene expression analysis of drought tolerance and cuticular wax biosynthesis in diploid and tetraploid induced wallflowers
inferred← citeshttps://doi.org/10.7287/peerj.15310v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Identification of ABF/AREB gene family in tomato (Solanum lycopersicum L.) and functional analysis of ABF/AREB in response to ABA and abiotic stresses (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15310v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Identification of ABF/AREB gene family in tomato (Solanum lycopersicum L.) and functional analysis of ABF/AREB in response to ABA and abiotic stresses (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15310v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Identification of ABF/AREB gene family in tomato (Solanum lycopersicum L.) and functional analysis of ABF/AREB in response to ABA and abiotic stresses (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15310v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Identification of ABF/AREB gene family in tomato (Solanum lycopersicum L.) and functional analysis of ABF/AREB in response to ABA and abiotic stresses (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.15310v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Identification of ABF/AREB gene family in tomato (Solanum lycopersicum L.) and functional analysis of ABF/AREB in response to ABA and abiotic stresses (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.15310v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Identification of ABF/AREB gene family in tomato (Solanum lycopersicum L.) and functional analysis of ABF/AREB in response to ABA and abiotic stresses (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.15310openalex-snapshot
Identification of ABF/AREB gene family in tomato ( Solanum lycopersicum L.) and functional analysis of ABF/AREB in response to ABA and abiotic stresses
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