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Multifaceted role of cycling DOF factor 3 (CDF3) in the regulation of flowering time and abiotic stress responses in Arabidopsis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Photosynthetic Carbon–Nitrogen Interactions: Modelling Inter-Pathway Control and Signalling
inferredcites →https://doi.org/10.1002/btpr.514openalex-snapshot
Transcription factors as tools to engineer enhanced drought stress tolerance in plants
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GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
inferredcites →https://doi.org/10.1007/bf00028874openalex-snapshot
Cloning of cDNAs for genes that are early-responsive to dehydration stress (ERDs) inArabidopsis thaliana L.: identification of three ERDs as HSP cognate genes
inferredcites →https://doi.org/10.1007/s00299-005-0061-xopenalex-snapshot
Involvement of GIGANTEA gene in the regulation of the cold stress response in Arabidopsis
inferredcites →https://doi.org/10.1007/s00299-007-0470-0openalex-snapshot
Enhanced tolerance to drought stress in transgenic rice plants overexpressing a small heat-shock protein, sHSP17.7
inferredcites →https://doi.org/10.1007/s00299-009-0813-0openalex-snapshot
Physiological roles of ERD10 in abiotic stresses and seed germination of Arabidopsis
inferredcites →https://doi.org/10.1007/s11103-013-0090-8openalex-snapshot
Overexpression of AtWRKY30 enhances abiotic stress tolerance during early growth stages in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.bbrc.2010.09.038openalex-snapshot
Arabidopsis DREB2C functions as a transcriptional activator of HsfA3 during the heat stress response
inferredcites →https://doi.org/10.1016/j.copbio.2010.03.002openalex-snapshot
More from less: plant growth under limited water
inferredcites →https://doi.org/10.1016/j.copbio.2014.11.023openalex-snapshot
Flowering time regulation in crops — what did we learn from Arabidopsis?
inferredcites →https://doi.org/10.1016/j.devcel.2009.06.015openalex-snapshot
Arabidopsis DOF Transcription Factors Act Redundantly to Reduce CONSTANS Expression and Are Essential for a Photoperiodic Flowering Response
inferredcites →https://doi.org/10.1016/j.pbi.2007.04.014openalex-snapshot
Regulatory metabolic networks in drought stress responses
inferredcites →https://doi.org/10.1016/j.pbi.2011.03.018openalex-snapshot
Programming desiccation-tolerance: from plants to seeds to resurrection plants
inferredcites →https://doi.org/10.1016/j.plantsci.2004.07.039openalex-snapshot
Proline as a measure of stress in tomato plants
inferredcites →https://doi.org/10.1016/j.plantsci.2013.03.016openalex-snapshot
The role of the DNA-binding One Zinc Finger (DOF) transcription factor family in plants
inferredcites →https://doi.org/10.1016/j.plaphy.2010.08.016openalex-snapshot
Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants
inferredcites →https://doi.org/10.1016/j.plaphy.2012.12.002openalex-snapshot
Proteomic analysis of spring freeze-stress responsive proteins in leaves of bread wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.1016/j.tplants.2004.03.006openalex-snapshot
Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response
inferredcites →https://doi.org/10.1016/j.tplants.2005.11.002openalex-snapshot
Abiotic stress, the field environment and stress combination
inferredcites →https://doi.org/10.1016/j.tplants.2010.08.002openalex-snapshot
Plant molecular stress responses face climate change
inferredcites →https://doi.org/10.1016/j.tplants.2011.12.006openalex-snapshot
Compartmentation of GABA metabolism raises intriguing questions
inferredcites →https://doi.org/10.1016/s0958-1669(03)00030-2openalex-snapshot
Molecular responses to drought, salinity and frost: common and different paths for plant protection
inferredcites →https://doi.org/10.1016/s1360-1385(02)02362-2openalex-snapshot
The Dof family of plant transcription factors
inferredcites →https://doi.org/10.1016/s1360-1385(99)01486-7openalex-snapshot
Metabolism and functions of gamma-aminobutyric acid
inferredcites →https://doi.org/10.1016/s1369-5266(03)00092-xopenalex-snapshot
Regulatory network of gene expression in the drought and cold stress responses
inferredcites →https://doi.org/10.1023/a:1006043914056openalex-snapshot
Effects of sucrose supply on growth and paraquat tolerance of the late-flowering gi-3 mutant
inferredcites →https://doi.org/10.1023/b:plan.0000009297.37235.4aopenalex-snapshot
An Arabidopsis thaliana T-DNA mutagenized population (GABI-Kat) for flanking sequence tag-based reverse genetics
inferredcites →https://doi.org/10.1023/b:plan.0000040902.06881.d4openalex-snapshot
Arabidopsis Transcriptional Activators CBF1, CBF2, and CBF3 have Matching Functional Activities
inferredcites →https://doi.org/10.1038/nprot.2007.199openalex-snapshot
Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis
inferredcites →https://doi.org/10.1042/0264-6021:3440503openalex-snapshot
Sugar/osmoticum levels modulate differential abscisic acid-independent expression of two stress-responsive sucrose synthase genes in Arabidopsis
inferredcites →https://doi.org/10.1042/bj20110060openalex-snapshot
The transcription factor AtDOF4.2 regulates shoot branching and seed coat formation in Arabidopsis
inferredcites →https://doi.org/10.1046/j.0960-7412.2001.01227.xopenalex-snapshot
Important roles of drought‐ and cold‐inducible genes for galactinol synthase in stress tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-3040.1999.00386.xopenalex-snapshot
The interaction between elevated carbon dioxide and nitrogen nutrition: the physiological and molecular background
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Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00363.xopenalex-snapshot
Diversity and similarity among recognition sequences of Dof transcription factors
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01165.xopenalex-snapshot
Maize VP1 complements Arabidopsisabi3 and confers a novel ABA/auxin interaction in roots
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01359.xopenalex-snapshot
Monitoring the expression profiles of 7000 Arabidopsis genes under drought, cold and high‐salinity stresses using a full‐length cDNA microarray
inferredcites →https://doi.org/10.1073/pnas.0402267101openalex-snapshot
Metabolic engineering with Dof1 transcription factor in plants: Improved nitrogen assimilation and growth under low-nitrogen conditions
inferredcites →https://doi.org/10.1073/pnas.0705639105openalex-snapshot
Arabidopsis CBF1 and CBF3 have a different function than CBF2 in cold acclimation and define different gene classes in the CBF regulon
inferredcites →https://doi.org/10.1073/pnas.1037532100openalex-snapshot
Mitochondrial succinic-semialdehyde dehydrogenase of the γ-aminobutyrate shunt is required to restrict levels of reactive oxygen intermediates in plants
inferredcites →https://doi.org/10.1073/pnas.1107161108openalex-snapshot
Integration of low temperature and light signaling during cold acclimation response in Arabidopsis
inferredcites →https://doi.org/10.1093/aob/mcn125openalex-snapshot
Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell
inferredcites →https://doi.org/10.1093/emboj/16.21.6535openalex-snapshot
The asymmetric distribution of the constituents of the Ran system is essential for transport into and out of the nucleus
inferredcites →https://doi.org/10.1093/emboj/18.17.4679openalex-snapshot
GIGANTEA: a circadian clock‐controlled gene that regulates photoperiodic flowering in Arabidopsis and encodes a protein with several possible membrane‐spanning domains
inferredcites →https://doi.org/10.1093/jxb/erl164openalex-snapshot
Gene networks involved in drought stress response and tolerance
inferredcites →https://doi.org/10.1093/jxb/erq167openalex-snapshot
Transcriptional profiles of drought-responsive genes in modulating transcription signal transduction, and biochemical pathways in tomato
inferredcites →https://doi.org/10.1093/jxb/ert451openalex-snapshot
Characterization of tomato Cycling Dof Factors reveals conserved and new functions in the control of flowering time and abiotic stress responses
inferredcites →https://doi.org/10.1093/nar/gkq310openalex-snapshot
agriGO: a GO analysis toolkit for the agricultural community
inferredcites →https://doi.org/10.1093/pcp/pce105openalex-snapshot
The Transcriptional Activation Domain of the Plant-Specific Dof1 Factor Functions in Plant, Animal, and Yeast Cells
inferredcites →https://doi.org/10.1093/pcp/pcn101openalex-snapshot
Arabidopsis Transcriptome Analysis under Drought, Cold, High-Salinity and ABA Treatment Conditions using a Tiling Array
inferredcites →https://doi.org/10.1104/pp.103.033431openalex-snapshot
When Defense Pathways Collide. The Response of Arabidopsis to a Combination of Drought and Heat Stress
inferredcites →https://doi.org/10.1104/pp.105.068254openalex-snapshot
The Zinc-Finger Protein Zat12 Plays a Central Role in Reactive Oxygen and Abiotic Stress Signaling in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.090795openalex-snapshot
Rapid Classification of Phenotypic Mutants of Arabidopsis via Metabolite Fingerprinting
inferredcites →https://doi.org/10.1104/pp.107.103101openalex-snapshot
Reduced Expression of Succinyl-Coenzyme A Ligase Can Be Compensated for by Up-Regulation of theγ-Aminobutyrate Shunt in Illuminated Tomato Leaves
inferredcites →https://doi.org/10.1104/pp.107.106989openalex-snapshot
Recombinational Cloning with Plant Gateway Vectors
inferredcites →https://doi.org/10.1104/pp.108.2.543openalex-snapshot
Calcium/Calmodulin Activation of Soybean Glutamate Decarboxylase
inferredcites →https://doi.org/10.1104/pp.110.161794openalex-snapshot
Molecular Basis of Plant Cold Acclimation: Insights Gained from Studying the CBF Cold Response Pathway
inferredcites →https://doi.org/10.1104/pp.113.216341openalex-snapshot
ETHYLENE RESPONSE FACTOR6 Acts as a Central Regulator of Leaf Growth under Water-Limiting Conditions in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.119.2.463openalex-snapshot
The Arabidopsis CBF Gene Family Is Composed of Three Genes Encoding AP2 Domain-Containing Proteins Whose Expression Is Regulated by Low Temperature but Not by Abscisic Acid or Dehydration1
inferredcites →https://doi.org/10.1105/tpc.000596openalex-snapshot
Cell Signaling during Cold, Drought, and Salt Stress
inferredcites →https://doi.org/10.1105/tpc.10.1.75openalex-snapshot
Involvement of Maize Dof Zinc Finger Proteins in Tissue-Specific and Light-Regulated Gene Expression
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.105.033464openalex-snapshot
Distinct Roles of GIGANTEA in Promoting Flowering and Regulating Circadian Rhythms in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.035881openalex-snapshot
Functional Analysis of anArabidopsisTranscription Factor, DREB2A, Involved in Drought-Responsive Gene Expression
inferredcites →https://doi.org/10.1105/tpc.105.039990openalex-snapshot
The Molecular Basis of Temperature Compensation in the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1105/tpc.108.058941openalex-snapshot
The Cold-Inducible CBF1 Factor–Dependent Signaling Pathway Modulates the Accumulation of the Growth-Repressing DELLA Proteins via Its Effect on Gibberellin Metabolism
inferredcites →https://doi.org/10.1105/tpc.108.062968openalex-snapshot
A Pivotal Role of the Basic Leucine Zipper Transcription Factor bZIP53 in the Regulation of Arabidopsis Seed Maturation Gene Expression Based on Heterodimerization and Protein Complex Formation
inferredcites →https://doi.org/10.1111/j.1365-3040.2004.01208.xopenalex-snapshot
Putative role of γ ‐aminobutyric acid (GABA) as a long‐distance signal in up‐regulation of nitrate uptake in Brassica napus L.
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02288.xopenalex-snapshot
Roles of the CBF2 and ZAT12 transcription factors in configuring the low temperature transcriptome of Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02437.xopenalex-snapshot
The Botany Array Resource: e‐Northerns, Expression Angling, and promoter analyses
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03573.xopenalex-snapshot
Differential regulation of two glutamine synthetase genes by a single Dof transcription factor
inferredcites →https://doi.org/10.1111/j.1399-3054.1962.tb08052.xopenalex-snapshot
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
inferredcites →https://doi.org/10.1111/j.1399-3054.2011.01451.xopenalex-snapshot
Genetic engineering of woody plants: current and future targets in a stressful environment
inferredcites →https://doi.org/10.1111/j.1467-7652.2011.00592.xopenalex-snapshot
Introduction of the ZmDof1 gene into rice enhances carbon and nitrogen assimilation under low‐nitrogen conditions
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02087.xopenalex-snapshot
Photosynthetic limitations in response to water stress and recovery in Mediterranean plants with different growth forms
inferredcites →https://doi.org/10.1111/jpi.12155openalex-snapshot
The cysteine2/histidine2‐type transcription factor ZINC FINGER OF ARABIDOPSIS THALIANA 6 ‐activated C‐ REPEAT ‐ BINDING FACTOR pathway is essential for melatonin‐mediated freezing stress resistance in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.12538openalex-snapshot
Transcription factor WRKY 46 regulates osmotic stress responses and stomatal movement independently in A rabidopsis
inferredcites →https://doi.org/10.1111/tpj.12759openalex-snapshot
The GI – CDF module of Arabidopsis affects freezing tolerance and growth as well as flowering
inferredcites →https://doi.org/10.1111/tpj.13091openalex-snapshot
Activation of autophagy by unfolded proteins during endoplasmic reticulum stress
inferredcites →https://doi.org/10.1126/science.1110586openalex-snapshot
FKF1 F-Box Protein Mediates Cyclic Degradation of a Repressor of CONSTANS in Arabidopsis
inferredcites →https://doi.org/10.1126/science.1146994openalex-snapshot
FKF1 and GIGANTEA Complex Formation Is Required for Day-Length Measurement in Arabidopsis
inferredcites →https://doi.org/10.1126/science.285.5433.1579openalex-snapshot
Control of Circadian Rhythms and Photoperiodic Flowering by the Arabidopsis GIGANTEA Gene
inferredcites →https://doi.org/10.1146/annurev.arplant.47.1.377openalex-snapshot
THE MOLECULAR BASIS OF DEHYDRATION TOLERANCE IN PLANTS
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/10.1146/annurev.arplant.57.032905.105444openalex-snapshot
TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092911openalex-snapshot
Mechanisms of Salinity Tolerance
inferredcites →https://doi.org/10.1186/1471-2148-3-17openalex-snapshot
Genome-wide comparative phylogenetic analysis of the rice and Arabidopsis Dof gene families
inferredcites →https://doi.org/10.1186/1471-2229-10-43openalex-snapshot
Small chloroplast-targeted DnaJ proteins are involved in optimization of photosynthetic reactions in Arabidopsis thaliana
inferredcites →https://doi.org/10.1186/1471-2229-12-202openalex-snapshot
The family of DOF transcription factors in Brachypodium distachyon: phylogenetic comparison with rice and barley DOFs and expression profiling
inferredcites →https://doi.org/10.1186/1756-0500-1-93openalex-snapshot
DNA-free RNA isolation protocols for Arabidopsis thaliana, including seeds and siliques
inferredcites →https://doi.org/10.1371/journal.pone.0021800openalex-snapshot
REVIGO Summarizes and Visualizes Long Lists of Gene Ontology Terms
inferredcites →https://doi.org/10.1371/journal.pone.0032124openalex-snapshot
Transcriptome Analyses of a Salt-Tolerant Cytokinin-Deficient Mutant Reveal Differential Regulation of Salt Stress Response by Cytokinin Deficiency
inferredcites →https://doi.org/10.21769/bioprotoc.1216openalex-snapshot
Salinity Assay in Arabidopsis
inferredcites →https://doi.org/10.4141/p99-003openalex-snapshot
Physiological mechanism of tolerance of Lycopersicon spp. exposed to salt stress
inferredcites →https://doi.org/10.5424/sjar/200806s1-391openalex-snapshot
Photoperiodic control of flowering time: a review
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Genome-Wide Identification and Expression Analysis of Dof Gene Family Reveal Their Involvement in Hormone Response and Abiotic Stresses in Sunflower (Helianthus Annuus L.)
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Advances in Plant Metabolomics
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Untargeted metabolomics of strawberry (Fragaria x ananassa ‘Camarosa’) fruit from plants grown under osmotic stress conditions
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Cycling DOF factor mediated seasonal regulation of sexual reproduction and cold response is not conserved in Physcomitrium patens
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Enzymatic Conversions of Glutamate and γ-Aminobutyric Acid as Indicators of Plant Stress Response
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An LRR-only protein regulates abscisic acid-mediated abiotic stress responses during Arabidopsis seed germination
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Multi-locus genome-wide association studies reveal the dynamic genetic architecture of flowering time in chrysanthemum
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CaCDF3 Positively Regulates Capsaicinoids Biosynthesis Under Drought Stress in Capsicum annuum
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Lysine positively regulates cold tolerance in tea plants through the induction of CsCDF1 transcription factor
inferred← citeshttps://doi.org/10.1016/j.jare.2026.07.029openalex-snapshot
ZmFKF1b antagonizes the bifunctional repressor ZmEREB214 to coordinate drought tolerance and flowering time in maize
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2026.02.005openalex-snapshot
CaDoF10, a DNA-binding with one finger transcription factor from pepper, act as a positive regulator of cold stress tolerance
inferred← citeshttps://doi.org/10.1016/j.jia.2025.09.007openalex-snapshot
Pleiotropic effects of overexpressing a legume-specific Cycling DOF Factor MsCDFc1 on flowering and forage quality in alfalfa
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153492openalex-snapshot
Transcriptomic study of the night break in Chenopodium rubrum reveals possible upstream regulators of the floral activator CrFTL1
inferred← citeshttps://doi.org/10.1016/j.molp.2023.09.011openalex-snapshot
The Dof transcription factor COG1 acts as a key regulator of plant biomass by promoting photosynthesis and starch accumulation
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.12.006openalex-snapshot
Climate change and the need for agricultural adaptation
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113214openalex-snapshot
Protein profiling of fast neutron soybean mutant seeds reveals differential accumulation of seed and iron storage proteins
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111608openalex-snapshot
GhMYB102 promotes drought resistance by regulating drought-responsive genes and ABA biosynthesis in cotton (Gossypium hirsutum L.)
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111880openalex-snapshot
RsCDF3, a member of Cycling Dof Factors, positively regulates cold tolerance via auto-regulation and repressing two RsRbohs transcription in radish (Raphanus sativus L.)
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112214openalex-snapshot
The non-canonically organized members of MIR395 gene family in Brassica juncea are associated with developmentally regulated, sulfate-stress responsive bidirectional promoters that exhibit orientation-dependent differential transcriptional activity
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.03.008openalex-snapshot
Characterization of two group III potato CDPKs, StCDPK22 and StCDPK24, that contain three EF-Hand motifs in their CLDs
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108607openalex-snapshot
Arabidopsis CDF3 transcription factor increases carbon and nitrogen assimilation and yield in trans-grafted tomato plants
inferred← citeshttps://doi.org/10.1016/j.sajb.2024.02.036openalex-snapshot
Prediction of drought regulating gene (s) in barley (Hordeum vulgare L.) using express sequence tags (ESTs) through in silico approaches
inferred← citeshttps://doi.org/10.1016/j.scienta.2019.03.007openalex-snapshot
Genome-wide identification of Dof transcription factors possibly associated with internal browning of postharvest pineapple fruits
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.112884openalex-snapshot
Identification and expression profiling of flowering-related microRNAs and their targets reveals complex regulatory networks associated with bolting time in spinach
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100990openalex-snapshot
Genome-wide identification of the Dof gene family in Carya illinoinensis and potential function analysis of CiDof22 in drought stress
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100417openalex-snapshot
Engineering drought and salinity tolerance traits in crops through CRISPR-mediated genome editing: Targets, tools, challenges, and perspectives
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101935openalex-snapshot
An indel in the FAD5 promoter confers cold tolerance by enhancing transcriptional activation of unsaturated fatty acid synthesis in grapevines
inferred← citeshttps://doi.org/10.1038/s41467-019-11228-3openalex-snapshot
Sequencing of Chinese castor lines reveals genetic signatures of selection and yield-associated loci
inferred← citeshttps://doi.org/10.1038/s41598-020-61758-wopenalex-snapshot
Specific functions for Mediator complex subunits from different modules in the transcriptional response of Arabidopsis thaliana to abiotic stress
inferred← citeshttps://doi.org/10.1038/s41598-020-67537-xopenalex-snapshot
The targeted overexpression of SlCDF4 in the fruit enhances tomato size and yield involving gibberellin signalling
inferred← citeshttps://doi.org/10.1038/s41598-024-75412-2openalex-snapshot
Exploring CDF gene family in wild potato under salinity stress unveils promising candidates for developing climate-resilient crops
inferred← citeshttps://doi.org/10.1039/d4en00997eopenalex-snapshot
Nano zinc oxide activates MdCDF2 to promote DNA replication and cell proliferation in apple calli
inferred← citeshttps://doi.org/10.1073/pnas.2009418117openalex-snapshot
Copy number variation of TdDof controls solid-stemmed architecture in wheat
inferred← citeshttps://doi.org/10.1079/9781800626911.0005openalex-snapshot
High-throughput Metabolomics for Uncovering Plant–Herbivore Interactions
inferred← citeshttps://doi.org/10.1089/dna.2020.5652openalex-snapshot
Genome-Wide Identification and Expression Analysis of the Dof Gene Family in Medicago sativa L. Under Various Abiotic Stresses
inferred← citeshttps://doi.org/10.1093/gigascience/giaf026openalex-snapshot
Phased high-quality genome of the gymnosperm Himalayan Yew assists in paclitaxel pathway exploration
inferred← citeshttps://doi.org/10.1093/hr/uhaf324openalex-snapshot
Map-based cloning and functional characterization reveal CDF3 as the causal gene for the flowering time phenotype in Brassica rapa and Brassica napus
inferred← citeshttps://doi.org/10.1093/jxb/eraa088openalex-snapshot
CDF transcription factors: plant regulators to deal with extreme environmental conditions
inferred← citeshttps://doi.org/10.1093/jxb/erae070openalex-snapshot
The transcription factor ThDOF8 binds to a novel cis-element and mediates molecular responses to salt stress in Tamarix hispida
inferred← citeshttps://doi.org/10.1093/jxb/erx285openalex-snapshot
Transcriptional control of strawberry ripening – two to tango
inferred← citeshttps://doi.org/10.1093/pcp/pcac102openalex-snapshot
GIGANTEA Is a Negative Regulator of Abscisic Acid Transcriptional Responses and Sensitivity in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pcae132openalex-snapshot
A seed-specific DNA-binding with One Finger transcription factor, RPBF, positively regulates galactinol synthase to maintain seed vigour in rice
inferred← citeshttps://doi.org/10.1093/plcell/koab113openalex-snapshot
Time of the day prioritizes the pool of translating mRNAs in response to heat stress
inferred← citeshttps://doi.org/10.1093/plcell/koaf083openalex-snapshot
The transcription factors DOF4.6 and XND1 jointly regulate root hydraulics and drought responses in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plcell/koaf208openalex-snapshot
A transcriptional roadmap of the yearly growth cycle in Populus trees
inferred← citeshttps://doi.org/10.1093/plcell/koag196openalex-snapshot
The mRNA covalent modification dihydrouridine regulates transcript turnover and photosynthetic capacity during plant abiotic stress
inferred← citeshttps://doi.org/10.1093/plphys/kiaf014openalex-snapshot
Cycling Dof Factor 3 mediates light-dependent ascorbate biosynthesis by activating GDP- l- galactose phosphorylase in Rosa roxburghii fruit
inferred← citeshttps://doi.org/10.1093/plphys/kiag542openalex-snapshot
CYCLING DOF FACTOR 2 functions as a positive regulator integrating gibberellin signaling and biosynthesis to drive bulb germination in Lilium
inferred← citeshttps://doi.org/10.1093/treephys/tpad023openalex-snapshot
Chromatin accessibility dynamics insight into crosstalk between regulatory landscapes in poplar responses to multiple treatments
inferred← citeshttps://doi.org/10.1101/2021.07.15.452498openalex-snapshot
Ammonium regulates the development of pine roots through hormonal crosstalk and differential expression of transcription factors in the apex
inferred← citeshttps://doi.org/10.1101/2024.04.25.591174openalex-snapshot
Predicting gene expression responses to environment in Arabidopsis thaliana using natural variation in DNA sequence
inferred← citeshttps://doi.org/10.1111/jipb.12990openalex-snapshot
Immediate transcriptional responses of Arabidopsis leaves to heat shock
inferred← citeshttps://doi.org/10.1111/nph.14703openalex-snapshot
The antiphasic regulatory module comprising CDF5 and its antisense RNA FLORE links the circadian clock to photoperiodic flowering
inferred← citeshttps://doi.org/10.1111/nph.20186openalex-snapshot
StCDF1 : A ‘jack of all trades’ clock output with a central role in regulating potato nitrate reduction activity
inferred← citeshttps://doi.org/10.1111/pbi.14011openalex-snapshot
A chromosome‐level genome assembly of radish (Raphanus sativus L.) reveals insights into genome adaptation and differential bolting regulation
inferred← citeshttps://doi.org/10.1111/pbi.14287openalex-snapshot
Glucose uptake from the rhizosphere mediated by MdDOF3 ‐ MdHT1 .2 regulates drought resistance in apple
inferred← citeshttps://doi.org/10.1111/pce.14214openalex-snapshot
Ammonium regulates the development of pine roots through hormonal crosstalk and differential expression of transcription factors in the apex
inferred← citeshttps://doi.org/10.1111/pce.70649openalex-snapshot
Integrated Multi‐Omic Analyses Uncover a Regulatory Link Between Photosynthesis and Drought Tolerance in Field‐Grown Sorghum
inferred← citeshttps://doi.org/10.1111/ppl.13119openalex-snapshot
The photoperiodic response of hypocotyl elongation involves regulation of CDF1 and CDF5 activity
inferred← citeshttps://doi.org/10.1111/ppl.13268openalex-snapshot
Transcription factors as key molecular target to strengthen the drought stress tolerance in plants
inferred← citeshttps://doi.org/10.1111/ppl.70182openalex-snapshot
Male sterility‐induced parthenocarpy arose during tomato domestication
inferred← citeshttps://doi.org/10.1111/ppl.70999openalex-snapshot
Genome‐Wide Identification and Functional Characterization of Dof Transcription Factors Involved in Salt Stress Responses in Taraxacum kok‐saghyz
inferred← citeshttps://doi.org/10.1111/tpj.14699openalex-snapshot
Heating quinoa shoots results in yield loss by inhibiting fruit production and delaying maturity
inferred← citeshttps://doi.org/10.1111/tpj.15093openalex-snapshot
RETRACTED: Potato CYCLING DOF FACTOR 1 and its lncRNA counterpart StFLORE link tuber development and drought response
inferred← citeshttps://doi.org/10.1111/tpj.17175openalex-snapshot
Rice OsDof12 enhances tolerance to drought stress by activating the phenylpropanoid pathway
inferred← citeshttps://doi.org/10.1111/tpj.70008openalex-snapshot
Transcription factor PgCDF2 enhances heat tolerance of Physalis grisea by activating heat shock transcription factors PgHSFA1 and PgHSFB3
inferred← citeshttps://doi.org/10.1111/tpj.70218openalex-snapshot
The IbDof2.1 – IbABF2 module regulates abscisic acid responses and proline biosynthesis to enhance drought tolerance in sweetpotato
inferred← citeshttps://doi.org/10.1111/tpj.70710openalex-snapshot
A novel domain of unknown function 707 protein coordinates root growth and drought tolerance
inferred← citeshttps://doi.org/10.11606/t.11.2023.tde-01112023-153705openalex-snapshot
Tolerância ao calor em batata: do fenótipo ao genótipo
inferred← citeshttps://doi.org/10.1186/s12863-025-01305-6openalex-snapshot
Genome-wide DNA polymorphisms in two peatland adapted Coffea liberica varieties
inferred← citeshttps://doi.org/10.1186/s12864-020-6691-0openalex-snapshot
Genome-wide analysis of wheat DNA-binding with one finger (Dof) transcription factor genes: evolutionary characteristics and diverse abiotic stress responses
inferred← citeshttps://doi.org/10.1186/s12864-021-08104-0openalex-snapshot
Genome-wide analysis of Dof transcription factors and their response to cold stress in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1186/s12864-024-10565-yopenalex-snapshot
Genome-wide identification and molecular evolution of Dof transcription factors in Cyperus esculentus
inferred← citeshttps://doi.org/10.1186/s12864-025-12321-2openalex-snapshot
DOF gene family in P. sativum (L.): comprehensive genomic identification, phylogenetic examination, evolutionary growth, and expression analysis
inferred← citeshttps://doi.org/10.1186/s12870-025-07548-wopenalex-snapshot
A comprehensive analysis to speculate the role of trithorax genes in photoperiod-mediated tuberization in potato and comparison with storage root crops
inferred← citeshttps://doi.org/10.1186/s12915-023-01705-zopenalex-snapshot
Interaction between phenylpropane metabolism and oil accumulation in the developing seed of Brassica napus revealed by high temporal-resolution transcriptomes
inferred← citeshttps://doi.org/10.1515/biol-2022-0084openalex-snapshot
Selection and functional identification of Dof genes expressed in response to nitrogen in Populus simonii × Populus nigra
inferred← citeshttps://doi.org/10.15252/embr.201948967openalex-snapshot
Transcription factor CDF4 promotes leaf senescence and floral organ abscission by regulating abscisic acid and reactive oxygen species pathways in Arabidopsis
inferred← citeshttps://doi.org/10.15407/frg2022.02.095openalex-snapshot
Effects of drought and high temperature on physiological and biochemical processes, and productivity of plants nanochelates
inferred← citeshttps://doi.org/10.17660/ejhs.2023/029openalex-snapshot
Onion AcCDF4 ectopia overexpression regulates flowering and abiotic stress response in Arabidopsis
inferred← citeshttps://doi.org/10.18174/636038openalex-snapshot
Tubers and time : Exploring the intricate link between tuberization and senescence
inferred← citeshttps://doi.org/10.20868/upm.thesis.77361openalex-snapshot
Molecular and physiological analyses of DOF/TCP factors in Systemic Nitrogen Signaling in Arabidopsis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1773094/v1openalex-snapshot
Isolation and characterization of a soybean transcription factor, GmDof4.2, improves transgenic tobacco drought tolerance
inferred← citeshttps://doi.org/10.21273/jashs05150-21openalex-snapshot
Identification of Dof Transcription Factors in the Genome of Rosa chinensis
inferred← citeshttps://doi.org/10.33540/894openalex-snapshot
Deciphering acclimation strategies to combined abiotic stresses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fchem.2018.00026openalex-snapshot
Heat and Drought Stresses in Crops and Approaches for Their Mitigation
inferred← citeshttps://doi.org/10.3389/fpls.2017.00660openalex-snapshot
Ectopic Expression of CDF3 Genes in Tomato Enhances Biomass Production and Yield under Salinity Stress Conditions
inferred← citeshttps://doi.org/10.3389/fpls.2019.01148openalex-snapshot
Overexpression of Medicago MtCDFd1_1 Causes Delayed Flowering in Medicago via Repression of MtFTa1 but Not MtCO-Like Genes
inferred← citeshttps://doi.org/10.3389/fpls.2019.01487openalex-snapshot
Automated Imaging, Tracking, and Analytics Pipeline for Differentiating Environmental Effects on Root Meristematic Cell Division
inferred← citeshttps://doi.org/10.3389/fpls.2020.601558openalex-snapshot
The Arabidopsis Transcription Factor CDF3 Is Involved in Nitrogen Responses and Improves Nitrogen Use Efficiency in Tomato
inferred← citeshttps://doi.org/10.3389/fpls.2022.844201openalex-snapshot
Emerging Roles of Plant DNA-Binding With One Finger Transcription Factors in Various Hormone and Stress Signaling Pathways
inferred← citeshttps://doi.org/10.3389/fpls.2022.919676openalex-snapshot
Clock-Controlled and Cold-Induced CYCLING DOF FACTOR6 Alters Growth and Development in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2022.956299openalex-snapshot
Intrinsically disordered protein, DNA binding with one finger transcription factor (OsDOF27) implicates thermotolerance in yeast and rice
inferred← citeshttps://doi.org/10.3389/fpls.2023.1010669openalex-snapshot
Ectopic expression of the AtCDF1 transcription factor in potato enhances tuber starch and amino acid contents and yield under open field conditions
inferred← citeshttps://doi.org/10.3389/fpls.2023.1044918openalex-snapshot
DOF transcription factors: Specific regulators of plant biological processes
inferred← citeshttps://doi.org/10.3389/fpls.2023.1140727openalex-snapshot
Genome-wide survey and expression analysis of Dof transcription factor family in sweetpotato shed light on their promising functions in stress tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2024.1329065openalex-snapshot
Dissection of the E8 locus in two early maturing Canadian soybean populations
inferred← citeshttps://doi.org/10.3389/fpls.2024.1463300openalex-snapshot
Integrated eQTL mapping approach reveals genomic regions regulating candidate genes of the E8-r3 locus in soybean
inferred← citeshttps://doi.org/10.3389/fpls.2025.1531399openalex-snapshot
Proteomes and ubiquitylomes reveal the regulation mechanism of cold tolerance mediated by OsGRF4 in rice
inferred← citeshttps://doi.org/10.3389/fpls.2025.1546092openalex-snapshot
The SlERF4-9-SlCDF1/3-SlAEC2/SlPIN5 module regulates tomato root morphogenesis
inferred← citeshttps://doi.org/10.3389/fpls.2025.1599849openalex-snapshot
Identification and expression profiling of the CoDof genes involved in fatty acid/lipid biosynthesis of tetraploid Camellia oleifera
inferred← citeshttps://doi.org/10.3390/agronomy10020294openalex-snapshot
Genome-Wide Identification, Structure Characterization, and Expression Profiling of Dof Transcription Factor Gene Family in Wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.3390/agronomy10111800openalex-snapshot
The Expression of ELF4-Like Genes Is Influenced by Light Quality in Petunia
inferred← citeshttps://doi.org/10.3390/agronomy8090186openalex-snapshot
Genome-Wide Identification and Expression Analysis of the Dof Transcription Factor Gene Family in Gossypium hirsutum L.
inferred← citeshttps://doi.org/10.3390/biology15201832openalex-snapshot
Genome-Wide Dissection of the Dof Transcription Factor Family in Senna tora: From Gene Identification to Expression Signatures
inferred← citeshttps://doi.org/10.3390/f11050542openalex-snapshot
Differential Metabolite Accumulation in Different Tissues of Gleditsia sinensis under Water Stress and Rehydration Conditions
inferred← citeshttps://doi.org/10.3390/genes16091108openalex-snapshot
Predicting Gene Expression Responses to Cold in Arabidopsis thaliana Using Natural Variation in DNA Sequence
inferred← citeshttps://doi.org/10.3390/horticulturae12030348openalex-snapshot
Characterization of the Dof Family Members in Citrus clementina (Hort. ex Tan.) and Functional Analysis of CcDof4 and CcDof6 in Phytophthora parasitica Resistance
inferred← citeshttps://doi.org/10.3390/ht7010007openalex-snapshot
When Transcriptomics and Metabolomics Work Hand in Hand: A Case Study Characterizing Plant CDF Transcription Factors
inferred← citeshttps://doi.org/10.3390/ijms18091859openalex-snapshot
Genome-Wide Transcriptome Analysis Reveals Conserved and Distinct Molecular Mechanisms of Al Resistance in Buckwheat (Fagopyrum esculentum Moench) Leaves
inferred← citeshttps://doi.org/10.3390/ijms20020424openalex-snapshot
Multifaceted Role of PheDof12-1 in the Regulation of Flowering Time and Abiotic Stress Responses in Moso Bamboo (Phyllostachys edulis)
inferred← citeshttps://doi.org/10.3390/ijms22115662openalex-snapshot
Plant Transcription Factors Involved in Drought and Associated Stresses
inferred← citeshttps://doi.org/10.3390/ijms231911229openalex-snapshot
Ectopic Expression of Arabidopsis thaliana zDof1.3 in Tomato (Solanum lycopersicum L.) Is Associated with Improved Greenhouse Productivity and Enhanced Carbon and Nitrogen Use
inferred← citeshttps://doi.org/10.3390/ijms231911768openalex-snapshot
Genome-Wide Identification of the DOF Gene Family Involved in Fruitlet Abscission in Areca catechu L.
inferred← citeshttps://doi.org/10.3390/ijms241512091openalex-snapshot
Characterization of Dof Transcription Factors and the Heat-Tolerant Function of PeDof-11 in Passion Fruit (Passiflora edulis)
inferred← citeshttps://doi.org/10.3390/ijms25063488openalex-snapshot
DNA-Binding with One Finger (Dof) Transcription Factor Gene Family Study Reveals Differential Stress-Responsive Transcription Factors in Contrasting Drought Tolerance Potato Species
inferred← citeshttps://doi.org/10.3390/ijms25147662openalex-snapshot
Genome-Based Identification of the Dof Gene Family in Three Cymbidium Species and Their Responses to Heat Stress in Cymbidium goeringii
inferred← citeshttps://doi.org/10.3390/ijms25169103openalex-snapshot
Genome-Wide Identification of the DOF Gene Family in Kiwifruit (Actinidia chinensis) and Functional Validation of AcDOF22 in Response to Drought Stress
inferred← citeshttps://doi.org/10.3390/ijms251910250openalex-snapshot
Identification of Genomic Regions Associated with Differences in Flowering Time and Inflorescence Architecture between Melastoma candidum and M. normale
inferred← citeshttps://doi.org/10.3390/ijms252011147openalex-snapshot
Identification and Characterization of the DOF Gene Family in Phoebe bournei and Its Role in Abiotic Stress—Drought, Heat and Light Stress
inferred← citeshttps://doi.org/10.3390/ijms26062396openalex-snapshot
Multi-Omics Association Analysis of DOF Transcription Factors Involved in the Drought Resistance of Wheat Induced by Strigolactone
inferred← citeshttps://doi.org/10.3390/ijms26062671openalex-snapshot
Genome-Wide Identification and Functional Characterization of the Dof Family in Dendrobium officinale
inferred← citeshttps://doi.org/10.3390/ijms26136192openalex-snapshot
Genome-Wide Analysis of the DNA-Binding with One Finger Gene Family Reveals Soybean Expression Pattern and Functional Analysis
inferred← citeshttps://doi.org/10.3390/ijms26178392openalex-snapshot
Sulfate Deficiency-Responsive MicroRNAs in Tomato Uncover an Expanded and Functionally Integrated Regulatory Network
inferred← citeshttps://doi.org/10.3390/metabo13030454openalex-snapshot
Data Science and Plant Metabolomics
inferred← citeshttps://doi.org/10.3390/plants10040709openalex-snapshot
Genome-Wide In Silico Identification and Comparative Analysis of Dof Gene Family in Brassica napus
inferred← citeshttps://doi.org/10.3390/plants10112409openalex-snapshot
Plants Metabolome Study: Emerging Tools and Techniques
inferred← citeshttps://doi.org/10.3390/plants11152057openalex-snapshot
Genome-Wide Identification and Expression Analysis of Dof Transcription Factors in Lotus (Nelumbo nucifera Gaertn.)
inferred← citeshttps://doi.org/10.3390/plants11243473openalex-snapshot
Transcriptome and Gene Regulatory Network Analyses Reveal New Transcription Factors in Mature Fruit Associated with Harvest Date in Prunus persica
inferred← citeshttps://doi.org/10.3390/plants12091831openalex-snapshot
Genome-Wide Identification and Expression Analysis of the Dof Transcription Factor in Annual Alfalfa Medicago polymorpha
inferred← citeshttps://doi.org/10.3390/plants12244103openalex-snapshot
Hydrangea arborescens ‘Annabelle’ Flower Formation and Flowering in the Current Year
inferred← citeshttps://doi.org/10.3390/plants13050603openalex-snapshot
A First Omics Data Integration Approach in Hass Avocados to Evaluate Rootstock–Scion Interactions: From Aerial and Root Plant Growth to Fruit Development
inferred← citeshttps://doi.org/10.3390/plants13142009openalex-snapshot
The Role of Liriodendron Dof Gene Family in Abiotic Stress Response
inferred← citeshttps://doi.org/10.3390/plants14111567openalex-snapshot
Genome-Wide Identification and Expression Analysis of the LbDof Transcription Factor Family Genes in Lycium barbarum
inferred← citeshttps://doi.org/10.3390/plants14121829openalex-snapshot
Genome-Wide Characterization and Functional Analysis of CsDOF Transcription Factors in Camellia sinensis cv. Tieguanyin Under Combined Heat–Drought Stress
inferred← citeshttps://doi.org/10.48130/opr-0024-0030openalex-snapshot
Genome-wide identification and characterization of Dof gene family in Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.53560/ppasb(60-3)905openalex-snapshot
Role of Dof Transcription Factors under Abiotic Stresses
inferred← citeshttps://doi.org/10.5747/ca.2018.v14.n4.a253openalex-snapshot
IN SILICO ANALYSIS OF THE Dof TRANSCRIPTION FACTOR FAMILY IN Coffea canephora
inferred← citeshttps://doi.org/10.6084/m9.figshare.24223798openalex-snapshot
Additional file 1 of Interaction between phenylpropane metabolism and oil accumulation in the developing seed of Brassica napus revealed by high temporal-resolution transcriptomes
inferred← citeshttps://doi.org/10.6084/m9.figshare.24223888openalex-snapshot
Additional file 2 of Interaction between phenylpropane metabolism and oil accumulation in the developing seed of Brassica napus revealed by high temporal-resolution transcriptomes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26743031openalex-snapshot
Additional file 1 of Genome-wide identification and molecular evolution of Dof transcription factors in Cyperus esculentus
inferred← citeshttps://doi.org/10.6084/m9.figshare.26743034openalex-snapshot
Additional file 2 of Genome-wide identification and molecular evolution of Dof transcription factors in Cyperus esculentus
inferred← citeshttps://doi.org/10.6084/m9.figshare.26743037openalex-snapshot
Additional file 3 of Genome-wide identification and molecular evolution of Dof transcription factors in Cyperus esculentus
inferred← citeshttps://doi.org/10.6084/m9.figshare.26743040openalex-snapshot
Additional file 4 of Genome-wide identification and molecular evolution of Dof transcription factors in Cyperus esculentus
inferred← citeshttps://doi.org/10.70675/7ddf8cbcza3fbz4a03z8708zea2205094580openalex-snapshot
Étude fonctionnelle d'un récepteur lectine kinase, LecRK-I.9 : un contrôle de la dynamique des parois chez Arabidopsis thaliana
inferred← citeshttps://doi.org/10.7717/peerj.6354openalex-snapshot
Genome-wide identification and comparative evolutionary analysis of the Dof transcription factor family in physic nut and castor bean
inferred← citeshttps://doi.org/10.7717/peerj.8358openalex-snapshot
Genome-wide characterization and expression analysis of theDofgene family related to abiotic stress in watermelon
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