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The MYB 96– HHP module integrates cold and abscisic acid signaling to activate the CBF – COR pathway in Arabidopsis

https://doi.org/10.1111/tpj.12866
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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/bf00028738openalex-snapshot
Cold acclimation and cold-regulated gene expression in ABA mutants of Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s00299-013-1414-5openalex-snapshot
Cross-talk between abscisic acid-dependent and abscisic acid-independent pathways during abiotic stress
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/s10535-010-0038-7openalex-snapshot
Transcription factors in plants and ABA dependent and independent abiotic stress signalling
inferredcites →https://doi.org/10.1007/s11033-011-0823-1openalex-snapshot
Signal transduction during cold, salt, and drought stresses in plants
inferredcites →https://doi.org/10.1007/s11103-015-0283-4openalex-snapshot
The Arabidopsis MYB96 transcription factor plays a role in seed dormancy
inferredcites →https://doi.org/10.1007/s12374-013-0903-yopenalex-snapshot
Cold stress signaling networks in Arabidopsis
inferredcites →https://doi.org/10.1016/j.bbagrm.2011.08.004openalex-snapshot
AP2/ERF family transcription factors in plant abiotic stress responses
inferredcites →https://doi.org/10.1016/j.gene.2008.10.016openalex-snapshot
Identification of ICE2, a gene involved in cold acclimation which determines freezing tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.pbi.2007.04.010openalex-snapshot
Interplay between cold-responsive gene regulation, metabolism and RNA processing during plant cold acclimation
inferredcites →https://doi.org/10.1016/j.tplants.2004.12.012openalex-snapshot
Organization of cis-acting regulatory elements in osmotic- and cold-stress-responsive promoters
inferredcites →https://doi.org/10.1016/j.ygeno.2012.06.004openalex-snapshot
Expression profiling of ABA pathway transcripts indicates crosstalk between abiotic and biotic stress responses in Arabidopsis
inferredcites →https://doi.org/10.1016/s1360-1385(01)01946-xopenalex-snapshot
Abiotic stress signalling pathways: specificity and cross-talk
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/10.1016/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:1006321900483openalex-snapshot
Organization and expression of two Arabidopsis DREB2 genes encoding DRE-binding proteins involved in dehydration- and high-salinity-responsive gene expression
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/10.1038/7036openalex-snapshot
Improving plant drought, salt, and freezing tolerance by gene transfer of a single stress-inducible transcription factor
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/10.1046/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.0303029101openalex-snapshot
CBF2/DREB1C is a negative regulator of CBF1/DREB1B and CBF3/DREB1A expression and plays a central role in stress tolerance in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0406069101openalex-snapshot
A prominent role for the CBF cold response pathway in configuring the low-temperature metabolome of Arabidopsis
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.0602874103openalex-snapshot
The negative regulator of plant cold responses, HOS1, is a RING E3 ligase that mediates the ubiquitination and degradation of ICE1
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.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/10.1074/jbc.275.3.1723openalex-snapshot
ABFs, a Family of ABA-responsive Element Binding Factors
inferredcites →https://doi.org/10.1074/jbc.m605895200openalex-snapshot
A R2R3 Type MYB Transcription Factor Is Involved in the Cold Regulation of CBF Genes and in Acquired Freezing Tolerance
inferredcites →https://doi.org/10.1093/jxb/erh005openalex-snapshot
Molecular genetic perspectives on cross-talk and specificity in abiotic stress signalling in plants
inferredcites →https://doi.org/10.1093/jxb/eri311openalex-snapshot
A novel gene family in Arabidopsis encoding putative heptahelical transmembrane proteins homologous to human adiponectin receptors and progestin receptors
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/erp039openalex-snapshot
HHP1 is involved in osmotic stress sensitivity in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erq162openalex-snapshot
HHP1, a novel signalling component in the cross-talk between the cold and osmotic signalling pathways in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/err279openalex-snapshot
Genetic analysis reveals a complex regulatory network modulating CBF gene expression and Arabidopsis response to abiotic stress
inferredcites →https://doi.org/10.1093/jxb/err460openalex-snapshot
Drought, salt, and temperature stress-induced metabolic rearrangements and regulatory networks
inferredcites →https://doi.org/10.1093/mp/ssm022openalex-snapshot
An Update on Abscisic Acid Signaling in Plants and More …
inferredcites →https://doi.org/10.1093/pcp/pcq112openalex-snapshot
Systemic low temperature signaling in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcr143openalex-snapshot
An ABRE Promoter Sequence is Involved in Osmotic Stress-Responsive Expression of the DREB2A Gene, Which Encodes a Transcription Factor Regulating Drought-Inducible Genes in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.1077503openalex-snapshot
ICE1: a regulator of cold-induced transcriptome and freezing tolerance in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.006478openalex-snapshot
Transcription Factor CBF4 Is a Regulator of Drought Adaptation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.008532openalex-snapshot
Transcriptome Changes for Arabidopsis in Response to Salt, Osmotic, and Cold Stress,
inferredcites →https://doi.org/10.1104/pp.103.025395openalex-snapshot
Regulation of Abscisic Acid Biosynthesis
inferredcites →https://doi.org/10.1104/pp.103.027169openalex-snapshot
Cold Induction of Arabidopsis CBF Genes Involves Multiple ICE (Inducer of CBF Expression) Promoter Elements and a Cold-Regulatory Circuit That Is Desensitized by Low Temperature
inferredcites →https://doi.org/10.1104/pp.104.043562openalex-snapshot
Abscisic Acid Induces CBF Gene Transcription and Subsequent Induction of Cold-Regulated Genes via the CRT Promoter Element
inferredcites →https://doi.org/10.1104/pp.104.058412openalex-snapshot
Quantitative Statistical Analysis of cis-Regulatory Sequences in ABA/VP1- and CBF/DREB1-Regulated Genes of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.4.1341openalex-snapshot
Alterations in Water Status, Endogenous Abscisic Acid Content, and Expression of rab18 Gene during the Development of Freezing Tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.107.1.141openalex-snapshot
Role of Abscisic Acid in Drought-Induced Freezing Tolerance, Cold Acclimation, and Accumulation of LT178 and RAB18 Proteins in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.108.122945openalex-snapshot
Putrescine Is Involved in Arabidopsis Freezing Tolerance and Cold Acclimation by Regulating Abscisic Acid Levels in Response to Low Temperature
inferredcites →https://doi.org/10.1104/pp.108.129791openalex-snapshot
Transcriptional Regulatory Networks in Response to Abiotic Stresses in Arabidopsis and Grasses
inferredcites →https://doi.org/10.1104/pp.109.144220openalex-snapshot
The MYB96 Transcription Factor Mediates Abscisic Acid Signaling during Drought Stress Response 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/10.1105/tpc.003483openalex-snapshot
Arabidopsis Transcriptome Profiling Indicates That Multiple Regulatory Pathways Are Activated during Cold Acclimation in Addition to the CBF Cold Response Pathway[W]
inferredcites →https://doi.org/10.1105/tpc.006130openalex-snapshot
Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) Function as Transcriptional Activators in Abscisic Acid Signaling
inferredcites →https://doi.org/10.1105/tpc.010101openalex-snapshot
The Arabidopsis LOS5/ABA3 Locus Encodes a Molybdenum Cofactor Sulfurase and Modulates Cold Stress– and Osmotic Stress–Responsive Gene Expression
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.105.035568openalex-snapshot
The Arabidopsis Cold-Responsive Transcriptome and Its Regulation by ICE1
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.106.048397openalex-snapshot
SIZ1-Mediated Sumoylation of ICE1 ControlsCBF3/DREB1AExpression and Freezing Tolerance inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.063958openalex-snapshot
Roles for Arabidopsis CAMTA Transcription Factors in Cold-Regulated Gene Expression and Freezing Tolerance
inferredcites →https://doi.org/10.1105/tpc.110.081059openalex-snapshot
The R2R3 MYB Transcription Factor DUO1 Activates a Male Germline-Specific Regulon Essential for Sperm Cell Differentiation inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.083485openalex-snapshot
The MYB96 Transcription Factor Regulates Cuticular Wax Biosynthesis under Drought Conditions inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.098723openalex-snapshot
A Self-Regulatory Circuit of CIRCADIAN CLOCK-ASSOCIATED1 Underlies the Circadian Clock Regulation of Temperature Responses in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.9.2063openalex-snapshot
The Arabidopsis LOS5/ABA3 Locus Encodes a Molybdenum Cofactor Sulfurase and Modulates Cold Stress- and Osmotic Stress-Responsive Gene Expression
inferredcites →https://doi.org/10.1105/tpc.9.11.1935openalex-snapshot
Genetic analysis of osmotic and cold stress signal transduction in Arabidopsis: interactions and convergence of abscisic acid-dependent and abscisic acid-independent pathways.
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.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.1469-8137.2010.03183.xopenalex-snapshot
MYB96‐mediated abscisic acid signals induce pathogen resistance response by promoting salicylic acid biosynthesis in Arabidopsis
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/10.1371/journal.pone.0026015openalex-snapshot
Chromatin Immunoprecipitation (ChIP): Revisiting the Efficacy of Sample Preparation, Sonication, Quantification of Sheared DNA, and Analysis via PCR
inferredcites →https://doi.org/10.2307/3870555openalex-snapshot
Genetic Analysis of Osmotic and Cold Stress Signal Transduction in Arabidopsis: Interactions and Convergence of Abscisic Acid-Dependent and Abscisic Acid-Independent Pathways
inferredcites →https://doi.org/10.2307/3871428openalex-snapshot
The Arabidopsis LOS5/ABA3 Locus Encodes a Molybdenum Cofactor Sulfurase and Modulates Cold Stress- and Osmotic Stress-Responsive Gene Expression
inferredcites →https://doi.org/10.3109/07388551.2010.505910openalex-snapshot
CBF-dependent signaling pathway: A key responder to low temperature stress in plants
inferredcites →https://doi.org/10.4161/psb.2.3.4156openalex-snapshot
Abscisic Acid and Abiotic Stress Signaling

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.4806954openalex-extracted
Genome-Wide Investigation of Myb Gene Family in Areca Catechu and Potential Roles of Actdf in Transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1002/fes3.484openalex-snapshot
Integrative physiological, transcriptome, and metabolome analyses reveal the associated genes and metabolites involved in cold stress response in common vetch ( Vicia sativa L.)
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Involvement of Plant Hormones in Cold Stress Tolerance
inferred← citeshttps://doi.org/10.1007/978-981-10-7479-0_11openalex-snapshot
Signalling During Cold Stress and Its Interplay with Transcriptional Regulation
inferred← citeshttps://doi.org/10.1007/978-981-13-1244-1_1openalex-snapshot
Gene Regulatory Networks Mediating Cold Acclimation: The CBF Pathway
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/10.1007/978-981-16-9037-2_2openalex-snapshot
Low Temperature Stress and Plant-Water Relationship: A Review
inferred← citeshttps://doi.org/10.1007/978-981-19-5817-5_1openalex-snapshot
Physiology and Molecular Biology of Abiotic Stress Tolerance in Legumes
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Transcriptomic Reprogramming in Plants: Insights into Gene Expression Modulation and Stress Adaptation
inferred← citeshttps://doi.org/10.1007/s00018-015-2089-6openalex-snapshot
Hormonal control of cold stress responses in plants
inferred← citeshttps://doi.org/10.1007/s00253-015-6966-6openalex-snapshot
Calmodulin-binding transcription activators and perspectives for applications in biotechnology
inferred← citeshttps://doi.org/10.1007/s00344-015-9565-yopenalex-snapshot
Overexpression of an MYB-Related Gene FvMYB1 from Fraxinus velutina Increases Tolerance to Salt Stress in Transgenic Tobacco
inferred← citeshttps://doi.org/10.1007/s00344-025-12032-8openalex-snapshot
Strigolactones as Central Integrators of Plant Development and Multistress Resilience
inferred← citeshttps://doi.org/10.1007/s00425-015-2366-5openalex-snapshot
Overexpression of a novel SbMYB15 from Salicornia brachiata confers salinity and dehydration tolerance by reduced oxidative damage and improved photosynthesis in transgenic tobacco
inferred← citeshttps://doi.org/10.1007/s00425-026-05082-zopenalex-snapshot
Transcription factor MYB102 regulates plant growth and tolerance to multiple abiotic stresses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00709-016-1004-9openalex-snapshot
Stress-responsive gene RsICE1 from Raphanus sativus increases cold tolerance in rice
inferred← citeshttps://doi.org/10.1007/s10725-024-01253-8openalex-snapshot
Advances in plant response to low-temperature stress
inferred← citeshttps://doi.org/10.1007/s11032-020-01187-9openalex-snapshot
Abscisic acid enhances tolerance to spring freeze stress and regulates the expression of ascorbate–glutathione biosynthesis-related genes and stress-responsive genes in common wheat
inferred← citeshttps://doi.org/10.1007/s11033-023-09051-7openalex-snapshot
Molecular switches in plant stress adaptation
inferred← citeshttps://doi.org/10.1007/s11033-024-10055-0openalex-snapshot
Genome-wide investigation of MYB gene family in Areca catechu and potential roles of AcTDF in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11103-015-0411-1openalex-snapshot
Overexpression of the MYB37 transcription factor enhances abscisic acid sensitivity, and improves both drought tolerance and seed productivity in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11105-024-01455-4openalex-snapshot
Expression Profiling of the 56 R2R3-MYB Family Genes in Response to Cold, Drought, and Salt Stress in Blue Honeysuckle (Lonicera caerulea L.)
inferred← citeshttps://doi.org/10.1007/s11240-016-1080-8openalex-snapshot
Overexpression of a heading Chinese cabbage ICE1 gene confers freezing tolerance in transgenic rice
inferred← citeshttps://doi.org/10.1007/s11540-023-09657-1openalex-snapshot
Comparative Transcriptomic Analysis of Different Potato Cultivars to Elucidate the Molecular Mechanisms Underlying Differences in Cold Resistance
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Comparative analysis of the structure, suberin and wax composition and key gene expression in the epidermis of ‘Dangshansuli’ pear and its russet mutant
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Advances in Understanding Cold Tolerance Mechanisms in Potato (Solanum Tuberosum L.): Physiological, Biochemical, Molecular, and Breeding Perspectives
inferred← citeshttps://doi.org/10.1007/s12298-026-01798-0openalex-snapshot
MYB transcription factors in plant cold stress adaptation: integrating phylogeny, signaling networks, and metabolic regulation
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Overexpression of the MYB transcription factor MYB28 or MYB99 confers hypersensitivity to abscisic acid in arabidopsis
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Transcriptome meta-analysis-based identification of hub transcription factors and RNA-binding proteins potentially orchestrating gene regulatory cascades and crosstalk in response to abiotic stresses in Arabidopsis thaliana
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Overlapping responses to multiple abiotic stresses in citrus: from mechanism understanding to genetic improvement
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inferred← citeshttps://doi.org/10.1016/j.ecoenv.2018.07.013openalex-snapshot
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ABA-regulated ploidy-related genes and non-structural carbon accumulation may underlie cold tolerance in tetraploid Fragaria moupinensis
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Transcriptional regulation and signalling of cold stress response in plants: An overview of current understanding
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Analysis of Lhcb gene family in rapeseed (Brassica napus L.) identifies a novel member “BnLhcb3.4” modulating cold tolerance
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Abscisic acid involved in trehalose improved melon photosynthesis via regulating oxidative stress tolerance and cell morphology structure under cold stress
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inferred← citeshttps://doi.org/10.1016/j.hpj.2017.12.001openalex-snapshot
Genomic Survey and Expression Profiling of the MYB Gene Family in Watermelon
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Unveiling the power of MYB transcription factors: Master regulators of multi-stress responses and development in cotton
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MYB transcription factors in plants: A comprehensive review of their discovery, structure, classification, functional diversity and regulatory mechanism
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Dynamic transcriptome profiling revealed key genes and pathways associated with cold stress in castor (Ricinus communis L.)
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Genome-wide analysis of the R2R3-MYB transcription factor gene family expressed in Juglans regia under abiotic and biotic stresses
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Integrated physiological, hormonal, and transcriptomic analyses reveal a novel E3 ubiquitin ligase-mediated cold acclimation mechanism for the acquisition of cold tolerance in sweet osmanthus
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DgbHLH2 positively regulates cold tolerance by activating DgGST expression to mediate ROS scavenging in chrysanthemum
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2022.128489openalex-snapshot
Low temperature tolerance is depressed in wild-type and abscisic acid-deficient mutant barley grown in Cd-contaminated soil
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Amur grape VaMYB4a mediates grapevine cold tolerance via dual regulation of CBF–COR and ABA pathways
inferred← citeshttps://doi.org/10.1016/j.jplph.2016.07.002openalex-snapshot
Increased STM expression is associated with drought tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.01.015openalex-snapshot
Ectopic expression of StCBF1and ScCBF1 have different functions in response to freezing and drought stresses in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111282openalex-snapshot
Interaction between MdWRKY55 and MdNAC17-L enhances salt tolerance in apple by activating MdNHX1 expression
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2024.112888openalex-snapshot
ROS- and CBF- mediated pathways are involved in chlorophyll degradation and anthocyanin accumulation enhanced by cool temperatures in ripening litchi fruits
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A cold-inducible MYB like transcription factor, CsHHO2, positively regulates chilling tolerance of cucumber fruit by enhancing CsGR-RBP3 expression
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2025.113687openalex-snapshot
Distinct post-harvest deterioration pathways caused by light vs dark storage of fresh-cut lettuce packed in modified atmosphere.
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.110892openalex-snapshot
The pepper MYB transcription factor CaMYB306 accelerates fruit coloration and negatively regulates cold resistance
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112764openalex-snapshot
Comprehensive analysis of MYB gene family and their expression under various stress conditions in Lilium pumilum
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113759openalex-snapshot
BcLhcb2.1, a Light-harvesting chlorophyll a/b-binding protein from Wucai, plays a positive regulatory role in the response to Abiotic Stress
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113879openalex-snapshot
Calcium chloride treatment delayed the softening of postharvest blueberries by regulating ABA biosynthesis and signal transduction
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100152openalex-snapshot
Role of phytohormones in regulating cold stress tolerance: Physiological and molecular approaches for developing cold-smart crop plants
inferred← citeshttps://doi.org/10.1016/j.xplc.2020.100040openalex-snapshot
Multifaceted Signaling Networks Mediated by Abscisic Acid Insensitive 4
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/10.1017/s0960258521000015openalex-snapshot
Characterization and expression quantitative trait loci analysis of TaABI4 , a pre-harvest sprouting related gene in wheat
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c09665openalex-snapshot
Functions of Basic Helix–Loop–Helix (bHLH) Proteins in the Regulation of Plant Responses to Cold, Drought, Salt, and Iron Deficiency: A Comprehensive Review
inferred← citeshttps://doi.org/10.1038/ncomms12525openalex-snapshot
The Arabidopsis MIEL1 E3 ligase negatively regulates ABA signalling by promoting protein turnover of MYB96
inferred← citeshttps://doi.org/10.1038/s41467-019-09417-1openalex-snapshot
MYB96 recruits the HDA15 protein to suppress negative regulators of ABA signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41467-026-70026-wopenalex-snapshot
Population genomics reveals association of transposable elements variants with climatic adaptation in wild Amur grape
inferred← citeshttps://doi.org/10.1038/s41598-018-27668-8openalex-snapshot
Nitric Oxide Controls Constitutive Freezing Tolerance in Arabidopsis by Attenuating the Levels of Osmoprotectants, Stress-Related Hormones and Anthocyanins
inferred← citeshttps://doi.org/10.1038/s41598-019-56797-xopenalex-snapshot
Acclimation, priming and memory in the response of Arabidopsis thaliana seedlings to cold stress
inferred← citeshttps://doi.org/10.1038/s41598-020-61512-2openalex-snapshot
Phenotypic and Transcriptomic Analysis of Two Pinellia ternata Varieties T2 line and T2Plus line
inferred← citeshttps://doi.org/10.1038/s41598-024-80143-5openalex-snapshot
CsWRKY29, a key transcription factor in tea plant for freezing tolerance, ABA sensitivity, and sugar metabolism
inferred← citeshttps://doi.org/10.1038/srep17620openalex-snapshot
ICE1 of Pyrus ussuriensis functions in cold tolerance by enhancing PuDREBa transcriptional levels through interacting with PuHHP1
inferred← citeshttps://doi.org/10.1038/srep35558openalex-snapshot
Small RNA-mediated responses to low- and high-temperature stresses in cotton
inferred← citeshttps://doi.org/10.1073/pnas.1819769116openalex-snapshot
Natural variation in the HAN1 gene confers chilling tolerance in rice and allowed adaptation to a temperate climate
inferred← citeshttps://doi.org/10.1080/10407782.2024.2302671openalex-snapshot
CAMTAs, a family of calmodulin-binding transcription factors, are versatile regulators of biotic and abiotic stress responses in plants
inferred← citeshttps://doi.org/10.1080/15592324.2022.2086733openalex-snapshot
Genome-wide identification and expression analysis of the CBF transcription factor family in Lolium perenne under abiotic stress
inferred← citeshttps://doi.org/10.1093/bbb/zbaf028openalex-snapshot
NtPhyA gene knockout enhances cold stress resistance in Nicotiana tabacum L
inferred← citeshttps://doi.org/10.1093/hr/uhab025openalex-snapshot
Photoprotection contributes to freezing tolerance as revealed by RNA-seq profiling ofRhododendronleaves during cold acclimation and deacclimation over time.
inferred← citeshttps://doi.org/10.1093/hr/uhac002openalex-snapshot
CmABF1 and CmCBF4 cooperatively regulate putrescine synthesis to improve cold tolerance of melon seedlings
inferred← citeshttps://doi.org/10.1093/hr/uhac040openalex-snapshot
Hierarchical transcription factor and regulatory network for drought response in Betula platyphylla
inferred← citeshttps://doi.org/10.1093/hr/uhac058openalex-snapshot
Evolution and functional diversification of R2R3-MYB transcription factors in plants
inferred← citeshttps://doi.org/10.1093/jxb/erab257openalex-snapshot
Temperature regulation of plant hormone signaling during stress and development
inferred← citeshttps://doi.org/10.1093/jxb/erab433openalex-snapshot
Abscisic acid insensitive 4 interacts with ICE1 and JAZ proteins to regulate ABA signaling-mediated cold tolerance in apple
inferred← citeshttps://doi.org/10.1093/jxb/erab554openalex-snapshot
Transcriptional regulation of triacylglycerol accumulation in plants under environmental stress conditions
inferred← citeshttps://doi.org/10.1093/jxb/erae123openalex-snapshot
Monosaccharide transporter OsMST6 is activated by transcription factor OsERF120 to enhance chilling tolerance in rice seedlings
inferred← citeshttps://doi.org/10.1093/jxb/erz115openalex-snapshot
Nitric oxide deficiency decreases C-repeat binding factor-dependent and -independent induction of cold acclimation
inferred← citeshttps://doi.org/10.1093/nar/gkv1463openalex-snapshot
Transcriptional regulatory networks inArabidopsis thalianaduring single and combined stresses
inferred← citeshttps://doi.org/10.1093/nar/gkx375openalex-snapshot
Environment-dependent regulation of spliceosome activity by the LSM2-8 complex in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pcz142openalex-snapshot
MaMYB4 Recruits Histone Deacetylase MaHDA2 and Modulates the Expression of ω-3 Fatty Acid Desaturase Genes during Cold Stress Response in Banana Fruit
inferred← citeshttps://doi.org/10.1093/pcp/pcz196openalex-snapshot
The Roots of Plant Frost Hardiness and Tolerance
inferred← citeshttps://doi.org/10.1093/plphys/kiaf586openalex-snapshot
The transcription factor MYB78 negatively regulates cold stress tolerance in Actinidia chinensis
inferred← citeshttps://doi.org/10.1093/plphys/kiag233openalex-snapshot
SlMYB30 relieves high vapor pressure deficit stress by modulating salicylic acid biosynthesis and stomatal morphology in tomato
inferred← citeshttps://doi.org/10.1093/plphys/kiag674openalex-snapshot
The transcription factor EIL1-MYB78 module negatively regulates cold tolerance in Actinidia chinensis
inferred← citeshttps://doi.org/10.1093/treephys/tpy038openalex-snapshot
Integrative transcriptional and metabolic analyses provide insights into cold spell response mechanisms in young shoots of the tea plant
inferred← citeshttps://doi.org/10.1093/treephys/tpz113openalex-snapshot
The poplar R2R3 MYB transcription factor PtrMYB94 coordinates with abscisic acid signaling to improve drought tolerance in plants
inferred← citeshttps://doi.org/10.1104/pp.16.01725openalex-snapshot
The OsMYB30 Transcription Factor Suppresses Cold Tolerance by Interacting with a JAZ Protein and Suppressing β -Amylase Expression
inferred← citeshttps://doi.org/10.1111/jipb.12515openalex-snapshot
The precise regulation of different COR genes by individual CBF transcription factors in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/nph.15240openalex-snapshot
The transcription factor Fc WRKY 40 of Fortunella crassifolia functions positively in salt tolerance through modulation of ion homeostasis and proline biosynthesis by directly regulating SOS 2 and P5 CS 1 homologs
inferred← citeshttps://doi.org/10.1111/nph.16549openalex-snapshot
OsTMF attenuates cold tolerance by affecting cell wall properties in rice
inferred← citeshttps://doi.org/10.1111/nph.71033openalex-snapshot
Transcription factor bZIP48 ‐ MYB96 module positively regulates cuticular wax synthesis by directly activating KCSs and CER3 genes in response to cold stress
inferred← citeshttps://doi.org/10.1111/pbi.12708openalex-snapshot
Pbr MYB 21, a novel MYB protein of Pyrus betulaefolia, functions in drought tolerance and modulates polyamine levels by regulating arginine decarboxylase gene
inferred← citeshttps://doi.org/10.1111/pbi.70201openalex-snapshot
Regulation of jasmonic acid signalling in tomato cold stress response: Insights into the MYB15 ‐ LOXD and MYB15 ‐ MYC2 ‐ LOXD regulatory modules
inferred← citeshttps://doi.org/10.1111/pbi.70635openalex-snapshot
SlMYB17 Antagonises the SlCBF Pathway to Negatively Regulate Tomato Chilling Tolerance
inferred← citeshttps://doi.org/10.1111/pce.12720openalex-snapshot
Growth temperature impact on leaf form and function in Arabidopsis thaliana ecotypes from northern and southern Europe
inferred← citeshttps://doi.org/10.1111/pce.12838openalex-snapshot
ERF105 is a transcription factor gene of Arabidopsis thaliana required for freezing tolerance and cold acclimation
inferred← citeshttps://doi.org/10.1111/pce.13868openalex-snapshot
The HY5 and MYB15 transcription factors positively regulate cold tolerance in tomato via the CBF pathway
inferred← citeshttps://doi.org/10.1111/pce.14796openalex-snapshot
ERF54 regulates cold tolerance in Rosa multiflora through DREB/COR signalling pathways
inferred← citeshttps://doi.org/10.1111/pce.15144openalex-snapshot
MYB Transcription Factor CDC5 Activates CBF3 Expression to Positively Regulate Freezing Tolerance via Cooperating With ICE1 and Histone Modification in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.15291openalex-snapshot
PhNH10 Suppresses Low Temperature Tolerance in Petunia Through the Abscisic Acid‐Dependent Pathway
inferred← citeshttps://doi.org/10.1111/pce.70415openalex-snapshot
BoMYC2 and BoAREB1 Interact With BoMYB2 to Respond to ABA Signaling and Drought Stress in Cabbage
inferred← citeshttps://doi.org/10.1111/plb.70118openalex-snapshot
RsMYB90, a R2R3‐MYB transcription factor, plays a positive role in regulating low temperature stress in radish
inferred← citeshttps://doi.org/10.1111/tpj.71107openalex-snapshot
A phosphatidic acid‐based retrograde signaling pathway responsive to abiotic stress in Arabidopsis
inferred← citeshttps://doi.org/10.1134/s0006297917100030openalex-snapshot
Gene regulation and signal transduction in the ICE–CBF–COR signaling pathway during cold stress in plants
inferred← citeshttps://doi.org/10.1186/s12864-022-09039-wopenalex-snapshot
A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.1186/s12864-024-10693-5openalex-snapshot
Genome-wide identification of R2R3-MYB transcription factor subfamily genes involved in salt stress in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1186/s12870-021-03083-6openalex-snapshot
Genome-wide analysis of MYB transcription factors and their responses to salt stress in Casuarina equisetifolia
inferred← citeshttps://doi.org/10.1186/s12870-022-03999-7openalex-snapshot
GhAAO2 was observed responding to NaHCO3 stress in cotton compared to AAO family genes
inferred← citeshttps://doi.org/10.1186/s12870-025-06721-5openalex-snapshot
The full-length transcriptome analysis of blueberry under different pH conditions
inferred← citeshttps://doi.org/10.1186/s12870-025-08083-4openalex-snapshot
Genome-wide identification, structural characterization, and gene expression analysis of the MYB transcription factor family in faba bean (Vicia faba L.)
inferred← citeshttps://doi.org/10.1186/s12870-026-08303-5openalex-snapshot
PbrMYB31 enhances abiotic stress tolerance by promoting suberin biosynthesis in Arabidopsis
inferred← citeshttps://doi.org/10.1371/journal.pone.0210672openalex-snapshot
Identification of new regulators through transcriptome analysis that regulate anthocyanin biosynthesis in apple leaves at low temperatures
inferred← citeshttps://doi.org/10.2174/1389202920666190129145439openalex-snapshot
OsmiR528 Enhances Cold Stress Tolerance by Repressing Expression of Stress Response-related Transcription Factor Genes in Plant Cells
inferred← citeshttps://doi.org/10.32615/bp.2023.018openalex-snapshot
RNA-Seq analysis of ground-cover chrysanthemum provides insights into the basis of natural low-temperature stress
inferred← citeshttps://doi.org/10.3389/fgene.2022.957505openalex-snapshot
Identification of Nitrogen Starvation-Responsive miRNAs to Reveal the miRNA-Mediated Regulatory Network in Betula luminifera
inferred← citeshttps://doi.org/10.3389/fpls.2018.00215openalex-snapshot
Arabidopsis PCaP2 Plays an Important Role in Chilling Tolerance and ABA Response by Activating CBF- and SnRK2-Mediated Transcriptional Regulatory Network
inferred← citeshttps://doi.org/10.3389/fpls.2020.00367openalex-snapshot
DEAR4, a Member of DREB/CBF Family, Positively Regulates Leaf Senescence and Response to Multiple Stressors in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2020.587620openalex-snapshot
ABA-Dependent and ABA-Independent Functions of RCAR5/PYL11 in Response to Cold Stress
inferred← citeshttps://doi.org/10.3389/fpls.2021.638788openalex-snapshot
The Halophyte Halostachys caspica AP2/ERF Transcription Factor HcTOE3 Positively Regulates Freezing Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2021.764625openalex-snapshot
Integration of Metabolome and Transcriptome Studies Reveals Flavonoids, Abscisic Acid, and Nitric Oxide Comodulating the Freezing Tolerance in Liriope spicata
inferred← citeshttps://doi.org/10.3389/fpls.2022.820439openalex-snapshot
Genome-Wide Identification and Expression Analysis of the R2R3-MYB Transcription Factor Family Revealed Their Potential Roles in the Flowering Process in Longan (Dimocarpus longan)
inferred← citeshttps://doi.org/10.3389/fpls.2022.855559openalex-snapshot
Calcium Mediated Cold Acclimation in Plants: Underlying Signaling and Molecular Mechanisms
inferred← citeshttps://doi.org/10.3390/agronomy11061146openalex-snapshot
Hormone Profiles and Antioxidant Activity of Cultivated and Wild Tomato Seedlings under Low-Temperature Stress
inferred← citeshttps://doi.org/10.3390/cells14020110openalex-snapshot
Plant Coping with Cold Stress: Molecular and Physiological Adaptive Mechanisms with Future Perspectives
inferred← citeshttps://doi.org/10.3390/f14112274openalex-snapshot
Genome-Wide Identification and Expression Analysis of the Walnut C-Repeat Binding Factor Gene Family under Low-Temperature Stress
inferred← citeshttps://doi.org/10.3390/genes12101638openalex-snapshot
Transcriptome Profiling of Maize (Zea mays L.) Leaves Reveals Key Cold-Responsive Genes, Transcription Factors, and Metabolic Pathways Regulating Cold Stress Tolerance at the Seedling Stage
inferred← citeshttps://doi.org/10.3390/genes13101695openalex-snapshot
Genome-Wide Analysis and Expression Profiles of the VOZ Gene Family in Quinoa (Chenopodium quinoa)
inferred← citeshttps://doi.org/10.3390/horticulturae11121495openalex-snapshot
Integrated Analysis of Transcriptome and Metabolome Provides Insights into Phenylpropanoid Biosynthesis of Blueberry Leaves in Response to Low-Temperature Stress
inferred← citeshttps://doi.org/10.3390/horticulturae12060711openalex-snapshot
Overexpression of CmMYBS3 Decreases Cold Tolerance in Ground Cover Chrysanthemum
inferred← citeshttps://doi.org/10.3390/horticulturae7120527openalex-snapshot
Gene Expression Analysis in Cold Stress Conditions Reveals BBX20 and CLO as Potential Biomarkers for Cold Tolerance in Almond
inferred← citeshttps://doi.org/10.3390/ijms19061634openalex-snapshot
Revisiting the Role of Plant Transcription Factors in the Battle against Abiotic Stress
inferred← citeshttps://doi.org/10.3390/ijms19103169openalex-snapshot
Multiple Regulatory Networks Are Activated during Cold Stress in Medicago sativa L.
inferred← citeshttps://doi.org/10.3390/ijms19123896openalex-snapshot
Calcium Signaling-Mediated Plant Response to Cold Stress
inferred← citeshttps://doi.org/10.3390/ijms21165727openalex-snapshot
AcoMYB4, an Ananas comosus L. MYB Transcription Factor, Functions in Osmotic Stress through Negative Regulation of ABA Signaling
inferred← citeshttps://doi.org/10.3390/ijms22116125openalex-snapshot
Multiple Functions of MYB Transcription Factors in Abiotic Stress Responses
inferred← citeshttps://doi.org/10.3390/ijms222111308openalex-snapshot
Transcriptomic and Metabolic Analyses Reveal the Mechanism of Ethylene Production in Stony Hard Peach Fruit during Cold Storage
inferred← citeshttps://doi.org/10.3390/ijms23031794openalex-snapshot
Overexpression of a Malus baccata MYB Transcription Factor Gene MbMYB4 Increases Cold and Drought Tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/ijms24032484openalex-snapshot
Genome-Wide Identification and Transcriptional Analysis of the MYB Gene Family in Pearl Millet (Pennisetum glaucum)
inferred← citeshttps://doi.org/10.3390/ijms24043346openalex-snapshot
The Role of Reactive Oxygen Species in Plant Response to Radiation
inferred← citeshttps://doi.org/10.3390/ijms24108670openalex-snapshot
BcMYB111 Responds to BcCBF2 and Induces Flavonol Biosynthesis to Enhance Tolerance under Cold Stress in Non-Heading Chinese Cabbage
inferred← citeshttps://doi.org/10.3390/ijms24119514openalex-snapshot
Cloning and Functional Characterization of Cold-Inducible MYB-like 17 Transcription Factor in Rapeseed (Brassica napus L.)
inferred← citeshttps://doi.org/10.3390/ijms241311090openalex-snapshot
Overexpression of TaMYB4 Confers Freezing Tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/ijms25063405openalex-snapshot
FvMYB108, a MYB Gene from Fragaria vesca, Positively Regulates Cold and Salt Tolerance of Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms26083518openalex-snapshot
Characterization of Critical Amino Acids in the Transport and Selectivity of the Plant Na+/H+ Exchanger Plasma Membrane SOS1
inferred← citeshttps://doi.org/10.3390/life16010017openalex-snapshot
Rising Demand for Winter Crops Under Climate Change: Breeding for Winter Hardiness in Autumn-Sown Legumes
inferred← citeshttps://doi.org/10.3390/plants10091864openalex-snapshot
Convergence and Divergence: Signal Perception and Transduction Mechanisms of Cold Stress in Arabidopsis and Rice
inferred← citeshttps://doi.org/10.3390/plants11070933openalex-snapshot
Cellular Protein Trafficking: A New Player in Low-Temperature Response Pathway
inferred← citeshttps://doi.org/10.3390/plants13162264openalex-snapshot
Overexpression of a ‘Paulownia fortunei’ MYB Factor Gene, PfMYB44, Increases Salt and Drought Tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/plants14040532openalex-snapshot
Calmodulin-Binding Transcription Factors: Roles in Plant Response to Abiotic Stresses
inferred← citeshttps://doi.org/10.4172/2376-0354.1000182openalex-snapshot
De novo Transcriptome Sequencing of Cold-treated Kentucky Bluegrass (Poa pratensis) and Analysis of the Genes Involved in Cold Tolerance
inferred← citeshttps://doi.org/10.4995/thesis/10251/192892openalex-snapshot
Caracterización fisiológica y molecular de la respuesta de patrones de cítricos a estrés por baja temperatura
inferred← citeshttps://doi.org/10.6084/m9.figshare.14936317openalex-snapshot
Additional file 1 of Genome-wide analysis of MYB transcription factors and their responses to salt stress in Casuarina equisetifolia
inferred← citeshttps://doi.org/10.6084/m9.figshare.14936320openalex-snapshot
Additional file 2 of Genome-wide analysis of MYB transcription factors and their responses to salt stress in Casuarina equisetifolia
inferred← citeshttps://doi.org/10.6084/m9.figshare.14936323openalex-snapshot
Additional file 3 of Genome-wide analysis of MYB transcription factors and their responses to salt stress in Casuarina equisetifolia
inferred← citeshttps://doi.org/10.6084/m9.figshare.14936326openalex-snapshot
Additional file 4 of Genome-wide analysis of MYB transcription factors and their responses to salt stress in Casuarina equisetifolia
inferred← citeshttps://doi.org/10.6084/m9.figshare.14936329openalex-snapshot
Additional file 5 of Genome-wide analysis of MYB transcription factors and their responses to salt stress in Casuarina equisetifolia
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604635openalex-snapshot
Additional file 1 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604638openalex-snapshot
Additional file 2 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604641openalex-snapshot
Additional file 3 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604644openalex-snapshot
Additional file 4 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604647openalex-snapshot
Additional file 5 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604650openalex-snapshot
Additional file 6 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604653openalex-snapshot
Additional file 7 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604656openalex-snapshot
Additional file 8 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604659openalex-snapshot
Additional file 9 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604662openalex-snapshot
Additional file 10 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604665openalex-snapshot
Additional file 11 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604668openalex-snapshot
Additional file 12 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604671openalex-snapshot
Additional file 13 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604674openalex-snapshot
Additional file 14 of A comparative transcriptomic analysis reveals a coordinated mechanism activated in response to cold acclimation in common vetch (Vicia sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604971openalex-snapshot
Additional file 1 of GhAAO2 was observed responding to NaHCO3 stress in cotton compared to AAO family genes
inferred← citeshttps://doi.org/10.6084/m9.figshare.22604974openalex-snapshot
Additional file 2 of GhAAO2 was observed responding to NaHCO3 stress in cotton compared to AAO family genes
inferred← citeshttps://doi.org/10.70675/9f4d0dc7zed7fz44eez989dzfc81f6717633openalex-snapshot
Nouveaux rôles du régulateur de l'immunité MYB30 dans le développement d'Arabidopsis thaliana
inferred← citeshttps://doi.org/10.70675/d9985fa0z7eddz401dzbecfz50d805b64d14openalex-snapshot
Molecular mechanisms of plant-xenobiotic interactions : involvement of stress, development and hormone signaling regulations
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.