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MPK3- and MPK6-Mediated ICE1 Phosphorylation Negatively Regulates ICE1 Stability and Freezing Tolerance in Arabidopsis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s10265-013-0576-0openalex-snapshot
Phosphorylation of Arabidopsis thaliana MEKK1 via Ca2+ signaling as a part of the cold stress response
inferredcites →https://doi.org/10.1016/j.cell.2009.03.038openalex-snapshot
Proteasome-Mediated Turnover of the Transcription Coactivator NPR1 Plays Dual Roles in Regulating Plant Immunity
inferredcites →https://doi.org/10.1016/j.chom.2015.07.005openalex-snapshot
Posttranslational Modifications of the Master Transcriptional Regulator NPR1 Enable Dynamic but Tight Control of Plant Immune Responses
inferredcites →https://doi.org/10.1016/j.devcel.2014.12.023openalex-snapshot
OST1 Kinase Modulates Freezing Tolerance by Enhancing ICE1 Stability in Arabidopsis
inferredcites →https://doi.org/10.1016/j.devcel.2015.02.022openalex-snapshot
The BASL Polarity Protein Controls a MAPK Signaling Feedback Loop in Asymmetric Cell Division
inferredcites →https://doi.org/10.1016/j.devcel.2017.09.024openalex-snapshot
MAP Kinase Cascades Regulate the Cold Response by Modulating ICE1 Protein Stability
inferredcites →https://doi.org/10.1016/j.molcel.2004.06.023openalex-snapshot
The MKK2 Pathway Mediates Cold and Salt Stress Signaling in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molcel.2017.02.016openalex-snapshot
Plasma Membrane CRPK1-Mediated Phosphorylation of 14-3-3 Proteins Induces Their Nuclear Import to Fine-Tune CBF Signaling during Cold Response
inferredcites →https://doi.org/10.1016/j.molp.2017.01.004openalex-snapshot
BZR1 Positively Regulates Freezing Tolerance via CBF-Dependent and CBF-Independent Pathways in Arabidopsis
inferredcites →https://doi.org/10.1016/j.plantsci.2011.03.011openalex-snapshot
CIPK7 is involved in cold response by interacting with CBL1 in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0248-4900(01)01156-xopenalex-snapshot
Regulation of MAP kinases by docking domains
inferredcites →https://doi.org/10.1016/s0968-0004(00)01627-3openalex-snapshot
Docking domains and substrate-specificity determination for MAP kinases
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00310.xopenalex-snapshot
Low temperature regulation of theArabidopsisCBF family of AP2 transcriptional activators as an early step in cold‐inducedCORgene expression
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00913.xopenalex-snapshot
Various abiotic stresses rapidly activate Arabidopsis MAP kinases ATMPK4 and ATMPK6
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.0810206106openalex-snapshot
Flg22 regulates the release of an ethylene response factor substrate from MAP kinase 6 in Arabidopsis thaliana via ethylene signaling
inferredcites →https://doi.org/10.1073/pnas.1211295109openalex-snapshot
Photoperiodic regulation of the C-repeat binding factor (CBF) cold acclimation pathway and freezing tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.152342599openalex-snapshot
The GSK3-like kinase BIN2 phosphorylates and destabilizes BZR1, a positive regulator of the brassinosteroid signaling pathway in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1611477113openalex-snapshot
Brassinosteroids participate in the control of basal and acquired freezing tolerance of plants
inferredcites →https://doi.org/10.1073/pnas.94.3.1035openalex-snapshot
Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit
inferredcites →https://doi.org/10.1074/jbc.270.25.14843openalex-snapshot
How MAP Kinases Are Regulated
inferredcites →https://doi.org/10.1074/jbc.m109.035659openalex-snapshot
A Calcium/Calmodulin-regulated Member of the Receptor-like Kinase Family Confers Cold Tolerance in Plants
inferredcites →https://doi.org/10.1074/jbc.m109495200openalex-snapshot
Cell Death Mediated by MAPK Is Associated with Hydrogen Peroxide Production in Arabidopsis
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/10.1074/jbc.m801392200openalex-snapshot
Activation of MAPK Kinase 9 Induces Ethylene and Camalexin Biosynthesis and Enhances Sensitivity to Salt Stress in Arabidopsis
inferredcites →https://doi.org/10.1093/nar/gkx417openalex-snapshot
Phosphorylation of the transcriptional repressor MYB15 by mitogen-activated protein kinase 6 is required for freezing tolerance 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/10.1101/gad.243675.114openalex-snapshot
BR-dependent phosphorylation modulates PIF4 transcriptional activity and shapes diurnal hypocotyl growth
inferredcites →https://doi.org/10.1104/pp.16.00533openalex-snapshot
Mutational Evidence for the Critical Role of CBF Transcription Factors in Cold Acclimation in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.006858openalex-snapshot
CIPK3 , a Calcium Sensor–Associated Protein Kinase That Regulates Abscisic Acid and Cold Signal Transduction in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.10.8.1391openalex-snapshot
Two Transcription Factors, DREB1 and DREB2, with an EREBP/AP2 DNA Binding Domain Separate Two Cellular Signal Transduction Pathways in Drought- and Low-Temperature-Responsive Gene Expression, Respectively, in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.104.026609openalex-snapshot
Phosphorylation of 1-Aminocyclopropane-1-Carboxylic Acid Synthase by MPK6, a Stress-Responsive Mitogen-Activated Protein Kinase, Induces Ethylene Biosynthesis in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.106.048298openalex-snapshot
Stomatal Development and Patterning Are Regulated by Environmentally Responsive Mitogen-Activated Protein Kinases 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.108.060848openalex-snapshot
SCREAM/ICE1 and SCREAM2 Specify Three Cell-State Transitional Steps Leading to Arabidopsis Stomatal Differentiation
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.109.070110openalex-snapshot
Novel and Expanded Roles for MAPK Signaling in Arabidopsis Stomatal Cell Fate Revealed by Cell Type–Specific Manipulations
inferredcites →https://doi.org/10.1105/tpc.111.084996openalex-snapshot
Phosphorylation of a WRKY Transcription Factor by Two Pathogen-Responsive MAPKs Drives Phytoalexin Biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.098640openalex-snapshot
Ethylene Signaling Negatively Regulates Freezing Tolerance by Repressing Expression of CBF and Type-A ARR Genes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.109074openalex-snapshot
Phosphorylation of an ERF Transcription Factor by Arabidopsis MPK3/MPK6 Regulates Plant Defense Gene Induction and Fungal Resistance
inferredcites →https://doi.org/10.1105/tpc.113.112631openalex-snapshot
Jasmonate Regulates the INDUCER OF CBF EXPRESSION–C-REPEAT BINDING FACTOR/DRE BINDING FACTOR1 Cascade and Freezing Tolerance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.128702openalex-snapshot
A Mitogen-Activated Protein Kinase Cascade Module, MKK3-MPK6 and MYC2, Is Involved in Blue Light-Mediated Seedling Development in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.16.00577openalex-snapshot
Regulation of Stomatal Immunity by Interdependent Functions of a Pathogen-Responsive MPK3/MPK6 Cascade and Abscisic Acid
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04589.xopenalex-snapshot
ICE1 Ser403 is necessary for protein stabilization and regulation of cold signaling and tolerance
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04659.xopenalex-snapshot
BON1 interacts with the protein kinases BIR1 and BAK1 in modulation of temperature‐dependent plant growth and cell death in Arabidopsis
inferredcites →https://doi.org/10.1111/nph.14088openalex-snapshot
The cbfs triple mutants reveal the essential functions of CBF s in cold acclimation and allow the definition of CBF regulons in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.12382openalex-snapshot
A chemical genetic approach demonstrates that MPK 3/ MPK 6 activation and NADPH oxidase‐mediated oxidative burst are two independent signaling events in plant immunity
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112252openalex-snapshot
Mitogen-Activated Protein Kinase Signaling in Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.571openalex-snapshot
PLANT COLD ACCLIMATION: Freezing Tolerance Genes and Regulatory Mechanisms
inferredcites →https://doi.org/10.1371/journal.pgen.1003422openalex-snapshot
Phosphorylation-Coupled Proteolysis of the Transcription Factor MYC2 Is Important for Jasmonate-Signaled Plant Immunity
inferredcites →https://doi.org/10.1371/journal.pgen.1004389openalex-snapshot
EDR1 Physically Interacts with MKK4/MKK5 and Negatively Regulates a MAP Kinase Cascade to Modulate Plant Innate Immunity
inferredcites →https://doi.org/10.4161/psb.2.4.3896openalex-snapshot
Arabidopsis MPK3, a Key Signalling Intermediate in Stomatal Function
inferredcites →https://doi.org/10.4161/psb.5.8.12225openalex-snapshot
Calcium/calmodulin-regulated receptor-like kinase CRLK1 interacts with MEKK1 in plants
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Sub4 Encoding Subtilisin-Like Protease Modulates Cold Tolerance in Rice Seedlings Through Cell Wall Modification
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0702openalex-snapshot
Phosphorylation‐Mediated Signalling in Plants
inferred← citeshttps://doi.org/10.1002/9781119541578.ch15openalex-snapshot
MAP Kinase as Regulators for Stress Responses in Plants
inferred← citeshttps://doi.org/10.1002/9781119541578.ch16openalex-snapshot
A Network View of MAP Kinase Pathways in Plant Defense Regulation
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Expand the Survival Limits of Crop Plants Under Cold Climate Region
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Abiotic Stress Tolerance in Plants by Genome Editing Applications
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A TaSnRK1α Modulates TaPAP6L‐Mediated Wheat Cold Tolerance through Regulating Endogenous Jasmonic Acid
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The MdHB7L–MdICE1L–MdHOS1 Module Fine‐Tunes Apple Cold Response via CBF‐Dependent and CBF‐Independent Pathways
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Genome‐wide association analysis of chilling‐tolerant germination in a new maize association mapping panel
inferred← citeshttps://doi.org/10.1007/978-1-0716-1625-3_2openalex-snapshot
Protein Phosphorylation Response to Abiotic Stress in Plants
inferred← citeshttps://doi.org/10.1007/978-1-0716-1625-3_3openalex-snapshot
Protein Phosphorylation in Plant Cell Signaling
inferred← citeshttps://doi.org/10.1007/978-3-030-01415-5_2openalex-snapshot
Molecular Genetic Approaches for the Identification of Candidate Cold Stress Tolerance Genes
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/s00122-019-03482-2openalex-snapshot
Dissecting the genetics of cold tolerance in a multiparental maize population
inferred← citeshttps://doi.org/10.1007/s00122-023-04455-2openalex-snapshot
Calcium signaling-mediated transcriptional reprogramming during abiotic stress response in plants
inferred← citeshttps://doi.org/10.1007/s00122-023-04506-8openalex-snapshot
OsMAPK6 positively regulates rice cold tolerance at seedling stage via phosphorylating and stabilizing OsICE1 and OsIPA1
inferred← citeshttps://doi.org/10.1007/s00122-024-04564-6openalex-snapshot
Identification of genetic loci and candidate genes underlying freezing tolerance in wheat seedlings
inferred← citeshttps://doi.org/10.1007/s00122-024-04697-8openalex-snapshot
Advances in functional studies of plant MYC transcription factors
inferred← citeshttps://doi.org/10.1007/s00122-025-04889-wopenalex-snapshot
OsBSK3 and OsBSK2 regulate grain size and leaf angle via MAPK signaling pathway in rice
inferred← citeshttps://doi.org/10.1007/s00299-019-02376-3openalex-snapshot
Cold acclimation by the CBF–COR pathway in a changing climate: Lessons from Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-019-02398-xopenalex-snapshot
The ICE-like transcription factor HbICE2 is involved in jasmonate-regulated cold tolerance in the rubber tree (Hevea brasiliensis)
inferred← citeshttps://doi.org/10.1007/s00299-019-02471-5openalex-snapshot
Banana MaBZR1/2 associate with MaMPK14 to modulate cell wall modifying genes during fruit ripening
inferred← citeshttps://doi.org/10.1007/s00299-022-02949-9openalex-snapshot
StICE1 enhances plant cold tolerance by directly upregulating StLTI6A expression
inferred← citeshttps://doi.org/10.1007/s00299-023-03093-8openalex-snapshot
Identification of hub genes that variate the qCSS12-mediated cold tolerance between indica and japonica rice using WGCNA
inferred← citeshttps://doi.org/10.1007/s00299-024-03382-wopenalex-snapshot
Ectopic expression of HvbHLH132 from hulless barley reduces cold tolerance in transgenic Arabidopsis thaliana
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Genome-wide identification of MYC transcription factors in Chrysanthemum morifolium and CmMYC25 promotes petal anthocyanin accumulation
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Trichoderma viride Tv-1511 Colonizes Arabidopsis Leaves and Promotes Arabidopsis Growth by Modulating the MAP Kinase 6-Mediated Activation of Plasma Membrane H+-ATPase
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Characterization of MAPK Gene Family in Moso Bamboo (Phyllostachys edulis) and Functional Analysis of PeMAPK8 Under Salt Stress
inferred← citeshttps://doi.org/10.1007/s00425-022-03858-7openalex-snapshot
The network centered on ICEs play roles in plant cold tolerance, growth and development
inferred← citeshttps://doi.org/10.1007/s00425-026-05055-2openalex-snapshot
VaWRKY26 transcription factor from Vitis amurensis negatively regulates plant cold tolerance
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Characterization of transcription activation domain of EcaICE1 and its interaction with EcaSIZ1 in Eucalyptus camaldulensis
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Phytotoxicity and the molecular response in yttrium oxide nanoparticle–treated Arabidopsis thaliana seedlings
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Regulation of plant epigenetic memory in response to cold and heat stress: towards climate resilient agriculture
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Genome-wide identification and cold stress expression of inducer of CBF expression (ICE) transcription factors in Taraxacum kok-saghyz
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Terpenoid indole alkaloid biosynthesis in Catharanthus roseus: effects and prospects of environmental factors in metabolic engineering
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Identification of novel microRNAs for cold deacclimation in barley
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SlMYB41 induced by exogenous brassinosteroids negatively regulates the cold resistance of tomato
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Advances in plant response to low-temperature stress
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ABA signal transduction and ROS metabolic balance play a key role in the drought resistance of safflower
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Functional genomics of the protein kinase superfamily from wheat
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OsCTP1 negatively regulates seedling cold tolerance in rice
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A novel basic helix-loop-helix transcription factor, ZjICE2 from Zoysia japonica confers abiotic stress tolerance to transgenic plants via activating the DREB/CBF regulon and enhancing ROS scavenging
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Genome-wide identification of MAPK cascade genes reveals the GhMAP3K14–GhMKK11–GhMPK31 pathway is involved in the drought response in cotton
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Characterisation of the ERF102 to ERF105 genes of Arabidopsis thaliana and their role in the response to cold stress
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Physiological Change and Transcriptome Analysis of Chinese Wild Vitis amurensis and Vitis vinifera in Response to Cold Stress
inferred← citeshttps://doi.org/10.1007/s11105-021-01324-4openalex-snapshot
Transcript Profiles Differentiate Cold Acclimation-Induced Processes in a Summer and Winter Biotype of Camelina
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Effects of MPK3 and MPK6 kinases on the chloroplast architecture and function induced by cold acclimation in Arabidopsis
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Mangifera indica (mango) ICE1s confer flowering and tolerance to multiple stresses in Arabidopsis thaliana
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HOS1 knockout enhances glucosinolate biosynthesis and activates multi-stress signaling in Arabidopsis callus
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Plant abiotic stress response and nutrient use efficiency
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Decades’ progress and prospects on maize functional genomics and molecular breeding
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AtLRRop2, an leucine-rich repeat-only protein, mediates cold stress response in Arabidopsis thaliana
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Overexpression of IbMPK3 increases low-temperature tolerance in transgenic sweetpotato
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Characteristics of the MAPK gene family in Zizania latifolia and MAPK3 role in response to fungal pathogen infection
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Heterologous expression of an Agropyron cristatum SnRK2 protein kinase gene (AcSnRK2.11) increases freezing tolerance in transgenic yeast and tobacco
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Expression of the W36, P5CS, P5CR, MAPK3, and MAPK6 genes and proline content in bread wheat genotypes under drought stress
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Candidate genes associated with low temperature tolerance in cucumber adult plants identified by combining GWAS & QTL mapping
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Lipid metabolism and MAPK-ICE1 cascade play crucial roles in cold tolerance of banana
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Hydrogen sulfide homeostasis in plants: An overview
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Approaches in stress mitigation of plants
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Mechanisms of sensing abiotic stress responses in plants
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Characterization of PyMAPK2, a D group mitogen-activated protein kinase gene from Pyropia yezoensis responding to various abiotic stress
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IbMPK3/IbMPK6-mediated IbSPF1 phosphorylation promotes cold stress tolerance in sweet potato
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A natural variant of COOL1 gene enhances cold tolerance for high-latitude adaptation in maize
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The OsbHLH002/OsICE1-OSH1 module orchestrates secondary cell wall formation in rice
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Protein phosphorylation: A molecular switch in plant signaling
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Phosphorylation of MAP18 by MPK6 orchestrates microtubule reorganization in Arabidopsis during adaptation to salt stress
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Calmodulins and calmodulin-like proteins-mediated plant organellar calcium signaling networks under abiotic stress
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ZmBARK1 as a low-temperature tolerance gene in maize germination
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Decoding post-translational modification for understanding stress tolerance in plant
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Inhibition of Arabidopsis stomatal development by plastoquinone oxidation
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Membrane-associated NRPM proteins are novel suppressors of stomatal production in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.devcel.2017.09.024openalex-snapshot
MAP Kinase Cascades Regulate the Cold Response by Modulating ICE1 Protein Stability
inferred← citeshttps://doi.org/10.1016/j.devcel.2017.10.032openalex-snapshot
MAP Kinase Signaling Turns to ICE
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PUB25 and PUB26 Promote Plant Freezing Tolerance by Degrading the Cold Signaling Negative Regulator MYB15
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Surviving and thriving: How plants perceive and respond to temperature stress
inferred← citeshttps://doi.org/10.1016/j.devcel.2022.09.012openalex-snapshot
Root twisting drives halotropism via stress-induced microtubule reorientation
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.04.001openalex-snapshot
Nitric oxide controls stomatal development and stress responses by inhibiting MPK6 phosphorylation via S-nitrosylation in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.11.011openalex-snapshot
Transcriptional and physiological analyses reveal the association of ROS metabolism with cold tolerance in tea plant
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104243openalex-snapshot
Transcriptional regulation and signalling of cold stress response in plants: An overview of current understanding
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104416openalex-snapshot
CBF1 and CBF4 in Solanum tuberosum L. differ in their effect on low-temperature tolerance and development
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The mitogen-activated protein kinase kinase MKK2 positively regulates constitutive cold resistance in the potato
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The interaction of CsWRKY4 and CsOCP3 with CsICE1 regulates CsCBF1/3 and mediates stress response in tea plant (Camellia sinensis)
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Comparative metabolomic analysis reveals the involvement of catechins in adaptation mechanism to cold stress in tea plant (Camellia sinensis var. sinensis)
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Recent insights into cell responses to cold stress in plants: Signaling, defence, and potential functions of phosphatidic acid
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105190openalex-snapshot
Low temperature stress-induced perception and molecular signaling pathways in plants
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2025.106143openalex-snapshot
The GPCR-type G protein PeuCOLD1 of Populus euphratica conferred the ability to resist low temperature stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2026.106403openalex-snapshot
Comprehensive analysis of Dendrobium catenatum C-repeat binding factor (CBF) family genes and the role of DcCBF1 in heat tolerance
inferred← citeshttps://doi.org/10.1016/j.heliyon.2021.e07889openalex-snapshot
Stomatal development and genetic expression in Arabidopsis thaliana L.
inferred← citeshttps://doi.org/10.1016/j.hpj.2021.03.005openalex-snapshot
Photoperiod- and temperature-mediated control of the ethylene response and winter dormancy induction in Prunus mume
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.123543openalex-snapshot
Comprehensive genome-wide identification and functional characterization of MAPK cascade gene families in Nelumbo
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.125231openalex-snapshot
The DREB transcription factor, a biomacromolecule, responds to abiotic stress by regulating the expression of stress-related genes
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.135331openalex-snapshot
γ-Aminobutyric acid mediated by MdCBF3- MdGAD1 mitigates low temperature damage in apple
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.138882openalex-snapshot
Comprehensive analysis of amino acid/auxin permease family genes reveal the positive role of GhAAAP128 in cotton tolerance to cold stress
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2026.152132openalex-snapshot
Functional characterization of VaMAPK9 in enhancing cold tolerance of Vitis amurensis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.114610openalex-snapshot
Dynamic transcriptome profiling revealed key genes and pathways associated with cold stress in castor (Ricinus communis L.)
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.114861openalex-snapshot
PeMPK7 is induced in an ROS-dependent manner and confers poplar para-hydroxybenzoic acid stress resistance through the removal of ROS
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.116709openalex-snapshot
Genome-wide analysis of the R2R3-MYB transcription factor gene family expressed in Juglans regia under abiotic and biotic stresses
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.116730openalex-snapshot
Regulatory network mediated by CmMKK5–CmMPK13 cascade response to phosphorus starvation in chrysanthemum
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106049openalex-snapshot
MKKK20 works as an upstream triple-kinase of MKK3-MPK6-MYC2 module in Arabidopsis seedling development
inferred← citeshttps://doi.org/10.1016/j.jare.2022.02.004openalex-snapshot
Insights into the plateau adaptation of Salvia castanea by comparative genomic and WGCNA analyses
inferred← citeshttps://doi.org/10.1016/j.jare.2026.07.023openalex-snapshot
Divergent regulation of DREB1A by ICE1 and ABF4 contributes to distinct cold adaptation in four turfgrass species
inferred← citeshttps://doi.org/10.1016/j.jia.2022.09.010openalex-snapshot
PpMAPK6 regulates peach bud endodormancy release through interactions with PpDAM6
inferred← citeshttps://doi.org/10.1016/j.jplph.2018.07.003openalex-snapshot
A C2H2 zinc-finger protein OsZFP213 interacts with OsMAPK3 to enhance salt tolerance in rice
inferred← citeshttps://doi.org/10.1016/j.jplph.2023.154076openalex-snapshot
Identification of Brassica rapa BrEBF1 homologs and their characterization in cold signaling
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154233openalex-snapshot
TaMAPK3 phosphorylates TaCBF and TaICE and plays a negative role in wheat freezing tolerance
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154743openalex-snapshot
The crucial roles of MAPK pathways in sophisticated salt stress responses in plants
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154785openalex-snapshot
The co-repressor protein HOS15 negatively regulates ethylene signaling via degradation of EIN3 during arabidopsis apical hook formation
inferred← citeshttps://doi.org/10.1016/j.jprot.2023.104923openalex-snapshot
Proteomics of wheat and barley cereals in response to environmental stresses: Current state and future challenges
inferred← citeshttps://doi.org/10.1016/j.jprot.2023.104994openalex-snapshot
Ubiquitylome analysis reveals the involvement of ubiquitination in the cold responses of banana seedling leaves
inferred← citeshttps://doi.org/10.1016/j.molp.2019.05.008openalex-snapshot
Phosphorylation of LTF1, an MYB Transcription Factor in Populus, Acts as a Sensory Switch Regulating Lignin Biosynthesis in Wood Cells
inferred← citeshttps://doi.org/10.1016/j.molp.2020.02.004openalex-snapshot
Molecular Regulation of Plant Responses to Environmental Temperatures
inferred← citeshttps://doi.org/10.1016/j.molp.2020.09.005openalex-snapshot
RGF1-RGI1, a Peptide-Receptor Complex, Regulates Arabidopsis Root Meristem Development via a MAPK Signaling Cascade
inferred← citeshttps://doi.org/10.1016/j.molp.2022.11.010openalex-snapshot
The MEKK1-MKK1/2-MPK4 cascade phosphorylates and stabilizes STOP1 to confer aluminum resistance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.molp.2023.04.004openalex-snapshot
Suppression of ETI by PTI priming to balance plant growth and defense through an MPK3/MPK6-WRKYs-PP2Cs module
inferred← citeshttps://doi.org/10.1016/j.molp.2023.07.005openalex-snapshot
Genetic and molecular exploration of maize environmental stress resilience: Toward sustainable agriculture
inferred← citeshttps://doi.org/10.1016/j.molp.2025.10.016openalex-snapshot
Monoculm1 confers cold tolerance at the seedling stage in rice
inferred← citeshttps://doi.org/10.1016/j.ncrops.2026.100125openalex-snapshot
Plant Survival under Adversity: Signaling Crosstalk and Transcriptional Regulation under Combined Drought and Cold Stress
inferred← citeshttps://doi.org/10.1016/j.pbi.2018.04.012openalex-snapshot
Conveying endogenous and exogenous signals: MAPK cascades in plant growth and defense
inferred← citeshttps://doi.org/10.1016/j.pbi.2026.102896openalex-snapshot
Mechanisms and flexibility in plant asymmetric cell division
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110375openalex-snapshot
Overexpression of an AP2/ERF family gene, BpERF13, in birch enhances cold tolerance through upregulating CBF genes and mitigating reactive oxygen species
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110753openalex-snapshot
A tomato dynein light chain gene SlLC6D is a negative regulator of chilling stress
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.110824openalex-snapshot
The apple MdPTI1L kinase is phosphorylated by MdOXI1 during S-RNase-induced reactive oxygen species signaling in pollen tubes
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.110927openalex-snapshot
Genome-wide analysis of the bZIP gene family and the role of AchnABF1 from postharvest kiwifruit (Actinidia chinensis cv. Hongyang) in osmotic and freezing stress adaptations
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111281openalex-snapshot
Enhanced brassinosteroid signaling via the overexpression of SlBRI1 positively regulates the chilling stress tolerance of tomato
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111621openalex-snapshot
JA-induced TaMPK6 enhanced the freeze tolerance of Arabidopsis thaliana through regulation of ICE-CBF-COR module and antioxidant enzyme system
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112020openalex-snapshot
Physiological and transcriptomic analysis revealed that the accumulation of reactive oxygen species caused the low temperature sensitivity of Liriodendron × sinoamericanum
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112475openalex-snapshot
Analysis of the SlRAF-like B gene family in tomato and the molecular mechanism of SlRAF7 in regulating cold stress resistance
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112513openalex-snapshot
Investigation of wheat cold response pathway regulated by TaICE41 and TaCBFⅣd-B9 through Brachypodium distachyon transformation
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112767openalex-snapshot
Evolution of mitogen-activated protein kinase in plants and AtMAPK6's role in heat stress response in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113020openalex-snapshot
Genome-wide identification of the HD-Zip gene family and functional study of AsHD-Zip49 under drought stress in oat (Avena sativa L.)
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113210openalex-snapshot
StICE1 activates StCBFs expression to regulate cold stress response in potato (Solanum tuberosum L.) seedlings
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.12.016openalex-snapshot
Differential regulation of the durum wheat MAPK phosphatase 1 by calmodulin, bivalent cations and possibly mitogen activated protein kinase 3
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.08.007openalex-snapshot
DlICE1, a stress-responsive gene from Dimocarpus longan, enhances cold tolerance in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.10.041openalex-snapshot
Chrysanthemum (Chrysanthemum morifolium) CmICE2 conferred freezing tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.03.020openalex-snapshot
Cloning and cold-resistance analyses of CfICE1 gene in Cryptomeria fortunei
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.07.023openalex-snapshot
Hydrogen sulfide and nitric oxide are involved in melatonin-induced salt tolerance in cucumber
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.107646openalex-snapshot
Sensing, signalling, and regulatory mechanism of cold-stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109290openalex-snapshot
MaMPK19, a key gene enhancing cold resistance by activating the CBF pathway in banana
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109454openalex-snapshot
Enhancement of cold tolerance in tea plants (Camellia sinensis) by glycine betaine accumulation through CsBADH overexpression
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109533openalex-snapshot
Identification of the grape MAPKKK gene family and functional analysis of the VaMAPKKK15 gene under low temperature stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109603openalex-snapshot
Hexokinase gene CsHXK4 positively regulates cold resistance in tea plants (Camellia sinensis)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109743openalex-snapshot
Comprehensive transcriptome analysis reveals StMAPK7 regulate cold response in potato
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109981openalex-snapshot
The sorghum SbMPK3-SbNAC074 module involved in salt tolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110250openalex-snapshot
The IbMYB52/IbARF11L-IbDRM1 module negatively regulates the root development of sweetpotato
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110778openalex-snapshot
Cold resistance identification and transcriptomic responses of rapeseed (Brassica napus L.) seedlings under cold stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110805openalex-snapshot
Molecular characterization of legume-lectin receptor-like kinase SIT genes in Brassica napus reveals the involvement of BnaA02.SIT3 in salt tolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111373openalex-snapshot
Cold-induced early flowering in tobacco: Insights from JA biosynthesis and signaling
inferred← citeshttps://doi.org/10.1016/j.plipres.2018.05.003openalex-snapshot
The phosphatidic acid paradox: Too many actions for one molecule class? Lessons from plants
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2021.111775openalex-snapshot
Ferulic acid enhances chilling tolerance in tomato fruit by up-regulating the gene expression of CBF transcriptional pathway in MAPK3-dependent manner
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2024.113090openalex-snapshot
Synergistic effects of SlCBF1 and ethylene signaling on the maintenance of tomatoes quality during long-term cold storage
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2024.113207openalex-snapshot
DIA-based phosphoproteomics profiling reveals rapid cold-responsive phosphorylation events in tomato fruit
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2025.114032openalex-snapshot
Heat treatment-induced PpbZIP43 regulates energy metabolism to enhance postharvest cold tolerance in peach fruit
inferred← citeshttps://doi.org/10.1016/j.scienta.2019.108775openalex-snapshot
Transcriptome profiling of Prunus persica branches reveals candidate genes potentially involved in freezing tolerance
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109468openalex-snapshot
Transcriptomics analysis unravels the response to low temperature in sensitive and tolerant eggplants
inferred← citeshttps://doi.org/10.1016/j.scienta.2021.109905openalex-snapshot
Genome-wide identification and expression analysis of bHLH transcription factor family in response to cold stress in sweet cherry (Prunus avium L.)
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112523openalex-snapshot
Transcriptome reveals molecular mechanism of cabbage response to low temperature stress and functional study of BoPYL8 gene
inferred← citeshttps://doi.org/10.1016/j.stress.2021.100028openalex-snapshot
Cold acclimation and prospects for cold-resilient crops
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101547openalex-snapshot
Functional characterization and molecular mechanism of cold-induced NtMPK4 in regulating cold stress responses of Nicotiana tabacum
inferred← citeshttps://doi.org/10.1016/j.tplants.2017.12.002openalex-snapshot
MAPping Kinase Regulation of ICE1 in Freezing Tolerance
inferred← citeshttps://doi.org/10.1016/j.tplants.2018.04.002openalex-snapshot
Molecular Regulation of CBF Signaling in Cold Acclimation
inferred← citeshttps://doi.org/10.1016/j.tplants.2018.08.002openalex-snapshot
The Quest for MAP Kinase Substrates: Gaining Momentum
inferred← citeshttps://doi.org/10.1016/j.tplants.2023.11.022openalex-snapshot
The arabidopsis bHLH transcription factor family
inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100628openalex-snapshot
MYB44 regulates PTI by promoting the expression of EIN2 and MPK3/6 in Arabidopsis
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c14021openalex-snapshot
SlBTF3-OST1-CBF1 Module Maintains Chloroplast Integrity under Cold Stress in Tomato ( Solanum lycopersicum )
inferred← citeshttps://doi.org/10.1038/s41421-022-00413-2openalex-snapshot
Chilling-induced phosphorylation of IPA1 by OsSAPK6 activates chilling tolerance responses in rice
inferred← citeshttps://doi.org/10.1038/s41438-021-00620-0openalex-snapshot
McMYB4 improves temperature adaptation by regulating phenylpropanoid metabolism and hormone signaling in apple
inferred← citeshttps://doi.org/10.1038/s41467-021-23112-0openalex-snapshot
The membrane-localized protein kinase MAP4K4/TOT3 regulates thermomorphogenesis
inferred← citeshttps://doi.org/10.1038/s41467-021-25001-yopenalex-snapshot
Natural variation in a type-A response regulator confers maize chilling tolerance
inferred← citeshttps://doi.org/10.1038/s41467-021-26827-2openalex-snapshot
MPK3- and MPK6-mediated VLN3 phosphorylation regulates actin dynamics during stomatal immunity in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41467-022-30254-2openalex-snapshot
Dichotomy of the BSL phosphatase signaling spatially regulates MAPK components in stomatal fate determination
inferred← citeshttps://doi.org/10.1038/s41467-024-46419-0openalex-snapshot
Natural variation of STKc_GSK3 kinase TaSG-D1 contributes to heat stress tolerance in Indian dwarf wheat
inferred← citeshttps://doi.org/10.1038/s41467-025-62887-4openalex-snapshot
Pangenome analysis of transposable element insertion polymorphisms reveals features underlying cold tolerance in rice
inferred← citeshttps://doi.org/10.1038/s41477-019-0440-xopenalex-snapshot
Bipartite anchoring of SCREAM enforces stomatal initiation by coupling MAP kinases to SPEECHLESS
inferred← citeshttps://doi.org/10.1038/s41477-019-0460-6openalex-snapshot
SCREAM in the making of stomata
inferred← citeshttps://doi.org/10.1038/s41477-022-01254-3openalex-snapshot
Natural polymorphism of ZmICE1 contributes to amino acid metabolism that impacts cold tolerance in maize
inferred← citeshttps://doi.org/10.1038/s41576-021-00413-0openalex-snapshot
Abiotic stress responses in plants
inferred← citeshttps://doi.org/10.1038/s41598-024-84491-0openalex-snapshot
Subtilisin-like protease 4 regulates cold tolerance through cell wall modification in rice
inferred← citeshttps://doi.org/10.1038/s41598-025-19801-1openalex-snapshot
Comparative transcriptome profiling reveals molecular mechanisms of freezing stress responses in cultivated and wild Cicer species
inferred← citeshttps://doi.org/10.1038/s41598-025-86057-0openalex-snapshot
PiERF1 regulates cold tolerance in Plumbago indica L. through ethylene signalling
inferred← citeshttps://doi.org/10.1038/s44319-026-00906-1openalex-snapshot
MPK3-mediated phosphorylation inactivates MYB4 to promote FIT-dependent iron acquisition
inferred← citeshttps://doi.org/10.1071/fp19163openalex-snapshot
A new morphological method to identify cold tolerance of melon at seedling stage
inferred← citeshttps://doi.org/10.1071/fp23144openalex-snapshot
Overexpression of TaMPK3 enhances freezing tolerance by increasing the expression of ICE-CBF-COR related genes in the Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1073/pnas.1814426116openalex-snapshot
F-box protein RAE1 regulates the stability of the aluminum-resistance transcription factor STOP1 in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.2004670118openalex-snapshot
Chromatin phosphoproteomics unravels a function for AT-hook motif nuclear localized protein AHL13 in PAMP-triggered immunity
inferred← citeshttps://doi.org/10.1073/pnas.2211102120openalex-snapshot
The OsBDR1-MPK3 module negatively regulates blast resistance by suppressing the jasmonate signaling and terpenoid biosynthesis pathway
inferred← citeshttps://doi.org/10.1073/pnas.2218503120openalex-snapshot
Dual regulations of cell cycle regulator DPa by auxin in Arabidopsis root distal stem cell maintenance
inferred← citeshttps://doi.org/10.1073/pnas.2510538122openalex-snapshot
An AINTEGUMENTA phosphoswitch controls bilateral stem cell activity during secondary growth
inferred← citeshttps://doi.org/10.1073/pnas.2530341123openalex-snapshot
Nitrogen–TOR targets a bivalent chromatin reader to modulate floral transition
inferred← citeshttps://doi.org/10.1080/07388551.2024.2344584openalex-snapshot
A close-up of regulatory networks and signaling pathways of MKK5 in biotic and abiotic stresses
inferred← citeshttps://doi.org/10.1080/15592324.2019.1573099openalex-snapshot
A calcium sensor calcineurin B-like 9 negatively regulates cold tolerance via calcium signaling in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1080/15592324.2020.1785668openalex-snapshot
The role of NAC transcription factor in plant cold response
inferred← citeshttps://doi.org/10.1080/15592324.2020.1814547openalex-snapshot
Overexpression of Arabidopsis ICE1 enhances yield and multiple abiotic stress tolerance in indica rice
inferred← citeshttps://doi.org/10.1080/21541264.2020.1820299openalex-snapshot
Unique and contrasting effects of light and temperature cues on plant transcriptional programs
inferred← citeshttps://doi.org/10.1093/hr/uhac171openalex-snapshot
Apple U-box-type E3 ubiquitin ligase MdPUB23 reduces cold-stress tolerance by degrading the cold-stress regulatory protein MdICE1
inferred← citeshttps://doi.org/10.1093/hr/uhac256openalex-snapshot
Thioredoxin h2 inhibits the MPKK5-MPK3 cascade to regulate the CBF–COR signaling pathway in Citrullus lanatus suffering chilling stress
inferred← citeshttps://doi.org/10.1093/hr/uhae297openalex-snapshot
The ubiquitin ligase VviPUB19 negatively regulates grape cold tolerance by affecting the stability of ICEs and CBFs
inferred← citeshttps://doi.org/10.1093/hr/uhaf200openalex-snapshot
MdMAPK6-mediated phosphorylation of MdWRKY9 regulates apple fruit ripening through interaction with MdERF5L
inferred← citeshttps://doi.org/10.1093/hr/uhaf350openalex-snapshot
MAPK regulates secondary metabolism and abiotic stress in horticultural and medicinal plants
inferred← citeshttps://doi.org/10.1093/jxb/eraa251openalex-snapshot
The HD-ZIP IV transcription factor GL2-LIKE regulates male flowering time and fertility in cucumber
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