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Quantitative phosphoproteomics identifies SnRK2 protein kinase substrates and reveals the effectors of abscisic acid action
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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/s00018-012-1087-1openalex-snapshot
Osmotic stress signaling via protein kinases
inferredcites →https://doi.org/10.1016/j.pbi.2005.11.010openalex-snapshot
Chromatin modifiers that control plant development
inferredcites →https://doi.org/10.1016/j.pbi.2012.08.003openalex-snapshot
Dynamic behavior of plastids related to environmental response
inferredcites →https://doi.org/10.1016/j.tplants.2009.03.006openalex-snapshot
The multifaceted role of ABA in disease resistance
inferredcites →https://doi.org/10.1016/j.virol.2008.07.033openalex-snapshot
Identification of an Arabidopsis thaliana protein that binds to tomato mosaic virus genomic RNA and inhibits its multiplication
inferredcites →https://doi.org/10.1016/s1534-5807(02)00229-0openalex-snapshot
A Calcium Sensor and Its Interacting Protein Kinase Are Global Regulators of Abscisic Acid Signaling in Arabidopsis
inferredcites →https://doi.org/10.1038/35021067openalex-snapshot
Calcium channels activated by hydrogen peroxide mediate abscisic acid signalling in guard cells
inferredcites →https://doi.org/10.1038/nature00936openalex-snapshot
Modulation of an RNA-binding protein by abscisic-acid-activated protein kinase
inferredcites →https://doi.org/10.1038/nature05176openalex-snapshot
The Mg-chelatase H subunit is an abscisic acid receptor
inferredcites →https://doi.org/10.1038/nature08599openalex-snapshot
In vitro reconstitution of an abscisic acid signalling pathway
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.0805207105openalex-snapshot
Reconstituting plant miRNA biogenesis
inferredcites →https://doi.org/10.1073/pnas.0903144106openalex-snapshot
Arabidopsis mutant deficient in 3 abscisic acid-activated protein kinases reveals critical roles in growth, reproduction, and stress
inferredcites →https://doi.org/10.1073/pnas.0907205106openalex-snapshot
MAP kinases MPK9 and MPK12 are preferentially expressed in guard cells and positively regulate ROS-mediated ABA signaling
inferredcites →https://doi.org/10.1073/pnas.1007879107openalex-snapshot
In planta changes in protein phosphorylation induced by the plant hormone abscisic acid
inferredcites →https://doi.org/10.1073/pnas.1010834107openalex-snapshot
The Plant Homeo Domain finger protein, VIN3-LIKE 2, is necessary for photoperiod-mediated epigenetic regulation of the floral repressor, MAF5
inferredcites →https://doi.org/10.1073/pnas.1018367108openalex-snapshot
Arabidopsis decuple mutant reveals the importance of SnRK2 kinases in osmotic stress responses in vivo
inferredcites →https://doi.org/10.1073/pnas.1118876109openalex-snapshot
FLOWERING BHLH transcriptional activators control expression of the photoperiodic flowering regulator CONSTANS in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1119418109openalex-snapshot
Sensitive kinase assay linked with phosphoproteomics for identifying direct kinase substrates
inferredcites →https://doi.org/10.1073/pnas.242607499openalex-snapshot
Mitogen-activated protein kinase signaling in postgermination arrest of development by abscisic acid
inferredcites →https://doi.org/10.1074/jbc.m405259200openalex-snapshot
Identification of Nine Sucrose Nonfermenting 1-related Protein Kinases 2 Activated by Hyperosmotic and Saline Stresses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/mcp.m110.000091openalex-snapshot
In-depth Analyses of Kinase-dependent Tyrosine Phosphoproteomes Based on Metal Ion-functionalized Soluble Nanopolymers
inferredcites →https://doi.org/10.1074/mcp.o113.027284openalex-snapshot
Quantitative Measurement of Phosphoproteome Response to Osmotic Stress in Arabidopsis Based on Library-Assisted eXtracted Ion Chromatogram (LAXIC)
inferredcites →https://doi.org/10.1093/jxb/erq151openalex-snapshot
ABA receptors: the START of a new paradigm in phytohormone signalling
inferredcites →https://doi.org/10.1093/jxb/err008openalex-snapshot
The avoidance and aggregative movements of mesophyll chloroplasts in C4 monocots in response to blue light and abscisic acid
inferredcites →https://doi.org/10.1093/jxb/ers059openalex-snapshot
HD2C interacts with HDA6 and is involved in ABA and salt stress response in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcp083openalex-snapshot
Three Arabidopsis SnRK2 Protein Kinases, SRK2D/SnRK2.2, SRK2E/SnRK2.6/OST1 and SRK2I/SnRK2.3, Involved in ABA Signaling are Essential for the Control of Seed Development and Dormancy
inferredcites →https://doi.org/10.1104/pp.108.124594openalex-snapshot
Protein Tyrosine Kinases and Protein Tyrosine Phosphatases Are Involved in Abscisic Acid-Dependent Processes in Arabidopsis Seeds and Suspension Cells
inferredcites →https://doi.org/10.1104/pp.110.155523openalex-snapshot
The Plant-Specific SR45 Protein Negatively Regulates Glucose and ABA Signaling during Early Seedling Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.158048openalex-snapshot
The Acidic A-Domain of Arabidopsis Toc159 Occurs as a Hyperphosphorylated Protein
inferredcites →https://doi.org/10.1104/pp.111.188789openalex-snapshot
Transcriptional Regulation of ArabidopsisMIR168aandARGONAUTE1Homeostasis in Abscisic Acid and Abiotic Stress Responses
inferredcites →https://doi.org/10.1104/pp.112.195578openalex-snapshot
Cooperative Function of PLDδ and PLDα1 in Abscisic Acid-Induced Stomatal Closure in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.021683openalex-snapshot
Proteomic Identification of Annexins, Calcium-Dependent Membrane Binding Proteins That Mediate Osmotic Stress and Abscisic Acid Signal Transduction in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.104.029926openalex-snapshot
A Putative Nucleoporin 96 Is Required for Both Basal Defense and Constitutive Resistance Responses Mediated by suppressor of npr1-1 , constitutive 1
inferredcites →https://doi.org/10.1105/tpc.105.033043openalex-snapshot
Role of an Arabidopsis AP2/EREBP-Type Transcriptional Repressor in Abscisic Acid and Drought Stress Responses
inferredcites →https://doi.org/10.1105/tpc.106.041566openalex-snapshot
TheArabidopsisSUPPRESSOR OF AUXIN RESISTANCE Proteins Are Nucleoporins with an Important Role in Hormone Signaling and Development
inferredcites →https://doi.org/10.1105/tpc.106.048538openalex-snapshot
Identification of Two Protein Kinases Required for Abscisic Acid Regulation of Seed Germination, Root Growth, and Gene Expression in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.049239openalex-snapshot
NUCLEAR PORE ANCHOR, theArabidopsisHomolog of Tpr/Mlp1/Mlp2/Megator, Is Involved in mRNA Export and SUMO Homeostasis and Affects Diverse Aspects of Plant Development
inferredcites →https://doi.org/10.1105/tpc.107.050666openalex-snapshot
Two Calcium-Dependent Protein Kinases, CPK4 and CPK11, Regulate Abscisic Acid Signal Transduction inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.110.074674openalex-snapshot
The Conserved Splicing Factor SUA Controls Alternative Splicing of the Developmental Regulator ABI3 in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.098574openalex-snapshot
Arabidopsis PYR/PYL/RCAR Receptors Play a Major Role in Quantitative Regulation of Stomatal Aperture and Transcriptional Response to Abscisic Acid
inferredcites →https://doi.org/10.1105/tpc.112.105114openalex-snapshot
The SWI2/SNF2 Chromatin Remodeling ATPase BRAHMA Represses Abscisic Acid Responses in the Absence of the Stress Stimulus in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.108191openalex-snapshot
ArabidopsisPaired Amphipathic Helix Proteins SNL1 and SNL2 Redundantly Regulate Primary Seed Dormancy via Abscisic Acid–Ethylene Antagonism Mediated by Histone Deacetylation
inferredcites →https://doi.org/10.1105/tpc.12.12.2351openalex-snapshot
A Mutation in the Arabidopsis HYL1 Gene Encoding a dsRNA Binding Protein Affects Responses to Abscisic Acid, Auxin, and Cytokinin
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02833.xopenalex-snapshot
Mutation of SAD2, an importin β‐domain protein in Arabidopsis, alters abscisic acid sensitivity
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03770.xopenalex-snapshot
FIERY1 regulates light‐mediated repression of cell elongation and flowering time via its 3′(2′),5′‐bisphosphate nucleotidase activity
inferredcites →https://doi.org/10.1126/science.1118642openalex-snapshot
Integration of Plant Responses to Environmentally Activated Phytohormonal Signals
inferredcites →https://doi.org/10.1126/science.1172408openalex-snapshot
Regulators of PP2C Phosphatase Activity Function as Abscisic Acid Sensors
inferredcites →https://doi.org/10.1126/science.1173041openalex-snapshot
Abscisic Acid Inhibits Type 2C Protein Phosphatases via the PYR/PYL Family of START Proteins
inferredcites →https://doi.org/10.1126/science.1215106openalex-snapshot
Molecular Mimicry Regulates ABA Signaling by SnRK2 Kinases and PP2C Phosphatases
inferredcites →https://doi.org/10.1126/scisignal.2003509openalex-snapshot
Genetics and Phosphoproteomics Reveal a Protein Phosphorylation Network in the Abscisic Acid Signaling Pathway in Arabidopsis thaliana
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112122openalex-snapshot
Abscisic Acid: Emergence of a Core Signaling Network
inferredcites →https://doi.org/10.1146/annurev-phyto-082712-102314openalex-snapshot
MAPK Cascades in Plant Disease Resistance Signaling
inferredcites →https://doi.org/10.1371/journal.pbio.0040327openalex-snapshot
CDPKs CPK6 and CPK3 Function in ABA Regulation of Guard Cell S-Type Anion- and Ca2+- Permeable Channels and Stomatal Closure
inferredcites →https://doi.org/10.1371/journal.pgen.1001225openalex-snapshot
Nucleolin Is Required for DNA Methylation State and the Expression of rRNA Gene Variants in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0013935openalex-snapshot
The Arabidopsis ABA-Activated Kinase OST1 Phosphorylates the bZIP Transcription Factor ABF3 and Creates a 14-3-3 Binding Site Involved in Its Turnover
inferredcites →https://doi.org/10.1371/journal.pone.0014012openalex-snapshot
Genetic Analyses of Interactions among Gibberellin, Abscisic Acid, and Brassinosteroids in the Control of Flowering Time in Arabidopsis thaliana
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Genome-Wide Identification of the Toc Gtpase Gene Family and Screening for Substrate Specificity of Sltoc34-1 in Tomato
inferred← citeshttps://doi.org/10.1002/1873-3468.14352openalex-snapshot
Shedding Light on the Role of Phosphorylation in Plant Autophagy
inferred← citeshttps://doi.org/10.1002/9781118889022.ch8openalex-snapshot
Mechanism of ABA Signaling in Response to Abiotic Stress in Plants
inferred← citeshttps://doi.org/10.1002/elps.201400153openalex-snapshot
Analytical challenges translating mass spectrometry‐based phosphoproteomics from discovery to clinical applications
inferred← citeshttps://doi.org/10.1002/elps.201400154openalex-snapshot
Phosphoproteomics in photosynthetic organisms
inferred← citeshttps://doi.org/10.1002/pmic.201400073openalex-snapshot
Phosphorylation‐dependent regulation of plant chromatin and chromatin‐associated proteins
inferred← citeshttps://doi.org/10.1002/pmic.201400384openalex-snapshot
Proteomic dissection of plant responses to various pathogens
inferred← citeshttps://doi.org/10.1002/pmic.201400403openalex-snapshot
Plant hormone signalling through the eye of the mass spectrometer
inferred← citeshttps://doi.org/10.1002/pmic.201400410openalex-snapshot
Recent advances and challenges in plant phosphoproteomics
inferred← citeshttps://doi.org/10.1002/tpg2.20358openalex-snapshot
Genomic approaches to enhance adaptive plasticity to cope with soil constraints amidst climate change in wheat
inferred← citeshttps://doi.org/10.1007/978-1-0716-0954-5_9openalex-snapshot
Identification of ABA Receptor Agonists Using a Multiplexed High-Throughput Chemical Screening
inferred← citeshttps://doi.org/10.1007/978-1-0716-1625-3_10openalex-snapshot
Plant Phosphopeptides Enrichment by Immobilized Metal Ion Affinity Chromatography
inferred← citeshttps://doi.org/10.1007/978-1-0716-1625-3_6openalex-snapshot
Universal Sample Preparation Workflow for Plant Phosphoproteomic Profiling
inferred← citeshttps://doi.org/10.1007/978-1-0716-2156-1_13openalex-snapshot
Phosphoproteomic Approaches to Evaluate ABA Signaling
inferred← citeshttps://doi.org/10.1007/978-1-4939-2211-6_3openalex-snapshot
Investigation of Plant Abiotic Stress Tolerance by Proteomics and Phosphoproteomics
inferred← citeshttps://doi.org/10.1007/978-1-4939-2540-7_3openalex-snapshot
Insights into the Small RNA-Mediated Networks in Response to Abiotic Stress in Plants
inferred← citeshttps://doi.org/10.1007/978-1-4939-2648-0_16openalex-snapshot
Databases for Plant Phosphoproteomics
inferred← citeshttps://doi.org/10.1007/978-1-4939-2648-0_3openalex-snapshot
Phosphoproteomics in Cereals
inferred← citeshttps://doi.org/10.1007/978-1-4939-2648-0_4openalex-snapshot
Screening of Kinase Substrates Using Kinase Knockout Mutants
inferred← citeshttps://doi.org/10.1007/978-1-4939-6859-6_10openalex-snapshot
Identification of MAPK Substrates Using Quantitative Phosphoproteomics
inferred← citeshttps://doi.org/10.1007/978-1-4939-7136-7_1openalex-snapshot
Epigenetics and RNA Processing: Connections to Drought, Salt, and ABA?
inferred← citeshttps://doi.org/10.1007/978-1-4939-7154-1_21openalex-snapshot
Identification of Plant Kinase Substrates Based on Kinase Assay-Linked Phosphoproteomics
inferred← citeshttps://doi.org/10.1007/978-3-030-48733-1_11openalex-snapshot
Role of Protein Phosphatases in Signaling, Potassium Transport, and Abiotic Stress Responses
inferred← citeshttps://doi.org/10.1007/978-3-030-58502-0_8openalex-snapshot
Annexin and Mechanosensitive Channel
inferred← citeshttps://doi.org/10.1007/978-3-319-43589-3_17openalex-snapshot
Plant SnRK1 Kinases: Structure, Regulation, and Function
inferred← citeshttps://doi.org/10.1007/978-3-319-49395-4_4openalex-snapshot
Plant Aquaporin Posttranslational Regulation
inferred← citeshttps://doi.org/10.1007/978-3-319-91352-0_8openalex-snapshot
Abscisic Acid Signaling and Biosynthesis: Protein Structures and Molecular Probes
inferred← citeshttps://doi.org/10.1007/978-94-017-9424-4_18openalex-snapshot
ABA and the Floral Transition
inferred← citeshttps://doi.org/10.1007/978-94-017-9424-4_8openalex-snapshot
Protein Kinases and Phosphatases Involved in ABA Signaling
inferred← citeshttps://doi.org/10.1007/978-981-19-9794-5_11openalex-snapshot
Insight into the Interaction of Strigolactones, Abscisic Acid, and Reactive Oxygen Species Signals
inferred← citeshttps://doi.org/10.1007/978-981-97-1699-9_22openalex-snapshot
Modern Crop Improvement Approaches for Developing Abiotic Stress-Tolerance in Plants
inferred← citeshttps://doi.org/10.1007/s00018-016-2376-xopenalex-snapshot
Regulation of mRNA decay in plant responses to salt and osmotic stress
inferred← citeshttps://doi.org/10.1007/s00299-015-1914-6openalex-snapshot
MdSOS2L1 phosphorylates MdVHA-B1 to modulate malate accumulation in response to salinity in apple
inferred← citeshttps://doi.org/10.1007/s00299-026-03766-0openalex-snapshot
Molecular characterization of SnRK2 gene family in Capsicum chinense and functional validation of CcSnRK2.5 under drought stress
inferred← citeshttps://doi.org/10.1007/s00425-023-04132-0openalex-snapshot
Plant serine/arginine-rich proteins: versatile players in RNA processing
inferred← citeshttps://doi.org/10.1007/s10535-018-0823-2openalex-snapshot
Salt oversensitivity derived from mutation breeding improves salinity tolerance in barley via ion homeostasis
inferred← citeshttps://doi.org/10.1007/s11103-016-0456-9openalex-snapshot
Genome-wide identification and homeolog-specific expression analysis of the SnRK2 genes in Brassica napus guard cells
inferred← citeshttps://doi.org/10.1007/s11103-016-0458-7openalex-snapshot
ABA and cytokinins: challenge and opportunity for plant stress research
inferred← citeshttps://doi.org/10.1007/s11103-017-0692-7openalex-snapshot
Interaction network of core ABA signaling components in maize
inferred← citeshttps://doi.org/10.1007/s11103-019-00908-9openalex-snapshot
Proteomic characterization of MPK4 signaling network and putative substrates
inferred← citeshttps://doi.org/10.1007/s11103-019-00941-8openalex-snapshot
The Arabidopsis kinase-associated protein phosphatase KAPP, interacting with protein kinases SnRK2.2/2.3/2.6, negatively regulates abscisic acid signaling
inferred← citeshttps://doi.org/10.1007/s11104-026-08515-6openalex-snapshot
Plant resilience under abiotic stress: all for one or one for all?
inferred← citeshttps://doi.org/10.1007/s11105-014-0718-0openalex-snapshot
Leucine-Rich Repeat Receptor-Like Kinase FON1 Regulates Drought Stress and Seed Germination by Activating the Expression of ABA-Responsive Genes in Rice
inferred← citeshttps://doi.org/10.1007/s11105-017-1034-2openalex-snapshot
SnRK2 Homologs in Gossypium and GhSnRK2.6 Improved Salt Tolerance in Transgenic Upland Cotton and Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11802-019-3799-4openalex-snapshot
Characterization and Expression Analysis of Protein Kinase C Gene from Dunaliella salina
inferred← citeshttps://doi.org/10.1007/s12374-026-09513-yopenalex-snapshot
Integrating Hormonal, Kinase and Transcription Factor Regulatory Networks in Plant Salinity Stress: Toward a Hierarchical Signal Integration Model
inferred← citeshttps://doi.org/10.1007/s13205-026-05055-9openalex-snapshot
Regulatory roles of alternative splicing (AS) and long non-coding RNAs (LncRNAs) in plant adaptation to abiotic stresses
inferred← citeshttps://doi.org/10.1007/s13258-020-00968-yopenalex-snapshot
The SnRK2 family in pepper (Capsicum annuum L.): genome-wide identification and expression analyses during fruit development and under abiotic stress
inferred← citeshttps://doi.org/10.1007/s13361-017-1603-5openalex-snapshot
Estimating the Efficiency of Phosphopeptide Identification by Tandem Mass Spectrometry
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Ectopic expression of an oat SnRK2 gene, AsSnRK2D, enhances dehydration and salinity tolerance in tobacco by modulating the expression of stress-related genes
inferred← citeshttps://doi.org/10.1007/s42994-020-00017-yopenalex-snapshot
FERONIA cytoplasmic domain: node of varied signal outputs
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Understanding the multifaceted role of ABA signaling in orchestrating plant developmental transition
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Integrative multi-omics approaches for crop abiotic stress tolerance
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Advances in biotechnology, genomics, and breeding strategies for enhancing drought resilience in sugar beet (Beta vulgaris L.)
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Phosphorylation Networks in the Abscisic Acid Signaling Pathway
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Engineering Signaling Molecules to Improve Abiotic Stress Tolerance in Crop Plants
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Conventional and biotechnological metabolic engineering approaches to enhancing abiotic stress tolerance in plants
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Plant signaling and signal transduction cascades in response to multiple abiotic stresses
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Structure and function of diverse abscisic acid receptors and coreceptors in modulating developmental and stress responses
inferred← citeshttps://doi.org/10.1016/bs.abr.2019.01.001openalex-snapshot
Posttranslational control of tetrapyrrole biosynthesis: Interacting proteins, chaperones, auxiliary factors
inferred← citeshttps://doi.org/10.1016/bs.abr.2019.09.015openalex-snapshot
Abscisic acid as a gateway for the crops of tomorrow
inferred← citeshttps://doi.org/10.1016/bs.abr.2019.10.001openalex-snapshot
ABA signaling in guard cells
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2016.07.001openalex-snapshot
Molecular Interactions Between Flowering Time and Abiotic Stress Pathways
inferred← citeshttps://doi.org/10.1016/bs.mie.2014.10.022openalex-snapshot
Sample Preparation for Phosphoproteomic Analysis of Circadian Time Series in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.agwat.2022.107911openalex-snapshot
Physiological response of winter wheat (Triticum aestivum L.) during vegetative growth to gradual, persistent and intermittent drought
inferred← citeshttps://doi.org/10.1016/j.algal.2025.104385openalex-snapshot
A PP2C-SnRK2-MnSOD module modulates ROS homeostasis in Ulva prolifera response to salt stress
inferred← citeshttps://doi.org/10.1016/j.bbagen.2016.08.017openalex-snapshot
Iron deficiency response gene Femu2 plays a positive role in protecting Chlamydomonas reinhardtii against salt stress
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2015.12.001openalex-snapshot
The E3 ubiquitin ligase CHIP mediates ubiquitination and proteasomal degradation of PRMT5
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2022.119224openalex-snapshot
Prokaryotic and eukaryotic traits support the biological role of the chloroplast outer envelope
inferred← citeshttps://doi.org/10.1016/j.bbapap.2015.12.008openalex-snapshot
Role of the proteome in phytohormonal signaling
inferred← citeshttps://doi.org/10.1016/j.cell.2016.08.029openalex-snapshot
Abiotic Stress Signaling and Responses in Plants
inferred← citeshttps://doi.org/10.1016/j.cellsig.2020.109799openalex-snapshot
Heterotrimeric G-proteins mediated hormonal responses in plants
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Control of grain size in rice by TGW3 phosphorylation of OsIAA10 through potentiation of OsIAA10-OsARF4-mediated auxin signaling
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115894openalex-snapshot
Rice B2 and B3 subgroup RAF kinases play central roles in both ABA and osmotic stress signaling
inferred← citeshttps://doi.org/10.1016/j.chembiol.2020.03.010openalex-snapshot
Specific Knockdown of α-Synuclein by Peptide-Directed Proteasome Degradation Rescued Its Associated Neurotoxicity
inferred← citeshttps://doi.org/10.1016/j.cj.2023.12.005openalex-snapshot
Drought-triggered repression of miR166 promotes drought tolerance in soybean
inferred← citeshttps://doi.org/10.1016/j.cj.2024.01.004openalex-snapshot
The CBL-interacting protein kinase OsCIPK1 phosphorylated by SAPK10 positively regulates responses to ABA and osmotic stress in rice
inferred← citeshttps://doi.org/10.1016/j.cj.2025.04.006openalex-snapshot
ABA-activated subclass III SnRK2s control kernel maturation in maize
inferred← citeshttps://doi.org/10.1016/j.devcel.2014.12.023openalex-snapshot
OST1 Kinase Modulates Freezing Tolerance by Enhancing ICE1 Stability in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.01.004openalex-snapshot
Increasing Freezing Tolerance: Kinase Regulation of ICE1
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.08.008openalex-snapshot
PUB25 and PUB26 Promote Plant Freezing Tolerance by Degrading the Cold Signaling Negative Regulator MYB15
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.10.012openalex-snapshot
Thriving under Stress: How Plants Balance Growth and the Stress Response
inferred← citeshttps://doi.org/10.1016/j.devcel.2022.09.012openalex-snapshot
Root twisting drives halotropism via stress-induced microtubule reorientation
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.10.004openalex-snapshot
Light-quality-directed plant growth strategy controlled by SnRK2s
inferred← citeshttps://doi.org/10.1016/j.devcel.2026.01.009openalex-snapshot
Moonlighting SnRK2s stabilize a bZIP-bHLH switch in light-instructed plant development
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105188openalex-snapshot
PDC1 is activated by ABF4 and inhibits seed germination by promoting ROS accumulation in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105541openalex-snapshot
Transcriptome uncovers BnaFBH3-mediated regulatory networks associated with tolerant to abiotic stress in Brassica napus
inferred← citeshttps://doi.org/10.1016/j.gene.2014.09.017openalex-snapshot
Genome-wide identification and expression profiling of the SnRK2 gene family in Malus prunifolia
inferred← citeshttps://doi.org/10.1016/j.gene.2018.12.070openalex-snapshot
Overexpression of a protein kinase gene MpSnRK2.10 from Malus prunifolia confers tolerance to drought stress in transgenic Arabidopsis thaliana and apple
inferred← citeshttps://doi.org/10.1016/j.gene.2022.146645openalex-snapshot
Proteomic analysis of Euryale ferox Salisb seeds at different developmental stages
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.125007openalex-snapshot
NtLTPI.38, a plasma membrane-localized protein, mediates lipid metabolism and salt tolerance in Nicotiana tabacum
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.135366openalex-snapshot
Comprehensive genomic analysis of CiPawPYL-PP2C-SnRK family genes in pecan (Carya illinoinensis) and functional characterization of CiPawSnRK2.1 under salt stress responses
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2026.152598openalex-snapshot
Genome-wide identification and functional characterization of drought-responsive U-box E3 ubiquitin ligase genes in Rosa chinensis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115030openalex-snapshot
Systematic analysis and comparison of CaLB genes reveal the functions of GhCaLB42 and GhCaLB123 in fiber development and abiotic stress in cotton
inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.120372openalex-snapshot
Alternative splicing of tanshinone synthesis genes and related splicing factors in Salvia miltiorrhiza in response to hormones
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.120560openalex-snapshot
Epigenetic regulation of switchgrass (Panicum virgatum L.) in multiple drought stresses
inferred← citeshttps://doi.org/10.1016/j.isci.2021.103547openalex-snapshot
Genetic and molecular mechanisms underlying mangrove adaptations to intertidal environments
inferred← citeshttps://doi.org/10.1016/j.jia.2026.05.013openalex-snapshot
SnRK1 orchestrates nitrogen remobilization by activating autophagy and repressing TOR during grain filling
inferred← citeshttps://doi.org/10.1016/j.jplph.2013.12.007openalex-snapshot
Abscisic acid and abiotic stress tolerance – Different tiers of regulation
inferred← citeshttps://doi.org/10.1016/j.jplph.2016.02.017openalex-snapshot
Analysis of the embryo proteome of sycamore (Acer pseudoplatanus L.) seeds reveals a distinct class of proteins regulating dormancy release
inferred← citeshttps://doi.org/10.1016/j.jplph.2016.07.016openalex-snapshot
Interactions of ABA signaling core components (SlPYLs, SlPP2Cs, and SlSnRK2s) in tomato (Solanum lycopersicon)
inferred← citeshttps://doi.org/10.1016/j.jplph.2018.01.011openalex-snapshot
Expression profiling of genes encoding ABA route components in response to dehydration or various light conditions in poplar buds and leaves
inferred← citeshttps://doi.org/10.1016/j.jplph.2018.03.022openalex-snapshot
Global insights of protein responses to cold stress in plants: Signaling, defence, and degradation
inferred← citeshttps://doi.org/10.1016/j.jplph.2020.153143openalex-snapshot
Expression profiling of the genes encoding ABA route components and the ACC oxidase isozymes in the senescing leaves of Populus tremula
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153587openalex-snapshot
Integrative proteomics and phosphoproteomics reveals phosphorylation networks involved in the maintenance and expression of embryogenic competence in sugarcane callus
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154471openalex-snapshot
Sugar sensors in plants: Orchestrators of growth, stress tolerance, and hormonal crosstalk
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154565openalex-snapshot
Revising the role of ABA as regulator of flowering and seed development
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154738openalex-snapshot
Phytochrome-interacting factors (PIFs): Integrating phytohormone signals at the nexus of development and stress adaptation
inferred← citeshttps://doi.org/10.1016/j.mcpro.2024.100762openalex-snapshot
TIMAHAC: Streamlined Tandem IMAC-HILIC Workflow for Simultaneous and High-Throughput Plant Phosphoproteomics and N-glycoproteomics
inferred← citeshttps://doi.org/10.1016/j.mcpro.2024.100804openalex-snapshot
DIA-Based Phosphoproteomics Identifies Early Phosphorylation Events in Response to EGTA and Mannitol in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.mcpro.2025.100926openalex-snapshot
Identifying Receptor Kinase Substrates Using an 8000 Peptide Kinase Client Library Enriched for Conserved Phosphorylation Sites
inferred← citeshttps://doi.org/10.1016/j.molcel.2017.12.002openalex-snapshot
Reciprocal Regulation of the TOR Kinase and ABA Receptor Balances Plant Growth and Stress Response
inferred← citeshttps://doi.org/10.1016/j.molp.2014.10.003openalex-snapshot
Dissection of miRNA Pathways Using Arabidopsis Mesophyll Protoplasts
inferred← citeshttps://doi.org/10.1016/j.molp.2014.12.005openalex-snapshot
The ABA-Deficiency Suppressor Locus HAS2 Encodes the PPR Protein LOI1/MEF11 Involved in Mitochondrial RNA Editing
inferred← citeshttps://doi.org/10.1016/j.molp.2015.09.015openalex-snapshot
Ubiquitin–Proteasome System in ABA Signaling: From Perception to Action
inferred← citeshttps://doi.org/10.1016/j.molp.2015.10.003openalex-snapshot
A Direct Link between Abscisic Acid Sensing and the Chromatin-Remodeling ATPase BRAHMA via Core ABA Signaling Pathway Components
inferred← citeshttps://doi.org/10.1016/j.molp.2018.05.001openalex-snapshot
The Antagonistic Action of Abscisic Acid and Cytokinin Signaling Mediates Drought Stress Response in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.pbi.2014.07.009openalex-snapshot
ABA-dependent and ABA-independent signaling in response to osmotic stress in plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2024.102592openalex-snapshot
How chromatin senses plant hormones
inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.09.013openalex-snapshot
At RAV1 and At RAV2 overexpression in cotton increases fiber length differentially under drought stress and delays flowering
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.111121openalex-snapshot
In vivo identification of putative CPK5 substrates in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111675openalex-snapshot
Substrate profiling of the Arabidopsis Ca2+-dependent protein kinase AtCPK4 and its Ricinus communis ortholog RcCDPK1
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.07.002openalex-snapshot
Comparative phosphoproteome analysis upon ethylene and abscisic acid treatment in Glycine max leaves
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.08.016openalex-snapshot
Phenological, morpho-physiological and proteomic responses of Triticum boeoticum to drought stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.08.019openalex-snapshot
A critical review on plant annexin: Structure, function, and mechanism
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.107931openalex-snapshot
Identification of tomato AHL gene families and functional analysis their roles in fruit development and abiotic stress response
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109331openalex-snapshot
Genome-wide identification of the Toc GTPase gene family in tomato and involvement of SlToc34-1 gene in fruit chloroplast development
inferred← citeshttps://doi.org/10.1016/j.rsci.2020.04.003openalex-snapshot
Protein Phosphorylation and Phosphoproteome: An Overview of Rice
inferred← citeshttps://doi.org/10.1016/j.scib.2023.08.017openalex-snapshot
Data-independent acquisition-based global phosphoproteomics reveal the diverse roles of casein kinase 1 in plant development
inferred← citeshttps://doi.org/10.1016/j.scienta.2019.108815openalex-snapshot
Improved salt-tolerance in Citrus macrophylla mutant rootstocks
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111175openalex-snapshot
Role of SnRK2s in grape berry development and stress response
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.143994openalex-snapshot
Adaptive roots of mangrove Avicennia marina: Structure and gene expressions analyses of pneumatophores
inferred← citeshttps://doi.org/10.1016/j.tplants.2015.04.001openalex-snapshot
Unnatural agrochemical ligands for engineered abscisic acid receptors
inferred← citeshttps://doi.org/10.1016/j.tplants.2016.04.004openalex-snapshot
The Role of MAPK Modules and ABA during Abiotic Stress Signaling
inferred← citeshttps://doi.org/10.1016/j.tplants.2017.08.009openalex-snapshot
Non-26S Proteasome Endomembrane Trafficking Pathways in ABA Signaling
inferred← citeshttps://doi.org/10.1016/j.tplants.2017.09.019openalex-snapshot
Alternative Splicing Control of Abiotic Stress Responses
inferred← citeshttps://doi.org/10.1016/j.tplants.2018.05.004openalex-snapshot
Mechanisms of Photodamage and Protein Turnover in Photoinhibition
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.04.008openalex-snapshot
Revisiting the Basal Role of ABA – Roles Outside of Stress
inferred← citeshttps://doi.org/10.1016/j.tplants.2020.03.013openalex-snapshot
Mass Spectrometry Untangles Plant Membrane Protein Signaling Networks
inferred← citeshttps://doi.org/10.1016/j.virusres.2024.199334openalex-snapshot
Comprehensive phytohormone metabolomic and transcriptomic analysis of tobacco (Nicotiana tabacum) infected by tomato spotted wilt virus (TSWV)
inferred← citeshttps://doi.org/10.1016/j.xplc.2020.100099openalex-snapshot
Abscisic Acid Connects Phytohormone Signaling with RNA Metabolic Pathways and Promotes an Antiviral Response that Is Evaded by a Self-Controlled RNA Virus
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100495openalex-snapshot
ABA signaling prevents phosphodegradation of the SR45 splicing factor to alleviate inhibition of early seedling development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.102038openalex-snapshot
Phosphate starvation primes plant immunity through an ABA–OsbZIP12–phytoalexin signaling network
inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.03.024openalex-snapshot
Hormonal control of the floral transition: Can one catch them all?
inferred← citeshttps://doi.org/10.1016/s2095-3119(18)62131-8openalex-snapshot
Effect of exogenous GA3 on flowering quality, endogenous hormones, and hormone- and flowering-associated gene expression in forcing-cultured tree peony (Paeonia suffruticosa)
inferred← citeshttps://doi.org/10.1016/s2095-3119(19)62830-3openalex-snapshot
TaSnRK2.4 is a vital regulator in control of thousand-kernel weight and response to abiotic stress in wheat
inferred← citeshttps://doi.org/10.1017/s0960258514000415openalex-snapshot
Regulation of seed dormancy by abscisic acid andDELAY OF GERMINATION 1
inferred← citeshttps://doi.org/10.1021/acs.analchem.3c00786openalex-snapshot
Suspension Trapping-Based Sample Preparation Workflow for In-Depth Plant Phosphoproteomics
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c02018openalex-snapshot
Caged Phytohormones: From Chemical Inactivation to Controlled Physiological Response
inferred← citeshttps://doi.org/10.1021/acs.jproteome.5b00574openalex-snapshot
Identification of Salmonella Typhimurium Deubiquitinase SseL Substrates by Immunoaffinity Enrichment and Quantitative Proteomic Analysis
inferred← citeshttps://doi.org/10.1021/acs.jproteome.6b00348openalex-snapshot
Up-to-Date Workflow for Plant (Phospho)proteomics Identifies Differential Drought-Responsive Phosphorylation Events in Maize Leaves
inferred← citeshttps://doi.org/10.1038/hortres.2016.29openalex-snapshot
Relative quantification of phosphoproteomic changes in grapevine (Vitis vinifera L.) leaves in response to abscisic acid
inferred← citeshttps://doi.org/10.1038/ncomms9139openalex-snapshot
An Arabidopsis PWI and RRM motif-containing protein is critical for pre-mRNA splicing and ABA responses
inferred← citeshttps://doi.org/10.1038/ncomms9630openalex-snapshot
Degradation of the ABA co-receptor ABI1 by PUB12/13 U-box E3 ligases
inferred← citeshttps://doi.org/10.1038/nplants.2016.204openalex-snapshot
ABA-unresponsive SnRK2 protein kinases regulate mRNA decay under osmotic stress in plants
inferred← citeshttps://doi.org/10.1038/nplants.2017.57openalex-snapshot
Root hydrotropism is controlled via a cortex-specific growth mechanism
inferred← citeshttps://doi.org/10.1038/s41467-020-14477-9openalex-snapshot
A RAF-SnRK2 kinase cascade mediates early osmotic stress signaling in higher plants
inferred← citeshttps://doi.org/10.1038/s41467-020-19977-2openalex-snapshot
Role of Raf-like kinases in SnRK2 activation and osmotic stress response in plants
inferred← citeshttps://doi.org/10.1038/s41467-024-49844-3openalex-snapshot
Multi-omics analysis of green lineage osmotic stress pathways unveils crucial roles of different cellular compartments
inferred← citeshttps://doi.org/10.1038/s41467-025-56008-4openalex-snapshot
CPK1 activates CNGCs through phosphorylation for Ca2+ signaling to promote root hair growth in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41580-022-00479-6openalex-snapshot
Plant hormone regulation of abiotic stress responses
inferred← citeshttps://doi.org/10.1038/s41598-017-16152-4openalex-snapshot
Molecular Characterization and Co-expression Analysis of the SnRK2 Gene Family in Sugarcane (Saccharum officinarum L.)
inferred← citeshttps://doi.org/10.1038/s42003-019-0281-1openalex-snapshot
SnRK2 protein kinases represent an ancient system in plants for adaptation to a terrestrial environment
inferred← citeshttps://doi.org/10.1038/s44319-025-00495-5openalex-snapshot
Cotyledon opening during seedling deetiolation is determined by ABA-mediated splicing regulation
inferred← citeshttps://doi.org/10.1038/srep03460openalex-snapshot
Global Screening of CK2 Kinase Substrates by an Integrated Phosphoproteomics Workflow
inferred← citeshttps://doi.org/10.1038/srep15626openalex-snapshot
Quantitative iTRAQ-based proteomic analysis of phosphoproteins and ABA-regulated phosphoproteins in maize leaves under osmotic stress
inferred← citeshttps://doi.org/10.1038/srep31697openalex-snapshot
Quantitative phosphoproteomics reveals the role of the AMPK plant ortholog SnRK1 as a metabolic master regulator under energy deprivation
inferred← citeshttps://doi.org/10.1038/srep42943openalex-snapshot
Methylated-antibody affinity purification to improve proteomic identification of plant RNA polymerase Pol V complex and the interacting proteins
inferred← citeshttps://doi.org/10.1039/c7an00985bopenalex-snapshot
Recent advances in phosphoproteomics and application to neurological diseases
inferred← citeshttps://doi.org/10.1042/bcj20160819openalex-snapshot
G protein subunit phosphorylation as a regulatory mechanism in heterotrimeric G protein signaling in mammals, yeast, and plants
inferred← citeshttps://doi.org/10.1042/bcj20170022openalex-snapshot
Revisiting paradigms of Ca2+ signaling protein kinase regulation in plants
inferred← citeshttps://doi.org/10.1042/bcj20190339openalex-snapshot
CBL–CIPK module-mediated phosphoregulation: facts and hypothesis
inferred← citeshttps://doi.org/10.1073/pnas.1316717111openalex-snapshot
GSK3-like kinases positively modulate abscisic acid signaling through phosphorylating subgroup III SnRK2s in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.1423481112openalex-snapshot
Nitric oxide negatively regulates abscisic acid signaling in guard cells by S-nitrosylation of OST1
inferred← citeshttps://doi.org/10.1073/pnas.1512779113openalex-snapshot
Calcium-dependent oligomerization of CAR proteins at cell membrane modulates ABA signaling
inferred← citeshttps://doi.org/10.1073/pnas.1819971116openalex-snapshot
Phosphoproteomics of Arabidopsis Highly ABA-Induced1 identifies AT-Hook–Like10 phosphorylation required for stress growth regulation
inferred← citeshttps://doi.org/10.1073/pnas.1906244116openalex-snapshot
Highly ABA-Induced 1 (HAI1)-Interacting protein HIN1 and drought acclimation-enhanced splicing efficiency at intron retention sites
inferred← citeshttps://doi.org/10.1073/pnas.1908677116openalex-snapshot
The MATH-BTB BPM3 and BPM5 subunits of Cullin3-RING E3 ubiquitin ligases target PP2CA and other clade A PP2Cs for degradation
inferred← citeshttps://doi.org/10.1073/pnas.1919901117openalex-snapshot
Mapping proteome-wide targets of protein kinases in plant stress responses
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.2010911118openalex-snapshot
Abscisic acid regulates secondary cell-wall formation and lignin deposition in Arabidopsis thaliana through phosphorylation of NST1
inferred← citeshttps://doi.org/10.1073/pnas.2100073118openalex-snapshot
Arabidopsis group C Raf-like protein kinases negatively regulate abscisic acid signaling and are direct substrates of SnRK2
inferred← citeshttps://doi.org/10.1073/pnas.2310670120openalex-snapshot
Distinct guard cell–specific remodeling of chromatin accessibility during abscisic acid– and CO 2 -dependent stomatal regulation
inferred← citeshttps://doi.org/10.1073/pnas.2537976123openalex-snapshot
CPKs are involved in Ca 2+ signaling encoding by enhancing OST1-initiated Ca 2+ influx for ABA-induced stomatal closure in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.2603627123openalex-snapshot
Rapid sensing and relaying of cellular hyperosmotic stress signals via RAF–SnRK2 core condensates
inferred← citeshttps://doi.org/10.1074/jbc.m116.751693openalex-snapshot
The Plant Hormone Abscisic Acid Is a Prosurvival Factor in Human and Murine Megakaryocytes
inferred← citeshttps://doi.org/10.1074/jbc.m117.776468openalex-snapshot
The novel chloroplast outer membrane kinase KOC1 is a required component of the plastid protein import machinery
inferred← citeshttps://doi.org/10.1074/mcp.m114.043307openalex-snapshot
Rapid Phosphoproteomic Effects of Abscisic Acid (ABA) on Wild-Type and ABA Receptor-Deficient A. thaliana Mutants*
inferred← citeshttps://doi.org/10.1074/mcp.tir118.000702openalex-snapshot
Universal Plant Phosphoproteomics Workflow and Its Application to Tomato Signaling in Response to Cold Stress*
inferred← citeshttps://doi.org/10.1080/07352689.2020.1770942openalex-snapshot
Emerging Functions of Plant Serine/Arginine-Rich (SR) Proteins: Lessons from Animals
inferred← citeshttps://doi.org/10.1080/15592324.2015.1031939openalex-snapshot
Nitric oxide suppresses the inhibitory effect of abscisic acid on seed germination by S-nitrosylation of SnRK2 proteins
inferred← citeshttps://doi.org/10.1080/15592324.2019.1642037openalex-snapshot
Phosphorylation regulates the activity of INDETERMINATE-DOMAIN (IDD/BIRD) proteins in response to diverse environmental conditions
inferred← citeshttps://doi.org/10.1080/15592324.2022.2071024openalex-snapshot
ABA activated SnRK2 kinases: an emerging role in plant growth and physiology
inferred← citeshttps://doi.org/10.1080/15592324.2026.2684387openalex-snapshot
Uncovering the role of ABI2 as a key regulator of flowering time in Arabidopsis
inferred← citeshttps://doi.org/10.1080/17429145.2020.1778110openalex-snapshot
AIW1 and AIW2, two ABA-induced WD40 repeat-containing transcription repressors function redundantly to regulate ABA and salt responses in Arabidopsis
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