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Cross-talk of calcium-dependent protein kinase and MAP kinase signaling

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1 of the 64 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1074/jbc.m805483200 (notice 2021-04-29).

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/jcp.21246openalex-snapshot
Mitogenic signaling pathways induced by G protein‐coupled receptors
inferredcites →https://doi.org/10.1002/pmic.200401282openalex-snapshot
Identification of Arabidopsis salt and osmotic stress responsive proteins using two‐dimensional difference gel electrophoresis and mass spectrometry
inferredcites →https://doi.org/10.1006/jmbi.2002.5426openalex-snapshot
N-terminal N -myristoylation of proteins: prediction of substrate proteins from amino acid sequence 1 1Edited by J. Thornton
inferredcites →https://doi.org/10.1007/978-1-59745-289-2_15openalex-snapshot
Functional Complementation of Yeast Mutants to Study Plant Signalling Pathways
inferredcites →https://doi.org/10.1007/s11103-007-9245-9openalex-snapshot
A chemical-genetic approach to elucidate protein kinase function in planta
inferredcites →https://doi.org/10.1016/j.cell.2004.07.016openalex-snapshot
MAP Kinase-Mediated Stress Relief that Precedes and Regulates the Timing of Transcriptional Induction
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.tplants.2008.06.006openalex-snapshot
Convergent energy and stress signaling
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/s0014-5793(98)01197-1openalex-snapshot
Identification of a possible MAP kinase cascade in Arabidopsis thaliana based on pairwise yeast two‐hybrid analysis and functional complementation tests of yeast mutants
inferredcites →https://doi.org/10.1016/s0092-8674(00)00213-0openalex-snapshot
Arabidopsis MAP Kinase 4 Negatively Regulates Systemic Acquired Resistance
inferredcites →https://doi.org/10.1016/s0898-6568(02)00007-4openalex-snapshot
Modulation of the Ras/Raf/MEK/ERK pathway by Ca2+, and Calmodulin
inferredcites →https://doi.org/10.1016/s1360-1385(00)01628-9openalex-snapshot
The role of calcium and activated oxygens as signals for controlling cross-tolerance
inferredcites →https://doi.org/10.1021/bi1003487openalex-snapshot
Kinetic Analysis of 14-3-3-Inhibited Arabidopsis thaliana Nitrate Reductase
inferredcites →https://doi.org/10.1038/352524a0openalex-snapshot
Transgenic plant aequorin reports the effects of touch and cold-shock and elicitors on cytoplasmic calcium
inferredcites →https://doi.org/10.1038/353170a0openalex-snapshot
Dissection of the protein kinase cascade by which nerve growth factor activates MAP kinases
inferredcites →https://doi.org/10.1038/415977aopenalex-snapshot
MAP kinase signalling cascade in Arabidopsis innate immunity
inferredcites →https://doi.org/10.1038/nature08794openalex-snapshot
Differential innate immune signalling via Ca2+ sensor protein kinases
inferredcites →https://doi.org/10.1038/nrm1679openalex-snapshot
Plants, symbiosis and parasites: a calcium signalling connection
inferredcites →https://doi.org/10.1038/nsmb.1795openalex-snapshot
Structures of apicomplexan calcium-dependent protein kinases reveal mechanism of activation by calcium
inferredcites →https://doi.org/10.1042/bj20080625openalex-snapshot
Arabidopsis MAPKs: a complex signalling network involved in multiple biological processes
inferredcites →https://doi.org/10.1042/bj20091147openalex-snapshot
Breaking the code: Ca2+ sensors in plant signalling
inferredcites →https://doi.org/10.1073/pnas.0502954102openalex-snapshot
Ethylene-mediated cross-talk between calcium-dependent protein kinase and MAPK signaling controls stress responses in plants
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.0912030107openalex-snapshot
Guard cell anion channel SLAC1 is regulated by CDPK protein kinases with distinct Ca 2+ affinities
inferredcites →https://doi.org/10.1073/pnas.091610798openalex-snapshot
Rck2, a member of the calmodulin-protein kinase family, links protein synthesis to high osmolarity MAP kinase signaling in budding yeast
inferredcites →https://doi.org/10.1073/pnas.132092099openalex-snapshot
Reconstitution in yeast of the Arabidopsis SOS signaling pathway for Na + homeostasis
inferredcites →https://doi.org/10.1074/jbc.m401099200openalex-snapshot
Dynamic Changes in the Localization of MAPK Cascade Components Controlling Pathogenesis-related (PR) Gene Expression during Innate Immunity in Parsley
inferredcites →https://doi.org/10.1074/jbc.m401501200openalex-snapshot
Calcium Activation of ERK Mediated by Calmodulin Kinase I
inferredcites →https://doi.org/10.1074/jbc.m702840200openalex-snapshot
Mitogen-activated Protein Kinase p38 Regulates the Wnt/Cyclic GMP/Ca2+ Non-canonical Pathway
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/10.1074/jbc.m805483200openalex-snapshot
Ca2+/Calmodulin-dependent Protein Kinase II Promotes Cell Cycle Progression by Directly Activating MEK1 and Subsequently Modulating p27 Phosphorylation
inferredcites →https://doi.org/10.1074/mcp.m600044-mcp200openalex-snapshot
Proteomics of Plant Detergent-resistant Membranes
inferredcites →https://doi.org/10.1074/mcp.m700099-mcp200openalex-snapshot
A High Content in Lipid-modified Peripheral Proteins and Integral Receptor Kinases Features in the Arabidopsis Plasma Membrane Proteome
inferredcites →https://doi.org/10.1093/emboj/20.20.5556openalex-snapshot
Calcium‐dependent protein kinases play an essential role in a plant defence response
inferredcites →https://doi.org/10.1093/jxb/erh012openalex-snapshot
From signal to cell polarity: mitogen-activated protein kinases as sensors and effectors of cytoskeleton dynamicity
inferredcites →https://doi.org/10.1093/jxb/erj212openalex-snapshot
Wounding increases salt tolerance in tomato plants: evidence on the participation of calmodulin-like activities in cross-tolerance signalling
inferredcites →https://doi.org/10.1093/mp/ssp109openalex-snapshot
Roles of Arabidopsis Patatin-Related Phospholipases A in Root Development Are Related to Auxin Responses and Phosphate Deficiency
inferredcites →https://doi.org/10.1094/mpmi-20-5-0589openalex-snapshot
The MAP Kinase Kinase MKK2 Affects Disease Resistance inArabidopsis
inferredcites →https://doi.org/10.1104/pp.010770openalex-snapshot
An Arabidopsis Calcium-Dependent Protein Kinase Is Associated with the Endoplasmic Reticulum
inferredcites →https://doi.org/10.1104/pp.102.011999openalex-snapshot
The Arabidopsis CDPK-SnRK Superfamily of Protein Kinases
inferredcites →https://doi.org/10.1104/pp.103.020008openalex-snapshot
Subcellular Targeting of Nine Calcium-Dependent Protein Kinase Isoforms from Arabidopsis
inferredcites →https://doi.org/10.1104/pp.105.069757openalex-snapshot
Arabidopsis Calcium-Dependent Protein Kinase AtCPK32 Interacts with ABF4, a Transcriptional Regulator of Abscisic Acid-Responsive Gene Expression, and Modulates Its Activity
inferredcites →https://doi.org/10.1105/tpc.106.049585openalex-snapshot
The PP2C-Type Phosphatase AP2C1, Which Negatively Regulates MPK4 and MPK6, Modulates Innate Immunity, Jasmonic Acid, and Ethylene Levels in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.050039openalex-snapshot
The Arabidopsis Mitogen-Activated Protein Kinase Kinase MKK3 Is Upstream of Group C Mitogen-Activated Protein Kinases and Participates in Pathogen Signaling
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.107.054296openalex-snapshot
Antagonistic Interaction between Systemic Acquired Resistance and the Abscisic Acid–Mediated Abiotic Stress Response in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.058123openalex-snapshot
Dual Fatty Acyl Modification Determines the Localization and Plasma Membrane Targeting of CBL/CIPK Ca2+ Signaling Complexes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.072686openalex-snapshot
Calcium Signals: The Lead Currency of Plant Information Processing
inferredcites →https://doi.org/10.1105/tpc.12.9.1667openalex-snapshot
SOS3 Function in Plant Salt Tolerance Requires N-Myristoylation and Calcium Binding
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02888.xopenalex-snapshot
The Arabidopsis MAP kinase kinase MKK1 participates in defence responses to the bacterial elicitor flagellin
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03404.xopenalex-snapshot
MAPK phosphorylation‐induced stabilization of ACS6 protein is mediated by the non‐catalytic C‐terminal domain, which also contains the cis‐determinant for rapid degradation by the 26S proteasome pathway
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03783.xopenalex-snapshot
Crosstalk between biotic and abiotic stress responses in tomato is mediated by the AIM1 transcription factor
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04046.xopenalex-snapshot
Arabidopsis MPK6 is involved in cell division plane control during early root development, and localizes to the pre-prophase band, phragmoplast, trans-Golgi network and plasma membrane
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04124.xopenalex-snapshot
Research on plant abiotic stress responses in the post‐genome era: past, present and future
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04255.xopenalex-snapshot
AtCPK1 calcium-dependent protein kinase mediates pathogen resistance in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04257.xopenalex-snapshot
The Ca2+-dependent protein kinase CPK3 is required for MAPK-independent salt-stress acclimation in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04316.xopenalex-snapshot
Turnover of LeACS2, a wound-inducible 1-aminocyclopropane-1-carboxylic acid synthase in tomato, is regulated by phosphorylation/dephosphorylation
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.55.031903.141627openalex-snapshot
DECODING Ca 2+ SIGNALS THROUGH PLANT PROTEIN KINASES
inferredcites →https://doi.org/10.1146/annurev.bi.57.070188.000441openalex-snapshot
THE BIOLOGY AND ENZYMOLOGY OF EUKARYOTIC PROTEIN ACYLATION
inferredcites →https://doi.org/10.1186/1471-2229-10-97openalex-snapshot
Regulation of Arabidopsis defense responses against Spodoptera littoralisby CPK-mediated calcium 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/10.4161/cc.7.23.7176openalex-snapshot
Experimental testing of predicted myristoylation targets involved in asymmetric cell division and calcium-dependent signalling

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.4765684openalex-extracted
Tacdpk1-5a, a Calcium-Dependent Protein Kinase Gene in T. Aestivum, Positively Regulate Drought Response Through Modulating Distinct Osmotic Stress Responsive-Associated Processes
inferred← citeshttps://doi.org/10.2139/ssrn.4854563openalex-extracted
Interaction of Biochar and Rhizobacterium Leclercia Adecarboxylata Alleviates Cadmium Toxicity in Glycine Max L Via Modulating Metal Flux and Metabolic Pathways
inferred← citeshttps://doi.org/10.1002/9781118889022.ch20openalex-snapshot
Redox Regulatory Networks in Response to Biotic Stress in Plants: A New Insight Through Chickpea‐ Fusarium Interplay
inferred← citeshttps://doi.org/10.1002/9781119541578.ch13openalex-snapshot
Casein Kinase2 and Its Dynamism in Abiotic Stress Management
inferred← citeshttps://doi.org/10.1002/9781119541578.ch7openalex-snapshot
Lipid Mediated Regulation of Protein Kinases
inferred← citeshttps://doi.org/10.1002/9783527675265.ch07openalex-snapshot
Current Concepts about Salinity and Salinity Tolerance in Plants
inferred← citeshttps://doi.org/10.1002/9783527694570.ch1openalex-snapshot
Abiotic Stress Signaling in Plants–An Overview
inferred← citeshttps://doi.org/10.1002/9783527694570.ch14openalex-snapshot
Brassinosteroids: Physiology and Stress Management in Plants
inferred← citeshttps://doi.org/10.1002/9783527694570.ch9openalex-snapshot
Role of Calcium‐Dependent Protein Kinases during Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.1002/csc2.70193openalex-snapshot
Proteomic insights on root and tuber crops’ response to abiotic stress—A review
inferred← citeshttps://doi.org/10.1002/jcb.25121openalex-snapshot
bZIP17 and bZIP60 Regulate the Expression of BiP3 and Other Salt Stress Responsive Genes in an UPR‐Independent Manner in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1002/jcb.26882openalex-snapshot
bZIP17 regulates the expression of genes related to seed storage and germination, reducing seed susceptibility to osmotic stress
inferred← citeshttps://doi.org/10.1007/978-1-4614-0815-4_14openalex-snapshot
Plant Signaling Under Abiotic Stress Environment
inferred← citeshttps://doi.org/10.1007/978-1-4614-6108-1_7openalex-snapshot
Salt Stress and MAPK Signaling in Plants
inferred← citeshttps://doi.org/10.1007/978-3-031-12990-2_9openalex-snapshot
The Role of Transcription Factors in Response to Biotic Stresses in Maize
inferred← citeshttps://doi.org/10.1007/978-3-031-59024-5_1openalex-snapshot
An Overview of Metal and Metalloid Toxicity and Signaling in Plants
inferred← citeshttps://doi.org/10.1007/978-3-032-01704-8_1openalex-snapshot
Unveiling Abiotic Stress Sensing and Regulatory Pathways for Enhanced Crop Resilience
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Advances in Breeding for Resistance to Insects
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Mammalian Neurotransmitter Are Important Signals Mediating Plant Morphogenesis
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Approach Towards Sustainable Crop Production by Utilizing Potential Microbiome
inferred← citeshttps://doi.org/10.1007/978-981-97-0672-3_2openalex-snapshot
Plant Response and Tolerance to Environmental Stresses
inferred← citeshttps://doi.org/10.1007/978-981-99-3334-1_9openalex-snapshot
Plant Phenolics Role in Bacterial Disease Stress Management in Plants
inferred← citeshttps://doi.org/10.1007/978-981-99-4370-8_10openalex-snapshot
Effect of Environmental Factors on Essential Oil Biosynthesis, Chemical Stability, and Yields
inferred← citeshttps://doi.org/10.1007/s00299-011-1130-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00299-013-1452-zopenalex-snapshot
Protein SUMOylation and plant abiotic stress signaling: in silico case study of rice RLKs, heat-shock and Ca2+-binding proteins
inferred← citeshttps://doi.org/10.1007/s00299-023-03019-4openalex-snapshot
A methane–cGMP module positively influences adventitious rooting
inferred← citeshttps://doi.org/10.1007/s00299-024-03344-2openalex-snapshot
TaCDPK1-5A positively regulates drought response through modulating osmotic stress responsive-associated processes in wheat (Triticum aestivum)
inferred← citeshttps://doi.org/10.1007/s00424-013-1390-1openalex-snapshot
Mechanism and synergism in epithelial fluid and electrolyte secretion
inferred← citeshttps://doi.org/10.1007/s00425-012-1732-9openalex-snapshot
The novel Solanum tuberosum calcium dependent protein kinase, StCDPK3, is expressed in actively growing organs
inferred← citeshttps://doi.org/10.1007/s10059-012-2299-9openalex-snapshot
Plant Stress Surveillance Monitored by ABA and Disease Signaling Interactions
inferred← citeshttps://doi.org/10.1007/s10535-016-0683-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10565-016-9345-xopenalex-snapshot
Differential effects of calcium on PI3K-Akt and HIF-1α survival pathways
inferred← citeshttps://doi.org/10.1007/s11105-012-0496-5openalex-snapshot
Characterization of the ZmCK1 Gene Encoding a Calcium-Dependent Protein Kinase Responsive to Multiple Abiotic Stresses in Maize
inferred← citeshttps://doi.org/10.1007/s11105-012-0513-8openalex-snapshot
Isolation and Characterization of a Calcium-Dependent Protein Kinase Gene, FvCDPK1, Responsive to Abiotic Stress in Woodland Strawberry (Fragaria vesca)
inferred← citeshttps://doi.org/10.1007/s11105-015-0897-3openalex-snapshot
Enhanced Tolerance to Chilling Stress in Tomato by Overexpression of a Mitogen-Activated Protein Kinase, SlMPK7
inferred← citeshttps://doi.org/10.1007/s11240-017-1320-6openalex-snapshot
Potential use of the DREB/ERF, MYB, NAC and WRKY transcription factors to improve abiotic and biotic stress in transgenic plants
inferred← citeshttps://doi.org/10.1007/s12033-012-9538-3openalex-snapshot
Bioengineering for Salinity Tolerance in Plants: State of the Art
inferred← citeshttps://doi.org/10.1007/s12042-015-9155-yopenalex-snapshot
RNA-Seq Transcriptome Analysis in Date Palm Suggests Multi-Dimensional Responses to Salinity Stress
inferred← citeshttps://doi.org/10.1007/s12892-025-00319-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13205-026-05008-2openalex-snapshot
Evolutionary analysis, structural characterization, and cultivar- and tissue-specific expression profiling of the CDPK gene family in turmeric (Curcuma longa L.)
inferred← citeshttps://doi.org/10.1007/s40362-014-0025-zopenalex-snapshot
The Role of Calmodulin and Related Proteins in Plant Cell Function: An Ever-Thickening Plot
inferred← citeshttps://doi.org/10.1007/s40502-026-01018-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s44154-021-00004-3openalex-snapshot
Regulation of biotic interactions and responses to abiotic stresses by MAP kinase pathways in plant pathogenic fungi
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Priming of plant’s immune system: the future sustainable approach for tea improvement
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inferred← citeshttps://doi.org/10.1016/b978-0-12-816451-8.00031-9openalex-snapshot
Heat Shock Proteins (Hsps) Mediated Signalling Pathways During Abiotic Stress Conditions
inferred← citeshttps://doi.org/10.1016/b978-0-12-819786-8.00013-xopenalex-snapshot
Carbon nanostructures: detection, controlling plant diseases and mycotoxins
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Plant response to heavy metal stress: an insight into the molecular mechanism of transcriptional regulation
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Exploring the role of beneficial elements in enhancing the resistance of plants to biotic stress
inferred← citeshttps://doi.org/10.1016/j.aquatox.2016.06.017openalex-snapshot
Copper-induced overexpression of genes encoding antioxidant system enzymes and metallothioneins involve the activation of CaMs, CDPKs and MEK1/2 in the marine alga Ulva compressa
inferred← citeshttps://doi.org/10.1016/j.bbapap.2014.11.006openalex-snapshot
Oxidation and phosphorylation of MAP kinase 4 cause protein aggregation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.151170openalex-snapshot
Soybean mitogen-activated protein kinase GmMPK6 enhances drought tolerance
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Role of copper in the enhancement of astaxanthin and lipid coaccumulation in Haematococcus pluvialis exposed to abiotic stress conditions
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Cross-regulation of cytoskeleton and calcium signaling at plant-pathogen interface
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Rice-Magnaporthe oryzae arms race: From effector diversification and NLR-mediated immunity to CRISPR-driven durable resistance
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Comparative transcriptomics reveals osmotic and ionic stress key genes contributing to the difference in the salinity tolerance of two pak choi cultivars
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Physiological and transcriptomic analyses reveal the effect of exogenous chitosan oligosaccharides on ‘Harumi’ fruit resistance to Penicillium digitatum
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Genome-wide identification of the calcium-dependent kinase CPK gene family in Salvia miltiorrhiza reveals that SmCPK24 promotes tanshinone biosynthesis
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Phosphoproteomics revealed salt stress tolerance mechanisms in the roots of sugar beet monomeric addition line M14
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Diltiazem disrupts Ca2+-homeostasis and exerts immunotoxic effects on a marine bivalve mollusc, the blood clam (Tegillarca granosa)
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High-quality assembled and annotated genomes of Nicotiana tabacum and Nicotiana benthamiana reveal chromosome evolution and changes in defense arsenals
inferred← citeshttps://doi.org/10.1016/j.plantsci.2013.09.014openalex-snapshot
ZmMKK1, a novel group A mitogen-activated protein kinase kinase gene in maize, conferred chilling stress tolerance and was involved in pathogen defense in transgenic tobacco
inferred← citeshttps://doi.org/10.1016/j.plantsci.2014.10.002openalex-snapshot
To grow or not to grow: A stressful decision for plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2017.06.005openalex-snapshot
Molecular and biochemical characterization of a Vigna mungo MAP kinase associated with Mungbean Yellow Mosaic India Virus infection and deciphering its role in restricting the virus multiplication
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113207openalex-snapshot
Calcium-dependent protein kinases play a key role in plant defense against pathogens and pests
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Integrated role of biochar and PGPR (Leclercia adecarboxylata HW04) in enhancing cadmium phytoremediation and stress tolerance in Glycine max L
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Postharvest Fumigation of (E)-2-Hexenal on Kiwifruit (Actinidia chinensis cv. ‘Haegeum’) Enhances Resistance to Botrytis cinerea
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Ethyl-Nα-lauroyl-L-arginate hydrochloride treatment inhibited the in vitro growth of Penicillium expansum and enhanced disease resistance in pear fruit
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The effect of arbuscular mycorrhizal fungus application on genes related to plant-pathogen interaction in different tissues of chickpea under alkali stress
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Melatonin in plants: A pleiotropic molecule for abiotic stresses and pathogens infection
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Life cycle and reproduction dynamics of Bangiales in response to environmental stresses
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Transcriptomic and Metabolic Analyses Provide New Insights into the Apple Fruit Quality Decline during Long-Term Cold Storage
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Identification and Validation of Inhibitor-Responsive Kinase Substrates Using a New Paradigm To Measure Kinase-Specific Protein Phosphorylation Index
inferred← citeshttps://doi.org/10.1038/s41598-025-10051-9openalex-snapshot
Proteomic analysis reveals dynamic expression related to malondialdehyde in cassava in response to cassava bacterial blight
inferred← citeshttps://doi.org/10.1038/s42003-025-09024-5openalex-snapshot
Reactive oxygen species-producing genes regulate mosquito midgut bacteria colonization, transcriptomic changes and cell repair
inferred← citeshttps://doi.org/10.1073/pnas.1814006115openalex-snapshot
Quantitative and functional posttranslational modification proteomics reveals that TREPH1 plays a role in plant touch-delayed bolting
inferred← citeshttps://doi.org/10.1080/15592324.2017.1388974openalex-snapshot
MAP kinases nomenclature: Time for curation
inferred← citeshttps://doi.org/10.1080/17429145.2011.640438openalex-snapshot
The new understanding ofArabidopsis thalianaproteins associated with salinity
inferred← citeshttps://doi.org/10.1089/omi.2011.0091openalex-snapshot
SnRK2 Protein Kinases—Key Regulators of Plant Response to Abiotic Stresses
inferred← citeshttps://doi.org/10.1093/jxb/erae033openalex-snapshot
Multiomics analyses reveal the central role of the nucleolus and its machinery during heat stress acclimation in Pinus radiata
inferred← citeshttps://doi.org/10.1093/jxb/err394openalex-snapshot
Plant organellar calcium signalling: an emerging field
inferred← citeshttps://doi.org/10.1093/jxb/ers366openalex-snapshot
ZmCPK11 is involved in abscisic acid-induced antioxidant defence and functions upstream of ZmMPK5 in abscisic acid signalling in maize
inferred← citeshttps://doi.org/10.1093/mp/sss158openalex-snapshot
Salt Stress Triggers Phosphorylation of the Arabidopsis Vacuolar K+ Channel TPK1 by Calcium-Dependent Protein Kinases (CDPKs)
inferred← citeshttps://doi.org/10.1093/pcp/pcaa084openalex-snapshot
Dissecting MicroRNA–mRNA Regulatory Networks Underlying Sulfur Assimilation and Cadmium Accumulation in Poplar Leaves
inferred← citeshttps://doi.org/10.1093/plphys/kiac587openalex-snapshot
Kinase MxMPK4-1 and calmodulin-binding protein MxIQM3 enhance apple root acidification during Fe deficiency
inferred← citeshttps://doi.org/10.1094/mpmi-09-18-0267-fiopenalex-snapshot
Regulation of Plant Immune Signaling by Calcium-Dependent Protein Kinases
inferred← citeshttps://doi.org/10.1105/tpc.113.111393openalex-snapshot
Golgi Traffic and Integrity Depend on N-Myristoyl Transferase-1 in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.114.126441openalex-snapshot
Direct Phosphorylation and Activation of a Mitogen-Activated Protein Kinase by a Calcium-Dependent Protein Kinase in Rice
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2012.04226.xopenalex-snapshot
StCDPK5 confers resistance to late blight pathogen but increases susceptibility to early blight pathogen in potato via reactive oxygen species burst
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2012.04239.xopenalex-snapshot
Low‐temperature perception leading to gene expression and cold tolerance in higher plants
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2012.04293.xopenalex-snapshot
Shaping the pathogen response by protein kinase triggered oxidative burst
inferred← citeshttps://doi.org/10.1111/jph.12066openalex-snapshot
Transcriptome Analysis of a Progeny of Somatic Hybrids of Cultivated Rice ( O ryza sativa L .) and Wild Rice ( O ryza meyeriana L .) With High Resistance to Bacterial Blight
inferred← citeshttps://doi.org/10.1111/mec.13566openalex-snapshot
Transcriptomic profiling of Alexandrium fundyense during physical interaction with or exposure to chemical signals from the parasite Amoebophrya
inferred← citeshttps://doi.org/10.1111/mec.16476openalex-snapshot
Pathogen exposure leads to a transcriptional downregulation of core cellular functions that may dampen the immune response in a macroalga
inferred← citeshttps://doi.org/10.1111/nph.19339openalex-snapshot
REVEILLE2 thermosensitive splicing: a molecular basis for the integration of nocturnal temperature information by the Arabidopsis circadian clock
inferred← citeshttps://doi.org/10.1111/pce.12414openalex-snapshot
ZmCPK 1, a calcium‐independent kinase member of the Z ea mays CDPK gene family, functions as a negative regulator in cold stress signalling
inferred← citeshttps://doi.org/10.1111/ppl.12579openalex-snapshot
A secreted chitinase‐like protein ( OsCLP ) supports root growth through calcium signaling inOryza sativa
inferred← citeshttps://doi.org/10.1111/ppl.12585openalex-snapshot
An osmotin from the resurrection plant Tripogon loliiformis ( TlOsm ) confers tolerance to multiple abiotic stresses in transgenic rice
inferred← citeshttps://doi.org/10.1111/ppl.12667openalex-snapshot
Prominent alterations of wild barley leaf transcriptome in response to individual and combined drought acclimation and heat shock conditions
inferred← citeshttps://doi.org/10.1134/s1021443726603095openalex-snapshot
Cold Shock Protein (EpCSP) from Exiguobacterium profundum Confers Enhanced Stress Tolerance to Drought and Cold in a Heterologous System
inferred← citeshttps://doi.org/10.1139/cjfr-2016-0356openalex-snapshot
Thigmomorphogenesis: changes in morphology, biochemistry, and levels of transcription in response to mechanical stress in Acacia koa
inferred← citeshttps://doi.org/10.11606/t.11.2021.tde-30112021-190722openalex-snapshot
O papel das nanopartículas de silício na mitigação do efeito da salinidade sobre a eletrofisiologia e na atividade fotossintética em plantas glicófitas e não acumuladora de silício
inferred← citeshttps://doi.org/10.1186/1471-2156-15-s1-s7openalex-snapshot
Transcriptome sequencing of transgenic poplar (Populus × euramericana 'Guariento') expressing multiple resistance genes
inferred← citeshttps://doi.org/10.1186/1471-2164-14-760openalex-snapshot
Differential expression of CPKs and cytosolic Ca2+ variation in resistant and susceptible apple cultivars (Malus x domestica) in response to the pathogen Erwinia amylovora and mechanical wounding
inferred← citeshttps://doi.org/10.1186/s12864-018-4830-7openalex-snapshot
Genome-wide transcriptome analysis and identification of benzothiadiazole-induced genes and pathways potentially associated with defense response in banana
inferred← citeshttps://doi.org/10.1186/s12864-020-6475-6openalex-snapshot
Genome-wide survey and expression analysis of calcium-dependent protein kinase (CDPK) in grass Brachypodium distachyon
inferred← citeshttps://doi.org/10.1186/s12870-016-0803-7openalex-snapshot
Salinity stress induces the production of 2-(2-phenylethyl)chromones and regulates novel classes of responsive genes involved in signal transduction in Aquilaria sinensis calli
inferred← citeshttps://doi.org/10.1186/s12870-019-1630-4openalex-snapshot
Full-length transcript sequencing and comparative transcriptomic analysis to evaluate the contribution of osmotic and ionic stress components towards salinity tolerance in the roots of cultivated alfalfa (Medicago sativa L.)
inferred← citeshttps://doi.org/10.1186/s12870-025-06402-3openalex-snapshot
Glycolysis and signal transduction participate in Lycium barbarum in response to NaCl stress through protein phosphorylation
inferred← citeshttps://doi.org/10.1371/journal.pone.0028565openalex-snapshot
Differential Expression of miRNAs in Response to Topping in Flue-Cured Tobacco (Nicotiana tabacum) Roots
inferred← citeshttps://doi.org/10.1371/journal.pone.0076392openalex-snapshot
CDPK1 from Ginger Promotes Salinity and Drought Stress Tolerance without Yield Penalty by Improving Growth and Photosynthesis in Nicotiana tabacum
inferred← citeshttps://doi.org/10.1371/journal.pone.0112269openalex-snapshot
Cloning of Gossypium hirsutum Sucrose Non-Fermenting 1-Related Protein Kinase 2 Gene (GhSnRK2) and Its Overexpression in Transgenic Arabidopsis Escalates Drought and Low Temperature Tolerance
inferred← citeshttps://doi.org/10.1631/jzus.b1900400openalex-snapshot
Salinity tolerance in barley during germination—homologs and potential genes
inferred← citeshttps://doi.org/10.18006/2023.11(1).41.53openalex-snapshot
Plant RNA-binding proteins as key players in abiotic stress physiology
inferred← citeshttps://doi.org/10.21203/rs.3.rs-243772/v1openalex-snapshot
Comparative Transcriptomics Reveals Osmotic and Ionic Stress Key Genes Contributing To Salinity Tolerance Differential in Two Pak Choi Cultivars
inferred← citeshttps://doi.org/10.2174/1389202918666170228141345openalex-snapshot
An Overview of Signaling Regulons During Cold Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.2174/1875036201811010012openalex-snapshot
Investigation of Drought and Salinity Tolerance Related Genes and their Regulatory Mechanisms in Arabidopsis (Arabidopsis thaliana)
inferred← citeshttps://doi.org/10.2174/1875036202013010039openalex-snapshot
Meta-Analysis of Expression of the Stress Tolerance Associated Genes and Uncover their Cis-Regulatory Elements in Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.30901/2658-6266-2023-4-o6openalex-snapshot
Evaluation of the GhMAPK gene expression level under salt stress in cotton cultivars
inferred← citeshttps://doi.org/10.3109/07388551.2012.672398openalex-snapshot
Ca2+signals: The versatile decoders of environmental cues
inferred← citeshttps://doi.org/10.3389/fpls.2012.00169openalex-snapshot
MAP Kinase Cascades in Arabidopsis Innate Immunity
inferred← citeshttps://doi.org/10.3389/fpls.2014.00178openalex-snapshot
The role of the cell wall in plant immunity
inferred← citeshttps://doi.org/10.3389/fpls.2014.00267openalex-snapshot
Phosphoinositide-signaling is one component of a robust plant defense response
inferred← citeshttps://doi.org/10.3389/fpls.2015.00420openalex-snapshot
Hydrogen peroxide priming modulates abiotic oxidative stress tolerance: insights from ROS detoxification and scavenging
inferred← citeshttps://doi.org/10.3389/fpls.2015.00737openalex-snapshot
Genome-wide identification and expression analysis of calcium-dependent protein kinase and its closely related kinase genes in Capsicum annuum
inferred← citeshttps://doi.org/10.3389/fpls.2017.02021openalex-snapshot
Transcript Profiling Identifies Gene Cohorts Controlled by Each Signal Regulating Trans-Differentiation of Epidermal Cells of Vicia faba Cotyledons to a Transfer Cell Phenotype
inferred← citeshttps://doi.org/10.3389/fpls.2018.00012openalex-snapshot
Traversing the Links between Heavy Metal Stress and Plant Signaling
inferred← citeshttps://doi.org/10.3389/fpls.2023.1138252openalex-snapshot
The captivating role of calcium in plant-microbe interaction
inferred← citeshttps://doi.org/10.3389/fpls.2024.1334996openalex-snapshot
Phenylpropane biosynthesis and alkaloid metabolism pathways involved in resistance of Amorphophallus spp. against soft rot disease
inferred← citeshttps://doi.org/10.3389/fpls.2025.1567412openalex-snapshot
Transcriptomic changes in donor soybean, dodder bridge, and the connected recipient soybean induced by cadmium addition
inferred← citeshttps://doi.org/10.3390/biochem6030027openalex-snapshot
STN7/STN8-Mediated Thylakoid Protein Phosphorylation: From Redox Signaling to Photosynthetic Acclimation Under Abiotic Stress
inferred← citeshttps://doi.org/10.3390/cimb48050474openalex-snapshot
Molecular Mechanisms of Plant Stress Tolerance: From Stress Perception to Phytohormonal Crosstalk and Transcriptional Regulation
inferred← citeshttps://doi.org/10.3390/genes14020293openalex-snapshot
Candidate Genes for Salt Tolerance in Forage Sorghum under Saline Conditions from Germination to Harvest Maturity
inferred← citeshttps://doi.org/10.3390/ijms20246173openalex-snapshot
Expression, Subcellular Localization, and Interactions of CPK Family Genes in Maize
inferred← citeshttps://doi.org/10.3390/ijms221910495openalex-snapshot
A Method for Assaying of Protein Kinase Activity In Vivo and Its Use in Studies of Signal Transduction in Strawberry Fruit Ripening
inferred← citeshttps://doi.org/10.3390/jdb9040047openalex-snapshot
The Organizer and Its Signaling in Embryonic Development
inferred← citeshttps://doi.org/10.3390/molecules26247610openalex-snapshot
AaTs-1: A Tetrapeptide from Androctonus australis Scorpion Venom, Inhibiting U87 Glioblastoma Cells Proliferation by p53 and FPRL-1 Up-Regulations
inferred← citeshttps://doi.org/10.3390/plants10081694openalex-snapshot
LEA13 and LEA30 Are Involved in Tolerance to Water Stress and Stomata Density in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/plants11223060openalex-snapshot
ZmDREB2.9 Gene in Maize (Zea mays L.): Genome-Wide Identification, Characterization, Expression, and Stress Response
inferred← citeshttps://doi.org/10.3390/plants15040555openalex-snapshot
Integrated Multi-Omics Analysis Revealed the Synergistic Regulatory Mechanisms of Salt Tolerance in Soybean (Kefeng 1)
inferred← citeshttps://doi.org/10.3390/plants3010160openalex-snapshot
Functions of Calcium-Dependent Protein Kinases in Plant Innate Immunity
inferred← citeshttps://doi.org/10.3390/plants3040458openalex-snapshot
Plant Responses to Simultaneous Biotic and Abiotic Stress: Molecular Mechanisms
inferred← citeshttps://doi.org/10.3892/mmr.2016.4862openalex-snapshot
The MAPK pathway is involved in the regulation of rapid pacing-induced ionic channel remodeling in rat atrial myocytes
inferred← citeshttps://doi.org/10.56739/jor.v35i1.137345openalex-snapshot
Versatile roles of ubiquitous calcium-dependent protein kinases (CDPKs) in plants
inferred← citeshttps://doi.org/10.5772/55865openalex-snapshot
Abiotic Stress in Plants
inferred← citeshttps://doi.org/10.64898/2026.01.27.701911openalex-snapshot
GCN5 restricts PRX-dependent lignin deposition during salt stress in Arabidopsis
inferred← citeshttps://doi.org/10.70675/069afadezcd0az4404zbb42z0159cebb1df6openalex-snapshot
Conception, synthèse et purification d’analogues de molécules de venin animal à action inhibitrice des cellules
inferred← citeshttps://doi.org/10.70675/6d4013bez90c4z4ac0z841azbd16ae72aa2fopenalex-snapshot
Implication de la paroi végétale et plus particulièrement des enzymes de modification des pectines dans la tolérance au stress salin chez Arabidopsis
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.7211openalex-snapshot
Transcription factors involved in abiotic stress responses in Maize ( Zea mays L.) and their roles in enhanced productivity in the post genomics era
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.