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Arabidopsis MAPKs: a complex signalling network involved in multiple biological processes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/bbrc.1998.9796openalex-snapshot
Isolation of ATMEKK1 (a MAP Kinase Kinase Kinase)-Interacting Proteins and Analysis of a MAP Kinase Cascade inArabidopsis
inferredcites →https://doi.org/10.1007/s004250050658openalex-snapshot
Harpin induces mitogen-activated protein kinase activity during defence responses in Arabidopsis thaliana suspension cultures
inferredcites →https://doi.org/10.1016/0092-8674(93)90119-bopenalex-snapshot
CTR1, a negative regulator of the ethylene response pathway in arabidopsis, encodes a member of the Raf family of protein kinases
inferredcites →https://doi.org/10.1016/j.bbapap.2007.07.002openalex-snapshot
Phosphorylation sites of Arabidopsis MAP kinase substrate 1 (MKS1)
inferredcites →https://doi.org/10.1016/j.cell.2006.02.047openalex-snapshot
Specific Bacterial Suppressors of MAMP Signaling Upstream of MAPKKK in Arabidopsis Innate Immunity
inferredcites →https://doi.org/10.1016/j.cell.2006.03.037openalex-snapshot
Perception of the Bacterial PAMP EF-Tu by the Receptor EFR Restricts Agrobacterium-Mediated Transformation
inferredcites →https://doi.org/10.1016/j.chom.2007.03.006openalex-snapshot
A Pseudomonas syringae Effector Inactivates MAPKs to Suppress PAMP-Induced Immunity in Plants
inferredcites →https://doi.org/10.1016/j.chom.2007.04.008openalex-snapshot
Intercepting Host MAPK Signaling Cascades by Bacterial Type III Effectors
inferredcites →https://doi.org/10.1016/j.envpol.2005.04.017openalex-snapshot
RNA interference-based (RNAi) suppression of AtMPK6, an Arabidopsis mitogen-activated protein kinase, results in hypersensitivity to ozone and misregulation of AtMPK3
inferredcites →https://doi.org/10.1016/j.febslet.2004.08.001openalex-snapshot
Involvement of MPK4 in osmotic stress response pathways in cell suspensions and plantlets of Arabidopsis thaliana: activation by hypoosmolarity and negative role in hyperosmolarity tolerance
inferredcites →https://doi.org/10.1016/j.febslet.2007.03.075openalex-snapshot
Diverse stress signals activate the C1 subgroup MAP kinases of Arabidopsis
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.plantsci.2006.06.009openalex-snapshot
Antagonistic interaction between MAP kinase and protein phosphatase 2C in stress recovery
inferredcites →https://doi.org/10.1016/j.tplants.2004.01.005openalex-snapshot
Reassessing the MAP3K and MAP4K relationships
inferredcites →https://doi.org/10.1016/s0014-5793(00)01565-9openalex-snapshot
The effect of ethylene on MAPKinase‐like activity in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0014-5793(02)03162-9openalex-snapshot
Different protein kinase families are activated by osmotic stresses in Arabidopsis thaliana cell suspensions
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/s0092-8674(00)80300-1openalex-snapshot
Activation of the Ethylene Gas Response Pathway in Arabidopsis by the Nuclear Protein ETHYLENE-INSENSITIVE3 and Related Proteins
inferredcites →https://doi.org/10.1016/s0092-8674(03)01067-5openalex-snapshot
A MAPKK Kinase Gene Regulates Extra-Embryonic Cell Fate in Arabidopsis
inferredcites →https://doi.org/10.1016/s1360-1385(02)02302-6openalex-snapshot
Mitogen-activated protein kinase cascades in plants: a new nomenclature
inferredcites →https://doi.org/10.1016/s1360-1385(03)00135-3openalex-snapshot
Reactive oxygen species and hormonal control of cell death
inferredcites →https://doi.org/10.1038/27240openalex-snapshot
Suppression of auxin signal transduction by a MAPK cascade in higher plants
inferredcites →https://doi.org/10.1038/35048692openalex-snapshot
Analysis of the genome sequence of the flowering plant Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/415977aopenalex-snapshot
MAP kinase signalling cascade in Arabidopsis innate immunity
inferredcites →https://doi.org/10.1038/cr.2008.29openalex-snapshot
Ethylene signaling is required for the acceleration of cell death induced by the activation of AtMEK5 in Arabidopsis
inferredcites →https://doi.org/10.1038/nature02353openalex-snapshot
OXI1 kinase is necessary for oxidative burst-mediated signalling in Arabidopsis
inferredcites →https://doi.org/10.1038/nature02485openalex-snapshot
Bacterial disease resistance in Arabidopsis through flagellin perception
inferredcites →https://doi.org/10.1038/nature03895openalex-snapshot
The map-based sequence of the rice genome
inferredcites →https://doi.org/10.1038/nature05999openalex-snapshot
A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence
inferredcites →https://doi.org/10.1038/nature06543openalex-snapshot
Dual control of nuclear EIN3 by bifurcate MAPK cascades in C2H4 signalling
inferredcites →https://doi.org/10.1038/sj.emboj.7600737openalex-snapshot
The MAP kinase substrate MKS1 is a regulator of plant defense responses
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.5010111.xopenalex-snapshot
Characterization of two cDNAs that encode MAP kinase homologues in Arabidopsis thaliana and analysis of the possible role of auxin in activating such kinase activities in cultured cells
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00265.xopenalex-snapshot
Plants have a sensitive perception system for the most conserved domain of bacterial flagellin
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00451.xopenalex-snapshot
A single locus determines sensitivity to bacterial flagellin in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00921.xopenalex-snapshot
Auxin induces mitogenic activated protein kinase (MAPK) activation in roots of Arabidopsis seedlings
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01065.xopenalex-snapshot
The protein kinases AtMAP3Kε1 and BnMAP3Kε1 are functional homologues of S. pombe cdc7p and may be involved in cell division
inferredcites →https://doi.org/10.1073/pnas.0705147104openalex-snapshot
CERK1, a LysM receptor kinase, is essential for chitin elicitor signaling in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0705306104openalex-snapshot
The receptor-like kinase SERK3/BAK1 is a central regulator of innate immunity in plants
inferredcites →https://doi.org/10.1073/pnas.252641899openalex-snapshot
NDP kinase 2 interacts with two oxidative stress-activated MAPKs to regulate cellular redox state and enhances multiple stress tolerance in transgenic plants
inferredcites →https://doi.org/10.1073/pnas.95.9.5401openalex-snapshot
Association of the Arabidopsis CTR1 Raf-like kinase with the ETR1 and ERS ethylene receptors
inferredcites →https://doi.org/10.1073/pnas.97.6.2940openalex-snapshot
Functional analysis of oxidative stress-activated mitogen-activated protein kinase cascade 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.m208200200openalex-snapshot
Mitogen-activated Protein Kinases Play an Essential Role in Oxidative Burst-independent Expression of Pathogenesis-related Genes in Parsley
inferredcites →https://doi.org/10.1074/jbc.m605293200openalex-snapshot
A Mitogen-activated Protein Kinase Kinase Kinase Mediates Reactive Oxygen Species Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m605319200openalex-snapshot
MEKK1 Is Required for MPK4 Activation and Regulates Tissue-specific and Temperature-dependent Cell Death in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m701888200openalex-snapshot
Arabidopsis MAPK Phosphatase 2 (MKP2) Positively Regulates Oxidative Stress Tolerance and Inactivates the MPK3 and MPK6 MAPKs
inferredcites →https://doi.org/10.1074/mcp.m500007-mcp200openalex-snapshot
High Throughput Identification of Potential Arabidopsis Mitogen-activated Protein Kinases Substrates
inferredcites →https://doi.org/10.1093/emboj/cdg131openalex-snapshot
A MAPK pathway mediates ethylene signaling in plants
inferredcites →https://doi.org/10.1093/jexbot/51.343.197openalex-snapshot
ABA activation of an MBP kinase in Pisum sativum epidermal peels correlates with stomatal responses to ABA
inferredcites →https://doi.org/10.1093/jxb/erm092openalex-snapshot
Mutational evidence that the Arabidopsis MAP kinase MPK6 is involved in anther, inflorescence, and embryo development
inferredcites →https://doi.org/10.1093/jxb/erm144openalex-snapshot
AtMEK1 mediates stress-induced gene expression of CAT1 catalase by triggering H2O2 production in Arabidopsis
inferredcites →https://doi.org/10.1094/mpmi-20-5-0589openalex-snapshot
The MAP Kinase Kinase MKK2 Affects Disease Resistance inArabidopsis
inferredcites →https://doi.org/10.1101/gad.12.23.3703openalex-snapshot
Nuclear events in ethylene signaling: a transcriptional cascade mediated by ETHYLENE-INSENSITIVE3 and ETHYLENE-RESPONSE-FACTOR1
inferredcites →https://doi.org/10.1104/pp.106.091389openalex-snapshot
MEKK1 Is Required for flg22-Induced MPK4 Activation in Arabidopsis Plants
inferredcites →https://doi.org/10.1104/pp.126.4.1579openalex-snapshot
Harpin Induces Activation of the Arabidopsis Mitogen-Activated Protein Kinases AtMPK4 and AtMPK6
inferredcites →https://doi.org/10.1105/tpc.001164openalex-snapshot
An Arabidopsis Mitogen-Activated Protein Kinase Kinase Kinase Gene Family Encodes Essential Positive Regulators of Cytokinesis
inferredcites →https://doi.org/10.1105/tpc.017046openalex-snapshot
IBR5, a Dual-Specificity Phosphatase-Like Protein Modulating Auxin and Abscisic Acid Responsiveness 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.104.026765openalex-snapshot
The N Terminus of Bacterial Elongation Factor Tu Elicits Innate Immunity in Arabidopsis Plants
inferredcites →https://doi.org/10.1105/tpc.105.037846openalex-snapshot
Increased Expression of MAP KINASE KINASE7 Causes Deficiency in Polar Auxin Transport and Leads to Plant Architectural Abnormality inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.044180openalex-snapshot
Phytotoxicity and Innate Immune Responses Induced by Nep1-Like Proteins
inferredcites →https://doi.org/10.1105/tpc.106.046581openalex-snapshot
The Mitogen-Activated Protein Kinase Cascade MKK3–MPK6 Is an Important Part of the Jasmonate Signal Transduction Pathway in Arabidopsis
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.106.049585openalex-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/10.1111/j.1365-313x.2004.02229.xopenalex-snapshot
Stress hormone‐independent activation and nuclear translocation of mitogen‐activated protein kinases in Arabidopsis thaliana during ozone exposure
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02806.xopenalex-snapshot
Arabidopsis MAP kinase 4 regulates salicylic acid‐ and jasmonic acid/ethylene‐dependent responses via EDS1 and PAD4
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02823.xopenalex-snapshot
The phs1‐3 mutation in a putative dual‐specificity protein tyrosine phosphatase gene provokes hypersensitive responses to abscisic acid in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02863.xopenalex-snapshot
The protein kinase genes MAP3K ɛ 1 and MAP3K ɛ 2 are required for pollen viability in Arabidopsis thaliana
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.2007.03192.xopenalex-snapshot
Quantitative phosphoproteomic analysis of plasma membrane proteins reveals regulatory mechanisms of plant innate immune responses
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03294.xopenalex-snapshot
Overexpression of Arabidopsis MAP kinase kinase 7 leads to activation of plant basal and systemic acquired resistance
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.1469-8137.2006.01953.xopenalex-snapshot
Guard cell‐specific inhibition of Arabidopsis MPK3 expression causes abnormal stomatal responses to abscisic acid and hydrogen peroxide
inferredcites →https://doi.org/10.1126/science.1096014openalex-snapshot
Stomatal Development and Pattern Controlled by a MAPKK Kinase
inferredcites →https://doi.org/10.1126/science.1148110openalex-snapshot
Trojan Horse Strategy in Agrobacterium Transformation: Abusing MAPK Defense Signaling
inferredcites →https://doi.org/10.1126/science.276.5321.2054openalex-snapshot
Receptor-Mediated Activation of a MAP Kinase in Pathogen Defense of Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.54.031902.134743openalex-snapshot
Protein Phosphatases in Plants
inferredcites →https://doi.org/10.1146/annurev.phyto.43.040204.135923openalex-snapshot
Contrasting Mechanisms of Defense Against Biotrophic and Necrotrophic Pathogens
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.4805372openalex-extracted
The Mapk Kinase Fvhog1 Regulates Fumonisin B1 Synthesis and Ca 2+ Homeostasis in Fusarium Verticillioides
inferred← citeshttps://doi.org/10.1002/1873-3468.12929openalex-snapshot
Coevolving MAPK and PID phosphosites indicate an ancient environmental control of PIN auxin transporters in land plants
inferred← citeshttps://doi.org/10.1002/1873-3468.13242openalex-snapshot
Identification of tyrosine autophosphorylation sites of Arabidopsis MEKK 1 and their involvement in the regulation of kinase activity
inferred← citeshttps://doi.org/10.1002/1873-3468.14753openalex-snapshot
MAP kinases may mediate regulation of the cell cycle in rice by E2F2 phosphorylation
inferred← citeshttps://doi.org/10.1002/2211-5463.13619openalex-snapshot
Specificity models in MAPK cascade signaling
inferred← citeshttps://doi.org/10.1002/9781118223086.ch7openalex-snapshot
EIN2 and EIN3 in Ethylene Signalling
inferred← citeshttps://doi.org/10.1002/9781118297674.ch73openalex-snapshot
The Response of Plants toward N ‐Acyl Homoserine Lactones of Quorum‐Sensing‐Active Bacteria in the Rhizosphere
inferred← citeshttps://doi.org/10.1002/9781118889022.ch27openalex-snapshot
Transcription Factors and Hormone‐Mediated Mechanisms Regulate Stomata Development and Responses Under Abiotic Stresses: An Overview
inferred← citeshttps://doi.org/10.1002/9781118889022.ch35openalex-snapshot
Mechanisms of Hormone Signaling in Plants Under Abioticand Biotic Stresses
inferred← citeshttps://doi.org/10.1002/9781118889022.ch9openalex-snapshot
Abscisic Acid Signaling and Involvement of Mitogen Activated Protein Kinases and Calcium‐Dependent Protein Kinases During Plant Abiotic Stress
inferred← citeshttps://doi.org/10.1002/9781119075691.ch71openalex-snapshot
Physiological and Molecular Aspects of Mechanisms Involved in Plant Response to Salt Stress
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0479openalex-snapshot
EIN 2 and EIN 3 in Ethylene Signalling
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0611openalex-snapshot
Abiotic Stress Responses are Governed by Reactive Oxygen Species and Age
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.ch18openalex-snapshot
Role of MAPK Cascade in Local and Systemic Immunity of Plants
inferred← citeshttps://doi.org/10.1002/9781119541578.ch19openalex-snapshot
Role of Plant Kinases in Combined Stress
inferred← citeshttps://doi.org/10.1002/9781119541578.ch7openalex-snapshot
Lipid Mediated Regulation of Protein Kinases
inferred← citeshttps://doi.org/10.1002/9781119949138.ch1openalex-snapshot
Innate Immunity: Pattern Recognition in Plants
inferred← citeshttps://doi.org/10.1002/9781394186457.ch6openalex-snapshot
Role of Signaling Molecules in Enhancing Abiotic Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1002/9783527628964.ch4openalex-snapshot
Stress Physiology of Higher Plants: Cross‐Talk between Abiotic and Biotic Stress Signaling
inferred← citeshttps://doi.org/10.1002/9783527632930.ch21openalex-snapshot
Make Your Best – MYB Transcription Factors for Improving Abiotic Stress Tolerance in Crops
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Current Concepts about Salinity and Salinity Tolerance in Plants
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Exploring Transcriptomic Microsatellite Markers in Hydrangea petiolaris (Hydrangeaceae): A Resource for Population Genetics and Functional Genomic Insights
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Plant phosphoproteomics: An update
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Reboot the system thanks to protein post‐translational modifications and proteome diversity: How quiescent seeds restart their metabolism to prepare seedling establishment
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Protein interactome analysis of 12 mitogen‐activated protein kinase kinase kinase in rice using a yeast two‐hybrid system
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Proteomic and phosphoproteomic analyses of chromatin‐associated proteins from Arabidopsis thaliana
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Genome‐wide identification and expression analysis reveals the drought‐response MAPK genes in peanut ( Arachis hypogaea L.)
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Abiotic Stress Responses in Plants: Present and Future
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Salt Stress and MAPK Signaling in Plants
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Signal Transduction and Regulatory Networks in Plant-Pathogen Interaction: A Proteomics Perspective
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In-Silico Approaches for Studying the MAP Kinase Signaling Pathways Involved in Resistance Against Alternaria Blight in Brassica
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Major Phytohormones Under Abiotic Stress
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Rapid Mutagenesis-Based Analysis of Phosphorylation Sites in Mitogen-Activated Protein Kinase Substrates
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Quantitative Phosphoproteomic Analysis Using iTRAQ Method
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Analysis of MAPK Activities Using MAPK-Specific Antibodies
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Role of Mitogen-Activated Protein Kinase Cascade in Combating Abiotic Stress in Plants
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The Omics of Cold Stress Responses in Plants
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iPTMnet: Integrative Bioinformatics for Studying PTM Networks
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Interplay Between Auxin and Cytokinin and Its Impact on Mitogen Activated Protein Kinase (MAPK)
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Mitogen-Activated Protein Kinase Activity and Reporter Gene Assays in Plants
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Type 2C Protein Phosphatases in Plant Signaling Pathways under Abiotic Stress
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Plant Protein Phosphatase 2C: Critical Negative Regulator of ABA Signaling
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Dissection of Physiological and Biochemical Bases of Drought Tolerance in Soybean (Glycine max) Using Recent Phenomics Approach
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Molecular Techniques for the Improvement of Abiotic Stress Tolerance in Plants
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Decoding of Calcium Signal Through Calmodulin: Calmodulin-Binding Proteins in Plants
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Cadmium and Copper Stress Induce a Cellular Oxidative Challenge Leading to Damage Versus Signalling
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The Cell Wall-Associated Kinases, WAKs, Regulate Cell Expansion and the Stress Response
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Plant Cell Wall Signaling in the Interaction with Plant-Parasitic Nematodes
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Exploring Oxidative Stress in Plants: Proteomic and Genomic Approaches
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Stress Signaling I: The Role of Abscisic Acid (ABA)
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Salicylic Acid-Mediated Abiotic Stress Tolerance
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Protein Kinases and Phosphatases Involved in ABA Signaling
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Marine Invertebrate Stress Responses to Virus Infection
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Abiotic Stress Signaling in Wheat Crop
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Role of Signaling Pathways in Improving Salt Stress in Plants
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Infection, Pathogenesis, and Disease Cycle
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Biochemical and Molecular Mechanisms of Abiotic Stress Tolerance
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Microbial Interactions in the Rhizosphere Contributing Crop Resilience to Biotic and Abiotic Stresses
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ABA: Metabolism, Regulation, and Functions in Crop Abiotic Stress Tolerance
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Genomics of Host–Pathogen Interaction
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Biometabolomics of Crucifer’s Host-Pathosystem
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Molecular Mechanisms Underpinning Signaling Function of ROS
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Plant Stress Responses: Past, Present, and Future
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Positive and negative peptide signals control stomatal density
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The molecular mechanism of zinc and cadmium stress response in plants
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QTL x environment modeling of malting barley preharvest sprouting
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Impact of the PGPB Enterobacter radicincitans DSM 16656 on Growth, Glucosinolate Profile, and Immune Responses of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-011-1064-4openalex-snapshot
Arabidopsis MAP kinase phosphatase 1 is phosphorylated and activated by its substrate AtMPK6
inferred← citeshttps://doi.org/10.1007/s00299-011-1116-9openalex-snapshot
ZmMKK4 regulates osmotic stress through reactive oxygen species scavenging in transgenic tobacco
inferred← citeshttps://doi.org/10.1007/s00299-011-1157-0openalex-snapshot
Arabidopsis MKKK20 is involved in osmotic stress response via regulation of MPK6 activity
inferred← citeshttps://doi.org/10.1007/s00299-011-1192-xopenalex-snapshot
Identification of a C2H2-type zinc finger transcription factor (ZAT10) from Arabidopsis as a substrate of MAP kinase
inferred← citeshttps://doi.org/10.1007/s00299-013-1481-7openalex-snapshot
Ectopic expression of a novel Ser/Thr protein kinase from cotton (Gossypium barbadense), enhances resistance to Verticillium dahliae infection and oxidative stress in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-015-1853-2openalex-snapshot
Wheat mitogen-activated protein kinase gene TaMPK4 improves plant tolerance to multiple stresses through modifying root growth, ROS metabolism, and nutrient acquisitions
inferred← citeshttps://doi.org/10.1007/s00299-018-2367-5openalex-snapshot
Mitogen-activated protein kinases MPK3 and MPK6 are required for stem cell maintenance in the Arabidopsis shoot apical meristem
inferred← citeshttps://doi.org/10.1007/s00299-020-02564-6openalex-snapshot
Characterization on TaMPK14, an MAPK family gene of wheat, in modulating N-starvation response through regulating N uptake and ROS homeostasis
inferred← citeshttps://doi.org/10.1007/s00299-021-02808-zopenalex-snapshot
WIPK–NtLTP4 pathway confers resistance to Ralstonia solanacearum in tobacco
inferred← citeshttps://doi.org/10.1007/s00299-024-03167-1openalex-snapshot
Comprehensive analysis of MAPK gene family in upland cotton (Gossypium hirsutum) and functional characterization of GhMPK31 in regulating defense response to insect infestation
inferred← citeshttps://doi.org/10.1007/s00299-025-03536-4openalex-snapshot
Transcriptional and phytohormonal responses to simulated animal grazing in Leymus chinensis
inferred← citeshttps://doi.org/10.1007/s00344-021-10529-6openalex-snapshot
Inoculation with Arbuscular Mycorrhizal Fungi Reinforces Tea Plant’s Tolerance to Salinity
inferred← citeshttps://doi.org/10.1007/s00344-022-10600-wopenalex-snapshot
The Characteristics of Solanum lycopersicum SlSPRH1 and its Negative Role in Thermotolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00344-023-11203-9openalex-snapshot
Signaling and Defence Mechanism of Jasmonic and Salicylic Acid Response in Pulse Crops: Role of WRKY Transcription Factors in Stress Response
inferred← citeshttps://doi.org/10.1007/s00344-025-11691-xopenalex-snapshot
Duplication and Functional Diversification of ANP3-Like Genes (MAPKKKs) in Rosaceae
inferred← citeshttps://doi.org/10.1007/s00425-011-1510-0openalex-snapshot
ZmMPK17, a novel maize group D MAP kinase gene, is involved in multiple stress responses
inferred← citeshttps://doi.org/10.1007/s00425-021-03804-zopenalex-snapshot
MAPK5 and MAPK10 overexpression influences strawberry fruit ripening, antioxidant capacity and resistance to Botrytis cinerea
inferred← citeshttps://doi.org/10.1007/s00425-022-04020-zopenalex-snapshot
Genome-wide identification of the mitogen-activated protein kinase kinase kinase (MAPKKK) in pear (Pyrus bretschneideri) and their functional analysis in response to black spot
inferred← citeshttps://doi.org/10.1007/s00425-023-04232-xopenalex-snapshot
A pervasive phosphorylation cascade modulation of plant transcription factors in response to abiotic stress
inferred← citeshttps://doi.org/10.1007/s00438-009-0446-6openalex-snapshot
A mitogen-activated protein kinase gene, AhMPK3 of peanut: molecular cloning, genomic organization, and heterologous expression conferring resistance against Spodoptera litura in tobacco
inferred← citeshttps://doi.org/10.1007/s00709-011-0316-zopenalex-snapshot
Calcium supplementation modulates arsenic-induced alterations and augments arsenic accumulation in callus cultures of Indian mustard (Brassica juncea (L.) Czern.)
inferred← citeshttps://doi.org/10.1007/s00709-015-0920-4openalex-snapshot
Abscisic-acid-dependent basic leucine zipper (bZIP) transcription factors in plant abiotic stress
inferred← citeshttps://doi.org/10.1007/s00709-019-01359-1openalex-snapshot
Development of efficient protocol for rice transformation overexpressing MAP kinase and their effect on root phenotypic traits
inferred← citeshttps://doi.org/10.1007/s10142-013-0356-xopenalex-snapshot
Drought stress responses in crops
inferred← citeshttps://doi.org/10.1007/s10142-025-01539-8openalex-snapshot
Unraveling key genes and pathways involved in Verticillium wilt resistance by integrative GWAS and transcriptomic approaches in Upland cotton
inferred← citeshttps://doi.org/10.1007/s10529-025-03567-7openalex-snapshot
Genome-wide screening of mitogen-activated protein kinase (MAPK) gene family and expression profile under heavy metal stress in Solanum lycopersicum
inferred← citeshttps://doi.org/10.1007/s10535-016-0683-6openalex-snapshot
Signal transduction and biotechnology in response to environmental stresses
inferred← citeshttps://doi.org/10.1007/s10658-015-0641-8openalex-snapshot
Expression analysis of MAP K 4 and MAP K 6 during pathogenesis of Alternaria blight in susceptible and tolerant genotypes of Brassica juncea
inferred← citeshttps://doi.org/10.1007/s10725-009-9403-yopenalex-snapshot
Effects of MAPKK inhibitor PD98059 on the gravitropism of primary roots of maize
inferred← citeshttps://doi.org/10.1007/s10725-010-9517-2openalex-snapshot
MEK/ERK inhibitor U0126 enhanced salt stress-induced programmed cell death in Thellungiella halophila suspension-cultured cells
inferred← citeshttps://doi.org/10.1007/s10725-022-00877-yopenalex-snapshot
Genome‑wide identification of MPK and MKK gene families and their responses to phytohormone treatment and abiotic stress in foxtail millet
inferred← citeshttps://doi.org/10.1007/s11032-013-9941-xopenalex-snapshot
Identification and expression profile analysis of the protein kinase gene superfamily in maize development
inferred← citeshttps://doi.org/10.1007/s11032-019-0998-zopenalex-snapshot
Fine mapping of wmv1551, a resistance gene to Watermelon mosaic virus in melon
inferred← citeshttps://doi.org/10.1007/s11032-020-01112-0openalex-snapshot
GWAS identifies two novel loci for photosynthetic traits related to phosphorus efficiency in soybean
inferred← citeshttps://doi.org/10.1007/s11032-022-01302-yopenalex-snapshot
Functional analysis of mitogen-activated protein kinases (MAPKs) in potato under biotic and abiotic stress
inferred← citeshttps://doi.org/10.1007/s11033-010-0066-6openalex-snapshot
Overexpression of maize mitogen-activated protein kinase gene, ZmSIMK1 in Arabidopsis increases tolerance to salt stress
inferred← citeshttps://doi.org/10.1007/s11033-010-0514-3openalex-snapshot
Expression analysis of five maize MAP kinase genes in response to various abiotic stresses and signal molecules
inferred← citeshttps://doi.org/10.1007/s11033-011-1232-1openalex-snapshot
Expression analysis of MAP2K9 and MAPK6 during pathogenesis of Alternaria blight in Arabidopsis thaliana ecotype Columbia
inferred← citeshttps://doi.org/10.1007/s11033-021-06570-zopenalex-snapshot
Molecular cloning and sequence analysis of a mitogen-activated protein kinase gene in the Antarctic yeast Rhodotorula mucilaginosa AN5
inferred← citeshttps://doi.org/10.1007/s11033-024-09551-0openalex-snapshot
Identification and analysis of MAPK cascade gene families of Camellia oleifera and their roles in response to cold stress
inferred← citeshttps://doi.org/10.1007/s11033-025-10285-wopenalex-snapshot
Utilizing CRISPR-based genetic modification for precise control of seed dormancy: progress, obstacles, and potential directions
inferred← citeshttps://doi.org/10.1007/s11103-010-9661-0openalex-snapshot
GhMPK7, a novel multiple stress-responsive cotton group C MAPK gene, has a role in broad spectrum disease resistance and plant development
inferred← citeshttps://doi.org/10.1007/s11103-011-9850-5openalex-snapshot
Transient MPK6 activation in response to oxygen deprivation and reoxygenation is mediated by mitochondria and aids seedling survival in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11103-013-0094-4openalex-snapshot
The yeast two-hybrid and related methods as powerful tools to study plant cell signalling
inferred← citeshttps://doi.org/10.1007/s11103-015-0295-0openalex-snapshot
An abscisic acid inducible Arabidopsis MAPKKK, MAPKKK18 regulates leaf senescence via its kinase activity
inferred← citeshttps://doi.org/10.1007/s11103-015-0333-yopenalex-snapshot
Overexpression of ZmMAPK1 enhances drought and heat stress in transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11103-018-0699-8openalex-snapshot
Mitogen activated protein kinase 6 and MAP kinase phosphatase 1 are involved in the response of Arabidopsis roots to l-glutamate
inferred← citeshttps://doi.org/10.1007/s11103-018-0713-1openalex-snapshot
The wheat TabZIP2 transcription factor is activated by the nutrient starvation-responsive SnRK3/CIPK protein kinase
inferred← citeshttps://doi.org/10.1007/s11103-020-00986-0openalex-snapshot
Genome-wide identification of MAPK cascade genes reveals the GhMAP3K14–GhMKK11–GhMPK31 pathway is involved in the drought response in cotton
inferred← citeshttps://doi.org/10.1007/s11104-013-1699-8openalex-snapshot
Mutation of mpk6 enhances cadmium tolerance in Arabidopsis plants by alleviating oxidative stress
inferred← citeshttps://doi.org/10.1007/s11104-019-04196-6openalex-snapshot
Comparative transcriptome analysis of cabbage (Brassica oleracea var. capitata) infected by Plasmodiophora brassicae reveals drastic defense response at secondary infection stage
inferred← citeshttps://doi.org/10.1007/s11105-010-0216-yopenalex-snapshot
PaPTP1, a Gene Encoding Protein Tyrosine Phosphatase from Orchid, Phalaenopsis amabilis, is Regulated During Floral Development and Induced by Wounding
inferred← citeshttps://doi.org/10.1007/s11105-015-0972-9openalex-snapshot
Curcuma longa Mitogen-Activated Protein Kinase 6 (ClMPK6) Stimulates the Defense Response Pathway and Enhances the Resistance to Necrotrophic Fungal Infection
inferred← citeshttps://doi.org/10.1007/s11105-018-1077-zopenalex-snapshot
The Role of MPK6 as Mediator of Ethylene/Jasmonic Acid Signaling in Serendipita indica-Colonized Arabidopsis Roots
inferred← citeshttps://doi.org/10.1007/s11120-021-00852-0openalex-snapshot
Effects of MPK3 and MPK6 kinases on the chloroplast architecture and function induced by cold acclimation in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11240-013-0366-3openalex-snapshot
Molecular cloning and characterization of the mitogen-activated protein kinase kinase gene (MKK4) and its promoter sequence from oilseed rape (Brassica campestris L.)
inferred← citeshttps://doi.org/10.1007/s11240-013-0392-1openalex-snapshot
GbMPK3, a mitogen-activated protein kinase from cotton, enhances drought and oxidative stress tolerance in tobacco
inferred← citeshttps://doi.org/10.1007/s11240-017-1216-5openalex-snapshot
CaMKK1 from Chenopodium album positively regulates salt and drought tolerance in transgenic tobacco
inferred← citeshttps://doi.org/10.1007/s11240-017-1358-5openalex-snapshot
Enhanced drought tolerance in tomato plants by overexpression of SlMAPK1
inferred← citeshttps://doi.org/10.1007/s11240-020-01948-6openalex-snapshot
Introduction of the Nicotiana protein kinase (NPK1) gene by combining Agrobacterium-mediated transformation and recurrent somatic embryogenesis to enhance salt tolerance in cauliflower
inferred← citeshttps://doi.org/10.1007/s11356-014-3739-1openalex-snapshot
Effect of salinity stress on plants and its tolerance strategies: a review
inferred← citeshttps://doi.org/10.1007/s11356-021-16843-6openalex-snapshot
Regulated strategies of cold-adapted microorganisms in response to cold: a review
inferred← citeshttps://doi.org/10.1007/s11427-010-4079-0openalex-snapshot
Expression pattern and core region analysis of AtMPK3 promoter in response to environmental stresses
inferred← citeshttps://doi.org/10.1007/s11738-009-0451-8openalex-snapshot
What happens in plant molecular responses to cold stress?
inferred← citeshttps://doi.org/10.1007/s11738-012-1160-2openalex-snapshot
Tomato SlMPK4 is required for resistance against Botrytis cinerea and tolerance to drought stress
inferred← citeshttps://doi.org/10.1007/s11738-015-2010-9openalex-snapshot
Genome-wide analysis of the barley MAPK gene family and its expression patterns in relation to Puccinia hordei infection
inferred← citeshttps://doi.org/10.1007/s11738-016-2332-2openalex-snapshot
Expression pattern and function of wheat mitogen-activated protein kinase (MPK) cascade genes under micronutrient-deprived conditions
inferred← citeshttps://doi.org/10.1007/s11738-018-2736-2openalex-snapshot
Enhanced tolerance to salt stress in highland barley seedlings (Hordeum vulgare ssp. vulgare) by gamma irradiation pretreatment
inferred← citeshttps://doi.org/10.1007/s11738-023-03545-4openalex-snapshot
Hydrogen peroxide participated in programmed cell death by mediating ethylene during the cryopreservation of Dendrobium nobile protocorm-like bodies
inferred← citeshttps://doi.org/10.1007/s11816-010-0152-1openalex-snapshot
Role of α-tocopherol in cellular signaling: α-tocopherol inhibits stress-induced mitogen-activated protein kinase activation
inferred← citeshttps://doi.org/10.1007/s11816-016-0412-9openalex-snapshot
Novel MAP kinase substrates identified by solid-phase phosphorylation screening in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s12298-025-01575-5openalex-snapshot
From perception to action: MAPKs in plant–virus interactions
inferred← citeshttps://doi.org/10.1007/s12374-016-0442-4openalex-snapshot
A positive transcription factor in osmotic stress tolerance, ZAT10, is regulated by MAP kinases in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s12892-025-00319-xopenalex-snapshot
What can CDPK provide as a bioengineering tool?
inferred← citeshttps://doi.org/10.1007/s13199-013-0246-yopenalex-snapshot
Piriformospora indica: a versatile root endophytic symbiont
inferred← citeshttps://doi.org/10.1007/s13258-014-0209-6openalex-snapshot
Soybean mitogen-activated protein kinase GMK2 is activated with GMK1 in Bradyrhizobium-Soybean interactions
inferred← citeshttps://doi.org/10.1007/s13562-014-0256-8openalex-snapshot
Characterization and expression analysis of mitogen-activated protein kinase cascade genes in wheat subjected to phosphorus and nitrogen deprivation, high salinity, and drought
inferred← citeshttps://doi.org/10.1007/s13562-020-00621-5openalex-snapshot
MKK3-MPK6-MYC2 module positively regulates ABA biosynthesis and signalling in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s43621-025-01718-4openalex-snapshot
Recent trends in transcriptional regulation of cold stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-799963-0.00019-8openalex-snapshot
Hydrogen Peroxide (H2O2) Generation, Scavenging and Signaling in Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-812689-9.00021-2openalex-snapshot
Involvement of Mitogen-Activated Protein Kinases in Abiotic Stress Responses in Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-816451-8.00001-0openalex-snapshot
Signaling Molecules in Ecophysiological Response Mechanisms of Salt-Stressed Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-816451-8.00030-7openalex-snapshot
Proteomics Insights Into Salt Stress Signaling in Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-818581-0.00013-9openalex-snapshot
Systems biology of crop improvement: Drought tolerance as a model to integrate molecular biology, physiology, and breeding
inferred← citeshttps://doi.org/10.1016/b978-0-323-90594-7.00012-0openalex-snapshot
The role of mitogen-activated protein kinases in stress signaling in plants
inferred← citeshttps://doi.org/10.1016/b978-0-443-13490-6.00026-6openalex-snapshot
Regulatory genes in water logging stress: submergence effect and postsubmergence recovery
inferred← citeshttps://doi.org/10.1016/b978-0-443-40320-0.00003-6openalex-snapshot
Biochemical and molecular responses of plants to urban air pollution
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.07.064openalex-snapshot
Arabidopsis MKK4 mediates osmotic-stress response via its regulation of MPK3 activity
inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.04.137openalex-snapshot
Phosphorylation by AtMPK6 is required for the biological function of AtMYB41 in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.06.019openalex-snapshot
Phosphorylation of the transcriptional regulator MYB44 by mitogen activated protein kinase regulates Arabidopsis seed germination
inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.12.039openalex-snapshot
Phosphorylation of the zinc finger transcriptional regulator ZAT6 by MPK6 regulates Arabidopsis seed germination under salt and osmotic stress
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.11.008openalex-snapshot
Identification of mitogen-activated protein kinase kinase gene family and MKK–MAPK interaction network in maize
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.01.104openalex-snapshot
Arabidopsis MAPKKK18 positively regulates drought stress resistance via downstream MAPKK3
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.04.065openalex-snapshot
The mitogen-activated protein kinase kinase 9 (MKK9) modulates nitrogen acquisition and anthocyanin accumulation under nitrogen-limiting condition in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.bbrep.2023.101620openalex-snapshot
Trancriptome data mining in combination with co-expression network analysis identifies the functional modules and critical regulators in Hordeum vulgare L. in response to cold stress
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2011.12.002openalex-snapshot
Improvement of stress tolerance in plants by genetic manipulation of mitogen-activated protein kinases
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2013.07.009openalex-snapshot
Crosstalk between secondary messengers, hormones and MAPK modules during abiotic stress signalling in plants
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2013.09.006openalex-snapshot
The role of ABA and MAPK signaling pathways in plant abiotic stress responses
inferred← citeshttps://doi.org/10.1016/j.cbd.2018.12.008openalex-snapshot
Liver transcriptome analysis and de novo annotation of the orange-spotted groupers (Epinephelus coioides) under cold stress
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112832openalex-snapshot
Banana MKK1 modulates fruit ripening via the MKK1-MPK6-3/11-4-bZIP21 module
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.126486openalex-snapshot
Hydrogen peroxide as a signalling molecule in plants and its crosstalk with other plant growth regulators under heavy metal stress
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2024.143438openalex-snapshot
Polyamines and hydrogen peroxide: Allies in plant resilience against abiotic stress
inferred← citeshttps://doi.org/10.1016/j.cj.2021.03.022openalex-snapshot
A gain-of-function mutation of OsMAPK6 leads to long grain in rice
inferred← citeshttps://doi.org/10.1016/j.cj.2025.12.012openalex-snapshot
OsMAP4K6 positively regulates salt tolerance via activating OsMKK6 in rice
inferred← citeshttps://doi.org/10.1016/j.cpb.2022.100239openalex-snapshot
Genomic and proteomic responses to drought stress and biotechnological interventions for enhanced drought tolerance in plants
inferred← citeshttps://doi.org/10.1016/j.csbj.2021.12.033openalex-snapshot
An allosteric regulation mechanism of Arabidopsis Serine/Threonine kinase 1 (SIK1) through phosphorylation
inferred← citeshttps://doi.org/10.1016/j.cub.2011.03.015openalex-snapshot
Evolution of Abscisic Acid Synthesis and Signaling Mechanisms
inferred← citeshttps://doi.org/10.1016/j.cyto.2012.06.317openalex-snapshot
BLyS expression and JNK activation may form a feedback loop to promote survival and proliferation of multiple myeloma cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.07.016openalex-snapshot
Modulators of Stomatal Lineage Signal Transduction Alter Membrane Contact Sites and Reveal Specialization among ERECTA Kinases
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.113017openalex-snapshot
Physiological and transcriptomic analyses reveal novel insights into the cultivar-specific response to alkaline stress in alfalfa (Medicago sativa L.)
inferred← citeshttps://doi.org/10.1016/j.ejop.2014.08.005openalex-snapshot
In silico identification and characterization of the MAPK family members of unicellular model eukaryote Tetrahymena thermophila
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2012.02.013openalex-snapshot
Primed plants do not forget
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2012.04.003openalex-snapshot
Exposure of Arabidopsis thaliana to Cd or Cu excess leads to oxidative stress mediated alterations in MAPKinase transcript levels
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2017.02.010openalex-snapshot
Abiotic stress: Interplay between ROS, hormones and MAPKs
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2019.103934openalex-snapshot
Functional characterization of Mitogen-Activated Protein Kinase Kinase (MAPKK) gene in Halophytic Salicornia europaea against salt stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104899openalex-snapshot
Synchronised interaction of carbon and nitrogen provides drought tolerance in Cyamopsis tetragonoloba
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105028openalex-snapshot
Oilseed rape MPK1 mediates reactive oxygen species-dependent cell death and jasmonic acid-induced leaf senescence
inferred← citeshttps://doi.org/10.1016/j.febslet.2014.04.032openalex-snapshot
Membrane rigidification functions upstream of the MEKK1‐MKK2‐MPK4 cascade during cold acclimation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.fsi.2024.110076openalex-snapshot
Comprehensive genome-wide identification and functional characterization of mapk gene family in northern snakeheads (Channa argus)
inferred← citeshttps://doi.org/10.1016/j.gene.2012.01.048openalex-snapshot
Genome-wide analysis of the mitogen-activated protein kinase gene family in Solanum lycopersicum
inferred← citeshttps://doi.org/10.1016/j.gene.2012.02.017openalex-snapshot
Characterization of an Abc1 kinase family gene OsABC1-2 conferring enhanced tolerance to dark-induced stress in rice
inferred← citeshttps://doi.org/10.1016/j.gene.2013.07.107openalex-snapshot
Genome-wide identification and expression analysis of MAPK and MAPKK gene family in Malus domestica
inferred← citeshttps://doi.org/10.1016/j.hpj.2023.02.003openalex-snapshot
Genome-wide identification of the mitogen-activated protein kinase kinases in pear and their functional analysis in response to black spot
inferred← citeshttps://doi.org/10.1016/j.hpj.2026.03.014openalex-snapshot
Engineering drought resilience in plants: integrating multi-omics, machine learning, and single-cell technologies for future food security
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.2024.132790openalex-snapshot
Pectin-associated immune responses in plant-microbe interactions: A review
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.138588openalex-snapshot
MYB proteins: Versatile regulators of plant development, stress responses, and secondary metabolite biosynthetic pathways
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144509openalex-snapshot
YcsE-mediated dephosphorylation of ComP regulates surfactin and iturin synthesis in Bacillus velezensis HN-1
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