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MEKK1/YDA-MKK4/5-MPK3/6 cascade is involved in extracellular ATP-regulated seedling growth of Arabidopsis thaliana
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1873-3468.14703openalex-snapshot
The intrinsically disordered C‐terminus of purinoceptor P2K1 fine‐tunes plant responses to extracellular ATP
inferredcites →https://doi.org/10.1007/s00709-020-01603-zopenalex-snapshot
Mitogen-activated protein kinase action in plant response to high-temperature stress: a mini review
inferredcites →https://doi.org/10.1007/s11103-010-9683-7openalex-snapshot
Both the stimulation and inhibition of root hair growth induced by extracellular nucleotides in Arabidopsis are mediated by nitric oxide and reactive oxygen species
inferredcites →https://doi.org/10.1016/j.celrep.2016.01.023openalex-snapshot
Ligand-Induced Receptor-like Kinase Complex Regulates Floral Organ Abscission in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2024.05.057openalex-snapshot
A multifaceted kinase axis regulates plant organ abscission through conserved signaling mechanisms
inferredcites →https://doi.org/10.1016/j.devcel.2017.09.024openalex-snapshot
MAP Kinase Cascades Regulate the Cold Response by Modulating ICE1 Protein Stability
inferredcites →https://doi.org/10.1016/j.febslet.2009.07.007openalex-snapshot
Touch induces ATP release in Arabidopsis roots that is modulated by the heterotrimeric G‐protein complex
inferredcites →https://doi.org/10.1016/j.jss.2017.03.025openalex-snapshot
Adenosine triphosphate as a molecular mediator of the vascular response to injury
inferredcites →https://doi.org/10.1016/j.molp.2020.01.001openalex-snapshot
YODA-HSP90 Module Regulates Phosphorylation-Dependent Inactivation of SPEECHLESS to Control Stomatal Development under Acute Heat Stress in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molp.2020.08.015openalex-snapshot
Stigma Receptivity Is Controlled by Functionally Redundant MAPK Pathway Components in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molp.2020.09.004openalex-snapshot
The YDA-MKK4/MKK5-MPK3/MPK6 Cascade Functions Downstream of the RGF1-RGI Ligand–Receptor Pair in Regulating Mitotic Activity in Root Apical Meristem
inferredcites →https://doi.org/10.1016/j.molp.2020.09.005openalex-snapshot
RGF1-RGI1, a Peptide-Receptor Complex, Regulates Arabidopsis Root Meristem Development via a MAPK Signaling Cascade
inferredcites →https://doi.org/10.1016/j.molp.2025.06.001openalex-snapshot
Activation of the CNGC2–CNGC4 channel complex by P2K1-mediated phosphorylation links extracellular ATP perception to calcium signaling in plant immunity
inferredcites →https://doi.org/10.1016/j.pbi.2018.04.012openalex-snapshot
Conveying endogenous and exogenous signals: MAPK cascades in plant growth and defense
inferredcites →https://doi.org/10.1016/j.plaphy.2024.108550openalex-snapshot
Adenosine triphosphate alleviates high temperature-enhanced glyphosate toxicity in maize seedlings
inferredcites →https://doi.org/10.1016/j.plaphy.2025.109684openalex-snapshot
Extracellular ATP receptors P2Ks are involved in regulating local and systemic stomatal responses to local environmental stimuli
inferredcites →https://doi.org/10.1016/j.tplants.2014.10.001openalex-snapshot
Mitogen-activated protein kinase cascades in signaling plant growth and development
inferredcites →https://doi.org/10.1016/j.tplants.2019.11.006openalex-snapshot
MAPK Signaling: Emerging Roles in Lateral Root Formation
inferredcites →https://doi.org/10.1073/pnas.1910916116openalex-snapshot
Noncanonical auxin signaling regulates cell division pattern during lateral root development
inferredcites →https://doi.org/10.1080/15592324.2024.2370706openalex-snapshot
FERONIA orchestrates P2K1-driven purinergic signaling in plant roots
inferredcites →https://doi.org/10.1093/jxb/erp091openalex-snapshot
Intersection of two signalling pathways: extracellular nucleotides regulate pollen germination and pollen tube growth via nitric oxide
inferredcites →https://doi.org/10.1093/mp/ssr095openalex-snapshot
Extracellular ATP Promotes Stomatal Opening of Arabidopsis thaliana through Heterotrimeric G Protein α Subunit and Reactive Oxygen Species
inferredcites →https://doi.org/10.1093/pcp/pcaa014openalex-snapshot
Redox-Responsive Transcription Factor 1 (RRFT1) Is Involved in Extracellular ATP-Regulated Arabidopsis thaliana Seedling Growth
inferredcites →https://doi.org/10.1093/plcell/koad029openalex-snapshot
The Raf-like MAPKKK INTEGRIN-LINKED KINASE 5 regulates purinergic receptor-mediated innate immunity in Arabidopsis
inferredcites →https://doi.org/10.1093/plcell/koad088openalex-snapshot
14-3-3 proteins facilitate the activation of MAP kinase cascades by upstream immunity-related kinases
inferredcites →https://doi.org/10.1093/plcell/koae225openalex-snapshot
Dual roles of the MPK3 and MPK6 mitogen-activated protein kinases in regulating Arabidopsis stomatal development
inferredcites →https://doi.org/10.1093/plphys/kiac393openalex-snapshot
Activation of indolic glucosinolate pathway by extracellular ATP in Arabidopsis
inferredcites →https://doi.org/10.1093/plphys/kiae415openalex-snapshot
Molecular traits of MAPK kinases and the regulatory mechanism of GhMAPKK5 alleviating drought/salt stress in cotton
inferredcites →https://doi.org/10.1104/pp.106.085670openalex-snapshot
Extracellular ATP in Plants. Visualization, Localization, and Analysis of Physiological Significance in Growth and Signaling
inferredcites →https://doi.org/10.1104/pp.17.01477openalex-snapshot
Extracellular ATP Acts on Jasmonate Signaling to Reinforce Plant Defense
inferredcites →https://doi.org/10.1104/pp.17.01757openalex-snapshot
BRASSINOSTEROID-SIGNALING KINASE1 Phosphorylates MAPKKK5 to Regulate Immunity in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.18.01301openalex-snapshot
Extracellular ATP Shapes a Defense-Related Transcriptome Both Independently and along with Other Defense Signaling Pathways
inferredcites →https://doi.org/10.1104/pp.19.01265openalex-snapshot
Arabidopsis Lectin Receptor Kinase P2K2 Is a Second Plant Receptor for Extracellular ATP and Contributes to Innate Immunity
inferredcites →https://doi.org/10.1105/tpc.104.023945openalex-snapshot
Evidence of a Novel Cell Signaling Role for Extracellular Adenosine Triphosphates and Diphosphates in Arabidopsis
inferredcites →https://doi.org/10.1111/1541-4337.13003openalex-snapshot
Advances in chilling injury of postharvest fruit and vegetable: Extracellular ATP aspects
inferredcites →https://doi.org/10.1111/jipb.12898openalex-snapshot
Plant immune signaling: Advancing on two frontiers
inferredcites →https://doi.org/10.1111/jipb.13150openalex-snapshot
The rice Raf‐like MAPKKK OsILA1 confers broad‐spectrum resistance to bacterial blight by suppressing the OsMAPKK4–OsMAPK6 cascade
inferredcites →https://doi.org/10.1111/jipb.13215openalex-snapshot
Mitogen‐activated protein kinase cascades in plant signaling
inferredcites →https://doi.org/10.1111/jipb.13309openalex-snapshot
Overlapping functions of YDA and MAPKKK3/MAPKKK5 upstream of MPK3/MPK6 in plant immunity and growth/development
inferredcites →https://doi.org/10.1111/nph.17987openalex-snapshot
Arabidopsis thaliana CYCLIC NUCLEOTIDE‐GATED CHANNEL2 mediates extracellular ATP signal transduction in root epidermis
inferredcites →https://doi.org/10.1111/nph.18350openalex-snapshot
ATP depletion plays a pivotal role in self‐incompatibility, revealing a link between cellular energy status, cytosolic acidification and actin remodelling in pollen tubes
inferredcites →https://doi.org/10.1111/nph.20235openalex-snapshot
The endosomal–vacuolar transport system acts as a docking platform for the Pmk1 MAP kinase signaling pathway in Magnaporthe oryzae
inferredcites →https://doi.org/10.1111/nph.70352openalex-snapshot
LRK10L3 and BAK1 are collaboratively involved in extracellular ATP ‐regulated seedling growth of Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/pce.15095openalex-snapshot
MAPKKK28 functions upstream of the MKK1‐MPK1 cascade to regulate abscisic acid responses in rice
inferredcites →https://doi.org/10.1111/pce.15381openalex-snapshot
ZjMAPKK4 Interacted With ZjNAC78 Regulates Cold Tolerance Response in Jujube
inferredcites →https://doi.org/10.1111/tpj.13737openalex-snapshot
Maternal control of embryogenesis by MPK6 and its upstream MKK4/MKK5 in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.16656openalex-snapshot
CPK28 is a modulator of purinergic signaling in plant growth and defense
inferredcites →https://doi.org/10.1111/tpj.70010openalex-snapshot
Nitrate activates an MKK3 ‐dependent MAPK module via NLP transcription factors in Arabidopsis
inferredcites →https://doi.org/10.1126/science.343.6168.290openalex-snapshot
Identification of a Plant Receptor for Extracellular ATP
inferredcites →https://doi.org/10.1146/annurev-phyto-082712-102314openalex-snapshot
MAPK Cascades in Plant Disease Resistance Signaling
inferredcites →https://doi.org/10.15252/embj.201694248openalex-snapshot
The Arabidopsis CERK1‐associated kinase PBL27 connects chitin perception to MAPK activation
inferredcites →https://doi.org/10.3390/ijms21228683openalex-snapshot
A Salt-Signaling Network Involving Ethylene, Extracellular ATP, Hydrogen Peroxide, and Calcium Mediates K+/Na+ Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.3390/ijms22020494openalex-snapshot
Annexin 1 Is a Component of eATP-Induced Cytosolic Calcium Elevation in Arabidopsis thaliana Roots
inferredcites →https://doi.org/10.3390/ijms242316688openalex-snapshot
The Plasma Membrane Purinoreceptor P2K1/DORN1 Is Essential in Stomatal Closure Evoked by Extracellular Diadenosine Tetraphosphate (Ap4A) in Arabidopsis thaliana
inferredcites →https://doi.org/10.4161/psb.5.8.12225openalex-snapshot
Calcium/calmodulin-regulated receptor-like kinase CRLK1 interacts with MEKK1 in plants
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