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The Arabidopsis thaliana lectin receptor kinase LecRK‐I.9 is required for full resistance to Pseudomonas syringae and affects jasmonate signalling
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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/pmic.200700938openalex-snapshot
Recent advances in plant cell wall proteomics
inferredcites →https://doi.org/10.1007/s00018-003-3394-zopenalex-snapshot
High affinity recognition of a Phytophthora protein by Arabidopsis via an RGD motif
inferredcites →https://doi.org/10.1016/j.bbagen.2005.04.004openalex-snapshot
Evidence for lectin activity of a plant receptor-like protein kinase by application of neoglycoproteins and bioinformatic algorithms
inferredcites →https://doi.org/10.1016/j.coi.2007.11.003openalex-snapshot
Pattern-recognition receptors in plant innate immunity
inferredcites →https://doi.org/10.1016/j.cub.2007.05.018openalex-snapshot
A Receptor-like Kinase Mediates the Response of Arabidopsis Cells to the Inhibition of Cellulose Synthesis
inferredcites →https://doi.org/10.1016/j.pbi.2005.07.003openalex-snapshot
Molecular players regulating the jasmonate signalling network
inferredcites →https://doi.org/10.1016/j.pbi.2009.07.013openalex-snapshot
The jasmonate pathway: the ligand, the receptor and the core signalling module
inferredcites →https://doi.org/10.1016/j.pbi.2014.04.007openalex-snapshot
Immune receptor complexes at the plant cell surface
inferredcites →https://doi.org/10.1016/j.plantsci.2012.12.019openalex-snapshot
Overexpression of L-type lectin-like protein kinase 1 confers pathogen resistance and regulates salinity response in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.tplants.2012.04.003openalex-snapshot
Plant LysM proteins: modules mediating symbiosis and immunity
inferredcites →https://doi.org/10.1023/a:1006136701595openalex-snapshot
Characterization of the Arabidopsis lecRK-a genes: members of a superfamily encoding putative receptors with an extracellular domain homologous to legume lectins
inferredcites →https://doi.org/10.1038/nchembio.161openalex-snapshot
(+)-7-iso-Jasmonoyl-L-isoleucine is the endogenous bioactive jasmonate
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00276.xopenalex-snapshot
High affinity RGD‐binding sites at the plasma membrane ofArabidopsis thalianalinks the cell wall
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0708139104openalex-snapshot
Regulation of tradeoffs between plant defenses against pathogens with different lifestyles
inferredcites →https://doi.org/10.1073/pnas.0711203105openalex-snapshot
Mapping methyl jasmonate-mediated transcriptional reprogramming of metabolism and cell cycle progression in cultured Arabidopsis cells
inferredcites →https://doi.org/10.1073/pnas.89.15.6837openalex-snapshot
Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana mutant.
inferredcites →https://doi.org/10.1080/07352689891304276openalex-snapshot
Plant Lectins: A Composite of Several Distinct Families of Structurally and Evolutionary Related Proteins with Diverse Biological Roles
inferredcites →https://doi.org/10.1093/aob/mct067openalex-snapshot
Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany
inferredcites →https://doi.org/10.1093/jxb/erp277openalex-snapshot
Arabidopsis L-type lectin receptor kinases: phylogeny, classification, and expression profiles
inferredcites →https://doi.org/10.1093/jxb/ers362openalex-snapshot
Signalling of Arabidopsis thaliana response to Pieris brassicae eggs shares similarities with PAMP-triggered immunity
inferredcites →https://doi.org/10.1094/mpmi-02-13-0044-ropenalex-snapshot
A Salicylic Acid–Induced Lectin-Like Protein Plays a Positive Role in the Effector-Triggered Immunity Response of Arabidopsis thaliana to Pseudomonas syringae Avr-Rpm1
inferredcites →https://doi.org/10.1094/mpmi-02-15-0025-ropenalex-snapshot
Arabidopsis Lectin Receptor Kinases LecRK-IX.1 and LecRK-IX.2 Are Functional Analogs in Regulating Phytophthora Resistance and Plant Cell Death
inferredcites →https://doi.org/10.1094/mpmi-06-14-0191-ropenalex-snapshot
Phenotypic Analyses of Arabidopsis T-DNA Insertion Lines and Expression Profiling Reveal That Multiple L-Type Lectin Receptor Kinases Are Involved in Plant Immunity
inferredcites →https://doi.org/10.1104/pp.105.066464openalex-snapshot
Lectin Receptor Kinases Participate in Protein-Protein Interactions to Mediate Plasma Membrane-Cell Wall Adhesions in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.2.567openalex-snapshot
COI1-Dependent Expression of an Arabidopsis Vegetative Storage Protein in Flowers and Siliques and in Response to Coronatine or Methyl Jasmonate
inferredcites →https://doi.org/10.1104/pp.111.175737openalex-snapshot
Cell Wall Damage-Induced Lignin Biosynthesis Is Regulated by a Reactive Oxygen Species- and Jasmonic Acid-Dependent Process in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.192641openalex-snapshot
Arabidopsis WRKY33 Is a Key Transcriptional Regulator of Hormonal and Metabolic Responses toward Botrytis cinerea Infection
inferredcites →https://doi.org/10.1105/tpc.002022openalex-snapshot
The Arabidopsis Mutant cev1 Links Cell Wall Signaling to Jasmonate and Ethylene Responses
inferredcites →https://doi.org/10.1105/tpc.104.022038openalex-snapshot
VASCULAR ASSOCIATED DEATH1, a Novel GRAM Domain–Containing Protein, Is a Regulator of Cell Death and Defense Responses in Vascular Tissues
inferredcites →https://doi.org/10.1105/tpc.105.037523openalex-snapshot
Physical and Functional Interactions between Pathogen-Induced Arabidopsis WRKY18, WRKY40, and WRKY60 Transcription Factors
inferredcites →https://doi.org/10.1105/tpc.106.048017openalex-snapshot
MYC2 Differentially Modulates Diverse Jasmonate-Dependent Functions in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.11.8.1393openalex-snapshot
Salicylic Acid Induction–Deficient Mutants of Arabidopsis Express PR-2 and PR-5 and Accumulate High Levels of Camalexin after Pathogen Inoculation
inferredcites →https://doi.org/10.1105/tpc.111.088229openalex-snapshot
Nicotiana attenuata LECTIN RECEPTOR KINASE1 Suppresses the Insect-Mediated Inhibition of Induced Defense Responses during Manduca sexta Herbivory
inferredcites →https://doi.org/10.1105/tpc.112.095778openalex-snapshot
The Lectin Receptor Kinase-VI.2 Is Required for Priming and Positively Regulates Arabidopsis Pattern-Triggered Immunity
inferredcites →https://doi.org/10.1105/tpc.112.108548openalex-snapshot
Salicylic Acid Suppresses Jasmonic Acid Signaling Downstream of SCFCOI1-JAZ by Targeting GCC Promoter Motifs via Transcription Factor ORA59
inferredcites →https://doi.org/10.1105/tpc.13.2.413openalex-snapshot
Plasma Membrane-Cell Wall Adhesion Is Required for Expression of Plant Defense Responses during Fungal Penetration
inferredcites →https://doi.org/10.1105/tpc.13.5.1025openalex-snapshot
The Arabidopsis Mutant cev1 Has Constitutively Active Jasmonate and Ethylene Signal Pathways and Enhanced Resistance to Pathogens
inferredcites →https://doi.org/10.1105/tpc.2.6.513openalex-snapshot
Exploiting the Triple Response of Arabidopsis to Identify Ethylene-Related Mutants
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02739.xopenalex-snapshot
A B‐lectin receptor kinase gene conferring rice blast resistance
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03052.xopenalex-snapshot
The AtGenExpress global stress expression data set: protocols, evaluation and model data analysis of UV‐B light, drought and cold stress responses
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03744.xopenalex-snapshot
Identification of cell‐wall stress as a hexose‐dependent and osmosensitive regulator of plant responses
inferredcites →https://doi.org/10.1111/nph.13117openalex-snapshot
Knowing your friends and foes – plant receptor‐like kinases as initiators of symbiosis or defence
inferredcites →https://doi.org/10.1126/science.280.5366.1091openalex-snapshot
COI1 : An Arabidopsis Gene Required for Jasmonate-Regulated Defense and Fertility
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-cellbio-092910-154055openalex-snapshot
Hormonal Modulation of Plant Immunity
inferredcites →https://doi.org/10.1146/annurev-phyto-073009-114447openalex-snapshot
Hormone Crosstalk in Plant Disease and Defense: More Than Just JASMONATE-SALICYLATE Antagonism
inferredcites →https://doi.org/10.1146/annurev-phyto-082712-102314openalex-snapshot
MAPK Cascades in Plant Disease Resistance Signaling
inferredcites →https://doi.org/10.1146/annurev-phyto-082712-102321openalex-snapshot
Pseudomonas syringae pv. tomato DC3000: A Model Pathogen for Probing Disease Susceptibility and Hormone Signaling in Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.48.1.355openalex-snapshot
BIOSYNTHESIS AND ACTION OF JASMONATES IN PLANTS
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105346openalex-snapshot
A Renaissance of Elicitors: Perception of Microbe-Associated Molecular Patterns and Danger Signals by Pattern-Recognition Receptors
inferredcites →https://doi.org/10.1371/journal.ppat.1001327openalex-snapshot
The Lectin Receptor Kinase LecRK-I.9 Is a Novel Phytophthora Resistance Component and a Potential Host Target for a RXLR Effector
inferredcites →https://doi.org/10.1371/journal.ppat.1002513openalex-snapshot
The Arabidopsis Lectin Receptor Kinase LecRK-V.5 Represses Stomatal Immunity Induced by Pseudomonas syringae pv. tomato DC3000
inferredcites →https://doi.org/10.2307/3870970openalex-snapshot
Salicylic Acid Induction-Deficient Mutants of Arabidopsis Express PR-2 and PR-5 and Accumulate High Levels of Camalexin after Pathogen Inoculation
inferredcites →https://doi.org/10.3389/fpls.2012.00280openalex-snapshot
Cell wall integrity signaling and innate immunity in plants
inferredcites →https://doi.org/10.3389/fpls.2013.00072openalex-snapshot
Nuclear jasmonate and salicylate signaling and crosstalk in defense against pathogens
inferredcites →https://doi.org/10.3389/fpls.2013.00124openalex-snapshot
Lectin receptor kinases in plant innate immunity
inferredcites →https://doi.org/10.3389/fpls.2014.00446openalex-snapshot
Extracellular ATP acts as a damage-associated molecular pattern (DAMP) signal in plants
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/1873-3468.14706openalex-snapshot
Phosphorylation by CIPK23 regulates the high‐affinity Mn transporter NRAMP1 in Arabidopsis
inferred← citeshttps://doi.org/10.1002/9781119541578.ch2openalex-snapshot
Lectin Receptor like Kinase
inferred← citeshttps://doi.org/10.1007/978-3-030-54478-2_3openalex-snapshot
Neurotransmitters in Signalling and Adaptation to Salinity Stress in Plants
inferred← citeshttps://doi.org/10.1007/s00425-021-03789-9openalex-snapshot
Identification and characterization of L-type lectin receptor-like kinases involved in Glycine max–Phytophthora sojae interaction
inferred← citeshttps://doi.org/10.1007/s00425-022-03839-wopenalex-snapshot
Extracellular ATP is involved in regulating Arabidopsis seed germination
inferred← citeshttps://doi.org/10.1007/s11103-021-01154-8openalex-snapshot
The transcriptome landscapes of citrus leaf in different developmental stages
inferred← citeshttps://doi.org/10.1007/s13258-019-00801-1openalex-snapshot
Pattern recognition receptors and their interactions with bacterial type III effectors in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-90594-7.00003-xopenalex-snapshot
Receptor-like kinases and their role in plant innate immunity
inferred← citeshttps://doi.org/10.1016/b978-0-323-90594-7.00014-4openalex-snapshot
Role of receptor-like kinases in plant-pathogen interaction
inferred← citeshttps://doi.org/10.1016/b978-0-323-91595-3.00025-2openalex-snapshot
Plant-pathogen interaction: Mechanisms and evolution
inferred← citeshttps://doi.org/10.1016/b978-0-443-30244-2.00011-7openalex-snapshot
Receptor-mediated endocytosis and autophagy in plants
inferred← citeshttps://doi.org/10.1016/j.cub.2025.03.072openalex-snapshot
Conserved role of the SERK-BIR module in development and immunity across land plants
inferred← citeshttps://doi.org/10.1016/j.mcpro.2025.100926openalex-snapshot
Identifying Receptor Kinase Substrates Using an 8000 Peptide Kinase Client Library Enriched for Conserved Phosphorylation Sites
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.111096openalex-snapshot
Review: The multiple roles of plant lectins
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112071openalex-snapshot
A novel lectin receptor kinase gene, AtG-LecRK-I.2, enhances bacterial pathogen resistance through regulation of stomatal immunity in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113323openalex-snapshot
StLecRK. IX and StLRPK1 form a complex with StBAK1 to positively regulate potato late blight resistance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.10.038openalex-snapshot
Recombinant N-glycosylation isoforms of Legume lectins: Production and purification from Nicotiana benthamiana leaves following RuBisCO depletion
inferred← citeshttps://doi.org/10.1016/j.pmpp.2025.102574openalex-snapshot
Susceptibility assessment and genetic analysis of cucumber genotypes to damping-off disease by Phytophthora melonis
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2020.111236openalex-snapshot
Characterization and function of banana DORN1s during fruit ripening and cold storage
inferred← citeshttps://doi.org/10.1016/j.tcsw.2022.100091openalex-snapshot
Plant lectins: Handymen at the cell surface
inferred← citeshttps://doi.org/10.1021/acs.jafc.6c05000openalex-snapshot
Cross-Talk Between a Nematode Effector–Targeted Metabolic Enzyme and a Lectin Receptor Kinase Regulates Wheat Immunity
inferred← citeshttps://doi.org/10.1038/s41467-017-02340-3openalex-snapshot
Extracellular ATP elicits DORN1-mediated RBOHD phosphorylation to regulate stomatal aperture
inferred← citeshttps://doi.org/10.1038/s41467-021-22854-1openalex-snapshot
S-acylation of P2K1 mediates extracellular ATP-induced immune signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41467-022-28150-wopenalex-snapshot
Activation of the plant mevalonate pathway by extracellular ATP
inferred← citeshttps://doi.org/10.1038/s41598-019-53444-3openalex-snapshot
Molecular and genetic analysis of defensive responses of Brassica juncea – B. fruticulosa introgression lines to Sclerotinia infection
inferred← citeshttps://doi.org/10.1042/bst20170371openalex-snapshot
Signaling through plant lectins: modulation of plant immunity and beyond
inferred← citeshttps://doi.org/10.1080/15592324.2018.1432229openalex-snapshot
A crosstalk between extracellular ATP and jasmonate signaling pathways for plant defense
inferred← citeshttps://doi.org/10.1080/15592324.2019.1659079openalex-snapshot
Transcriptomic perspective on extracellular ATP signaling: a few curious trifles
inferred← citeshttps://doi.org/10.1080/15592324.2021.1940019openalex-snapshot
VvXYLP02 confers gray mold resistance by amplifying jasmonate signaling pathway in Vitis vinifera
inferred← citeshttps://doi.org/10.1093/aob/mcz135openalex-snapshot
DORN1/P2K1 and purino-calcium signalling in plants: making waves with extracellular ATP
inferred← citeshttps://doi.org/10.1093/femsre/fuaf029openalex-snapshot
Purine-based infochemicals and immunometabolites: a comparative review of emerging signaling pathways in plants and animals
inferred← citeshttps://doi.org/10.1093/hr/uhac010openalex-snapshot
Potato StLecRK-IV.1 negatively regulates late blight resistance by affecting the stability of a positive regulator StTET8
inferred← citeshttps://doi.org/10.1093/jxb/erae520openalex-snapshot
Receptor kinase LecRK-I.9 regulates cell wall remodelling during lateral root formation in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/eraf025openalex-snapshot
The Arabidopsis e ATP receptor DORN1 and CNGC19 calcium channel act in tandem to regulate plant defense upon Spodoptera litura herbivory
inferred← citeshttps://doi.org/10.1093/plcell/koad029openalex-snapshot
The Raf-like MAPKKK INTEGRIN-LINKED KINASE 5 regulates purinergic receptor-mediated innate immunity in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiac393openalex-snapshot
Activation of indolic glucosinolate pathway by extracellular ATP in Arabidopsis
inferred← citeshttps://doi.org/10.1094/phyto-03-23-0104-rvwopenalex-snapshot
Damage-Associated Molecular Patterns and Systemic Signaling
inferred← citeshttps://doi.org/10.1101/2022.04.19.488815openalex-snapshot
The mitogen-activated protein kinase kinase kinase, ILK5, regulates plant purinergic receptor-mediated, innate immunity
inferred← citeshttps://doi.org/10.1101/2024.01.31.578125openalex-snapshot
Receptor kinase LecRK-I.9 regulates cell wall remodelling and signalling during lateral root formation in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2024.07.17.603821openalex-snapshot
MENTOR: Multiplex Embedding of Networks for Team-Based Omics Research
inferred← citeshttps://doi.org/10.1101/2025.08.14.670329openalex-snapshot
A molecular glue in plants: The lectin domain of LecRK-I.9 creates persistent plasma membrane - cell wall connections
inferred← citeshttps://doi.org/10.1104/pp.17.00404openalex-snapshot
A Lectin Receptor-Like Kinase Mediates Pattern-Triggered Salicylic Acid Signaling
inferred← citeshttps://doi.org/10.1104/pp.17.01477openalex-snapshot
Extracellular ATP Acts on Jasmonate Signaling to Reinforce Plant Defense
inferred← citeshttps://doi.org/10.1104/pp.18.01301openalex-snapshot
Extracellular ATP Shapes a Defense-Related Transcriptome Both Independently and along with Other Defense Signaling Pathways
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/jipb.12897openalex-snapshot
Lectin receptor kinase OsLecRK‐S.7 is required for pollen development and male fertility
inferred← citeshttps://doi.org/10.1111/mpp.12916openalex-snapshot
Phosphate excess increases susceptibility to pathogen infection in rice
inferred← citeshttps://doi.org/10.1111/nph.18868openalex-snapshot
Extracellular ATP sensing in living plant tissues with a genetically encoded, ratiometric fluorescent sensor
inferred← citeshttps://doi.org/10.1111/nph.70624openalex-snapshot
Arabidopsis thaliana Cyclic Nucleotide‐Gated Channel 19 is involved in root extracellular ATP and Pep1 signalling
inferred← citeshttps://doi.org/10.1111/nph.71383openalex-snapshot
Defective cuticle‐derived signals enhance extracellular ATP response and plant immunity
inferred← citeshttps://doi.org/10.1111/pbi.13650openalex-snapshot
A large‐scale genomic association analysis identifies a fragment in Dt11 chromosome conferring cotton Verticillium wilt resistance
inferred← citeshttps://doi.org/10.1111/pbi.70006openalex-snapshot
Extracellular ATP : an emerging multifaceted regulator of plant fitness
inferred← citeshttps://doi.org/10.1111/tpj.13807openalex-snapshot
Plant cell wall‐mediated immunity: cell wall changes trigger disease resistance responses
inferred← citeshttps://doi.org/10.1111/tpj.15636openalex-snapshot
Cyclic nucleotide‐gated ion channel 6 is involved in extracellular ATP signaling and plant immunity
inferred← citeshttps://doi.org/10.1111/tpj.16656openalex-snapshot
CPK28 is a modulator of purinergic signaling in plant growth and defense
inferred← citeshttps://doi.org/10.1111/tpj.70232openalex-snapshot
γ‐Aminobutyric acid modulates terpene biosynthesis through the ATG8a ‐mediated pathway
inferred← citeshttps://doi.org/10.1186/s12864-018-4606-0openalex-snapshot
Classification and phylogenetic analyses of the Arabidopsis and tomato G-type lectin receptor kinases
inferred← citeshttps://doi.org/10.1186/s12870-023-04300-0openalex-snapshot
The Arabidopsis thaliana onset of leaf death 12 mutation in the lectin receptor kinase P2K2 results in an autoimmune phenotype
inferred← citeshttps://doi.org/10.1186/s43897-025-00168-wopenalex-snapshot
Apyrase in horticultural crops: insights into growth, stress adaptation and quality regulation
inferred← citeshttps://doi.org/10.1199/tab.0188openalex-snapshot
Oomycetes Used in Arabidopsis Research.
inferred← citeshttps://doi.org/10.1360/ssv-2025-0334openalex-snapshot
Research progress on the release, degradation, perception and downstream signaling pathways of plant extracellular ATP
inferred← citeshttps://doi.org/10.1371/journal.ppat.1006433openalex-snapshot
L-type lectin receptor kinases: New forces in plant immunity
inferred← citeshttps://doi.org/10.1371/journal.ppat.1013664openalex-snapshot
A bacterial effector protein targets plant ferredoxin-NADP+ reductase to promote infection
inferred← citeshttps://doi.org/10.15252/embr.201847430openalex-snapshot
Serendipita indica E5′NT modulates extracellular nucleotide levels in the plant apoplast and affects fungal colonization
inferred← citeshttps://doi.org/10.20868/upm.thesis.68069openalex-snapshot
La proteína quinasa YODA regula respuestas de inmunidad y la resistencia a patógenos de Arabidopsis thaliana y tomate (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1252039openalex-snapshot
Plant immune receptors interact with hemibiotrophic pathogens to activate plant immunity
inferred← citeshttps://doi.org/10.3389/fpls.2017.01522openalex-snapshot
Heterotrimeric G Protein-Regulated Ca2+ Influx and PIN2 Asymmetric Distribution Are Involved in Arabidopsis thaliana Roots' Avoidance Response to Extracellular ATP
inferred← citeshttps://doi.org/10.3389/fpls.2019.00036openalex-snapshot
Messages From the Past: New Insights in Plant Lectin Evolution
inferred← citeshttps://doi.org/10.3389/fpls.2019.00623openalex-snapshot
The Arabidopsis Lectin Receptor Kinase LecRK-I.8 Is Involved in Insect Egg Perception
inferred← citeshttps://doi.org/10.3389/fpls.2020.00225openalex-snapshot
High Resolution Mapping of a Hordeum bulbosum-Derived Powdery Mildew Resistance Locus in Barley Using Distinct Homologous Introgression Lines
inferred← citeshttps://doi.org/10.3389/fpls.2020.572920openalex-snapshot
Purinoceptor P2K1/DORN1 Enhances Plant Resistance Against a Soilborne Fungal Pathogen, Rhizoctonia solani
inferred← citeshttps://doi.org/10.3389/fpls.2021.788514openalex-snapshot
Damage Signaling by Extracellular Nucleotides: A Role for Cyclic Nucleotides in Elevating Cytosolic Free Calcium?
inferred← citeshttps://doi.org/10.3389/fpls.2021.793989openalex-snapshot
Preharvest UV-C Hormesis Induces Key Genes Associated With Homeostasis, Growth and Defense in Lettuce Inoculated With Xanthomonas campestris pv. vitians
inferred← citeshttps://doi.org/10.3389/fpls.2022.1098146openalex-snapshot
Phosphate-deprivation and damage signalling by extracellular ATP
inferred← citeshttps://doi.org/10.3389/fpls.2022.963263openalex-snapshot
Genome-wide identification and functional exploration of the legume lectin genes in Brassica napus and their roles in Sclerotinia disease resistance
inferred← citeshttps://doi.org/10.3389/fpls.2023.1183335openalex-snapshot
A histochemical reporter system to study extracellular ATP response in plants
inferred← citeshttps://doi.org/10.3389/fpls.2023.1201805openalex-snapshot
Ligand recognition and signal transduction by lectin receptor-like kinases in plant immunity
inferred← citeshttps://doi.org/10.3389/fpls.2024.1372361openalex-snapshot
Unveiling orphan receptor-like kinases in plants: novel client discovery using high-confidence library predictions in the Kinase–Client (KiC) assay
inferred← citeshttps://doi.org/10.3390/agronomy11081672openalex-snapshot
VaCRK2 Mediates Gray Mold Resistance in Vitis amurensis by Activating the Jasmonate Signaling Pathway
inferred← citeshttps://doi.org/10.3390/agronomy9040188openalex-snapshot
Cereal Root Interactions with Soilborne Pathogens—From Trait to Gene and Back
inferred← citeshttps://doi.org/10.3390/cells9020345openalex-snapshot
New Insight into Plant Signaling: Extracellular ATP and Uncommon Nucleotides
inferred← citeshttps://doi.org/10.3390/ijms18061164openalex-snapshot
Plant Lectins and Lectin Receptor-Like Kinases: How Do They Sense the Outside?
inferred← citeshttps://doi.org/10.3390/ijms19030717openalex-snapshot
Comparative Transcriptome Profiling of Rice Near-Isogenic Line Carrying Xa23 under Infection of Xanthomonas oryzae pv. oryzae
inferred← citeshttps://doi.org/10.3390/ijms19113590openalex-snapshot
Role of Ca2+ in Mediating Plant Responses to Extracellular ATP and ADP
inferred← citeshttps://doi.org/10.3390/ijms24087417openalex-snapshot
Signals and Their Perception for Remodelling, Adjustment and Repair of the Plant Cell Wall
inferred← citeshttps://doi.org/10.3390/plants14121884openalex-snapshot
Comprehensive Genome-Wide Characterization of L-Type Lectin Receptor-like Kinase (L-LecRLK) Genes in Wheat (Triticum aestivum L.) and Their Response to Abiotic Stress
inferred← citeshttps://doi.org/10.3390/plants14152277openalex-snapshot
Identification of Auxin-Associated Genes in Wheat Through Comparative Transcriptome Analysis and Validation of the Candidate Receptor-like Kinase Gene TaPBL7-2B in Arabidopsis
inferred← citeshttps://doi.org/10.3390/stresses5030054openalex-snapshot
Selective and Mild Transcriptional Modulation of Lectin Genes in Soy Leaves Under Drought Stress
inferred← citeshttps://doi.org/10.36462/h.biosci.20219openalex-snapshot
blkn, a novel Medicago truncatula mutant achieving black nodule phenotype
inferred← citeshttps://doi.org/10.6084/m9.figshare.23280999openalex-snapshot
Additional file 1 of The Arabidopsis thaliana onset of leaf death 12 mutation in the lectin receptor kinase P2K2 results in an autoimmune phenotype
inferred← citeshttps://doi.org/10.70675/7ddf8cbcza3fbz4a03z8708zea2205094580openalex-snapshot
Étude fonctionnelle d'un récepteur lectine kinase, LecRK-I.9 : un contrôle de la dynamique des parois chez Arabidopsis thaliana
inferred← citeshttps://doi.org/10.70675/fa6f60bdzb6a5z41d8za5edz0913d0875eaeopenalex-snapshot
Identification du xyloglucane comme nouvel éliciteur oligosaccharidique stimulant l’immunité de Vitis vinifera et d’Arabidopsis thaliana et caractérisation de deux récepteurs aux chito-oligosaccharides chez la vigne (VvLYK1-1 et VvLYK1-2)
inferred← citeshttps://doi.org/10.7554/elife.92913openalex-snapshot
Soil-borne fungi alter the apoplastic purinergic signaling in plants by deregulating the homeostasis of extracellular ATP and its metabolite adenosine
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