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Mitogen activated protein kinases function as a cohort during a plant defense response
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/978-3-540-49166-8_6openalex-snapshot
Pathogen-Induced MAP Kinases in Tobacco
inferredcites →https://doi.org/10.1007/978-3-642-86659-3openalex-snapshot
Evolution by Gene Duplication
inferredcites →https://doi.org/10.1007/s00299-013-1389-2openalex-snapshot
OsMPK3 positively regulates the JA signaling pathway and plant resistance to a chewing herbivore in rice
inferredcites →https://doi.org/10.1007/s00299-015-1901-yopenalex-snapshot
PAD4, LSD1 and EDS1 regulate drought tolerance, plant biomass production, and cell wall properties
inferredcites →https://doi.org/10.1007/s00299-016-1955-5openalex-snapshot
Erratum to: PAD4, LSD1 and EDS1 regulate drought tolerance, plant biomass production, and cell wall properties
inferredcites →https://doi.org/10.1007/s00425-007-0578-zopenalex-snapshot
Laser capture microdissection (LCM) and comparative microarray expression analysis of syncytial cells isolated from incompatible and compatible soybean (Glycine max) roots infected by the soybean cyst nematode (Heterodera glycines)
inferredcites →https://doi.org/10.1007/s00425-007-0581-4openalex-snapshot
A time-course comparative microarray analysis of an incompatible and compatible response by Glycine max (soybean) to Heterodera glycines (soybean cyst nematode) infection
inferredcites →https://doi.org/10.1007/s00425-009-0926-2openalex-snapshot
A correlation between host-mediated expression of parasite genes as tandem inverted repeats and abrogation of development of female Heterodera glycines cyst formation during infection of Glycine max
inferredcites →https://doi.org/10.1007/s00425-013-1840-1openalex-snapshot
Engineered resistance and hypersusceptibility through functional metabolic studies of 100 genes in soybean to its major pathogen, the soybean cyst nematode
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/10.1007/s00709-017-1157-1openalex-snapshot
Involvement of metabolic components, volatile compounds, PR proteins, and mechanical strengthening in multilayer protection of cucumber plants against Rhizoctonia solani activated by Trichoderma atroviride TRS25
inferredcites →https://doi.org/10.1007/s10142-012-0278-zopenalex-snapshot
Co-expression of soybean Dicer-like genes in response to stress and development
inferredcites →https://doi.org/10.1007/s10142-013-0349-9openalex-snapshot
Genome-wide identification and expression analysis of the mitogen-activated protein kinase gene family from banana suggest involvement of specific members in different stages of fruit ripening
inferredcites →https://doi.org/10.1007/s11103-009-9539-1openalex-snapshot
A gene expression analysis of syncytia laser microdissected from the roots of the Glycine max (soybean) genotype PI 548402 (Peking) undergoing a resistant reaction after infection by Heterodera glycines (soybean cyst nematode)
inferredcites →https://doi.org/10.1007/s11103-010-9715-3openalex-snapshot
Differences in gene expression amplitude overlie a conserved transcriptomic program occurring between the rapid and potent localized resistant reaction at the syncytium of the Glycine max genotype Peking (PI 548402) as compared to the prolonged and potent resistant reaction of PI 88788
inferredcites →https://doi.org/10.1007/s11103-011-9828-3openalex-snapshot
Mapping cell fate decisions that occur during soybean defense responses
inferredcites →https://doi.org/10.1007/s11103-012-9932-zopenalex-snapshot
The expression of a naturally occurring, truncated allele of an α-SNAP gene suppresses plant parasitic nematode infection
inferredcites →https://doi.org/10.1007/s11103-014-0172-2openalex-snapshot
Syntaxin 31 functions in Glycine max resistance to the plant parasitic nematode Heterodera glycines
inferredcites →https://doi.org/10.1007/s11103-015-0391-1openalex-snapshot
Functional analysis of NtMPK2 uncovers its positive role in response to Pseudomonas syringae pv. tomato DC3000 in tobacco
inferredcites →https://doi.org/10.1007/s11240-007-9323-3openalex-snapshot
MiniMax, a new diminutive Glycine max genotype with a rapid life cycle, embryogenic potential and transformation capabilities
inferredcites →https://doi.org/10.1016/0003-9861(89)90120-3openalex-snapshot
Interaction of folylpolyglutamates with enzymes in one-carbon metabolism
inferredcites →https://doi.org/10.1016/0092-8674(80)90128-2openalex-snapshot
Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway
inferredcites →https://doi.org/10.1016/0092-8674(84)90430-6openalex-snapshot
Transformation of several species of higher plants by agrobacterium rhizogenes: Sexual transmission of the transformed genotype and phenotype
inferredcites →https://doi.org/10.1016/0092-8674(90)90482-topenalex-snapshot
SNAPs, a family of NSF attachment proteins involved in intracellular membrane fusion in animals and yeast
inferredcites →https://doi.org/10.1016/0092-8674(94)90218-6openalex-snapshot
Arabidopsis mutants simulating disease resistance response
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.2009.05.019openalex-snapshot
Regulation of Cell Death and Innate Immunity by Two Receptor-like Kinases in Arabidopsis
inferredcites →https://doi.org/10.1016/j.chom.2010.03.007openalex-snapshot
Receptor-like Cytoplasmic Kinases Integrate Signaling from Multiple Plant Immune Receptors and Are Targeted by a Pseudomonas syringae Effector
inferredcites →https://doi.org/10.1016/j.chom.2012.01.015openalex-snapshot
Disruption of PAMP-Induced MAP Kinase Cascade by a Pseudomonas syringae Effector Activates Plant Immunity Mediated by the NB-LRR Protein SUMM2
inferredcites →https://doi.org/10.1016/j.chom.2014.09.004openalex-snapshot
A Plant Phosphoswitch Platform Repeatedly Targeted by Type III Effector Proteins Regulates the Output of Both Tiers of Plant Immune Receptors
inferredcites →https://doi.org/10.1016/j.chom.2017.03.005openalex-snapshot
Matching NLR Immune Receptors to Autoimmunity in camta3 Mutants Using Antimorphic NLR Alleles
inferredcites →https://doi.org/10.1016/j.ejcb.2009.11.001openalex-snapshot
The multifunctional leucine-rich repeat receptor kinase BAK1 is implicated in Arabidopsis development and immunity
inferredcites →https://doi.org/10.1016/j.febslet.2007.05.083openalex-snapshot
Genetic interaction and phenotypic analysis of the Arabidopsis MAP kinase pathway mutations mekk1 and mpk4 suggests signaling pathway complexity
inferredcites →https://doi.org/10.1016/j.molcel.2011.02.029openalex-snapshot
Calmodulin-Dependent Activation of MAP Kinase for ROS Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1016/j.pbi.2005.05.010openalex-snapshot
Plant immunity: the EDS1 regulatory node
inferredcites →https://doi.org/10.1016/j.pbi.2010.04.007openalex-snapshot
NB-LRR proteins: pairs, pieces, perception, partners, and pathways
inferredcites →https://doi.org/10.1016/j.plaphy.2009.12.003openalex-snapshot
Syncytium gene expression in Glycine max[PI 88788] roots undergoing a resistant reaction to the parasitic nematode Heterodera glycines
inferredcites →https://doi.org/10.1016/j.plaphy.2017.02.022openalex-snapshot
A Glycine max homolog of NON-RACE SPECIFIC DISEASE RESISTANCE 1 (NDR1) alters defense gene expression while functioning during a resistance response to different root pathogens in different genetic backgrounds
inferredcites →https://doi.org/10.1016/j.plaphy.2017.10.004openalex-snapshot
A harpin elicitor induces the expression of a coiled-coil nucleotide binding leucine rich repeat (CC-NB-LRR) defense signaling gene and others functioning during defense to parasitic nematodes
inferredcites →https://doi.org/10.1016/j.tplants.2009.12.001openalex-snapshot
Convergence and specificity in the Arabidopsis MAPK nexus
inferredcites →https://doi.org/10.1016/s0006-291x(86)80457-0openalex-snapshot
Muscle proteins related to microtubule associated protein-2 are substrates for an insulin-stimulatable kinase
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)80357-8openalex-snapshot
A Putative Leucine-Rich Repeat Receptor Kinase Involved in Brassinosteroid Signal Transduction
inferredcites →https://doi.org/10.1016/s0092-8674(00)80993-9openalex-snapshot
Cytokinesis in the Arabidopsis Embryo Involves the Syntaxin-Related KNOLLE Gene Product
inferredcites →https://doi.org/10.1016/s0092-8674(00)81911-xopenalex-snapshot
A Novel Zinc Finger Protein Is Encoded by the Arabidopsis LSD1 Gene and Functions as a Negative Regulator of Plant Cell Death
inferredcites →https://doi.org/10.1016/s0092-8674(02)00661-xopenalex-snapshot
RIN4 Interacts with Pseudomonas syringae Type III Effector Molecules and Is Required for RPM1-Mediated Resistance in Arabidopsis
inferredcites →https://doi.org/10.1016/s0092-8674(02)00812-7openalex-snapshot
BAK1, an Arabidopsis LRR Receptor-like Protein Kinase, Interacts with BRI1 and Modulates Brassinosteroid Signaling
inferredcites →https://doi.org/10.1016/s0092-8674(02)00814-0openalex-snapshot
BRI1/BAK1, a Receptor Kinase Pair Mediating Brassinosteroid Signaling
inferredcites →https://doi.org/10.1016/s0092-8674(03)00036-9openalex-snapshot
Initiation of RPS2-Specified Disease Resistance in Arabidopsis Is Coupled to the AvrRpt2-Directed Elimination of RIN4
inferredcites →https://doi.org/10.1016/s0092-8674(03)00040-0openalex-snapshot
Arabidopsis RIN4 Is a Target of the Type III Virulence Effector AvrRpt2 and Modulates RPS2-Mediated Resistance
inferredcites →https://doi.org/10.1016/s1360-1385(01)02103-3openalex-snapshot
MAPK cascades in plant defense signaling
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/s1369-5266(02)00285-6openalex-snapshot
Complexity, Cross Talk and Integration of Plant MAP Kinase Signalling
inferredcites →https://doi.org/10.1038/343651a0openalex-snapshot
Requirement for integration of signals from two distinct phosphorylation pathways for activation of MAP kinase
inferredcites →https://doi.org/10.1038/35048507openalex-snapshot
Sequence and analysis of chromosome 5 of the plant Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/35107108openalex-snapshot
Isochorismate synthase is required to synthesize salicylic acid for plant defence
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/cr.2008.300openalex-snapshot
MEKK1, MKK1/MKK2 and MPK4 function together in a mitogen-activated protein kinase cascade to regulate innate immunity in plants
inferredcites →https://doi.org/10.1038/emboj.2008.147openalex-snapshot
Arabidopsis MAP kinase 4 regulates gene expression through transcription factor release in the nucleus
inferredcites →https://doi.org/10.1038/emboj.2008.37openalex-snapshot
Munc18a controls SNARE assembly through its interaction with the syntaxin N‐peptide
inferredcites →https://doi.org/10.1038/nature02076openalex-snapshot
SNARE-protein-mediated disease resistance at the plant cell wall
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/nature06151openalex-snapshot
Gene duplication and the adaptive evolution of a classic genetic switch
inferredcites →https://doi.org/10.1038/nature08670openalex-snapshot
Genome sequence of the palaeopolyploid soybean
inferredcites →https://doi.org/10.1038/nmeth.1701openalex-snapshot
SignalP 4.0: discriminating signal peptides from transmembrane regions
inferredcites →https://doi.org/10.1038/nrg928openalex-snapshot
Splitting pairs: the diverging fates of duplicated genes
inferredcites →https://doi.org/10.1038/nrm715openalex-snapshot
MAPK-regulated transcription: a continuously variable gene switch?
inferredcites →https://doi.org/10.1038/sj.emboj.7601312openalex-snapshot
bZIP10‐LSD1 antagonism modulates basal defense and cell death in Arabidopsis following infection
inferredcites →https://doi.org/10.1038/srep28306openalex-snapshot
Comparative proteomic study of Arabidopsis mutants mpk4 and mpk6
inferredcites →https://doi.org/10.1038/srep30050openalex-snapshot
Molecular evolution and expression divergence of the Populus euphratica Hsf genes provide insight into the stress acclimation of desert poplar
inferredcites →https://doi.org/10.1042/bj20141176openalex-snapshot
Activation of AtMPK9 through autophosphorylation that makes it independent of the canonical MAPK cascades
inferredcites →https://doi.org/10.1042/bj2820821openalex-snapshot
Xyloglucan endotransglycosylase, a new wall-loosening enzyme activity from plants
inferredcites →https://doi.org/10.1042/bj3300115openalex-snapshot
Harpin and hydrogen peroxide both initiate programmed cell death but have differential effects on defence gene expression in Arabidopsis suspension cultures
inferredcites →https://doi.org/10.1046/j.0960-7412.2001.01225.xopenalex-snapshot
Runaway cell death, but not basal disease resistance, in lsd1 is SA‐ and NIM1/NPR1‐dependent
inferredcites →https://doi.org/10.1046/j.0960-7412.2001.01227.xopenalex-snapshot
Important roles of drought‐ and cold‐inducible genes for galactinol synthase in stress tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.0960-7412.2001.01229.xopenalex-snapshot
Arabidopsis RPP4 is a member of the RPP5 multigene family of TIR‐NB‐LRR genes and confers downy mildew resistance through multiple signalling components
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.10040591.xopenalex-snapshot
hrp gene‐dependent induction of hin1: a plant gene activated rapidly by both harpins and the avrPto gene‐mediated signal
inferredcites →https://doi.org/10.1073/pnas.0500792102openalex-snapshot
The Pseudomonas syringae effector AvrRpt2 cleaves its C-terminally acylated target, RIN4, from Arabidopsis membranes to block RPM1 activation
inferredcites →https://doi.org/10.1073/pnas.0700344104openalex-snapshot
Tomato MAPKs LeMPK1, LeMPK2, and LeMPK3 function in the systemin-mediated defense response against herbivorous insects
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.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.0909705107openalex-snapshot
A receptor-like cytoplasmic kinase, BIK1, associates with a flagellin receptor complex to initiate plant innate immunity
inferredcites →https://doi.org/10.1073/pnas.1003619107openalex-snapshot
A regulon conserved in monocot and dicot plants defines a functional module in antifungal plant immunity
inferredcites →https://doi.org/10.1073/pnas.1130421100openalex-snapshot
Antagonistic control of oxidative stress-induced cell death in Arabidopsis by two related, plant-specific zinc finger proteins
inferredcites →https://doi.org/10.1073/pnas.1215543110openalex-snapshot
BIK1 interacts with PEPRs to mediate ethylene-induced immunity
inferredcites →https://doi.org/10.1073/pnas.1302154110openalex-snapshot
Inverse modulation of plant immune and brassinosteroid signaling pathways by the receptor-like cytoplasmic kinase BIK1
inferredcites →https://doi.org/10.1073/pnas.1318817111openalex-snapshot
Tyrosine phosphorylation of protein kinase complex BAK1/BIK1 mediates Arabidopsis innate immunity
inferredcites →https://doi.org/10.1073/pnas.1511182112openalex-snapshot
Spatial and temporal regulation of biosynthesis of the plant immune signal salicylic acid
inferredcites →https://doi.org/10.1073/pnas.86.18.6940openalex-snapshot
Evidence that pp42, a major tyrosine kinase target protein, is a mitogen-activated serine/threonine protein kinase.
inferredcites →https://doi.org/10.1073/pnas.92.14.6597openalex-snapshot
NDR1, a locus of Arabidopsis thaliana that is required for disease resistance to both a bacterial and a fungal pathogen.
inferredcites →https://doi.org/10.1073/pnas.93.19.10078openalex-snapshot
Ultrasensitivity in the mitogen-activated protein kinase cascade.
inferredcites →https://doi.org/10.1073/pnas.94.6.2122openalex-snapshot
Removal of a cryptic intron and subcellular localization of green fluorescent protein are required to mark transgenic Arabidopsis plants brightly
inferredcites →https://doi.org/10.1073/pnas.95.17.10306openalex-snapshot
Different requirements for EDS1 and NDR1 by disease resistance genes define at least two R gene-mediated signaling pathways in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.96.6.3292openalex-snapshot
EDS1 , an essential component of R gene-mediated disease resistance in Arabidopsis has homology to eukaryotic lipases
inferredcites →https://doi.org/10.1074/jbc.275.11.7521openalex-snapshot
Microbial Elicitors Induce Activation and Dual Phosphorylation of the Arabidopsis thaliana MAPK 6
inferredcites →https://doi.org/10.1074/jbc.m114.617274openalex-snapshot
Members of the Plant CRK Superfamily Are Capable of Trans- and Autophosphorylation of Tyrosine Residues
inferredcites →https://doi.org/10.1074/jbc.m909267199openalex-snapshot
Tobacco Transcription Factor TGA2.2 Is the Main Component of as-1-binding Factor ASF-1 and Is Involved in Salicylic Acid- and Auxin-inducible Expression of as-1-containing Target Promoters
inferredcites →https://doi.org/10.1080/15592324.2016.1274481openalex-snapshot
Components of the SNARE-containing regulon are co-regulated in root cells undergoing defense
inferredcites →https://doi.org/10.1080/15592324.2017.1356533openalex-snapshot
Constitutive activity of the Arabidopsis MAP Kinase 3 confers resistance to Pseudomonas syringae and drives robust immune responses
inferredcites →https://doi.org/10.1080/17429145.2016.1195891openalex-snapshot
Co-regulation of theGlycine maxsoluble N-ethylmaleimide-sensitive fusion protein attachment protein receptor (SNARE)-containing regulon occurs during defense to a root pathogen
inferredcites →https://doi.org/10.1083/jcb.109.6.3039openalex-snapshot
The identification of a novel synaptosomal-associated protein, SNAP-25, differentially expressed by neuronal subpopulations.
inferredcites →https://doi.org/10.1083/jcb.200107126openalex-snapshot
Functional characterization of the KNOLLE-interacting t-SNARE AtSNAP33 and its role in plant cytokinesis
inferredcites →https://doi.org/10.1091/mbc.e04-02-0140openalex-snapshot
The PEN1 Syntaxin Defines a Novel Cellular Compartment upon Fungal Attack and Is Required for the Timely Assembly of Papillae
inferredcites →https://doi.org/10.1093/jxb/erq227openalex-snapshot
Transcriptome analysis of Hpa1Xoo transformed cotton revealed constitutive expression of genes in multiple signalling pathways related to disease resistance
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/10.1093/jxb/ert368openalex-snapshot
Arabidopsis thaliana mitogen-activated protein kinase 6 is involved in seed formation and modulation of primary and lateral root development
inferredcites →https://doi.org/10.1093/jxb/erv440openalex-snapshot
Plant resistance against the parasitic nematodeHeterodera schachtiiis mediated by MPK3 and MPK6 kinases, which are controlled by the MAPK phosphatase AP2C1 in Arabidopsis
inferredcites →https://doi.org/10.1093/nar/gkh378openalex-snapshot
PrediSi: prediction of signal peptides and their cleavage positions
inferredcites →https://doi.org/10.1093/nar/gkm256openalex-snapshot
Advantages of combined transmembrane topology and signal peptide prediction--the Phobius web server
inferredcites →https://doi.org/10.1093/nar/gkp798openalex-snapshot
SoyBase, the USDA-ARS soybean genetics and genomics database
inferredcites →https://doi.org/10.1093/nar/gkr944openalex-snapshot
Phytozome: a comparative platform for green plant genomics
inferredcites →https://doi.org/10.1093/pcp/pce123openalex-snapshot
Oxidative Stress Activates ATMPK6, an Arabidopsis Homologue of MAP Kinase
inferredcites →https://doi.org/10.1094/mpmi-07-10-0150openalex-snapshot
Bacterial Effector HopF2 Suppresses Arabidopsis Innate Immunity at the Plasma Membrane
inferredcites →https://doi.org/10.1094/mpmi-11-11-0281openalex-snapshot
Activation of the Arabidopsis thaliana Mitogen-Activated Protein Kinase MPK11 by the Flagellin-Derived Elicitor Peptide, flg22
inferredcites →https://doi.org/10.1094/mpmi-11-13-0350-ropenalex-snapshot
Positive and Negative Roles for Soybean MPK6 in Regulating Defense Responses
inferredcites →https://doi.org/10.1094/mpmi-19-0530openalex-snapshot
Molecular Analysis of the Rice MAP Kinase Gene Family in Relation to Magnaporthe grisea Infection
inferredcites →https://doi.org/10.1094/mpmi-22-3-0235openalex-snapshot
Overexpression of Brassica napus MPK4 Enhances Resistance to Sclerotinia sclerotiorum in Oilseed Rape
inferredcites →https://doi.org/10.1094/mpmi-23-7-0940openalex-snapshot
Effector-Triggered and Pathogen-Associated Molecular Pattern–Triggered Immunity Differentially Contribute to Basal Resistance to Pseudomonas syringae
inferredcites →https://doi.org/10.1094/mpmi.1999.12.11.1022openalex-snapshot
LSD1 Regulates Salicylic Acid Induction of Copper Zinc Superoxide Dismutase in Arabidopsis thaliana
inferredcites →https://doi.org/10.1094/mpmi.2001.14.10.1131openalex-snapshot
Activation of an EDS1-Mediated R -Gene Pathway in the snc1 Mutant Leads to Constitutive, NPR1-Independent Pathogen Resistance
inferredcites →https://doi.org/10.1104/pp.103.027979openalex-snapshot
A Gateway Cloning Vector Set for High-Throughput Functional Analysis of Genes in Planta
inferredcites →https://doi.org/10.1104/pp.103.038059openalex-snapshot
Biosynthesis of the Nitrile Glucosides Rhodiocyanoside A and D and the Cyanogenic Glucosides Lotaustralin and Linamarin in Lotus japonicus
inferredcites →https://doi.org/10.1104/pp.104.043646openalex-snapshot
LESION SIMULATING DISEASE 1 Is Required for Acclimation to Conditions That Promote Excess Excitation Energy
inferredcites →https://doi.org/10.1104/pp.106.080697openalex-snapshot
Activation of Ntf4, a Tobacco Mitogen-Activated Protein Kinase, during Plant Defense Response and Its Involvement in Hypersensitive Response-Like Cell Death
inferredcites →https://doi.org/10.1104/pp.106.082107openalex-snapshot
Characterization of a Mitogen-Activated Protein Kinase Gene from Cucumber Required for Trichoderma-Conferred Plant Resistance
inferredcites →https://doi.org/10.1104/pp.106.095299openalex-snapshot
Genetic Interactions of TGA Transcription Factors in the Regulation of Pathogenesis-Related Genes and Disease Resistance in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.157610openalex-snapshot
A Gain-of-Function Mutation in the Arabidopsis Disease Resistance Gene RPP4 Confers Sensitivity to Low Temperature
inferredcites →https://doi.org/10.1104/pp.111.174003openalex-snapshot
Arabidopsis MPK3 and MPK6 Play Different Roles in Basal and Oligogalacturonide- or Flagellin-Induced Resistance against Botrytis cinerea
inferredcites →https://doi.org/10.1104/pp.111.185686openalex-snapshot
Soybean Homologs of MPK4 Negatively Regulate Defense Responses and Positively Regulate Growth and Development
inferredcites →https://doi.org/10.1104/pp.112.208116openalex-snapshot
LESION SIMULATING DISEASE1, ENHANCED DISEASE SUSCEPTIBILITY1, and PHYTOALEXIN DEFICIENT4 Conditionally Regulate Cellular Signaling Homeostasis, Photosynthesis, Water Use Efficiency, and Seed Yield in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.114.245944openalex-snapshot
Distinct Roles for Mitogen-Activated Protein Kinase Signaling and CALMODULIN-BINDING TRANSCRIPTIONAL ACTIVATOR3 in Regulating the Peak Time and Amplitude of the Plant General Stress Response
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/10.1104/pp.17.00378openalex-snapshot
Constitutively Active Arabidopsis MAP Kinase 3 Triggers Defense Responses Involving Salicylic Acid and SUMM2 Resistance Protein
inferredcites →https://doi.org/10.1105/tpc.008714openalex-snapshot
Disease Resistance and Abiotic Stress Tolerance in Rice Are Inversely Modulated by an Abscisic Acid–Inducible Mitogen-Activated Protein Kinase[W]
inferredcites →https://doi.org/10.1105/tpc.010085openalex-snapshot
The Disease Resistance Signaling Components EDS1 and PAD4 Are Essential Regulators of the Cell Death Pathway Controlled by LSD1 in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.015842openalex-snapshot
A Gain-of-Function Mutation in a Plant Disease Resistance Gene Leads to Constitutive Activation of Downstream Signal Transduction Pathways in suppressor of npr1-1 , constitutive 1
inferredcites →https://doi.org/10.1105/tpc.104.024117openalex-snapshot
Arabidopsis RIN4 Negatively Regulates Disease Resistance Mediated by RPS2 and RPM1 Downstream or Independent of the NDR1 Signal Modulator and Is Not Required for the Virulence Functions of Bacterial Type III Effectors AvrRpt2 or AvrRpm1
inferredcites →https://doi.org/10.1105/tpc.105.035576openalex-snapshot
The Membrane-Anchored BOTRYTIS-INDUCED KINASE1 Plays Distinct Roles in Arabidopsis Resistance to Necrotrophic and Biotrophic Pathogens
inferredcites →https://doi.org/10.1105/tpc.105.038372openalex-snapshot
ArabidopsisPEN3/PDR8, an ATP Binding Cassette Transporter, Contributes to Nonhost Resistance to Inappropriate Pathogens That Enter by Direct Penetration
inferredcites →https://doi.org/10.1105/tpc.105.039982openalex-snapshot
Salicylic Acid–Independent ENHANCED DISEASE SUSCEPTIBILITY1 Signaling in Arabidopsis Immunity and Cell Death Is Regulated by the Monooxygenase FMO1 and the Nudix Hydrolase NUDT7
inferredcites →https://doi.org/10.1105/tpc.106.044693openalex-snapshot
NDR1 Interaction with RIN4 Mediates the Differential Activation of Multiple Disease Resistance Pathways in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.048843openalex-snapshot
Lysigenous Aerenchyma Formation in Arabidopsis Is Controlled by LESION SIMULATING DISEASE1
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.108.059618openalex-snapshot
Chloroplast Signaling andLESION SIMULATING DISEASE1Regulate Crosstalk between Light Acclimation and Immunity inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.11.12.2419openalex-snapshot
Arabidopsis PAD3 , a Gene Required for Camalexin Biosynthesis, Encodes a Putative Cytochrome P450 Monooxygenase
inferredcites →https://doi.org/10.1105/tpc.110.077164openalex-snapshot
The MAP Kinase MPK4 Is Required for Cytokinesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.110.082602openalex-snapshot
Of PAMPs and Effectors: The Blurred PTI-ETI Dichotomy
inferredcites →https://doi.org/10.1105/tpc.111.084301openalex-snapshot
The Arabidopsis Leucine-Rich Repeat Receptor–Like Kinases BAK1/SERK3 and BKK1/SERK4 Are Required for Innate Immunity to Hemibiotrophic and Biotrophic Pathogens
inferredcites →https://doi.org/10.1105/tpc.112.101253openalex-snapshot
Constitutively Active Mitogen-Activated Protein Kinase Versions Reveal Functions of Arabidopsis MPK4 in Pathogen Defense Signaling
inferredcites →https://doi.org/10.1105/tpc.114.131185openalex-snapshot
Quantitative Peptidomics Study Reveals That a Wound-Induced Peptide from PR-1 Regulates Immune Signaling in Tomato
inferredcites →https://doi.org/10.1105/tpc.13.10.2211openalex-snapshot
The Disease Resistance Signaling Components EDS1 and PAD4 Are Essential Regulators of the Cell Death Pathway Controlled by LSD1 in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.5.1079openalex-snapshot
A Harpin Binding Site in Tobacco Plasma Membranes Mediates Activation of the Pathogenesis-Related Gene HIN1 Independent of Extracellular Calcium but Dependent on Mitogen-Activated Protein Kinase Activity
inferredcites →https://doi.org/10.1105/tpc.5.8.865openalex-snapshot
RPS2, an Arabidopsis disease resistance locus specifying recognition of Pseudomonas syringae strains expressing the avirulence gene avrRpt2.
inferredcites →https://doi.org/10.1105/tpc.6.11.1583openalex-snapshot
Characterization of an Arabidopsis Mutant That Is Nonresponsive to Inducers of Systemic Acquired Resistance.
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02382.xopenalex-snapshot
SIPK signaling controls multiple components of harpin‐induced cell death in tobacco
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02454.xopenalex-snapshot
Ex vitro composite plants: an inexpensive, rapid method for root biology
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.2006.02961.xopenalex-snapshot
A SNARE‐protein has opposing functions in penetration resistance and defence signalling pathways
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03369.xopenalex-snapshot
Interplay between MAMP‐triggered and SA‐mediated defense responses
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04318.xopenalex-snapshot
Mitogen-activated protein kinase 3 and 6 regulate Botrytis cinerea-induced ethylene production in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1432-0436.1987.tb00154.xopenalex-snapshot
HLAMP – a conjugate of hippuryllysine and AMP which contains a phosphoamide bond – stimulates chemotaxis in Dictyostelium discoideum
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03275.xopenalex-snapshot
The Arabidopsis LSD1 gene plays an important role in the regulation of low temperature‐dependent cell death
inferredcites →https://doi.org/10.1111/nph.13821openalex-snapshot
TNL ‐mediated immunity in A rabidopsis requires complex regulation of the redundant ADR 1 gene family
inferredcites →https://doi.org/10.1111/nph.14216openalex-snapshot
Temperature‐dependent autoimmunity mediated by chs1 requires its neighboring TNL gene SOC 3
inferredcites →https://doi.org/10.1111/nph.14842openalex-snapshot
A cerato‐platanin protein SsCP1 targets plant PR1 and contributes to virulence of Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1111/nph.14943openalex-snapshot
A dominant‐interfering camta3 mutation compromises primary transcriptional outputs mediated by both cell surface and intracellular immune receptors in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/pce.12288openalex-snapshot
LESION SIMULATING DISEASE 1 and ENHANCED DISEASE SUSCEPTIBILITY 1 differentially regulate UV ‐ C ‐induced photooxidative stress signalling and programmed cell death in A rabidopsis thaliana
inferredcites →https://doi.org/10.1111/pce.12994openalex-snapshot
The dual role of LESION SIMULATING DISEASE 1 as a condition‐dependent scaffold protein and transcription regulator
inferredcites →https://doi.org/10.1111/tpj.12381openalex-snapshot
The P seudomonas syringae effector HopF2 suppresses Arabidopsis immunity by targeting BAK 1
inferredcites →https://doi.org/10.1111/tpj.12571openalex-snapshot
Role of the penetration‐resistance genes PEN 1, PEN 2 and PEN 3 in the hypersensitive response and race‐specific resistance in A rabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.12707openalex-snapshot
Insect eggs induce a systemic acquired resistance in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.13012openalex-snapshot
Identification and genome organization of saponin pathway genes from a wild crucifer, and their use for transient production of saponins in Nicotiana benthamiana
inferredcites →https://doi.org/10.1126/science.1119409openalex-snapshot
Pre- and Postinvasion Defenses Both Contribute to Nonhost Resistance in Arabidopsis
inferredcites →https://doi.org/10.1126/science.1203877openalex-snapshot
Evidence for Network Evolution in an Arabidopsis Interactome Map
inferredcites →https://doi.org/10.1126/science.1211641openalex-snapshot
Arabidopsis EDS1 Connects Pathogen Effector Recognition to Cell Compartment–Specific Immune Responses
inferredcites →https://doi.org/10.1126/science.1228746openalex-snapshot
Copy Number Variation of Multiple Genes at Rhg1 Mediates Nematode Resistance in Soybean
inferredcites →https://doi.org/10.1126/science.1250322openalex-snapshot
A Chloroplast Retrograde Signal Regulates Nuclear Alternative Splicing
inferredcites →https://doi.org/10.1126/science.1621099openalex-snapshot
Harpin, Elicitor of the Hypersensitive Response Produced by the Plant Pathogen Erwinia amylovora
inferredcites →https://doi.org/10.1126/science.273.5283.1853openalex-snapshot
Initiation of Runaway Cell Death in an Arabidopsis Mutant by Extracellular Superoxide
inferredcites →https://doi.org/10.1126/science.274.5294.1853openalex-snapshot
The Metal-Insulator Transition in Correlated Disordered Systems
inferredcites →https://doi.org/10.1126/science.278.5345.1963openalex-snapshot
NDR1 , a Pathogen-Induced Component Required for Arabidopsis Disease Resistance
inferredcites →https://doi.org/10.1126/science.290.5494.1151openalex-snapshot
The Evolutionary Fate and Consequences of Duplicate Genes
inferredcites →https://doi.org/10.1126/science.7638602openalex-snapshot
Structure of the Arabidopsis RPM1 Gene Enabling Dual Specificity Disease Resistance
inferredcites →https://doi.org/10.1128/aem.61.8.2879-2884.1995openalex-snapshot
Universal PCR primers for detection of phytopathogenic Agrobacterium strains
inferredcites →https://doi.org/10.1128/jb.175.24.7958-7967.1993openalex-snapshot
HrpI of Erwinia amylovora functions in secretion of harpin and is a member of a new protein family
inferredcites →https://doi.org/10.1128/jb.180.19.5211-5217.1998openalex-snapshot
The Pseudomonas syringae pv. tomato HrpW Protein Has Domains Similar to Harpins and Pectate Lyases and Can Elicit the Plant Hypersensitive Response and Bind to Pectate
inferredcites →https://doi.org/10.1139/g96-123openalex-snapshot
Cytological expression of early response to infection by Heterodera glycines Ichinohe in resistant PI 437654 soybean
inferredcites →https://doi.org/10.1146/annurev.phyto.050908.135202openalex-snapshot
Salicylic Acid, a Multifaceted Hormone to Combat Disease
inferredcites →https://doi.org/10.1155/2010/491217openalex-snapshot
Microarray Detection Call Methodology as a Means to Identify and Compare Transcripts Expressed within Syncytial Cells from Soybean (Glycine max) Roots Undergoing Resistant and Susceptible Reactions to the Soybean Cyst Nematode (Heterodera glycines)
inferredcites →https://doi.org/10.1186/1471-2105-7-85openalex-snapshot
Statistical analysis of real-time PCR data
inferredcites →https://doi.org/10.1186/gb-2014-15-6-r87openalex-snapshot
Functional analysis of Arabidopsisimmune-related MAPKs uncovers a role for MPK3 as negative regulator of inducible defences
inferredcites →https://doi.org/10.1186/s12864-015-1244-7openalex-snapshot
Identification of new members of the MAPK gene family in plants shows diverse conserved domains and novel activation loop variants
inferredcites →https://doi.org/10.1186/s12864-016-2460-5openalex-snapshot
A rice LSD1-like-type ZFP gene OsLOL5 enhances saline-alkaline tolerance in transgenic Arabidopsis thaliana, yeast and rice
inferredcites →https://doi.org/10.1214/aoms/1177730491openalex-snapshot
On a Test of Whether one of Two Random Variables is Stochastically Larger than the Other
inferredcites →https://doi.org/10.1242/jcs.202838openalex-snapshot
Signal motif-dependent ER export of the Qc-SNARE BET12 interacts with MEMB12 and affects PR1 trafficking in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pgen.1002046openalex-snapshot
Phosphorylation-Dependent Differential Regulation of Plant Growth, Cell Death, and Innate Immunity by the Regulatory Receptor-Like Kinase BAK1
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