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MYC2 influences salicylic acid biosynthesis and defense against bacterial pathogens in Arabidopsis thaliana
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9781118867716openalex-snapshot
Plant Pathogen Resistance Biotechnology
inferredcites →https://doi.org/10.1002/9781118867716.ch3openalex-snapshot
Application of Antimicrobial Proteins and Peptides in Developing Disease‐Resistant Plants
inferredcites →https://doi.org/10.1002/embj.201284303openalex-snapshot
The Arabidopsis PEPR pathway couples local and systemic plant immunity
inferredcites →https://doi.org/10.1007/s00425-004-1272-zopenalex-snapshot
Light conditions influence specific defence responses in incompatible plant?pathogen interactions: uncoupling systemic resistance from salicylic acid and PR-1 accumulation
inferredcites →https://doi.org/10.1007/s00425-010-1265-zopenalex-snapshot
Salicylate-mediated suppression of jasmonate-responsive gene expression in Arabidopsis is targeted downstream of the jasmonate biosynthesis pathway
inferredcites →https://doi.org/10.1007/s12038-014-9498-9openalex-snapshot
Identification of plant defence regulators through transcriptional profiling of Arabidopsis thaliana cdd1 mutant
inferredcites →https://doi.org/10.1007/s12038-017-9703-8openalex-snapshot
Rice MYC2 (OsMYC2) modulates light-dependent seedling phenotype, disease defence but not ABA signalling
inferredcites →https://doi.org/10.1016/j.chom.2011.01.009openalex-snapshot
Specific Threonine Phosphorylation of a Host Target by Two Unrelated Type III Effectors Activates a Host Innate Immune Receptor in Plants
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.febslet.2011.04.039openalex-snapshot
Salicylic acid and its location in response to biotic and abiotic stress
inferredcites →https://doi.org/10.1016/j.it.2014.05.004openalex-snapshot
Plant pattern-recognition receptors
inferredcites →https://doi.org/10.1016/j.jplph.2013.12.015openalex-snapshot
The Arabidopsis thaliana At4g13040 gene, a unique member of the AP2/EREBP family, is a positive regulator for salicylic acid accumulation and basal defense against bacterial pathogens
inferredcites →https://doi.org/10.1016/j.molp.2018.05.007openalex-snapshot
Antagonism of Transcription Factor MYC2 by EDS1/PAD4 Complexes Bolsters Salicylic Acid Defense in Arabidopsis Effector-Triggered Immunity
inferredcites →https://doi.org/10.1016/j.pbi.2004.07.005openalex-snapshot
NPR1, all things considered
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.plaphy.2018.10.026openalex-snapshot
APD1, the unique member of Arabidopsis AP2 family influences systemic acquired resistance and ethylene-jasmonic acid signaling
inferredcites →https://doi.org/10.1016/j.tplants.2012.02.010openalex-snapshot
Evolution of jasmonate and salicylate signal crosstalk
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(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/10.1038/35107108openalex-snapshot
Isochorismate synthase is required to synthesize salicylic acid for plant defence
inferredcites →https://doi.org/10.1038/415977aopenalex-snapshot
MAP kinase signalling cascade in Arabidopsis innate immunity
inferredcites →https://doi.org/10.1038/nprot.2007.132openalex-snapshot
Gene splicing and mutagenesis by PCR-driven overlap extension
inferredcites →https://doi.org/10.1038/nprot.2008.38openalex-snapshot
Chromatin immunoprecipitation (ChIP) coupled to detection by quantitative real-time PCR to study transcription factor binding to DNA in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/nprot.2008.66openalex-snapshot
An efficient chromatin immunoprecipitation (ChIP) protocol for studying histone modifications in Arabidopsis plants
inferredcites →https://doi.org/10.1073/pnas.1005225107openalex-snapshot
Control of salicylic acid synthesis and systemic acquired resistance by two members of a plant-specific family of transcription factors
inferredcites →https://doi.org/10.1073/pnas.1216780110openalex-snapshot
Layered pattern receptor signaling via ethylene and endogenous elicitor peptides during Arabidopsis immunity to bacterial infection
inferredcites →https://doi.org/10.1073/pnas.1911758116openalex-snapshot
A MYC2/MYC3/MYC4-dependent transcription factor network regulates water spray-responsive gene expression and jasmonate levels
inferredcites →https://doi.org/10.1073/pnas.96.23.13583openalex-snapshot
Arabidopsis thaliana PAD4 encodes a lipase-like gene that is important for salicylic acid signaling
inferredcites →https://doi.org/10.1074/jbc.m109.097394openalex-snapshot
Perception of the Arabidopsis Danger Signal Peptide 1 Involves the Pattern Recognition Receptor AtPEPR1 and Its Close Homologue AtPEPR2
inferredcites →https://doi.org/10.1074/jbc.m605193200openalex-snapshot
Arabidopsis Isochorismate Synthase Functional in Pathogen-induced Salicylate Biosynthesis Exhibits Properties Consistent with a Role in Diverse Stress Responses
inferredcites →https://doi.org/10.1079/9781845935740.0000openalex-snapshot
Molecular plant-microbe interactions
inferredcites →https://doi.org/10.1093/nar/gkl1006openalex-snapshot
AthaMap web tools for the analysis and identification of co-regulated genes
inferredcites →https://doi.org/10.1093/pcp/pch085openalex-snapshot
Antagonistic Interactions between the SA and JA Signaling Pathways in Arabidopsis Modulate Expression of Defense Genes and Gene-for-Gene Resistance to Cucumber Mosaic Virus
inferredcites →https://doi.org/10.1093/pcp/pcr063openalex-snapshot
Tobacco MYC2 Regulates Jasmonate-Inducible Nicotine Biosynthesis Genes Directly and By Way of the NIC2-Locus ERF Genes
inferredcites →https://doi.org/10.1094/mpmi-04-13-0096-ropenalex-snapshot
Arabidopsis thaliana FLOWERING LOCUS D Is Required for Systemic Acquired Resistance
inferredcites →https://doi.org/10.1094/mpmi-08-17-0208-ropenalex-snapshot
AtOZF1 Positively Regulates Defense Against Bacterial Pathogens and NPR1-Independent Salicylic Acid Signaling
inferredcites →https://doi.org/10.1094/mpmi-19-0789openalex-snapshot
The Arabidopsis thaliana JASMONATE INSENSITIVE 1 Gene Is Required for Suppression of Salicylic Acid-Dependent Defenses During Infection by Pseudomonas syringae
inferredcites →https://doi.org/10.1094/mpmi.1997.10.1.69openalex-snapshot
Characterization of aSalicylicAcid-Insensitive Mutant (sai1) ofArabidopsis thaliana, Identified in a Selective Screen Utilizing the SA-Inducible Expression of thetms2Gene
inferredcites →https://doi.org/10.1097/00024382-200209000-00016openalex-snapshot
Annual Review of Cell and Developmental Biology 2001
inferredcites →https://doi.org/10.1104/pp.108.121392openalex-snapshot
Kinetics of Salicylate-Mediated Suppression of Jasmonate Signaling Reveal a Role for Redox Modulation
inferredcites →https://doi.org/10.1104/pp.108.133926openalex-snapshot
Ethylene Modulates the Role of NONEXPRESSOR OF PATHOGENESIS-RELATED GENES1 in Cross Talk between Salicylate and Jasmonate Signaling
inferredcites →https://doi.org/10.1104/pp.17.01579openalex-snapshot
The Polycomb-Group Repressor MEDEA Attenuates Pathogen 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/10.1105/tpc.022319openalex-snapshot
JASMONATE-INSENSITIVE1 Encodes a MYC Transcription Factor Essential to Discriminate between Different Jasmonate-Regulated Defense Responses in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.105.032060openalex-snapshot
A Basic Helix-Loop-Helix Transcription Factor in Arabidopsis, MYC2, Acts as a Repressor of Blue Light–Mediated Photomorphogenic Growth
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.113.122002openalex-snapshot
Jasmonate-Activated MYC2 Represses ETHYLENE INSENSITIVE3 Activity to Antagonize Ethylene-Promoted Apical Hook Formation inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.16.00953openalex-snapshot
MYC2 Orchestrates a Hierarchical Transcriptional Cascade That Regulates Jasmonate-Mediated Plant Immunity in Tomato
inferredcites →https://doi.org/10.1111/j.1364-3703.2004.00242.xopenalex-snapshot
The jasmonate‐insensitive mutant jin1 shows increased resistance to biotrophic as well as necrotrophic pathogens
inferredcites →https://doi.org/10.1111/j.1753-4887.1981.tb06752.xopenalex-snapshot
Proceedings of the National Academy of Sciences of the United States of America
inferredcites →https://doi.org/10.1111/jipb.12524openalex-snapshot
ORA59 and EIN3 interaction couples jasmonate‐ethylene synergistic action to antagonistic salicylic acid regulation of PDF expression
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.12803openalex-snapshot
TCP transcription factors are critical for the coordinated regulation of ISOCHORISMATE SYNTHASE 1 expression in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.12899openalex-snapshot
Interaction of MYC 2 and GBF 1 results in functional antagonism in blue light‐mediated Arabidopsis seedling development
inferredcites →https://doi.org/10.1111/tpj.13030openalex-snapshot
Jasmonic acid promotes degreening via MYC 2/3/4‐ and ANAC 019/055/072‐mediated regulation of major chlorophyll catabolic genes
inferredcites →https://doi.org/10.1111/tpj.13608openalex-snapshot
GBF 1 differentially regulates CAT 2 and PAD 4 transcription to promote pathogen defense in Arabidopsis thaliana
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154055openalex-snapshot
Hormonal Modulation of Plant Immunity
inferredcites →https://doi.org/10.1186/1471-2229-11-89openalex-snapshot
WRKY Transcription Factors Involved in Activation of SA Biosynthesis Genes
inferredcites →https://doi.org/10.1371/journal.pgen.1003244openalex-snapshot
A Quartet of PIF bHLH Factors Provides a Transcriptionally Centered Signaling Hub That Regulates Seedling Morphogenesis through Differential Expression-Patterning of Shared Target Genes in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pgen.1004389openalex-snapshot
EDR1 Physically Interacts with MKK4/MKK5 and Negatively Regulates a MAP Kinase Cascade to Modulate Plant Innate Immunity
inferredcites →https://doi.org/10.1371/journal.ppat.1000301openalex-snapshot
Arabidopsis CaM Binding Protein CBP60g Contributes to MAMP-Induced SA Accumulation and Is Involved in Disease Resistance against Pseudomonas syringae
inferredcites →https://doi.org/10.1385/1-59745-003-0:225openalex-snapshot
Transient Expression Assay by Agroinfiltration of Leaves
inferredcites →https://doi.org/10.14348/molcells.2019.2433openalex-snapshot
Role of RIN4 in Regulating PAMP-Triggered Immunity and Effector-Triggered Immunity: Current Status and Future Perspectives.
inferredcites →https://doi.org/10.4161/psb.25679openalex-snapshot
MYC2 differentially regulates GATA-box conaining promoters during seedling development inArabidopsis
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.4822038openalex-extracted
Konjac Glucomannan Oligosaccharides (Kgmos) Preparation and Disclose its Immunomodulatory Impact on Arabidopsis Thaliana Against Pst Dc3000
inferred← citeshttps://doi.org/10.2139/ssrn.4879950openalex-extracted
Konjac Glucomannan Oligosaccharides (Kgmos) Preparation and Disclose its Immunomodulatory Impact on Arabidopsis Thaliana Against Pst Dc3000
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Identification of the sweet orange ( Citrus sinensis ) bHLH gene family and the role of CsbHLH55 and CsbHLH87 in regulating salt stress
inferred← citeshttps://doi.org/10.1007/s00122-022-04212-xopenalex-snapshot
Sigma factor binding protein 1 (CsSIB1) is a putative candidate of the major-effect QTL dm5.3 for downy mildew resistance in cucumber (Cucumis sativus)
inferred← citeshttps://doi.org/10.1007/s00299-022-02861-2openalex-snapshot
MTO1-RESPONDING DOWN 1 (MRD1) is a transcriptional target of OZF1 for promoting salicylic acid-mediated defense in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-026-03740-wopenalex-snapshot
The BoMYC2-BoD27 cascade regulates branching by influencing the content of strigolactones in ornamental kale
inferred← citeshttps://doi.org/10.1007/s00344-024-11446-0openalex-snapshot
Disruption in Jasmonic Acid Biosynthesis Influences Metabolism of Other Hormones in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s10658-023-02660-9openalex-snapshot
Evaluation of salicylic acid (SA) signaling pathways and molecular markers in Trichoderma-treated plants under salinity and Fusarium stresses. A Review
inferred← citeshttps://doi.org/10.1007/s12298-023-01364-yopenalex-snapshot
Light signaling as cellular integrator of multiple environmental cues in plants
inferred← citeshttps://doi.org/10.1007/s12298-025-01688-xopenalex-snapshot
Deciphering the immune blueprint: a holistic view of Arabidopsis (host) responses to hemibiotrophic pathogen Pseudomonas syringae pv. tomato DC 3000
inferred← citeshttps://doi.org/10.1007/s12374-025-09462-yopenalex-snapshot
The Roles of MYC2 Transcription Factor in JA-Signaling Pathway in Plants
inferred← citeshttps://doi.org/10.1007/s13562-025-00959-8openalex-snapshot
Comparative transcriptomic analysis provides insight into the key regulatory pathways and differentially expressed genes in Pyrus pyrifolia. 'Mixue'
inferred← citeshttps://doi.org/10.1007/s44281-025-00067-6openalex-snapshot
CsLOB1 impairs kumquat immunity to citrus canker by reprogramming cell development and defense responses
inferred← citeshttps://doi.org/10.1016/b978-0-323-95375-7.00006-9openalex-snapshot
Salicylic acid biosynthesis for hormone crosstalk and plant development
inferred← citeshttps://doi.org/10.1016/j.gene.2022.146336openalex-snapshot
Identification and expression analysis of arabinogalactan protein genes in cotton reveal the function of GhAGP15 in Verticillium dahliae resistance
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148622openalex-snapshot
CRISPR/Cas9-mediated knockout of NtMYC2a gene involved in resistance to bacterial wilt in tobacco
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.114928openalex-snapshot
Genome-wide investigation of bHLH genes and expression analysis under salt and hormonal treatments in Andrographis paniculata
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.124097openalex-snapshot
JA-GhMYC2-GhWIND1-A transcriptional cascade promotes cotton callus enlargement
inferred← citeshttps://doi.org/10.1016/j.ncrops.2023.11.003openalex-snapshot
The central role of transcription factors in bridging biotic and abiotic stress responses for plants’ resilience
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112407openalex-snapshot
A review of the interaction mechanisms between jasmonic acid (JA) and various plant hormones, as well as the core regulatory role of MYC2
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109356openalex-snapshot
Silencing CsMAP65-2 and CsMAP65-3 in cucumber reduces susceptibility to Meloidogyne incognita
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2023.112260openalex-snapshot
Transcription factor CsERF1B regulates postharvest citrus fruit resistance to Penicillium digitatum
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c07067openalex-snapshot
Preparation and Functional Characterization of Konjac Glucomannan Oligosaccharide as an Immunomodulator Against Pst DC3000 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/s42003-026-09667-yopenalex-snapshot
The core clock transcription factor TOC1 binds directly to defence gene promoters regulating immunity in Arabidopsis
inferred← citeshttps://doi.org/10.1071/fp23155openalex-snapshot
Methylglyoxal metabolism is altered during defence response in pigeonpea (Cajanus cajan (L.) Millsp.) against the spotted pod borer (Maruca vitrata)
inferred← citeshttps://doi.org/10.1093/jxb/erae323openalex-snapshot
The concerted function of a novel class of transcription factors, ZBFs, in light, jasmonate, and abscisic acid signaling pathways
inferred← citeshttps://doi.org/10.1093/jxb/erag172openalex-snapshot
An Arabidopsis receptor-like kinase mediates competitive plant–plant interactions
inferred← citeshttps://doi.org/10.1093/pcp/pcad075openalex-snapshot
Glucosinolate Catabolism Maintains Glucosinolate Profiles and Transport in Sulfur-Starved Arabidopsis
inferred← citeshttps://doi.org/10.1093/plcell/koaf285openalex-snapshot
The EDR1–PP2A phospho-regulatory module fine-tunes MYC2-mediated plant disease resistance
inferred← citeshttps://doi.org/10.1094/mpmi-02-22-0049-ropenalex-snapshot
Involvement ofArabidopsisAcyl Carrier Protein 1 in PAMP-Triggered Immunity
inferred← citeshttps://doi.org/10.1101/2022.11.07.515491openalex-snapshot
The grape powdery mildew resistance loci Ren2, Ren3, Ren4D, Ren4U, Run1, Run1.2b, Run2.1 , and Run2.2 activate different transcriptional responses to Erysiphe necator
inferred← citeshttps://doi.org/10.1101/2023.03.31.535076openalex-snapshot
Changes in Protein Turn-over rates Regulate Tryptophan and Glucosinolate Biosynthesis, IAA Transport and Photosynthesis in Arabidopsis Growth and Defense Transitions
inferred← citeshttps://doi.org/10.1111/pbi.70177openalex-snapshot
PpMYC2 and PpJAM2 /3 antagonistically regulate lignin synthesis to cope with the disease in peach fruit
inferred← citeshttps://doi.org/10.1111/pce.14812openalex-snapshot
External jasmonic acid isoleucine mediates amplification of plant elicitor peptide receptor (PEPR) and jasmonate‐based immune signalling
inferred← citeshttps://doi.org/10.1111/pce.15561openalex-snapshot
A Stem‐Specific Cell Death‐Inducing Cyclo‐Dipeptide From Woody Plant Pathogen Valsa mali Modulates Plant Immune Response
inferred← citeshttps://doi.org/10.1111/ppl.70102openalex-snapshot
LDL2 and PAO5 genes are essential for systemic acquired resistance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/ppl.70304openalex-snapshot
MeJA and Post‐Harvest Storage of Fruits and Vegetables and Metabolite Synthesis in Plants
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Seaweed‐Derived Oligosaccharides Confer Broad‐Spectrum Antiviral Defenses in Tomato and Arabidopsis Plants
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RSI1 / FLD and its epigenetic target RRTF1 are essential for the retention of infection memory in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1186/s12864-024-10297-zopenalex-snapshot
Genome-wide identification of ZmMYC2 binding sites and target genes in maize
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Mechanisms of systemic resistance to pathogen infection in plants and their potential application in forestry
inferred← citeshttps://doi.org/10.1186/s12915-023-01739-3openalex-snapshot
Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
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An efficient screening system of disease-resistant genes from wild apple, Malus sieversii in response to Valsa mali pathogenic fungus
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BnaA07.SUC2 regulated by BnaA05.MYC2 in jasmonate pathway promotes oilseed rape susceptibility to Plasmodiophora brassicae
inferred← citeshttps://doi.org/10.32604/phyton.2022.023733openalex-snapshot
The Role of Salicylic Acid Signal in Plant Growth, Development and Abiotic Stress
inferred← citeshttps://doi.org/10.3389/fpls.2022.1017840openalex-snapshot
Genome-wide identification and expression of TIFY family in cassava (Manihot esculenta Crantz)
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The grape powdery mildew resistance loci Ren2, Ren3, Ren4D, Ren4U, Run1, Run1.2b, Run2.1, and Run2.2 activate different transcriptional responses to Erysiphe necator
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The Multifaceted Roles of MYC2 in Plants: Toward Transcriptional Reprogramming and Stress Tolerance by Jasmonate Signaling
inferred← citeshttps://doi.org/10.3390/cimb45040179openalex-snapshot
Transcriptomics Reveals the Molecular Basis for Methyl Jasmonate to Promote the Synthesis of Monoterpenoids in Schizonepeta tenuifolia Briq.
inferred← citeshttps://doi.org/10.3390/foods12142750openalex-snapshot
CRISPR/Cas9-Mediated SlATG5 Mutagenesis Reduces the Resistance of Tomato Fruit to Botrytis cinerea
inferred← citeshttps://doi.org/10.3390/horticulturae11060565openalex-snapshot
Chitin Oligomers from Alternaria alternata Induce Activation of Signal Transduction Pathways by Ethylene, Jasmonic Acid, and Salicylic Acid in Solanum lycopersicum Fruits
inferred← citeshttps://doi.org/10.3390/ijms24043511openalex-snapshot
MYC2: A Master Switch for Plant Physiological Processes and Specialized Metabolite Synthesis
inferred← citeshttps://doi.org/10.3390/plants12030620openalex-snapshot
Genome-Wide Identification of bHLH Transcription Factor Family in Malus sieversii and Functional Exploration of MsbHLH155.1 Gene under Valsa Canker Infection
inferred← citeshttps://doi.org/10.3390/plants14081255openalex-snapshot
The Role of MYC2 Transcription Factors in Plant Secondary Metabolism and Stress Response Mechanisms
inferred← citeshttps://doi.org/10.48130/vegres-0024-0026openalex-snapshot
Reframing agriculture by light: the role of light-mediated jasmonates/salicylic acid regulation in plant defense, development and beyond
inferred← citeshttps://doi.org/10.6084/m9.figshare.24531942openalex-snapshot
Additional file 1 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.24532326openalex-snapshot
Additional file 2 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637633openalex-snapshot
Additional file 3 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637636openalex-snapshot
Additional file 4 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637639openalex-snapshot
Additional file 5 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637642openalex-snapshot
Additional file 6 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637645openalex-snapshot
Additional file 7 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637648openalex-snapshot
Additional file 8 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637651openalex-snapshot
Additional file 9 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637654openalex-snapshot
Additional file 10 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637657openalex-snapshot
Additional file 11 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637660openalex-snapshot
Additional file 12 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637663openalex-snapshot
Additional file 13 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637666openalex-snapshot
Additional file 14 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26648721openalex-snapshot
Additional file 1 of An efficient screening system of disease-resistant genes from wild apple, Malus sieversii in response to Valsa mali pathogenic fungus
inferred← citeshttps://doi.org/10.6084/m9.figshare.26648724openalex-snapshot
Additional file 2 of An efficient screening system of disease-resistant genes from wild apple, Malus sieversii in response to Valsa mali pathogenic fungus
inferred← citeshttps://doi.org/10.6084/m9.figshare.26648727openalex-snapshot
Additional file 3 of An efficient screening system of disease-resistant genes from wild apple, Malus sieversii in response to Valsa mali pathogenic fungus
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