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Maize Kernel Development Stage the Primary Factor in Differential Gene Expression in Response to Two Methods of Field Inoculation with Aspergillus flavus

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s10142-002-0046-6openalex-snapshot
DNA array profiling of gene expression changes during maize embryo development
inferredcites →https://doi.org/10.1016/j.biocel.2014.09.026openalex-snapshot
Structural analysis of glyceraldehyde-3-phosphate dehydrogenase functional diversity
inferredcites →https://doi.org/10.1016/j.jcs.2016.01.013openalex-snapshot
Transition from vitreous to floury endosperm in maize ( Zea mays L.) kernels is related to protein and starch gradients
inferredcites →https://doi.org/10.1016/j.pep.2016.06.014openalex-snapshot
Purification and characterization of glyceraldehyde-3-phosphate-dehydrogenase (GAPDH) from pea seeds
inferredcites →https://doi.org/10.1016/j.phytochem.2007.03.022openalex-snapshot
Down-regulation of hydroxycinnamoyl CoA: Shikimate hydroxycinnamoyl transferase in transgenic alfalfa affects lignification, development and forage quality
inferredcites →https://doi.org/10.1016/j.pmpp.2009.10.004openalex-snapshot
Maize seed chitinase is modified by a protein secreted by Bipolaris zeicola
inferredcites →https://doi.org/10.1016/j.ygeno.2007.12.002openalex-snapshot
Genome-wide analysis of gene expression profiles during the kernel development of maize (Zea mays L.)
inferredcites →https://doi.org/10.1016/s0022-2836(02)01103-8openalex-snapshot
The Three-dimensional Solution Structure of NaD1, a New Floral Defensin from Nicotiana alata and its Application to a Homology Model of the Crop Defense Protein alfAFP
inferredcites →https://doi.org/10.1016/s0891-5849(00)00398-1openalex-snapshot
Oxidative stress as a prerequisite for aflatoxin production by Aspergillus parasiticus
inferredcites →https://doi.org/10.1016/s0960-9822(00)00560-1openalex-snapshot
The hypersensitive response facilitates plant infection by the necrotrophic pathogen Botrytis cinerea
inferredcites →https://doi.org/10.1038/ni1410openalex-snapshot
Plant NBS-LRR proteins in pathogen sensing and host defense
inferredcites →https://doi.org/10.1038/nprot.2013.084openalex-snapshot
De novo transcript sequence reconstruction from RNA-Seq: reference generation and analysis with Trinity
inferredcites →https://doi.org/10.1073/pnas.1011739108openalex-snapshot
Multivariate analysis of maize disease resistances suggests a pleiotropic genetic basis and implicates a GST gene
inferredcites →https://doi.org/10.1073/pnas.142284999openalex-snapshot
The barley stem rust-resistance gene Rpg1 is a novel disease-resistance gene with homology to receptor kinases
inferredcites →https://doi.org/10.1073/pnas.96.24.14165openalex-snapshot
Transgenic tobacco plants with reduced capability to detoxify reactive oxygen intermediates are hyperresponsive to pathogen infection
inferredcites →https://doi.org/10.1074/jbc.m310029200openalex-snapshot
Molecular Chaperone Hsp90 Associates with Resistance Protein N and Its Signaling Proteins SGT1 and Rar1 to Modulate an Innate Immune Response in Plants
inferredcites →https://doi.org/10.1080/07352689209382320openalex-snapshot
Aflatoxin in maize
inferredcites →https://doi.org/10.1080/08905439409549875openalex-snapshot
Phenolic compounds in peanut seeds: Enhanced elicitation by chitosan and effects on growth and aflatoxin b1production byaspergillus flavus
inferredcites →https://doi.org/10.1080/08905439409549876openalex-snapshot
Effects of chitosan andaspergillus flawson isozymes related to phenouc compound synthesis and protein profiles of peanut seeds
inferredcites →https://doi.org/10.1080/08905439509549885openalex-snapshot
Phenolic compounds in peanut seeds: Enhanced elicitation by chitosan and effects on growth and aflatoxin B1production byAspergillus flavus
inferredcites →https://doi.org/10.1093/bib/bbs046openalex-snapshot
A comprehensive evaluation of normalization methods for Illumina high-throughput RNA sequencing data analysis
inferredcites →https://doi.org/10.1093/jexbot/53.372.1305openalex-snapshot
Regulation and function of ascorbate peroxidase isoenzymes
inferredcites →https://doi.org/10.1093/nar/gkn201openalex-snapshot
NCBI BLAST: a better web interface
inferredcites →https://doi.org/10.1093/nar/gkt1140openalex-snapshot
Activities at the Universal Protein Resource (UniProt)
inferredcites →https://doi.org/10.1093/nar/gkt1223openalex-snapshot
Pfam: the protein families database
inferredcites →https://doi.org/10.1094/mpmi-20-8-0900openalex-snapshot
Identification of 118 Arabidopsis Transcription Factor and 30 Ubiquitin-Ligase Genes Responding to Chitin, a Plant-Defense Elicitor
inferredcites →https://doi.org/10.1094/mpmi-21-12-1515openalex-snapshot
Lr34-Mediated Leaf Rust Resistance in Wheat: Transcript Profiling Reveals a High Energetic Demand Supported by Transient Recruitment of Multiple Metabolic Pathways
inferredcites →https://doi.org/10.1094/mpmi-21-5-0507openalex-snapshot
Plant Receptor-Like Serine Threonine Kinases: Roles in Signaling and Plant Defense
inferredcites →https://doi.org/10.1094/mpmi.2002.15.9.963openalex-snapshot
Characterization of Early, Chitin-Induced Gene Expression in Arabidopsis
inferredcites →https://doi.org/10.1094/pd-73-0313openalex-snapshot
Evaluation of Field Inoculation Techniques for Screening Maize Genotypes Against Kernel Infection by Aspergillus flavus in Mississippi
inferredcites →https://doi.org/10.1094/pd-78-0123openalex-snapshot
Kernel Infection and Aflatoxin Production in Maize byAspergillus flavusRelative to Inoculation and Harvest Dates
inferredcites →https://doi.org/10.1094/pdis-93-11-1163openalex-snapshot
Aspergillus flavus Biomass in Maize Estimated by Quantitative Real-Time Polymerase Chain Reaction Is Strongly Correlated with Aflatoxin Concentration
inferredcites →https://doi.org/10.1094/phyto-09-10-0261openalex-snapshot
Gene Expression Profile and Response to Maize Kernels by Aspergillus flavus
inferredcites →https://doi.org/10.1094/phyto-100-7-0645openalex-snapshot
Allozyme-Specific Modification of a Maize Seed Chitinase by a Protein Secreted by the Fungal Pathogen Stenocarpella maydis
inferredcites →https://doi.org/10.1094/phyto-74-1284openalex-snapshot
Preharvest Infection of Corn Silks and Kernels byAspergillus flavus
inferredcites →https://doi.org/10.1104/pp.108.131144openalex-snapshot
Identification of an Apoplastic Protein Involved in the Initial Phase of Salt Stress Response in Rice Root by Two-Dimensional Electrophoresis
inferredcites →https://doi.org/10.1104/pp.113.214874openalex-snapshot
The Differential Transcription Network between Embryo and Endosperm in the Early Developing Maize Seed
inferredcites →https://doi.org/10.1105/tpc.003905openalex-snapshot
Maize Opaque Endosperm Mutations Create Extensive Changes in Patterns of Gene Expression[W]
inferredcites →https://doi.org/10.1105/tpc.010240openalex-snapshot
Genomics Analysis of Genes Expressed in Maize Endosperm Identifies Novel Seed Proteins and Clarifies Patterns of Zein Gene Expression
inferredcites →https://doi.org/10.1105/tpc.11.3.431openalex-snapshot
The Involvement of Cysteine Proteases and Protease Inhibitor Genes in the Regulation of Programmed Cell Death in Plants
inferredcites →https://doi.org/10.1105/tpc.112.102855openalex-snapshot
Genome-Wide Analysis Uncovers Regulation of Long Intergenic Noncoding RNAs in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.134858openalex-snapshot
Genome-Wide Characterization of cis -Acting DNA Targets Reveals the Transcriptional Regulatory Framework of Opaque2 in Maize
inferredcites →https://doi.org/10.1105/tpc.7.4.407openalex-snapshot
The brown midrib3 (bm3) mutation in maize occurs in the gene encoding caffeic acid O-methyltransferase.
inferredcites →https://doi.org/10.1111/j.1364-3703.2007.00419.xopenalex-snapshot
The role of plant defence proteins in fungal pathogenesis
inferredcites →https://doi.org/10.1111/j.1365-2672.2005.02637.xopenalex-snapshot
Aflatoxin biosynthesis gene clusters and flanking regions
inferredcites →https://doi.org/10.1111/j.2517-6161.1995.tb02031.xopenalex-snapshot
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
inferredcites →https://doi.org/10.1111/mpp.12056openalex-snapshot
Localization, morphology and transcriptional profile of A spergillus flavus during seed colonization
inferredcites →https://doi.org/10.1111/mpp.12224openalex-snapshot
Tissue‐specific gene expression in maize seeds during colonization by A spergillus flavus and F usarium verticillioides
inferredcites →https://doi.org/10.1111/tpj.12101openalex-snapshot
The maize lipoxygenase, Zm LOX 10 , mediates green leaf volatile, jasmonate and herbivore‐induced plant volatile production for defense against insect attack
inferredcites →https://doi.org/10.1126/science.1178534openalex-snapshot
The B73 Maize Genome: Complexity, Diversity, and Dynamics
inferredcites →https://doi.org/10.1128/aem.00738-15openalex-snapshot
Genetic Analysis of the Aspergillus flavus Vegetative Compatibility Group to Which a Biological Control Agent That Limits Aflatoxin Contamination in U.S. Crops Belongs
inferredcites →https://doi.org/10.1128/aem.70.3.1253-1262.2004openalex-snapshot
Clustered Pathway Genes in Aflatoxin Biosynthesis
inferredcites →https://doi.org/10.1146/annurev.phyto.43.040204.135923openalex-snapshot
Contrasting Mechanisms of Defense Against Biotrophic and Necrotrophic Pathogens
inferredcites →https://doi.org/10.1155/2008/496957openalex-snapshot
MaizeGDB: The Maize Model Organism Database for Basic, Translational, and Applied Research
inferredcites →https://doi.org/10.1186/1471-2180-11-169openalex-snapshot
The cross-pathway control system regulates production of the secondary metabolite toxin, sirodesmin PL, in the ascomycete, Leptosphaeria maculans
inferredcites →https://doi.org/10.1186/s12870-016-0713-8openalex-snapshot
Two members of TaRLK family confer powdery mildew resistance in common wheat
inferredcites →https://doi.org/10.1371/journal.pone.0036892openalex-snapshot
Identification of Maize Genes Associated with Host Plant Resistance or Susceptibility to Aspergillus flavus Infection and Aflatoxin Accumulation
inferredcites →https://doi.org/10.1371/journal.pone.0117737openalex-snapshot
Genome Wide Association Study for Drought, Aflatoxin Resistance, and Important Agronomic Traits of Maize Hybrids in the Sub-Tropics
inferredcites →https://doi.org/10.1371/journal.pone.0126185openalex-snapshot
Characterization of the Maize Chitinase Genes and Their Effect on Aspergillus flavus and Aflatoxin Accumulation Resistance
inferredcites →https://doi.org/10.1371/journal.pone.0131080openalex-snapshot
Biodiversity on the Rocks: Macrofauna Inhabiting Authigenic Carbonate at Costa Rica Methane Seeps
inferredcites →https://doi.org/10.1371/journal.pone.0181265openalex-snapshot
Characterization of the maize lipoxygenase gene family in relation to aflatoxin accumulation resistance
inferredcites →https://doi.org/10.1515/bc.2007.030openalex-snapshot
Purification, characterization, and molecular gene cloning of an antifungal protein from Ginkgo biloba seeds
inferredcites →https://doi.org/10.2134/agronj1991.00021962008300030018xopenalex-snapshot
Aflatoxin in Corn Hybrids Field Inoculated with Aspergillus flavus
inferredcites →https://doi.org/10.2134/agronj2004.0565openalex-snapshot
Aflatoxin Accumulation in Maize Hybrids of Different Maturities
inferredcites →https://doi.org/10.2135/cropsci1987.0011183x002700050007xopenalex-snapshot
Independent Inheritance of Genes Conditioning Resistance to Phytophthora Root Rot from Diploid and Tetraploid Alfalfa1
inferredcites →https://doi.org/10.2135/cropsci1987.0011183x002700050007xaopenalex-snapshot
Inheritance of Aflatoxin B1 Levels in Maize Kernels under Modified Natural Inoculation with Aspergillus flavus1
inferredcites →https://doi.org/10.2135/cropsci1990.0011183x003000060080xopenalex-snapshot
Registration of Mp313E Parental Line of Maize
inferredcites →https://doi.org/10.2135/cropsci2001.4141374-axopenalex-snapshot
Registration of Maize Germplasm Line Mp715
inferredcites →https://doi.org/10.2135/cropsci2002.1894openalex-snapshot
Aflatoxin Accumulation of White and Yellow Maize Inbreds in Diallel Crosses
inferredcites →https://doi.org/10.2135/cropsci2004.1036aopenalex-snapshot
Registration of Tx772 Maize
inferredcites →https://doi.org/10.2135/cropsci2012.10.0616openalex-snapshot
Phenotypic and Genetic Characterization of a Maize Association Mapping Panel Developed for the Identification of New Sources of Resistance to Aspergillus flavus and Aflatoxin Accumulation
inferredcites →https://doi.org/10.2135/cropsci2013.04.0249openalex-snapshot
Quantitative Trait Loci Influencing Mycotoxin Contamination of Maize: Analysis by Linkage Mapping, Characterization of Near‐Isogenic Lines, and Meta‐Analysis
inferredcites →https://doi.org/10.2135/cropsci2016.06.0519openalex-snapshot
Identification of Resistance to Aflatoxin Accumulation and Yield Potential in Maize Hybrids in the Southeast Regional Aflatoxin Trials (SERAT)
inferredcites →https://doi.org/10.2307/3870079openalex-snapshot
The brown midrib3 (bm3) Mutation in Maize Occurs in the Gene Encoding Caffeic Acid O-Methyltransferase
inferredcites →https://doi.org/10.2307/3871509openalex-snapshot
Genomics Analysis of Genes Expressed in Maize Endosperm Identifies Novel Seed Proteins and Clarifies Patterns of Zein Gene Expression
inferredcites →https://doi.org/10.3389/fmicb.2014.00040openalex-snapshot
Environmental influences on maize-Aspergillus flavus interactions and aflatoxin production
inferredcites →https://doi.org/10.3389/fmicb.2014.00384openalex-snapshot
Aspergillus flavus infection induces transcriptional and physical changes in developing maize kernels
inferredcites →https://doi.org/10.3389/fmicb.2016.02048openalex-snapshot
Responses of Aspergillus flavus to Oxidative Stress Are Related to Fungal Development Regulator, Antioxidant Enzyme, and Secondary Metabolite Biosynthetic Gene Expression
inferredcites →https://doi.org/10.3389/fpls.2013.00044openalex-snapshot
Hexose Kinases and Their Role in Sugar-Sensing and Plant Development
inferredcites →https://doi.org/10.3389/fpls.2017.00503openalex-snapshot
Expression Profiling Coupled with In-silico Mapping Identifies Candidate Genes for Reducing Aflatoxin Accumulation in Maize
inferredcites →https://doi.org/10.3390/ijms131215706openalex-snapshot
Heat Shock Protein 90 in Plants: Molecular Mechanisms and Roles in Stress Responses
inferredcites →https://doi.org/10.3390/toxins3060538openalex-snapshot
Expression Analysis of Stress-Related Genes in Kernels of Different Maize (Zea mays L.) Inbred Lines with Different Resistance to Aflatoxin Contamination
inferredcites →https://doi.org/10.3835/plantgenome2012.09.0025openalex-snapshot
Maize Metabolic Network Construction and Transcriptome Analysis
inferredcites →https://doi.org/10.3923/ppj.2006.115.124openalex-snapshot
Resistance Mechanisms to Aspergillus flavus Infection and Aflatoxin Contamination in Peanut (Arachis hypogaea)

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/csc2.20710openalex-snapshot
Control of aflatoxin using atoxigenic strains and irrigation management is complicated by maize hybrid diversity
inferred← citeshttps://doi.org/10.1007/s13205-026-04726-xopenalex-snapshot
The essential role of methylation in maize (Zea mays) defense against the seed-colonizing fungus Aspergillus flavus
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