| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Ana Butron | Q63229849 |
| Rogelio Santiago | Q38590301 | ||
| P2093 | author name string | Ana Cao | |
| P2860 | cites work | Comparison of Fumonisin Concentrations in Kernels of Transgenic Bt Maize Hybrids and Nontransgenic Hybrids. | Q64979430 |
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| Fumonisin B1 contamination of home-grown corn in high-risk areas for esophageal and liver cancer in China | Q79963986 | ||
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| Maize kernel antioxidants and their potential involvement in Fusarium ear rot resistance | Q86364028 | ||
| Evaluation of Maize Inbred Lines for Resistance to Fusarium Ear Rot and Fumonisin Accumulation in Grain in Tropical Africa | Q91708370 | ||
| Evaluation of Food-Grade Dent Corn Hybrids for Severity of Fusarium Ear Rot and Fumonisin Accumulation in Grain | Q91837226 | ||
| Evaluation of Inoculation Techniques for Fusarium Ear Rot and Fumonisin Contamination of Corn | Q91974740 | ||
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| Exposure to fumonisins and the occurrence of neural tube defects along the Texas-Mexico border | Q25257385 | ||
| Fungus- and wound-induced accumulation of mRNA containing a class II chitinase of the pathogenesis-related protein 4 (PR-4) family of maize | Q28165352 | ||
| Flavonoids and isoflavonoids - a gold mine for metabolic engineering. | Q30322980 | ||
| Integrating toxin gene expression, growth and fumonisin B1 and B2 production by a strain of Fusarium verticillioides under different environmental factors | Q30630827 | ||
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| Effect of temperature and water activity on the production of fumonisins by Aspergillus niger and different Fusarium species | Q33521528 | ||
| Recent progress toward understanding biosynthesis of the amylopectin crystal | Q33888413 | ||
| Functional genomic analysis of constitutive and inducible defense responses to Fusarium verticillioides infection in maize genotypes with contrasting ear rot resistance | Q34130287 | ||
| The myb-homologous P gene controls phlobaphene pigmentation in maize floral organs by directly activating a flavonoid biosynthetic gene subset. | Q34350049 | ||
| Modeling effects of environment, insect damage, and Bt genotypes on fumonisin accumulation in maize in Argentina and the Philippines | Q34558892 | ||
| Transcriptional and metabolic changes associated to the infection by Fusarium verticillioides in maize inbreds with contrasting ear rot resistance | Q34700440 | ||
| Genome-wide association study of Fusarium ear rot disease in the U.S.A. maize inbred line collection. | Q34998271 | ||
| Starch synthesis in the cereal endosperm. | Q35130122 | ||
| Natural incidence of Fusarium species and fumonisins B1 and B2 associated with maize kernels from nine provinces in China in 2012. | Q35332130 | ||
| A public platform for the verification of the phenotypic effect of candidate genes for resistance to aflatoxin accumulation and Aspergillus flavus infection in maize | Q35459093 | ||
| The dent stage of maize kernels is the most conducive for fumonisin biosynthesis under field conditions | Q35599160 | ||
| Current models for starch synthesis and the sugary enhancer1 (se1) mutation in Zea mays | Q35832371 | ||
| Fumonisin-producing strains of Fusarium: a review of their ecophysiology | Q35871774 | ||
| Inactivation of the lipoxygenase ZmLOX3 increases susceptibility of maize to Aspergillus spp. | Q35983605 | ||
| Fusarium species and fumonisins associated with maize kernels produced in Rio Grande do Sul State for the 2008/09 and 2009/10 growing seasons | Q37244502 | ||
| A genome-wide association study reveals genes associated with fusarium ear rot resistance in a maize core diversity panel. | Q37272965 | ||
| Fatty acids and early detection of pathogens. | Q38120912 | ||
| Natural occurrence of Fusarium and subsequent fumonisin contamination in preharvest and stored maize in Benin, West Africa | Q38998748 | ||
| Differential effect of environmental conditions on the growth and regulation of the fumonisin biosynthetic gene FUM1 in the maize pathogens and fumonisin producers Fusarium verticillioides and Fusarium proliferatum | Q39221568 | ||
| Associations of planting date, drought stress, and insects with Fusarium ear rot and fumonisin B1 contamination in California maize | Q39340616 | ||
| Production of fumonisin analogs by Fusarium species. | Q39653438 | ||
| Role of the European corn borer (Ostrinia nubilalis) on contamination of maize with 13 Fusarium mycotoxins | Q41722735 | ||
| Relationship between solute and matric potential stress, temperature, growth, and FUM1 gene expression in two Fusarium verticillioides strains from Spain | Q41885375 | ||
| Is it possible to control fumonisin contamination in maize kernels by using genotypes resistant to the Mediterranean corn borer? | Q42005977 | ||
| Field control of Fusarium ear rot, Ostrinia nubilalis (Hübner), and fumonisins in maize kernels | Q42017968 | ||
| Biotic and abiotic factors limiting efficacy of Bt corn in indirectly reducing mycotoxin levels in commercial fields | Q42053010 | ||
| Differential gene expression in kernels and silks of maize lines with contrasting levels of ear rot resistance after Fusarium verticillioides infection. | Q42474725 | ||
| Transcriptional activation of a maize calcium-dependent protein kinase gene in response to fungal elicitors and infection | Q42502482 | ||
| Role of accelerated style senescence in pathogen defense | Q42732723 | ||
| Population parameters for resistance to Fusarium graminearum and Fusarium verticillioides ear rot among large sets of early, mid-late and late maturing European maize (Zea mays L.) inbred lines | Q43207630 | ||
| Biology of maize kernel infection by Fusarium verticillioides | Q43230842 | ||
| Survey of Fusarium moniliforme (F. verticillioides) and production of fumonisin B1 in cereal grains and oilseeds in Zimbabwe | Q43853716 | ||
| Fungal growth and fusarium mycotoxin content in isogenic traditional maize and genetically modified maize grown in France and Spain | Q43878061 | ||
| Effect of flavonoid pigments on the accumulation of fumonisin B1 in the maize kernel. | Q44036322 | ||
| Aflatoxin and fumonisin contamination of commercial corn (Zea mays) hybrids in Mississippi | Q44109711 | ||
| Natural occurrence of Fusarium species, fumonisin production by toxigenic strains, and concentrations of fumonisins B1, and B2 in conventional and organic maize grown in Spain. | Q44127678 | ||
| Accumulation of fumonisins B1 and B2 in freshly harvested Brazilian commercial maize at three locations during two nonconsecutive seasons | Q44371177 | ||
| Some traditional herbal medicines, some mycotoxins, naphthalene and styrene. | Q44398593 | ||
| Breeding maize for resistance to ear rot caused by Fusarium moniliforme | Q44655002 | ||
| Comparison of fumonisin B1 biosynthesis in maize germ and degermed kernels by Fusarium verticillioides | Q44661787 | ||
| Identification of Maize Kernel Endosperm Proteins Associated with Resistance to Aflatoxin Contamination by Aspergillus flavus | Q44863300 | ||
| Logistic regression modeling of cropping systems to predict fumonisin contamination in maize | Q44987556 | ||
| Ferulic acid, an efficient inhibitor of type B trichothecene biosynthesis and Tri gene expression in Fusarium liquid cultures. | Q46106002 | ||
| Role of maize hybrids and their chemical composition in Fusarium infection and fumonisin production | Q46121975 | ||
| Extracellular cross-linking of maize arabinoxylans by oxidation of feruloyl esters to form oligoferuloyl esters and ether-like bonds | Q46156766 | ||
| Fumonisins in maize in relation to climate, planting time and hybrids in two agroecological zones in Zambia | Q46251674 | ||
| Sources of resistance to fumonisin accumulation in grain and fusarium ear and kernel rot of corn | Q46303059 | ||
| Infection and Fumonisin Production by Fusarium verticillioides in Developing Maize Kernels | Q46303142 | ||
| A mathematical simulation of growth of fusarium in maize ears after artificial inoculation | Q46303707 | ||
| Fumonisin B2 production by Aspergillus niger. | Q46398778 | ||
| Effect of water activity and temperature on growth and the relationship between fumonisin production and the radial growth of Fusarium verticillioides and Fusarium proliferatum on corn | Q46492040 | ||
| Worldwide survey of fumonisin contamination of corn and corn-based products. | Q46544132 | ||
| Maternal fumonisin exposure and risk for neural tube defects: mechanisms in an in vivo mouse model | Q46549802 | ||
| Giberella fujikuroi species complex isolated from maize and wheat in Iran: distribution, molecular identification and fumonisin B1 in vitro biosynthesis. | Q46738840 | ||
| Covariation between line and testcross performance for reduced mycotoxin concentrations in European maize after silk channel inoculation of two Fusarium species | Q46748541 | ||
| Amylopectin induces fumonisin B1 production by Fusarium verticillioides during colonization of maize kernels | Q46944165 | ||
| The influence of local factors on the prediction of fumonisin contamination in maize. | Q51454748 | ||
| Disruption of a maize 9-lipoxygenase results in increased resistance to fungal pathogens and reduced levels of contamination with mycotoxin fumonisin. | Q52581524 | ||
| Reduced fusarium ear rot and symptomless infection in kernels of maize genetically engineered for European corn borer resistance. | Q52694877 | ||
| Influence of agricultural practices on the contamination of maize by fumonisin mycotoxins. | Q52697393 | ||
| Environmental factors related to fungal infection and fumonisin accumulation during the development and drying of white maize kernels. | Q52754887 | ||
| Critical environmental and genotypic factors for Fusarium verticillioides infection, fungal growth and fumonisin contamination in maize grown in northwestern Spain. | Q52767465 | ||
| The fumonisin B1 content in corn from North China, a high-risk area of esophageal cancer. | Q53407758 | ||
| Fumonisins: Toxicokinetics, mechanism of action and toxicity | Q55110902 | ||
| Interaction of Fusarium graminearum and F. moniliforme in Maize Ears: Disease Progress, Fungal Biomass, and Mycotoxin Accumulation | Q57221381 | ||
| Importance of Different Pathways for Maize Kernel Infection by Fusarium moniliforme | Q57221914 | ||
| Diallel Analysis of Resistance to Fusarium Ear Rot and Fumonisin Contamination in Maize | Q57430627 | ||
| Selection for Reduced Fusarium Ear Rot and Fumonisin Content in Advanced Backcross Maize Lines and Their Topcross Hybrids | Q57438564 | ||
| Maize lipids play a pivotal role in the fumonisin accumulation | Q57819258 | ||
| Effects of temperature and water activity on FUM2 and FUM21 gene expression and fumonisin B production in Fusarium verticillioides | Q58080001 | ||
| Resistant and susceptible maize genotypes activate different transcriptional responses against Fusarium verticillioides | Q58080028 | ||
| Dynamic of water activity in maize hybrids is crucial for fumonisin contamination in kernels | Q58080039 | ||
| Evaluation of broad spectrum sources of resistance to Fusarium verticillioides and advanced maize breeding lines | Q58080067 | ||
| Effect of environmental conditions on spore production by Fusarium verticillioides, the causal agent of maize ear rot | Q58080077 | ||
| Fumonisin B1 Contamination of Cereals and Risk of Esophageal Cancer in a High Risk Area in Northeastern Iran | Q58440665 | ||
| Relationship between fumonisin production andFUMgene expression inFusarium verticillioidesunder different environmental conditions | Q58924306 | ||
| Differential activation of defense genes and enzymes in maize genotypes with contrasting levels of resistance to Fusarium verticillioides | Q58924308 | ||
| Epidemiology of Toxigenic Fungi and their Associated Mycotoxins for Some Mediterranean Crops | Q58924353 | ||
| Aggressiveness and mycotoxin production of eight isolates each of Fusarium graminearum and Fusarium verticillioides for ear rot on susceptible and resistant early maize inbred lines | Q59905701 | ||
| Genetic Variation for Resistance to Ear Rots and Mycotoxins Contamination in Early European Maize Inbred Lines | Q59905812 | ||
| Methods for preventing, decontaminating and minimizing the toxicity of mycotoxins in feeds | Q60305537 | ||
| Characterization of Fusarium verticillioides strains isolated from maize in Italy: Fumonisin production, pathogenicity and genetic variability | Q61733453 | ||
| Resistance in Maize Inbred Lines to Fusarium verticillioides and Fumonisin Accumulation in South Africa | Q61798027 | ||
| Progress in understanding the biosynthesis of amylose | Q62570634 | ||
| P275 | copyright license | Creative Commons Attribution | Q6905323 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | mycotoxins | Q422449 |
| eukaryote | Q19088 | ||
| hydrocarbon | Q43648 | ||
| agronomics | Q56299227 | ||
| disease resistance | Q60790177 | ||
| P304 | page(s) | 3267-3296 | |
| P577 | publication date | 2015-08-01 | |
| 2015-08-20 | |||
| P1433 | published in | Toxins | Q15724569 |
| P1476 | title | Genetic Factors Involved in Fumonisin Accumulation in Maize Kernels and Their Implications in Maize Agronomic Management and Breeding | |
| P478 | volume | 7 |
| Q64883706 | A Genome Wide Association Study Reveals Markers and Genes Associated with Resistance to Fusarium verticillioides Infection of Seedlings in a Maize Diversity Panel. |
| Q37285660 | Confirmation and Fine Mapping of a Major QTL for Aflatoxin Resistance in Maize Using a Combination of Linkage and Association Mapping |
| Q64079681 | Differences in Ear Rot Resistance and -Produced Fumonisin Contamination Between Polish Currently and Historically Used Maize Inbred Lines |
| Q39271390 | Fusarium diseases of maize associated with mycotoxin contamination of agricultural products intended to be used for food and feed. |
| Q64083616 | Genome-wide association analysis for fumonisin content in maize kernels |
| Q36256315 | QTL mapping and candidate genes for resistance to Fusarium ear rot and fumonisin contamination in maize |
| Q40576850 | The effect of enhanced carotenoid content of transgenic maize grain on fungal colonization and mycotoxin content |
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