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1. Full Text 3D “honeycomb” cell/carbon nanofiber/gelatin methacryloyl (GelMA) modified screen-printed electrode for electrochemical assessment of the combined toxicity of deoxynivalenol family mycotoxins
by Wei, Kaimin and Sun, Jiadi and Gao, Qing and Yang, Xingxing and Ye, Yongli and Ji, Jian and Sun, Xiulan
Bioelectrochemistry (Amsterdam, Netherlands), ISSN 1567-5394, 06/2021, Volume 139, pp. 107743 - 107743
Electrochemistry | Deoxynivalenol | 3-Acetyl-deoxynivalenol | 15-Acetyl-deoxynivalenol | Toxicity | 3D printing | Index Medicus
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2. Full Text A Fusarium graminearum strain-comparative proteomic approach identifies regulatory changes triggered by agmatine
by Pasquali, M and Serchi, T and Cocco, E and Leclercq, C.C and Planchon, S and Guignard, C and Renaut, J and Hoffmann, L
Journal of proteomics, ISSN 1874-3919, 03/2016, Volume 137, pp. 107 - 116
Nivalenol | Glutamic acid | 2D-DIGE | Strain diversity | Polyamine regulation | 15-acetylated deoxynivalenol | Deoxynivalenol | 3-acetylated deoxynivalenol | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Biochemical Research Methods | Science & Technology | Proteome - biosynthesis | Fungal Proteins - biosynthesis | Species Specificity | Fusarium - metabolism | Proteomics | Trichothecenes - biosynthesis | Proteins | Safety and security measures | Comparative analysis | Food | Index Medicus
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3. Full Text Evaluation of the toxicity and chemical alterations of deoxynivalenol degradation products under ozone treatment
by Yang, Yang and Xu, Yun and Wu, Shang and Qiu, Tianyu and Blaženović, Ivana and Sun, Jiadi and Zhang, Yinzhi and Sun, Xiulan and Ji, Jian
Food control, ISSN 0956-7135, 06/2021, Volume 124, p. 107937
Metabolomics | Ozone | Cytotoxicity | Deoxynivalenol | Structure
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4. Full Text Genetic approaches to chemotype determination in type B-trichothecene producing Fusaria
by Pasquali, Matias and Migheli, Quirico
International journal of food microbiology, ISSN 0168-1605, 10/2014, Volume 189, pp. 164 - 182
Nivalenol | Fusarium culmorum | TRI genes | Acetylated deoxynivalenol | Deoxynivalenol | Fusarium graminearum species complex | Food Science & Technology | Life Sciences & Biomedicine | Microbiology | Science & Technology | Fundamental and applied biological sciences. Psychology | Food industries | Food microbiology | Biological and medical sciences | Gene Expression Regulation, Fungal | Trichothecenes - classification | Humans | Vegetables - microbiology | Food Safety | Trichothecenes - analysis | Trichothecenes - biosynthesis | Edible Grain - microbiology | Fruit - microbiology | Genes, Fungal | Fusarium - classification | Fusarium - genetics | Fusarium - pathogenicity | Mycological Typing Techniques | Genetic research | Index Medicus
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5. Full Text Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats
by Nagl, Veronika and Schwartz, Heidi and Krska, Rudolf and Moll, Wulf-Dieter and Knasmüller, Siegfried and Ritzmann, Mathias and Adam, Gerhard and Berthiller, Franz
Toxicology letters, ISSN 0378-4274, 09/2012, Volume 213, Issue 3, pp. 367 - 373
Urine | Conjugated mycotoxins | Deoxynivalenol | Feces | Rodent | ADME | Life Sciences & Biomedicine | Toxicology | Science & Technology | Plant poisons toxicology | Biological and medical sciences | Medical sciences | Glucuronides - pharmacokinetics | Biological Availability | Male | Glucosides - pharmacokinetics | Chromatography, High Pressure Liquid | Tandem Mass Spectrometry | Spectrometry, Mass, Electrospray Ionization | Biotransformation | Reproducibility of Results | Glucosides - urine | Glucosides - toxicity | Risk Assessment | Administration, Oral | Rats | Trichothecenes - pharmacokinetics | Digestion | Trichothecenes - administration & dosage | Rats, Sprague-Dawley | Hydrolysis | Trichothecenes - toxicity | Animals | Feces - chemistry | Intestines - microbiology | Glucosides - administration & dosage | Trichothecenes - urine | Oncology, Experimental | Physiological aspects | Nitriles | Liquid chromatography | Universities and colleges | Research | Mass spectrometry | Cancer | Index Medicus | MS, mass spectrometry | RA, apparent recovery | JECFA, Joint FAO | LOQ, limit of quantification | Z14G, zearalenone-14-β-d-glucoside | b.w., body weight | enhancement | HPLC, high performance liquid chromatography | WHO Expert Committee on Food Additives | ACN, acetonitrile | RE, recovery of the extraction step | MeOH, methanol | DON-GlcA, deoxynivalenol-glucuronide | SRM, selected reaction monitoring | DP, declustering potential | DON, deoxynivalenol | DOM-1-GlcA, DOM-1-glucuronide | D3G, deoxynivalenol-3-β-d-glucoside | SSE, signal suppression | CE, collision energy | SPE, solid phase extraction | MS, tandem mass spectrometry | DOM-1, de-epoxy deoxynivalenol | LOD, limit of detection
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6. Full Text The effect of agmatine on trichothecene type B and zearalenone production in Fusarium graminearum, F. culmorum and F. poae
by Pasquali, Matias and Cocco, Emmanuelle and Guignard, Cédric and Hoffmann, Lucien
PeerJ (San Francisco, CA), ISSN 2167-8359, 2016, Volume 2016, Issue 2, pp. e1672 - e1672
Nivalenol | 15-acetylaed deoxynivalenol | Fusarenon-X | Toxin induction | Zearalenone | Deoxynivalenol | 3-acetylated deoxynivalenol | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fungi | Oxidative stress | Genes | Genomes | Genetic diversity | Polyamines | Species | Agmatine | Wheat | Food
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7. Full Text Enzyme-linked immunosorbent assay in analysis of deoxynivalenol: Investigation of the impact of samplematrix on results accuracy
by Dzuman, Zbynek and Vaclavikova, Marta and Polisenska, Ivana and Veprikova, Zdenka and Fenclova, Marie and Zachariasova, Milena and Hajslova, Jana
Analytical and bioanalytical chemistry, ISSN 1618-2642, 2014, Volume 406, Issue 2, pp. 505 - 514
LC-MS/MS | Cereals | Cross-reactivity | Deoxynivalenol metabolites | Deoxynivalenol | ELISA
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8. Full Text Deoxynivalenol in food and feed: occurrence and exposure
European Food Safety Authority
EFSA journal, ISSN 1831-4732, 10/2013, Volume 11, Issue 10, p. n/a
food and feed | 15‐acetyldeoxynivalenol | deoxynivalenol | deoxynivalenol‐3‐glucoside | exposure | occurrence | 3‐acetyldeoxynivalenol | 15-acetyldeoxynivalenol | deoxynivalenol-3-glucoside | 3-acetyldeoxynivalenol
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