Moniliformin (BioDeep_00000003271)

   

human metabolite blood metabolite natural product


代谢物信息卡片


3-hydroxycyclobut-3-ene-1,2-dione

化学式: C4H2O3 (98.0004)
中文名称: 1-羟环丁-1-烯-3,4-二酮
谱图信息: 最多检出来源 Homo sapiens(blood) 98.48%

分子结构信息

SMILES: C1=C(C(=O)C1=O)O
InChI: InChI=1S/C4H2O3/c5-2-1-3(6)4(2)7/h1,5H

描述信息

同义名列表

4 个代谢物同义名

3-hydroxycyclobut-3-ene-1,2-dione; Moniliformin, potassium salt; Moniliformin, sodium salt; Moniliformin



数据库引用编号

12 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

11 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 9 ABCB1, ALB, CAT, HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, TFPT
Endosome membrane 2 CD1A, TFRC
Endoplasmic reticulum membrane 1 HSP90B1
Nucleus 9 ALB, HDAC1, HDAC11, HDAC2, HDAC3, HDAC6, HDAC8, HSP90B1, TFPT
cytosol 8 ALB, CAT, CD44, GPT, HDAC1, HDAC3, HDAC6, HSP90B1
dendrite 1 HDAC6
centrosome 2 ALB, HDAC6
nucleoplasm 6 HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, TFPT
Cell membrane 7 ABCB1, CCR7, CD1A, CD44, CD80, CD86, TFRC
Cell projection, axon 1 HDAC6
Multi-pass membrane protein 2 ABCB1, CCR7
Synapse 1 ACAN
cell surface 6 ABCB1, CCR7, CD44, CD80, CD86, TFRC
glutamatergic synapse 2 ACAN, TFRC
Golgi apparatus 3 ALB, CD44, HDAC3
neuronal cell body 1 HDAC1
smooth endoplasmic reticulum 1 HSP90B1
Cytoplasm, cytosol 1 HDAC3
endosome 1 TFRC
plasma membrane 9 ABCB1, CCR7, CD1A, CD44, CD80, CD86, HDAC11, HDAC3, TFRC
Membrane 9 ABCB1, CAT, CD1A, CD44, CD80, CD86, HDAC2, HSP90B1, TFRC
apical plasma membrane 2 ABCB1, CD44
axon 1 HDAC6
basolateral plasma membrane 2 CD44, TFRC
caveola 1 HDAC6
extracellular exosome 8 ABCB1, ALB, CAT, CD44, CD86, GPT, HSP90B1, TFRC
endoplasmic reticulum 2 ALB, HSP90B1
extracellular space 5 ACAN, ALB, CD1A, IL10, TFRC
lysosomal lumen 1 ACAN
perinuclear region of cytoplasm 3 HDAC6, HSP90B1, TFRC
mitochondrion 2 CAT, CCR7
protein-containing complex 5 ALB, CAT, HDAC1, HDAC2, HSP90B1
intracellular membrane-bounded organelle 2 CAT, TFRC
ESC/E(Z) complex 1 HDAC2
Single-pass type I membrane protein 4 CD1A, CD44, CD80, CD86
Secreted 3 ALB, CD44, IL10
extracellular region 7 ACAN, ALB, CAT, CD44, HSP90B1, IL10, TFRC
Single-pass membrane protein 1 CD44
mitochondrial matrix 1 CAT
anchoring junction 1 ALB
Cell projection, cilium 1 HDAC6
centriolar satellite 1 CD86
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 HDAC6
external side of plasma membrane 5 CCR7, CD1A, CD80, CD86, TFRC
Extracellular vesicle 1 TFRC
Secreted, extracellular space, extracellular matrix 1 ACAN
multivesicular body 1 HDAC6
perikaryon 1 HDAC6
cytoplasmic vesicle 1 TFRC
axon cytoplasm 1 HDAC6
midbody 1 HSP90B1
Early endosome 1 TFRC
clathrin-coated pit 1 TFRC
recycling endosome 1 TFRC
Single-pass type II membrane protein 1 TFRC
Apical cell membrane 1 ABCB1
heterochromatin 1 HDAC1
Membrane raft 1 CD1A
Cytoplasm, cytoskeleton 1 HDAC6
focal adhesion 3 CAT, CD44, HSP90B1
microtubule 1 HDAC6
GABA-ergic synapse 1 ACAN
Peroxisome 1 CAT
basement membrane 1 ACAN
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
collagen-containing extracellular matrix 2 ACAN, HSP90B1
ciliary basal body 2 ALB, HDAC6
chromatin 3 HDAC1, HDAC2, HDAC3
cell leading edge 1 HDAC6
microtubule associated complex 1 HDAC6
cell projection 1 CD44
mitotic spindle 1 HDAC3
Chromosome 2 HDAC3, HDAC8
Cytoplasm, cytoskeleton, cilium basal body 1 HDAC6
centriole 1 ALB
spindle pole 1 ALB
chromosome, telomeric region 1 HDAC2
nuclear chromosome 1 HDAC8
actin filament 1 TFPT
blood microparticle 2 ALB, TFRC
Recycling endosome membrane 1 TFRC
microvillus 1 CD44
Cell projection, microvillus 1 CD44
Cell projection, dendrite 1 HDAC6
Melanosome 2 HSP90B1, TFRC
sperm plasma membrane 1 HSP90B1
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
HFE-transferrin receptor complex 1 TFRC
secretory granule membrane 1 CD44
Golgi lumen 1 ACAN
endoplasmic reticulum lumen 2 ALB, HSP90B1
transcription repressor complex 2 HDAC1, HDAC3
platelet alpha granule lumen 1 ALB
histone deacetylase complex 6 HDAC1, HDAC11, HDAC2, HDAC3, HDAC6, HDAC8
NuRD complex 2 HDAC1, HDAC2
perineuronal net 1 ACAN
aggresome 1 HDAC6
clathrin-coated endocytic vesicle membrane 1 TFRC
Sarcoplasmic reticulum lumen 1 HSP90B1
Sin3-type complex 2 HDAC1, HDAC2
external side of apical plasma membrane 1 ABCB1
postsynaptic recycling endosome membrane 1 TFRC
lamellipodium membrane 1 CD44
Ino80 complex 1 TFPT
endocytic vesicle lumen 1 HSP90B1
[Transferrin receptor protein 1, serum form]: Secreted 1 TFRC
catalase complex 1 CAT
inclusion body 1 HDAC6
macrophage migration inhibitory factor receptor complex 1 CD44
endoplasmic reticulum chaperone complex 1 HSP90B1
protein complex involved in cell adhesion 1 CD80
perisynaptic extracellular matrix 1 ACAN
ciliary transition fiber 1 ALB


文献列表

  • Massimo Blandino, Valentina Scarpino, Giulio Testa, Francesca Vanara, Amedeo Reyneri. The Effect of Foliar Fungicide and Insecticide Application on the Contamination of Fumonisins, Moniliformin and Deoxynivalenol in Maize Used for Food Purposes. Toxins. 2022 06; 14(7):. doi: 10.3390/toxins14070422. [PMID: 35878160]
  • Magda Formela-Luboińska, Dorota Remlein-Starosta, Agnieszka Waśkiewicz, Zbigniew Karolewski, Jan Bocianowski, Łukasz Stępień, Mateusz Labudda, Philippe Jeandet, Iwona Morkunas. The Role of Saccharides in the Mechanisms of Pathogenicity of Fusarium oxysporum f. sp. lupini in Yellow Lupine (Lupinus luteus L.). International journal of molecular sciences. 2020 Oct; 21(19):. doi: 10.3390/ijms21197258. [PMID: 33019571]
  • Hester F Vismer, Gordon S Shephard, Liana van der Westhuizen, Pamella Mngqawa, Vuyiswa Bushula-Njah, John F Leslie. Mycotoxins produced by Fusarium proliferatum and F. pseudonygamai on maize, sorghum and pearl millet grains in vitro. International journal of food microbiology. 2019 May; 296(?):31-36. doi: 10.1016/j.ijfoodmicro.2019.02.016. [PMID: 30826540]
  • Ł Stępień, K Gromadzka, J Chełkowski, A Basińska-Barczak, J Lalak-Kańczugowska. Diversity and mycotoxin production by Fusarium temperatum and Fusarium subglutinans as causal agents of pre-harvest Fusarium maize ear rot in Poland. Journal of applied genetics. 2019 Feb; 60(1):113-121. doi: 10.1007/s13353-018-0478-x. [PMID: 30430379]
  • Gabriela A Pena, Lilia R Cavaglieri, Sofía N Chulze. Fusarium species and moniliformin occurrence in sorghum grains used as ingredient for animal feed in Argentina. Journal of the science of food and agriculture. 2019 Jan; 99(1):47-54. doi: 10.1002/jsfa.9140. [PMID: 29797405]
  • Veli Hietaniemi, Sari Rämö, Tapani Yli-Mattila, Marika Jestoi, Sari Peltonen, Mirja Kartio, Elina Sieviläinen, Tauno Koivisto, Päivi Parikka. Updated survey of Fusarium species and toxins in Finnish cereal grains. Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment. 2016 May; 33(5):831-48. doi: 10.1080/19440049.2016.1162112. [PMID: 27002810]
  • Martina Jonsson, Janne Atosuo, Marika Jestoi, Alexis V Nathanail, Ulla-Maija Kokkonen, Marjukka Anttila, Pertti Koivisto, Esa-Matti Lilius, Kimmo Peltonen. Repeated dose 28-day oral toxicity study of moniliformin in rats. Toxicology letters. 2015 Feb; 233(1):38-44. doi: 10.1016/j.toxlet.2014.11.006. [PMID: 25482064]
  • Ksenija Nesic, Snezana Ivanovic, Vladimir Nesic. Fusarial toxins: secondary metabolites of Fusarium fungi. Reviews of environmental contamination and toxicology. 2014; 228(?):101-20. doi: 10.1007/978-3-319-01619-1_5. [PMID: 24162094]
  • Łukasz Stępień, Grzegorz Koczyk, Agnieszka Waśkiewicz. Diversity of Fusarium species and mycotoxins contaminating pineapple. Journal of applied genetics. 2013 Aug; 54(3):367-80. doi: 10.1007/s13353-013-0146-0. [PMID: 23572446]
  • Tom Gräfenhan, Susan K Patrick, Mike Roscoe, Robert Trelka, Don Gaba, Jason M Chan, Twylla McKendry, Randy M Clear, Sheryl A Tittlemier. Fusarium damage in cereal grains from Western Canada. 1. Phylogenetic analysis of moniliformin-producing fusarium species and their natural occurrence in mycotoxin-contaminated wheat, oats, and rye. Journal of agricultural and food chemistry. 2013 Jun; 61(23):5425-37. doi: 10.1021/jf400651p. [PMID: 23683177]
  • Martina Jonsson, Marika Jestoi, Alexis V Nathanail, Ulla-Maija Kokkonen, Marjukka Anttila, Pertti Koivisto, Pirkko Karhunen, Kimmo Peltonen. Application of OECD Guideline 423 in assessing the acute oral toxicity of moniliformin. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2013 Mar; 53(?):27-32. doi: 10.1016/j.fct.2012.11.023. [PMID: 23201451]
  • Agnieszka Waśkiewicz, Łukasz Stępień. Mycotoxins biosynthesized by plant-derived Fusarium isolates. Arhiv za higijenu rada i toksikologiju. 2012 Dec; 63(4):437-46. doi: 10.2478/10004-1254-63-2012-2230. [PMID: 23334038]
  • Lidia Irzykowska, Jan Bocianowski, Agnieszka Waśkiewicz, Zbigniew Weber, Zbigniew Karolewski, Piotr Goliński, Marian Kostecki, Witold Irzykowski. Genetic variation of Fusarium oxysporum isolates forming fumonisin B(1) and moniliformin. Journal of applied genetics. 2012 May; 53(2):237-47. doi: 10.1007/s13353-012-0087-z. [PMID: 22367665]
  • Łukasz Stępień, Karolina Gromadzka, Jerzy Chełkowski. Polymorphism of mycotoxin biosynthetic genes among Fusarium equiseti isolates from Italy and Poland. Journal of applied genetics. 2012 May; 53(2):227-36. doi: 10.1007/s13353-012-0085-1. [PMID: 22354659]
  • Alberto González, M de Los Ángeles Cabrera, M Josefa Henríquez, Rodrigo A Contreras, Bernardo Morales, Alejandra Moenne. Cross talk among calcium, hydrogen peroxide, and nitric oxide and activation of gene expression involving calmodulins and calcium-dependent protein kinases in Ulva compressa exposed to copper excess. Plant physiology. 2012 Mar; 158(3):1451-62. doi: 10.1104/pp.111.191759. [PMID: 22234999]
  • H J van der Fels-Klerx, T C de Rijk, C J H Booij, P W Goedhart, E A M Boers, C Zhao, C Waalwijk, H G J Mol, T A J van der Lee. Occurrence of Fusarium Head Blight species and Fusarium mycotoxins in winter wheat in the Netherlands in 2009. Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment. 2012; 29(11):1716-26. doi: 10.1080/19440049.2012.685891. [PMID: 22624849]
  • Philipp Wiemann, Sabine Albermann, Eva-Maria Niehaus, Lena Studt, Katharina W von Bargen, Nelson L Brock, Hans-Ulrich Humpf, Jeroen S Dickschat, Bettina Tudzynski. The Sfp-type 4'-phosphopantetheinyl transferase Ppt1 of Fusarium fujikuroi controls development, secondary metabolism and pathogenicity. PloS one. 2012; 7(5):e37519. doi: 10.1371/journal.pone.0037519. [PMID: 22662164]
  • Yazmid Reyes-Dominguez, Stefan Boedi, Michael Sulyok, Gerlinde Wiesenberger, Norbert Stoppacher, Rudolf Krska, Joseph Strauss. Heterochromatin influences the secondary metabolite profile in the plant pathogen Fusarium graminearum. Fungal genetics and biology : FG & B. 2012 Jan; 49(1):39-47. doi: 10.1016/j.fgb.2011.11.002. [PMID: 22100541]
  • Y Yang, N Bouras, J Yang, R J Howard, S E Strelkov. Mycotoxin production by isolates of Fusarium lactis from greenhouse sweet pepper (Capsicum annuum). International journal of food microbiology. 2011 Dec; 151(2):150-6. doi: 10.1016/j.ijfoodmicro.2011.08.013. [PMID: 21903288]
  • Daniela S Christ, Bernward Märländer, Mark Varrelmann. Characterization and mycotoxigenic potential of Fusarium species in freshly harvested and stored sugar beet in Europe. Phytopathology. 2011 Nov; 101(11):1330-7. doi: 10.1094/phyto-01-11-0002. [PMID: 21770776]
  • Daniela S Christ, Ruben Gödecke, Andreas von Tiedemann, Mark Varrelmann. Pathogenicity, symptom development, and mycotoxin formation in wheat by Fusarium species frequently isolated from sugar beet. Phytopathology. 2011 Nov; 101(11):1338-45. doi: 10.1094/phyto-01-11-0003. [PMID: 21635142]
  • Lukasz Stępień, Grzegorz Koczyk, Agnieszka Waśkiewicz. Genetic and phenotypic variation of Fusarium proliferatum isolates from different host species. Journal of applied genetics. 2011 Nov; 52(4):487-96. doi: 10.1007/s13353-011-0059-8. [PMID: 21796391]
  • Jian-Hua Wang, Mbacke Ndoye, Jing-Bo Zhang, He-Ping Li, Yu-Cai Liao. Population structure and genetic diversity of the Fusarium graminearum species complex. Toxins. 2011 08; 3(8):1020-37. doi: 10.3390/toxins3081020. [PMID: 22069755]
  • Dolores Fernández-Ortuño, Sarah L Atkins, Bart A Fraaije. The use of a CYP51C gene based PCR-RFLP assay for simultaneous detection and identification of Fusarium avenaceum and F. tricinctum in wheat. International journal of food microbiology. 2011 Jan; 145(1):370-4. doi: 10.1016/j.ijfoodmicro.2011.01.011. [PMID: 21269719]
  • Tomasz Kulik, Agnieszka Pszczółkowska, Maciej Lojko. Multilocus phylogenetics show high intraspecific variability within Fusarium avenaceum. International journal of molecular sciences. 2011; 12(9):5626-40. doi: 10.3390/ijms12095626. [PMID: 22016614]
  • P Golinski, A Waskiewicz, H Wisniewska, I Kiecana, E Mielniczuk, K Gromadzka, M Kostecki, J Bocianowski, E Rymaniak. Reaction of winter wheat (Triticum aestivum L.) cultivars to infection with Fusarium spp.: mycotoxin contamination in grain and chaff. Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment. 2010 Jul; 27(7):1015-24. doi: 10.1080/19440041003702208. [PMID: 20432094]
  • A Waskiewicz, P Golinski, Z Karolewski, L Irzykowska, J Bocianowski, M Kostecki, Z Weber. Formation of fumonisins and other secondary metabolites by Fusarium oxysporum and F. proliferatum: a comparative study. Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment. 2010 May; 27(5):608-15. doi: 10.1080/19440040903551947. [PMID: 20455157]
  • Kerry O'Donnell, Cécile Gueidan, Stacy Sink, Peter R Johnston, Pedro W Crous, Anthony Glenn, Ron Riley, Nicholas C Zitomer, Patrick Colyer, Cees Waalwijk, Theo van der Lee, Antonio Moretti, Seogchan Kang, Hye-Seon Kim, David M Geiser, Jean H Juba, Robert P Baayen, Matthew G Cromey, Sean Bithell, Deanna A Sutton, Kerstin Skovgaard, Randy Ploetz, H Corby Kistler, Monica Elliott, Mike Davis, Brice A J Sarver. A two-locus DNA sequence database for typing plant and human pathogens within the Fusarium oxysporum species complex. Fungal genetics and biology : FG & B. 2009 Dec; 46(12):936-48. doi: 10.1016/j.fgb.2009.08.006. [PMID: 19715767]
  • Jens Laurids Sørensen, Richard Kerry Phipps, Kristian Fog Nielsen, Hans-Josef Schroers, Jana Frank, Ulf Thrane. Analysis of Fusarium avenaceum metabolites produced during wet apple core rot. Journal of agricultural and food chemistry. 2009 Feb; 57(4):1632-9. doi: 10.1021/jf802926u. [PMID: 19170495]
  • Nora A Foroud, François Eudes. Trichothecenes in cereal grains. International journal of molecular sciences. 2009 Jan; 10(1):147-173. doi: 10.3390/ijms10010147. [PMID: 19333439]
  • D Sharma, R K Asrani, D R Ledoux, N Jindal, G E Rottinghaus, V K Gupta. Individual and combined effects of fumonisin b1 and moniliformin on clinicopathological and cell-mediated immune response in Japanese quail. Poultry science. 2008 Jun; 87(6):1039-51. doi: 10.3382/ps.2007-00204. [PMID: 18492990]
  • Tomasz Kulik. Detection of Fusarium tricinctum from cereal grain using PCR assay. Journal of applied genetics. 2008; 49(3):305-11. doi: 10.1007/bf03195628. [PMID: 18670068]
  • Irma Morales-Rodríguez, María de J Yañez-Morales, Hilda V Silva-Rojas, Gabino García-de-Los-Santos, Doralinda A Guzmán-de-Peña. Biodiversity of Fusarium species in Mexico associated with ear rot in maize, and their identification using a phylogenetic approach. Mycopathologia. 2007 Jan; 163(1):31-9. doi: 10.1007/s11046-006-0082-1. [PMID: 17216329]
  • Silvio Uhlig, Marika Jestoi, Ann Kristin Knutsen, Berit T Heier. Multiple regression analysis as a tool for the identification of relations between semi-quantitative LC-MS data and cytotoxicity of extracts of the fungus Fusarium avenaceum (syn. F. arthrosporioides). Toxicon : official journal of the International Society on Toxinology. 2006 Oct; 48(5):567-79. doi: 10.1016/j.toxicon.2006.07.007. [PMID: 16908037]
  • Anne E Desjardins, Chris M Maragos, Robert H Proctor. Maize ear rot and moniliformin contamination by cryptic species of Fusarium subglutinans. Journal of agricultural and food chemistry. 2006 Sep; 54(19):7383-90. doi: 10.1021/jf0612272. [PMID: 16968109]
  • H Saremi, S M Okhovvat. Mycotoxin producing Fusarium species associated with plant disease on potato, wheat, corn and animal diseases in northwest Iran. Communications in agricultural and applied biological sciences. 2006; 71(3 Pt B):1175-85. doi: . [PMID: 17390876]
  • Silvio Uhlig, Arno C Gutleb, Ulf Thrane, Arne Flåøyen. Identification of cytotoxic principles from Fusarium avenaceum using bioassay-guided fractionation. Toxicon : official journal of the International Society on Toxinology. 2005 Aug; 46(2):150-9. doi: 10.1016/j.toxicon.2005.03.005. [PMID: 15946720]
  • Stefan Malonek, Christiane Bömke, Erich Bornberg-Bauer, María C Rojas, Peter Hedden, Paul Hopkins, Bettina Tudzynski. Distribution of gibberellin biosynthetic genes and gibberellin production in the Gibberella fujikuroi species complex. Phytochemistry. 2005 Jun; 66(11):1296-311. doi: 10.1016/j.phytochem.2005.04.012. [PMID: 15925394]
  • T Javed, R M Bunte, M A Dombrink-Kurtzman, J L Richard, G A Bennett, L M Côté, W B Buck. Comparative pathologic changes in broiler chicks on feed amended with Fusarium proliferatum culture material or purified fumonisin B1 and moniliformin. Mycopathologia. 2005 Jun; 159(4):553-64. doi: 10.1007/s11046-005-4518-9. [PMID: 15983742]
  • John F Leslie, Kurt A Zeller, Sandra C Lamprecht, John P Rheeder, Walter F O Marasas. Toxicity, pathogenicity, and genetic differentiation of five species of fusarium from sorghum and millet. Phytopathology. 2005 Mar; 95(3):275-83. doi: 10.1094/phyto-95-0275. [PMID: 18943121]
  • D R Ledoux, J N Broomhead, A J Bermudez, G E Rottinghaus. Individual and combined effects of the Fusarium mycotoxins fumonisin B1 and moniliformin in broiler chicks. Avian diseases. 2003 Oct; 47(4):1368-75. doi: 10.1637/7028. [PMID: 14708984]
  • Juan Manuel Bravo, Sonia Campo, Isabel Murillo, Mária Coca, Blanca San Segundo. Fungus- and wound-induced accumulation of mRNA containing a class II chitinase of the pathogenesis-related protein 4 (PR-4) family of maize. Plant molecular biology. 2003 Jul; 52(4):745-59. doi: 10.1023/a:1025016416951. [PMID: 13677464]
  • Faik Atroshi, Aldo Rizzo, Tuomas Westermarck, Terhi Ali-Vehmas. Antioxidant nutrients and mycotoxins. Toxicology. 2002 Nov; 180(2):151-67. doi: 10.1016/s0300-483x(02)00388-8. [PMID: 12324191]
  • J N Broomhead, D R Ledoux, A J Bermudez, G E Rottinghaus. Chronic effects of moniliformin in broiler and turkeys fed dietary treatments to market age. Avian diseases. 2002 Oct; 46(4):901-8. doi: 10.1637/0005-2086(2002)046[0901:ceomib]2.0.co;2. [PMID: 12495051]
  • D Abramson, B McCallum, D M Smith, A Tekauz. Moniliformin in barley inoculated with Fusarium avenaceum. Food additives and contaminants. 2002 Aug; 19(8):765-9. doi: 10.1080/02652030210136991. [PMID: 12227940]
  • Ellen Morrison, Barbara Kosiak, Alberto Ritieni, Are H Aastveit, Silvio Uhlig, Aksel Bernhoft. Mycotoxin production by Fusarium avenaceum strains isolated from Norwegian grain and the cytotoxicity of rice culture extracts to porcine kidney epithelial cells. Journal of agricultural and food chemistry. 2002 May; 50(10):3070-5. doi: 10.1021/jf011532h. [PMID: 11982443]
  • B Harvey, Thomas S Edrington, Leon F Kubena, George E Rottinghaus, James R Turk, Kenneth J Genovese, Richard L Ziprin, David J Nisbet. Toxicity of fumonisin from Fusarium verticillioides culture material and moniliformin from Fusarium fujikuroi culture material when fed singly and in combination to growing barrows. Journal of food protection. 2002 Feb; 65(2):373-7. doi: 10.4315/0362-028x-65.2.373. [PMID: 11848570]
  • R B Harvey, T S Edrington, L F Kubena, G E Rottinghaus, J R Turk, K J Genovese, D J Nisbet. Toxicity of moniliformin from Fusarium fujikuroi culture material to growing barrows. Journal of food protection. 2001 Nov; 64(11):1780-4. doi: 10.4315/0362-028x-64.11.1780. [PMID: 11726159]
  • T H Lin, S J Chang, C C Chen, J P Wang, L T Tsao. Two phenanthraquinones from Dendrobium moniliforme. Journal of natural products. 2001 Aug; 64(8):1084-6. doi: 10.1021/np010016i. [PMID: 11520233]
  • W Mubatanhema, M O Moss, M J Frank, D M Wilson. Prevalence of Fusarium species of the Liseola section on Zimbabwean corn and their ability to produce the mycotoxins zearalenone, moniliformin and fumonisin B1. Mycopathologia. 1999 Dec; 148(3):157-63. doi: 10.1023/a:1007146419501. [PMID: 11189767]
  • C M Morris, Y C Li, D R Ledoux, A J Bermudez, G E Rottinghaus. The individual and combined effects of feeding moniliformin, supplied by Fusarium fujikuroi culture material, and deoxynivalenol in young turkey poults. Poultry science. 1999 Aug; 78(8):1110-5. doi: 10.1093/ps/78.8.1110. [PMID: 10472836]
  • M K Morgan, S D Fitzgerald, G E Rottinghaus, S J Bursian, R J Aulerich. Toxic effects to mink of moniliformin extracted from Fusarium fujikuroi culture material. Veterinary and human toxicology. 1999 Feb; 41(1):1-5. doi: . [PMID: 9949474]
  • H K Abbas, R D Cartwright, W Xie, C J Mirocha, J L Richard, T J Dvorak, G L Sciumbato, W T Shier. Mycotoxin production by Fusarium proliferatum isolates from rice with Fusarium sheath rot disease. Mycopathologia. 1999; 147(2):97-104. doi: 10.1023/a:1007147813326. [PMID: 10967968]
  • M K Morgan, S J Bursian, G E Rottinghaus, G A Bennett, J A Render, R J Aulerich. Subacute and reproductive effects in mink from exposure to Fusarium fujikuroi culture material (M-1214) containing known concentrations of moniliformin. Archives of environmental contamination and toxicology. 1998 Oct; 35(3):513-7. doi: 10.1007/s002449900410. [PMID: 9732485]
  • R B Harvey, L F Kubena, G E Rottinghaus, J R Turk, H H Casper, S A Buckley. Moniliformin from Fusarium fujikuroi culture material and deoxynivalenol from naturally contaminated wheat incorporated into diets of broiler chicks. Avian diseases. 1997 Oct; 41(4):957-63. doi: . [PMID: 9454932]
  • L F Kubena, R B Harvey, S A Buckley, T S Edrington, G E Rottinghaus. Individual and combined effects of moniliformin present in Fusarium fujikuroi culture material and aflatoxin in broiler chicks. Poultry science. 1997 Feb; 76(2):265-70. doi: 10.1093/ps/76.2.265. [PMID: 9057205]
  • R Y Reams, H L Thacker, D D Harrington, M N Novilla, G E Rottinghaus, G A Bennett, J Horn. A sudden death syndrome induced in poults and chicks fed diets containing Fusarium fujikuroi with known concentrations of moniliformin. Avian diseases. 1997 Jan; 41(1):20-35. doi: . [PMID: 9087317]
  • H Lew, J Chelkowski, P Pronczuk, W Edinger. Occurrence of the mycotoxin moniliformin in maize (Zea mays L.) ears infected by Fusarium subglutinans (Wollenw. & Reinking) Nelson et al. Food additives and contaminants. 1996 Apr; 13(3):321-4. doi: 10.1080/02652039609374414. [PMID: 8718747]
  • J F Leslie, W F Marasas, G S Shephard, E W Sydenham, S Stockenström, P G Thiel. Duckling toxicity and the production of fumonisin and moniliformin by isolates in the A and E mating populations of Gibberella fujikuroi (Fusarium moniliforme). Applied and environmental microbiology. 1996 Apr; 62(4):1182-7. doi: 10.1128/aem.62.4.1182-1187.1996. [PMID: 8919779]
  • M A Qureshi, J D Garlich, W M Hagler, D Weinstock. Fusarium proliferatum culture material alters several production and immune performance parameters in White Leghorn chickens. Immunopharmacology and immunotoxicology. 1995 Nov; 17(4):791-804. doi: 10.3109/08923979509037197. [PMID: 8537614]
  • T Javed, M A Dombrink-Kurtzman, J L Richard, G A Bennett, L M Côté, W B Buck. Serohematologic alterations in broiler chicks on feed amended with Fusarium proliferatum culture material on fumonisin B1 and moniliformin. Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc. 1995 Oct; 7(4):520-6. doi: 10.1177/104063879500700417. [PMID: 8580176]
  • J O Hall, T Javed, G A Bennett, J L Richard, M A Dombrink-Kurtzman, L M Côté, W B Buck. Serum vitamin A (retinol) reduction in broiler chicks on feed amended with Fusarium proliferatum culture material or fumonisin B1 and moniliformin. Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc. 1995 Jul; 7(3):416-8. doi: 10.1177/104063879500700326. [PMID: 7578467]
  • J Schumacher, J Mullen, R Shelby, S Lenz, D C Ruffin, B W Kemppainen. An investigation of the role of Fusarium moniliforme in duodenitis/proximal jejunitis of horses. Veterinary and human toxicology. 1995 Feb; 37(1):39-45. doi: NULL. [PMID: 7709589]
  • R F Vesonder, H Gasdorf, R E Peterson. Comparison of the cytotoxicities of Fusarium metabolites and Alternaria metabolite AAL-toxin to cultured mammalian cell lines. Archives of environmental contamination and toxicology. 1993 May; 24(4):473-7. doi: 10.1007/bf01146164. [PMID: 8507101]
  • J M Casacuberta, D Raventós, P Puigdoménech, B San Segundo. Expression of the gene encoding the PR-like protein PRms in germinating maize embryos. Molecular & general genetics : MGG. 1992 Jul; 234(1):97-104. doi: 10.1007/bf00272350. [PMID: 1495490]
  • H K Abbas, C J Mirocha, R F Vesonder, R Gunther. Acute toxic effects of an isolate of moniliformin-producing Fusarium oxysporum and purified moniliformin on rats. Archives of environmental contamination and toxicology. 1990 May; 19(3):433-6. doi: 10.1007/bf01054989. [PMID: 2353842]