STERIGMATOCYSTIN

STERIGMATOCYSTIN is a lipid of Polyketides (PK) class. Sterigmatocystin is associated with abnormalities such as CLEFT LIP, CONGENITAL HEALED, Exanthema and Lung diseases. The involved functions are known as sterigmatocystin biosynthetic process, Signal, secondary metabolic process, Biosynthetic Pathways and Anabolism. Sterigmatocystin often locates in Genital system, SAGA complex, Chromosomes, germ tube and Extracellular. The associated genes with STERIGMATOCYSTIN are Genome, Genes, vif, Homologous Gene, Genes, Regulator and Gene Clusters. The related lipids are hexanoic acid, Fatty Acids and Fatty Acids, Unsaturated.

Cross Reference

Introduction

To understand associated biological information of STERIGMATOCYSTIN, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with STERIGMATOCYSTIN?

STERIGMATOCYSTIN is suspected in CLEFT LIP, CONGENITAL HEALED, Exanthema, Lung diseases and other diseases in descending order of the highest number of associated sentences.

Related references are mostly published in these journals:

Disease Cross reference Weighted score Related literature
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Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with STERIGMATOCYSTIN

MeSH term MeSH ID Detail
Adenocarcinoma D000230 166 associated lipids
Adenoma D000236 40 associated lipids
Body Weight D001835 333 associated lipids
Cattle Diseases D002418 24 associated lipids
Cell Transformation, Neoplastic D002471 126 associated lipids
Esophageal Neoplasms D004938 20 associated lipids
Gastritis D005756 27 associated lipids
Hemangiosarcoma D006394 4 associated lipids
Liver Diseases D008107 31 associated lipids
Liver Neoplasms, Experimental D008114 46 associated lipids
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PubChem Associated disorders and diseases

What pathways are associated with STERIGMATOCYSTIN

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with STERIGMATOCYSTIN?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
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What functions are associated with STERIGMATOCYSTIN?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with STERIGMATOCYSTIN?

Related references are published most in these journals:

Lipid concept Cross reference Weighted score Related literatures
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What genes are associated with STERIGMATOCYSTIN?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with STERIGMATOCYSTIN?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with STERIGMATOCYSTIN

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Per page 10 20 50 100 | Total 527
Authors Title Published Journal PubMed Link
Shimizu M et al. Hydrolase controls cellular NAD, sirtuin, and secondary metabolites. 2012 Mol. Cell. Biol. pmid:22801369
Kocić-Tanackov S et al. Effects of onion (Allium cepa L.) and garlic (Allium sativum L.) essential oils on the Aspergillus versicolor growth and sterigmatocystin production. 2012 J. Food Sci. pmid:22497489
Liu Y et al. Sterigmatocystin alters the number of FoxP3+ regulatory T cells and plasmacytoid dendritic cells in BALB/c mice. 2012 Food Chem. Toxicol. pmid:22429820
Jakšić D et al. Cytotoxicity and genotoxicity of versicolorins and 5-methoxysterigmatocystin in A549 cells. 2012 Arch. Toxicol. pmid:22648070
Laskowski-Peak MC et al. VEA1 is required for cleistothecial formation and virulence in Histoplasma capsulatum. 2012 Fungal Genet. Biol. pmid:22841690
Ramamoorthy V et al. veA-dependent RNA-pol II transcription elongation factor-like protein, RtfA, is associated with secondary metabolism and morphological development in Aspergillus nidulans. 2012 Mol. Microbiol. pmid:22783880
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Bartoszewska M et al. The significance of peroxisomes in secondary metabolite biosynthesis in filamentous fungi. 2011 Biotechnol. Lett. pmid:21660569
Bansal J et al. Surveys of rice sold in Canada for aflatoxins, ochratoxin A and fumonisins. 2011 Food Addit Contam Part A Chem Anal Control Expo Risk Assess pmid:21623501
Samson RA et al. New taxa in Aspergillus section Usti. 2011 Stud. Mycol. pmid:21892244
Varga J et al. Two new aflatoxin producing species, and an overview of Aspergillus section Flavi. 2011 Stud. Mycol. pmid:21892243
Boenisch MJ and Schäfer W Fusarium graminearum forms mycotoxin producing infection structures on wheat. 2011 BMC Plant Biol. pmid:21798058
Pauly JL and Paszkiewicz G Cigarette smoke, bacteria, mold, microbial toxins, and chronic lung inflammation. 2011 J Oncol pmid:21772847
Trienens M and Rohlfs M Experimental evolution of defense against a competitive mold confers reduced sensitivity to fungal toxins but no increased resistance in Drosophila larvae. 2011 BMC Evol. Biol. pmid:21756302
Khaldi N and Wolfe KH Evolutionary Origins of the Fumonisin Secondary Metabolite Gene Cluster in Fusarium verticillioides and Aspergillus niger. 2011 Int J Evol Biol pmid:21716743
Gerbaldo GA et al. Surveillance of Aflatoxin and Microbiota Related to Brewer's Grain Destined for Swine Feed in Argentina. 2011 Vet Med Int pmid:21547231
Freitas-Silva O et al. Tracing fungi secondary metabolites in Brazil nuts using LC-MS/MS. 2011 Drug Metab Lett pmid:21722090
Cai GH et al. Fungal DNA, allergens, mycotoxins and associations with asthmatic symptoms among pupils in schools from Johor Bahru, Malaysia. 2011 Pediatr Allergy Immunol pmid:21457336