| MeSH term | MeSH ID | Detail |
|---|---|---|
| Adenocarcinoma | D000230 | 166 associated lipids |
| Lung Neoplasms | D008175 | 171 associated lipids |
| Cattle Diseases | D002418 | 24 associated lipids |
| Body Weight | D001835 | 333 associated lipids |
| Esophageal Neoplasms | D004938 | 20 associated lipids |
| Precancerous Conditions | D011230 | 48 associated lipids |
| Gastritis | D005756 | 27 associated lipids |
| Liver Diseases | D008107 | 31 associated lipids |
| Weight Gain | D015430 | 101 associated lipids |
| Cell Transformation, Neoplastic | D002471 | 126 associated lipids |
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
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 PathwaysWhat cellular locations are associated with STERIGMATOCYSTIN?
Visualization in cellular structure
Associated locations are in red color. Not associated locations are in black.
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
Download all related citations| Authors | Title | Published | Journal | PubMed Link |
|---|---|---|---|---|
| Chang PK et al. | Deletion of the Aspergillus flavus orthologue of A. nidulans fluG reduces conidiation and promotes production of sclerotia but does not abolish aflatoxin biosynthesis. | 2012 | Appl. Environ. Microbiol. | pmid:22904054 |
| 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 |
| Reyes-Dominguez Y et al. | Heterochromatin influences the secondary metabolite profile in the plant pathogen Fusarium graminearum. | 2012 | Fungal Genet. Biol. | pmid:22100541 |
| Huţanaşu C et al. | [High levels of sterigmatocystin in patients with chronic liver diseases]. | 2011 Jan-Mar | Rev Med Chir Soc Med Nat Iasi | pmid:21688557 |
| Rank C et al. | Distribution of sterigmatocystin in filamentous fungi. | 2011 Apr-May | Fungal Biol | pmid:21530923 |
| Bartoszewska M et al. | The significance of peroxisomes in secondary metabolite biosynthesis in filamentous fungi. | 2011 | Biotechnol. Lett. | pmid:21660569 |
| Zeng H et al. | Conversion of 11-hydroxy-O-methylsterigmatocystin to aflatoxin G1 in Aspergillus parasiticus. | 2011 | Appl. Microbiol. Biotechnol. | pmid:21153813 |
| Nasmith CG et al. | Tri6 is a global transcription regulator in the phytopathogen Fusarium graminearum. | 2011 | PLoS Pathog. | pmid:21980289 |
| 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 |
| 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 |