MeSH term | MeSH ID | Detail |
---|---|---|
Diabetes Mellitus, Type 2 | D003924 | 87 associated lipids |
Diabetes Mellitus, Experimental | D003921 | 85 associated lipids |
Arteriosclerosis | D001161 | 86 associated lipids |
Hyperlipidemias | D006949 | 73 associated lipids |
1-octadecanoyl-sn-glycero-3-phosphocholine is a lipid of Glycerophospholipids (GP) class. 1-octadecanoyl-sn-glycero-3-phosphocholine is associated with abnormalities such as Septicemia. The involved functions are known as Phosphorylation, MAP kinase activity, Phagocytosis, protein serine/threonine kinase activity and Uptake. The associated genes with 1-octadecanoyl-sn-glycero-3-phosphocholine are FPR1 gene and OLR1 gene. The related lipids are Lysophosphatidylcholines.
To understand associated biological information of 1-octadecanoyl-sn-glycero-3-phosphocholine, 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.
1-octadecanoyl-sn-glycero-3-phosphocholine is suspected in Septicemia and other diseases in descending order of the highest number of associated sentences.
Disease | Cross reference | Weighted score | Related literature |
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We collected disease MeSH terms mapped to the references associated with 1-octadecanoyl-sn-glycero-3-phosphocholine
MeSH term | MeSH ID | Detail |
---|---|---|
Diabetes Mellitus, Type 2 | D003924 | 87 associated lipids |
Diabetes Mellitus, Experimental | D003921 | 85 associated lipids |
Arteriosclerosis | D001161 | 86 associated lipids |
Hyperlipidemias | D006949 | 73 associated lipids |
There are no associated biomedical information in the current reference collection.
There are no associated biomedical information in the current reference collection.
Function | Cross reference | Weighted score | Related literatures |
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Lipid concept | Cross reference | Weighted score | Related literatures |
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Gene | Cross reference | Weighted score | Related literatures |
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There are no associated biomedical information in the current reference collection.
Authors | Title | Published | Journal | PubMed Link |
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Nagy-Szakal D et al. | Insights into myalgic encephalomyelitis/chronic fatigue syndrome phenotypes through comprehensive metabolomics. | 2018 | Sci Rep | pmid:29968805 |
Quan H et al. | Stearoyl lysophosphatidylcholine enhances the phagocytic ability of macrophages through the AMP-activated protein kinase/p38 mitogen activated protein kinase pathway. | 2016 | Int. Immunopharmacol. | pmid:27517519 |
Yang Y et al. | Lipidomic analyses of female mice lacking hepatic lipase and endothelial lipase indicate selective modulation of plasma lipid species. | 2014 | Lipids | pmid:24777581 |
Zhang X et al. | Towards an understanding of the release behavior of temperature-sensitive liposomes: a possible explanation of the "pseudoequilibrium" release behavior at the phase transition temperature. | 2013 | J Liposome Res | pmid:23510297 |
Jung JH et al. | Inactivation of HDAC3 and STAT3 is critically involved in 1-stearoyl-sn-glycero-3-phosphocholine-induced apoptosis in chronic myelogenous leukemia K562 cells. | 2013 | Cell Biochem. Biophys. | pmid:23729004 |
Flasiński M et al. | Comparative characteristics of membrane-active single-chained ether phospholipids: PAF and lyso-PAF in Langmuir monolayers. | 2012 | J Phys Chem B | pmid:22316066 |
Shim J et al. | Morphological effect of lipid carriers on permeation of lidocaine hydrochloride through lipid membranes. | 2010 | Int J Pharm | pmid:20060459 |
Schaeffer DF et al. | LOX-1 augments oxLDL uptake by lysoPC-stimulated murine macrophages but is not required for oxLDL clearance from plasma. | 2009 | J. Lipid Res. | pmid:19359704 |
Tang D et al. | Quercetin prevents LPS-induced high-mobility group box 1 release and proinflammatory function. | 2009 | Am. J. Respir. Cell Mol. Biol. | pmid:19265175 |
Soga T et al. | Lysophosphatidylcholine enhances glucose-dependent insulin secretion via an orphan G-protein-coupled receptor. | 2005 | Biochem. Biophys. Res. Commun. | pmid:15607732 |