MeSH term | MeSH ID | Detail |
---|---|---|
Sudden Infant Death | D013398 | 3 associated lipids |
Zellweger Syndrome | D015211 | 39 associated lipids |
Metabolic Syndrome | D024821 | 44 associated lipids |
Polycystic Kidney Diseases | D007690 | 12 associated lipids |
Lignoceric acid is a lipid of Fatty Acyls (FA) class. Lignoceric acid is associated with abnormalities such as Adrenoleukodystrophy and Peroxisomal Disorders. The involved functions are known as Anabolism, establishment and maintenance of localization, Saturated, Process and long-chain-fatty-acid-CoA ligase activity. Lignoceric acid often locates in Membrane, Microsomes, Plasma membrane, peroxisome and Mitochondria. The associated genes with Lignoceric acid are SLC27A1 gene, CD36 gene, F10 gene, INHA gene and ABCD1 gene. The related lipids are Sphingolipids, Fatty Acids, erucic acid, inositolphosphoceramides and Palmitates.
To understand associated biological information of Lignoceric acid, 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.
Lignoceric acid is suspected in Peroxisomal Disorders, Adrenoleukodystrophy 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 Lignoceric acid
MeSH term | MeSH ID | Detail |
---|---|---|
Sudden Infant Death | D013398 | 3 associated lipids |
Zellweger Syndrome | D015211 | 39 associated lipids |
Metabolic Syndrome | D024821 | 44 associated lipids |
Polycystic Kidney Diseases | D007690 | 12 associated lipids |
There are no associated biomedical information in the current reference collection.
Associated locations are in red color. Not associated locations are in black.
Location | Cross reference | Weighted score | Related literatures |
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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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pmid: | ||||
Tanaka K et al. | Very long-chain fatty acids in erythrocyte membrane phospholipids in adrenoleukodystrophy. | 1989 | Acta Paediatr Jpn | pmid:2516693 |
Ogino T et al. | Metabolic studies of adrenoleukodystrophy. | 1978 | Adv. Exp. Med. Biol. | pmid:696482 |
Lemaitre RN et al. | Plasma phospholipid very-long-chain saturated fatty acids and incident diabetes in older adults: the Cardiovascular Health Study. | 2015 | Am. J. Clin. Nutr. | pmid:25787996 |
Poll-The BT et al. | A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy). | 1988 | Am. J. Hum. Genet. | pmid:2894756 |
Suzuki Y et al. | D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder. | 1997 | Am. J. Hum. Genet. | pmid:9345094 |
Jaffe R et al. | Neonatal adrenoleukodystrophy: clinical, pathologic, and biochemical delineation of a syndrome affecting both males and females. | 1982 | Am. J. Pathol. | pmid:7091298 |
Carneheim C et al. | Rare fatty acids in brown fat are substrates for thermogenesis during arousal from hibernation. | 1989 | Am. J. Physiol. | pmid:2912207 |
Noland RC et al. | Peroxisomal-mitochondrial oxidation in a rodent model of obesity-associated insulin resistance. | 2007 | Am. J. Physiol. Endocrinol. Metab. | pmid:17638705 |
Agazzi ME et al. | In-house validation of an improved sample extraction and clean-up method for GC determination of isomers of nervonic acid in meat products. | 2003 | Anal Bioanal Chem | pmid:12732919 |