| MeSH term | MeSH ID | Detail |
|---|---|---|
| Body Weight | D001835 | 333 associated lipids |
| Abnormalities, Multiple | D000015 | 13 associated lipids |
| Adrenoleukodystrophy | D000326 | 29 associated lipids |
| Refsum Disease | D012035 | 19 associated lipids |
| Cholestasis | D002779 | 23 associated lipids |
| Lipid Metabolism, Inborn Errors | D008052 | 26 associated lipids |
| Brain Diseases, Metabolic, Inborn | D020739 | 10 associated lipids |
| Peroxisomal Disorders | D018901 | 5 associated lipids |
| Brain Damage, Chronic | D001925 | 6 associated lipids |
| Chondrodysplasia Punctata | D002806 | 8 associated lipids |
Pristanic acid
Pristanic acid is a lipid of Prenol Lipids (PR) class. Pristanic acid is associated with abnormalities such as Refsum Disease, Peroxisomal Disorders, Hereditary Diseases, Peripheral Neuropathy and Sensory neuropathy. The involved functions are known as physiological aspects, Regulation, Pathogenesis, Oxidation and Peroxisome Proliferator-activated Receptor Activity [MoA]. Pristanic acid often locates in peroxisome, Body tissue, Mitochondria, Membrane of peroxisome and Organelles. The associated genes with Pristanic acid are PSG5 gene, LGALS4 gene, PEX2 gene, ACSL4 gene and ACSL1 Gene. The related lipids are pristanic acid, Fatty Acids, branched chain fatty acid, Plasmalogens and 3-hydroxypristanic acid.
Cross Reference
Introduction
To understand associated biological information of Pristanic 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.
What diseases are associated with Pristanic acid?
Pristanic acid is suspected in Peroxisomal Disorders, Refsum Disease, Protein Deficiency, Retinitis Pigmentosa, Enzyme Deficiency, Hereditary 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 Pristanic acid
PubChem Associated disorders and diseases
What pathways are associated with Pristanic acid
Lipid pathways are not clear in current pathway databases. We organized associated pathways with Pristanic acid through full-text articles, including metabolic pathways or pathways of biological mechanisms.
Related references are published most in these journals:
| Pathway name | Related literatures |
|---|
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PubChem Biomolecular Interactions and Pathways
Link to PubChem Biomolecular Interactions and PathwaysWhat cellular locations are associated with Pristanic acid?
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 Pristanic acid?
Related references are published most in these journals:
| Function | Cross reference | Weighted score | Related literatures |
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What lipids are associated with Pristanic acid?
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 Pristanic acid?
Related references are published most in these journals:
| Gene | Cross reference | Weighted score | Related literatures |
|---|
What common seen animal models are associated with Pristanic acid?
There are no associated biomedical information in the current reference collection.
NCBI Entrez Crosslinks
All references with Pristanic acid
Download all related citations| Authors | Title | Published | Journal | PubMed Link |
|---|---|---|---|---|
| Wanders RJ et al. | Clinical and biochemical characteristics of peroxisomal disorders: an update. | 1994 | Eur. J. Pediatr. | pmid:7957386 |
| ten Brink HJ et al. | Heterogeneity in di/trihydroxycholestanoic acidaemia. | 1994 | Ann. Clin. Biochem. | pmid:8060102 |
| Singh H et al. | Peroxisomal beta-oxidation of branched chain fatty acids in rat liver. Evidence that carnitine palmitoyltransferase I prevents transport of branched chain fatty acids into mitochondria. | 1994 | J. Biol. Chem. | pmid:8144536 |
| Pahan K et al. | Phytanic acid alpha-oxidation in rat liver mitochondria. | 1994 | Biochim. Biophys. Acta | pmid:7803482 |
| ten Brink HJ et al. | Diagnosis of peroxisomal disorders by analysis of phytanic and pristanic acids in stored blood spots collected at neonatal screening. | 1993 | Clin. Chem. | pmid:8375069 |
| Schmitt K et al. | [Zellweger syndrome, neonatal adrenoleukodystrophy or infantile Refsum's disease in a case with generalized peroxisome defect?]. | 1993 | Wien. Klin. Wochenschr. | pmid:7687405 |
| Singh I et al. | Refsum disease: a defect in the alpha-oxidation of phytanic acid in peroxisomes. | 1993 | J. Lipid Res. | pmid:7504046 |
| Wanders RJ et al. | Characteristics and subcellular localization of pristanoyl-CoA synthetase in rat liver. | 1992 | Biochim. Biophys. Acta | pmid:1596515 |
| ten Brink HJ et al. | Pristanic acid and phytanic acid in plasma from patients with peroxisomal disorders: stable isotope dilution analysis with electron capture negative ion mass fragmentography. | 1992 | J. Lipid Res. | pmid:1372637 |
| Chow CW et al. | Autopsy findings in two siblings with infantile Refsum disease. | 1992 | Acta Neuropathol. | pmid:1373019 |
| ten Brink HJ et al. | In vivo study of phytanic acid alpha-oxidation in classic Refsum's disease and chondrodysplasia punctata. | 1992 | Pediatr. Res. | pmid:1282700 |
| Singh I et al. | Phytanic acid alpha-oxidation in human cultured skin fibroblasts. | 1992 | Biochim. Biophys. Acta | pmid:1463774 |
| Wanders RJ et al. | Activation and oxidation of pristanic acid in rat liver: identification of a distinct, clofibrate non-inducible pristanoyl-CoA oxidase. | 1992 | Prog. Clin. Biol. Res. | pmid:1438370 |
| Wanders RJ et al. | Molecular analysis of disorders of peroxisomal beta-oxidation. | 1992 | Prog. Clin. Biol. Res. | pmid:1438395 |
| Singh H et al. | Peroxisomal beta-oxidation of branched chain fatty acids in human skin fibroblasts. | 1992 | J. Lipid Res. | pmid:1464743 |
| ten Brink HJ et al. | Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disorders. | 1992 | J. Lipid Res. | pmid:1385561 |
| ten Brink HJ et al. | Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: evidence for a distinct peroxisomal pristanyl-CoA oxidase. | 1991 | J. Inherit. Metab. Dis. | pmid:1779614 |
| Kase BF et al. | Separation of phytanic and pristanic acid by high-pressure liquid chromatography: application of the method. | 1991 | Anal. Biochem. | pmid:1888042 |
| ten Brink HJ et al. | Pristanic acid and phytanic acid in plasma from patients with a single peroxisomal enzyme deficiency. | 1991 | J. Inherit. Metab. Dis. | pmid:1722861 |
| Poulos A et al. | Defective oxidation of pristanic acid by fibroblasts from patients with disorders in propionic acid metabolism. | 1990 | Clin. Genet. | pmid:2311265 |
| Harris HM et al. | Phytanic acid, pristanic acid, and very-long-chain fatty acid methyl esters measured simultaneously by capillary gas chromatography. | 1989 | Clin. Chem. | pmid:2702761 |
| Poulos A et al. | Accumulation of pristanic acid (2, 6, 10, 14 tetramethylpentadecanoic acid) in the plasma of patients with generalised peroxisomal dysfunction. | 1988 | Eur. J. Pediatr. | pmid:2452737 |
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