oleic acid has been researched along with Lipid Metabolism, Inborn Error in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (44.44) | 18.7374 |
| 1990's | 4 (44.44) | 18.2507 |
| 2000's | 1 (11.11) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Coleman, RA; Igal, RA | 2 |
| Bonham, JR; Clark, S; Downing, M; Manning, NJ; Olpin, SE; Pollitt, RJ | 1 |
| Roe, CR; Roe, DS; Sharma, S; Vianey-Saban, C; Zabot, MT | 1 |
| Coleman, RA; Grunfeld, C; Placezk, D; Williams, ML | 1 |
| Billaudel, S; De Lisle, B; Douste-Blazy, L; Maret, A; Mussini, JM; Negre, A; Radom, J; Salvayre, R | 1 |
| Douste-Blazy, L; Maret, A; Negre, A; Radom, J; Salvayre, R | 1 |
| Slotte, JP | 1 |
| Brady, RO; Patel, SC; Pentchev, PG; Suresh, S; Weintroub, H | 1 |
9 other study(ies) available for oleic acid and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
Acylglycerol recycling from triacylglycerol to phospholipid, not lipase activity, is defective in neutral lipid storage disease fibroblasts.
Topics: Acylation; Carbon Radioisotopes; Cells, Cultured; Fibroblasts; Glycerides; Humans; Hydrolysis; Lipase; Lipid Metabolism, Inborn Errors; Oleic Acid; Oleic Acids; Phospholipids; Triazenes; Triglycerides | 1996 |
Neutral lipid storage disease: a genetic disorder with abnormalities in the regulation of phospholipid metabolism.
Topics: Cells, Cultured; Choline; Cytidine Diphosphate; Cytidine Diphosphate Choline; Diglycerides; Ethanolamine; Ethanolamines; Fibroblasts; Glycerol; Homeostasis; Humans; Lipid Metabolism, Inborn Errors; Oleic Acid; Phosphatidylcholines; Phosphatidylinositols; Phosphatidylserines; Phospholipids; Sphingomyelins; Triglycerides | 1998 |
The use of [9,10-3H]myristate, [9,10-3H]palmitate and [9,10-3H]oleate for the detection and diagnosis of medium and long-chain fatty acid oxidation disorders in intact cultured fibroblasts.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Cells, Cultured; Fatty Acid Desaturases; Fibroblasts; Humans; Lipid Metabolism, Inborn Errors; Myristic Acid; Oleic Acid; Palmitic Acid; Tritium | 1999 |
Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Acyl-CoA Dehydrogenases; Adult; Carnitine; Case-Control Studies; Cells, Cultured; Child; Child, Preschool; Fatty Acids, Unsaturated; Female; Fibroblasts; Humans; Infant, Newborn; Isomerism; Lipid Metabolism, Inborn Errors; Oleic Acid; Oleic Acids; Oxidation-Reduction; Substrate Specificity | 2001 |
Neutral lipid storage disease: a possible functional defect in phospholipid- linked triacylglycerol metabolism.
Topics: Acetates; Cells, Cultured; Genes, Recessive; Glycolipids; Humans; In Vitro Techniques; Lipase; Lipid Metabolism, Inborn Errors; Male; Oleic Acid; Oleic Acids; Phospholipids; Plasmalogens; Triglycerides | 1991 |
Biochemical and ultrastructural features of human fibroblasts cultured from a new variant of type 3 lipid storage myopathy.
Topics: Autoradiography; Cells, Cultured; Cholesterol; Fibroblasts; Humans; Kinetics; Lipid Metabolism, Inborn Errors; Lipids; Microscopy, Electron; Microscopy, Fluorescence; Muscular Diseases; Oleic Acid; Oleic Acids; Phospholipids; Skin; Triglycerides; Vacuoles | 1988 |
Extracellular origin of the lipid lysosomal storage in cultured fibroblasts from Wolman's disease.
Topics: Cells, Cultured; Fibroblasts; Humans; Kinetics; Lipase; Lipid Metabolism; Lipid Metabolism, Inborn Errors; Oleic Acid; Oleic Acids; Reference Values; Skin; Tritium | 1987 |
Intracellular processing of exogenously derived non-lipoprotein [3H]cholesterol in normal and mutant human skin fibroblasts deficient in acid sterol ester hydrolase.
Topics: Amides; Carboxylic Ester Hydrolases; Cell-Free System; Cells, Cultured; Cholesterol; Cholesterol Esters; Fibroblasts; Humans; Lipid Metabolism, Inborn Errors; Mutation; Oleic Acid; Oleic Acids; Organosilicon Compounds; Sterol Esterase; Sterol O-Acyltransferase | 1987 |
Impaired cholesterol esterification in primary brain cultures of the lysosomal cholesterol storage disorder (LCSD) mouse mutant.
Topics: Animals; Brain; Cells, Cultured; Cholesterol; Cholesterol Esters; Female; Homozygote; Lipid Metabolism, Inborn Errors; Lysosomes; Male; Mice; Mice, Mutant Strains; Mutation; Oleic Acid; Oleic Acids; Triolein; Tritium | 1987 |