L-octanoylcarnitine is a lipid of Fatty Acyls (FA) class.
We collected disease MeSH terms mapped to the references associated with L-octanoylcarnitine
| MeSH term | MeSH ID | Detail |
|---|---|---|
| Lipid Metabolism, Inborn Errors | D008052 | 26 associated lipids |
| Metabolic Diseases | D008659 | 12 associated lipids |
| Starvation | D013217 | 47 associated lipids |
| Ventricular Dysfunction, Left | D018487 | 33 associated lipids |
| Insulin Resistance | D007333 | 99 associated lipids |
| Thinness | D013851 | 11 associated lipids |
| Heart Failure, Systolic | D054143 | 3 associated lipids |
| Authors | Title | Published | Journal | PubMed Link |
|---|---|---|---|---|
| Millington DS et al. | Valproylcarnitine: a novel drug metabolite identified by fast atom bombardment and thermospray liquid chromatography-mass spectrometry. | 1985 | Clin. Chim. Acta | pmid:3919970 |
| Roe CR et al. | Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes. | 1986 | J. Pediatr. | pmid:3944676 |
| Roe CR et al. | Diagnostic and therapeutic implications of medium-chain acylcarnitines in the medium-chain acyl-coA dehydrogenase deficiency. | 1985 | Pediatr. Res. | pmid:4000772 |
| Duran M et al. | Octanoylglucuronide excretion in patients with a defective oxidation of medium-chain fatty acids. | 1985 | Clin. Chim. Acta | pmid:4064333 |
| Chalmers RA et al. | Urinary excretion of l-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency of l-carnitine. | 1984 | Pediatr. Res. | pmid:6441143 |
| Kim CS et al. | L-carnitine: therapeutic strategy for metabolic encephalopathy. | 1984 | Brain Res. | pmid:6478235 |
| Nakatani T et al. | Effects of (+)-octanoylcarnitine on deoxyribonucleic acid synthesis in regenerating rabbit liver. | 1982 | Clin. Sci. | pmid:7060336 |
| Nakatani T et al. | Changes in predominant energy substrate after hepatectomy. | 1981 | Life Sci. | pmid:7219046 |
| Parameswaran M and Arinze IJ | Phosphoenolpyruvate synthesis by fetal guinea-pig liver mitochondria. | 1981 | Biochim. Biophys. Acta | pmid:7225415 |
| Nakatani T et al. | Differences in predominant energy substrate in relation to the resected hepatic mass in the phase immediately after hepatectomy. | 1981 | J. Lab. Clin. Med. | pmid:7229515 |
| Davis-van Thienen W and Davis EJ | The effects of energetic steady state, pyruvate concentration, and octanoyl-(--)-carnitine on the relative rates of carboxylation and decarboxylation of pyruvate by rat liver mitochondria. | 1981 | J. Biol. Chem. | pmid:7263658 |
| Jones CT | Is there a gloxylate cycle in the liver of the fetal guinea pig? | 1980 | Biochem. Biophys. Res. Commun. | pmid:7417292 |
| Zammit VA | The effect of glucagon treatment and starvation of virgin and lactating rats on the rates of oxidation of octanoyl-L-carnitine and octanoate by isolated liver mitochondria. | 1980 | Biochem. J. | pmid:7470052 |
| Ziadeh R et al. | Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies. | 1995 | Pediatr. Res. | pmid:7603790 |
| Minkler PE and Hoppel CL | Quantification of free carnitine, individual short- and medium-chain acylcarnitines, and total carnitine in plasma by high-performance liquid chromatography. | 1993 | Anal. Biochem. | pmid:8214594 |
| Van Hove JL et al. | Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood. | 1993 | Am. J. Hum. Genet. | pmid:8488845 |
| Schmidt-Sommerfeld E et al. | Detection of inborn errors of fatty acid oxidation from acylcarnitine analysis of plasma and blood spots with the radioisotopic exchange-high-performance liquid chromatographic method. | 1993 | J. Pediatr. | pmid:8496747 |
| Zangar RC and Novak RF | Effects of fatty acids and ketone bodies on cytochromes P450 2B, 4A, and 2E1 expression in primary cultured rat hepatocytes. | 1997 | Arch. Biochem. Biophys. | pmid:9016816 |
| Chace DH et al. | Rapid diagnosis of MCAD deficiency: quantitative analysis of octanoylcarnitine and other acylcarnitines in newborn blood spots by tandem mass spectrometry. | 1997 | Clin. Chem. | pmid:9365395 |
| Clayton PT et al. | Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry. | 1998 | Arch. Dis. Child. | pmid:9797589 |